Aminoglycosides

mitochondrially encoded 12S RNA ; Homo sapiens







7 Article(s)
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1 34032273 Clinical Pharmacogenetics Implementation Consortium Guideline for the Use of Aminoglycosides Based on MT-RNR1 Genotype. 2022 Feb 5
2 32630724 A Novel Approach for the Identification of Pharmacogenetic Variants in MT-RNR1 through Next-Generation Sequencing Off-Target Data. 2020 Jul 2 1
3 30523288 The prevalence of mitochondrial mutations associated with aminoglycoside-induced deafness in ethnic Latvian population: the appraisal of the evidence. 2019 Mar 3
4 27397648 Allele-specific PCR for detecting the deafness-associated mitochondrial 12S rRNA mutations. 2016 Oct 10 1
5 26168747 A meta-analysis and systematic review of the prevalence of mitochondrially encoded 12S RNA in the general population: Is there a role for screening neonates requiring aminoglycosides? 2015 Apr-Jun 1
6 23969527 Association between idiopathic hearing loss and mitochondrial DNA mutations: a study on 169 hearing-impaired subjects. 2013 Oct 1
7 20111055 Extensive and rapid screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss. 2010 Mar 1