검색어 : 통합검색[G1555]
총 291건 중 291건 출력
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101
- Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation
- Lu, J.; Qian, Y.; Li, Z.; Yang, A.; Zhu, Y.; Li, R.; Yang, L.; Tang, X.; Chen, B.; Ding, Y.; Li, Y.; You, J.; Zheng, J.; Tao, Z.; Zhao, F.; Wang, J.; Sun, D.; Zhao, J.; Meng, Y.; Guan, M.X.; ; (Mitochondrion, v.10, 2010, pp.69-81)
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102
- Mitochondrial 12S rRNA A1555G mutation associated with nonsyn-dromic hearing loss in twenty-five Han Chinese pedigrees : Mitochondrial 12S rRNA A1555G mutation associated with nonsyn-dromic hearing loss in twenty-five Han Chinese pedigrees
- PENG, Guang-Hua; ZHENG, Bin-Jiao; FANG, Fang; WU, Yue; LIANG, Ling-Zhi; ZHENG, Jing; NAN, Ben-Yu; YU, Xiao; TANG, Xiao-Wen; ZHU, Yi; LU, Jian-Xin; CHEN, Bo-Bei; GUAN, Min-Xin; ; (遺傳 = Hereditas, v.35, 2013, pp.62-72)
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103
- Predisposición familiar a la ototoxicidad de los aminoglucósidos debido a la mutación A1555G del ADN mitocondrial
- Gallo-Terá n, Jaime; Morales-Angulo, Carmelo; del Castillo, Ignacio; Á ngel Moreno-Pelayo, Miguel; Mazó n, Á ngel; Moreno, Felipe; ; (Medicina clínica, v.121, 2003, pp.216-218)
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104
- Contribution of the tRNA<sup>Ile</sup> 4317A→G mutation to the phenotypic manifestation of the deafness-associated mitochondrial 12S rRNA 1555A→G mutation
- Meng, Feilong; He, Zheyun; Tang, Xiaowen; Zheng, Jing; Jin, Xiaofen; Zhu, Yi; Ren, Xiaoyan; Zhou, Mi; Wang, Meng; Gong, Shasha; Mo, Jun Qin; Shu, Qiang; Guan, Min-Xin; From the Division of Medical Genetics and Genomics, The Children's Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang 310052, China,; the Attardi Institute of Mitochondrial Biomedicine, School of Life Sciences, and; the Attardi Institute of Mitochondrial Biomedicine, School of Life Sciences, and; From the Division of Medical Genetics and Genomics, The Children's Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang 310052, China,; the Institute of Genetics,; Department of Otolaryngology, The First Affiliated Hospital, Wenzhou Medical University, Wenzhou, Zhejiang 325035, China,; the Attardi Institute of Mitochondrial Biomedicine, School of Life Sciences, and; From the Division of Medical Genetics and Genomics, The Children's Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang 310052, China,; From the Division of Medical Genetics and Genomics, The Children's Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang 310; (The Journal of biological chemistry, v.293, 2018, pp.3321-3334)
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105
- Molecular Investigation of the A1555G Mitochondrial Mutation in Brazilian Patients~!2009-04-10~!2010-01-19~!2010-06-18~!
- Piatto Vania B.; Maniglia Luciano P.; Silva Magali A.O.M.; Maniglia Jose Victor; ; (The Open Otorhinolaryngology Journal, v.4, 2010, pp.68-72)
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106
- The mitochondrial transfer RNAAsp A7551G mutation may contribute to the clinical expression of deafness associated with the A1555G mutation in a pedigree with hearing impairment
- Zhang Jing; Lu Bo; Xia Wei‑Wei; Fang Bin; Ding Xiao‑Xia; Hu Guang‑Wei; Department of Otolaryngology, Zhoushan Hospital, Zhejiang University School of Medicine, Zhoushan, Zhejiang 316021, P.R. China; Department of Otolaryngology, Zhoushan Hospital, Zhejiang University School of Medicine, Zhoushan, Zhejiang 316021, P.R. China; Department of Otolaryngology, Zhoushan Hospital, Zhejiang University School of Medicine, Zhoushan, Zhejiang 316021, P.R. China; Department of Otolaryngology, Zhoushan Hospital, Zhejiang University School of Medicine, Zhoushan, Zhejiang 316021, P.R. China; Central Laboratory, Hangzhou First People' s Hospital, Hangzhou, Zhejiang 310006, P.R. China; Department of Otolaryngology, Zhoushan Hospital, Zhejiang University School of Medicine, Zhoushan, Zhejiang 316021, P.R. China; (Molecular Medicine Reports, v., 2018, )
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107
- Sequence analysis of the connexin 26 genes from a deafness family with A1555G mutation in huaiyin
- ZHANG, Haijun; School, of Medicine; Southeast, University); XU, Chunhong; School, of Medicine; Southeast, University); ZHANG, Yiju; ZHAO, Suying; School, of Medicine; Southeast, University); GENG, Xuexia; SHAN, Yunfeng; School, of Medicine; Southeast, University); FAN, Gang; XING, Guangqian; SHAN, Xiangnian; School, of Medicine; Southeast, University); BU, Xingkuan; Genetics Research Cente; Genetics Research Cente; Genetics Research Cente; Genetics Research Cente; Genetics Research Cente; (中華耳鼻咽喉頭頸外科雜誌 = Chinese journal of otorhinolaryngology head and neck surgery, v.40, 2005, pp.678-683)
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108
- Mitochondrial tRNA<SUP>Glu</SUP> A14693G variant may modulate the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in a Han Chinese family
- Ding, Y.; Li, Y.; You, J.; Yang, L.; Chen, B.; Lu, J.; Guan, M.-X.; ; (Genetic and genomic medicine, v.2009, 2009, pp.241-250)
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109
- On the Variable Nebul of Hind (N.G.C. 1555) and Struve (N.G.C. 1554) in Taurus, and on the Nebulous Condition of the Variable Star T Tauri
- Barnard E. E.; ; (Monthly Notices of the Royal Astronomical Society, v.55, 1895, pp.442-453)
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110
- Observations of Hind's Variable Nebula in Taurus (N.G.C. 1555), made with the 40 inch Refractor of the Yerkes Observatory
- Barnard E. E.; ; (Monthly Notices of the Royal Astronomical Society, v.59, 1899, pp.372-376)
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