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Literature DB >> 2736791

Unique inheritance of streptomycin-induced deafness.

Abstract

Analysis of reported families which include two or more members with streptomycin-induced hearing loss reveals that the trait of high susceptibility of cochlea to streptomycin is transmitted primarily through females. This is not explained by ordinary Mendelian inheritance; rather it is best understood by extranuclear inheritance.

Entities: Chemical Disease

Mesh：

Substances：
Streptomycin

Year: 1989 PMID： 2736791

Source DB: PubMed Journal: Clin Genet ISSN： 0009-9163 Impact factor: 4.438

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Cited

13 in total

1. Heterogenous point mutations in the mitochondrial tRNA Ser(UCN) precursor coexisting with the A1555G mutation in deaf students from Mongolia.

Authors: A Pandya; X J Xia; R Erdenetungalag; M Amendola; B Landa; J Radnaabazar; B Dangaasuren; G Van Tuyle; W E Nance
Journal: Am J Hum Genet Date: 1999-12 Impact factor: 11.025

Review 2. Drug-induced tinnitus and other hearing disorders.

Authors: H Seligmann; L Podoshin; J Ben-David; M Fradis; M Goldsher
Journal: Drug Saf Date: 1996-03 Impact factor: 5.606

3. Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss.

Authors: Zhiyuan Li; Ronghua Li; Jianfu Chen; Zhisu Liao; Yi Zhu; Yaping Qian; Sudao Xiong; Selena Heman-Ackah; Jianbo Wu; Daniel I Choo; Min-Xin Guan
Journal: Hum Genet Date: 2005-04-20 Impact factor: 4.132

4. Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity.

Authors: A Pandya; X Xia; J Radnaabazar; J Batsuuri; B Dangaansuren; N Fischel-Ghodsian; W E Nance
Journal: J Med Genet Date: 1997-02 Impact factor: 6.318

Review 5. Proposed molecular and cellular mechanism for aminoglycoside ototoxicity.

Authors: T Hutchin; G Cortopassi
Journal: Antimicrob Agents Chemother Date: 1994-11 Impact factor: 5.191

6. The prevalence of mitochondrial mutations associated with aminoglycoside-induced deafness in ethnic Latvian population: the appraisal of the evidence.

Authors: Viktorija Igumnova; Lauma Veidemane; Anda Vīksna; Valentina Capligina; Egija Zole; Renate Ranka
Journal: J Hum Genet Date: 2018-12-06 Impact factor: 3.172

Unique inheritance of streptomycin-induced deafness.

1. Heterogenous point mutations in the mitochondrial tRNA Ser(UCN) precursor coexisting with the A1555G mutation in deaf students from Mongolia.

Review 2. Drug-induced tinnitus and other hearing disorders.

3. Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss.

4. Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity.

Review 5. Proposed molecular and cellular mechanism for aminoglycoside ototoxicity.

6. The prevalence of mitochondrial mutations associated with aminoglycoside-induced deafness in ethnic Latvian population: the appraisal of the evidence.

7. Audiological and genetic features of the mtDNA mutations.

8. Noise-induced hearing loss in mice treated with antiretroviral drugs.

Review 9. [Mitochondrial hearing impairment. Background, genetic predisposition and possibilities for diagnosis].

10. A six-generation Chinese family in haplogroup B4C1C exhibits high penetrance of 1555A > G-induced hearing Loss.