subject area of
- A frameshift mitochondrial complex I gene mutation in a patient with dystonia and cataracts: is the mutation pathogenic? Journal Articles
- A heteroplasmic mitochondrial complex I gene mutation in adult-onset dystonia Journal Articles
- Bacterial Inactivation of the Anticancer Drug Doxorubicin Journal Articles
- Control of oxygen free radical formation from mitochondrial complex I: roles for protein kinase A and pyruvate dehydrogenase kinase Journal Articles
-
Exercise‐stimulated interleukin‐15 is controlled by
AMPK and regulates skin metabolism and aging Journal Articles - Exome sequencing identifies complex I NDUFV2 mutations as a novel cause of Leigh syndrome Journal Articles
- Leigh syndrome associated with mitochondrial complex I deficiency due to novel mutations In NDUFV1 and NDUFS2 Journal Articles
- Massage Therapy Attenuates Inflammatory Signaling After Exercise-Induced Muscle Damage Journal Articles
- Perifascicular atrophic fibers in childhood dermatomyositis with particular reference to mitochondrial changes Journal Articles
- Repopulation of ?0 cells with mitochondria from a patient with a mitochondrial DNA point mutation in tRNAGly results in respiratory chain dysfunction Journal Articles
- Severe infantile leigh syndrome associated with a rare mitochondrial ND6 mutation, m.14487T>C Journal Articles
- Single-locus species delimitation: a test of the mixed Yule–coalescent model, with an empirical application to Philippine round-leaf bats Journal Articles
- TPNH-cytochrome c reductase and nitrate reductase in mutant and wild type Neurospora and Aspergillus Journal Articles
- Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes Journal Articles