Kay Elizabeth Davies - Publications

University of Oxford, Oxford, United Kingdom 
Muscular Dystrophy, Ataxia

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Year Citation  Score
2020 Chatzopoulou M, Emer E, Lecci C, Rowley JA, Casagrande AS, Moir L, Squire SE, Davies SG, Harriman S, Wynne GM, Wilson FX, Davies KE, Russell AJ. Decreasing HepG2 Cytotoxicity by Lowering the Lipophilicity of Benzo[d]oxazolephosphinate Ester Utrophin Modulators. Acs Medicinal Chemistry Letters. 11: 2421-2427. PMID 33335663 DOI: 10.1021/acsmedchemlett.0c00405  0.48
2020 Lovering RM, Iyer SR, Edwards B, Davies KE. Alterations of neuromuscular junctions in Duchenne muscular dystrophy. Neuroscience Letters. 135304. PMID 32818587 DOI: 10.1016/j.neulet.2020.135304  1
2020 Babbs A, Berg A, Chatzopoulou M, Davies KE, Davies SG, Edwards B, Elsey DJ, Emer E, Figuccia ALA, Fletcher AM, Guiraud S, Harriman S, Moir L, Robinson N, Rowley JA, et al. Synthesis of SMT022357 enantiomers and evaluation in a Duchenne muscular dystrophy mouse model. Tetrahedron. 76: 130819. PMID 32713969 DOI: 10.1016/j.tet.2019.130819  1
2020 Babbs A, Berg A, Chatzopoulou M, Davies KE, Davies SG, Edwards B, Elsey D, Emer E, Guiraud S, Harriman S, Lecci C, Moir L, Peters D, Robinson N, Rowley J, et al. 2-Arylbenzo[d]oxazole phosphinate esters as second-generation modulators of utrophin for the treatment of Duchenne Muscular Dystrophy. Journal of Medicinal Chemistry. PMID 32551645 DOI: 10.1021/acs.jmedchem.0c00807  1
2019 Wilkinson IVL, Perkins KJ, Dugdale H, Moir L, Vuorinen A, Chatzopoulou M, Squire SE, Monecke S, Lomow A, Geese M, Charles PD, Burch P, Tinsley JM, Wynne GM, Davies SG, ... ... Davies KE, et al. Chemical Proteomics and Phenotypic Profiling Identifies the Aryl Hydrocarbon Receptor as a Molecular Target of the Utrophin Modulator Ezutromid. Angewandte Chemie (International Ed. in English). PMID 31755636 DOI: 10.1002/anie.201912392  0.48
2019 Williamson MG, Finelli MJ, Sleigh JN, Reddington A, Gordon D, Talbot K, Davies KE, Oliver PL. Neuronal over-expression of Oxr1 is protective against ALS-associated mutant TDP-43 mislocalisation in motor neurons and neuromuscular defects in vivo. Human Molecular Genetics. PMID 31642482 DOI: 10.1093/hmg/ddz190  1
2019 Pomatto LCD, Sun PY, Yu K, Gullapalli S, Bwiza CP, Sisliyan C, Wong S, Zhang H, Forman HJ, Oliver PL, Davies KE, Davies KJA. Limitations to adaptive homeostasis in an hyperoxia-induced model of accelerated ageing. Redox Biology. 24: 101194. PMID 31022673 DOI: 10.1016/j.redox.2019.101194  1
2019 Guiraud S, Edwards B, Babbs A, Squire SE, Berg A, Moir L, Wood MJ, Davies KE. The potential of utrophin and dystrophin combination therapies for Duchenne muscular dystrophy. Human Molecular Genetics. PMID 30990876 DOI: 10.1093/hmg/ddz049  1
2019 Guiraud S, Davies KE. Regenerative biomarkers for Duchenne muscular dystrophy. Neural Regeneration Research. 14: 1317-1320. PMID 30964048 DOI: 10.4103/1673-5374.253534  0.56
2019 Davies KE, Guiraud S. Micro-dystrophin Genes Bring Hope of an Effective Therapy for Duchenne Muscular Dystrophy. Molecular Therapy : the Journal of the American Society of Gene Therapy. 27: 486-488. PMID 30765324 DOI: 10.1016/j.ymthe.2019.01.019  0.56
2019 Muntoni F, Tejura B, Spinty S, Roper H, Hughes I, Layton G, Davies KE, Harriman S, Tinsley J. A Phase 1b Trial to Assess the Pharmacokinetics of Ezutromid in Pediatric Duchenne Muscular Dystrophy Patients on a Balanced Diet. Clinical Pharmacology in Drug Development. PMID 30650257 DOI: 10.1002/cpdd.642  0.32
2018 Kennedy TL, Guiraud S, Edwards B, Squire S, Moir L, Babbs A, Odom G, Golebiowski D, Schneider J, Chamberlain JS, Davies KE. Micro-utrophin Improves Cardiac and Skeletal Muscle Function of Severely Affected D2/ Mice. Molecular Therapy. Methods & Clinical Development. 11: 92-105. PMID 30417024 DOI: 10.1016/j.omtm.2018.10.005  1
2018 Guiraud S, Edwards B, Squire SE, Moir L, Berg A, Babbs A, Ramadan N, Wood MJ, Davies KE. Embryonic myosin is a regeneration marker to monitor utrophin based therapies for DMD. Human Molecular Genetics. PMID 30304405 DOI: 10.1093/hmg/ddy353  1
2018 Ang G, McKillop LE, Purple R, Blanco-Duque C, Peirson SN, Foster RG, Harrison PJ, Sprengel R, Davies KE, Oliver PL, Bannerman DM, Vyazovskiy VV. Absent sleep EEG spindle activity in GluA1 (Gria1) knockout mice: relevance to neuropsychiatric disorders. Translational Psychiatry. 8: 154. PMID 30108203 DOI: 10.1038/s41398-018-0199-2  1
2018 Perkins KJ, Davies KE. Alternative utrophin mRNAs contribute to phenotypic differences between dystrophin-deficient mice and Duchenne muscular dystrophy. Febs Letters. PMID 29772070 DOI: 10.1002/1873-3468.13099  0.44
2017 Kennedy TL, Moir L, Hemming S, Edwards B, Squire S, Davies K, Guiraud S. Utrophin influences mitochondrial pathology and oxidative stress in dystrophic muscle. Skeletal Muscle. 7: 22. PMID 29065908 DOI: 10.1186/s13395-017-0139-5  1
2017 Guiraud S, Davies KE. Pharmacological advances for treatment in Duchenne muscular dystrophy. Current Opinion in Pharmacology. 34: 36-48. PMID 28486179 DOI: 10.1016/j.coph.2017.04.002  0.56
2017 Guiraud S, Edwards B, Squire SE, Babbs A, Shah N, Berg A, Chen H, Davies KE. Identification of serum protein biomarkers for utrophin based DMD therapy. Scientific Reports. 7: 43697. PMID 28252048 DOI: 10.1016/j.nmd.2017.06.269  1
2016 Wu Y, Davies KE, Oliver PL. The antioxidant protein Oxr1 influences aspects of mitochondrial morphology. Free Radical Biology & Medicine. PMID 27036366 DOI: 10.1016/j.freeradbiomed.2016.03.029  1
2016 Janghra N, Morgan JE, Sewry CA, Wilson FX, Davies KE, Muntoni F, Tinsley J. Correlation of Utrophin Levels with the Dystrophin Protein Complex and Muscle Fibre Regeneration in Duchenne and Becker Muscular Dystrophy Muscle Biopsies. Plos One. 11: e0150818. PMID 26974331 DOI: 10.1371/journal.pone.0150818  0.32
2015 Finelli MJ, Sanchez-Pulido L, Liu KX, Davies KE, Oliver PL. The evolutionarily conserved Tre2/Bub2/Cdc16 (TBC), Lysin motif (LysM), Domain catalytic (TLDc) domain is neuroprotective against oxidative stress. The Journal of Biological Chemistry. PMID 26668325 DOI: 10.1074/jbc.M115.685222  1
2015 Pembroke WG, Babbs A, Davies K, Ponting CP, Oliver PL. Temporal transcriptomics suggest that twin-peaking genes reset the clock. Elife. 4. PMID 26523393 DOI: 10.7554/eLife.10518  1
2015 Richardson K, Livieratos A, Dumbill R, Hughes S, Ang G, Smith DA, Morris L, Brown LA, Peirson SN, Platt FM, Davies KE, Oliver PL. Circadian profiling in two mouse models of lysosomal storage disorders; Niemann Pick type-C and Sandhoff disease. Behavioural Brain Research. 297: 213-223. PMID 26467605 DOI: 10.1016/j.bbr.2015.10.021  1
2015 Guiraud S, Chen H, Burns DT, Davies KE. Advances in genetic therapeutic strategies for Duchenne muscular dystrophy. Experimental Physiology. PMID 26140505 DOI: 10.1113/EP085308  1
2015 Guiraud S, Aartsma-Rus A, Vieira NM, Davies KE, van Ommen GJ, Kunkel LM. The Pathogenesis and Therapy of Muscular Dystrophies. Annual Review of Genomics and Human Genetics. PMID 26048046 DOI: 10.1146/annurev-genom-090314-025003  1
2015 Davies K. Keep the directive that protects research animals. Nature. 521: 7. PMID 25951248 DOI: 10.1038/521007a  1
2015 Guiraud S, Squire SE, Edwards B, Chen H, Burns DT, Shah N, Babbs A, Davies SG, Wynne GM, Russell AJ, Elsey D, Wilson FX, Tinsley JM, Davies KE. Second-generation compound for the modulation of utrophin in the therapy of DMD. Human Molecular Genetics. 24: 4212-24. PMID 25935002 DOI: 10.1093/hmg/ddv154  1
2015 Dulneva A, Lee S, Oliver PL, Di Gleria K, Kessler BM, Davies KE, Becker EB. The mutant Moonwalker TRPC3 channel links calcium signaling to lipid metabolism in the developing cerebellum. Human Molecular Genetics. 24: 4114-25. PMID 25908616 DOI: 10.1093/hmg/ddv150  1
2015 Finelli MJ, Liu KX, Wu Y, Oliver PL, Davies KE. Oxr1 improves pathogenic cellular features of ALS-associated FUS and TDP-43 mutations. Human Molecular Genetics. 24: 3529-44. PMID 25792726 DOI: 10.1093/hmg/ddv104  1
2015 Liu KX, Edwards B, Lee S, Finelli MJ, Davies B, Davies KE, Oliver PL. Neuron-specific antioxidant OXR1 extends survival of a mouse model of amyotrophic lateral sclerosis. Brain : a Journal of Neurology. 138: 1167-81. PMID 25753484 DOI: 10.1093/brain/awv039  1
2015 Tan SC, Gomes RS, Yeoh KK, Perbellini F, Malandraki-Miller S, Ambrose L, Heather LC, Faggian G, Schofield CJ, Davies KE, Clarke K, Carr CA. Preconditioning of cardiosphere-derived cells with hypoxia or prolyl-4-hydroxylase inhibitors increases stemness and decreases reliance on oxidative metabolism. Cell Transplantation. PMID 25751158 DOI: 10.3727/096368915X687697  1
2015 Tinsley J, Robinson N, Davies KE. Safety, tolerability, and pharmacokinetics of SMT C1100, a 2-arylbenzoxazole utrophin modulator, following single- and multiple-dose administration to healthy male adult volunteers. Journal of Clinical Pharmacology. 55: 698-707. PMID 25651188 DOI: 10.1002/jcph.468  1
2015 Goyenvalle A, Griffith G, Babbs A, El Andaloussi S, Ezzat K, Avril A, Dugovic B, Chaussenot R, Ferry A, Voit T, Amthor H, Bühr C, Schürch S, Wood MJ, Davies KE, et al. Functional correction in mouse models of muscular dystrophy using exon-skipping tricyclo-DNA oligomers. Nature Medicine. 21: 270-5. PMID 25642938 DOI: 10.1038/nm.3765  1
2015 Davies K. Interview with Professor Kay Davies Future Neurology. 10: 305-307. DOI: 10.2217/fnl.15.24  1
2014 Moore JM, Oliver PL, Finelli MJ, Lee S, Lickiss T, Molnár Z, Davies KE. Laf4/Aff3, a gene involved in intellectual disability, is required for cellular migration in the mouse cerebral cortex. Plos One. 9: e105933. PMID 25162227 DOI: 10.1371/journal.pone.0105933  1
2014 Paton L, Bitoun E, Kenyon J, Priestman DA, Oliver PL, Edwards B, Platt FM, Davies KE. A novel mouse model of a patient mucolipidosis II mutation recapitulates disease pathology. The Journal of Biological Chemistry. 289: 26709-21. PMID 25107912 DOI: 10.1074/jbc.M114.586156  1
2014 Turner BJ, Alfazema N, Sheean RK, Sleigh JN, Davies KE, Horne MK, Talbot K. Overexpression of survival motor neuron improves neuromuscular function and motor neuron survival in mutant SOD1 mice. Neurobiology of Aging. 35: 906-15. PMID 24210254 DOI: 10.1016/j.neurobiolaging.2013.09.030  1
2014 Taylor TN, Potgieter D, Anwar S, Senior SL, Janezic S, Threlfell S, Ryan B, Parkkinen L, Deltheil T, Cioroch M, Livieratos A, Oliver PL, Jennings KA, Davies KE, Ansorge O, et al. Region-specific deficits in dopamine, but not norepinephrine, signaling in a novel A30P α-synuclein BAC transgenic mouse. Neurobiology of Disease. 62: 193-207. PMID 24121116 DOI: 10.1016/j.nbd.2013.10.005  1
2014 Sleigh JN, Barreiro-Iglesias A, Oliver PL, Biba A, Becker T, Davies KE, Becker CG, Talbot K. Chondrolectin affects cell survival and neuronal outgrowth in in vitro and in vivo models of spinal muscular atrophy. Human Molecular Genetics. 23: 855-69. PMID 24067532 DOI: 10.1093/hmg/ddt477  1
2014 Van Rossen E, Liu Z, Blijweert D, Eysackers N, Mannaerts I, Schroyen B, El Taghdouini A, Edwards B, Davies KE, Sokal E, Najimi M, Reynaert H, van Grunsven LA. Syncoilin is an intermediate filament protein in activated hepatic stellate cells. Histochemistry and Cell Biology. 141: 85-99. PMID 24043511 DOI: 10.1007/s00418-013-1142-5  1
2013 Davies K. The era of genomic medicine. Clinical Medicine (London, England). 13: 594-601. PMID 24298109 DOI: 10.7861/clinmedicine.13-6-594  1
2013 Le Hir M, Goyenvalle A, Peccate C, Précigout G, Davies KE, Voit T, Garcia L, Lorain S. AAV genome loss from dystrophic mouse muscles during AAV-U7 snRNA-mediated exon-skipping therapy. Molecular Therapy : the Journal of the American Society of Gene Therapy. 21: 1551-8. PMID 23752313 DOI: 10.1038/mt.2013.121  1
2013 Ravenscroft G, McNamara E, Griffiths LM, Papadimitriou JM, Hardeman EC, Bakker AJ, Davies KE, Laing NG, Nowak KJ. Cardiac α-actin over-expression therapy in dominant ACTA1 disease. Human Molecular Genetics. 22: 3987-97. PMID 23736297 DOI: 10.1093/hmg/ddt252  1
