Showing results (11-20 of 86) with videos related to
Sort By:
Pageof 9
Arquivos De Neuro-Psiquiatria|December 1, 1994
[Periodic paralysis. Clinical analysis in 20 patients]C H Tengan, A S De Oliveira, A A GabbaiJournal of Neurology, Neurosurgery, and Psychiatry|February 18, 2004
The exercise test as a monitor of disease status in hypokalaemic periodic paralysisC H Tengan, A C Antunes, A A Gabbai, et al.The Journal of Biological Chemistry|May 29, 1999
Titrating the effects of mitochondrial complex I impairment in the cell physiologyA Barrientos, C T MoraesHuman Molecular Genetics|December 26, 2001
Manipulating mitochondrial DNA heteroplasmy by a mitochondrially targeted restriction endonucleaseS Srivastava, C T MoraesProceedings of the National Academy of Sciences of the United States of America|August 19, 1997
Expanding the functional human mitochondrial DNA database by the establishment of primate xenomitochondrial cybridsL Kenyon, C T MoraesThe Journal of Biological Chemistry|March 4, 2000
Lack of oxidative phosphorylation and low mitochondrial membrane potential decrease susceptibility to apoptosis and do not modulate the protective effect of Bcl-x(L) in osteosarcoma cellsR Dey, C T MoraesHuman Molecular Genetics|September 16, 1998
Simultaneous transfer of mitochondrial DNA and single chromosomes in somatic cells: a novel approach for the study of defects in nuclear-mitochondrial communicationA Barrientos, C T MoraesMolecular and Cellular Biology|December 31, 1997
A disease-associated G5703A mutation in human mitochondrial DNA causes a conformational change and a marked decrease in steady-state levels of mitochondrial tRNA(Asn)H Hao, C T MoraesThe Journal of Biological Chemistry|January 26, 1996
Functional and molecular mitochondrial abnormalities associated with a C --> T transition at position 3256 of the human mitochondrial genome. The effects of a pathogenic mitochondrial tRNA point mutation in organelle translation and RNA processingH Hao, C T MoraesPageof 9