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

Elaine M Cleary

Showing results (1-10 of 6) with videos related to

Pageof 1
Sort By:
Nature Communications|January 13, 2015
Human iPSC-derived motoneurons harbouring TARDBP or C9ORF72 ALS mutations are dysfunctional despite maintaining viabilityAnna-Claire Devlin, Karen Burr, Shyamanga Borooah, et al.
Molecular and Cellular Probes|June 12, 2016
Improved PCR based methods for detecting C9orf72 hexanucleotide repeat expansionsElaine M Cleary, Suvankar Pal, Tara Azam, et al.
Stem Cells (Dayton, Ohio)|January 15, 2016
Maturation and electrophysiological properties of human pluripotent stem cell-derived oligodendrocytesMatthew R Livesey, Dario Magnani, Elaine M Cleary, 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.
Nature Communications|January 26, 2018
C9ORF72 repeat expansion causes vulnerability of motor neurons to Ca<sup>2+</sup>-permeable AMPA receptor-mediated excitotoxicityBhuvaneish T Selvaraj, Matthew R Livesey, Chen Zhao, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Nature Communications|January 13, 2015
Human iPSC-derived motoneurons harbouring TARDBP or C9ORF72 ALS mutations are dysfunctional despite maintaining viabilityAnna-Claire Devlin, Karen Burr, Shyamanga Borooah, et al.
Molecular and Cellular Probes|June 12, 2016
Improved PCR based methods for detecting C9orf72 hexanucleotide repeat expansionsElaine M Cleary, Suvankar Pal, Tara Azam, et al.
Stem Cells (Dayton, Ohio)|January 15, 2016
Maturation and electrophysiological properties of human pluripotent stem cell-derived oligodendrocytesMatthew R Livesey, Dario Magnani, Elaine M Cleary, 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.
Nature Communications|January 26, 2018
C9ORF72 repeat expansion causes vulnerability of motor neurons to Ca<sup>2+</sup>-permeable AMPA receptor-mediated excitotoxicityBhuvaneish T Selvaraj, Matthew R Livesey, Chen Zhao, et al.
Pageof 1