2013 Fairclough RJ, Wood MJ, Davies KE. Therapy for Duchenne muscular dystrophy: renewed optimism from genetic approaches. Nature Reviews. Genetics. 14: 373-8. PMID 23609411 DOI: 10.1038/nrg3460  1
2013 Sleigh JN, Grice SJ, Davies KE, Talbot K. Spinal muscular atrophy at the crossroads of basic science and therapy. Neuromuscular Disorders : Nmd. 23: 96. PMID 22981697 DOI: 10.1016/j.nmd.2012.08.008  1
2012 Perkins KJ, Davies KE. Recent advances in Duchenne muscular dystrophy. Degenerative Neurological and Neuromuscular Disease. 2: 141-164. PMID 30890885 DOI: 10.2147/DNND.S26637  0.44
2012 Eckenfelder A, Tordo J, Babbs A, Davies KE, Goyenvalle A, Danos O. The Cellular Processing Capacity Limits the Amounts of Chimeric U7 snRNA Available for Antisense Delivery. Molecular Therapy. Nucleic Acids. 1: e31. PMID 23344083 DOI: 10.1038/mtna.2012.24  1
2012 Oliver PL, Davies KE. New insights into behaviour using mouse ENU mutagenesis. Human Molecular Genetics. 21: R72-81. PMID 22892373 DOI: 10.1093/hmg/dds318  1
2012 Fairclough RJ, Perkins KJ, Davies KE. Pharmacologically targeting the primary defect and downstream pathology in Duchenne muscular dystrophy. Current Gene Therapy. 12: 206-44. PMID 22571500 DOI: 10.2174/156652312800840595  1
2012 Pritchett D, Wulff K, Oliver PL, Bannerman DM, Davies KE, Harrison PJ, Peirson SN, Foster RG. Evaluating the links between schizophrenia and sleep and circadian rhythm disruption. Journal of Neural Transmission (Vienna, Austria : 1996). 119: 1061-75. PMID 22569850 DOI: 10.1007/s00702-012-0817-8  1
2012 Gehrig SM, van der Poel C, Sayer TA, Schertzer JD, Henstridge DC, Church JE, Lamon S, Russell AP, Davies KE, Febbraio MA, Lynch GS. Hsp72 preserves muscle function and slows progression of severe muscular dystrophy. Nature. 484: 394-8. PMID 22495301 DOI: 10.1038/nature10980  1
2012 Goyenvalle A, Babbs A, Wright J, Wilkins V, Powell D, Garcia L, Davies KE. Rescue of severely affected dystrophin/utrophin-deficient mice through scAAV-U7snRNA-mediated exon skipping. Human Molecular Genetics. 21: 2559-71. PMID 22388933 DOI: 10.1093/hmg/dds082  1
2012 Goyenvalle A, Wright J, Babbs A, Wilkins V, Garcia L, Davies KE. Engineering multiple U7snRNA constructs to induce single and multiexon-skipping for Duchenne muscular dystrophy. Molecular Therapy : the Journal of the American Society of Gene Therapy. 20: 1212-21. PMID 22354379 DOI: 10.1038/mt.2012.26  1
2012 Oliver PL, Sobczyk MV, Maywood ES, Edwards B, Lee S, Livieratos A, Oster H, Butler R, Godinho SI, Wulff K, Peirson SN, Fisher SP, Chesham JE, Smith JW, Hastings MH, ... Davies KE, et al. Disrupted circadian rhythms in a mouse model of schizophrenia. Current Biology : Cb. 22: 314-9. PMID 22264613 DOI: 10.1016/j.cub.2011.12.051  1
2012 Stuckey DJ, Carr CA, Camelliti P, Tyler DJ, Davies KE, Clarke K. In vivo MRI characterization of progressive cardiac dysfunction in the mdx mouse model of muscular dystrophy. Plos One. 7: e28569. PMID 22235247 DOI: 10.1371/journal.pone.0028569  1
2012 Tan SC, Carr CA, Yeoh KK, Schofield CJ, Davies KE, Clarke K. Identification of valid housekeeping genes for quantitative RT-PCR analysis of cardiosphere-derived cells preconditioned under hypoxia or with prolyl-4-hydroxylase inhibitors. Molecular Biology Reports. 39: 4857-67. PMID 22065248 DOI: 10.1007/s11033-011-1281-5  1
2011 Ravenscroft G, Jackaman C, Sewry CA, McNamara E, Squire SE, Potter AC, Papadimitriou J, Griffiths LM, Bakker AJ, Davies KE, Laing NG, Nowak KJ. Actin nemaline myopathy mouse reproduces disease, suggests other actin disease phenotypes and provides cautionary note on muscle transgene expression. Plos One. 6: e28699. PMID 22174871 DOI: 10.1371/journal.pone.0028699  1
2011 Oliver PL, Finelli MJ, Edwards B, Bitoun E, Butts DL, Becker EB, Cheeseman MT, Davies B, Davies KE. Oxr1 is essential for protection against oxidative stress-induced neurodegeneration. Plos Genetics. 7: e1002338. PMID 22028674 DOI: 10.1371/journal.pgen.1002338  1
2011 Fairclough RJ, Bareja A, Davies KE. Progress in therapy for Duchenne muscular dystrophy. Experimental Physiology. 96: 1101-13. PMID 21804140 DOI: 10.1113/expphysiol.2010.053025  1
2011 Goyenvalle A, Davies KE. Challenges to oligonucleotides-based therapeutics for Duchenne muscular dystrophy. Skeletal Muscle. 1: 8. PMID 21798085 DOI: 10.1186/2044-5040-1-8  1
2011 Vernes SC, Oliver PL, Spiteri E, Lockstone HE, Puliyadi R, Taylor JM, Ho J, Mombereau C, Brewer A, Lowy E, Nicod J, Groszer M, Baban D, Sahgal N, Cazier JB, ... ... Davies KE, et al. Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain. Plos Genetics. 7: e1002145. PMID 21765815 DOI: 10.1371/journal.pgen.1002145  1
2011 Tinsley JM, Fairclough RJ, Storer R, Wilkes FJ, Potter AC, Squire SE, Powell DS, Cozzoli A, Capogrosso RF, Lambert A, Wilson FX, Wren SP, De Luca A, Davies KE. Daily treatment with SMTC1100, a novel small molecule utrophin upregulator, dramatically reduces the dystrophic symptoms in the mdx mouse. Plos One. 6: e19189. PMID 21573153 DOI: 10.1371/journal.pone.0019189  1
2011 Pichavant C, Aartsma-Rus A, Clemens PR, Davies KE, Dickson G, Takeda S, Wilton SD, Wolff JA, Wooddell CI, Xiao X, Tremblay JP. Current status of pharmaceutical and genetic therapeutic approaches to treat DMD. Molecular Therapy : the Journal of the American Society of Gene Therapy. 19: 830-40. PMID 21468001 DOI: 10.1038/mt.2011.59  1
2011 Chancellor DR, Davies KE, De Moor O, Dorgan CR, Johnson PD, Lambert AG, Lawrence D, Lecci C, Maillol C, Middleton PJ, Nugent G, Poignant SD, Potter AC, Price PD, Pye RJ, et al. Discovery of 2-arylbenzoxazoles as upregulators of utrophin production for the treatment of Duchenne muscular dystrophy. Journal of Medicinal Chemistry. 54: 3241-50. PMID 21456623 DOI: 10.1021/jm200135z  1
2011 Goyenvalle A, Seto JT, Davies KE, Chamberlain J. Therapeutic approaches to muscular dystrophy. Human Molecular Genetics. 20: R69-78. PMID 21436158 DOI: 10.1093/hmg/ddr105  1
2011 Becker EB, Fogel BL, Rajakulendran S, Dulneva A, Hanna MG, Perlman SL, Geschwind DH, Davies KE. Candidate screening of the TRPC3 gene in cerebellar ataxia. Cerebellum (London, England). 10: 296-9. PMID 21321808 DOI: 10.1007/s12311-011-0253-6  1
2011 Ravenscroft G, Jackaman C, Bringans S, Papadimitriou JM, Griffiths LM, McNamara E, Bakker AJ, Davies KE, Laing NG, Nowak KJ. Mouse models of dominant ACTA1 disease recapitulate human disease and provide insight into therapies. Brain : a Journal of Neurology. 134: 1101-15. PMID 21303860 DOI: 10.1093/brain/awr004  1
2011 Goyenvalle A, Davies KE. Engineering exon-skipping vectors expressing U7 snRNA constructs for Duchenne muscular dystrophy gene therapy. Methods in Molecular Biology (Clifton, N.J.). 709: 179-96. PMID 21194028 DOI: 10.1007/978-1-61737-982-6_11  1
2011 Crisp A, Yin H, Goyenvalle A, Betts C, Moulton HM, Seow Y, Babbs A, Merritt T, Saleh AF, Gait MJ, Stuckey DJ, Clarke K, Davies KE, Wood MJ. Diaphragm rescue alone prevents heart dysfunction in dystrophic mice. Human Molecular Genetics. 20: 413-21. PMID 21062902 DOI: 10.1093/hmg/ddq477  1
2010 Chodroff RA, Goodstadt L, Sirey TM, Oliver PL, Davies KE, Green ED, Molnár Z, Ponting CP. Long noncoding RNA genes: conservation of sequence and brain expression among diverse amniotes. Genome Biology. 11: R72. PMID 20624288 DOI: 10.1186/gb-2010-11-7-r72  1
2010 Danos O, Davies K, Lehn P, Mulligan R. The ARRIVE guidelines, a welcome improvement to standards for reporting animal research. The Journal of Gene Medicine. 12: 559-60. PMID 20603891 DOI: 10.1002/jgm.1472  1
2010 Clarke WT, Edwards B, McCullagh KJ, Kemp MW, Moorwood C, Sherman DL, Burgess M, Davies KE. Syncoilin modulates peripherin filament networks and is necessary for large-calibre motor neurons. Journal of Cell Science. 123: 2543-52. PMID 20587592 DOI: 10.1242/jcs.059113  1
2010 Li D, Bareja A, Judge L, Yue Y, Lai Y, Fairclough R, Davies KE, Chamberlain JS, Duan D. Sarcolemmal nNOS anchoring reveals a qualitative difference between dystrophin and utrophin. Journal of Cell Science. 123: 2008-13. PMID 20483958 DOI: 10.1242/jcs.064808  1
2010 Turner BJ, Ackerley S, Davies KE, Talbot K. Dismutase-competent SOD1 mutant accumulation in myelinating Schwann cells is not detrimental to normal or transgenic ALS model mice. Human Molecular Genetics. 19: 815-24. PMID 20008901 DOI: 10.1093/hmg/ddp550  1
2010 Goyenvalle A, Babbs A, Powell D, Kole R, Fletcher S, Wilton SD, Davies KE. Prevention of dystrophic pathology in severely affected dystrophin/utrophin-deficient mice by morpholino-oligomer-mediated exon-skipping. Molecular Therapy : the Journal of the American Society of Gene Therapy. 18: 198-205. PMID 19844193 DOI: 10.1038/mt.2009.248  1
2009 Goyenvalle A, Babbs A, van Ommen GB, Garcia L, Davies KE. Enhanced Exon-skipping Induced by U7 snRNA Carrying a Splicing Silencer Sequence: Promising Tool for DMD Therapy. Molecular Therapy : the Journal of the American Society of Gene Therapy. 17: 1234-1240. PMID 28178473 DOI: 10.1038/mt.2009.113  0.48
2009 Bäumer D, Lee S, Nicholson G, Davies JL, Parkinson NJ, Murray LM, Gillingwater TH, Ansorge O, Davies KE, Talbot K. Alternative splicing events are a late feature of pathology in a mouse model of spinal muscular atrophy. Plos Genetics. 5: e1000773. PMID 20019802 DOI: 10.1371/journal.pgen.1000773  1
2009 Bitoun E, Finelli MJ, Oliver PL, Lee S, Davies KE. AF4 is a critical regulator of the IGF-1 signaling pathway during Purkinje cell development. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 15366-74. PMID 20007461 DOI: 10.1523/JNEUROSCI.5188-09.2009  1
2009 Oliver PL, Davies KE. Interaction between environmental and genetic factors modulates schizophrenic endophenotypes in the Snap-25 mouse mutant blind-drunk. Human Molecular Genetics. 18: 4576-89. PMID 19729413 DOI: 10.1093/hmg/ddp425  1
2009 Davies K, Wynshaw-Boris A. Human genetics: conceptual and practical advances in the post-genome era Current Opinion in Genetics and Development. 19: 193-195. PMID 19481439 DOI: 10.1016/j.gde.2009.05.002  1
2009 Nowak KJ, Ravenscroft G, Jackaman C, Filipovska A, Davies SM, Lim EM, Squire SE, Potter AC, Baker E, Clément S, Sewry CA, Fabian V, Crawford K, Lessard JL, Griffiths LM, ... ... Davies KE, et al. Rescue of skeletal muscle alpha-actin-null mice by cardiac (fetal) alpha-actin. The Journal of Cell Biology. 185: 903-15. PMID 19468071 DOI: 10.1083/jcb.200812132  1
2009 Goyenvalle A, Babbs A, van Ommen GJ, Garcia L, Davies KE. Enhanced exon-skipping induced by U7 snRNA carrying a splicing silencer sequence: Promising tool for DMD therapy. Molecular Therapy : the Journal of the American Society of Gene Therapy. 17: 1234-40. PMID 19455105 DOI: 10.1038/mt.2009.113  1
2009 Becker EB, Oliver PL, Glitsch MD, Banks GT, Achilli F, Hardy A, Nolan PM, Fisher EM, Davies KE. A point mutation in TRPC3 causes abnormal Purkinje cell development and cerebellar ataxia in moonwalker mice. Proceedings of the National Academy of Sciences of the United States of America. 106: 6706-11. PMID 19351902 DOI: 10.1073/pnas.0810599106  1
2009 Bitoun E, Davies KE. The robotic mouse: understanding the role of AF4, a cofactor of transcriptional elongation and chromatin remodelling, in purkinje cell function. Cerebellum (London, England). 8: 175-83. PMID 19340490 DOI: 10.1007/s12311-009-0101-0  1
2009 Turner BJ, Parkinson NJ, Davies KE, Talbot K. Survival motor neuron deficiency enhances progression in an amyotrophic lateral sclerosis mouse model. Neurobiology of Disease. 34: 511-7. PMID 19332122 DOI: 10.1016/j.nbd.2009.03.005  1
2009 Court FA, Hewitt JE, Davies K, Patton BL, Uncini A, Wrabetz L, Feltri ML. A laminin-2, dystroglycan, utrophin axis is required for compartmentalization and elongation of myelin segments Journal of Neuroscience. 29: 3908-3919. PMID 19321787 DOI: 10.1523/JNEUROSCI.5672-08.2009  1
2009 Kemp MW, Edwards B, Burgess M, Clarke WT, Nicholson G, Parry DA, Davies KE. Syncoilin isoform organization and differential expression in murine striated muscle. Journal of Structural Biology. 165: 196-203. PMID 19070665 DOI: 10.1016/j.jsb.2008.11.002  1
