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American Journal of Human Genetics
|
July 31, 1998
Mitochondrial neurogastrointestinal encephalomyopathy syndrome maps to chromosome 22q13.32-qter
M Hirano, J Garcia-de-Yebenes, A C Jones, et al.
Mitochondrion
|
May 4, 2010
Coexistence of mitochondrial and nuclear DNA mutations in a woman with mitochondrial encephalomyopathy and double cortex
Carmela Scuderi, Eugenia Borgione, Filippa Castello, et al.
Nature
|
October 8, 2011
Pathogenic exon-trapping by SVA retrotransposon and rescue in Fukuyama muscular dystrophy
Mariko Taniguchi-Ikeda, Kazuhiro Kobayashi, Motoi Kanagawa, et al.
Neurology
|
November 23, 2000
Different brain networks mediate task performance in normal aging and AD: defining compensation
Y Stern, J R Moeller, K E Anderson, et al.
The Journal of Physical Chemistry. A
|
February 15, 2023
Attochemistry Regulation of Charge Migration
Aderonke S Folorunso, François Mauger, Kyle A Hamer, et al.
Journal of Inherited Metabolic Disease
|
October 27, 2004
Congenital cardiomyopathy and pulmonary hypertension: another fatal variant of cytochrome-c oxidase deficiency
C P Venditti, M C Harris, D Huff, et al.
Human Molecular Genetics
|
March 22, 2007
Missense mutation of the COQ2 gene causes defects of bioenergetics and de novo pyrimidine synthesis
José M López-Martín, Leonardo Salviati, Eva Trevisson, et al.
Redox Biology
|
January 11, 2024
The impact of physical activity on promoter-specific methylation of genes involved in the redox-status and disease progression: A longitudinal study on post-surgery female breast cancer patients undergoing medical treatment
Chantalle Moulton, Arianna Murri, Gianmarco Benotti, et al.
Neurology
|
April 12, 2003
Cerebellar ataxia and coenzyme Q10 deficiency
C Lamperti, A Naini, M Hirano, et al.
Physical Review Letters
|
March 2, 2019
Diffractive Imaging of C_{60} Structural Deformations Induced by Intense Femtosecond Midinfrared Laser Fields
Harald Fuest, Yu Hang Lai, Cosmin I Blaga, et al.
Page
of 95
Search research articles
Search
Showing results (801-810 of 942) with videos related to
Sort By:
Page
of 95
American Journal of Human Genetics
|
July 31, 1998
Mitochondrial neurogastrointestinal encephalomyopathy syndrome maps to chromosome 22q13.32-qter
M Hirano, J Garcia-de-Yebenes, A C Jones, et al.
Mitochondrion
|
May 4, 2010
Coexistence of mitochondrial and nuclear DNA mutations in a woman with mitochondrial encephalomyopathy and double cortex
Carmela Scuderi, Eugenia Borgione, Filippa Castello, et al.
Nature
|
October 8, 2011
Pathogenic exon-trapping by SVA retrotransposon and rescue in Fukuyama muscular dystrophy
Mariko Taniguchi-Ikeda, Kazuhiro Kobayashi, Motoi Kanagawa, et al.
Neurology
|
November 23, 2000
Different brain networks mediate task performance in normal aging and AD: defining compensation
Y Stern, J R Moeller, K E Anderson, et al.
The Journal of Physical Chemistry. A
|
February 15, 2023
Attochemistry Regulation of Charge Migration
Aderonke S Folorunso, François Mauger, Kyle A Hamer, et al.
Journal of Inherited Metabolic Disease
|
October 27, 2004
Congenital cardiomyopathy and pulmonary hypertension: another fatal variant of cytochrome-c oxidase deficiency
C P Venditti, M C Harris, D Huff, et al.
Human Molecular Genetics
|
March 22, 2007
Missense mutation of the COQ2 gene causes defects of bioenergetics and de novo pyrimidine synthesis
José M López-Martín, Leonardo Salviati, Eva Trevisson, et al.
Redox Biology
|
January 11, 2024
The impact of physical activity on promoter-specific methylation of genes involved in the redox-status and disease progression: A longitudinal study on post-surgery female breast cancer patients undergoing medical treatment
Chantalle Moulton, Arianna Murri, Gianmarco Benotti, et al.
Neurology
|
April 12, 2003
Cerebellar ataxia and coenzyme Q10 deficiency
C Lamperti, A Naini, M Hirano, et al.
Physical Review Letters
|
March 2, 2019
Diffractive Imaging of C_{60} Structural Deformations Induced by Intense Femtosecond Midinfrared Laser Fields
Harald Fuest, Yu Hang Lai, Cosmin I Blaga, et al.
Page
of 95