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Pediatric Research
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January 23, 2003
Mutation screening in patients with isolated cytochrome c oxidase deficiency
Sabrina Sacconi, Leonardo Salviati, Carolyn M Sue, et al.
Nature
|
March 9, 2012
Imaging ultrafast molecular dynamics with laser-induced electron diffraction
Cosmin I Blaga, Junliang Xu, Anthony D DiChiara, et al.
Free Radical Biology & Medicine
|
May 14, 2023
Steady-state redox status in circulating extracellular vesicles: A proof-of-principle study on the role of fitness level and short-term aerobic training in healthy young males
Veronica Lisi, Chantalle Moulton, Cristina Fantini, et al.
Oxidative Medicine and Cellular Longevity
|
December 2, 2021
Systemic Response of Antioxidants, Heat Shock Proteins, and Inflammatory Biomarkers to Short-Lasting Exercise Training in Healthy Male Subjects
Ivan Dimauro, Elisa Grazioli, Veronica Lisi, et al.
AIDS Research and Human Retroviruses
|
December 15, 2010
Short communication: transplacental nucleoside analogue exposure and mitochondrial parameters in HIV-uninfected children
Susan B Brogly, Salvatore DiMauro, Russell B Van Dyke, et al.
Ecology and Evolution
|
January 11, 2017
Blood serum retinol levels in Asinara white donkeys reflect albinism-induced metabolic adaptation to photoperiod at Mediterranean latitudes
Maria Grazia Cappai, Maria Grazia Antonietta Lunesu, Francesca Accioni, et al.
Redox Biology
|
November 7, 2016
Resistance training and redox homeostasis: Correlation with age-associated genomic changes
Ivan Dimauro, Mattia Scalabrin, Cristina Fantini, et al.
Archives of Neurology
|
August 16, 2006
Clinical spectrum of mitochondrial DNA depletion due to mutations in the thymidine kinase 2 gene
Maryam Oskoui, Guido Davidzon, Juan Pascual, et al.
Archives of Neurology
|
September 17, 2003
Clinical and genetic heterogeneity in progressive external ophthalmoplegia due to mutations in polymerase gamma
Massimiliano Filosto, Michelangelo Mancuso, Yutaka Nishigaki, et al.
Neurology
|
January 13, 2012
Muscle phosphorylase kinase deficiency: a neutral metabolic variant or a disease?
N Preisler, M C Orngreen, A Echaniz-Laguna, et al.
Page
of 95
Search research articles
Search
Showing results (691-700 of 942) with videos related to
Sort By:
Page
of 95
Pediatric Research
|
January 23, 2003
Mutation screening in patients with isolated cytochrome c oxidase deficiency
Sabrina Sacconi, Leonardo Salviati, Carolyn M Sue, et al.
Nature
|
March 9, 2012
Imaging ultrafast molecular dynamics with laser-induced electron diffraction
Cosmin I Blaga, Junliang Xu, Anthony D DiChiara, et al.
Free Radical Biology & Medicine
|
May 14, 2023
Steady-state redox status in circulating extracellular vesicles: A proof-of-principle study on the role of fitness level and short-term aerobic training in healthy young males
Veronica Lisi, Chantalle Moulton, Cristina Fantini, et al.
Oxidative Medicine and Cellular Longevity
|
December 2, 2021
Systemic Response of Antioxidants, Heat Shock Proteins, and Inflammatory Biomarkers to Short-Lasting Exercise Training in Healthy Male Subjects
Ivan Dimauro, Elisa Grazioli, Veronica Lisi, et al.
AIDS Research and Human Retroviruses
|
December 15, 2010
Short communication: transplacental nucleoside analogue exposure and mitochondrial parameters in HIV-uninfected children
Susan B Brogly, Salvatore DiMauro, Russell B Van Dyke, et al.
Ecology and Evolution
|
January 11, 2017
Blood serum retinol levels in Asinara white donkeys reflect albinism-induced metabolic adaptation to photoperiod at Mediterranean latitudes
Maria Grazia Cappai, Maria Grazia Antonietta Lunesu, Francesca Accioni, et al.
Redox Biology
|
November 7, 2016
Resistance training and redox homeostasis: Correlation with age-associated genomic changes
Ivan Dimauro, Mattia Scalabrin, Cristina Fantini, et al.
Archives of Neurology
|
August 16, 2006
Clinical spectrum of mitochondrial DNA depletion due to mutations in the thymidine kinase 2 gene
Maryam Oskoui, Guido Davidzon, Juan Pascual, et al.
Archives of Neurology
|
September 17, 2003
Clinical and genetic heterogeneity in progressive external ophthalmoplegia due to mutations in polymerase gamma
Massimiliano Filosto, Michelangelo Mancuso, Yutaka Nishigaki, et al.
Neurology
|
January 13, 2012
Muscle phosphorylase kinase deficiency: a neutral metabolic variant or a disease?
N Preisler, M C Orngreen, A Echaniz-Laguna, et al.
Page
of 95