2009 Hoerder-Suabedissen A, Wang WZ, Lee S, Davies KE, Goffinet AM, Raki? S, Parnavelas J, Reim K, Nicoli? M, Paulsen O, Molnár Z. Novel markers reveal subpopulations of subplate neurons in the murine cerebral cortex. Cerebral Cortex (New York, N.Y. : 1991). 19: 1738-50. PMID 19008461 DOI: 10.1093/cercor/bhn195  1
2009 Briese M, Esmaeili B, Fraboulet S, Burt EC, Christodoulou S, Towers PR, Davies KE, Sattelle DB. Deletion of smn-1, the Caenorhabditis elegans ortholog of the spinal muscular atrophy gene, results in locomotor dysfunction and reduced lifespan. Human Molecular Genetics. 18: 97-104. PMID 18829666 DOI: 10.1093/hmg/ddn320  1
2008 Cauchi RJ, Davies KE, Liu JL. A motor function for the DEAD-box RNA helicase, Gemin3, in Drosophila. Plos Genetics. 4: e1000265. PMID 19023405 DOI: 10.1371/journal.pgen.1000265  1
2008 Vernes SC, Newbury DF, Abrahams BS, Winchester L, Nicod J, Groszer M, Alarcón M, Oliver PL, Davies KE, Geschwind DH, Monaco AP, Fisher SE. A functional genetic link between distinct developmental language disorders. The New England Journal of Medicine. 359: 2337-45. PMID 18987363 DOI: 10.1056/NEJMoa0802828  1
2008 Johnson RD, Oliver PL, Davies KE. SNARE proteins and schizophrenia: linking synaptic and neurodevelopmental hypotheses. Acta Biochimica Polonica. 55: 619-28. PMID 18985177  1
2008 McCullagh KJ, Edwards B, Kemp MW, Giles LC, Burgess M, Davies KE. Analysis of skeletal muscle function in the C57BL6/SV129 syncoilin knockout mouse. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 19: 339-51. PMID 18594912 DOI: 10.1007/s00335-008-9120-2  1
2008 Doran G, Davies KE, Talbot K. Activation of mutant protein kinase Cgamma leads to aberrant sequestration and impairment of its cellular function. Biochemical and Biophysical Research Communications. 372: 447-53. PMID 18503760 DOI: 10.1016/j.bbrc.2008.05.072  1
2008 Talbot K, Davies KE. Is good housekeeping the key to motor neuron survival? Cell. 133: 572-4. PMID 18485864 DOI: 10.1016/j.cell.2008.05.002  1
2008 Toms C, Jessup H, Thompson C, Baban D, Davies K, Powrie F. Gpr83 expression is not required for the maintenance of intestinal immune homeostasis and regulation of T-cell-dependent colitis Immunology. 125: 302-312. PMID 18479351 DOI: 10.1111/j.1365-2567.2008.02857.x  1
2008 Gulston MK, Rubtsov DV, Atherton HJ, Clarke K, Davies KE, Lilley KS, Griffin JL. A combined metabolomic and proteomic investigation of the effects of a failure to express dystrophin in the mouse heart. Journal of Proteome Research. 7: 2069-77. PMID 18386883 DOI: 10.1021/pr800070p  1
2008 Baban D, Davies KE. Microarray analysis of mdx mice expressing high levels of utrophin: therapeutic implications for dystrophin deficiency. Neuromuscular Disorders : Nmd. 18: 239-47. PMID 18343112 DOI: 10.1016/j.nmd.2007.11.011  1
2008 't Hoen PA, de Meijer EJ, Boer JM, Vossen RH, Turk R, Maatman RG, Davies KE, van Ommen GJ, van Deutekom JC, den Dunnen JT. Generation and characterization of transgenic mice with the full-length human DMD gene. The Journal of Biological Chemistry. 283: 5899-907. PMID 18083704 DOI: 10.1074/jbc.M709410200  1
2007 Kemp MW, Davies KE. The role of intermediate filament proteins in the development of neurological disease. Critical Reviews in Neurobiology. 19: 1-27. PMID 19166389  1
2007 Talbot K, Davies KE. Chapter 7 Spinal muscular atrophies and hereditary motor neuropathies. Handbook of Clinical Neurology. 82: 141-53. PMID 18808892 DOI: 10.1016/S0072-9752(07)80010-8  1
2007 Molnár Z, Hoerder-Suabedissen A, Wang WZ, DeProto J, Davies K, Lee S, Jacobs EC, Campagnoni AT, Paulsen O, Piñon MC, Cheung AF. Genes involved in the formation of the earliest cortical circuits. Novartis Foundation Symposium. 288: 212-24; discussion 2. PMID 18494261 DOI: 10.1002/9780470994030.ch15  1
2007 Davies KE, Grounds MD. Modified patient stem cells as prelude to autologous treatment of muscular dystrophy. Cell Stem Cell. 1: 595-6. PMID 18371397 DOI: 10.1016/j.stem.2007.11.003  1
2007 Vernes SC, Spiteri E, Nicod J, Groszer M, Taylor JM, Davies KE, Geschwind DH, Fisher SE. High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders. American Journal of Human Genetics. 81: 1232-50. PMID 17999362 DOI: 10.1086/522238  1
2007 Trülzsch B, Garnett C, Davies K, Wood M. Knockdown of SMN by RNA interference induces apoptosis in differentiated P19 neural stem cells. Brain Research. 1183: 1-9. PMID 17976539 DOI: 10.1016/j.brainres.2007.09.025  1
2007 Mattei E, Corbi N, Di Certo MG, Strimpakos G, Severini C, Onori A, Desantis A, Libri V, Buontempo S, Floridi A, Fanciulli M, Baban D, Davies KE, Passananti C. Utrophin up-regulation by an artificial transcription factor in transgenic mice. Plos One. 2: e774. PMID 17712422 DOI: 10.1371/journal.pone.0000774  1
2007 McCullagh KJ, Edwards B, Poon E, Lovering RM, Paulin D, Davies KE. Intermediate filament-like protein syncoilin in normal and myopathic striated muscle. Neuromuscular Disorders : Nmd. 17: 970-9. PMID 17629480 DOI: 10.1016/j.nmd.2007.06.004  1
2007 Oliver PL, Keays DA, Davies KE. Behavioural characterisation of the robotic mouse mutant. Behavioural Brain Research. 181: 239-47. PMID 17532061 DOI: 10.1016/j.bbr.2007.04.012  1
2007 Oliver PL, Bitoun E, Davies KE. Comparative genetic analysis: the utility of mouse genetic systems for studying human monogenic disease. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 18: 412-24. PMID 17514509 DOI: 10.1007/s00335-007-9014-8  1
2007 Hodges A, Sharrocks K, Edelmann M, Baban D, Moris A, Schwartz O, Drakesmith H, Davies K, Kessler B, McMichael A, Simmons A. Activation of the lectin DC-SIGN induces an immature dendritic cell phenotype triggering Rho-GTPase activity required for HIV-1 replication. Nature Immunology. 8: 569-77. PMID 17496896 DOI: 10.1038/ni1470  1
2007 Davies KE, Khurana TS. A new way to regulate the NMJ. Nature Medicine. 13: 538-9. PMID 17479096 DOI: 10.1038/nm0507-538  1
2007 Rezniczek GA, Konieczny P, Nikolic B, Reipert S, Schneller D, Abrahamsberg C, Davies KE, Winder SJ, Wiche G. Plectin 1f scaffolding at the sarcolemma of dystrophic (mdx) muscle fibers through multiple interactions with beta-dystroglycan. The Journal of Cell Biology. 176: 965-77. PMID 17389230 DOI: 10.1083/jcb.200604179  1
2007 Li Y, Huang J, Zhao YL, He J, Wang W, Davies KE, Nosé V, Xiao S. UTRN on chromosome 6q24 is mutated in multiple tumors. Oncogene. 26: 6220-8. PMID 17384672 DOI: 10.1038/sj.onc.1210432  1
2007 Grounds MD, Davies KE. The allure of stem cell therapy for muscular dystrophy. Neuromuscular Disorders : Nmd. 17: 206-8. PMID 17306535 DOI: 10.1016/j.nmd.2007.01.007  1
2007 Jeans AF, Oliver PL, Johnson R, Capogna M, Vikman J, Molnár Z, Babbs A, Partridge CJ, Salehi A, Bengtsson M, Eliasson L, Rorsman P, Davies KE. A dominant mutation in Snap25 causes impaired vesicle trafficking, sensorimotor gating, and ataxia in the blind-drunk mouse. Proceedings of the National Academy of Sciences of the United States of America. 104: 2431-6. PMID 17283335 DOI: 10.1073/pnas.0610222104  1
2007 Keays DA, Tian G, Poirier K, Huang GJ, Siebold C, Cleak J, Oliver PL, Fray M, Harvey RJ, Molnár Z, Piñon MC, Dear N, Valdar W, Brown SD, Davies KE, et al. Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans. Cell. 128: 45-57. PMID 17218254 DOI: 10.1016/j.cell.2006.12.017  1
2007 Martin-Rendon E, Hale SJ, Ryan D, Baban D, Forde SP, Roubelakis M, Sweeney D, Moukayed M, Harris AL, Davies K, Watt SM. Transcriptional profiling of human cord blood CD133+ and cultured bone marrow mesenchymal stem cells in response to hypoxia. Stem Cells (Dayton, Ohio). 25: 1003-12. PMID 17185612 DOI: 10.1634/stemcells.2006-0398  1
2007 Bitoun E, Oliver PL, Davies KE. The mixed-lineage leukemia fusion partner AF4 stimulates RNA polymerase II transcriptional elongation and mediates coordinated chromatin remodeling. Human Molecular Genetics. 16: 92-106. PMID 17135274 DOI: 10.1093/hmg/ddl444  1
2006 Davies KE, Grounds MD. Treating muscular dystrophy with stem cells? Cell. 127: 1304-6. PMID 17190595 DOI: 10.1016/j.cell.2006.12.010  1
2006 Vernes SC, Nicod J, Elahi FM, Coventry JA, Kenny N, Coupe AM, Bird LE, Davies KE, Fisher SE. Functional genetic analysis of mutations implicated in a human speech and language disorder. Human Molecular Genetics. 15: 3154-67. PMID 16984964 DOI: 10.1093/hmg/ddl392  1
2006 Davies KE, Nowak KJ. Molecular mechanisms of muscular dystrophies: old and new players. Nature Reviews. Molecular Cell Biology. 7: 762-73. PMID 16971897 DOI: 10.1038/nrm2024  1
2006 Towers PR, Lescure P, Baban D, Malek JA, Duarte J, Jones E, Davies KE, Ségalat L, Sattelle DB. Gene expression profiling studies on Caenorhabditis elegans dystrophin mutants dys-1(cx-35) and dys-1(cx18). Genomics. 88: 642-9. PMID 16962739 DOI: 10.1016/j.ygeno.2006.07.014  1
2006 Yokota T, Lu QL, Morgan JE, Davies KE, Fisher R, Takeda S, Partridge TA. Expansion of revertant fibers in dystrophic mdx muscles reflects activity of muscle precursor cells and serves as an index of muscle regeneration. Journal of Cell Science. 119: 2679-87. PMID 16757519 DOI: 10.1242/jcs.03000  1
2006 Jiang Y, Oliver P, Davies KE, Platt N. Identification and characterization of murine SCARA5, a novel class A scavenger receptor that is expressed by populations of epithelial cells. The Journal of Biological Chemistry. 281: 11834-45. PMID 16407294 DOI: 10.1074/jbc.M507599200  1
2006 Ackerley S, James PA, Kalli A, French S, Davies KE, Talbot K. A mutation in the small heat-shock protein HSPB1 leading to distal hereditary motor neuronopathy disrupts neurofilament assembly and the axonal transport of specific cellular cargoes. Human Molecular Genetics. 15: 347-54. PMID 16368711 DOI: 10.1093/hmg/ddi452  1
2006 Wilding JR, Lygate CA, Davies KE, Neubauer S, Clarke K. MLP accumulation and remodelling in the infarcted rat heart. European Journal of Heart Failure. 8: 343-6. PMID 16330255 DOI: 10.1016/j.ejheart.2005.10.006  1
2005 Hirst RC, McCullagh KJ, Davies KE. Utrophin upregulation in Duchenne muscular dystrophy. Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology / Edited by the Gaetano Conte Academy For the Study of Striated Muscle Diseases. 24: 209-16. PMID 16629055  1
2005 Bitoun E, Davies KE. The robotic mouse: unravelling the function of AF4 in the cerebellum. Cerebellum (London, England). 4: 250-60. PMID 16321881 DOI: 10.1080/14734220500325897  1
2005 Sewry CA, Nowak KJ, Ehmsen JT, Davies KE. A and B utrophin in human muscle and sarcolemmal A-utrophin associated with tumours. Neuromuscular Disorders : Nmd. 15: 779-85. PMID 16198105 DOI: 10.1016/j.nmd.2005.08.002  1
2005 Brown SC, Torelli S, Ugo I, De Biasia F, Howman EV, Poon E, Britton J, Davies KE, Muntoni F. Syncoilin upregulation in muscle of patients with neuromuscular disease. Muscle & Nerve. 32: 715-25. PMID 16124004 DOI: 10.1002/mus.20431  1
2005 Davies KE. Regulation of utrophin in transgenic mice. Neuromuscular Disorders : Nmd. 15: 648; author reply 64. PMID 16081285 DOI: 10.1016/j.nmd.2005.06.013  1
2005 Oliver PL, Davies KE. Analysis of human neurological disorders using mutagenesis in the mouse. Clinical Science (London, England : 1979). 108: 385-97. PMID 15831088 DOI: 10.1042/CS20050041  1
2005 Nowak K, McCullagh K, Poon E, Davies KE. Muscular dystrophies related to the cytoskeleton/nuclear envelope. Novartis Foundation Symposium. 264: 98-111; discussion 1. PMID 15773750  1
2005 Wilding JR, Schneider JE, Sang AE, Davies KE, Neubauer S, Clarke K. Dystrophin- and MLP-deficient mouse hearts: marked differences in morphology and function, but similar accumulation of cytoskeletal proteins. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 19: 79-81. PMID 15494447 DOI: 10.1096/fj.04-1731fje  1
2005 Davies KE. Editorial Human Molecular Genetics. 14: 1243. DOI: 10.1093/hmg/ddi150  1
2004 Moore CJ, Daly EM, Tassone F, Tysoe C, Schmitz N, Ng V, Chitnis X, McGuire P, Suckling J, Davies KE, Hagerman RJ, Hagerman PJ, Murphy KC, Murphy DG. The effect of pre-mutation of X chromosome CGG trinucleotide repeats on brain anatomy. Brain : a Journal of Neurology. 127: 2672-81. PMID 15483045 DOI: 10.1093/brain/awh256  1
