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Proceedings of the National Academy of Sciences of the United States of America
|
November 20, 2013
RAN proteins and RNA foci from antisense transcripts in C9ORF72 ALS and frontotemporal dementia
Tao Zu, Yuanjing Liu, Monica Bañez-Coronel, et al.
Annals of Clinical and Translational Neurology
|
September 19, 2020
Dominant mutations in ITPR3 cause Charcot-Marie-Tooth disease
Julius Rönkkö, Svetlana Molchanova, Anya Revah-Politi, et al.
Annals of Neurology
|
December 24, 2016
Proteomics of rimmed vacuoles define new risk allele in inclusion body myositis
Anne-Katrin Güttsches, Stefen Brady, Kathryn Krause, et al.
Neurobiology of Aging
|
January 17, 2017
Genetic epidemiology of motor neuron disease-associated variants in the Scottish population
Holly A Black, Danielle J Leighton, Elaine M Cleary, et al.
Neurobiology of Aging
|
June 14, 2017
Corrigendum to "Genetic epidemiology of motor neuron disease-associated variants in the Scottish population." [Neurobiol. Aging 51 (2017) 178.e11-178.e20]
Holly A Black, Danielle J Leighton, Elaine M Cleary, et al.
Acta Neuropathologica
|
November 13, 2014
Hypermethylation of repeat expanded C9orf72 is a clinical and molecular disease modifier
Jenny Russ, Elaine Y Liu, Kathryn Wu, et al.
Neurobiology of Disease
|
June 8, 2013
Dynein mutations associated with hereditary motor neuropathies impair mitochondrial morphology and function with age
Judith Eschbach, Jérôme Sinniger, Jamal Bouitbir, et al.
Muscle & Nerve
|
September 19, 2024
Access for ALL in ALS: A large-scale, inclusive, collaborative consortium to unlock the molecular and genetic mechanisms of amyotrophic lateral sclerosis
James D Berry, Sabrina Paganoni, Matthew B Harms, et al.
Science Translational Medicine
|
October 25, 2013
Targeting RNA foci in iPSC-derived motor neurons from ALS patients with a C9ORF72 repeat expansion
Dhruv Sareen, Jacqueline G O'Rourke, Pratap Meera, et al.
Genome Research
|
April 4, 2019
A new approach for rare variation collapsing on functional protein domains implicates specific genic regions in ALS
Sahar Gelfman, Sarah Dugger, Cristiane de Araujo Martins Moreno, et al.
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of 7
Search research articles
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Showing results (31-40 of 68) with videos related to
Sort By:
Page
of 7
Proceedings of the National Academy of Sciences of the United States of America
|
November 20, 2013
RAN proteins and RNA foci from antisense transcripts in C9ORF72 ALS and frontotemporal dementia
Tao Zu, Yuanjing Liu, Monica Bañez-Coronel, et al.
Annals of Clinical and Translational Neurology
|
September 19, 2020
Dominant mutations in ITPR3 cause Charcot-Marie-Tooth disease
Julius Rönkkö, Svetlana Molchanova, Anya Revah-Politi, et al.
Annals of Neurology
|
December 24, 2016
Proteomics of rimmed vacuoles define new risk allele in inclusion body myositis
Anne-Katrin Güttsches, Stefen Brady, Kathryn Krause, et al.
Neurobiology of Aging
|
January 17, 2017
Genetic epidemiology of motor neuron disease-associated variants in the Scottish population
Holly A Black, Danielle J Leighton, Elaine M Cleary, et al.
Neurobiology of Aging
|
June 14, 2017
Corrigendum to "Genetic epidemiology of motor neuron disease-associated variants in the Scottish population." [Neurobiol. Aging 51 (2017) 178.e11-178.e20]
Holly A Black, Danielle J Leighton, Elaine M Cleary, et al.
Acta Neuropathologica
|
November 13, 2014
Hypermethylation of repeat expanded C9orf72 is a clinical and molecular disease modifier
Jenny Russ, Elaine Y Liu, Kathryn Wu, et al.
Neurobiology of Disease
|
June 8, 2013
Dynein mutations associated with hereditary motor neuropathies impair mitochondrial morphology and function with age
Judith Eschbach, Jérôme Sinniger, Jamal Bouitbir, et al.
Muscle & Nerve
|
September 19, 2024
Access for ALL in ALS: A large-scale, inclusive, collaborative consortium to unlock the molecular and genetic mechanisms of amyotrophic lateral sclerosis
James D Berry, Sabrina Paganoni, Matthew B Harms, et al.
Science Translational Medicine
|
October 25, 2013
Targeting RNA foci in iPSC-derived motor neurons from ALS patients with a C9ORF72 repeat expansion
Dhruv Sareen, Jacqueline G O'Rourke, Pratap Meera, et al.
Genome Research
|
April 4, 2019
A new approach for rare variation collapsing on functional protein domains implicates specific genic regions in ALS
Sahar Gelfman, Sarah Dugger, Cristiane de Araujo Martins Moreno, et al.
Page
of 7