Výsledky vyhledávání - Stuart Pickering‐Brown
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5′ Splice Site Mutations in tau Associated with the Inherited Dementia FTDP-17 Affect a Stem-Loop Structure That Regulates Alternative Splicing of Exon 10 Autor Andrew Grover, Henry Houlden, Matt Baker, Jennifer Adamson, Jada Lewis, Guy Prihar, Stuart Pickering‐Brown, Karen Duff, Mike Hutton
Vydáno 1999Artigo -
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Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known... Autor Stuart Pickering‐Brown, Sara Rollinson, Daniel du Plessis, Karen Morrison, Anoop Varma, Anna Richardson, David Neary, Julie S. Snowden, David Mann
Vydáno 2008Artigo -
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TDP-43 protein in plasma may index TDP-43 brain pathology in Alzheimer’s disease and frontotemporal lobar degeneration Autor Penelope G. Foulds, Erica McAuley, Linda Gibbons, Yvonne S. Davidson, Stuart Pickering‐Brown, David Neary, Julie S. Snowden, David Allsop, David Mann
Vydáno 2008Artigo -
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UBAP1 Is a Component of an Endosome-Specific ESCRT-I Complex that Is Essential for MVB Sorting Autor Flavia Stefani, Ling Zhang, Sandra Taylor, Johanna Donovan, Sara Rollinson, Aurelie Doyotte, Kim Brownhill, Janis M. Bennion, Stuart Pickering‐Brown, Philip Woodman
Vydáno 2011Artigo -
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Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotype Autor Ian R. Mackenzie, Atik Baborie, Stuart Pickering‐Brown, Daniel du Plessis, Evelyn Jaros, Robert H. Perry, David Neary, Julie S. Snowden, David Mann
Vydáno 2006Artigo -
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Phosphorylated TDP-43 pathology and hippocampal sclerosis in progressive supranuclear palsy Autor Osamu Yokota, Yvonne S. Davidson, Eileen H. Bigio, Hideki Ishizu, Seishi Terada, Tetsuaki Arai, Masato Hasegawa, Haruhiko Akiyama, Stephen Sikkink, Stuart Pickering‐Brown, David Mann
Vydáno 2010Artigo -
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Genomewide association study in cervical dystonia demonstrates possible association with sodium leak channel Autor Kin Y. Mok, Susanne A. Schneider, Daniah Trabzuni, María Stamelou, Mark J. Edwards, Dalia Kasperavičiūtė, Stuart Pickering‐Brown, Monty Silverdale, John Hardy, Kailash P. Bhatia
Vydáno 2013Artigo -
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Dipeptide repeat proteins are present in the p62 positive inclusions in patients with frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9OR... Autor David Mann, Sara Rollinson, Andrew Robinson, Janis Bennion Callister, J. C. Thompson, Julie S. Snowden, Tania Gendron, Leonard Petrucelli, Masami Masuda‐Suzukake, Masato Hasegawa, Yvonne S. Davidson, Stuart Pickering‐Brown
Vydáno 2013Artigo -
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Antisense RNA foci in the motor neurons of C9ORF72-ALS patients are associated with TDP-43 proteinopathy Autor Johnathan Cooper‐Knock, Adrian Higginbottom, Matthew J. Stopford, J. Robin Highley, Paul G. Ince, Stephen B. Wharton, Stuart Pickering‐Brown, Janine Kirby, Guillaume M. Hautbergue, Pamela J. Shaw
Vydáno 2015Artigo -
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Accumulation of dipeptide repeat proteins predates that of <scp>TDP</scp>‐43 in frontotemporal lobar degeneration associated with hexanucleotide repeat expansions in <scp><i>C9ORF7... Autor Atik Baborie, Timothy D. Griffiths, Evelyn Jaros, Robert Perry, Ian G. McKeith, David J. Burn, Masami Masuda‐Suzukake, Masato Hasegawa, Sara Rollinson, Stuart Pickering‐Brown, Andrew Robinson, Yvonne S. Davidson, David Mann
Vydáno 2014Artigo -
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Frontotemporal dementia with Pick‐type histology associated with Q336R mutation in the tau gene Autor Stuart Pickering‐Brown, Matthew Baker, Takashi Nonaka, Keiichi Ikeda, Suvasini Sharma, J. M. MacKenzie, Sharon Simpson, Joan Moore, Julie S. Snowden, R. de Silva, Tamás Révész, Masato Hasegawa, M. Hutton, David Mann
Vydáno 2004Artigo -
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Inherited frontotemporal dementia in nine British families associated with intronic mutations in the tau gene Autor Stuart Pickering‐Brown, Anna Richardson, Julie S. Snowden, A. M. McDonagh, Alistair Burns, W. Braude, Matthew Baker, W.‐K. Liu, S. -H. Yen, John Hardy, M. Hutton, Yvonne Davies, David Allsop, David Craufurd, David Neary, David Mann
Vydáno 2002Artigo
Vyhledávací nástroje:
Související témata
Medicine
Disease
Biology
Dementia
Genetics
Gene
Pathology
Frontotemporal dementia
Frontotemporal lobar degeneration
Allele
C9orf72
Neuroscience
Alzheimer's disease
Amyotrophic lateral sclerosis
Internal medicine
Genotype
Single-nucleotide polymorphism
Psychology
Genome-wide association study
Trinucleotide repeat expansion
Mutation
Genetic association
Locus (genetics)
Neurodegeneration
Cell biology
Dementia with Lewy bodies
Haplotype
Computational biology
Exon
Parkinson's disease