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Gene Therapy
|
June 29, 2007
Modulating mtDNA heteroplasmy by mitochondria-targeted restriction endonucleases in a 'differential multiple cleavage-site' model
S R Bacman, S L Williams, D Hernandez, et al.
Brain Research. Molecular Brain Research
|
December 3, 1999
Dopamine transporter mRNA in autopsy studies of chronic cocaine users
L Chen, D M Segal, C T Moraes, et al.
Molecular Biology and Evolution
|
October 6, 2000
Cytochrome c oxidase assembly in primates is sensitive to small evolutionary variations in amino acid sequence
A Barrientos, S Müller, R Dey, et al.
American Journal of Human Genetics
|
May 1, 1995
Segregation patterns of a novel mutation in the mitochondrial tRNA glutamic acid gene associated with myopathy and diabetes mellitus
H Hao, E Bonilla, G Manfredi, et al.
Gene Therapy
|
March 12, 2010
Organ-specific shifts in mtDNA heteroplasmy following systemic delivery of a mitochondria-targeted restriction endonuclease
S R Bacman, S L Williams, S Garcia, et al.
American Journal of Human Genetics
|
May 1, 1992
The mitochondrial tRNA(Leu(UUR)) mutation in mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS): genetic, biochemical, and morphological correlations in skeletal muscle
C T Moraes, E Ricci, E Bonilla, et al.
Biochemical Pharmacology
|
December 8, 2000
Rho(0) tumor cells: a model for studying whether mitochondria are targets for rhodamine 123, doxorubicin, and other drugs
Y Hu, C T Moraes, N Savaraj, et al.
Annals of Neurology
|
November 18, 2000
An out-of-frame cytochrome b gene deletion from a patient with parkinsonism is associated with impaired complex III assembly and an increase in free radical production
M Rana, I de Coo, F Diaz, et al.
American Journal of Human Genetics
|
December 1, 1992
A new mtDNA mutation in the tRNA(Lys) gene associated with myoclonic epilepsy and ragged-red fibers (MERRF)
G Silvestri, C T Moraes, S Shanske, et al.
Human Molecular Genetics
|
January 1, 1994
Distribution of wild-type and common deletion forms of mtDNA in normal and respiration-deficient muscle fibers from patients with mitochondrial myopathy
M Sciacco, E Bonilla, E A Schon, et al.
Page
of 9
Search research articles
Search
Showing results (31-40 of 88) with videos related to
Sort By:
Page
of 9
Gene Therapy
|
June 29, 2007
Modulating mtDNA heteroplasmy by mitochondria-targeted restriction endonucleases in a 'differential multiple cleavage-site' model
S R Bacman, S L Williams, D Hernandez, et al.
Brain Research. Molecular Brain Research
|
December 3, 1999
Dopamine transporter mRNA in autopsy studies of chronic cocaine users
L Chen, D M Segal, C T Moraes, et al.
Molecular Biology and Evolution
|
October 6, 2000
Cytochrome c oxidase assembly in primates is sensitive to small evolutionary variations in amino acid sequence
A Barrientos, S Müller, R Dey, et al.
American Journal of Human Genetics
|
May 1, 1995
Segregation patterns of a novel mutation in the mitochondrial tRNA glutamic acid gene associated with myopathy and diabetes mellitus
H Hao, E Bonilla, G Manfredi, et al.
Gene Therapy
|
March 12, 2010
Organ-specific shifts in mtDNA heteroplasmy following systemic delivery of a mitochondria-targeted restriction endonuclease
S R Bacman, S L Williams, S Garcia, et al.
American Journal of Human Genetics
|
May 1, 1992
The mitochondrial tRNA(Leu(UUR)) mutation in mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS): genetic, biochemical, and morphological correlations in skeletal muscle
C T Moraes, E Ricci, E Bonilla, et al.
Biochemical Pharmacology
|
December 8, 2000
Rho(0) tumor cells: a model for studying whether mitochondria are targets for rhodamine 123, doxorubicin, and other drugs
Y Hu, C T Moraes, N Savaraj, et al.
Annals of Neurology
|
November 18, 2000
An out-of-frame cytochrome b gene deletion from a patient with parkinsonism is associated with impaired complex III assembly and an increase in free radical production
M Rana, I de Coo, F Diaz, et al.
American Journal of Human Genetics
|
December 1, 1992
A new mtDNA mutation in the tRNA(Lys) gene associated with myoclonic epilepsy and ragged-red fibers (MERRF)
G Silvestri, C T Moraes, S Shanske, et al.
Human Molecular Genetics
|
January 1, 1994
Distribution of wild-type and common deletion forms of mtDNA in normal and respiration-deficient muscle fibers from patients with mitochondrial myopathy
M Sciacco, E Bonilla, E A Schon, et al.
Page
of 9