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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.American Journal of Medical Genetics|December 1, 1991
Mitochondrial DNA deletion in a girl with manifestations of Kearns-Sayre and Lowe syndromes: an example of phenotypic mimicry?C T Moraes, M Zeviani, E A Schon, 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.Neurology|April 1, 1995
High levels of mitochondrial DNA with an unstable 260-bp duplication in a patient with a mitochondrial myopathyG Manfredi, S Servidei, E Bonilla, et al.Gut|October 24, 2007
Pathophysiology and fate of hepatocytes in a mouse model of mitochondrial hepatopathiesF Diaz, S Garcia, D Hernandez, et al.Neurology|September 1, 1988
Deletions of mitochondrial DNA in Kearns-Sayre syndromeM Zeviani, C T Moraes, S DiMauro, et al.Neuromuscular Disorders : NMD|September 1, 1995
A new mutation associated with MELAS is located in a mitochondrial DNA polypeptide-coding geneG Manfredi, E A Schon, C T Moraes, et al.Cardiovascular Research|March 23, 2000
Mitochondrial function in heart muscle from patients with idiopathic dilated cardiomyopathyD Jarreta, J Orús, A Barrientos, et al.Biochimica Et Biophysica Acta|November 22, 1985
Isolation and characterization of a heparin with high anticoagulant activity from Anomalocardia brasilianaC P Dietrich, J F de Paiva, C T Moraes, et al.Cellular and Molecular Biology (Noisy-Le-Grand, France)|June 10, 1998
Structure of heparan sulfate: identification of variable and constant oligosaccharide domains in eight heparan sulfates of different originsC P Dietrich, I L Tersariol, L Toma, et al.Pageof 9