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Mitochondrion
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August 27, 2005
Identification of a proximal promoter region critical for the expression of the beta-F1-ATPase gene during Drosophila melanogaster development
C Ugalde, P Ochoa, M L Pérez, et al.
Advances in Space Research : the Official Journal of the Committee on Space Research (COSPAR)
|
January 1, 1992
Microgravity effects on Drosophila melanogaster development and aging: comparative analysis of the results of the Fly experiment in the Biokosmos 9 biosatellite flight
R Marco, J González-Jurado, M Calleja, et al.
Advances in Space Research : the Official Journal of the Committee on Space Research (COSPAR)
|
January 1, 1994
Arthropod model systems for studying complex biological processes in the space environment
R Marco, E de Juan, I Ushakov, et al.
Neurology
|
February 5, 1999
A double mutation (A8296G and G8363A) in the mitochondrial DNA tRNA (Lys) gene associated with myoclonus epilepsy with ragged-red fibers
J Arenas, Y Campos, B Bornstein, et al.
Neuromuscular Disorders : NMD
|
October 4, 2005
Increased muscle nucleoside levels associated with a novel frameshift mutation in the thymidine phosphorylase gene in a Spanish patient with MNGIE
A Blazquez, M A Martín, M C Lara, et al.
Neuromuscular Disorders : NMD
|
June 19, 2001
A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with ocular myopathy
Y Campos, J Gámez, A García, et al.
Neurology
|
October 10, 2001
Mitochondrial dysfunction associated with a mutation in the Notch3 gene in a CADASIL family
P de la Peña, B Bornstein, P del Hoyo, et al.
Human Mutation
|
March 26, 2003
Mutation analysis in 16 patients with mtDNA depletion
R Carrozzo, B Bornstein, S Lucioli, et al.
Annals of Neurology
|
September 18, 2001
Early-onset multisystem mitochondrial disorder caused by a nonsense mutation in the mitochondrial DNA cytochrome C oxidase II gene
Y Campos, A García-Redondo, M A Fernández-Moreno, et al.
Neurology
|
January 15, 2003
Myoglobinuria and COX deficiency in a patient taking cerivastatin and gemfibrozil
J Arenas, M A Fernández-Moreno, J A Molina, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 41) with videos related to
Sort By:
Page
of 5
Mitochondrion
|
August 27, 2005
Identification of a proximal promoter region critical for the expression of the beta-F1-ATPase gene during Drosophila melanogaster development
C Ugalde, P Ochoa, M L Pérez, et al.
Advances in Space Research : the Official Journal of the Committee on Space Research (COSPAR)
|
January 1, 1992
Microgravity effects on Drosophila melanogaster development and aging: comparative analysis of the results of the Fly experiment in the Biokosmos 9 biosatellite flight
R Marco, J González-Jurado, M Calleja, et al.
Advances in Space Research : the Official Journal of the Committee on Space Research (COSPAR)
|
January 1, 1994
Arthropod model systems for studying complex biological processes in the space environment
R Marco, E de Juan, I Ushakov, et al.
Neurology
|
February 5, 1999
A double mutation (A8296G and G8363A) in the mitochondrial DNA tRNA (Lys) gene associated with myoclonus epilepsy with ragged-red fibers
J Arenas, Y Campos, B Bornstein, et al.
Neuromuscular Disorders : NMD
|
October 4, 2005
Increased muscle nucleoside levels associated with a novel frameshift mutation in the thymidine phosphorylase gene in a Spanish patient with MNGIE
A Blazquez, M A Martín, M C Lara, et al.
Neuromuscular Disorders : NMD
|
June 19, 2001
A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with ocular myopathy
Y Campos, J Gámez, A García, et al.
Neurology
|
October 10, 2001
Mitochondrial dysfunction associated with a mutation in the Notch3 gene in a CADASIL family
P de la Peña, B Bornstein, P del Hoyo, et al.
Human Mutation
|
March 26, 2003
Mutation analysis in 16 patients with mtDNA depletion
R Carrozzo, B Bornstein, S Lucioli, et al.
Annals of Neurology
|
September 18, 2001
Early-onset multisystem mitochondrial disorder caused by a nonsense mutation in the mitochondrial DNA cytochrome C oxidase II gene
Y Campos, A García-Redondo, M A Fernández-Moreno, et al.
Neurology
|
January 15, 2003
Myoglobinuria and COX deficiency in a patient taking cerivastatin and gemfibrozil
J Arenas, M A Fernández-Moreno, J A Molina, et al.
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of 5