Functional analysis of lymphoblast and cybrid mitochondria containing the 3460, 11778, or 14484 Leber's hereditary optic neuropathy mitochondrial DNA mutation.
about
Differential production of superoxide by neuronal mitochondriaCytoplasmic hybrid (cybrid) cell lines as a practical model for mitochondriopathiesNoninvasive diagnostics of mitochondrial disorders in isolated lymphocytes with high resolution respirometryFunctional Characterization of Three Concomitant MtDNA LHON Mutations Shows No Synergistic Effect on Mitochondrial ActivityA mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicineMitochondrial oxidative phosphorylation in autosomal dominant optic atrophy.Mitochondrial disorders and the eye.Inherited mitochondrial DNA variants can affect complement, inflammation and apoptosis pathways: insights into mitochondrial-nuclear interactions.Decylubiquinone increases mitochondrial function in synaptosomesMitochondrial oxidative phosphorylation compensation may preserve vision in patients with OPA1-linked autosomal dominant optic atrophy.Leber hereditary optic neuropathyMitochondrial optic neuropathies - disease mechanisms and therapeutic strategies.Profiling the mitochondrial proteome of Leber's Hereditary Optic Neuropathy (LHON) in Thailand: down-regulation of bioenergetics and mitochondrial protein quality control pathways in fibroblasts with the 11778G>A mutationMitochondrial DNA variant associated with Leber hereditary optic neuropathy and high-altitude Tibetans.A very large Brazilian pedigree with 11778 Leber's hereditary optic neuropathyMitochondrial defects in neurodegenerative disease.T cell activation markers and African mitochondrial DNA haplogroups among non-Hispanic black participants in AIDS clinical trials group study 384.Cell and animal models of mtDNA biology: progress and prospects.Epidemiology and penetrance of Leber hereditary optic neuropathy in Finland.Electrophile and oxidant damage of mitochondrial DNA leading to rapid evolution of homoplasmic mutations.Molecular and bioenergetic differences between cells with African versus European inherited mitochondrial DNA haplogroups: implications for population susceptibility to diseases.LHON: Mitochondrial Mutations and More.Bioenergetic origins of complexity and disease.Increase of mitochondrial DNA in blood cells of patients with Leber's hereditary optic neuropathy with 11778 mutationIncreased relative mitochondrial DNA content in leucocytes of patients with NAION.Measurement of Systemic Mitochondrial Function in Advanced Primary Open-Angle Glaucoma and Leber Hereditary Optic Neuropathy.Molecular genetic basis of primary inherited optic neuropathies.Assessing heteroplasmic load in Leber's hereditary optic neuropathy mutation 3460G->A/MT-ND1 with a real-time PCR quantitative approach.Leber's hereditary optic neuropathy is associated with the T3866C mutation in mitochondrial ND1 gene in three Han Chinese Families.Genetic and Clinical Analyses of DOA and LHON in 304 Chinese Patients with Suspected Childhood-Onset Hereditary Optic Neuropathy.Colour vision defects in asymptomatic carriers of the Leber's hereditary optic neuropathy (LHON) mtDNA 11778 mutation from a large Brazilian LHON pedigree: a case-control study.Leber hereditary optic neuropathy and oxidative stress.Mouse mtDNA mutant model of Leber hereditary optic neuropathy.Mechanisms of retinal ganglion specific-cell death in Leber hereditary optic neuropathy.Evidence for Detrimental Cross Interactions between Reactive Oxygen and Nitrogen Species in Leber's Hereditary Optic Neuropathy Cells.Phosphorylated neurofilament heavy chain is a marker of neurodegeneration in Leber hereditary optic neuropathy (LHON)Study of mitochondrial respiratory defects on reprogramming to human induced pluripotent stem cells.Inherited mitochondrial optic neuropathies.Mitochondrial Haplogroups as a Risk Factor for Herpes Zoster.Relaxation of selective constraints on avian mitochondrial DNA following the degeneration of flight ability.
P2860
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P2860
Functional analysis of lymphoblast and cybrid mitochondria containing the 3460, 11778, or 14484 Leber's hereditary optic neuropathy mitochondrial DNA mutation.
description
2000 nî lūn-bûn
@nan
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
2000年论文
@zh
2000年论文
@zh-cn
name
Functional analysis of lymphob ...... hy mitochondrial DNA mutation.
@en
type
label
Functional analysis of lymphob ...... hy mitochondrial DNA mutation.
@en
prefLabel
Functional analysis of lymphob ...... hy mitochondrial DNA mutation.
@en
P2093
P2860
P356
P1476
Functional analysis of lymphob ...... hy mitochondrial DNA mutation.
@en
P2093
P2860
P304
39831-39836
P356
10.1074/JBC.M006476200
P407
P577
2000-12-01T00:00:00Z