| Year |
Citation |
Score |
| 2024 |
Bucknor EMV, Johnson E, Efthymiou S, Alvi JR, Sultan T, Houlden H, Maroofian R, Karimiani EG, Finelli MJ, Oliver PL. Neuroinflammation and Lysosomal Abnormalities Characterise the Essential Role for Oxidation Resistance 1 in the Developing and Adult Cerebellum. Antioxidants (Basel, Switzerland). 13. PMID 38929124 DOI: 10.3390/antiox13060685 |
0.788 |
|
| 2021 |
Ang G, Brown LA, Tam SKE, Davies KE, Foster RG, Harrison PJ, Sprengel R, Vyazovskiy VV, Oliver PL, Bannerman DM, Peirson SN. Deletion of AMPA receptor GluA1 subunit gene (Gria1) causes circadian rhythm disruption and aberrant responses to environmental cues. Translational Psychiatry. 11: 588. PMID 34782594 DOI: 10.1038/s41398-021-01690-3 |
0.556 |
|
| 2020 |
Castroflorio E, den Hoed J, Svistunova D, Finelli MJ, Cebrian-Serrano A, Corrochano S, Bassett AR, Davies B, Oliver PL. The Ncoa7 locus regulates V-ATPase formation and function, neurodevelopment and behaviour. Cellular and Molecular Life Sciences : Cmls. PMID 33340069 DOI: 10.1007/s00018-020-03721-6 |
0.757 |
|
| 2020 |
Simpson DSA, Oliver PL. ROS Generation in Microglia: Understanding Oxidative Stress and Inflammation in Neurodegenerative Disease. Antioxidants (Basel, Switzerland). 9. PMID 32823544 DOI: 10.3390/Antiox9080743 |
0.361 |
|
| 2019 |
Hunn BHM, Vingill S, Threlfell S, Alegre-Abarrategui J, Magdelyns M, Deltheil T, Bengoa-Vergniory N, Oliver PL, Cioroch M, Doig NM, Bannerman DM, Cragg SJ, Wade-Martins R. Impairment of Macroautophagy in Dopamine Neurons Has Opposing Effects on Parkinsonian Pathology and Behavior. Cell Reports. 29: 920-931.e7. PMID 31644913 DOI: 10.1016/J.Celrep.2019.09.029 |
0.301 |
|
| 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 |
0.8 |
|
| 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 |
0.587 |
|
| 2019 |
Stewart M, Lau P, Banks G, Bains RS, Castroflorio E, Oliver PL, Dixon CL, Kruer MC, Kullmann DM, Acevedo-Arozena A, Wells SE, Corrochano S, Nolan PM. Loss of disrupts synaptic AMPA receptor function, and results in neurodevelopmental, motor, cognitive and electrographical abnormalities. Disease Models & Mechanisms. PMID 30692144 DOI: 10.1242/Dmm.036806 |
0.398 |
|
| 2018 |
Svistunova DM, Simon JN, Rembeza E, Crabtree M, Yue WW, Oliver PL, Finelli MJ. Oxidation resistance 1 regulates post-translational modifications of peroxiredoxin 2 in the cerebellum. Free Radical Biology & Medicine. PMID 30389497 DOI: 10.1016/J.Freeradbiomed.2018.10.447 |
0.761 |
|
| 2018 |
Finelli MJ, Aprile D, Castroflorio E, Jeans A, Moschetta M, Chessum L, Degiacomi MT, Grasegger J, Lupien-Meilleur A, Bassett A, Rossignol E, Campeau PM, Bowl MR, Benfenati F, Fassio A, ... Oliver PL, et al. The epilepsy-associated protein TBC1D24 is required for normal development, survival and vesicle trafficking in mammalian neurons. Human Molecular Genetics. PMID 30335140 DOI: 10.1093/Hmg/Ddy370 |
0.778 |
|
| 2018 |
Gordon D, Dafinca R, Scaber J, Alegre-Abarrategui J, Farrimond L, Scott C, Biggs D, Kent L, Oliver PL, Davies B, Ansorge O, Wade-Martins R, Talbot K. Single-copy expression of an amyotrophic lateral sclerosis-linked TDP-43 mutation (M337V) in BAC transgenic mice leads to altered stress granule dynamics and progressive motor dysfunction. Neurobiology of Disease. PMID 30290270 DOI: 10.1016/J.Nbd.2018.09.024 |