2004 Anderson KN, Baban D, Oliver PL, Potter A, Davies KE. Expression profiling in spinal muscular atrophy reveals an RNA binding protein deficit. Neuromuscular Disorders : Nmd. 14: 711-22. PMID 15482955 DOI: 10.1016/j.nmd.2004.08.009  1
2004 Nowak KJ, Davies KE. Duchenne muscular dystrophy and dystrophin: pathogenesis and opportunities for treatment. Embo Reports. 5: 872-6. PMID 15470384 DOI: 10.1038/sj.embor.7400221  1
2004 Oliver PL, Bitoun E, Clark J, Jones EL, Davies KE. Mediation of Af4 protein function in the cerebellum by Siah proteins. Proceedings of the National Academy of Sciences of the United States of America. 101: 14901-6. PMID 15459319 DOI: 10.1073/pnas.0406196101  1
2004 Ilkovski B, Nowak KJ, Domazetovska A, Maxwell AL, Clement S, Davies KE, Laing NG, North KN, Cooper ST. Evidence for a dominant-negative effect in ACTA1 nemaline myopathy caused by abnormal folding, aggregation and altered polymerization of mutant actin isoforms. Human Molecular Genetics. 13: 1727-43. PMID 15198992 DOI: 10.1093/hmg/ddh185  1
2004 Anderson KN, Potter AC, Piccenna LG, Quah AK, Davies KE, Cheema SS. Isolation and culture of motor neurons from the newborn mouse spinal cord. Brain Research. Brain Research Protocols. 12: 132-6. PMID 15013463 DOI: 10.1016/j.brainresprot.2003.10.001  1
2004 Ishikawa-Sakurai M, Yoshida M, Imamura M, Davies KE, Ozawa E. ZZ domain is essentially required for the physiological binding of dystrophin and utrophin to beta-dystroglycan. Human Molecular Genetics. 13: 693-702. PMID 14962982 DOI: 10.1093/hmg/ddh087  1
2004 Weir AP, Morgan JE, Davies KE. A-utrophin up-regulation in mdx skeletal muscle is independent of regeneration. Neuromuscular Disorders : Nmd. 14: 19-23. PMID 14659408 DOI: 10.1016/j.nmd.2003.09.004  1
2003 Vargas JD, Herpers B, McKie AT, Gledhill S, McDonnell J, van den Heuvel M, Davies KE, Ponting CP. Stromal cell-derived receptor 2 and cytochrome b561 are functional ferric reductases. Biochimica Et Biophysica Acta. 1651: 116-23. PMID 14499595 DOI: 10.1016/S1570-9639(03)00242-5  1
2003 Moghadaszadeh B, Albrechtsen R, Guo LT, Zaik M, Kawaguchi N, Borup RH, Kronqvist P, Schroder HD, Davies KE, Voit T, Nielsen FC, Engvall E, Wewer UM. Compensation for dystrophin-deficiency: ADAM12 overexpression in skeletal muscle results in increased alpha 7 integrin, utrophin and associated glycoproteins. Human Molecular Genetics. 12: 2467-79. PMID 12915458 DOI: 10.1093/hmg/ddg264  1
2003 Anderson K, Potter A, Baban D, Davies KE. Protein expression changes in spinal muscular atrophy revealed with a novel antibody array technology. Brain : a Journal of Neurology. 126: 2052-64. PMID 12847076 DOI: 10.1093/brain/awg208  1
2003 Talbot K, Davies K. Musculoskeletal diseases: from complex genetics to therapy. Current Opinion in Pharmacology. 3: 277-9. PMID 12810192 DOI: 10.1016/S1471-4892(03)00044-4  1
2003 Chan YB, Miguel-Aliaga I, Franks C, Thomas N, Trülzsch B, Sattelle DB, Davies KE, van den Heuvel M. Neuromuscular defects in a Drosophila survival motor neuron gene mutant. Human Molecular Genetics. 12: 1367-76. PMID 12783845  1
2003 Khurana TS, Davies KE. Pharmacological strategies for muscular dystrophy. Nature Reviews. Drug Discovery. 2: 379-90. PMID 12750741 DOI: 10.1038/nrd1085  1
2003 Cerletti M, Negri T, Cozzi F, Colpo R, Andreetta F, Croci D, Davies KE, Cornelio F, Pozza O, Karpati G, Gilbert R, Mora M. Dystrophic phenotype of canine X-linked muscular dystrophy is mitigated by adenovirus-mediated utrophin gene transfer. Gene Therapy. 10: 750-7. PMID 12704413 DOI: 10.1038/sj.gt.3301941  1
2003 Perkins KJ, Davies KE. Ets, Ap-1 and GATA factor families regulate the utrophin B promoter: potential regulatory mechanisms for endothelial-specific expression. Febs Letters. 538: 168-72. PMID 12633873 DOI: 10.1016/S0014-5793(03)00175-3  1
2003 Isaacs AM, Oliver PL, Jones EL, Jeans A, Potter A, Hovik BH, Nolan PM, Vizor L, Glenister P, Simon AK, Gray IC, Spurr NK, Brown SD, Hunter AJ, Davies KE. A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouse. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 23: 1631-7. PMID 12629167  1
2003 Howman EV, Sullivan N, Poon EP, Britton JE, Hilton-Jones D, Davies KE. Syncoilin accumulation in two patients with desmin-related myopathy. Neuromuscular Disorders : Nmd. 13: 42-8. PMID 12467731 DOI: 10.1016/S0960-8966(02)00181-5  1
2003 Talbot K, Davies KE. Chapter 16 Spinal Muscular Atrophy Blue Books of Practical Neurology. 28: 401-424,cp1-cp2. DOI: 10.1016/S1877-3419(09)70117-5  1
2002 Squire S, Raymackers JM, Vandebrouck C, Potter A, Tinsley J, Fisher R, Gillis JM, Davies KE. Prevention of pathology in mdx mice by expression of utrophin: analysis using an inducible transgenic expression system. Human Molecular Genetics. 11: 3333-44. PMID 12471059 DOI: 10.1093/hmg/11.26.3333  1
2002 Isaacs AM, Jeans A, Oliver PL, Vizor L, Brown SD, Hunter AJ, Davies KE. Identification of a new Pmp22 mouse mutant and trafficking analysis of a Pmp22 allelic series suggesting that protein aggregates may be protective in Pmp22-associated peripheral neuropathy. Molecular and Cellular Neurosciences. 21: 114-25. PMID 12359155 DOI: 10.1006/mcne.2002.1158  1
2002 Weir AP, Burton EA, Harrod G, Davies KE. A- and B-utrophin have different expression patterns and are differentially up-regulated in mdx muscle. The Journal of Biological Chemistry. 277: 45285-90. PMID 12235137 DOI: 10.1074/jbc.M205177200  1
2002 Perkins KJ, Davies KE. The role of utrophin in the potential therapy of Duchenne muscular dystrophy. Neuromuscular Disorders : Nmd. 12: S78-89. PMID 12206801 DOI: 10.1016/S0960-8966(02)00087-1  1
2002 Vargas JD, Culetto E, Ponting CP, Miguel-Aliaga I, Davies KE, Sattelle DB. Cloning and developmental expression analysis of ltd-1, the Caenorhabditis elegans homologue of the mouse kyphoscoliosis (ky) gene. Mechanisms of Development. 117: 289-92. PMID 12204272 DOI: 10.1016/S0925-4773(02)00182-X  1
2002 Rybakova IN, Patel JR, Davies KE, Yurchenco PD, Ervasti JM. Utrophin binds laterally along actin filaments and can couple costameric actin with sarcolemma when overexpressed in dystrophin-deficient muscle. Molecular Biology of the Cell. 13: 1512-21. PMID 12006649 DOI: 10.1091/mbc.01-09-0446  1
2002 Blake DJ, Weir A, Newey SE, Davies KE. Function and genetics of dystrophin and dystrophin-related proteins in muscle. Physiological Reviews. 82: 291-329. PMID 11917091 DOI: 10.1152/physrev.00028.2001  1
2002 Cole MA, Rafael JA, Taylor DJ, Lodi R, Davies KE, Styles P. A quantitative study of bioenergetics in skeletal muscle lacking utrophin and dystrophin. Neuromuscular Disorders : Nmd. 12: 247-57. PMID 11801396 DOI: 10.1016/S0960-8966(01)00278-4  1
2002 Burton EA, Davies KE. Muscular dystrophy--reason for optimism? Cell. 108: 5-8. PMID 11792315 DOI: 10.1016/S0092-8674(01)00626-2  1
2002 Poon E, Howman EV, Newey SE, Davies KE. Association of syncoilin and desmin: linking intermediate filament proteins to the dystrophin-associated protein complex. The Journal of Biological Chemistry. 277: 3433-9. PMID 11694502 DOI: 10.1074/jbc.M105273200  1
2001 Culle MJ, Walsh JM, Tinsle JM, Fisher R, Davies KE. Immunogold confirmation that utrophin is localized to the normal position of dystrophin in dystrophin-negative transgenic mouse muscle. The Histochemical Journal. 33: 579-83. PMID 12005030 DOI: 10.1023/A:1014964127156  1
2001 Perkins KJ, Burton EA, Davies KE. The role of basal and myogenic factors in the transcriptional activation of utrophin promoter A: implications for therapeutic up-regulation in Duchenne muscular dystrophy. Nucleic Acids Research. 29: 4843-50. PMID 11726694  1
2001 Fisher R, Tinsley JM, Phelps SR, Squire SE, Townsend ER, Martin JE, Davies KE. Non-toxic ubiquitous over-expression of utrophin in the mdx mouse. Neuromuscular Disorders : Nmd. 11: 713-21. PMID 11595513 DOI: 10.1016/S0960-8966(01)00220-6  1
2001 Loh NY, Nebenius-Oosthuizen D, Blake DJ, Smith AJ, Davies KE. Role of beta-dystrobrevin in nonmuscle dystrophin-associated protein complex-like complexes in kidney and liver. Molecular and Cellular Biology. 21: 7442-8. PMID 11585924 DOI: 10.1128/MCB.21.21.7442-7448.2001  1
2001 Talbot K, Davies KE. Spinal muscular atrophy. Seminars in Neurology. 21: 189-97. PMID 11442327 DOI: 10.1055/s-2001-15264  1
2001 Skordis LA, Dunckley MG, Burglen L, Campbell L, Talbot K, Patel S, Melki J, Davies KE, Dubowitz V, Muntoni F. Characterisation of novel point mutations in the survival motor neuron gene SMN, in three patients with SMA. Human Genetics. 108: 356-7. PMID 11379882 DOI: 10.1007/s004390100497  1
2001 Nakamura A, Harrod GV, Davies KE. Activation of calcineurin and stress activated protein kinase/p38-mitogen activated protein kinase in hearts of utrophin-dystrophin knockout mice. Neuromuscular Disorders : Nmd. 11: 251-9. PMID 11297940 DOI: 10.1016/S0960-8966(00)00201-7  1
2001 Newey SE, Gramolini AO, Wu J, Holzfeind P, Jasmin BJ, Davies KE, Blake DJ. A novel mechanism for modulating synaptic gene expression: differential localization of alpha-dystrobrevin transcripts in skeletal muscle. Molecular and Cellular Neurosciences. 17: 127-40. PMID 11161474 DOI: 10.1006/mcne.2000.0918  1
2001 Newey SE, Howman EV, Ponting CP, Benson MA, Nawrotzki R, Loh NY, Davies KE, Blake DJ. Syncoilin, a novel member of the intermediate filament superfamily that interacts with alpha-dystrobrevin in skeletal muscle. The Journal of Biological Chemistry. 276: 6645-55. PMID 11053421 DOI: 10.1074/jbc.M008305200  1
2001 Moore CJ, Daly E, Tassone F, Jacobs PA, Davies KE, Murphy KC, Murphy KGM. Neuroanatomical effect of FMR1 gene mRNA in premutation carriers of Fragile X syndrome American Journal of Medical Genetics - Neuropsychiatric Genetics. 105: 585.  1
2000 Hopkins JC, Bia BL, Crilley JG, Boehm EA, Sang AE, Tinsley JM, King LM, Radda GK, Davies KE, Clarke K. Muscular dystrophy: from gene to patient. Magma (New York, N.Y.). 11: 7-9. PMID 11186993 DOI: 10.1016/S1352-8661(00)00099-5  1
2000 Miguel-Aliaga I, Chan YB, Davies KE, van den Heuvel M. Disruption of SMN function by ectopic expression of the human SMN gene in Drosophila. Febs Letters. 486: 99-102. PMID 11113446 DOI: 10.1016/S0014-5793(00)02243-2  1
2000 Newey SE, Benson MA, Ponting CP, Davies KE, Blake DJ. Alternative splicing of dystrobrevin regulates the stoichiometry of syntrophin binding to the dystrophin protein complex. Current Biology : Cb. 10: 1295-8. PMID 11069112 DOI: 10.1016/S0960-9822(00)00760-0  1
2000 Rafael JA, Nitta Y, Peters J, Davies KE. Testing of SHIRPA, a mouse phenotypic assessment protocol, on Dmd(mdx) and Dmd(mdx3cv) dystrophin-deficient mice. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 11: 725-8. PMID 10967129 DOI: 10.1007/s003350010149  1
2000 Isaacs AM, Davies KE, Hunter AJ, Nolan PM, Vizor L, Peters J, Gale DG, Kelsell DP, Latham ID, Chase JM, Fisher EM, Bouzyk MM, Potter A, Masih M, Walsh FS, et al. Identification of two new Pmp22 mouse mutants using large-scale mutagenesis and a novel rapid mapping strategy. Human Molecular Genetics. 9: 1865-71. PMID 10915775  1
2000 Loh NY, Newey SE, Davies KE, Blake DJ. Assembly of multiple dystrobrevin-containing complexes in the kidney. Journal of Cell Science. 113: 2715-24. PMID 10893187  1
2000 Corbi N, Libri V, Fanciulli M, Tinsley JM, Davies KE, Passananti C. The artificial zinc finger coding gene 'Jazz' binds the utrophin promoter and activates transcription. Gene Therapy. 7: 1076-83. PMID 10871758 DOI: 10.1038/sj.gt.3301204  1
2000 Rafael JA, Townsend ER, Squire SE, Potter AC, Chamberlain JS, Davies KE. Dystrophin and utrophin influence fiber type composition and post-synaptic membrane structure. Human Molecular Genetics. 9: 1357-67. PMID 10814717 DOI: 10.1093/HMG/9.9.1357  1
2000 Rodrigues NR, Theodosiou AM, Nesbit MA, Campbell L, Tandle AT, Saranath D, Davies KE. Characterization of Ngef, a novel member of the Dbl family of genes expressed predominantly in the caudate nucleus. Genomics. 65: 53-61. PMID 10777665 DOI: 10.1006/geno.2000.6138  1
2000 Campbell L, Hunter KM, Mohaghegh P, Tinsley JM, Brasch MA, Davies KE. Direct interaction of Smn with dp103, a putative RNA helicase: a role for Smn in transcription regulation? Human Molecular Genetics. 9: 1093-100. PMID 10767334  1
