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The Journal of Biological Chemistry|March 25, 2020
<i>COQ11</i> deletion mitigates respiratory deficiency caused by mutations in the gene encoding the coenzyme Q chaperone protein Coq10Michelle C Bradley, Krista Yang, Lucía Fernández-Del-Río, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 4, 2019
Insula serotonin 2A receptor binding and gene expression contribute to serotonin transporter polymorphism anxious phenotype in primatesAndrea M Santangelo, Steve J Sawiak, Tim Fryer, et al.
Journal of Lipid Research|May 4, 2019
Human COQ10A and COQ10B are distinct lipid-binding START domain proteins required for coenzyme Q functionHui S Tsui, Nguyen V B Pham, Brendan R Amer, et al.
Epilepsy & Behavior : E&B|December 9, 2023
Epilepsy monitoring unit practices and safety among NAEC epilepsy centers: A census surveyAnto I Bagić, Stephanie M Ahrens, Kevin E Chapman, et al.
Neuromuscular Disorders : NMD|June 21, 2011
A study of FHL1, BAG3, MATR3, PTRF and TCAP in Australian muscular dystrophy patientsLeigh B Waddell, Jenny Tran, Xi F Zheng, et al.
Plos Genetics|April 26, 2008
Primary coenzyme Q deficiency in Pdss2 mutant mice causes isolated renal diseaseMin Peng, Marni J Falk, Volker H Haase, et al.
Journal of Immunology (Baltimore, Md. : 1950)|September 5, 2008
Lipids including cholesteryl linoleate and cholesteryl arachidonate contribute to the inherent antibacterial activity of human nasal fluidThai Q Do, Safiehkhatoon Moshkani, Patricia Castillo, et al.
Annals of Neurology|October 7, 2004
Actin mutations are one cause of congenital fibre type disproportionNigel G Laing, Nigel F Clarke, Danielle E Dye, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 6, 2016
Control of inflammation by stromal Hedgehog pathway activation restrains colitisJohn J Lee, Michael E Rothenberg, E Scott Seeley, et al.
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