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Nature Medicine|July 30, 1999
A calcium signaling defect in the pathogenesis of a mitochondrial DNA inherited oxidative phosphorylation deficiencyM Brini, P Pinton, M P King, et al.EMBO Molecular Medicine|January 6, 2010
Modulation of mitochondrial protein phosphorylation by soluble adenylyl cyclase ameliorates cytochrome oxidase defectsRebeca Acin-Perez, Eric Salazar, Sonja Brosel, et al.International Archives of Allergy and Applied Immunology|January 1, 1990
A contiguous network of dendritic antigen-presenting cells within the respiratory epitheliumP G Holt, M A Schon-Hegrad, J Oliver, et al.Human Molecular Genetics|March 1, 1994
Extremely high levels of mutant mtDNAs co-localize with cytochrome c oxidase-negative ragged-red fibers in patients harboring a point mutation at nt 3243V Petruzzella, C T Moraes, M C Sano, et al.Science (New York, N.Y.)|September 13, 2021
Mitochondrial disease: Replace or edit?Eli Y Adashi, Donald S Rubenstein, Jim A Mossman, et al.American Journal of Respiratory and Critical Care Medicine|June 1, 1994
Functional analysis of human bronchial mucosal T cells extracted with interleukin-2J W Upham, C McMenamin, M A Schon-Hegrad, et al.Neurology|May 1, 1994
A T-->C mutation at nt 8993 of mitochondrial DNA in a child with Leigh syndromeF M Santorelli, S Shanske, K D Jain, et al.Journal of the Neurological Sciences|March 12, 2005
Hypocitrullinemia in patients with MELAS: an insight into the "MELAS paradox"Ali Naini, Petra Kaufmann, Sara Shanske, et al.Aging Cell|July 18, 2006
Does premature aging of the mtDNA mutator mouse prove that mtDNA mutations are involved in natural aging?Konstantin Khrapko, Yevgenya Kraytsberg, Aubrey D N J de Grey, et al.Nature Genetics|August 1, 1992
Molecular analysis of the muscle pathology associated with mitochondrial DNA deletionsC T Moraes, E Ricci, V Petruzzella, et al.Pageof 22