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Research Database: Mitochondria

Research Database
(Jeng 2007) Maintenance of mtDNA copy number and expression are essential for mitochondrial function and cell growth
(Belikova 2007) Oxygen consumption of human peripheral blood mononuclear cells in severe sepsis
(Ecktay 2007) Physiological role of mitochondrial uncoupling proteins
(Short 2007) Enhancement of muscle mitochondrial function by growth hormone
(Romano 2007) Variable outcome of GH administration in respiratory chain deficiency
(Hakimi 2007) Over-expression of PEPCK-C in skeletal muscle repatterns energy metabolism in mice
(Brosnan 2007) Creatine: Endogenous Metabolite, Dietary, and Therapeutic Supplement
(Burgess 2006) Diminished hepatic gluconeogenesis via defects in TCA flux in PGC-1alpha deficient mice
(Lazoff 2006) Long-lasting neural and behavioral effects of iron deficiency in infancy
(Roe 2006) Anaplerotic diet therapy in inherited metabolic disease
(Brunengraber 2006) Anaplerotic molecules - current and future
(Beard 2003) Pre- and postweaning iron deficiency alters myelination in Sprague-Dawley rats
(Ackrell 2002) Cytopathies involving mitochondrial complex II
(Barisic 2002) Effects of creatine in patient with MELAS phenotype and associated nephropathy
(Baysal 2001) Phenotypic dichotomy in mitochondrial complex II genetic disorders
(de Deungria 2000) Perinatal iron deficiency decreases COX activity in neonatal rat brain
(Wyss 2000) Creatine and creatinine metabolism
(Vergani 1999) Riboflavin therapy and biochemical heterogeneity in two adult lipid storage myopathies
(Rubio-Gozalbo 1997) Favourable clinical course in an infant with severe complex III deficiency
(Hagenfeldt 1994) Creatine treatment in MELAS
(Plioplys 1993) L-carnitine as a treatment for Rett syndrome
(Bernsen 1993) Treatment of complex I deficiency with riboflavin
(Campos 1993) Muscle carnitine deficiency and lipid storage myopathy in mitochondrial myopathy
(Giovannini 1991) Is carnitine essential in children?
(Korenke 1990) Isolated and combined complex I deficiencies in muscle of children with mitochondrial myopathies
(White 1990) Acetyl-L-carnitine as a precursor of acetylcholine
(DiMauro 1987) Mitochondrial myopathies
(Di Donato 1986) Systemic carnitine deficiency due to lack of electron transfer flavoprotein:ubiquinone oxidoreductase