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

Peter Bross

Showing results (51-60 of 94) with videos related to

Pageof 10
Sort By:
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|June 11, 2003
Approval summary: imatinib mesylate capsules for treatment of adult patients with newly diagnosed philadelphia chromosome-positive chronic myelogenous leukemia in chronic phaseJohn R Johnson, Peter Bross, Martin Cohen, et al.
BMC Gastroenterology|February 7, 2026
Energy metabolism alteration and gene expression reprogramming in a cell model of high fat load non-alcoholic fatty liver diseaseTianran Zhou, Yuhang Zhou, Cagla Cömert, et al.
Annals of the New York Academy of Sciences|June 29, 2006
Heat-shock protein 70 genes and human longevity: a view from DenmarkRipudaman Singh, Steen Kølvraa, Peter Bross, et al.
Plos One|December 11, 2012
Identification of elements that dictate the specificity of mitochondrial Hsp60 for its co-chaperoninAvital Parnas, Shahar Nisemblat, Celeste Weiss, et al.
Metabolism: Clinical and Experimental|December 17, 2009
Metabolic profiling of heat or anoxic stress in mouse C2C12 myotubes using multinuclear magnetic resonance spectroscopyIda K Straadt, Jette F Young, Bent O Petersen, et al.
Journal of Inherited Metabolic Disease|January 11, 2012
Heterozygosity for an in-frame deletion causes glutaryl-CoA dehydrogenase deficiency in a patient detected by newborn screening: investigation of the effect of the mutant allelePeter Bross, Jane B Frederiksen, Anne S Bie, et al.
Cell Stress & Chaperones|April 16, 2010
Inactivation of the hereditary spastic paraplegia-associated Hspd1 gene encoding the Hsp60 chaperone results in early embryonic lethality in miceJane H Christensen, Marit N Nielsen, Jakob Hansen, et al.
Plos One|September 9, 2014
Ethylmalonic encephalopathy ETHE1 R163W/R163Q mutations alter protein stability and redox properties of the iron centreBárbara J Henriques, Tânia G Lucas, João V Rodrigues, et al.
Human Genetics|August 14, 2016
Genomic structure of the human mitochondrial chaperonin genes: HSP60 and HSP10 are localised head to head on chromosome 2 separated by a bidirectional promoterJens J Hansen, Peter Bross, Majken Westergaard, et al.
Human Genetics|December 17, 2002
Genomic structure of the human mitochondrial chaperonin genes: HSP60 and HSP10 are localised head to head on chromosome 2 separated by a bidirectional promoterJens J Hansen, Peter Bross, Majken Westergaard, et al.
Pageof 10

Showing results (51-60 of 94) with videos related to

Sort By:
Pageof 10
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|June 11, 2003
Approval summary: imatinib mesylate capsules for treatment of adult patients with newly diagnosed philadelphia chromosome-positive chronic myelogenous leukemia in chronic phaseJohn R Johnson, Peter Bross, Martin Cohen, et al.
BMC Gastroenterology|February 7, 2026
Energy metabolism alteration and gene expression reprogramming in a cell model of high fat load non-alcoholic fatty liver diseaseTianran Zhou, Yuhang Zhou, Cagla Cömert, et al.
Annals of the New York Academy of Sciences|June 29, 2006
Heat-shock protein 70 genes and human longevity: a view from DenmarkRipudaman Singh, Steen Kølvraa, Peter Bross, et al.
Plos One|December 11, 2012
Identification of elements that dictate the specificity of mitochondrial Hsp60 for its co-chaperoninAvital Parnas, Shahar Nisemblat, Celeste Weiss, et al.
Metabolism: Clinical and Experimental|December 17, 2009
Metabolic profiling of heat or anoxic stress in mouse C2C12 myotubes using multinuclear magnetic resonance spectroscopyIda K Straadt, Jette F Young, Bent O Petersen, et al.
Journal of Inherited Metabolic Disease|January 11, 2012
Heterozygosity for an in-frame deletion causes glutaryl-CoA dehydrogenase deficiency in a patient detected by newborn screening: investigation of the effect of the mutant allelePeter Bross, Jane B Frederiksen, Anne S Bie, et al.
Cell Stress & Chaperones|April 16, 2010
Inactivation of the hereditary spastic paraplegia-associated Hspd1 gene encoding the Hsp60 chaperone results in early embryonic lethality in miceJane H Christensen, Marit N Nielsen, Jakob Hansen, et al.
Plos One|September 9, 2014
Ethylmalonic encephalopathy ETHE1 R163W/R163Q mutations alter protein stability and redox properties of the iron centreBárbara J Henriques, Tânia G Lucas, João V Rodrigues, et al.
Human Genetics|August 14, 2016
Genomic structure of the human mitochondrial chaperonin genes: HSP60 and HSP10 are localised head to head on chromosome 2 separated by a bidirectional promoterJens J Hansen, Peter Bross, Majken Westergaard, et al.
Human Genetics|December 17, 2002
Genomic structure of the human mitochondrial chaperonin genes: HSP60 and HSP10 are localised head to head on chromosome 2 separated by a bidirectional promoterJens J Hansen, Peter Bross, Majken Westergaard, et al.
Pageof 10