Pathogenic expression of homoplasmic mtDNA mutations needs a complex nuclear-mitochondrial interaction.
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Mitochondrial diabetes in children: seek and you will find itThe background of mitochondrial DNA haplogroup J increases the sensitivity of Leber's hereditary optic neuropathy cells to 2,5-hexanedione toxicityAnalysis of mitochondrial DNA variations in Indian patients with congenital cataractMitochondrial disease in autism spectrum disorder patients: a cohort analysisCardiac involvement in mitochondrial DNA disease: clinical spectrum, diagnosis, and management.Analysis of mitochondrial DNA sequences in childhood encephalomyopathies reveals new disease-associated variantsA reduced number of mtSNPs saturates mitochondrial DNA haplotype diversity of worldwide population groupsLong survival in patients with leigh syndrome and the m.10191T>C mutation in MT-ND3 : a case report and review of the literature.Mutational analysis of whole mitochondrial DNA in patients with MELAS and MERRF diseases.The optic nerve: a "mito-window" on mitochondrial neurodegenerationA mitochondrial mutation A4401G is involved in the pathogenesis of left ventricular hypertrophy in Chinese hypertensivesRole of mtDNA haplogroups in the prevalence of osteoarthritis in different geographic populations: a meta-analysisOestrogens ameliorate mitochondrial dysfunction in Leber's hereditary optic neuropathy.Characterization of macular thickness changes in Leber's hereditary optic neuropathy by optical coherence tomography.A cluster of metabolic defects caused by mutation in a mitochondrial tRNA.An Incompatibility between a mitochondrial tRNA and its nuclear-encoded tRNA synthetase compromises development and fitness in Drosophila.Mito-nuclear co-evolution: the positive and negative sides of functional ancient mutationsAn MRPS12 mutation modifies aminoglycoside sensitivity caused by 12S rRNA mutations.Efficient mitochondrial biogenesis drives incomplete penetrance in Leber's hereditary optic neuropathy.Association of a citrate synthase missense mutation with age-related hearing loss in A/J miceHuman extraocular muscles in mitochondrial diseases: comparing chronic progressive external ophthalmoplegia with Leber's hereditary optic neuropathy.Grand rounds: could occupational exposure to n-hexane and other solvents precipitate visual failure in leber hereditary optic neuropathy?Direct linkage of mitochondrial genome variation to risk factors for type 2 diabetes in conplastic strains.Assessing heteroplasmic load in Leber's hereditary optic neuropathy mutation 3460G->A/MT-ND1 with a real-time PCR quantitative approach.Neuron-specific enolase is elevated in asymptomatic carriers of Leber's hereditary optic neuropathy.Cigarette toxicity triggers Leber's hereditary optic neuropathy by affecting mtDNA copy number, oxidative phosphorylation and ROS detoxification pathwaysThe role of mitochondria in inherited neurodegenerative diseases.Overexpression of human mitochondrial valyl tRNA synthetase can partially restore levels of cognate mt-tRNAVal carrying the pathogenic C25U mutationMitochondrial DNA variations in Madras motor neuron diseaseEvidence for nuclear modifier gene in mitochondrial cardiomyopathy.Pathogenic mutations of nuclear genes associated with mitochondrial disorders.Novel mitochondrial DNA mutations responsible for maternally inherited nonsyndromic hearing loss.Characterization of retinal nerve fiber layer thickness changes associated with Leber's hereditary optic neuropathy by optical coherence tomography.Strain-specific nuclear genetic background differentially affects mitochondria-related phenotypes in Saccharomyces cerevisiaeIL-1β hampers glucose-stimulated insulin secretion in Cohen diabetic rat islets through mitochondrial cytochrome c oxidase inhibition by nitric oxide.Fifteen novel mutations in the mitochondrial NADH dehydrogenase subunit 1, 2, 3, 4, 4L, 5 and 6 genes from Iranian patients with Leber's hereditary optic neuropathy (LHON).The G1888A variant in the mitochondrial 16S rRNA gene may be associated with Type 2 diabetes in Caucasian-Brazilian patients from southern Brazil.Detection of low levels of the mitochondrial tRNALeu(UUR) 3243A>G mutation in blood derived from patients with diabetes.Parsing the differences in affected with LHON: genetic versus environmental triggers of disease conversion.A comparative analysis approach to determining the pathogenicity of mitochondrial tRNA mutations.
P2860
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P2860
Pathogenic expression of homoplasmic mtDNA mutations needs a complex nuclear-mitochondrial interaction.
description
2003 nî lūn-bûn
@nan
2003 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Pathogenic expression of homop ...... ear-mitochondrial interaction.
@ast
Pathogenic expression of homop ...... ear-mitochondrial interaction.
@en
type
label
Pathogenic expression of homop ...... ear-mitochondrial interaction.
@ast
Pathogenic expression of homop ...... ear-mitochondrial interaction.
@en
prefLabel
Pathogenic expression of homop ...... ear-mitochondrial interaction.
@ast
Pathogenic expression of homop ...... ear-mitochondrial interaction.
@en
P1433
P1476
Pathogenic expression of homop ...... ear-mitochondrial interaction.
@en
P2093
Giulia d'Amati
P304
P356
10.1016/S0168-9525(03)00072-6
P577
2003-05-01T00:00:00Z