검색어 : 통합검색[G1555]
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61
- Mitochondrial DNA G7444A mutation may influence the phenotypic manifestation of the deafness-associated 12S rRNA A1555G mutation : Mitochondrial DNA G7444A mutation may influence the phenotypic manifestation of the deafness-associated 12S rRNA A1555G mutation
- YANG, Ai-Fen; ; (遺傳 = Hereditas, v.30, 2008, pp.728-734)
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62
- Audiological Follow-Up of Children with the m.1555A>G Mutation in Mitochondrial DNA
- Hä kli, Sanna; Luotonen, Mirja; Sorri, Martti; Majamaa, Kari; Department of Otorhinolaryngology and; Department of Otorhinolaryngology and; Otorhinolaryngology and; Clinical Research Center, Oulu University Hospital, and Departments of; (Audiology & neuro-otology, v.18, 2012, pp.23-30)
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63
- Mitochondrial tRNAIle A4317G mutation may influence the pheno-typic manifestation of deafness-associated 12S rRNA A1555G mutation : Mitochondrial tRNAIle A4317G mutation may influence the pheno-typic manifestation of deafness-associated 12S rRNA A1555G mutation
- LIANG, Ling-Zhi; WU, Yue; YANG, Ya-Ling; CAI, Qin; XIAO, Hong-Li; ZHENG, Jing; ZHENG, Bin-Jiao; TANG, Xiao-Wen; ZHU, Yi; LU, Jian-Xin; GUAN, Min-Xin; ; (遺傳 = Hereditas, v.35, 2013, pp.752-760)
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64
- Isepamicin Sulfate-Induced Sensorineural Hearing Loss in Patients with the 1555 A→G Mitochondrial Mutation
- Usami, Shin-ichi; Abe, Satoko; Tono, Tetsuya; Komune, Shizuo; Kimberling, William J.; Shinkawa, Hideichi; Department of Otorhinolaryngology, Hirosaki University School of Medicine, Hirosaki,; Department of Otorhinolaryngology, Hirosaki University School of Medicine, Hirosaki,; Department of Otorhinolaryngology, Miyazaki Medical College, Miyazaki, Japan; ; Department of Otorhinolaryngology, Miyazaki Medical College, Miyazaki, Japan; ; Department of Genetics, Boys Town National Research Hospital, Omaha, Nebr., USA; Department of Otorhinolaryngology, Hirosaki University School of Medicine, Hirosaki,; (ORL : Journal for Oto-Rhino-Laryngology, Head and Neck Surgery, v.60, 1998, pp.164-169)
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65
- Study of mitochondrial DNA A1555G mutation among nonsyndromic hearing impairment in Chinese population
- OU, Qishui; CHENG, Zujian; CHEN, Jing; YANG, Bin; JIANG, Ling; YE, Shengnan; Department of Laboratory Medicine, First Affiliated Hospital, Department of Gene Diagnostic Research, Department of Laboratory Medicine Fujian Medical University; Department of Laboratory Medicine, First Affiliated Hospital, Department of Gene Diagnostic Research, Department of Laboratory Medicine Fujian Medical University; Department of Laboratory Medicine, First Affiliated Hospital, Department of Gene Diagnostic Research, Department of Laboratory Medicine Fujian Medical University; Department of Laboratory Medicine, First Affiliated Hospital, Department of Gene Diagnostic Research, Department of Laboratory Medicine Fujian Medical University; Department of Laboratory Medicine, First Affiliated Hospital, Department of Gene Diagnostic Research, Department of Laboratory Medicine Fujian Medical University; Department of Laboratory Medicine, First Affiliated Hospital, Department of Gene Diagnostic Research, Department of Laboratory Medicine Fujian Medical University; (中華檢驗醫學雜志 = Chinese journal of laboratory medicine, v.30, 2007, pp.273-275)
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66
- Cosegregation of the mitochondrial DNA A1555G and G4309A mutations results in deafness and mitochondrial myopathy
- Campos, Y.; Garcí a, A.; Ló pez, A.; Jimé nez, S.; Rubio, J.C.; Del Hoyo, P.; Bustos, F.; Martí n, M.A.; Cabello, A.; Ricoy, J.R.; Arenas, J.; ; (Muscle & nerve, v.25, 2002, pp.185-188)
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67
- Frequency of the mitochondrial A1555G mutation in Iranian patients with nonsyndromic hearing impairment
- Zohour, M. Montazer; ; (Indian journal of science and technology, v.5, 2012, pp.1-6)
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68
- P251 Analysis of screening for the m.1555A>G mutation at annual review
- Dooney, M.K.; Baker-Wardle, K.; ; (Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society, v.23, 2024, pp.S145)
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69
- Extremely low penetrance of hearing loss in four Chinese families with the mitochondrial 12S rRNA A1555G mutation
- Young, Wie-Yen; Zhao, Lidong; Qian, Yaping; Wang, Qiuju; Li, Ning; Greinwald Jr., John H.; Guan Jr., Min-Xin; Institute of Otolaryngology, Chinese PLA General Hospital, Beijing, China; Institute of Otolaryngology, Chinese PLA General Hospital, Beijing, China; Division and Program in Human Genetics, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, USA; Institute of Otolaryngology, Chinese PLA General Hospital, Beijing, China; State Key Laboratory of Agricultural Biological Technique, China Agricultural University, Beijing, China; Center for Hearing and Deafness Research, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, USA; Division and Program in Human Genetics, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, USA; (Biochemical and biophysical research communications, v.328, 2005, pp.1244-1251)
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70
- A maternal hereditary deafness pedigree of the A1555G mitochondrial mutation, causing aminoglycoside ototoxicity predisposition
- Bai, Y-H; Ren, C-C; Gong, X-R; Meng, L-P; ; (The journal of laryngology and otology, v.122, 2008, pp.1037-1041)
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