0.618 |
|
| 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 |
0.562 |
|
| 2018 |
Finelli MJ, Paramo T, Pires E, Ryan BJ, Wade-Martins R, Biggin PC, McCullagh J, Oliver PL. Oxidation Resistance 1 Modulates Glycolytic Pathways in the Cerebellum via an Interaction with Glucose-6-Phosphate Isomerase. Molecular Neurobiology. PMID 29905912 DOI: 10.1007/S12035-018-1174-X |
0.745 |
|
| 2018 |
Merkulova M, Păunescu TG, Nair AV, Wang CY, Capen DE, Oliver PL, Breton S, Brown D. Targeted Deletion of the Ncoa7 Gene Results in Incomplete Distal Renal Tubular Acidosis in Mice. American Journal of Physiology. Renal Physiology. PMID 29384414 DOI: 10.1152/Ajprenal.00407.2017 |
0.351 |
|
| 2017 |
Finelli MJ, Oliver PL. TLDc proteins: new players in the oxidative stress response and neurological disease. Mammalian Genome : Official Journal of the International Mammalian Genome Society. PMID 28707022 DOI: 10.1007/S00335-017-9706-7 |
0.757 |
|
| 2017 |
Vargas-Caballero M, Denk F, Wobst HJ, Arch E, Pegasiou CM, Oliver PL, Shipton OA, Paulsen O, Wade-Martins R. Wild-Type, but Not Mutant N296H, Human Tau Restores Aβ-Mediated Inhibition of LTP in Tau(-/-) mice. Frontiers in Neuroscience. 11: 201. PMID 28484365 DOI: 10.3389/Fnins.2017.00201 |
0.339 |
|
| 2017 |
Wobst HJ, Denk F, Oliver PL, Livieratos A, Taylor TN, Knudsen MH, Bengoa-Vergniory N, Bannerman D, Wade-Martins R. Increased 4R tau expression and behavioural changes in a novel MAPT-N296H genomic mouse model of tauopathy. Scientific Reports. 7: 43198. PMID 28233851 DOI: 10.1038/Srep43198 |
0.379 |
|
| 2017 |
Clayton EL, Mancuso R, Nielsen TT, Mizielinska S, Holmes H, Powell N, Norona F, Overgaard Larsen J, Milioto C, Wilson KM, Lythgoe MF, Ourselin S, Nielsen JE, Johannsen P, Holm I, ... ... Oliver PL, et al. Early microgliosis precedes neuronal loss and behavioural impairment in mice with a frontotemporal dementia-causing CHMP2B mutation. Human Molecular Genetics. PMID 28093491 DOI: 10.1093/Hmg/Ddx003 |
0.435 |
|
| 2016 |
Fisher SP, Cui N, McKillop LE, Gemignani J, Bannerman DM, Oliver PL, Peirson SN, Vyazovskiy VV. Stereotypic wheel running decreases cortical activity in mice. Nature Communications. 7: 13138. PMID 27748455 DOI: 10.1038/Ncomms13138 |
0.3 |
|
| 2016 |
Balestrini S, Milh M, Castiglioni C, Lüthy K, Finelli MJ, Verstreken P, Cardon A, Stražišar BG, Holder JL, Lesca G, Mancardi MM, Poulat AL, Repetto GM, Banka S, Bilo L, ... ... Oliver PL, et al. TBC1D24 genotype-phenotype correlation: Epilepsies and other neurologic features. Neurology. PMID 27281533 DOI: 10.1212/Wnl.0000000000002807 |
0.722 |
|
| 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 |
0.621 |
|
| 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 |
0.788 |
|
| 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 |
0.596 |
|
| 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 |
0.634 |
|
| 2015 |
Parsons MJ, Brancaccio M, Sethi S, Maywood ES, Satija R, Edwards JK, Jagannath A, Couch Y, Finelli MJ, Smyllie NJ, Esapa C, Butler R, Barnard AR, Chesham JE, Saito S, ... ... Oliver PL, et al. The Regulatory Factor ZFHX3 Modifies Circadian Function in SCN via an AT Motif-Driven Axis. Cell. 162: 607-21. PMID 26232227 DOI: 10.1016/J.Cell.2015.06.060 |
0.751 |
|
| 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 |
