Contact and support
Need help, have a question, or want to contact the ResearchHub team?
© 2026 ResearchHub. Built for responsible scholarly connection.
Privacy-aware community infrastructureResearch graph
References from 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?. Local targets link to admitted publications; unresolved targets remain external evidence.
genenames. org: the HGNC resources in 2011
10.1093/nar/gkq892 · 2011 · External reference
Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness
10.1038/ng0793-289 · 1993 · External reference
Molecular analysis of the mitochondrial 12S rRNA and tRNASer(UCN) genes in paediatric subjects with non-syndromic hearing loss
10.1136/jmg.2004.020230 · 2004 · External reference
Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip
10.1038/sj.ejhg.5201891 · 2007 · External reference
Mutation analysis of mitochondrial DNA 12SrRNA and tRNASer(UCN) genes in non-syndromic hearing loss patients
10.1016/j.mito.2008.08.001 · 2008 · External reference
Prevalence of the mitochondrial A 1555G mutation in Moroccan patients with non-syndromic hearing loss
10.1016/j.ijporl.2010.06.008 · 2010 · External reference
Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss
10.1016/j.mito.2010.01.007 · 2010 · External reference
Mitochondrial DNA mutations in patients with postlingual, nonsyndromic hearing impairment
10.1038/sj.ejhg.5201250 · 2005 · External reference
Investigation of mitochondrial sequence variants associated with aminoglycoside-induced ototoxicity in South African TB patients on aminoglycosides
10.1016/j.bbrc.2010.02.075 · 2010 · External reference
The prevalence of mitochondrial mutations associated with aminoglycoside-induced sensorineural hearing loss in an NICU population
10.1002/lary.21778 · 2011 · External reference
Analysis of mitochondrial 12S rRNA and tRNA(Ser(UCN)) genes in patients with nonsyndromic sensorineural hearing loss from various regions of Russia
2009 · External reference
Mitochondrial DNA mutation screening in South Florida
2010 · External reference
Unique spectrum of GJB2 mutations in Mexico
10.1016/j.ijporl.2012.08.005 · 2012 · External reference
The spectrum of hearing loss due to mitochondrial DNA defects
10.1093/brain/123.1.82 · 2000 · External reference
Mitochondrial deafness alleles confer misreading of the genetic code
10.1073/pnas.0707265105 · 2008 · External reference
A rapid method for detection of five known mutations associated with aminoglycoside-induced deafness
10.1186/1471-2350-10-2 · 2009 · External reference
Extensive and rapid screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss
10.1038/jhg.2009.143 · 2010 · External reference
The societal costs of severe to profound hearing loss in the United States
10.1017/s0266462300103162 · 2000 · External reference
Meta-analysis of prevalence
10.1136/jech-2013-203104 · 2013 · External reference
C1494T mitochondrial DNA mutation, hearing loss, and aminoglycosides antibiotics
2009 · External reference
Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment of aminoglycosides
10.1086/301676 · 1998 · External reference
Very low penetrance of hearing loss in seven Han Chinese pedigrees carrying the deafness-associated 12S rRNA A1555G mutation
10.1016/j.gene.2007.01.001 · 2007 · External reference
Aminoglycoside ototoxicity in Nicaraguan children: Patient risk factors and mitochondrial DNA results
10.1016/j.otohns.2008.09.027 · 2009 · External reference
Mitochondrial haplotype and phenotype of 13 Chinese families may suggest multi-original evolution of mitochondrial C1494T mutation
10.1016/j.mito.2009.07.006 · 2009 · External reference
Molecular and clinical characterization of the variable phenotype in Korean families with hearing loss associated with the mitochondrial A1555G mutation
10.1371/journal.pone.0042463 · 2012 · External reference
Prevalence and clinical features of the mitochondrial m.1555A>G mutation in Taiwanese patients with idiopathic sensorineural hearing loss and association of haplogroup F with low penetrance in three families
10.1097/aud.0b013e318047941e · 2007 · External reference
Screening of the general Polish population for deafness-associated mutations in mitochondrial 12S rRNA and tRNA Ser(UCN) genes
10.1089/gtmb.2008.0098 · 2009 · External reference
Heteroplasmy for the 1555A>G mutation in the mitochondrial 12S rRNA gene in six Spanish families with non-syndromic hearing loss
10.1136/jmg.40.8.632 · 2003 · External reference
Screening of the mitochondrial A1555G mutation in patients with sensorineural hearing loss
10.1016/s1808-8694(15)31384-7 · 2008 · External reference
