{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,3,28]],"date-time":"2024-03-28T11:13:52Z","timestamp":1711624432626},"reference-count":19,"publisher":"Spandidos Publications","issue":"6","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2015,12]]},"DOI":"10.3892\/mmr.2015.4484","type":"journal-article","created":{"date-parts":[[2015,10,26]],"date-time":"2015-10-26T03:28:01Z","timestamp":1445830081000},"page":"8176-8178","source":"Crossref","is-referenced-by-count":4,"title":["Mitochondrial COI\/tRNASer(UCN) G7444A mutation may be associated with aminoglycoside-induced and non-syndromic hearing impairment"],"prefix":"10.3892","volume":"12","author":[{"given":"QI","family":"LIU","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"PING","family":"LIU","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"YU","family":"DING","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"XUE-JUN","family":"DONG","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"ZONG-XIN","family":"WANG","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"YAN-ER","family":"QIAN","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"QING","family":"WANG","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"GUO-CAN","family":"YANG","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"2249","published-online":{"date-parts":[[2012,10,26]]},"reference":[{"key":"key20180108023034_b1-mmr-12-06-8176","doi-asserted-by":"crossref","first-page":"277","DOI":"10.1038\/nrg2309","article-title":"Quiet as a mouse: Dissecting the molecular and genetic basis of hearing","volume":"9","author":"Brown","year":"2008","journal-title":"Nat Rev Genet"},{"key":"key20180108023034_b2-mmr-12-06-8176","doi-asserted-by":"crossref","first-page":"27","DOI":"10.1517\/14622416.6.1.27","article-title":"Genetic factors in aminoglycoside toxicity","volume":"6","author":"Fischel-Ghodsian","year":"2005","journal-title":"Pharmacogenomics"},{"key":"key20180108023034_b3-mmr-12-06-8176","first-page":"211","article-title":"Prevalence of mitochondrial 12S rRNA mutations associated with aminoglycoside ototoxicity","volume":"105","author":"Guan","year":"2005","journal-title":"Volta Rev"},{"key":"key20180108023034_b4-mmr-12-06-8176","doi-asserted-by":"crossref","first-page":"632","DOI":"10.1136\/jmg.40.8.632","article-title":"Heteroplasmy for the 1555A>G mutation in the mitochondrial 12S rRNA gene in six Spanish families with non-syndromic hearing loss","volume":"40","author":"del Castillo","year":"2003","journal-title":"J Med Genet"},{"key":"key20180108023034_b5-mmr-12-06-8176","doi-asserted-by":"crossref","first-page":"1244","DOI":"10.1016\/j.bbrc.2005.01.085","article-title":"Extremely low penetrance of hearing loss in four Chinese families with the mitochondrial 12S rRNA A1555G mutation","volume":"328","author":"Young","year":"2005","journal-title":"Biochem Biophys Res Commun"},{"key":"key20180108023034_b6-mmr-12-06-8176","doi-asserted-by":"crossref","first-page":"967","DOI":"10.1016\/j.bbrc.2005.08.199","article-title":"Clinical evaluation and mitochondrial DNA sequence analysis in two Chinese families with aminoglycoside-induced and non-syndromic hearing loss","volume":"336","author":"Zhao","year":"2005","journal-title":"Biochem Biophys Res Commun"},{"key":"key20180108023034_b7-mmr-12-06-8176","doi-asserted-by":"crossref","first-page":"1421","DOI":"10.1093\/hmg\/4.8.1421","article-title":"Maternally inherited hearing loss, ataxia and myoclonus associated with a novel point mutation in mitochondrial tRNASer(UCN) gene","volume":"4","author":"Tiranti","year":"1995","journal-title":"Hum Mol Genet"},{"key":"key20180108023034_b8-mmr-12-06-8176","doi-asserted-by":"crossref","first-page":"4174","DOI":"10.1093\/nar\/21.18.4174","article-title":"A molecular basis for human hypersensitivity to aminoglycoside antibiotics","volume":"21","author":"Hutchin","year":"1993","journal-title":"Nucleic Acids Res"},{"key":"key20180108023034_b9-mmr-12-06-8176","doi-asserted-by":"crossref","first-page":"615","DOI":"10.1136\/jmg.2004.020230","article-title":"Molecular analysis of mitochondrial 12S rRNA and tRNASer(UCN) genes in paediatric subjects with nonsyndromic hearing