검색어 : 통합검색[G1555]
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121
- GJB2 and mitochondrial A1555G gene mutations in nonsyndromic profound hearing loss and carrier frequencies in healthy individuals
- Baysal, Elif; Bayazit, Yildirim A.; Ceylaner, Serdar; Alatas, Necat; Donmez, Buket; Ceylaner, Gulay; San, Imran; Korkmaz, Baki; Yilmaz, Akin; Menevse, Adnan; Altunyay, Senay; Gunduz, Bulent; Goksu, Nebil; Arslan, Ahmet; Ekmekci, Abdullah; ; (Journal of genetics, v.87, 2008, pp.53-57)
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122
- Analysis of mitochondrial DNA heteroplasmic mutations A1555G, C3256T, T3336C, С5178А, G12315A, G13513A, G14459A, G14846А and G15059A in CHD patients with the history of myocardial infarction
- Mitrofanov, K.Y.; Zhelankin, A.V.; Shiganova, G.M.; Sazonova, M.A.; Bobryshev, Y.V.; Postnov, A.Y.; Sobenin I.@?., I.A.; Orekhov, A.N.; ; (Experimental and molecular pathology, v.100, 2016, pp.87-91)
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123
- Global prevalence of the mitochondrial MT-RNR1 A1555G variant in non-syndromic hearing loss: A systematic review and meta-analysis
- Baoai Han; Wenqing Wang; Han Wu; Juanjuan Hu; Liu Sun; Yun Zhu; Alan G. Cheng; Haiying Sun; ; (Neuroscience, v.570, 2025, pp.16-26)
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124
- Patients with <i>CDH23</i> mutations and the 1555A>G mitochondrial mutation are good candidates for electric acoustic stimulation (EAS)
- Usami, Shin-Ichi; Miyagawa, Maiko; Nishio, Shin-Ya; Moteki, Hideaki; Takumi, Yutaka; Suzuki, Mika; Kitano, Yoko; Iwasaki, Satoshi; Department of Otorhinolaryngology, Shinshu University School of Medicine, Matsumoto, Japan; Department of Otorhinolaryngology, Shinshu University School of Medicine, Matsumoto, Japan; Department of Otorhinolaryngology, Shinshu University School of Medicine, Matsumoto, Japan; Department of Otorhinolaryngology, Shinshu University School of Medicine, Matsumoto, Japan; Department of Otorhinolaryngology, Shinshu University School of Medicine, Matsumoto, Japan; Department of Otorhinolaryngology, Shinshu University School of Medicine, Matsumoto, Japan; School of Health Sciences, Tokai University, Isehara, Japan; Department of Hearing Implant Sciences, Shinshu University School of Medicine, Matsumoto, Japan; (Acta oto-laryngologica, v.132, 2012, pp.377-384)
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125
- <i>GJB2</i>,<i>SLC26A4</i>and mitochondrial DNA A1555G mutations in prelingual deafness in Northern Chinese subjects
- Guo, Yu-Fen; Guo, Yu-Fen; Liu, Xiao-Wen; Guan, Jing; Han, Ming-Kun; Wang, Da-Yong; Zhao, Ya-Li; Rao, Shao-Qi; Wang, Qiu-ju; ; (Acta oto-laryngologica, v.128, 2008, pp.297-303)
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126
- The frequency in New Zealand of a mitochondrial DNA mutation (1555 A to G) associated with aminoglycoside-induced hearing loss.
- Scrimshaw, B J; Faed, J M; Tate, W P; Yun, K; ; (New Zealand medical journal, v.112, 1999, pp.216-217)
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127
- GJB2 and mitochondrial DNA 1555A>G mutations in students with hearing loss in the Hubei Province of China
- Chen, G.; He, F.; Fu, S.; Dong, J.; Department of Medical Genetics, Tongji Medical College, Huazhong University of Science and Technology, 13 Hangkong Road, Wuhan 430030, China; (International journal of pediatric otorhinolaryngology, v.75, 2011, pp.1156-1159)
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128
- Prevalence of the A1555G (12S rRNA) and tRNA Ser(UCN) mitochondrial mutations in hearing-impaired Brazilian patients
- Abreu-Silva, R.S.; Lezirovitz, K.; Braga, M.C.C.; Spinelli, M.; Pirana, S.; Della-Rosa, V.A.; Otto, P.A.; Mingroni-Netto, R.C.; Universidade de Sã o Paulo, Brasil; Universidade de Sã o Paulo, Brasil; Universidade Estadual de Maringá , Brasil; Pontifí cia Universidade Cató lica de Sã o Paulo, Brasil; Pontifí cia Universidade Cató lica de Sã o Paulo, Brasil; Universidade Estadual de Maringá , Brasil; Universidade de Sã o Paulo, Brasil; Universidade de Sã o Paulo, Brasil; (Brazilian journal of medical and biological research = Revista brasileira de pesquisas médicas e biológicas, v.39, 2006, pp.219-226)
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129
- 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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130
- Screening of A1555G mDNA Variant Using U-TOP™HL Genotyping Kit in Korean Family with Progressive Hearing Loss
- Ahn, Jung Hyun; Byun, Kwang Hyun; Jung, Bo Kyeung; Lee, Min Young; ; (Korean journal of otorhinolaryngology-head and neck surgery, v.64, 2021, pp.108-113)
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