0.757 |
|
| 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 |
0.801 |
|
| 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 |
0.789 |
|
| 2015 |
Pembroke WG, Babbs A, Davies KE, Ponting CP, Oliver PL. Author response: Temporal transcriptomics suggest that twin-peaking genes reset the clock Elife. DOI: 10.7554/Elife.10518.033 |
0.559 |
|
| 2014 |
Tan JY, Vance KW, Varela MA, Sirey T, Watson LM, Curtis HJ, Marinello M, Alves S, Steinkraus BR, Cooper S, Nesterova T, Brockdorff N, Fulga TA, Brice A, Sittler A, ... Oliver PL, et al. Cross-talking noncoding RNAs contribute to cell-specific neurodegeneration in SCA7. Nature Structural & Molecular Biology. 21: 955-61. PMID 25306109 DOI: 10.1038/Nsmb.2902 |
0.421 |
|
| 2014 |
Oliver PL, Chodroff RA, Gosal A, Edwards B, Cheung AF, Gomez-Rodriguez J, Elliot G, Garrett LJ, Lickiss T, Szele F, Green ED, Molnár Z, Ponting CP. Disruption of Visc-2, a Brain-Expressed Conserved Long Noncoding RNA, Does Not Elicit an Overt Anatomical or Behavioral Phenotype. Cerebral Cortex (New York, N.Y. : 1991). PMID 25209608 DOI: 10.1093/Cercor/Bhu196 |
0.568 |
|
| 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 |
0.799 |
|
| 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 |
0.808 |
|
| 2014 |
Vance KW, Sansom SN, Lee S, Chalei V, Kong L, Cooper SE, Oliver PL, Ponting CP. The long non-coding RNA Paupar regulates the expression of both local and distal genes. The Embo Journal. 33: 296-311. PMID 24488179 DOI: 10.1002/Embj.201386225 |
0.352 |
|
| 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 |
0.602 |
|
| 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 |
0.783 |
|
| 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 |
0.655 |
|
| 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 |
0.552 |
|
| 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, 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 |
0.603 |
|
| 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 |
0.77 |
|
| 2011 |
Kwok AS, Phadwal K, Turner BJ, Oliver PL, Raw A, Simon AK, Talbot K, Agashe VR. HspB8 mutation causing hereditary distal motor neuropathy impairs lysosomal delivery of autophagosomes. Journal of Neurochemistry. 119: 1155-61. PMID 21985219 DOI: 10.1111/J.1471-4159.2011.07521.X |
0.583 |
|
| 2011 |
Keane TM, Goodstadt L, Danecek P, White MA, Wong K, Yalcin B, Heger A, Agam A, Slater G, Goodson M, Furlotte NA, Eskin E, Nellåker C, Whitley H, Cleak J, ... ... Oliver PL, et al. Mouse genomic variation and its effect on phenotypes and gene regulation. Nature. 477: 289-94. PMID 21921910 DOI: 10.1038/Nature10413 |
0.343 |
|
| 2011 |
Edwards A, Treiber CD, Breuss M, Pidsley R, Huang GJ, Cleak J, Oliver PL, Flint J, Keays DA. Cytoarchitectural disruption of the superior colliculus and an enlarged acoustic startle response in the Tuba1a mutant mouse. Neuroscience. 195: 191-200. PMID 21875651 DOI: 10.1016/J.Neuroscience.2011.08.035 |
0.407 |
|
| 2011 |
Belgard TG, Marques AC, Oliver PL, Abaan HO, Sirey TM, Hoerder-Suabedissen A, GarcÃa-Moreno F, Molnár Z, Margulies EH, Ponting CP. A transcriptomic atlas of mouse neocortical layers. Neuron. 71: 605-16. PMID 21867878 DOI: 10.1016/J.Neuron.2011.06.039 |
0.507 |
|
| 2011 |
