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Seminars in Cell & Developmental Biology|December 12, 2001
Reactive oxygen species and mitochondrial diseasesI G Kirkinezos, C T MoraesJournal of Neurology, Neurosurgery, and Psychiatry|March 18, 2006
Frequency of dystrophic muscle abnormalities in chronic progressive external ophthalmoplegia: analysis of 86 patientsB H Kiyomoto, C H Tengan, C K Costa, et al.Molecular Biology of the Cell|October 8, 1999
Mechanisms of human mitochondrial DNA maintenance: the determining role of primary sequence and length over functionC T Moraes, L Kenyon, H HaoAmerican Journal of Human Genetics|June 1, 1997
Functional and structural features of a tandem duplication of the human mtDNA promoter regionH Hao, G Manfredi, C T MoraesThe Journal of Biological Chemistry|June 11, 1998
Human xenomitochondrial cybrids. Cellular models of mitochondrial complex I deficiencyA Barrientos, L Kenyon, C T MoraesThe Journal of Biological Chemistry|July 26, 2000
Functional constraints of nuclear-mitochondrial DNA interactions in xenomitochondrial rodent cell linesR Dey, A Barrientos, C T MoraesArquivos De Neuro-Psiquiatria|December 1, 1994
[Distal renal tubular acidosis presenting with rhabdomyolysis]E Zanoteli, A S De Oliveira, C H Tengan, et al.Biochemistry|March 8, 1988
Structural characterization of several galactofuranose-containing, high-mannose-type oligosaccharides present in glycoproteins of the trypanosomatid Leptomonas samueliC T Moraes, M Bosch, A J ParodiHuman Molecular Genetics|May 20, 1999
Suppression of a mitochondrial tRNA gene mutation phenotype associated with changes in the nuclear backgroundH Hao, L E Morrison, C T MoraesJournal of Internal Medicine|March 17, 2020
DNA-editing enzymes as potential treatments for heteroplasmic mtDNA diseasesU Zekonyte, S R Bacman, C T MoraesPageof 9