Pages that link to "Q34145936"

The following pages link to The A1555G mutation in the 12S rRNA gene of human mtDNA: recurrent origins and founder events in families affected by sensorineural deafness (Q34145936):

Displaying 44 items.

• The molecular dissection of mtDNA haplogroup H confirms that the Franco-Cantabrian glacial refuge was a major source for the European gene pool (Q24534129) (← links)
• Platinum-induced ototoxicity in children: a consensus review on mechanisms, predisposition, and protection, including a new International Society of Pediatric Oncology Boston ototoxicity scale (Q24615296) (← links)
• Mitochondrial DNA transit between West Asia and North Africa inferred from U6 phylogeography (Q24658426) (← links)
• Y-chromosome and mtDNA polymorphisms in Iraq, a crossroad of the early human dispersal and of post-Neolithic migrations (Q28202529) (← links)
• A six-generation Chinese family in haplogroup B4C1C exhibits high penetrance of 1555A > G-induced hearing Loss (Q30479483) (← links)
• 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. (Q30485662) (← links)
• Molecular and clinical characterization of the variable phenotype in Korean families with hearing loss associated with the mitochondrial A1555G mutation (Q31083642) (← links)
• MRPS18CP2 alleles and DEFA3 absence as putative chromosome 8p23.1 modifiers of hearing loss due to mtDNA mutation A1555G in the 12S rRNA gene (Q33312080) (← links)
• Mitochondrial DNA haplogroups do not play a role in the variable phenotypic presentation of the A3243G mutation (Q33904943) (← links)
• Do the four clades of the mtDNA haplogroup L2 evolve at different rates? (Q34044867) (← links)
• Candidate locus for a nuclear modifier gene for maternally inherited deafness (Q34390627) (← links)
• The transmission of mitochondrial DNA following assisted reproductive techniques (Q34484088) (← links)
• Pathogenic expression of homoplasmic mtDNA mutations needs a complex nuclear-mitochondrial interaction (Q35113387) (← links)
• Disorders of mitochondrial protein synthesis (Q35203201) (← links)
• The potential risks of abnormal transmission of mtDNA through assisted reproductive technologies. (Q35647363) (← links)
• Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss is associated with the 12S rRNA C1494T mutation in three Han Chinese pedigrees (Q36054556) (← links)
• Co-occurrence of m.1555A>G and m.11778G>A mitochondrial DNA mutations in two Indian families with strikingly different clinical penetrance of Leber hereditary optic neuropathy (Q36954801) (← links)
• Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation (Q37455749) (← links)
• The relationship between pluripotency and mitochondrial DNA proliferation during early embryo development and embryonic stem cell differentiation (Q37517401) (← links)
• Are GJB2 mutations an aggravating factor in the phenotypic expression of mitochondrial non-syndromic deafness? (Q37714312) (← links)
• Mitochondrial 12S rRNA mutations associated with aminoglycoside ototoxicity (Q37806816) (← links)
• Rational use of aminoglycosides--review and recommendations by the Swedish Reference Group for Antibiotics (SRGA). (Q38070006) (← links)
• A reappraisal of complete mtDNA variation in East Asian families with hearing impairment (Q42491866) (← links)
• Mutations in the mitochondrial tRNA Ser(UCN) and in the GJB2 (connexin 26) gene are not modifiers of the age at onset or severity of hearing loss in Spanish patients with the 12S rRNA A1555G mutation (Q42698112) (← links)
• Mitochondrial DNA mutations in patients with postlingual, nonsyndromic hearing impairment (Q43784130) (← links)
• Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutation. (Q44020891) (← links)
• Mitochondrial DNA nucleotide changes C14482G and C14482A in the ND6 gene are pathogenic for Leber's hereditary optic neuropathy. (Q44060092) (← links)
• [Prevalence of the 35delG mutation in the GJB2 gene, del (GJB6-D13S1830) in the GJB6 gene, Q829X in the OTOF gene and A1555G in the mitochondrial 12S rRNA gene in subjects with non-syndromic sensorineural hearing impairment of congenital/childhood o (Q44086737) (← links)
• Influence of mtDNA genetic variation on antibiotic therapy. (Q44375134) (← links)
• PharmGKB summary: very important pharmacogene information for MT-RNR1. (Q45957328) (← links)
• Genetic susceptibility to aminoglycoside ototoxicity: how many are at risk? (Q46500420) (← links)
• Frequency of mtDNA A1555G and A7445G mutations among children with prelingual deafness in Turkey (Q48355437) (← links)
• Complete mitochondrial genome analysis and clinical documentation of a five-generational Indian family with mitochondrial 1555A>G mutation and postlingual hearing loss (Q50425808) (← links)
• Unique penetrance of hearing loss in a five-generation Chinese family with the mitochondrial 12S rRNA 1555A > G mutation (Q50434325) (← links)
• Familial susceptibility to aminoglycoside ototoxicity due to the A1555G mutation in the mitochondrial DNA (Q50482926) (← links)
• Audiometric features of familial hearing impairment transmitted by mitochondrial inheritance (A1555G) (Q50484776) (← links)
• The A1555G mtDNA mutation in Danish hearing-impaired patients: frequency and clinical signs (Q50486160) (← links)
• Second family with hearing impairment linked to 19q13 and refined DFNA4 localisation (Q50488284) (← links)
• Molecular characterization of six Chinese families with m.3460G>A and Leber hereditary optic neuropathy (Q51577298) (← links)
• Mitochondrial toxicity of tobacco smoke and air pollution. (Q52757992) (← links)
• Mitochondrial DNA mutations associated with aminoglycoside induced ototoxicity. (Q55223565) (← links)
• mtDNA Population Variants and Neurodegenerative Diseases (Q58122630) (← links)
• The prevalence of mitochondrial mutations associated with aminoglycoside-induced deafness in ethnic Latvian population: the appraisal of the evidence (Q90317812) (← links)
• Screening for mitochondrial 12S rRNA C1494T mutation in 655 patients with non-syndromic hearing loss: An observational study (Q90712112) (← links)