Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss is associated with the 12S rRNA C1494T mutation in three Han Chinese pedigrees.
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Mitochondrial diabetes in children: seek and you will find itMechanisms of aminoglycoside ototoxicity and targets of hair cell protection.Very low penetrance of Leber's hereditary optic neuropathy in five Han Chinese families carrying the ND1 G3460A mutation.Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing lossMitochondrial 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 mutationFrequency and spectrum of mitochondrial 12S rRNA variants in 440 Han Chinese hearing impaired pediatric subjects from two otology clinicsAminoglycoside stress together with the 12S rRNA 1494C>T mutation leads to mitophagy.An MRPS12 mutation modifies aminoglycoside sensitivity caused by 12S rRNA mutations.The ND4 G11696A mutation may influence the phenotypic manifestation of the deafness-associated 12S rRNA A1555G mutation in a four-generation Chinese family.Aminoglycosides: molecular insights on the recognition of RNA and aminoglycoside mimics.The role of mitochondrial DNA mutations in hearing loss.PharmGKB summary: very important pharmacogene information for MT-RNR1.Maternally transmitted aminoglycoside-induced and non-syndromic hearing loss caused by the 1494C > T mutation in the mitochondrial 12S rRNA gene in two Chinese families.Rapid screening for the mitochondrial DNA C1494T mutation in a deaf population in China using real-time quantitative PCR.Mitochondrial tRNAThr 15891C>G mutation was not associated with Leber's hereditary optic neuropathy in Han Chinese patients.The analysis of mitochondrial DNA haplogroups and variants for in vitro fertilization failure in a Han Chinese population.Mitochondrial DNA mutations associated with aminoglycoside induced ototoxicity.
P2860
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P2860
Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss is associated with the 12S rRNA C1494T mutation in three Han Chinese pedigrees.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Maternally inherited aminoglyc ...... n three Han Chinese pedigrees.
@ast
Maternally inherited aminoglyc ...... n three Han Chinese pedigrees.
@en
type
label
Maternally inherited aminoglyc ...... n three Han Chinese pedigrees.
@ast
Maternally inherited aminoglyc ...... n three Han Chinese pedigrees.
@en
prefLabel
Maternally inherited aminoglyc ...... n three Han Chinese pedigrees.
@ast
Maternally inherited aminoglyc ...... n three Han Chinese pedigrees.
@en
P2093
P2860
P1433
P1476
Maternally inherited aminoglyc ...... n three Han Chinese pedigrees.
@en
P2093
Aifen Yang
Asami Tsushima
Dongmei Sun
Jianfu Chen
Jianxin Lu
Jianyue Zhao
Jinbao Feng
Jindan Wang
P2860
P356
10.1016/J.GENE.2007.06.009
P407
P577
2007-06-20T00:00:00Z