Mitochondrial DNA mutations in diseases of energy metabolism.
about
Treatment for mitochondrial disordersTreatment for mitochondrial disordersStatin adverse effects : a review of the literature and evidence for a mitochondrial mechanismMitochondrial DNA haplogroups influence AIDS progressionRegulation of neuronal bioenergy homeostasis by glutamateMitochondrial disease in superoxide dismutase 2 mutant miceMitochondrial DNA sequence variation is associated with free-living activity energy expenditure in the elderlyMitochondrial DNA does not appear to influence the congenital onset type of myotonic dystrophy.Inherited mitochondrial DNA variants can affect complement, inflammation and apoptosis pathways: insights into mitochondrial-nuclear interactions.Mitochondrial disorders. A diagnostic challenge in clinical chemistry.Oxidative stress induced age dependent meibomian gland dysfunction in Cu, Zn-superoxide dismutase-1 (Sod1) knockout miceNonneutral mitochondrial DNA variation in humans and chimpanzeesMitochondrial base excision repair assaysMitochondria as all-round players of the calcium game.Human mitochondrial genetics.Introduction of an additional pathway for lactate oxidation in the treatment of lactic acidosis and mitochondrial dysfunction in Caenorhabditis elegans.Mitochondrial-nuclear epistasis: implications for human aging and longevity.Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population.Mitochondrial DNA haplogroups confer differences in risk for age-related macular degeneration: a case control study.Mitochondrial DNA variants mediate energy production and expression levels for CFH, C3 and EFEMP1 genes: implications for age-related macular degeneration.Organization and expression of the mitochondrial genome in the Nicotiana sylvestris CMSII mutantMitochondrial diabetes mellitus.Molecular and bioenergetic differences between cells with African versus European inherited mitochondrial DNA haplogroups: implications for population susceptibility to diseases.Stable heteroplasmy at the single-cell level is facilitated by intercellular exchange of mtDNA.Mitochondrial mutations and polymorphisms in psychiatric disorders.Tissue-specific implications of mitochondrial alterations in aging.Use of transmitochondrial cybrids to assign a complex I defect to the mitochondrial DNA-encoded NADH dehydrogenase subunit 6 gene mutation at nucleotide pair 14459 that causes Leber hereditary optic neuropathy and dystonia.Skeletal muscle action of estrogen receptor α is critical for the maintenance of mitochondrial function and metabolic homeostasis in femalesMitochondrial DNA haplogroups influence lipoatrophy after highly active antiretroviral therapyDisruption of cytochrome c oxidase function induces the Warburg effect and metabolic reprogramming.Increased expression of ApoE and protection from amyloid-beta toxicity in transmitochondrial cybrids with haplogroup K mtDNA.Quantitative PCR-based measurement of nuclear and mitochondrial DNA damage and repair in mammalian cells.Involvement of mitochondria in endoplasmic reticulum stress-induced apoptotic cell death pathway triggered by the prion peptide PrP(106-126).Marked increase in the number and variety of mitochondrial DNA rearrangements in aging human skeletal muscle.The universality of bioenergetic disease. Age-associated cellular bioenergetic degradation and amelioration therapy.Maternally inherited diabetes and deafness: a new diabetes subtype.Relationship of genotype to phenotype in fibroblast-derived transmitochondrial cell lines carrying the 3243 mutation associated with the MELAS encephalomyopathy: shift towards mutant genotype and role of mtDNA copy number.Effect of a polymorphism in the ND1 mitochondrial gene on human skeletal muscle mitochondrial function.The Role of Mitochondria in AMD: Current Knowledge and Future Applications.Audiological assessment in patients with mitochondrial myopathy.
P2860
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P2860
Mitochondrial DNA mutations in diseases of energy metabolism.
description
1994 nî lūn-bûn
@nan
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
1994年论文
@zh
1994年论文
@zh-cn
name
Mitochondrial DNA mutations in diseases of energy metabolism.
@en
type
label
Mitochondrial DNA mutations in diseases of energy metabolism.
@en
prefLabel
Mitochondrial DNA mutations in diseases of energy metabolism.
@en
P356
P1476
Mitochondrial DNA mutations in diseases of energy metabolism.
@en
P2093
D C Wallace
P2888
P304
P356
10.1007/BF00763096
P577
1994-06-01T00:00:00Z