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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|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.Journal of Agricultural and Food Chemistry|January 16, 2010
Oxidative stress-induced metabolic changes in mouse C2C12 myotubes studied with high-resolution 13C, 1H, and 31P NMR spectroscopyIda K Straadt, Jette F Young, Bent O Petersen, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 20, 2024
FDA Approval Summary: Nadofaragene Firadenovec-vncg for Bacillus Calmette-Guérin-Unresponsive Non-Muscle-Invasive Bladder CancerLaronna Colbert, Yuxia Jia, Anurag Sharma, et al.Journal of the Neurological Sciences|May 9, 2009
Sequence variants in SPAST, SPG3A and HSPD1 in hereditary spastic paraplegiaKirsten Svenstrup, Peter Bross, Pernille Koefoed, et al.American Journal of Human Genetics|January 20, 2015
CLPB variants associated with autosomal-recessive mitochondrial disorder with cataract, neutropenia, epilepsy, and methylglutaconic aciduriaCarol Saunders, Laurie Smith, Flemming Wibrand, et al.American Journal of Human Genetics|March 19, 2002
Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60Jens Jacob Hansen, Alexandra Dürr, Isabelle Cournu-Rebeix, et al.Pageof 9