Pages that link to "Q37071065"
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The following pages link to Biochemical characterization of the mitochondrial tRNASer(UCN) T7511C mutation associated with nonsyndromic deafness (Q37071065):
Displaying 50 items.
- Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutations (Q24669653) (← links)
- Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss (Q24791654) (← links)
- Frequency of mitochondrial mutations in non-syndromic hearing loss as well as possibly responsible variants found by whole mitochondrial genome screening (Q28660527) (← links)
- Human 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 diabetes (Q33826223) (← links)
- A deafness-associated tRNAHis mutation alters the mitochondrial function, ROS production and membrane potential. (Q33843127) (← links)
- Mitochondrial tRNAThr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese families (Q34000668) (← links)
- Mitochondrial transfer RNAMet 4435A>G mutation is associated with maternally inherited hypertension in a Chinese pedigree (Q34007628) (← links)
- Failures in mitochondrial tRNAMet and tRNAGln metabolism caused by the novel 4401A>G mutation are involved in essential hypertension in a Han Chinese Family (Q34007647) (← links)
- Dual-mode recognition of noncanonical tRNAs(Ser) by seryl-tRNA synthetase in mammalian mitochondria (Q34116221) (← links)
- Aminoglycoside stress together with the 12S rRNA 1494C>T mutation leads to mitophagy (Q34634692) (← links)
- Absence of GJB2 gene mutations, the GJB6 deletion (GJB6-D13S1830) and four common mitochondrial mutations in nonsyndromic genetic hearing loss in a South African population (Q34999808) (← links)
- Noncanonical secondary structure stabilizes mitochondrial tRNA(Ser(UCN)) by reducing the entropic cost of tertiary folding. (Q35447374) (← links)
- Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss is associated with the 12S rRNA C1494T mutation in three Han Chinese pedigrees (Q36054556) (← links)
- TRNA mutations that affect decoding fidelity deregulate development and the proteostasis network in zebrafish (Q36191817) (← links)
- Mitochondrial DNA and disease (Q36194900) (← links)
- Association of nuclear and mitochondrial genes with audiological examinations in Iranian patients with nonaminoglycoside antibiotics-induced hearing loss (Q36551100) (← links)
- 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 (Q36553950) (← links)
- Mitochondrial rRNA and tRNA and hearing function (Q36697530) (← links)
- Noncoding RNAs and RNA editing in brain development, functional diversification, and neurological disease (Q36872209) (← links)
- A Hypertension-Associated tRNAAla Mutation Alters tRNA Metabolism and Mitochondrial Function. (Q37073167) (← links)
- Coronary heart disease is associated with a mutation in mitochondrial tRNA. (Q37193896) (← links)
- Variants in mitochondrial tRNA gene may not be associated with thyroid carcinoma (Q37262055) (← links)
- Association between idiopathic hearing loss and mitochondrial DNA mutations: a study on 169 hearing-impaired subjects (Q37265644) (← links)
- Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation (Q37455749) (← links)
- A deafness-associated tRNAAsp mutation alters the m1G37 modification, aminoacylation and stability of tRNAAsp and mitochondrial function. (Q37507554) (← links)
- Mitochondrial 12S rRNA mutations associated with aminoglycoside ototoxicity (Q37806816) (← links)
- The role of mitochondrial DNA mutations in hearing loss (Q38100717) (← links)
- A Deafness- and Diabetes-associated tRNA Mutation Causes Deficient Pseudouridinylation at Position 55 in tRNAGlu and Mitochondrial Dysfunction. (Q38752245) (← links)
- The exome sequencing identified the mutation in YARS2 encoding the mitochondrial tyrosyl-tRNA synthetase as a nuclear modifier for the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation (Q38813517) (← links)
- A novel mitochondrial tRNA(Ala) gene variant causes chronic progressive external ophthalmoplegia in a patient with Huntington disease. (Q38961648) (← links)
- Leber's Hereditary Optic Neuropathy Is Associated with the T12338C Mutation in Mitochondrial ND5 Gene in Six Han Chinese Families (Q39809744) (← links)
- Biochemical Evidence for a Nuclear Modifier Allele (A10S) in TRMU (Methylaminomethyl-2-thiouridylate-methyltransferase) Related to Mitochondrial tRNA Modification in the Phenotypic Manifestation of Deafness-associated 12S rRNA Mutation (Q40386722) (← links)
- Mutational Analysis of Mitochondrial tRNA Genes in Patients with Asthma (Q41886199) (← links)
- Mutation in MTO1 involved in tRNA modification impairs mitochondrial RNA metabolism in the yeast Saccharomyces cerevisiae (Q41972180) (← links)
- A reappraisal of complete mtDNA variation in East Asian families with hearing impairment (Q42491866) (← links)
- Mitochondrial tRNA(Glu) A14693G variant may modulate the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in a Han Chinese family (Q43666060) (← links)
- Mitochondrial tRNA mutations are associated with maternally inherited hypertension in two Han Chinese pedigrees (Q45738904) (← links)
- A hypertension-associated mitochondrial DNA mutation introduces an m1G37 modification into tRNAMet, altering its structure and function (Q46244954) (← links)
- Contribution of the tRNAIle 4317A>G mutation to the phenotypic manifestation of the deafness-associated mitochondrial 12S rRNA 1555A>G mutation (Q47653533) (← links)
- Application of next‑generation sequencing to identify mitochondrial mutations: Study on m.7511T>C in patients with hearing loss (Q49209858) (← links)
- The contribution of the mitochondrial COI/tRNA(Ser(UCN)) gene mutations to non-syndromic and aminoglycoside-induced hearing loss in Polish patients (Q50433773) (← links)
- Maternally inherited hearing loss is associated with the novel mitochondrial tRNA Ser(UCN) 7505T>C mutation in a Han Chinese family (Q50439126) (← links)
- Isolated hearing loss associated with T7511C mutation in mitochondrial DNA. (Q50452310) (← links)
- Transition m.3308T>C in the ND1 gene is associated with left ventricular hypertrabeculation/noncompaction (Q51456831) (← links)
- Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutation. (Q55404336) (← links)
- Tinnitus in patients with hearing loss due to mitochondrial DNA pathogenic variants (Q60492813) (← links)
- Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside-induced and nonsyndromic hearing loss (Q81191060) (← links)
- The mitochondrial <I>ND5</I> T12338C mutation may be associ-ated with Leber’s hereditary optic neuropathy in two Chinese fami-lies (Q83829873) (← links)
- Mutations in mitochondrial DNA associated with hypertension (Q84998195) (← links)
- Hypertension-associated mitochondrial DNA 4401A>G mutation caused the aberrant processing of tRNAMet, all 8 tRNAs and ND6 mRNA in the light-strand transcript (Q90029316) (← links)