James Nicholas Sleigh - Publications

Affiliations: 
University College London, London, United Kingdom 
Area:
neuromuscular disease, motor neuron, sensory neuron, neuromuscular junction, neuropathy, Charcot-Marie-Tooth, spinal muscular atrophy

37 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Sleigh JN, Mech AM, Aktar T, Zhang Y, Schiavo G. Altered Sensory Neuron Development in CMT2D Mice Is Site-Specific and Linked to Increased GlyRS Levels. Frontiers in Cellular Neuroscience. 14: 232. PMID 32848623 DOI: 10.3389/fncel.2020.00232  1
2020 Tosolini AP, Sleigh JN. Intramuscular Delivery of Gene Therapy for Targeting the Nervous System. Frontiers in Molecular Neuroscience. 13: 129. PMID 32765219 DOI: 10.3389/fnmol.2020.00129  1
2020 Sleigh JN, Mech AM, Schiavo G. Developmental demands contribute to early neuromuscular degeneration in CMT2D mice. Cell Death & Disease. 11: 564. PMID 32703932 DOI: 10.1038/s41419-020-02798-y  1
2020 Sleigh JN, West SJ, Schiavo G. A video protocol for rapid dissection of mouse dorsal root ganglia from defined spinal levels. Bmc Research Notes. 13: 302. PMID 32580748 DOI: 10.1186/s13104-020-05147-6  1
2020 Mech AM, Brown AL, Schiavo G, Sleigh JN. Morphological variability is greater at developing than mature mouse neuromuscular junctions. Journal of Anatomy. PMID 32533580 DOI: 10.1111/joa.13228  1
2020 Sleigh JN, Tosolini AP, Schiavo G. In Vivo Imaging of Anterograde and Retrograde Axonal Transport in Rodent Peripheral Nerves. Methods in Molecular Biology (Clifton, N.J.). 2143: 271-292. PMID 32524487 DOI: 10.1007/978-1-0716-0585-1_20  1
2020 Sleigh JN, Tosolini AP, Gordon D, Devoy A, Fratta P, Fisher EMC, Talbot K, Schiavo G. Mice Carrying ALS Mutant TDP-43, but Not Mutant FUS, Display In Vivo Defects in Axonal Transport of Signaling Endosomes. Cell Reports. 30: 3655-3662.e2. PMID 32187538 DOI: 10.1016/j.celrep.2020.02.078  1
2020 Rossor AM, Sleigh JN, Groves M, Muntoni F, Reilly MM, Hoogenraad CC, Schiavo G. Loss of BICD2 in muscle drives motor neuron loss in a developmental form of spinal muscular atrophy. Acta Neuropathologica Communications. 8: 34. PMID 32183910 DOI: 10.1186/s40478-020-00909-6  1
2019 Surana S, Villarroel-Campos D, Lazo OM, Moretto E, Tosolini AP, Rhymes ER, Richter S, Sleigh JN, Schiavo G. The evolution of the axonal transport toolkit. Traffic (Copenhagen, Denmark). PMID 31670447 DOI: 10.1111/tra.12710  1
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  0.52
2019 Sleigh JN, Rossor AM, Fellows AD, Tosolini AP, Schiavo G. Axonal transport and neurological disease. Nature Reviews. Neurology. PMID 31558780 DOI: 10.1038/s41582-019-0257-2  1
2019 Kalinski AL, Kar AN, Craver J, Tosolini AP, Sleigh JN, Lee SJ, Hawthorne A, Brito-Vargas P, Miller-Randolph S, Passino R, Shi L, Wong VSC, Picci C, Smith DS, Willis DE, et al. Deacetylation of Miro1 by HDAC6 blocks mitochondrial transport and mediates axon growth inhibition. The Journal of Cell Biology. PMID 31068376 DOI: 10.1083/jcb.201702187  1
2018 Shorrock HK, van der Hoorn D, Boyd PJ, Llavero Hurtado M, Lamont DJ, Wirth B, Sleigh JN, Schiavo G, Wishart TM, Groen EJN, Gillingwater TH. UBA1/GARS-dependent pathways drive sensory-motor connectivity defects in spinal muscular atrophy. Brain : a Journal of Neurology. 141: 2878-2894. PMID 30239612 DOI: 10.1093/brain/awy237  1
2018 Grice SJ, Sleigh JN, Zameel Cader M. Plexin-Semaphorin Signaling Modifies Neuromuscular Defects in aModel of Peripheral Neuropathy. Frontiers in Molecular Neuroscience. 11: 55. PMID 29520219 DOI: 10.3389/fnmol.2018.00055  0.52
2018 Rossor AM, Reilly MM, Sleigh JN. Antisense oligonucleotides and other genetic therapies made simple. Practical Neurology. PMID 29455156 DOI: 10.1136/practneurol-2017-001764  0.72
2018 Soliman E, Bianchi F, Sleigh JN, George JH, Cader MZ, Cui Z, Ye H. Aligned electrospun fibers for neural patterning. Biotechnology Letters. PMID 29313254 DOI: 10.1007/s10529-017-2494-z  0.48
2017 Tosolini AP, Sleigh JN. Motor Neuron Gene Therapy: Lessons from Spinal Muscular Atrophy for Amyotrophic Lateral Sclerosis. Frontiers in Molecular Neuroscience. 10: 405. PMID 29270111 DOI: 10.3389/fnmol.2017.00405  1
2017 Soliman E, Bianchi F, Sleigh JN, George JH, Cader MZ, Cui Z, Ye H. Engineered method for directional growth of muscle sheets on electrospun fibers. Journal of Biomedical Materials Research. Part A. PMID 29266766 DOI: 10.1002/jbm.a.36312  0.48
2017 Sleigh JN, Gómez-Martín A, Wei N, Bai G, Yang XL, Schiavo G. Neuropilin 1 sequestration by neuropathogenic mutant glycyl-tRNA synthetase is permissive to vascular homeostasis. Scientific Reports. 7: 9216. PMID 28835631 DOI: 10.1038/s41598-017-10005-w  1
