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

Mashiat Khan

Showing results (1-10 of 5) with videos related to

Pageof 1
Sort By:
Biology|February 25, 2022
Selective Loss of MATR3 in Spinal Interneurons, Upper Motor Neurons and Hippocampal CA1 Neurons in a MATR3 S85C Knock-In Mouse Model of Amyotrophic Lateral SclerosisJustin You, Katarina Maksimovic, Jooyun Lee, et al.
Biochemical and Biophysical Research Communications|June 28, 2021
MATR3 F115C knock-in mice do not exhibit motor defects or neuropathological features of ALSRebekah van Bruggen, Katarina Maksimovic, Justin You, et al.
Nature Communications|October 21, 2020
Selective neuronal degeneration in MATR3 S85C knock-in mouse model of early-stage ALSChing Serena Kao, Rebekah van Bruggen, Jihye Rachel Kim, et al.
FEBS Letters|February 6, 2024
MATR3 pathogenic variants differentially impair its cryptic splicing repression functionMashiat Khan, Xiao Xiao Lily Chen, Michelle Dias, et al.
FEBS Letters|June 10, 2020
Knockdown of genes involved in axonal transport enhances the toxicity of human neuromuscular disease-linked MATR3 mutations in DrosophilaMelody Zhao, Ching Serena Kao, Claudia Arndt, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Biology|February 25, 2022
Selective Loss of MATR3 in Spinal Interneurons, Upper Motor Neurons and Hippocampal CA1 Neurons in a MATR3 S85C Knock-In Mouse Model of Amyotrophic Lateral SclerosisJustin You, Katarina Maksimovic, Jooyun Lee, et al.
Biochemical and Biophysical Research Communications|June 28, 2021
MATR3 F115C knock-in mice do not exhibit motor defects or neuropathological features of ALSRebekah van Bruggen, Katarina Maksimovic, Justin You, et al.
Nature Communications|October 21, 2020
Selective neuronal degeneration in MATR3 S85C knock-in mouse model of early-stage ALSChing Serena Kao, Rebekah van Bruggen, Jihye Rachel Kim, et al.
FEBS Letters|February 6, 2024
MATR3 pathogenic variants differentially impair its cryptic splicing repression functionMashiat Khan, Xiao Xiao Lily Chen, Michelle Dias, et al.
FEBS Letters|June 10, 2020
Knockdown of genes involved in axonal transport enhances the toxicity of human neuromuscular disease-linked MATR3 mutations in DrosophilaMelody Zhao, Ching Serena Kao, Claudia Arndt, et al.
Pageof 1