Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss. - Wikidata - awgldk - TriplyDB

Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss.

Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss.

http://www.wikidata.org/entity/Q34703553

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The phylogeny of the four pan-American MtDNA haplogroups: implications for evolutionary and disease studies Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutations Frequency of mitochondrial mutations in non-syndromic hearing loss as well as possibly responsible variants found by whole mitochondrial genome screening Establishment of a Flexible Real-Time Polymerase Chain Reaction-Based Platform for Detecting Prevalent Deafness Mutations Associated with Variable Degree of Sensorineural Hearing Loss in Koreans.Modifiers of hearing impairment in humans and mice.Molecular and clinical characterisation of three Spanish families with maternally inherited non-syndromic hearing loss caused by the 1494C->T mutation in the mitochondrial 12S rRNA gene.Molecular and clinical characterization of the variable phenotype in Korean families with hearing loss associated with the mitochondrial A1555G mutation.Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss Mutational analysis of whole mitochondrial DNA in patients with MELAS and MERRF diseases.Mitochondrial tRNAThr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese families.Systematic analysis of mitochondrial genes associated with hearing loss in the Japanese population: dHPLC reveals a new candidate mutation Frequency and spectrum of mitochondrial 12S rRNA variants in 440 Han Chinese hearing impaired pediatric subjects from two otology clinics Systematic analysis of the clinical and biochemical characteristics of maternally inherited hypertension in Chinese Han families associated with mitochondrial.Genetic mutations in non-syndromic deafness patients of Uyghur and Han Chinese ethnicities in Xinjiang, China: a comparative study Hearing in 44-45 year olds with m.1555A>G, a genetic mutation predisposing to aminoglycoside-induced deafness: a population based cohort study.The genetic bases for non-syndromic hearing loss among Chinese Molecular investigation of pediatric portuguese patients with sensorineural hearing loss.Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss is associated with the 12S rRNA C1494T mutation in three Han Chinese pedigrees.Antibiotics and the ribosome.Association of nuclear and mitochondrial genes with audiological examinations in Iranian patients with nonaminoglycoside antibiotics-induced hearing loss Genetic counseling for patients with nonsyndromic hearing impairment directed by gene analysis Mitochondrial rRNA and tRNA and hearing function.Genetic mutations of GJB2 and mitochondrial 12S rRNA in nonsyndromic hearing loss in Jiangsu Province of China.A rapid method for detection of five known mutations associated with aminoglycoside-induced deafness.The ND4 G11696A mutation may influence the phenotypic manifestation of the deafness-associated 12S rRNA A1555G mutation in a four-generation Chinese family.Association between idiopathic hearing loss and mitochondrial DNA mutations: a study on 169 hearing-impaired subjects.Genetics of aminoglycoside-induced and prelingual non-syndromic mitochondrial hearing impairment: a review.Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation.Screening of mitochondrial mutations in Tunisian patients with mitochondrial disorders: an overview study.Highly sensitive and reproducible silicon-based surface-enhanced Raman scattering sensors for real applications.GJB2 and MTRNR1 contributions in children with hearing impairment from Northern Cameroon.Genetic Epidemiology of Mitochondrial Pathogenic Variants Causing Nonsyndromic Hearing Loss in a Large Cohort of South Indian Hearing Impaired Individuals.Mitochondrial mutations associated with aminoglycoside ototoxicity and hearing loss susceptibility identified by meta-analysis.Mitochondrial Sensorineural Hearing Loss: A Retrospective Study and a Description of Cochlear Implantation in a MELAS Patient.Pathogenicity of two COQ7 mutations and responses to 2,4-dihydroxybenzoate bypass treatment Audiological and genetic features of the mtDNA mutations.PharmGKB summary: very important pharmacogene information for MT-RNR1.Aminoglycoside ototoxicity in Nicaraguan children: patient risk factors and mitochondrial DNA results.Dynamic Editome of Zebrafish under Aminoglycosides Treatment and Its Potential Involvement in Ototoxicity.GJB2 and mitochondrial 12S rRNA susceptibility mutations in sudden deafness.

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P2860

Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss.

http://www.wikidata.org/entity/Q34703553

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2005 nî lūn-bûn

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2005 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2005 թվականի ապրիլին հրատարակված գիտական հոդված

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Mutational analysis of the mit ...... nd non-syndromic hearing loss.

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Daniel I Choo

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Jianbo Wu

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Jianfu Chen

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Min-Xin Guan

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Ronghua Li

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Selena Heman-Ackah

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Sudao Xiong

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Yaping Qian

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Yi Zhu

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Zhisu Liao

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P2860

Automating the identification of DNA variations using quality-based fluorescence re-sequencing: analysis of the human mitochondrial genome

Sequence and organization of the human mitochondrial genome

Sequence and gene organization of mouse mitochondrial DNA

Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family

Nuclear background determines biochemical phenotype in the deafness-associated mitochondrial 12S rRNA mutation.

Genetic aspects of antibiotic induced deafness: mitochondrial inheritance.

Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity

Genetic factors in aminoglycoside toxicity.

Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment of aminoglycosides.

Genetics, genomics and gene discovery in the auditory system.

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