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Biochemical and Molecular Medicine|June 1, 1996
Detection and analysis of mitochondrial DNA deletions by whole genome PCRC H Tengan, C T MoraesBiochimica Et Biophysica Acta|April 18, 1998
Duplication and triplication with staggered breakpoints in human mitochondrial DNAC H Tengan, C T MoraesMutation Research|October 23, 1997
Oxidative phosphorylation dysfunction does not increase the rate of accumulation of age-related mtDNA deletions in skeletal muscleC H Tengan, A A Gabbai, S Shanske, et al.Neuromuscular Disorders : NMD|September 21, 2000
A novel myopathy-associated mitochondrial DNA mutation altering the conserved size of the tRNA(Gln) anticodon loopR Dey, C H Tengan, M P Morita, et al.Journal of the Neurological Sciences|February 7, 1998
Mitochondrial DNA defects in Brazilian patients with chronic progressive external ophthalmoplegiaB H Kiyomoto, C H Tengan, C T Moraes, et al.The Journal of Clinical Endocrinology and Metabolism|January 22, 1998
Mitochondrial encephalomyopathy and hypoparathyroidism associated with a duplication and a deletion of mitochondrial deoxyribonucleic acidC H Tengan, B H Kiyomoto, M S Rocha, et al.Muscle & Nerve. Supplement|January 1, 1995
Phenotype-genotype correlations in skeletal muscle of patients with mtDNA deletionsC T Moraes, M Sciacco, E Ricci, et al.Trends in Genetics : TIG|March 29, 2001
What regulates mitochondrial DNA copy number in animal cells?C T MoraesPageof 9