검색어 : 통합검색[G1555]
총 291건 중 291건 출력
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191
- [Mitochondrial tRNA(Thr)T15943C mutation may be a new position that affects the phenotypic expression of deafness associated 12s rRNA A1555G mutation].
- Xiao, Hongli; He, Zheyun; Gao, Yinglong; Yang, Yaling; Zheng, Jing; Cai, Zhaoyang; Zheng, Binjiao; Tang, Xiaowen; Guan, Minxin; ; (中華醫學遺傳學雜誌 = Chinese journal of medical genetics, v.32, 2015, pp.163-168)
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192
- [Study of mtDNA 12S rRNA A1555G, GJB2, GJB3 gene mutation in Uighur and Han people with hereditary nonsyndromic hearing loss in Xinjiang.]
- Li, Yan-Hua; Jiang, Hua; Yang, Li-Juan; Xu, Hong-Xia; Li, Hui; Li, Hui-Wu; Luo, Yong-Hai; Wang, Chang-Wei; Zou, Guang-Hua; ; (中華耳鼻咽喉頭頸外科雜誌 = Chinese journal of otorhinolaryngology head and neck surgery, v.45, 2010, pp.645-651)
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193
- Lack of a modulative factor in locus 8p23 in a Finnish family with nonsyndromic sensorineural hearing loss associated with the 1555A>G mitochondrial DNA mutation
- Finnilä , Saara; Majamaa, Kari; [1] 1Department of Neurology, University of Oulu, Oulu, Finland [2] 2Department of Medical Biochemistry and Molecular Biology, University of Oulu, Oulu, Finland [3] 3Biocenter, University of Oulu, Oulu, Finland; [1] 1Department of Neurology, University of Oulu, Oulu, Finland [2] 2Department of Medical Biochemistry and Molecular Biology, University of Oulu, Oulu, Finland [3] 3Biocenter, University of Oulu, Oulu, Finland; (European journal of human genetics : EJHG, v.11, 2003, pp.652-658)
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194
- Genetic and clinical analysis of nonsyndromic hearing impairment in pediatric and adult cases
- Xing, J; Liu, X; Tian, Y; Tan, J; Zhao, H; Ear, Nose and Throat Department, The Central Hospital of Zhumadian, Zhumadian City, Henan Province, People’s Republic of China; Ear, Nose and Throat Department, The Central Hospital of Zhumadian, Zhumadian City, Henan Province, People’s Republic of China; Ear, Nose and Throat Department, The Central Hospital of Zhumadian, Zhumadian City, Henan Province, People’s Republic of China; Ear, Nose and Throat Department, The Central Hospital of Zhumadian, Zhumadian City, Henan Province, People’s Republic of China; (Balkan journal of medical genetics : BJMG, v.19, 2016, pp.35-42)
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195
- A novel mitochondrial mutation, 1556C→T, in a Japanese patient with streptomycin-induced tinnitus
- Tanimoto, Hitoshi; Nishio, Hisahide; Matsuo, Masafumi; Nibu, Ken-Ichi; From the Department of Otolaryngology--Head and Neck Surgery Kobe University Graduate School of Medicine Kobe Japan; Department of Environmental Health and Safety, Division of Public Health Kobe University Graduate School of Medicine Kobe Japan; Department of Pediatrics Kobe University Graduate School of Medicine Kobe Japan; From the Department of Otolaryngology--Head and Neck Surgery Kobe University Graduate School of Medicine Kobe Japan; (Acta oto-laryngologica, v.124, 2004, pp.258-261)
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196
- Mutant mtDNA at 1555 A to G in 12S rRNA Gene and Hypersusceptibility of Mitochondrial Translation to Streptomycin Can Be Co-Transferred to ρ<SUP>0</SUP>HeLa Cells
- Inoue, K.; Takai, D.; Soejima, A.; Isobe, K.; Yamasoba, T.; Oka, Y.; Goto, Y.i.; Hayashi, J.I.; ; (Biochemical and biophysical research communications, v.223, 1996, pp.496-501)
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197
- Molecular epidemiological analysis of mitochondrial DNA12SrRNA A1555G, <i>GJB2,</i> and <i>SLC26A4</i> mutations in sporadic outpatients with nonsyndromic sensorineural hearing loss in China
- Ji, Yu-bin; Han, Dong-Yi; Lan, Lan; Wang, Da-Yong; Zong, Liang; Zhao, Fei-Fan; Liu, Qiong; Benedict-Alderfer, Cindy; Zheng, Qing-yin; Wang, Qiu-Ju; Department of Otolaryngology/Head and Neck Surgery, Chinese PLA Institute of Otolaryngology, Chinese PLA General Hospital, Beijing, China; Department of Otolaryngology/Head and Neck Surgery, Chinese PLA Institute of Otolaryngology, Chinese PLA General Hospital, Beijing, China; Department of Otolaryngology/Head and Neck Surgery, Chinese PLA Institute of Otolaryngology, Chinese PLA General Hospital, Beijing, China; Department of Otolaryngology/Head and Neck Surgery, Chinese PLA Institute of Otolaryngology, Chinese PLA General Hospital, Beijing, China; Department of Otolaryngology/Head and Neck Surgery, Chinese PLA Institute of Otolaryngology, Chinese PLA General Hospital, Beijing, China; Department of Otolaryngology/Head and Neck Surgery, Chinese PLA Institute of Otolaryngology, Chinese PLA General Hospital, Beijing, China; Department of Otolaryngology/Head and Neck Surgery, Chinese PLA Institute of Otolaryngology, Chinese PLA General Hospital, Beijing, China; Department of Otolar; (Acta oto-laryngologica, v.131, 2011, pp.124-129)
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198
- Improvement of a Rapid and Highly Sensitive Method for the Diagnosis of the Mitochondrial m.1555A>G Mutation Based on a Single-Stranded Tag Hybridization Chromatographic Printed-Array Strip
- Isaka, Yuichi; Nishio, Shin-ya; Hishinuma, Eiji; Hiratsuka, Masahiro; Usami, Shin-ichi; Department of Hearing Implant Sciences and Shinshu University School of Medicine, Matsumoto, Japan.; Department of Hearing Implant Sciences and Shinshu University School of Medicine, Matsumoto, Japan.; Laboratory of Pharmacotherapy of Life-Style Related Diseases, Graduate School of Pharmaceutical Sciences, Tohoku University, Sendai, Japan.; Laboratory of Pharmacotherapy of Life-Style Related Diseases, Graduate School of Pharmaceutical Sciences, Tohoku University, Sendai, Japan.; Department of Hearing Implant Sciences and Shinshu University School of Medicine, Matsumoto, Japan.; (Genetic testing and molecular biomarkers, v.25, 2021, pp.79-83)
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199
- Indentation of a half-space with a rigid indentor - Voyiadjis, G Z; Buckner, N E Int J Num Meth Engng V19, N10, Oct 1983, P1555-1578
- ; ; (International journal of rock mechanics and mining sciences & geomechanics abstracts, v.21, 1984, pp.211)
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200
- Mutations in the Mitochondrial tRNA Ser(UCN) and in the GJB2 (Connexin 26) Gene Are Not Modifiers of the Age at Onset or Severity of Hearing Loss in Spanish Patients with the 12S rRNA A1555G Mutation
- Lopez-Bigas, N.; Rabionet, R.; Martinez, E.; Bravo, O.; Girons, J.; Borragan, A.; Pellicer, M.; Arbones, M.L.; Estivill, X.; ; (American journal of human genetics, v.66, 2000, pp.1465-1467)
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