검색어 : 통합검색[G1555]
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131
- Connexin 26 gene (GJB2) mutation modulates the severity of hearing loss associated with the 1555A→G mitochondrial mutation
- Abe, Satoko; Kelley, Philip M.; Kimberling, William J.; Usami, Shin-ichi; Department of Otorhinolaryngology, Hirosaki University School of Medicine, Hirosaki, Japan; Department of Genetics, Boys Town National Research Hospital, Omaha, Nebraska; Department of Genetics, Boys Town National Research Hospital, Omaha, Nebraska; Department of Otorhinolaryngology, Shinshu University School of Medicine, Matsumoto, Japan; (American journal of medical genetics, v.103, 2001, pp.334-338)
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132
- Mutation A1555G in the 12S rRNA gene and its epidemiological importance in German, Hungarian, and Polish patients
- Kupka, Susan; Tó th, Tí mea; Wró bel, Maciej; Zeiß ler, Ulrike; Szyfter, Witold; Szyfter, Krzysztof; Niedzielska, Grazyna; Bal, Jerzy; Zenner, Hans-Peter; Sziklai, Istvá n; Blin, Nikolaus; Pfister, Markus; ; (Human mutation, v.19, 2002, pp.308-309)
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133
- Co-segregation of the T1095C with the A1555G mutation of the mitochondrial 12S rRNA gene in a patient with non-syndromic hearing loss
- Dai, D.; Lu, Y.; Chen, Z.; Wei, Q.; Cao, X.; Xing, G.; ; (Biochemical and biophysical research communications, v.377, 2008, pp.1152-1155)
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134
- Familial Progressive Sensorineural Deafness Is Mainly Due to the mtDNA A1555G Mutation and Is Enhanced by Treatment with Aminoglycosides
- ; ; (American journal of human genetics, v.62, 1998, pp.27-35)
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135
- Correction to: Prevalence of the mitochondrial 1555 A>G and 1494 C>T mutations in a community-dwelling population in Japan
- Maeda, Yasunori; Sasaki, Akira; Kasai, Shuya; Goto, Shinichi; Nishio, Shin-ya; Sawada, Kaori; Tokuda, Itoyo; Itoh, Ken; Usami, Shin-ichi; Matsubara, Atsushi; Department of Otorhinolaryngology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan; Department of Otorhinolaryngology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan; Department of Stress Response Science, Center for Advanced Medical Research, Hirosaki University Graduate School of Medicine, Hirosaki, Japan; Department of Otorhinolaryngology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan; Department of Otorhinolaryngology, Shinshu University School of Medicine, Matsumoto, Japan; Department of Social Medicine, Hirosaki University School of Medicine, Hirosaki, Japan; Department of Social Medicine, Hirosaki University School of Medicine, Hirosaki, Japan; Department of Stress Response Science, Center for Advanced Medical Research, Hirosaki University Graduate School of Medicine, Hirosaki, Japan; Department of Otorhinolaryngology, Shinshu University School of Medicine, Matsumoto, Japan; Department of Otorhinolaryngology, Hirosak; (Human genome variation, v.7, 2020, pp.36)
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136
- [Analysis of GJB2 gene and mitochondrial DNA A1555G mutations in 16 families with non-syndromic hearing loss].
- Wang, Wei; Cheng, Hong-bo; Yang, Nian; Shi, Yi-chao; Liu, Jin-zhi; Li, Qin; Yang, Shen-min; Shen, Li-yan; Liu, Min-juan; Chen, Ying; Li, Hong; ; (中華醫學遺傳學雜誌 = Chinese journal of medical genetics, v.29, 2012, pp.388-392)
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137
- Large-scale screening of mtDNA A1555G mutation in China and its significance in prevention of aminoglycoside antibiotic induced deafness
- Liu, Xin; Dai, Pu; Huang, Deliang; Yuan, Huijun; Li, Weimin; Cao, Juyang; Yu, Fei; Zhang, Ruining; Lin, Hongyan; Zhu, Xiuhui; He, Yong; Yu, Youjun; Yao, Kun; Department of Otolaryngology, General Hospital of People＇s Liberation Army; Department of Otolaryngology, General Hospital of People＇s Liberation Army; Department of Otolaryngology, General Hospital of People＇s Liberation Army; Department of Otolaryngology, General Hospital of People＇s Liberation Army; Department of Otolaryngology, General Hospital of People＇s Liberation Army; Department of Otolaryngology, General Hospital of People＇s Liberation Army; Department of Otolaryngology, General Hospital of People＇s Liberation Army; (中華醫學雜誌 = National medical journal of China, v.86, 2006, pp.1318-1322)
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138
- Genedrive kit for detecting single nucleotide polymorphism m.1555A>G in neonates and their mothers: a systematic review and cost-effectiveness analysis
- Shabaninejad Hosein; Kenny Ryan PW; Robinson Tomos; Stoniute Akvile; O’Keefe Hannah; Still Madeleine; Thornton Christopher; Pearson Fiona; Beyer Fiona; Meader Nick; ; (Health Technology Assessment, v., 2024, pp.1-75)
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139
- Unique penetrance of hearing loss in a five-generation Chinese family with the mitochondrial 12S rRNA 1555A > G mutation
- Men, Meichao; Jiang, Lu; Wang, Honghan; Liu, Yalan; Hu, Zhengmao; He, Chufeng; Feng, Yong; Department of Otolaryngology, Head and Neck Surgery, Xiangya Hospital, Central South University, Changsha City, Hunan Province; Department of Otolaryngology, Head and Neck Surgery, Xiangya Hospital, Central South University, Changsha City, Hunan Province; Department of Otolaryngology, Head and Neck Surgery, Xiangya Hospital, Central South University, Changsha City, Hunan Province; State Key Laboratory of Medical Genetics of China, Central South University, Changsha City, Hunan Province, China; State Key Laboratory of Medical Genetics of China, Central South University, Changsha City, Hunan Province, China; Department of Otolaryngology, Head and Neck Surgery, Xiangya Hospital, Central South University, Changsha City, Hunan Province; Department of Otolaryngology, Head and Neck Surgery, Xiangya Hospital, Central South University, Changsha City, Hunan Province; (Acta oto-laryngologica, v.131, 2011, pp.970-975)
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140
- Prevalencia de la mutación A1555G del gen MTRNR1 en pacientes con hipoacusia postlocutiva sin antecedentes familiares de sordera
- Morales Angulo, Carmelo; Gallo-Terá n, Jaime; Señ aris, Blanca; Fontalva, Ana; Gonzá lez-Aguado, Rocí o; Ferná ndez-Luna, José Luis; ; (Acta otorrinolaringológica española, v.62, 2011, pp.83-86)
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