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The 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 processing
H Hao, C T Moraes
Methods in Enzymology
|
January 1, 1996
Detection and analysis of mitochondrial DNA and RNA in muscle by in situ hybridization and single-fiber PCR
C T Moraes, E A Schon
Seminars in Cell & Developmental Biology
|
December 12, 2001
Reactive oxygen species and mitochondrial diseases
I G Kirkinezos, C T Moraes
Biochemical and Molecular Medicine
|
June 1, 1996
Detection and analysis of mitochondrial DNA deletions by whole genome PCR
C H Tengan, C T Moraes
Biochimica Et Biophysica Acta
|
April 18, 1998
Duplication and triplication with staggered breakpoints in human mitochondrial DNA
C H Tengan, C T Moraes
Molecular Biology of the Cell
|
October 8, 1999
Mechanisms of human mitochondrial DNA maintenance: the determining role of primary sequence and length over function
C T Moraes, L Kenyon, H Hao
Methods in Cell Biology
|
May 31, 2001
Transmitochondrial technology in animal cells
C T Moraes, R Dey, A Barrientos
American Journal of Human Genetics
|
June 1, 1997
Functional and structural features of a tandem duplication of the human mtDNA promoter region
H Hao, G Manfredi, C T Moraes
The Journal of Biological Chemistry
|
June 11, 1998
Human xenomitochondrial cybrids. Cellular models of mitochondrial complex I deficiency
A Barrientos, L Kenyon, C T Moraes
The Journal of Biological Chemistry
|
July 26, 2000
Functional constraints of nuclear-mitochondrial DNA interactions in xenomitochondrial rodent cell lines
R Dey, A Barrientos, C T Moraes
Page
of 9
Search research articles
Search
Showing results (11-20 of 88) with videos related to
Sort By:
Page
of 9
The 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 processing
H Hao, C T Moraes
Methods in Enzymology
|
January 1, 1996
Detection and analysis of mitochondrial DNA and RNA in muscle by in situ hybridization and single-fiber PCR
C T Moraes, E A Schon
Seminars in Cell & Developmental Biology
|
December 12, 2001
Reactive oxygen species and mitochondrial diseases
I G Kirkinezos, C T Moraes
Biochemical and Molecular Medicine
|
June 1, 1996
Detection and analysis of mitochondrial DNA deletions by whole genome PCR
C H Tengan, C T Moraes
Biochimica Et Biophysica Acta
|
April 18, 1998
Duplication and triplication with staggered breakpoints in human mitochondrial DNA
C H Tengan, C T Moraes
Molecular Biology of the Cell
|
October 8, 1999
Mechanisms of human mitochondrial DNA maintenance: the determining role of primary sequence and length over function
C T Moraes, L Kenyon, H Hao
Methods in Cell Biology
|
May 31, 2001
Transmitochondrial technology in animal cells
C T Moraes, R Dey, A Barrientos
American Journal of Human Genetics
|
June 1, 1997
Functional and structural features of a tandem duplication of the human mtDNA promoter region
H Hao, G Manfredi, C T Moraes
The Journal of Biological Chemistry
|
June 11, 1998
Human xenomitochondrial cybrids. Cellular models of mitochondrial complex I deficiency
A Barrientos, L Kenyon, C T Moraes
The Journal of Biological Chemistry
|
July 26, 2000
Functional constraints of nuclear-mitochondrial DNA interactions in xenomitochondrial rodent cell lines
R Dey, A Barrientos, C T Moraes
Page
of 9