The ND4 G11696A mutation may influence the phenotypic manifestation of the deafness-associated 12S rRNA A1555G mutation in a four-generation Chinese family

Zhisu Liao; Jianyue Zhao; Yi Zhu; Li Yang; Aifen Yang; Dongmei Sun; Zhongnong Zhao; Xinjian Wang; Zhihua Tao; Xiaowen Tang; Jindan Wang; Minqiang Guan; Jiafu Chen; Zhiyuan Li; Jianxin Lu; Min-Xin Guan

doi:10.1016/j.bbrc.2007.08.034

The ND4 G11696A mutation may influence the phenotypic manifestation of the deafness-associated 12S rRNA A1555G mutation in a four-generation Chinese family

Biochemical and Biophysical Research Communications ◽

10.1016/j.bbrc.2007.08.034 ◽

2007 ◽

Vol 362 (3) ◽

pp. 670-676 ◽

Cited By ~ 10

Author(s):

Zhisu Liao ◽

Jianyue Zhao ◽

Yi Zhu ◽

Li Yang ◽

Aifen Yang ◽

...

Keyword(s):

Chinese Family ◽

12S Rrna ◽

A1555g Mutation ◽

Phenotypic Manifestation

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Mitochondrial tRNAGlu A14693G variant may modulate the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in a Han Chinese family

Journal of Genetics and Genomics ◽

10.1016/s1673-8527(08)60111-3 ◽

2009 ◽

Vol 36 (4) ◽

pp. 241-250 ◽

Cited By ~ 16

Author(s):

Yu Ding ◽

Yongyan Li ◽

Junyan You ◽

Li Yang ◽

Bobei Chen ◽

...

Keyword(s):

Han Chinese ◽

Chinese Family ◽

12S Rrna ◽

A1555g Mutation ◽

Phenotypic Manifestation

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Cosegregation of C-insertion at position 961 with the A1555G mutation of the mitochondrial 12S rRNA gene in a large Chinese family with maternally inherited hearing loss

American Journal of Medical Genetics ◽

10.1002/ajmg.a.20305 ◽

2003 ◽

Vol 124A (2) ◽

pp. 113-117 ◽

Cited By ~ 106

Author(s):

Ronghua Li ◽

Guangqian Xing ◽

Ming Yan ◽

Xing Cao ◽

Xue-Zhong Liu ◽

...

Keyword(s):

Hearing Loss ◽

Chinese Family ◽

12S Rrna ◽

Rrna Gene ◽

A1555g Mutation ◽

12S Rrna Gene ◽

Mitochondrial 12S Rrna

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53. Mitochondrial tRNAThr G15927A variant may modulate the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation

Mitochondrion ◽

10.1016/j.mito.2008.12.047 ◽

2009 ◽

Vol 9 (1) ◽

pp. 74

Author(s):

Xinjian Wang ◽

Jianxin Lu ◽

Aifen Yang ◽

Li Yang ◽

Yi Zhu ◽

...

Keyword(s):

12S Rrna ◽

A1555g Mutation ◽

Phenotypic Manifestation

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Mitochondrial COX2 G7598A Mutation May Have a Modifying Role in the Phenotypic Manifestation of Aminoglycoside Antibiotic-Induced Deafness Associated with 12S rRNA A1555G Mutation in a Han Chinese Pedigree

Genetic Testing and Molecular Biomarkers ◽

10.1089/gtmb.2012.0251 ◽

2013 ◽

Vol 17 (2) ◽

pp. 122-130 ◽

Cited By ~ 5

Author(s):

Tianbin Chen ◽

Qicai Liu ◽

Ling Jiang ◽

Can Liu ◽

Qishui Ou

Keyword(s):

Aminoglycoside Antibiotic ◽

Han Chinese ◽

12S Rrna ◽

A1555g Mutation ◽

Phenotypic Manifestation

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Mitochondrial ND5 T12338C, tRNACys T5802C, and tRNAThr G15927A variants may have a modifying role in the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese pedigrees

American Journal of Medical Genetics Part A ◽

10.1002/ajmg.a.32285 ◽

2008 ◽

Vol 146A (10) ◽

pp. 1248-1258 ◽

Cited By ~ 33

Author(s):

Bobei Chen ◽

Dongmei Sun ◽

Li Yang ◽

Chuqin Zhang ◽

Aifen Yang ◽

...

Keyword(s):

Han Chinese ◽

12S Rrna ◽

A1555g Mutation ◽

Phenotypic Manifestation

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The mitochondrial tRNAAla 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

Biochemical and Biophysical Research Communications ◽

10.1016/j.bbrc.2007.03.199 ◽

2007 ◽

Vol 357 (2) ◽

pp. 554-560 ◽

Cited By ~ 26

Author(s):

Dongyi Han ◽

Pu Dai ◽

Qingwen Zhu ◽

Xin Liu ◽

Deliang Huang ◽

...

Keyword(s):

Hearing Loss ◽

Chinese Family ◽

12S Rrna ◽

Phenotypic Manifestation

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Cosegregation of the G7444A mutation in the mitochondrial COI/tRNASer(UCN) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside-induced and nonsyndromic hearing loss

American Journal of Medical Genetics Part A ◽

10.1002/ajmg.a.30952 ◽

2005 ◽

Vol 138A (2) ◽

pp. 133-140 ◽

Cited By ~ 68

Author(s):

Huijun Yuan ◽

Yaping Qian ◽

Yanjun Xu ◽

Juyang Cao ◽

Linna Bai ◽

...

Keyword(s):

Hearing Loss ◽

Chinese Family ◽

12S Rrna ◽

Nonsyndromic Hearing Loss ◽

Mitochondrial Coi ◽

A1555g Mutation

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Mitochondrial DNA G7444A mutation may influence the phenotypic manifestation of the deafness-associated 12S rRNA A1555G mutation

Hereditas (Beijing) ◽

10.3724/sp.j.1005.2008.00728 ◽

2008 ◽

Vol 30 (6) ◽

pp. 728-734 ◽

Cited By ~ 2

Author(s):

Ai-Fen YANG

Keyword(s):

Mitochondrial Dna ◽

12S Rrna ◽

A1555g Mutation ◽

Phenotypic Manifestation

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Mitochondrial tRNAThr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese families

Pharmacogenetics and Genomics ◽

10.1097/fpc.0b013e3283131661 ◽

2008 ◽

Vol 18 (12) ◽

pp. 1059-1070 ◽

Cited By ~ 40

Author(s):

Xinjian Wang ◽

Jianxin Lu ◽

Yi Zhu ◽

Aifen Yang ◽

Li Yang ◽

...

Keyword(s):

12S Rrna ◽

Chinese Families ◽

A1555g Mutation ◽

Phenotypic Manifestation

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Mitochondrial TrnaThr G15927A mutation may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation

Hereditas (Beijing) ◽

10.3724/sp.j.1005.2008.01287 ◽

2008 ◽

Vol 30 (10) ◽

pp. 1287-1294 ◽

Cited By ~ 1

Author(s):

Xiao-Wen TANG

Keyword(s):

12S Rrna ◽

Mitochondrial Trna ◽

A1555g Mutation ◽

Phenotypic Manifestation

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