2000 Owen N, Doe CL, Mellor J, Davies KE. Characterization of the Schizosaccharomyces pombe orthologue of the human survival motor neuron (SMN) protein. Human Molecular Genetics. 9: 675-84. PMID 10749974  1
2000 Wakefield PM, Tinsley JM, Wood MJ, Gilbert R, Karpati G, Davies KE. Prevention of the dystrophic phenotype in dystrophin/utrophin-deficient muscle following adenovirus-mediated transfer of a utrophin minigene. Gene Therapy. 7: 201-4. PMID 10694796 DOI: 10.1038/sj.gt.3301066  1
2000 Miller WJ, Skinner JA, Foss GS, Davies KE. Localization of the fragile X mental retardation 2 (FMR2) protein in mammalian brain. The European Journal of Neuroscience. 12: 381-4. PMID 10651894 DOI: 10.1046/j.1460-9568.2000.00921.x  1
1999 Burton EA, Tinsley JM, Holzfeind PJ, Rodrigues NR, Davies KE. A second promoter provides an alternative target for therapeutic up-regulation of utrophin in Duchenne muscular dystrophy. Proceedings of the National Academy of Sciences of the United States of America. 96: 14025-30. PMID 10570192  1
1999 Miguel-Aliaga I, Culetto E, Walker DS, Baylis HA, Sattelle DB, Davies KE. The Caenorhabditis elegans orthologue of the human gene responsible for spinal muscular atrophy is a maternal product critical for germline maturation and embryonic viability. Human Molecular Genetics. 8: 2133-43. PMID 10545592 DOI: 10.1093/hmg/8.12.2133  1
1999 Bia BL, Cassidy PJ, Young ME, Rafael JA, Leighton B, Davies KE, Radda GK, Clarke K. Decreased myocardial nNOS, increased iNOS and abnormal ECGs in mouse models of Duchenne muscular dystrophy. Journal of Molecular and Cellular Cardiology. 31: 1857-62. PMID 10525423 DOI: 10.1006/jmcc.1999.1018  1
1999 Mohaghegh P, Rodrigues NR, Owen N, Ponting CP, Le TT, Burghes AH, Davies KE. Analysis of mutations in the tudor domain of the survival motor neuron protein SMN. European Journal of Human Genetics : Ejhg. 7: 519-25. PMID 10439956 DOI: 10.1038/sj.ejhg.5200346  1
1999 Zerres K, Davies KE. 59th ENMC International Workshop: Spinal Muscular Atrophies: recent progress and revised diagnostic criteria 17-19 April 1998, Soestduinen, The Netherlands. Neuromuscular Disorders : Nmd. 9: 272-8. PMID 10399757 DOI: 10.1016/S0960-8966(99)00016-4  1
1999 Gilbert R, Nalbantoglu J, Petrof BJ, Ebihara S, Guibinga GH, Tinsley JM, Kamen A, Massie B, Davies KE, Karpati G. Adenovirus-mediated utrophin gene transfer mitigates the dystrophic phenotype of mdx mouse muscles. Human Gene Therapy. 10: 1299-310. PMID 10365661 DOI: 10.1089/10430349950017987  1
1999 Rafael JA, Trickett JI, Potter AC, Davies KE. Dystrophin and utrophin do not play crucial roles in nonmuscle tissues in mice. Muscle & Nerve. 22: 517-9. PMID 10204788 DOI: 10.1002/(SICI)1097-4598(199904)22:4<517::AID-MUS14>3.0.CO;2-6  1
1999 Gramolini AO, Angus LM, Schaeffer L, Burton EA, Tinsley JM, Davies KE, Changeux JP, Jasmin BJ. Induction of utrophin gene expression by heregulin in skeletal muscle cells: role of the N-box motif and GA binding protein. Proceedings of the National Academy of Sciences of the United States of America. 96: 3223-7. PMID 10077665 DOI: 10.1073/pnas.96.6.3223  1
1999 Holzfeind PJ, Ambrose HJ, Newey SE, Nawrotzki RA, Blake DJ, Davies KE. Tissue-selective expression of alpha-dystrobrevin is determined by multiple promoters. The Journal of Biological Chemistry. 274: 6250-8. PMID 10037712 DOI: 10.1074/jbc.274.10.6250  1
1998 Trump D, Dixon PH, Mumm S, Wooding C, Davies KE, Schlessinger D, Whyte MP, Thakker RV. Localisation of X linked recessive idiopathic hypoparathyroidism to a 1.5 Mb region on Xq26-q27. Journal of Medical Genetics. 35: 905-9. PMID 9832036  1
1998 Talbot K, Miguel-Aliaga I, Mohaghegh P, Ponting CP, Davies KE. Characterization of a gene encoding survival motor neuron (SMN)-related protein, a constituent of the spliceosome complex. Human Molecular Genetics. 7: 2149-56. PMID 9817934  1
1998 Taylor JE, Thomas NH, Lewis CM, Abbs SJ, Rodrigues NR, Davies KE, Mathew CG. Correlation of SMNt and SMNc gene copy number with age of onset and survival in spinal muscular atrophy. European Journal of Human Genetics : Ejhg. 6: 467-74. PMID 9801871 DOI: 10.1038/sj.ejhg.5200210  1
1998 Loh NY, Ambrose HJ, Guay-Woodford LM, DasGupta S, Nawrotzki RA, Blake DJ, Davies KE. Genomic organization and refined mapping of the mouse beta-dystrobrevin gene. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 9: 857-62. PMID 9799833 DOI: 10.1007/s003359900883  1
1998 Goudemant JF, Deconinck N, Tinsley JM, Demeure R, Robert A, Davies KE, Gillis JM. Expression of truncated utrophin improves pH recovery in exercising muscles of dystrophic mdx mice: a 31P NMR study. Neuromuscular Disorders : Nmd. 8: 371-9. PMID 9713853 DOI: 10.1016/S0960-8966(98)00049-2  1
1998 Deconinck N, Rafael JA, Beckers-Bleukx G, Kahn D, Deconinck AE, Davies KE, Gillis JM. Consequences of the combined deficiency in dystrophin and utrophin on the mechanical properties and myosin composition of some limb and respiratory muscles of the mouse. Neuromuscular Disorders : Nmd. 8: 362-70. PMID 9713852 DOI: 10.1016/S0960-8966(98)00048-0  1
1998 Nawrotzki R, Loh NY, Ruegg MA, Davies KE, Blake DJ. Characterisation of alpha-dystrobrevin in muscle. Journal of Cell Science. 111: 2595-605. PMID 9701558  1
1998 Willard HF, Davies KE. Genetics of disease Complex genetics, complex diseases Current Opinion in Genetics & Development. 8: 271-3. PMID 9690994  0.32
1998 Campbell L, Daniels RJ, Dubowitz V, Davies KE. Maternal mosaicism for a second mutational event in a type I spinal muscular atrophy family. American Journal of Human Genetics. 63: 37-44. PMID 9634516 DOI: 10.1086/301918  1
1998 Ward CL, Davies KE. Genetic modelling of muscular dystrophies. Neuropathology and Applied Neurobiology. 24: 96-100. PMID 9634204 DOI: 10.1046/j.1365-2990.1998.00005.x  1
1998 Porter JD, Rafael JA, Ragusa RJ, Brueckner JK, Trickett JI, Davies KE. The sparing of extraocular muscle in dystrophinopathy is lost in mice lacking utrophin and dystrophin. Journal of Cell Science. 111: 1801-11. PMID 9625743  1
1998 Vater R, Young C, Anderson LV, Lindsay S, Blake DJ, Davies KE, Zuellig R, Slater CR. Utrophin mRNA expression in muscle is not restricted to the neuromuscular junction. Molecular and Cellular Neurosciences. 10: 229-42. PMID 9604203 DOI: 10.1006/mcne.1998.0661  1
1998 Rafael JA, Tinsley JM, Potter AC, Deconinck AE, Davies KE. Skeletal muscle-specific expression of a utrophin transgene rescues utrophin-dystrophin deficient mice. Nature Genetics. 19: 79-82. PMID 9590295 DOI: 10.1038/ng0598-79  1
1998 Chakrabarti L, Bristulf J, Foss GS, Davies KE. Expression of the murine homologue of FMR2 in mouse brain and during development. Human Molecular Genetics. 7: 441-8. PMID 9467002 DOI: 10.1093/hmg/7.3.441  1
1998 Gilbert R, Nalbanoglu J, Tinsley JM, Massie B, Davies KE, Karpati G. Efficient utrophin expression following adenovirus gene transfer in dystrophic muscle. Biochemical and Biophysical Research Communications. 242: 244-7. PMID 9439643 DOI: 10.1006/bbrc.1997.7936  1
1998 Gramolini AO, Burton EA, Tinsley JM, Ferns MJ, Cartaud A, Cartaud J, Davies KE, Lunde JA, Jasmin BJ. Muscle and neural isoforms of agrin increase utrophin expression in cultured myotubes via a transcriptional regulatory mechanism. The Journal of Biological Chemistry. 273: 736-43. PMID 9422725 DOI: 10.1074/jbc.273.2.736  1
1998 Blake DJ, Nawrotzki R, Loh NY, Górecki DC, Davies KE. beta-dystrobrevin, a member of the dystrophin-related protein family. Proceedings of the National Academy of Sciences of the United States of America. 95: 241-6. PMID 9419360 DOI: 10.1073/pnas.95.1.241  1
1998 Willard HF, Davies KE. Complex genetics, complex diseases: Editorial overview Current Opinion in Genetics and Development. 8: 271-273. DOI: 10.1016/S0959-437X(98)80080-4  1
1997 Davies KE. Challenges in Duchenne muscular dystrophy. Neuromuscular Disorders : Nmd. 7: 482-6. PMID 9447604 DOI: 10.1016/S0960-8966(97)00107-7  1
1997 Ritchie RJ, Chakrabarti L, Knight SJ, Harding RM, Davies KE. Population genetics of the FRAXE and FRAXF GCC repeats, and a novel CGG repeat, in Xq28. American Journal of Medical Genetics. 73: 463-9. PMID 9415475 DOI: 10.1002/(SICI)1096-8628(19971231)73:4<463::AID-AJMG16>3.0.CO;2-P  1
1997 Deconinck AE, Rafael JA, Skinner JA, Brown SC, Potter AC, Metzinger L, Watt DJ, Dickson JG, Tinsley JM, Davies KE. Utrophin-dystrophin-deficient mice as a model for Duchenne muscular dystrophy. Cell. 90: 717-27. PMID 9288751 DOI: 10.1016/S0092-8674(00)80532-2  1
1997 Ponting CP, Phillips C, Davies KE, Blake DJ. PDZ domains: targeting signalling molecules to sub-membranous sites. Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology. 19: 469-79. PMID 9204764 DOI: 10.1002/bies.950190606  1
1997 Nesbit MA, Hodges MD, Campbell L, de Meulemeester TM, Alders M, Rodrigues NR, Talbot K, Theodosiou AM, Mannens MA, Nakamura Y, Little PF, Davies KE. Genomic organization and chromosomal localization of a member of the MAP kinase phosphatase gene family to human chromosome 11p15.5 and a pseudogene to 10q11.2. Genomics. 42: 284-94. PMID 9192849 DOI: 10.1006/geno.1997.4737  1
1997 Talbot K, Rodrigues NR, Ignatius J, Muntoni F, Davies KE. Gene conversion at the SMN locus in autosomal recessive spinal muscular atrophy does not predict a mild phenotype. Neuromuscular Disorders : Nmd. 7: 198-201. PMID 9185185 DOI: 10.1016/S0960-8966(97)00450-1  1
1997 Talbot K, Ponting CP, Theodosiou AM, Rodrigues NR, Surtees R, Mountford R, Davies KE. Missense mutation clustering in the survival motor neuron gene: a role for a conserved tyrosine and glycine rich region of the protein in RNA metabolism? Human Molecular Genetics. 6: 497-500. PMID 9147655 DOI: 10.1093/hmg/6.3.497  1
1997 Chakrabarti L, Davies KE. Fragile X syndrome. Current Opinion in Neurology. 10: 142-7. PMID 9146995  1
1997 Ambrose HJ, Blake DJ, Nawrotzki RA, Davies KE. Genomic organization of the mouse dystrobrevin gene: comparative analysis with the dystrophin gene. Genomics. 39: 359-69. PMID 9119373 DOI: 10.1006/geno.1996.4515  1
1997 Gramolini AO, Dennis CL, Tinsley JM, Robertson GS, Cartaud J, Davies KE, Jasmin BJ. Local transcriptional control of utrophin expression at the neuromuscular synapse. The Journal of Biological Chemistry. 272: 8117-20. PMID 9079621 DOI: 10.1074/jbc.272.13.8117  1
1997 Deconinck AE, Potter AC, Tinsley JM, Wood SJ, Vater R, Young C, Metzinger L, Vincent A, Slater CR, Davies KE. Postsynaptic abnormalities at the neuromuscular junctions of utrophin-deficient mice. The Journal of Cell Biology. 136: 883-94. PMID 9049253 DOI: 10.1083/jcb.136.4.883  1
1996 Tinsley JM, Potter AC, Phelps SR, Fisher R, Trickett JI, Davies KE. Amelioration of the dystrophic phenotype of mdx mice using a truncated utrophin transgene. Nature. 384: 349-53. PMID 8934518 DOI: 10.1038/384349a0  1
1996 Rodrigues NR, Owen N, Talbot K, Patel S, Muntoni F, Ignatius J, Dubowitz V, Davies KE. Gene deletions in spinal muscular atrophy. Journal of Medical Genetics. 33: 93-6. PMID 8929942  1
1996 Blake DJ, Tinsley JM, Davies KE. Utrophin: a structural and functional comparison to dystrophin. Brain Pathology (Zurich, Switzerland). 6: 37-47. PMID 8866746  1
1996 Ponting CP, Blake DJ, Davies KE, Kendrick-Jones J, Winder SJ. ZZ and TAZ: new putative zinc fingers in dystrophin and other proteins. Trends in Biochemical Sciences. 21: 11-13. PMID 8848831 DOI: 10.1016/0968-0004(96)80878-4  1
1996 Holden JJ, Julien-Inalsingh C, Chalifoux M, Wing M, Scott E, Fidler K, Swift I, Maidment B, Knight SJ, Davies KE, White BN. Trinucleotide repeat expansion in the FRAXE locus is not common among institutionalized individuals with non-specific developmental disabilities. American Journal of Medical Genetics. 64: 420-3. PMID 8844096 DOI: 10.1002/(SICI)1096-8628(19960809)64:2<420::AID-AJMG37>3.0.CO;2-F  1
1996 Rodrigues NR, Talbot K, Davies KE. Molecular genetics of autosomal recessive spinal muscular atrophy. Molecular Medicine (Cambridge, Mass.). 2: 400-4. PMID 8827710  1
