Výsledky vyhledávání - Christopher E. Shaw
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Progressive loss of PAX6, TBR2, NEUROD and TBR1 mRNA gradients correlates with translocation of EMX2 to the cortical plate during human cortical development Autor Nadhim Bayatti, Subrot Sarma, Christopher E. Shaw, J A Eyre, Demetrius A. Vouyiouklis, Susan Lindsay, Gavin J. Clowry
Vydáno 2008Artigo -
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Amyotrophic lateral sclerosis-associated mutant VAPBP56S perturbs calcium homeostasis to disrupt axonal transport of mitochondria Autor Gábor M. Mórotz, Kurt J. De Vos, Alessio Vagnoni, Steven Ackerley, Christopher E. Shaw, Christopher C.J. Miller
Vydáno 2012Artigo -
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D90A-SOD1 mediated amyotrophic lateral sclerosis: A single founder for all cases with evidence for aCis-acting disease modifier in the recessive haplotype Autor M. Parton, Wendy Broom, Peter M. Andersen, Ammar Al‐Chalabi, P. Nigel Leigh, John Powell, Christopher E. Shaw
Vydáno 2002Artigo -
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Dipeptide repeat protein inclusions are rare in the spinal cord and almost absent from motor neurons in C9ORF72 mutant amyotrophic lateral sclerosis and are unlikely to cause their... Autor Jorge Gomez-Deza, Youn‐Bok Lee, Claire Troakes, Matthew Nolan, Safa Al‐Sarraj, Jean‐Marc Gallo, Christopher E. Shaw
Vydáno 2015Artigo -
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Mitochondrial abnormalities and disruption of the neuromuscular junction precede the clinical phenotype and motor neuron loss in hFUSWT transgenic mice Autor Eva So, Jacqueline C. Mitchell, Caroline Memmi, George Chennell, Gema Vizcay‐Barrena, Leanne Allison, Christopher E. Shaw, Caroline Vance
Vydáno 2017Artigo -
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Neurofilament heavy chain side arm phosphorylation regulates axonal transport of neurofilaments Autor Steven Ackerley, Paul Thornhill, Andrew J. Grierson, Janet Brownlees, Brian H. Anderton, P. Nigel Leigh, Christopher E. Shaw, Christopher C.J. Miller
Vydáno 2003Artigo -
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Low index-to-ring finger length ratio in sporadic ALS supports prenatally defined motor neuronal vulnerability Autor Umesh Vivekananda, Z.-R. Manjalay, Jeban Ganesalingam, Jeffrey A. Simms, Christopher E. Shaw, P. Nigel Leigh, Martin R. Turner, Ammar Al‐Chalabi
Vydáno 2011Artigo
Vyhledávací nástroje:
Související témata
Medicine
Biology
Disease
Gene
Amyotrophic lateral sclerosis
Genetics
Pathology
Internal medicine
Neuroscience
Cell biology
Dementia
Frontotemporal dementia
Mutation
Allele
Genotype
C9orf72
Psychology
Single-nucleotide polymorphism
SOD1
Genome-wide association study
Mutant
Neurodegeneration
Trinucleotide repeat expansion
Phenotype
RNA
Genetic association
Physical medicine and rehabilitation
Frontotemporal lobar degeneration
Motor neuron
TARDBP