subject area of
- A frameshift mitochondrial complex I gene mutation in a patient with dystonia and cataracts: is the mutation pathogenic? Academic Article
- A heteroplasmic mitochondrial complex I gene mutation in adult-onset dystonia Academic Article
- Bacterial Inactivation of the Anticancer Drug Doxorubicin Academic Article
- Control of oxygen free radical formation from mitochondrial complex I: roles for protein kinase A and pyruvate dehydrogenase kinase Academic Article
- Exercise‐stimulated interleukin‐15 is controlled by AMPK and regulates skin metabolism and aging Academic Article
- Exome sequencing identifies complex I NDUFV2 mutations as a novel cause of Leigh syndrome Academic Article
- Leigh syndrome associated with mitochondrial complex I deficiency due to novel mutations In NDUFV1 and NDUFS2 Academic Article
- Massage Therapy Attenuates Inflammatory Signaling After Exercise-Induced Muscle Damage Academic Article
- Perifascicular atrophic fibers in childhood dermatomyositis with particular reference to mitochondrial changes Academic Article
- Repopulation of ?0 cells with mitochondria from a patient with a mitochondrial DNA point mutation in tRNAGly results in respiratory chain dysfunction Academic Article
- Severe infantile leigh syndrome associated with a rare mitochondrialND6mutation, m.14487T>C Academic Article
- Single-locus species delimitation: a test of the mixed Yule–coalescent model, with an empirical application to Philippine round-leaf bats Academic Article
- TPNH-cytochrome c reductase and nitrate reductase in mutant and wild type Neurospora and Aspergillus Academic Article
- Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes Academic Article