1996 Chakrabarti L, Knight SJ, Flannery AV, Davies KE. A candidate gene for mild mental handicap at the FRAXE fragile site. Human Molecular Genetics. 5: 275-82. PMID 8824884 DOI: 10.1093/hmg/5.2.275  1
1996 Coleman MP, Ambrose HJ, Carrel L, Németh AH, Willard HF, Davies KE. A novel gene, DXS8237E, lies within 20 kb upstream of UBE1 in Xp11.23 and has a different X inactivation status. Genomics. 31: 135-8. PMID 8808293 DOI: 10.1006/geno.1996.0022  1
1996 Rowe PS, Goulding JN, Francis F, Oudet C, Econs MJ, Hanauer A, Lehrach H, Read AP, Mountford RC, Summerfield T, Weissenbach J, Fraser W, Drezner MK, Davies KE, O'Riordan JL. The gene for X-linked hypophosphataemic rickets maps to a 200-300kb region in Xp22.1, and is located on a single YAC containing a putative vitamin D response element (VDRE). Human Genetics. 97: 345-52. PMID 8786079  1
1996 Morrison KE, Qureshi SJ, Anderson S, Borrett JP, Theodosiou A, Rodrigues N, Blake D, Nesbit A, Davies KE, Porteous DJ, Brookes AJ. Novel transcribed sequences represented in the complex genomic region 5q13. Biochimica Et Biophysica Acta. 1308: 97-102. PMID 8764824 DOI: 10.1016/0167-4781(96)00097-8  1
1996 Theodosiou AM, Rodrigues NR, Nesbit MA, Ambrose HJ, Paterson H, McLellan-Arnold E, Boyd Y, Leversha MA, Owen N, Blake DJ, Ashworth A, Davies KE. A member of the MAP kinase phosphatase gene family in mouse containing a complex trinucleotide repeat in the coding region. Human Molecular Genetics. 5: 675-84. PMID 8733137  0.56
1996 Knight SJ, Ritchie RJ, Chakrabarti L, Cross G, Taylor GR, Mueller RF, Hurst J, Paterson J, Yates JR, Dow DJ, Davies KE. A study of FRAXE in mentally retarded individuals referred for fragile X syndrome (FRAXA) testing in the United Kingdom. American Journal of Human Genetics. 58: 906-13. PMID 8651274  1
1996 Dennis CL, Tinsley JM, Deconinck AE, Davies KE. Molecular and functional analysis of the utrophin promoter. Nucleic Acids Research. 24: 1646-52. PMID 8649981 DOI: 10.1093/nar/24.9.1646  1
1996 Blake DJ, Nawrotzki R, Peters MF, Froehner SC, Davies KE. Isoform diversity of dystrobrevin, the murine 87-kDa postsynaptic protein. The Journal of Biological Chemistry. 271: 7802-10. PMID 8631824 DOI: 10.1074/jbc.271.13.7802  1
1995 Winder SJ, Hemmings L, Bolton SJ, Maciver SK, Tinsley JM, Davies KE, Critchley DR, Kendrick-Jones J. Calmodulin regulation of utrophin actin binding. Biochemical Society Transactions. 23: 397S. PMID 8566285  1
1995 Nguyen TM, Helliwell TR, Simmons C, Winder SJ, Kendrick-Jones J, Davies KE, Morris GE. Full-length and short forms of utrophin, the dystrophin-related protein. Febs Letters. 358: 262-6. PMID 7843413 DOI: 10.1016/0014-5793(94)01441-3  1
1995 Blake DJ, Tinsley JM, Davies KE, Knight AE, Winder SJ, Kendrick-Jones J. Coiled-coil regions in the carboxy-terminal domains of dystrophin and related proteins: potentials for protein-protein interactions. Trends in Biochemical Sciences. 20: 133-5. PMID 7770909 DOI: 10.1016/S0968-0004(00)88986-0  1
1995 Partridge TA, Davies KE. Myoblast-based gene therapies. British Medical Bulletin. 51: 123-37. PMID 7767639  1
1995 Daniels RJ, Campbell L, Rodrigues NR, Francis MJ, Morrison KE, McLean M, MacKenzie A, Ignatius J, Dubowitz V, Davies KE. Genomic rearrangements in childhood spinal muscular atrophy: linkage disequilibrium with a null allele. Journal of Medical Genetics. 32: 93-6. PMID 7760328  1
1995 Brown CJ, Miller AP, Carrel L, Rupert JL, Davies KE, Willard HF. The DXS423E gene in Xp11.21 escapes X chromosome inactivation. Human Molecular Genetics. 4: 251-5. PMID 7757075 DOI: 10.1093/hmg/4.2.251  1
1995 Rocques PJ, Clark J, Ball S, Crew J, Gill S, Christodoulou Z, Borts RH, Louis EJ, Davies KE, Cooper CS. The human SB1.8 gene (DXS423E) encodes a putative chromosome segregation protein conserved in lower eukaryotes and prokaryotes. Human Molecular Genetics. 4: 243-9. PMID 7757074 DOI: 10.1093/HMG/4.2.243  1
1995 Winder SJ, Hemmings L, Maciver SK, Bolton SJ, Tinsley JM, Davies KE, Critchley DR, Kendrick-Jones J. Utrophin actin binding domain: analysis of actin binding and cellular targeting. Journal of Cell Science. 108: 63-71. PMID 7738117  1
1995 Blake DJ, Schofield JN, Zuellig RA, Górecki DC, Phelps SR, Barnard EA, Edwards YH, Davies KE. G-utrophin, the autosomal homologue of dystrophin Dp116, is expressed in sensory ganglia and brain. Proceedings of the National Academy of Sciences of the United States of America. 92: 3697-701. PMID 7731967  1
1995 Rodrigues NR, Campbell L, Owen N, Rodeck CH, Davies KE. Prenatal diagnosis of spinal muscular atrophy by gene deletion analysis. Lancet. 345: 1049. PMID 7723516  0.56
1995 Dubowitz V, Daniels RJ, Davies KE. Olivopontocerebellar hypoplasia with anterior horn cell involvement (SMA) does not localize to chromosome 5q. Neuromuscular Disorders : Nmd. 5: 25-9. PMID 7719137 DOI: 10.1016/0960-8966(94)00043-9  1
1995 Slaney SF, Wilkie AO, Hirst MC, Charlton R, McKinley M, Pointon J, Christodoulou Z, Huson SM, Davies KE. DNA testing for fragile X syndrome in schools for learning difficulties. Archives of Disease in Childhood. 72: 33-7. PMID 7717734  0.36
1995 Rodrigues NR, Owen N, Talbot K, Ignatius J, Dubowitz V, Davies KE. Deletions in the survival motor neuron gene on 5q13 in autosomal recessive spinal muscular atrophy. Human Molecular Genetics. 4: 631-4. PMID 7633412 DOI: 10.1093/hmg/4.4.631  1
1995 Davies KE, Tinsley JM, Blake DJ. Molecular analysis of Duchenne muscular dystrophy: past, present, and future. Annals of the New York Academy of Sciences. 758: 287-96. PMID 7625698 DOI: 10.1111/j.1749-6632.1995.tb24834.x  1
1995 Flannery AV, Hirst MC, Knight SJ, Ritchie RJ, Davies KE. The fragile X syndrome. Biochimica Et Biophysica Acta. 1271: 293-303. PMID 7605796 DOI: 10.1016/0925-4439(95)00046-7  1
1995 Jasmin BJ, Alameddine H, Lunde JA, Stetzkowski-Marden F, Collin H, Tinsley JM, Davies KE, Tomé FM, Parry DJ, Cartaud J. Expression of utrophin and its mRNA in denervated mdx mouse muscle. Febs Letters. 374: 393-8. PMID 7589578 DOI: 10.1016/0014-5793(95)01131-W  1
1995 Francis MJ, Nesbit MA, Theodosiou AM, Rodrigues NR, Campbell L, Christodoulou Z, Qureshi SJ, Porteous DJ, Brookes AJ, Davies KE. Mapping of retrotransposon sequences in the unstable region surrounding the spinal muscular atrophy locus in 5q13. Genomics. 27: 366-9. PMID 7558009 DOI: 10.1006/geno.1995.1059  0.56
1994 Blake DJ, Tinsley JM, Davies KE. The emerging family of dystrophin-related proteins. Trends in Cell Biology. 4: 19-23. PMID 14731825 DOI: 10.1016/0962-8924(94)90034-5  1
1994 Mérette C, Brzustowicz LM, Daniels RJ, Davies KE, Gilliam TC, Melki J, Munnich A, Pericak-Vance MA, Siddique T, Voosen B. An investigation of genetic heterogeneity and linkage disequilibrium in 161 families with spinal muscular atrophy. Genomics. 21: 27-33. PMID 8088801 DOI: 10.1006/geno.1994.1220  1
1994 Tinsley JM, Blake DJ, Zuellig RA, Davies KE. Increasing complexity of the dystrophin-associated protein complex. Proceedings of the National Academy of Sciences of the United States of America. 91: 8307-13. PMID 8078878  1
1994 Knight SJ, Voelckel MA, Hirst MC, Flannery AV, Moncla A, Davies KE. Triplet repeat expansion at the FRAXE locus and X-linked mild mental handicap. American Journal of Human Genetics. 55: 81-6. PMID 8023854  1
1994 Blair HJ, Hirst MC, MacKinnon R, Davies KE, Boyd Y. Evaluation of human microdissection clones from the FRAXA region as tools for comparative mapping in the mouse: isolation of a conserved genomic clone close to FMR1. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 5: 584-7. PMID 8000145 DOI: 10.1007/BF00354936  1
1994 Schofield JN, Blake DJ, Simmons C, Morris GE, Tinsley JM, Davies KE, Edwards YH. Apo-dystrophin-1 and apo-dystrophin-2, products of the Duchenne muscular dystrophy locus: expression during mouse embryogenesis and in cultured cell lines. Human Molecular Genetics. 3: 1309-16. PMID 7987307  1
1994 Theodosiou AM, Morrison KE, Nesbit AM, Daniels RJ, Campbell L, Francis MJ, Christodoulou Z, Davies KE. Complex repetitive arrangements of gene sequence in the candidate region of the spinal muscular atrophy gene in 5q13. American Journal of Human Genetics. 55: 1209-17. PMID 7977382  1
1994 Hirst MC, Grewal PK, Davies KE. Precursor arrays for triplet repeat expansion at the fragile X locus. Human Molecular Genetics. 3: 1553-60. PMID 7833910 DOI: 10.1093/hmg/3.9.1553  1
1993 Tinsley JM, Blake DJ, Davies KE. Apo-dystrophin-3: a 2.2kb transcript from the DMD locus encoding the dystrophin glycoprotein binding site. Human Molecular Genetics. 2: 521-4. PMID 8518789 DOI: 10.1093/hmg/2.5.521  1
1993 Karpati G, Carpenter S, Morris GE, Davies KE, Guerin C, Holland P. Localization and quantitation of the chromosome 6-encoded dystrophin-related protein in normal and pathological human muscle. Journal of Neuropathology and Experimental Neurology. 52: 119-28. PMID 8440993  1
1993 Hirst MC, Knight SJ, Christodoulou Z, Grewal PK, Fryns JP, Davies KE. Origins of the fragile X syndrome mutation. Journal of Medical Genetics. 30: 647-50. PMID 8411050  0.36
1993 Clerk A, Morris GE, Dubowitz V, Davies KE, Sewry CA. Dystrophin-related protein, utrophin, in normal and dystrophic human fetal skeletal muscle. The Histochemical Journal. 25: 554-61. PMID 8407365 DOI: 10.1007/BF00173053  1
1993 Thompson TG, Morrison KE, Kleyn P, Bengtsson U, Gilliam TC, Davies KE, Wasmuth JJ, McPherson JD. High resolution physical map of the region surrounding the spinal muscular atrophy gene. Human Molecular Genetics. 2: 1169-76. PMID 8401498 DOI: 10.1093/hmg/2.8.1169  1
1993 Morrison KE, Daniels RJ, Suthers GK, Flynn GA, Francis MJ, Grewal PK, Dennis C, Buckle V, Ignatius J, Dubowitz V. Two novel microsatellite markers for prenatal prediction of spinal muscular atrophy (SMA). Human Genetics. 92: 133-8. PMID 8370578 DOI: 10.1007/BF00219680  1
1993 Tinsley JM, Blake DJ, Pearce M, Knight AE, Kendrick-Jones J, Davies KE. Dystrophin and related proteins. Current Opinion in Genetics & Development. 3: 484-90. PMID 8353425 DOI: 10.1016/0959-437X(93)90124-8  1
1993 Love DR, Byth BC, Tinsley JM, Blake DJ, Davies KE. Dystrophin and dystrophin-related proteins: a review of protein and RNA studies. Neuromuscular Disorders : Nmd. 3: 5-21. PMID 8329888 DOI: 10.1016/0960-8966(93)90037-K  1
1993 Le TT, Nguyen TM, Love DR, Helliwell TR, Davies KE, Morris GE. Monoclonal antibodies against the muscle-specific N-terminus of dystrophin: characterization of dystrophin in a muscular dystrophy patient with a frameshift deletion of exons 3-7. American Journal of Human Genetics. 53: 131-9. PMID 8317478  1
1993 Knox-Macaulay HH, Bashawri L, Davies KE. X linked recessive thrombocytopenia. Journal of Medical Genetics. 30: 968-9. PMID 8301658  1
1993 Pearce M, Blake DJ, Tinsley JM, Byth BC, Campbell L, Monaco AP, Davies KE. The utrophin and dystrophin genes share similarities in genomic structure. Human Molecular Genetics. 2: 1765-72. PMID 8281135 DOI: 10.1093/hmg/2.11.1765  1
1993 Morrison KE, Daniels RJ, Campbell L, McPherson J, Davies KE. Dinucleotide repeat polymorphism proximal to the spinal muscular atrophy region at D5S681. Human Molecular Genetics. 2: 1753. PMID 8268953 DOI: 10.1093/hmg/2.10.1753  1
1993 Gangadharan U, Maconochie MK, Davies KE, Brown SD. Isolation and characterization of a genomic clone from the murine utrophin locus. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 4: 608-11. PMID 8268660 DOI: 10.1007/BF00361394  1
1993 Tinsley JM, Davies KE. Utrophin: a potential replacement for dystrophin? Neuromuscular Disorders : Nmd. 3: 537-9. PMID 8186707 DOI: 10.1016/0960-8966(93)90111-V  1
1993 Rowe PS, Goulding J, Read A, Mountford R, Hanauer A, Oudet C, Whyte MP, Meier-Ewert S, Lehrach H, Davies KE. New markers for linkage analysis of X-linked hypophosphataemic rickets. Human Genetics. 91: 571-5. PMID 8101831 DOI: 10.1007/BF00205082  1
1993 Németh AH, Hunter N, Coleman MP, Borts RH, Louis EJ, Davies KE. Rescue of a single yeast artificial chromosome from a cotransformation event utilizing segregation at meiosis. Genetic Analysis, Techniques and Applications. 10: 123-7. PMID 8043304  0.36