loss","volume":"41","author":"Li","year":"2004","journal-title":"J Med Genet"},{"key":"key20180108023034_b10-mmr-12-06-8176","doi-asserted-by":"crossref","first-page":"167","DOI":"10.1089\/gtmb.2008.0098","article-title":"Screening of the general Polish population for deafness-associated mutations in mitochondrial 12S rRNA and tRNA Ser(UCN) genes","volume":"13","author":"Rydzanicz","year":"2009","journal-title":"Genet Test Mol Biomarkers"},{"key":"key20180108023034_b11-mmr-12-06-8176","doi-asserted-by":"crossref","first-page":"967","DOI":"10.1093\/nar\/26.4.967","article-title":"Automating the identification of DNA variations using quality-based fluorescence re-sequencing: Analysis of the human mitochondrial genome","volume":"26","author":"Rieder","year":"1998","journal-title":"Nucleic Acids Res"},{"key":"key20180108023034_b12-mmr-12-06-8176","doi-asserted-by":"crossref","first-page":"147","DOI":"10.1038\/13779","article-title":"Reanalysis and revision of the cambridge reference sequence for human mitochondrial DNA","volume":"23","author":"Andrews","year":"1999","journal-title":"Nat Genet"},{"key":"key20180108023034_b13-mmr-12-06-8176","doi-asserted-by":"crossref","first-page":"289","DOI":"10.1038\/ng0793-289","article-title":"Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness","volume":"4","author":"Prezant","year":"1993","journal-title":"Nat Genet"},{"key":"key20180108023034_b14-mmr-12-06-8176","doi-asserted-by":"crossref","first-page":"1072","DOI":"10.1002\/humu.20378","article-title":"Evidence for adaptive selection acting on the tRNA and rRNA genes of human mitochondrial DNA","volume":"27","author":"Ruiz-Pesini","year":"2006","journal-title":"Hum Mutat"},{"key":"key20180108023034_b15-mmr-12-06-8176","doi-asserted-by":"crossref","first-page":"588","DOI":"10.1007\/s10528-013-9589-6","article-title":"The role of mitochondrial DNA mutations in hearing loss","volume":"51","author":"Ding","year":"2013","journal-title":"Biochem Genet"},{"key":"key20180108023034_b16-mmr-12-06-8176","doi-asserted-by":"crossref","first-page":"963","DOI":"10.1093\/hmg\/5.7.963","article-title":"Biochemical evidence for nuclear gene involvement in phenotype of non-syndromic deafness associated with mitochondrial 12S rRNA mutation","volume":"5","author":"Guan","year":"1996","journal-title":"Hum Mol Genet"},{"key":"key20180108023034_b17-mmr-12-06-8176","doi-asserted-by":"crossref","first-page":"69","DOI":"10.1016\/j.mito.2009.09.007","article-title":"Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation","volume":"10","author":"Lu","year":"2010","journal-title":"Mitochondrion"},{"key":"key20180108023034_b18-mmr-12-06-8176","doi-asserted-by":"crossref","first-page":"311","DOI":"10.1002\/humu.1380060405","article-title":"Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations","volume":"6","author":"Brown","year":"1995","journal-title":"Hum Mutat"},{"key":"key20180108023034_b19-mmr-12-06-8176","doi-asserted-by":"crossref","first-page":"5868","DOI":"10.1128\/MCB.18.10.5868","article-title":"The deafness-associated mitochondrial DNA mutation at position 7445, which affects tRNASer(UCN) precursor processing, has long-range effects on NADH dehydrogenase ND6 subunit gene expression","volume":"18","author":"Guan","year":"1998","journal-title":"Mol Cell Biol"}],"container-title":["Molecular Medicine Reports"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/spandidos-publications.com\/10.3892\/mmr.2015.4484\/download","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2018,1,7]],"date-time":"2018-01-07T23:39:17Z","timestamp":1515368357000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.spandidos-publications.com\/10.3892\/mmr.2015.4484"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2012,10,26]]},"references-count":19,"journal-issue":{"issue":"6","published-online":{"date-parts":[[2012,10,26]]},"published-print":{"date-parts":[[2015,12]]}},"alternative-id":["10.3892\/mmr.2015.4484"],"URL":"https:\/\/doi.org\/10.3892\/mmr.2015.4484","relation":{},"ISSN":["1791-2997","1791-3004"],"issn-type":[{"value":"1791-2997","type":"print"},{"value":"1791-3004","type":"electronic"}],"subject":[],"published":{"date-parts":[[2012,10,26]]}}}