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

Bross

Showing results (551-560 of 779) with videos related to

Pageof 78
Sort By:
Molecular Metabolism|August 15, 2024
HSP60 chaperone deficiency disrupts the mitochondrial matrix proteome and dysregulates cholesterol synthesisCagla Cömert, Kasper Kjær-Sørensen, Jakob Hansen, et al.
European Journal of Biochemistry|October 14, 2004
The Y42H mutation in medium-chain acyl-CoA dehydrogenase, which is prevalent in babies identified by MS/MS-based newborn screening, is temperature sensitiveLinda O'Reilly, Peter Bross, Thomas J Corydon, et al.
The Journal of Pediatrics|February 5, 2021
Hepatic Steatosis is Negatively Associated with Bone Mineral Density in ChildrenLauren F Chun, Elizabeth L Yu, Mary Catherine Sawh, et al.
Stem Cells and Development|October 28, 2016
Mitochondrial Spare Respiratory Capacity Is Negatively Correlated with Nuclear Reprogramming EfficiencyYan Zhou, Rasha Abdelkadhem Al-Saaidi, Paula Fernandez-Guerra, et al.
American Journal of Human Genetics|October 3, 2000
Isolated 2-methylbutyrylglycinuria caused by short/branched-chain acyl-CoA dehydrogenase deficiency: identification of a new enzyme defect, resolution of its molecular basis, and evidence for distinct acyl-CoA dehydrogenases in isoleucine and valine metabolismB S Andresen, E Christensen, T J Corydon, et al.
Translational Psychiatry|August 8, 2022
The psychiatric risk gene BRD1 modulates mitochondrial bioenergetics by transcriptional regulationVeerle Paternoster, Cagla Cömert, Louise Sand Kirk, et al.
BMC Plant Biology|September 20, 2015
Transcriptome analysis of 20 taxonomically related benzylisoquinoline alkaloid-producing plantsJillian M Hagel, Jeremy S Morris, Eun-Jeong Lee, et al.
Circulation. Cardiovascular Genetics|April 8, 2014
Truncating plakophilin-2 mutations in arrhythmogenic cardiomyopathy are associated with protein haploinsufficiency in both myocardium and epidermisTorsten B Rasmussen, Peter H Nissen, Johan Palmfeldt, et al.
Human Mutation|February 6, 2013
Mutated desmoglein-2 proteins are incorporated into desmosomes and exhibit dominant-negative effects in arrhythmogenic right ventricular cardiomyopathyTorsten B Rasmussen, Johan Palmfeldt, Peter H Nissen, et al.
Journal of Andrology|April 9, 2011
Reexamination of pharmacokinetics of oral testosterone undecanoate in hypogonadal men with a new self-emulsifying formulationAnthony Y Yin, Michelle Htun, Ronald S Swerdloff, et al.
Pageof 78

Showing results (551-560 of 779) with videos related to

Sort By:
Pageof 78
Molecular Metabolism|August 15, 2024
HSP60 chaperone deficiency disrupts the mitochondrial matrix proteome and dysregulates cholesterol synthesisCagla Cömert, Kasper Kjær-Sørensen, Jakob Hansen, et al.
European Journal of Biochemistry|October 14, 2004
The Y42H mutation in medium-chain acyl-CoA dehydrogenase, which is prevalent in babies identified by MS/MS-based newborn screening, is temperature sensitiveLinda O'Reilly, Peter Bross, Thomas J Corydon, et al.
The Journal of Pediatrics|February 5, 2021
Hepatic Steatosis is Negatively Associated with Bone Mineral Density in ChildrenLauren F Chun, Elizabeth L Yu, Mary Catherine Sawh, et al.
Stem Cells and Development|October 28, 2016
Mitochondrial Spare Respiratory Capacity Is Negatively Correlated with Nuclear Reprogramming EfficiencyYan Zhou, Rasha Abdelkadhem Al-Saaidi, Paula Fernandez-Guerra, et al.
American Journal of Human Genetics|October 3, 2000
Isolated 2-methylbutyrylglycinuria caused by short/branched-chain acyl-CoA dehydrogenase deficiency: identification of a new enzyme defect, resolution of its molecular basis, and evidence for distinct acyl-CoA dehydrogenases in isoleucine and valine metabolismB S Andresen, E Christensen, T J Corydon, et al.
Translational Psychiatry|August 8, 2022
The psychiatric risk gene BRD1 modulates mitochondrial bioenergetics by transcriptional regulationVeerle Paternoster, Cagla Cömert, Louise Sand Kirk, et al.
BMC Plant Biology|September 20, 2015
Transcriptome analysis of 20 taxonomically related benzylisoquinoline alkaloid-producing plantsJillian M Hagel, Jeremy S Morris, Eun-Jeong Lee, et al.
Circulation. Cardiovascular Genetics|April 8, 2014
Truncating plakophilin-2 mutations in arrhythmogenic cardiomyopathy are associated with protein haploinsufficiency in both myocardium and epidermisTorsten B Rasmussen, Peter H Nissen, Johan Palmfeldt, et al.
Human Mutation|February 6, 2013
Mutated desmoglein-2 proteins are incorporated into desmosomes and exhibit dominant-negative effects in arrhythmogenic right ventricular cardiomyopathyTorsten B Rasmussen, Johan Palmfeldt, Peter H Nissen, et al.
Journal of Andrology|April 9, 2011
Reexamination of pharmacokinetics of oral testosterone undecanoate in hypogonadal men with a new self-emulsifying formulationAnthony Y Yin, Michelle Htun, Ronald S Swerdloff, et al.
Pageof 78