1992 Dunckley MG, Love DR, Davies KE, Walsh FS, Morris GE, Dickson G. Retroviral-mediated transfer of a dystrophin minigene into mdx mouse myoblasts in vitro. Febs Letters. 296: 128-34. PMID 1733767 DOI: 10.1016/0014-5793(92)80363-L  1
1992 Laval SH, Blair HJ, Hirst MC, Davies KE, Boyd Y. Mapping of FMR1, the gene implicated in fragile X-linked mental retardation, on the mouse X chromosome. Genomics. 12: 818-21. PMID 1572655 DOI: 10.1016/0888-7543(92)90315-J  1
1992 Suthers GK, Davies KE. Phenotypic heterogeneity and the single gene. American Journal of Human Genetics. 50: 887-91. PMID 1570841  1
1992 Morrison KE, Daniels RJ, Suthers GK, Flynn GA, Francis MJ, Buckle VJ, Davies KE. High-resolution genetic map around the spinal muscular atrophy (SMA) locus on chromosome 5. American Journal of Human Genetics. 50: 520-7. PMID 1539593  1
1992 Davies KE. Human genetics. The costs of instability. Nature. 356: 15. PMID 1538769 DOI: 10.1038/356015a0  1
1992 Hirst MC, Knight SM, Nakahori Y, Roche A, Davies KE. Molecular analysis of the fragile X syndrome. Journal of Inherited Metabolic Disease. 15: 532-8. PMID 1528014 DOI: 10.1007/BF01799612  1
1992 Helliwell TR, Man NT, Morris GE, Davies KE. The dystrophin-related protein, utrophin, is expressed on the sarcolemma of regenerating human skeletal muscle fibres in dystrophies and inflammatory myopathies. Neuromuscular Disorders : Nmd. 2: 177-84. PMID 1483043 DOI: 10.1016/0960-8966(92)90004-P  1
1992 Tinsley JM, Blake DJ, Roche A, Fairbrother U, Riss J, Byth BC, Knight AE, Kendrick-Jones J, Suthers GK, Love DR. Primary structure of dystrophin-related protein. Nature. 360: 591-3. PMID 1461283 DOI: 10.1038/360591a0  1
1992 Suthers GK, Huson SM, Davies KE. Instability versus predictability: the molecular diagnosis of myotonic dystrophy. Journal of Medical Genetics. 29: 761-5. PMID 1453422  1
1992 Nguyen TM, Le TT, Blake DJ, Davies KE, Morris GE. Utrophin, the autosomal homologue of dystrophin, is widely-expressed and membrane-associated in cultured cell lines. Febs Letters. 313: 19-22. PMID 1426262 DOI: 10.1016/0014-5793(92)81174-K  1
1992 Knight SJ, Hirst MC, Davies KE. Molecular analysis of the fragile X syndrome. Disease Markers. 10: 1-5. PMID 1424438  1
1992 Hirst MC, Bassett JH, Roche A, Davies KE. Preparation of radiolabelled hybridization probes by STS labelling. Trends in Genetics : Tig. 8: 6-7. PMID 1369736 DOI: 10.1016/0168-9525(92)90005-O  1
1992 Byth BC, Love DR, Murray JC, Davies KE. Localization of two new DNA markers on the linkage map of human chromosome 6q. Cytogenetics and Cell Genetics. 60: 216-8. PMID 1354595 DOI: 10.1159/000133342  1
1992 Rowe PS, Read AP, Mountford R, Benham F, Kruse TA, Camerino G, Davies KE, O'Riordan JL. Three DNA markers for hypophosphataemic rickets. Human Genetics. 89: 539-42. PMID 1353055 DOI: 10.1007/BF00219180  1
1992 Wöhrle D, Hirst MC, Kennerknecht I, Davies KE, Steinbach P. Genotype mosaicism in fragile X fetal tissues. Human Genetics. 89: 114-6. PMID 1349561 DOI: 10.1007/BF00207057  1
1992 Hirst MC, Knight SJ, Bell MV, Super M, Davies KE. The fragile X syndrome. Clinical Science (London, England : 1979). 83: 255-64. PMID 1327643  1
1992 Blake DJ, Love DR, Tinsley J, Morris GE, Turley H, Gatter K, Dickson G, Edwards YH, Davies KE. Characterization of a 4.8kb transcript from the Duchenne muscular dystrophy locus expressed in Schwannoma cells. Human Molecular Genetics. 1: 103-9. PMID 1301145 DOI: 10.1093/hmg/1.2.103  1
1992 Wells DJ, Wells KE, Walsh FS, Davies KE, Goldspink G, Love DR, Chan-Thomas P, Dunckley MG, Piper T, Dickson G. Human dystrophin expression corrects the myopathic phenotype in transgenic mdx mice. Human Molecular Genetics. 1: 35-40. PMID 1301134  1
1992 Munsat TL, Davies KE. International SMA consortium meeting. (26-28 June 1992, Bonn, Germany). Neuromuscular Disorders : Nmd. 2: 423-8. PMID 1300191 DOI: 10.1016/S0960-8966(06)80015-5  1
1991 Love DR, England SB, Speer A, Marsden RF, Bloomfield JF, Roche AL, Cross GS, Mountford RC, Smith TJ, Davies KE. Sequences of junction fragments in the deletion-prone region of the dystrophin gene. Genomics. 10: 57-67. PMID 2045110 DOI: 10.1016/0888-7543(91)90484-V  1
1991 Ledbetter SA, Schwartz CE, Davies KE, Ledbetter DH. New somatic cell hybrids for physical mapping in distal Xq and the fragile X region American Journal of Medical Genetics. 38: 418-420. PMID 2018083 DOI: 10.1002/ajmg.1320380254  1
1991 Love DR, Morris GE, Ellis JM, Fairbrother U, Marsden RF, Bloomfield JF, Edwards YH, Slater CP, Parry DJ, Davies KE. Tissue distribution of the dystrophin-related gene product and expression in the mdx and dy mouse. Proceedings of the National Academy of Sciences of the United States of America. 88: 3243-7. PMID 2014247  1
1991 Passos-Bueno MR, Terwilliger J, Ott J, Vainzof M, Love DR, Davies KE, Zatz M. Linkage analysis in families with autosomal recessive limb-girdle muscular dystrophy (LGMD) and 6q probes flanking the dystrophin-related sequence. American Journal of Medical Genetics. 38: 140-6. PMID 2012126 DOI: 10.1002/ajmg.1320380130  1
1991 Dickson G, Love DR, Davies KE, Wells KE, Piper TA, Walsh FS. Human dystrophin gene transfer: production and expression of a functional recombinant DNA-based gene. Human Genetics. 88: 53-8. PMID 1959926 DOI: 10.1007/BF00204929  1
1991 Acsadi G, Dickson G, Love DR, Jani A, Walsh FS, Gurusinghe A, Wolff JA, Davies KE. Human dystrophin expression in mdx mice after intramuscular injection of DNA constructs. Nature. 352: 815-8. PMID 1881437 DOI: 10.1038/352815a0  1
1991 Davies KE, Thomas NH, Daniels RJ, Dubowitz V. Molecular studies of spinal muscular atrophy. Neuromuscular Disorders : Nmd. 1: 83-5. PMID 1822785 DOI: 10.1016/0960-8966(91)90053-U  1
1991 Coleman MP, Murray JC, Willard HF, Nolan KF, Reid KB, Blake DJ, Lindsay S, Bhattacharya SS, Wright A, Davies KE. Genetic and physical mapping around the properdin P gene. Genomics. 11: 991-6. PMID 1783405 DOI: 10.1016/0888-7543(91)90024-9  0.32
1991 Love DR, Flint TJ, Genet SA, Middleton-Price HR, Davies KE. Becker muscular dystrophy patient with a large intragenic dystrophin deletion: implications for functional minigenes and gene therapy. Journal of Medical Genetics. 28: 860-4. PMID 1757963  1
1991 Hirst MC, Nakahori Y, Knight SJ, Schwartz C, Thibodeau SN, Roche A, Flint TJ, Connor JM, Fryns JP, Davies KE. Genotype prediction in the fragile X syndrome. Journal of Medical Genetics. 28: 824-9. PMID 1757957  1
1991 Nguyen TM, Ellis JM, Love DR, Davies KE, Gatter KC, Dickson G, Morris GE. Localization of the DMDL gene-encoded dystrophin-related protein using a panel of nineteen monoclonal antibodies: presence at neuromuscular junctions, in the sarcolemma of dystrophic skeletal muscle, in vascular and other smooth muscles, and in proliferating brain cell lines. The Journal of Cell Biology. 115: 1695-700. PMID 1757469  1
1991 Lafrenière RG, Brown CJ, Powers VE, Carrel L, Davies KE, Barker DF, Willard HF. Physical mapping of 60 DNA markers in the p21.1----q21.3 region of the human X chromosome. Genomics. 11: 352-63. PMID 1685139 DOI: 10.1016/0888-7543(91)90143-3  1
1991 Byth BC, Love DR, Passos-Bueno MR, Davies KE. A new DNA marker, D6S129, identifies a HindIII polymorphism on chromosome 6q. Nucleic Acids Research. 19: 4310. PMID 1678512 DOI: 10.1093/nar/19.15.4310-a  1
1991 Delisi LE, Crow TJ, Davies KE, Terwilliger JD, Ott J, Ram R, Flint T, Boccio A. No genetic linkage detected for schizophrenia to Xq27-q28. The British Journal of Psychiatry : the Journal of Mental Science. 158: 630-4. PMID 1677599  1
1991 Davies KE, Mandel JL, Monaco AP, Nussbaum RL, Willard HF. Report of the committee on the genetic constitution of the X chromosome Cytogenetics and Cell Genetics. 58: 853-966. DOI: 10.1159/000132662  1
1991 Davies KE, Craig IW. Report of the second X Chromosome Workshop Oxford, UK, January 6-7, 1991 Genomics. 10: 842-846. DOI: 10.1016/0888-7543(91)90473-R  1
1990 England SB, Nicholson LVB, Johnson MA, Forrest SM, Love DR, Zubrzycka-Gaarn EE, Bulman DE, Harris JB, Davies KE. Very mild muscular dystrophy associated with the deletion of 46% of dystrophin Nature. 343: 180-182. PMID 2404210 DOI: 10.1038/343180A0  1
1990 Brzustowicz LM, Lehner T, Castilla LH, Penchaszadeh GK, Wilhelmsen KC, Daniels R, Davies KE, Leppert M, Ziter F, Wood D, Dubowitz V, Zerres K, Hausmanowa-Petrusewicz I, Ott J, Munsat TL, et al. Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q1 1.2-13.3 Nature. 344: 540-541. PMID 2320125 DOI: 10.1038/344540A0  1
1990 Love DR, Flint TJ, Marsden RF, Bloomfield JF, Daniels RJ, Forrest SM, Gabrielli O, Giorgi P, Novelli G, Davies KE. Characterization of deletions in the dystrophin gene giving mild phenotypes American Journal of Medical Genetics. 37: 136-142. PMID 2240031 DOI: 10.1002/ajmg.1320370132  1
1990 Buckle VJ, Guenet JL, Simon-Chazottes D, Love DR, Davies KE. Localisation of a dystrophin-related autosomal gene to 6q24 in man, and to mouse chromosome 10 in the region of the dystrophia muscularis (dy) locus Human Genetics. 85: 324-326. PMID 2203673 DOI: 10.1007/BF00206755  1
1990 Passos-Bueno MR, Rapaport D, Love D, Flint T, Bortolini ER, Zatz M, Davies KE. Screening of deletions in the dystrophin gene with the cDNA probes Cf23a, Cf56a, and Cf115. Journal of Medical Genetics. 27: 145-50. PMID 2182872 DOI: 10.1136/jmg.27.3.145  1
1990 Love DR, Bloomfield JF, Kenwrick SJ, Yates JRW, Davies KE. Physical mapping distal to the DMD locus Genomics. 8: 106-112. PMID 2081587 DOI: 10.1016/0888-7543(90)90231-I  1
1990 Thakker RV, Davies KE, Read AP, Tippett P, Wooding C, Flint T, Woob S, Kruse TA, Whyte MP, O'Riordan JLH. Linkage analysis of two cloned DNA sequences, DXS197 and DXS207, in hypophosphatemic rickets families Genomics. 8: 189-193. PMID 1979046 DOI: 10.1016/0888-7543(90)90271-U  1
1990 Thakker RV, Davies KE, Whyte MP, Wooding C, O'Riordan JLH. Mapping the gene causing X-linked recessive idiopathic hypoparathyroidism to Xq26-Xq27 by linkage studies Journal of Clinical Investigation. 86: 40-45. PMID 1973175 DOI: 10.1172/JCI114712  1
1990 Gilliam TC, Brzustowicz LM, Castilla LH, Lehner T, Penchaszadeh GK, Daniels RJ, Byth BC, Knowles J, Hislop JE, Shapira Y, Dubowitz V, Munsat TL, Ott J, Davies KE. Genetic homogeneity between acute and chronic forms of spinal muscular atrophy Nature. 345: 823-825. PMID 1972783 DOI: 10.1038/345823A0  1
1989 Winter RM, Davies KE, Bell MV, Huson SM, Patterson MN. MASA syndrome: further clinical delineation and chromosomal localisation Human Genetics. 82: 367-370. PMID 2737668 DOI: 10.1007/BF00273999  1
1989 Hirst MC, Watson JeV, Davies KE. The use of filter-bound DNA fragments as templates for radiolabelling by random priming Nucleic Acids Research. 17: 2872. PMID 2717420 DOI: 10.1093/nar/17.7.2872  1
1989 Love DR, Forrest SM, Smith TJ, England S, Flint T, Davies KE, Speer A. Molecular analysis of duschenne and becker muscular dystrophies British Medical Bulletin. 45: 659-680. PMID 2688822 DOI: 10.1093/OXFORDJOURNALS.BMB.A072351  1
1989 Suthers GK, Davies KE, Baker E, Sutherland GR. Taqi RFLP identified by probe 1A1 [DXS374] at Xq28 Nucleic Acids Research. 17: 8901. PMID 2573886 DOI: 10.1093/nar/17.21.8901  1
1989 Bell MV, Patterson MN, Dorkins HR, Davies KE. Physical mapping of DXS134 close to the DXS52 locus Human Genetics. 82: 27-30. PMID 2565864 DOI: 10.1007/BF00288266  1
1989 Clarke A, Davies KE, Gardner-Medwin D, Burn J, Hudgson P. Xp21 DNA PROBE IN DIAGNOSIS OF MUSCULAR DYSTROPHY AND SPINAL MUSCULAR ATROPHY The Lancet. 333: 443. PMID 2563824 DOI: 10.1016/S0140-6736(89)90044-5  1
1989 Love DR, Hill DF, Dickson G, Spurr NK, Byth BC, Marsden RF, Walsh FS, Edwards YH, Davies KE. An autosomal transcript in skeletal muscle with homology to dystrophin. Nature. 339: 55-8. PMID 2541343 DOI: 10.1038/339055a0  1
1988 Forrest SM, Cross GS, Flint T, Speer A, Robson KJH, Davies KE. Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies Genomics. 2: 109-114. PMID 3410474 DOI: 10.1016/0888-7543(88)90091-2  1
