検索結果 - 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 著者: Andrew Grover, Henry Houlden, Matt Baker, Jennifer Adamson, Jada Lewis, Guy Prihar, Stuart Pickering‐Brown, Karen Duff, Mike Hutton
出版事項 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... 著者: Stuart Pickering‐Brown, Sara Rollinson, Daniel du Plessis, Karen Morrison, Anoop Varma, Anna Richardson, David Neary, Julie S. Snowden, David Mann
出版事項 2008Artigo -
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TDP-43 protein in plasma may index TDP-43 brain pathology in Alzheimer’s disease and frontotemporal lobar degeneration 著者: Penelope G. Foulds, Erica McAuley, Linda Gibbons, Yvonne S. Davidson, Stuart Pickering‐Brown, David Neary, Julie S. Snowden, David Allsop, David Mann
出版事項 2008Artigo -
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Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotype 著者: Ian R. Mackenzie, Atik Baborie, Stuart Pickering‐Brown, Daniel du Plessis, Evelyn Jaros, Robert H. Perry, David Neary, Julie S. Snowden, David Mann
出版事項 2006Artigo -
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Phosphorylated TDP-43 pathology and hippocampal sclerosis in progressive supranuclear palsy 著者: 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
出版事項 2010Artigo -
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Genomewide association study in cervical dystonia demonstrates possible association with sodium leak channel 著者: 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
出版事項 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... 著者: 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
出版事項 2013Artigo -
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Antisense RNA foci in the motor neurons of C9ORF72-ALS patients are associated with TDP-43 proteinopathy 著者: 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
出版事項 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... 著者: 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
出版事項 2014Artigo -
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Frontotemporal dementia with Pick‐type histology associated with Q336R mutation in the tau gene 著者: 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
出版事項 2004Artigo -
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Inherited frontotemporal dementia in nine British families associated with intronic mutations in the tau gene 著者: 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
出版事項 2002Artigo
関連主題
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