Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
Cell Metabolism|September 7, 2010
Acyl-CoA dehydrogenase 9 is required for the biogenesis of oxidative phosphorylation complex IJessica Nouws, Leo Nijtmans, Sander M Houten, et al.
Human Molecular Genetics|July 11, 2014
A mutation in the human CBP4 ortholog UQCC3 impairs complex III assembly, activity and cytochrome b stabilityBas F J Wanschers, Radek Szklarczyk, Mariël A M van den Brand, et al.
Human Molecular Genetics|April 12, 2012
Gene identification in the congenital disorders of glycosylation type I by whole-exome sequencingSharita Timal, Alexander Hoischen, Ludwig Lehle, et al.
AIDS (London, England)|April 2, 2025
Dolutegravir plus lamivudine downregulates cellular stress responses versus three-drug HIV RegimensVictoria Rios-Vazquez, Wilhelm A J W Vos, Marc J T Blaauw, et al.
Brain : a Journal of Neurology|February 1, 2022
ZBTB11 dysfunction: spectrum of brain abnormalities, biochemical signature and cellular consequencesDulika Sumathipala, Petter Strømme, Zohreh Fattahi, et al.
Annals of Clinical and Translational Neurology|January 10, 2015
Mutations in PTRH2 cause novel infantile-onset multisystem disease with intellectual disability, microcephaly, progressive ataxia, and muscle weaknessHao Hu, Michelle L Matter, Lina Issa-Jahns, et al.
American Journal of Human Genetics|July 7, 2009
Deficiency of Dol-P-Man synthase subunit DPM3 bridges the congenital disorders of glycosylation with the dystroglycanopathiesDirk J Lefeber, Johannes Schönberger, Eva Morava, et al.
Nature Genetics|December 20, 2017
Mutations in SELENBP1, encoding a novel human methanethiol oxidase, cause extraoral halitosisArjan Pol, G Herma Renkema, Albert Tangerman, et al.
The Journal of Clinical Investigation|May 4, 2021
C2orf69 mutations disrupt mitochondrial function and cause a multisystem human disorder with recurring autoinflammationEva Lausberg, Sebastian Gießelmann, Joseph P Dewulf, et al.
Pageof 4