Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Matthew B Harms

Showing results (31-40 of 68) with videos related to

Pageof 7
Sort By:
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 dementiaTao 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 diseaseJulius 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 myositisAnne-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 populationHolly 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 modifierJenny 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 ageJudith 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 sclerosisJames 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 expansionDhruv 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 ALSSahar Gelfman, Sarah Dugger, Cristiane de Araujo Martins Moreno, et al.
Pageof 7

Showing results (31-40 of 68) with videos related to

Sort By:
Pageof 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 dementiaTao 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 diseaseJulius 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 myositisAnne-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 populationHolly 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 modifierJenny 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 ageJudith 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 sclerosisJames 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 expansionDhruv 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 ALSSahar Gelfman, Sarah Dugger, Cristiane de Araujo Martins Moreno, et al.
Pageof 7