The deafness-associated mitochondrial DNA mutation at position 7445, which affects tRNASer(UCN) precursor processing, has long-range effects on NADH dehydrogenase subunit ND6 gene expression.
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Human mtDNA haplogroups associated with high or reduced spermatozoa motilityMutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutationsFunctional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing lossMitochondrial tRNA mutations and diseaseComprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China.Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese familyMitochondrial deafness mutations reviewed.Low penetrance of Leber's hereditary optic neuropathy in ten Han Chinese families carrying the ND6 T11484C mutationVery low penetrance of Leber's hereditary optic neuropathy in five Han Chinese families carrying the ND1 G3460A mutation.A nuclear-mitochondrial DNA interaction affecting hearing impairment in miceHuman mitochondrial leucyl-tRNA synthetase corrects mitochondrial dysfunctions due to the tRNALeu(UUR) A3243G mutation, associated with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like symptoms and diabetesA deafness-associated tRNAHis mutation alters the mitochondrial function, ROS production and membrane potential.Characterization of mitochondrial mRNAs in codfish reveals unique features compared to mammals.Evolution meets disease: penetrance and functional epistasis of mitochondrial tRNA mutations.The RNase P associated with HeLa cell mitochondria contains an essential RNA component identical in sequence to that of the nuclear RNase P.Maternally inherited hearing impairment.Mitochondrial tRNAThr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese families.Mitochondrial transfer RNAMet 4435A>G mutation is associated with maternally inherited hypertension in a Chinese pedigree.Failures in mitochondrial tRNAMet and tRNAGln metabolism caused by the novel 4401A>G mutation are involved in essential hypertension in a Han Chinese Family.Human mitochondrial mRNAs--like members of all families, similar but differentPathology-related substitutions in human mitochondrial tRNA(Ile) reduce precursor 3' end processing efficiency in vitroMitochondrial threshold effects.The human mitochondrial transcriptomeDisorders of mitochondrial protein synthesis.Epigenetics, epidemiology and mitochondrial DNA diseases.Mitochondrial tRNA 3' end metabolism and human disease.Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss is associated with the 12S rRNA C1494T mutation in three Han Chinese pedigrees.Mitochondrial DNA Heteroplasmy Associations With Neurosensory and Mobility Function in Elderly Adults.The Effect of a Novel c.820C>T (Arg274Trp) Mutation in the Mitofusin 2 Gene on Fibroblast Metabolism and Clinical Manifestation in a Patient.Mitochondrial COX2 G7598A mutation may have a modifying role in the phenotypic manifestation of aminoglycoside antibiotic-induced deafness associated with 12S rRNA A1555G mutation in a Han Chinese pedigree.Mitochondrial rRNA and tRNA and hearing function.Biochemical characterization of the mitochondrial tRNASer(UCN) T7511C mutation associated with nonsyndromic deafnessA Hypertension-Associated tRNAAla Mutation Alters tRNA Metabolism and Mitochondrial Function.Coronary heart disease is associated with a mutation in mitochondrial tRNA.Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation.A deafness-associated tRNAAsp mutation alters the m1G37 modification, aminoacylation and stability of tRNAAsp and mitochondrial function.tRNASer(CGA) differentially regulates expression of wild-type and codon-modified papillomavirus L1 genes.Mitochondrial tRNA variants in Chinese subjects with coronary heart diseaseThe clinical and audiologic features of hearing loss due to mitochondrial mutations.The role of mitochondrial DNA mutations in hearing loss.
P2860
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P2860
The deafness-associated mitochondrial DNA mutation at position 7445, which affects tRNASer(UCN) precursor processing, has long-range effects on NADH dehydrogenase subunit ND6 gene expression.
description
1998 nî lūn-bûn
@nan
1998 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
The deafness-associated mitoch ...... e subunit ND6 gene expression.
@ast
The deafness-associated mitoch ...... e subunit ND6 gene expression.
@en
type
label
The deafness-associated mitoch ...... e subunit ND6 gene expression.
@ast
The deafness-associated mitoch ...... e subunit ND6 gene expression.
@en
prefLabel
The deafness-associated mitoch ...... e subunit ND6 gene expression.
@ast
The deafness-associated mitoch ...... e subunit ND6 gene expression.
@en
P2093
P2860
P356
P1476
The deafness-associated mitoch ...... se subunit ND6 gene expression
@en
P2093
N Fischel-Ghodsian
R S Puranam
P2860
P304
P356
10.1128/MCB.18.10.5868
P407
P577
1998-10-01T00:00:00Z