Хайлтын үр дүнгүүд - Johnathan Cooper‐Knock
- 46-н 1 - 20 үр дүнгүүдийг харуулж байна
- Дараагийн хуудас руу очих
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Genetics of Familial Amyotrophic Lateral Sclerosis -н Feneberg Emily, J. Joanna, Johnathan Cooper‐Knock, J. Pamela, Janine Kirby
Хэвлэсэн 2012Capítulo de Livro -
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Simultaneous and independent detection of C9ORF72 alleles with low and high number of GGGGCC repeats using an optimised protocol of Southern blot hybridisation -н Vladimir L. Buchman, Johnathan Cooper‐Knock, Natalie Connor‐Robson, Adrian Higginbottom, Janine Kirby, O D Razinskaya, Natalia Ninkina, Pamela J. Shaw
Хэвлэсэн 2013Artigo -
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The gut microbiome: a key player in the complexity of amyotrophic lateral sclerosis (ALS) -н Sarah Boddy, Ilaria Giovannelli, Matilde Sassani, Johnathan Cooper‐Knock, M Snyder, Eran Segal, Eran Elinav, Lynne Barker, Pamela J. Shaw, Christopher McDermott
Хэвлэсэн 2021Revisão -
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Oligodendrocyte pathology exceeds axonal pathology in white matter in human amyotrophic lateral sclerosis -н Alejandro Lorente Pons, Adrian Higginbottom, Johnathan Cooper‐Knock, Aziza Alrafiah, Ebtisam A. Al-ofi, Janine Kirby, Pamela J. Shaw, Jonathan Wood, J. Robin Highley
Хэвлэсэн 2020Artigo -
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Physical exercise is a risk factor for amyotrophic lateral sclerosis: Convergent evidence from Mendelian randomisation, transcriptomics and risk genotypes -н Thomas Julian, Nicholas Glascow, Adrian Barry, Tobias Moll, Calum Harvey, Yann C. Klimentidis, Michelle Newell, Sai Zhang, M Snyder, Johnathan Cooper‐Knock, Pamela J. Shaw
Хэвлэсэн 2021Artigo -
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Serum miRNAs miR-206, 143-3p and 374b-5p as potential biomarkers for amyotrophic lateral sclerosis (ALS) -н Rachel Waller, Gerald Goodall, Marta Milo, Johnathan Cooper‐Knock, Marc Da Costa, Esther Hobson, Mbombe Kazoka, Helen Wollff, Paul R. Heath, Pamela J. Shaw, Janine Kirby
Хэвлэсэн 2017Artigo -
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Long non-coding RNA Neat1 regulates adaptive behavioural response to stress in mice -н Michail S. Kukharsky, Natalia Ninkina, Haiyan An, Vsevolod Telezhkin, Wenbin Wei, Camille Rabesahala de Meritens, Johnathan Cooper‐Knock, Shinichi Nakagawa, Tetsuro Hirose, Vladimir L. Buchman, Tatyana A. Shelkovnikova
Хэвлэсэн 2020Artigo -
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Mendelian Randomization Study With Clinical Follow‐Up Links Metabolites to Risk and Severity of Pulmonary Arterial Hypertension -н Elham Alhathli, Thomas Julian, Zain Girach, A. A. Roger Thompson, Christopher J. Rhodes, Stefan Gräf, Niamh Errington, Martin R. Wilkins, Allan Lawrie, Dennis Wang, Johnathan Cooper‐Knock
Хэвлэсэн 2024Artigo -
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Antisense RNA foci in the motor neurons of C9ORF72-ALS patients are associated with TDP-43 proteinopathy -н 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
Хэвлэсэн 2015Artigo -
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A review of Mendelian randomization in amyotrophic lateral sclerosis -н Thomas Julian, Sarah Boddy, Mahjabin Islam, Julian Kurz, Katherine J. Whittaker, Tobias Moll, Calum Harvey, Sai Zhang, M Snyder, Christopher McDermott, Johnathan Cooper‐Knock, Pamela J. Shaw
Хэвлэсэн 2021Revisão -
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C9ORF72 GGGGCC Expanded Repeats Produce Splicing Dysregulation which Correlates with Disease Severity in Amyotrophic Lateral Sclerosis -н Johnathan Cooper‐Knock, Joanna J. Bury, Paul R. Heath, Matthew Wyles, Adrian Higginbottom, Catherine Gelsthorpe, J. Robin Highley, Guillaume M. Hautbergue, Magnus Rattray, Janine Kirby, Pamela J. Shaw
Хэвлэсэн 2015Artigo -
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A bacterial artificial chromosome mouse model of amyotrophic lateral sclerosis manifests ‘space cadet syndrome’ on two FVB backgrounds -н Shirlene Badger, Ian Coldicott, Ergita Kyrgiou-Balli, Adrian Higginbottom, Chloé Moutin, Kamallia Mohd Imran, John C. C. Day, Johnathan Cooper‐Knock, Richard J. Mead, James J. P. Alix
Хэвлэсэн 2025Artigo
Хайх хэрэгслүүд:
Холбогдох сэдвүүд
Biology
Medicine
Disease
Genetics
Gene
Amyotrophic lateral sclerosis
Pathology
C9orf72
Internal medicine
Dementia
Frontotemporal dementia
Neuroscience
Allele
Genotype
Trinucleotide repeat expansion
Bioinformatics
Single-nucleotide polymorphism
Computational biology
Phenotype
Gene expression
Neurodegeneration
Genome-wide association study
Immunology
Cell biology
Genetic variants
Mendelian randomization
RNA
Transcriptome
Mendelian inheritance
Messenger RNA