1988 Kenwrick SJ, Smith TJ, England S, Collins F, Davies KE. Localisation of the endpoints of deletions in the 5′ region of the duchenne gene using a sequence isolated by chromosome jumping Nucleic Acids Research. 16: 1305-1317. PMID 3347492 DOI: 10.1093/nar/16.4.1305  1
1988 Read AP, Mountford RC, Forrest SM, Kenwrick SJ, Davies KE, Harris R. Patterns of exon deletions in Duchenne and Becker muscular dystrophy Human Genetics. 80: 152-156. PMID 3169738 DOI: 10.1007/BF00702859  1
1988 Davies KE, Smith TJ, Bundey S, Read AP, Flint T, Bell M, Speer A. Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosome Journal of Medical Genetics. 25: 9-13. PMID 3162536 DOI: 10.1136/jmg.25.1.9  1
1988 Dickson G, Pizzey JA, Elsom VE, Love D, Davies KE, Walsh FS. Distinct dystrophin mRNA species are expressed in embryonic and adult mouse skeletal muscle. Febs Letters. 242: 47-52. PMID 3060377 DOI: 10.1016/0014-5793(88)80982-7  1
1988 Ryder-Cook AS, Sicinski P, Thomas K, Davies KE, Worton RG, Barnard EA, Darlison MG, Barnard PJ. Localization of the mdx mutation within the mouse dystrophin gene. The Embo Journal. 7: 3017-21. PMID 2903046  1
1987 Davies KE, Gusella JF, Tsui LC, Williamson R, Page DC, Ferguson-Smith MA. Valuable libraries. Nature. 326: 124. PMID 3821885 DOI: 10.1038/326124e0  0.84
1987 Smith TJ, Forrest SM, Cross GS, Davies KE. Duchenne and becker muscular dystrophy mutations: Analysis using 2.6 kb of muscle cDNA from the 5′ end of the gene Nucleic Acids Research. 15: 9761-9769. PMID 3697082 DOI: 10.1093/nar/15.23.9761  1
1987 Davies KE, Mandel JL, Weissenbach J, Fellous M. Report of the committee on the genetic constitution of the X and Y chromosomes. Cytogenetics and Cell Genetics. 46: 277-315. PMID 3507278 DOI: 10.1159/000132481  1
1987 Forrest SM, Smith TJ, Cross GS, Read AP, Thomas NS, Mountford RC, Harper PS, Geirsson RT, Davies KE. Effective strategy for prenatal prediction of Duchenne and Becker muscular dystrophy. Lancet (London, England). 2: 1294-7. PMID 2890901 DOI: 10.1016/S0140-6736(87)91192-5  1
1987 Thakker RV, Read AP, Davies KE, Whyte MP, Weksberg R, Glorieux F, Davies M, Mountford RC, Harris R, King A, Kim GS, Fraser D, Kooh SW, O'Riordan JLH. Bridging markers defining the map position of X linked hypophosphataemic rickets Journal of Medical Genetics. 24: 756-760. PMID 2828625 DOI: 10.1136/jmg.24.12.756  1
1987 Robbins TP, Scambler PJ, Davies KE, Williamson R. An anonymous clone E9pl (D4S112) localised to 4q26-qter detects an Msp I RFLP. Nucleic Acids Research. 15: 8122. PMID 2444927 DOI: 10.1093/nar/15.19.8122  1
1986 Davies KE. DNA studies of X-linked mental retardation associated with a fragile site at Xq27 American Journal of Medical Genetics. 23: 633-642. PMID 3513572 DOI: 10.1002/AJMG.1320230157  1
1986 Schwartz M, Christensen E, Christensen NC, Skovby F, Davies KE, Old JM. Detection and exclusion of carriers of ornithine transcarbamylase deficiency by RFLP analysis. Clinical Genetics. 29: 449-52. PMID 3017613 DOI: 10.1111/j.1399-0004.1986.tb00520.x  1
1986 Read AP, Thakker RV, Davies KE, Mountford RC, Brenton DP, Davies M, Glorieux F, Harris R, Hendy GN, King A, McGlade S, Peacock CJ, Smith R, O'Riordan JLH. Mapping of human X-linked hypophosphataemic rickets by multilocus linkage analysis Human Genetics. 73: 267-270. PMID 3015770 DOI: 10.1007/BF00401242  1
1986 Moss PAH, Davies KE, Boni C, Mallet J, Reeders ST. Linkage of tyrosine hydroxylase to four other markers on the short arm of chromosome 11 Nucleic Acids Research. 14: 9927-9932. PMID 2880337 DOI: 10.1093/nar/14.24.9927  1
1986 Lindlof M, Kaariainen H, Davies KE, De La Chapelle A. Carrier detection and prenatal diagnosis in X linked muscular dystrophy using restriction fragment length polymorphisms Journal of Medical Genetics. 23: 560-572. PMID 2879928 DOI: 10.1136/jmg.23.6.560  1
1986 Old JM, Davies KE. Prenatal diagnosis of Duchenne muscular dystrophy by DNA analysis Journal of Medical Genetics. 23: 556-559. PMID 2879927 DOI: 10.1136/jmg.23.6.556  1
1986 Davies KE, Williamson R. Towards a complete linkage map of the human X chromosome. Horizons in Biochemistry and Biophysics. 8: 1-50. PMID 2875929  1
1985 Pembrey ME, Winter RM, Davies KE. A premutation that generates a defect at crossing over explains the inheritance of fragile X mental retardation American Journal of Medical Genetics. 21: 709-717. PMID 4040705 DOI: 10.1002/AJMG.1320210413  1
1985 Donald JA, Wallis SC, Kessling A, Tippett P, Robson EB, Ball S, Davies KE, Scambler P, Berg K, Heiberg A. Linkage relationships of the gene for apolipoprotein CII with loci on chromosome 19. Human Genetics. 69: 39-43. PMID 3855405 DOI: 10.1007/BF00295527  0.36
1985 Davies KE, Briand P, Ionasescu V, Ionasescu G, Williamson R, Brown C, Cavard C, Cathelineau L. Gene for OTC: characterisation and linkage to Duchenne muscular dystrophy. Nucleic Acids Research. 13: 155-65. PMID 3839070  0.84
1985 Reeders ST, Breuning MH, Davies KE, Nicholls RD, Jarman AP, Higgs DR, Pearson PL, Weatherall DJ. A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16. Nature. 317: 542-4. PMID 2995836 DOI: 10.1038/317542a0  1
1985 Davies KE. Molecular genetics of the human X chromosome Journal of Medical Genetics. 22: 243-249. PMID 2995673 DOI: 10.1136/jmg.22.4.243  1
1985 Brown CS, Thomas NS, Sarfarazi M, Davies KE, Kunkel L, Pearson PL, Kingston HM, Shaw DJ, Harper PS. Genetic linkage relationships of seven DNA probes with Duchenne and Becker muscular dystrophy. Human Genetics. 71: 62-74. PMID 2993158 DOI: 10.1007/BF00295671  1
1985 Ingle C, Williamson R, de la Chapelle A, Herva RR, Haapala K, Bates G, Willard HF, Pearson P, Davies KE. Mapping DNA sequences in a human X-chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutation. American Journal of Human Genetics. 37: 451-62. PMID 2988331  1
1985 Scambler P, Robbins T, Gilliam C, Boylston A, Tippett P, Williamson R, Davies KE. Linkage studies between polymorphic markers on chromosome 4 and cystic fibrosis. Human Genetics. 69: 250-4. PMID 2984105  0.84
1985 Old JM, Briand PL, Purvis-Smith S, Howard NJ, Wilcken B, Hammond J, Pearson P, Cathelineau L, Williamson R, Davies KE. Prenatal exclusion of ornithine transcarbamylase deficiency by direct gene analysis. Lancet (London, England). 1: 73-5. PMID 2857026  0.84
1984 Pembrey ME, Davies KE, Winter RM, Elles RG, Williamson R, Fazzone TA, Walker C. Clinical use of DNA markers linked to the gene for Duchenne muscular dystrophy. Archives of Disease in Childhood. 59: 208-16. PMID 6585184  0.84
1984 Hartley DA, Davies KE, Drayna D, White RL, Williamson R. A cytological map of the human X chromosome--evidence for non-random recombination. Nucleic Acids Research. 12: 5277-85. PMID 6547776 DOI: 10.1093/nar/12.13.5277  1
1984 Williamson R, Davies KE, Donald J, Gilliam C, Wallis S, Humphries S. The implications of genetic variation in human pathology. Biochemical Society Symposium. 49: 183-8. PMID 6400491  1
1984 Rappold GA, Cremer T, Hager HD, Davies KE, Müller CR, Yang T. Sex chromosome positions in human interphase nuclei as studied by in situ hybridization with chromosome specific DNA probes Human Genetics. 67: 317-325. PMID 6336321 DOI: 10.1007/BF00291361  1
1984 Wieacker P, Davies KE, Cooke HJ, Pearson PL, Williamson R, Bhattacharya S, Zimmer J, Ropers HH. Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybrids. American Journal of Human Genetics. 36: 265-76. PMID 6324578  0.84
1984 Davies KE, Harper K, Bonthron D, Krumlauf R, Polkey A, Pembrey ME, Williamson R. Use of a chromosome 21 cloned DNA probe for the analysis of non-disjunction in Down syndrome. Human Genetics. 66: 54-6. PMID 6230306 DOI: 10.1007/BF00275186  1
1984 Gilliam TC, Scambler P, Robbins T, Ingle C, Williamson R, Davies KE. The positions of three restriction fragment length polymorphisms on chromosome 4 relative to known genetic markers. Human Genetics. 68: 154-8. PMID 6094335 DOI: 10.1007/BF00279306  1
1983 Wieacker P, Wienker TF, Dallapiccola B, Bender K, Davies KE, Ropers HH. Linkage relationships between Retinoschisis, Xg, and a cloned DNA sequence from the distal short arm of the X chromosome. Human Genetics. 64: 143-5. PMID 6885047 DOI: 10.1007/BF00327111  1
1983 Harper PS, O'Brien T, Murray JM, Davies KE, Pearson P, Williamson R. The use of linked DNA polymorphisms for genotype prediction in families with Duchenne muscular dystrophy. Journal of Medical Genetics. 20: 252-4. PMID 6684693  0.84
1983 O'Brien T, Harper PS, Davies KE, Murray JM, Sarfarazi M, Williamson R. Absence of genetic heterogeneity in Duchenne muscular dystrophy shown by a linkage study using two cloned DNA sequences. Journal of Medical Genetics. 20: 249-51. PMID 6684692 DOI: 10.1136/jmg.20.4.249  1
1983 Davies KE, Jackson J, Williamson R, Harper PS, Ball S, Sarfarazi M, Meredith L, Fey G. Linkage analysis of myotonic dystrophy and sequences on chromosome 19 using a cloned complement 3 gene probe. Journal of Medical Genetics. 20: 259-63. PMID 6620325 DOI: 10.1136/jmg.20.4.259  0.84
1983 Sarfarazi M, Harper PS, Kingston HM, Murray JM, O'Brien T, Davies KE, Williamson R, Tippett P, Sanger R. Genetic linkage relationship between the Xg blood group system and two X chromosome DNA polymorphisms in families with Duchenne and Becker muscular dystrophy. Human Genetics. 65: 169-71. PMID 6317539 DOI: 10.1007/BF00286656  1
1983 Davies KE, Pearson PL, Harper PS, Murray JM, O'Brien T, Sarfarazi M, Williamson R. Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome. Nucleic Acids Research. 11: 2303-12. PMID 6304647 DOI: 10.1093/nar/11.8.2303  0.84
1983 Wieacker P, Davies KE, Mevorah B, Ropers HH. Linkage studies in a family with X-linked recessive ichthyosis employing a cloned DNA sequence from the distal short arm of the X chromosome Human Genetics. 63: 113-116. PMID 6301973 DOI: 10.1007/BF00291528  1
1983 Kingston HM, Harper PS, Pearson PL, Davies KE, Williamson R, Page D. Localisation of gene for Becker muscular dystrophy. Lancet (London, England). 2: 1200. PMID 6139558  0.84
1983 Davies KE, Harper PS, Williamson R. Cloned gene probes for carrier detection in muscular dystrophy. Lancet (London, England). 2: 108. PMID 6134944 DOI: 10.1016/S0140-6736(83)90095-8  1
1983 Davies KE, Gilliam TC, Williamson R. Cystic fibrosis is not caused by a defect in the gene coding for human complement C3. Molecular Biology & Medicine. 1: 185-90. PMID 6094950  1
1982 Murray JM, Davies KE, Harper PS, Meredith L, Mueller CR, Williamson R. Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy. Nature. 300: 69-71. PMID 6982420  0.84
1982 Hill ME, Davies KE, Harper P, Williamson R. The Mendelian inheritance of a human X chromosome-specific DNA sequence polymorphism and its use in linkage studies of genetic disease. Human Genetics. 60: 222-6. PMID 6286461 DOI: 10.1007/BF00303007  1
1981 Davies KE. The application of DNA recombinant technology to the analysis of the human genome and genetic disease Human Genetics. 58: 351-357. PMID 7035333 DOI: 10.1007/BF00282814  1
1981 Annesley M, Davies KE, Kumar NM, Walker IO. The characterisation of a 5-s 'monosome' fraction from chromatin of physarum polycephalum Nucleic Acids Research. 9: 831-839. PMID 7015286 DOI: 10.1093/nar/9.4.831  1
1981 Davies KE, Young BD, Elles RG, Hill ME, Williamson R. Cloning of a representative genomic library of the human X chromosome after sorting by flow cytometry. Nature. 293: 374-6. PMID 6456416 DOI: 10.1038/293374a0  1
1981 Crampton JM, Davies KE, Knapp TF. The occurrence of families of repetitive sequences in a library of cloned cDNA from human lymphocytes Nucleic Acids Research. 9: 3821-3834. PMID 6169012 DOI: 10.1093/nar/9.15.3821  1
1978 Butler MJ, Davies KE, Walker IO. The structure of nucleolar chromatin in physarum polycephalum Nucleic Acids Research. 5: 667-678. PMID 565509 DOI: 10.1093/nar/5.3.667  1
1978 Davies KE, Walker IO. Control of RNA transcription in nuclei and nucleoli of Physarum polycephalum Febs Letters. 86: 303-306. PMID 564291 DOI: 10.1016/0014-5793(78)80585-7  1
1974 Davies KE, Walker IO. The solubility of calf thymus chromatin in sodium chloride Nucleic Acids Research. 1: 129-140. PMID 10793666 DOI: 10.1093/nar/1.1.129  1
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