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Mitochondrion|February 9, 2016
Megaconial muscular dystrophy caused by mitochondrial membrane homeostasis defect, new insights from skeletal and heart muscle analysesArnaud V Vanlander, Laura Muiño Mosquera, Joseph Panzer, et al.American Journal of Human Genetics|September 7, 2002
GRACILE syndrome, a lethal metabolic disorder with iron overload, is caused by a point mutation in BCS1LIlona Visapää, Vineta Fellman, Jouni Vesa, et al.Annals of Neurology|January 31, 2003
A new leukoencephalopathy with brainstem and spinal cord involvement and high lactateMarjo S van der Knaap, Patrick van der Voorn, Frederik Barkhof, et al.Biochimica Et Biophysica Acta|December 3, 2014
Mitochondria in peroxisome-deficient hepatocytes exhibit impaired respiration, depleted DNA, and PGC-1α independent proliferationAnnelies Peeters, Abhijit Babaji Shinde, Ruud Dirkx, et al.BMC Cancer|August 28, 2004
No evidence for involvement of SDHD in neuroblastoma pathogenesisKatleen De Preter, Jo Vandesompele, Jasmien Hoebeeck, et al.EMBO Molecular Medicine|January 6, 2010
Parkinson's disease mutations in PINK1 result in decreased Complex I activity and deficient synaptic functionVanessa A Morais, Patrik Verstreken, Anne Roethig, et al.Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|April 1, 2006
Linezolid-induced inhibition of mitochondrial protein synthesisAn S De Vriese, Rudy Van Coster, Joel Smet, et al.BMC Clinical Pathology|June 9, 2009
Mitochondrial mosaics in the liver of 3 infants with mtDNA defectsFrank Roels, Patrick Verloo, François Eyskens, et al.Journal of Synchrotron Radiation|December 24, 2019
Nanoscopic X-ray imaging and quantification of the iron cellular architecture within single fibroblasts of Friedreich's ataxia patientsBjörn De Samber, Tom Vanden Berghe, Eline Meul, et al.Archives of Disease in Childhood|March 26, 2010
Mitochondrial encephalocardio-myopathy with early neonatal onset due to TMEM70 mutationTomás Honzík, Markéta Tesarová, Johannes A Mayr, et al.Pageof 13