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

Rima Rozen

Showing results (101-110 of 106) with videos related to

Pageof 11
Sort By:
You have reached the last page of results.This site can display upto 106 results.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|September 2, 2022
The <i>677C > T</i> variant in methylenetetrahydrofolate reductase causes morphological and functional cerebrovascular deficits in miceAlaina M Reagan, Karen E Christensen, Leah C Graham, et al.
Human Molecular Genetics|January 11, 2017
High dietary folate in pregnant mice leads to pseudo-MTHFR deficiency and altered methyl metabolism, with embryonic growth delay and short-term memory impairment in offspringRenata H Bahous, Nafisa M Jadavji, Liyuan Deng, et al.
Cell Metabolism|June 4, 2015
Epigenome-wide association of liver methylation patterns and complex metabolic traits in miceLuz D Orozco, Marco Morselli, Liudmilla Rubbi, et al.
JAMA Neurology|May 7, 2014
Severe methylenetetrahydrofolate reductase deficiency: clinical clues to a potentially treatable cause of adult-onset hereditary spastic paraplegiaAlexander Lossos, Omri Teltsh, Tsipi Milman, et al.
American Journal of Human Genetics|July 2, 2021
Shifting landscapes of human MTHFR missense-variant effectsJochen Weile, Nishka Kishore, Song Sun, et al.
Molecular Genetics and Metabolism|July 20, 2010
A novel transgenic mouse model of CBS-deficient homocystinuria does not incur hepatic steatosis or fibrosis and exhibits a hypercoagulative phenotype that is ameliorated by betaine treatmentKenneth N Maclean, Jakub Sikora, Viktor Kožich, et al.
Pageof 11

Showing results (101-110 of 106) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 106 results.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|September 2, 2022
The <i>677C > T</i> variant in methylenetetrahydrofolate reductase causes morphological and functional cerebrovascular deficits in miceAlaina M Reagan, Karen E Christensen, Leah C Graham, et al.
Human Molecular Genetics|January 11, 2017
High dietary folate in pregnant mice leads to pseudo-MTHFR deficiency and altered methyl metabolism, with embryonic growth delay and short-term memory impairment in offspringRenata H Bahous, Nafisa M Jadavji, Liyuan Deng, et al.
Cell Metabolism|June 4, 2015
Epigenome-wide association of liver methylation patterns and complex metabolic traits in miceLuz D Orozco, Marco Morselli, Liudmilla Rubbi, et al.
JAMA Neurology|May 7, 2014
Severe methylenetetrahydrofolate reductase deficiency: clinical clues to a potentially treatable cause of adult-onset hereditary spastic paraplegiaAlexander Lossos, Omri Teltsh, Tsipi Milman, et al.
American Journal of Human Genetics|July 2, 2021
Shifting landscapes of human MTHFR missense-variant effectsJochen Weile, Nishka Kishore, Song Sun, et al.
Molecular Genetics and Metabolism|July 20, 2010
A novel transgenic mouse model of CBS-deficient homocystinuria does not incur hepatic steatosis or fibrosis and exhibits a hypercoagulative phenotype that is ameliorated by betaine treatmentKenneth N Maclean, Jakub Sikora, Viktor Kožich, et al.
Pageof 11