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
10.1136/jmg.2006.042440 · 2006 · External reference
Carrier frequency of the 35delG and A1555G deafness mutations in the Argentinean population. Impact on the newborn hearing screening
10.1016/j.ijporl.2006.12.015 · 2007 · External reference
Genetic mutations and aminoglycoside-induced ototoxicity in neonates
10.1016/j.otohns.2010.01.030 · 2010 · External reference
Prevalence of A1555G mitochondrial mutation in Chinese newborns and the correlation with neonatal hearing screening
10.1016/j.ijporl.2011.01.013 · 2011 · External reference
A maternal hereditary deafness pedigree of the A1555G mitochondrial mutation, causing aminoglycoside ototoxicity predisposition
10.1017/s0022215107001648 · 2008 · External reference
Newborn hearing concurrent gene screening can improve care for hearing loss: A study on 14,913 Chinese newborns
10.1016/j.ijporl.2011.01.016 · 2011 · External reference
Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: Implication for early detection and prevention of deafness
10.1016/j.bbrc.2005.11.156 · 2006 · External reference
Combination of hearing screening and genetic screening for deafness-susceptibility genes in newborns
10.3892/etm.2013.1406 · 2014 · External reference
Efficient discrimination of three hotspot mutations associated with aminoglycoside antibiotics induced deafness in the mitochondrial 12S rRNA by on/off switch
2013 · External reference
A novel method of detecting mitochondrial C1494T and A1555G mutations by using the base-quenched probe technique in a single PCR assay
2012 · External reference
Novel multiplex primer extension and denaturing high-performance liquid chromatography for genotyping of the deafness gene mutations
2011 · External reference
Mutation analysis of the entire mitochondrial genome using denaturing high performance liquid chromatography
10.1093/nar/28.20.e89 · 2000 · External reference
Rapid screening for the mitochondrial DNA C1494T mutation in a deaf population in China using real-time quantitative PCR
2012 · External reference
The mitochondrial tRNA (Ala) T5628C variant may have a modifying role in the phenotypic manifestation of the 12S rRNA C1494T mutation in a large Chinese family with hearing loss
10.1016/j.bbrc.2007.03.199 · 2007 · External reference
Nuclear background determines biochemical phenotype in the deafness-associated mitochondrial 12S rRNA mutation
10.1093/hmg/10.6.573 · 2001 · External reference
Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss
10.1093/nar/gki262 · 2005 · External reference
Evidence for complex nuclear inheritance in a pedigree with nonsyndromic deafness due to a homoplasmic mitochondrial mutation
10.1002/(sici)1096-8628(19980605)77:5<421::aid-ajmg13>3.0.co;2-k · 1998 · External reference
Mitochondrial deafness mutations reviewed
10.1002/(sici)1098-1004(1999)13:4<261::aid-humu1>3.0.co;2-w · 1999 · External reference
Variants in mitochondrial tRNAGlu, tRNAArg, and tRNAThr may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese families with hearing loss
10.1002/ajmg.a.31434 · 2006 · External reference
Mitochondrial 12S rRNA A1555G mutation associated with nonsyndromic hearing loss in twenty-five Han Chinese pedigrees
10.3724/sp.j.1005.2013.00062 · 2013 · External reference
Interaction of aminoglycosides with human mitochondrial 12S rRNA carrying the deafness-associated mutation
10.1128/aac.00965-08 · 2009 · External reference
Mitochondrial tRNAThr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese families
10.1097/fpc.0b013e3283131661 · 2008 · External reference
Aminoglycoside antibiotics
10.1159/000013861 · 2000 · External reference
Gentamicin vestibulotoxicity
10.1177/019459989411100506 · 1994 · External reference
Recovery from vestibular ototoxicity
10.1097/00129492-200109000-00018 · 2001 · External reference
Experience with a once-daily aminoglycoside program administered to 2,184 adult patients
10.1128/aac.39.3.650 · 1995 · External reference
Gentamicin ototoxicity: Clinical features and the effect on the human vestibulo-ocular reflex
10.1080/00016480600606673 · 2006 · External reference
Aminoglycosides-50 years on
1995 · External reference
Ototoxicity of amikacin
10.1128/aac.9.6.956 · 1976 · External reference
Cochlear alterations in deaf and unaffected subjects carrying the deafness-associated A1555G mutation in the mitochondrial 12S rRNA gene
10.1016/j.bbrc.2006.03.143 · 2006 · External reference
Structural insights into translational fidelity
10.1146/annurev.biochem.74.061903.155440 · 2005 · External reference