Oliver PL. Challenges of analysing gene-environment interactions in mouse models of schizophrenia. Thescientificworldjournal. 11: 1411-20. PMID 21789475 DOI: 10.1100/Tsw.2011.128 |
0.367 |
|
| 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, 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 |
0.657 |
|
| 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 |
0.66 |
|
| 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 |
0.776 |
|
| 2009 |
Oliver PL, Goodstadt L, Bayes JJ, Birtle Z, Roach KC, Phadnis N, Beatson SA, Lunter G, Malik HS, Ponting CP. Accelerated evolution of the Prdm9 speciation gene across diverse metazoan taxa. Plos Genetics. 5: e1000753. PMID 19997497 DOI: 10.1371/Journal.Pgen.1000753 |
0.334 |
|
| 2009 |
Deakin IH, Law AJ, Oliver PL, Schwab MH, Nave KA, Harrison PJ, Bannerman DM. Behavioural characterization of neuregulin 1 type I overexpressing transgenic mice. Neuroreport. 20: 1523-8. PMID 19829162 DOI: 10.1097/Wnr.0B013E328330F6E7 |
0.329 |
|
| 2009 |
Mackenzie FE, Parker A, Parkinson NJ, Oliver PL, Brooker D, Underhill P, Lukashkina VA, Lukashkin AN, Holmes C, Brown SD. Analysis of the mouse mutant Cloth-ears shows a role for the voltage-gated sodium channel Scn8a in peripheral neural hearing loss. Genes, Brain, and Behavior. 8: 699-713. PMID 19737145 DOI: 10.1111/J.1601-183X.2009.00514.X |
0.412 |
|
| 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 |
0.631 |
|
| 2009 |
Ponjavic J, Oliver PL, Lunter G, Ponting CP. Genomic and transcriptional co-localization of protein-coding and long non-coding RNA pairs in the developing brain. Plos Genetics. 5: e1000617. PMID 19696892 DOI: 10.1371/Journal.Pgen.1000617 |
0.328 |
|
| 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 |
0.767 |
|
| 2009 |
Ponting CP, Oliver PL, Reik W. Evolution and functions of long noncoding RNAs. Cell. 136: 629-41. PMID 19239885 DOI: 10.1016/J.Cell.2009.02.006 |
0.304 |
|
| 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 |
0.578 |
|
| 2008 |
Johnson RD, Oliver PL, Davies KE. SNARE proteins and schizophrenia: linking synaptic and neurodevelopmental hypotheses. Acta Biochimica Polonica. 55: 619-28. PMID 18985177 DOI: 10.18388/Abp.2008_3022 |
0.572 |
|
| 2008 |
Fullerton JM, Willis-Owen SA, Yalcin B, Shifman S, Copley RR, Miller SR, Bhomra A, Davidson S, Oliver PL, Mott R, Flint J. Human-mouse quantitative trait locus concordance and the dissection of a human neuroticism locus. Biological Psychiatry. 63: 874-83. PMID 18083140 DOI: 10.1016/J.Biopsych.2007.10.019 |
0.334 |
|
| 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 |
0.6 |
|
| 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 |
0.796 |
|
| 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 |
0.711 |
|
| 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 |
0.71 |
|
| 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 |
0.78 |
|
| 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 |
0.563 |
|
| 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 |
0.669 |
|
| 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 |
0.615 |
|
| 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 |
0.778 |
|
| 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 DOI: 10.1523/Jneurosci.23-05-01631.2003 |
0.656 |
|
| 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: 10.1042/Cs104041P |
0.641 |
|
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