2017 Sleigh JN, Dawes JM, West SJ, Wei N, Spaulding EL, Gómez-Martín A, Zhang Q, Burgess RW, Cader MZ, Talbot K, Yang XL, Bennett DL, Schiavo G. Trk receptor signaling and sensory neuron fate are perturbed in human neuropathy caused by Gars mutations. Proceedings of the National Academy of Sciences of the United States of America. PMID 28351971 DOI: 10.1073/pnas.1614557114  1
2017 Sleigh JN, Vagnoni A, Twelvetrees AE, Schiavo G. Methodological advances in imaging intravital axonal transport. F1000research. 6: 200. PMID 28344778 DOI: 10.12688/f1000research.10433.1  1
2016 Hammond SM, Hazell G, Shabanpoor F, Saleh AF, Bowerman M, Sleigh JN, Meijboom KE, Zhou H, Muntoni F, Talbot K, Gait MJ, Wood MJ. Systemic peptide-mediated oligonucleotide therapy improves long-term survival in spinal muscular atrophy. Proceedings of the National Academy of Sciences of the United States of America. PMID 27621445 DOI: 10.1073/pnas.1605731113  0.52
2016 Spaulding EL, Sleigh JN, Morelli KH, Pinter MJ, Burgess RW, Seburn KL. Synaptic Deficits at Neuromuscular Junctions in Two Mouse Models of Charcot-Marie-Tooth Type 2d. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 36: 3254-67. PMID 26985035 DOI: 10.1523/JNEUROSCI.1762-15.2016  0.48
2016 Sleigh JN, Weir GA, Schiavo G. A simple, step-by-step dissection protocol for the rapid isolation of mouse dorsal root ganglia. Bmc Research Notes. 9: 82. PMID 26864470 DOI: 10.1186/s13104-016-1915-8  1
2016 Gibbs KL, Kalmar B, Sleigh JN, Greensmith L, Schiavo G. In vivo imaging of axonal transport in murine motor and sensory neurons. Journal of Neuroscience Methods. 257: 26-33. PMID 26424507 DOI: 10.1016/j.jneumeth.2015.09.018  0.84
2015 Somers E, Lees RD, Hoban K, Sleigh JN, Zhou H, Muntoni F, Talbot K, Gillingwater TH, Parson SH. Vascular defects and spinal cord hypoxia in spinal muscular atrophy. Annals of Neurology. PMID 26506088 DOI: 10.1002/ana.24549  0.84
2015 Grice SJ, Sleigh JN, Motley WW, Liu JL, Burgess RW, Talbot K, Cader MZ. Dominant, toxic gain-of-function mutations in gars lead to non-cell autonomous neuropathology. Human Molecular Genetics. 24: 4397-406. PMID 25972375 DOI: 10.1093/hmg/ddv176  0.52
2014 Sleigh JN, Burgess RW, Gillingwater TH, Cader MZ. Morphological analysis of neuromuscular junction development and degeneration in rodent lumbrical muscles. Journal of Neuroscience Methods. 227: 159-65. PMID 24530702 DOI: 10.1016/j.jneumeth.2014.02.005  0.84
2014 Sleigh JN, Grice SJ, Burgess RW, Talbot K, Cader MZ. Neuromuscular junction maturation defects precede impaired lower motor neuron connectivity in Charcot-Marie-Tooth type 2D mice. Human Molecular Genetics. 23: 2639-50. PMID 24368416 DOI: 10.1093/hmg/ddt659  0.84
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  0.84
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  0.84
2013 Bogdanik LP, Sleigh JN, Tian C, Samuels ME, Bedard K, Seburn KL, Burgess RW. Loss of the E3 ubiquitin ligase LRSAM1 sensitizes peripheral axons to degeneration in a mouse model of Charcot-Marie-Tooth disease. Disease Models & Mechanisms. 6: 780-92. PMID 23519028 DOI: 10.1242/dmm.010942  0.84
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  0.84
2011 Grice SJ, Sleigh JN, Liu JL, Sattelle DB. Invertebrate models of spinal muscular atrophy: insights into mechanisms and potential therapeutics. Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology. 33: 956-65. PMID 22009672 DOI: 10.1002/bies.201100082  0.84
2011 Sleigh JN, Gillingwater TH, Talbot K. The contribution of mouse models to understanding the pathogenesis of spinal muscular atrophy. Disease Models & Mechanisms. 4: 457-67. PMID 21708901 DOI: 10.1242/dmm.007245  0.84
2011 Sleigh JN, Buckingham SD, Esmaeili B, Viswanathan M, Cuppen E, Westlund BM, Sattelle DB. A novel Caenorhabditis elegans allele, smn-1(cb131), mimicking a mild form of spinal muscular atrophy, provides a convenient drug screening platform highlighting new and pre-approved compounds. Human Molecular Genetics. 20: 245-60. PMID 20962036 DOI: 10.1093/hmg/ddq459  0.84
2010 Dimitriadi M, Sleigh JN, Walker A, Chang HC, Sen A, Kalloo G, Harris J, Barsby T, Walsh MB, Satterlee JS, Li C, Van Vactor D, Artavanis-Tsakonas S, Hart AC. Conserved genes act as modifiers of invertebrate SMN loss of function defects. Plos Genetics. 6: e1001172. PMID 21124729 DOI: 10.1371/journal.pgen.1001172  0.84
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