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C T Moraes

Showing results (21-30 of 88) with videos related to

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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 Parodi
Human 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 Moraes
Journal of Internal Medicine|March 17, 2020
DNA-editing enzymes as potential treatments for heteroplasmic mtDNA diseasesU Zekonyte, S R Bacman, C T Moraes
Neurology|July 23, 1998
Cybrids in Alzheimer's disease: a cellular model of the disease?E A Schon, E A Shoubridge, C T Moraes
Brain Research. Molecular Brain Research|May 1, 1997
Up-regulation of D3 dopamine receptor mRNA in the nucleus accumbens of human cocaine fatalitiesD M Segal, C T Moraes, D C Mash
Somatic Cell and Molecular Genetics|September 1, 1992
Structural and functional mitochondrial abnormalities associated with high levels of partially deleted mitochondrial DNAs in somatic cell hybridsS Sancho, C T Moraes, K Tanji, et al.
Neurology|May 1, 1994
Clinical and morphologic features of a myopathy associated with a point mutation in the mitochondrial tRNA(Pro) geneV V Ionasescu, M Hart, S DiMauro, et al.
Gene Therapy|December 2, 2011
Manipulation of mtDNA heteroplasmy in all striated muscles of newborn mice by AAV9-mediated delivery of a mitochondria-targeted restriction endonucleaseS R Bacman, S L Williams, D Duan, et al.
Biochemical and Biophysical Research Communications|April 28, 1989
Heteroplasmy of mitochondrial genomes in clonal cultures from patients with Kearns-Sayre syndromeC T Moraes, E A Schon, S DiMauro, et al.
Neurology|May 1, 1996
A MERRF/PEO overlap syndrome associated with the mitochondrial DNA 3243 mutationA Verma, C T Moraes, R T Shebert, et al.
Pageof 9

Showing results (21-30 of 88) with videos related to

Sort By:
Pageof 9
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 Parodi
Human 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 Moraes
Journal of Internal Medicine|March 17, 2020
DNA-editing enzymes as potential treatments for heteroplasmic mtDNA diseasesU Zekonyte, S R Bacman, C T Moraes
Neurology|July 23, 1998
Cybrids in Alzheimer's disease: a cellular model of the disease?E A Schon, E A Shoubridge, C T Moraes
Brain Research. Molecular Brain Research|May 1, 1997
Up-regulation of D3 dopamine receptor mRNA in the nucleus accumbens of human cocaine fatalitiesD M Segal, C T Moraes, D C Mash
Somatic Cell and Molecular Genetics|September 1, 1992
Structural and functional mitochondrial abnormalities associated with high levels of partially deleted mitochondrial DNAs in somatic cell hybridsS Sancho, C T Moraes, K Tanji, et al.
Neurology|May 1, 1994
Clinical and morphologic features of a myopathy associated with a point mutation in the mitochondrial tRNA(Pro) geneV V Ionasescu, M Hart, S DiMauro, et al.
Gene Therapy|December 2, 2011
Manipulation of mtDNA heteroplasmy in all striated muscles of newborn mice by AAV9-mediated delivery of a mitochondria-targeted restriction endonucleaseS R Bacman, S L Williams, D Duan, et al.
Biochemical and Biophysical Research Communications|April 28, 1989
Heteroplasmy of mitochondrial genomes in clonal cultures from patients with Kearns-Sayre syndromeC T Moraes, E A Schon, S DiMauro, et al.
Neurology|May 1, 1996
A MERRF/PEO overlap syndrome associated with the mitochondrial DNA 3243 mutationA Verma, C T Moraes, R T Shebert, et al.
Pageof 9