검색어 : 통합검색[G1555]
총 291건 중 291건 출력
, 21/30 페이지
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201
- Mitochondrial ND5 T12338C, tRNA<sup>Cys</sup> T5802C, and tRNA<sup>Thr</sup> G15927A variants may have a modifying role in the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese pedigrees
- Chen, Bobei; Sun, Dongmei; Yang, Li; Zhang, Chuqin; Yang, Aifen; Zhu, Yi; Zhao, Jianyue; Chen, Yingying; Guan, Minqiang; Wang, Xinjian; Li, Ronghua; Tang, Xiaowen; Wang, Jindan; Tao, Zhihua; Lu, Jianxin; Guan, Min-Xin; Department of Otolaryngology, The Second Affiliated Hospital, Wenzhou Medical College, Wenzhou, Zhejiang, China; Zhejiang Provincial Key Laboratory of Medical Genetics, School of Life Sciences, Wenzhou Medical College, Wenzhou, Zhejiang, China; Division of Human Genetics and Center for Hearing and Deafness Research, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio; Department of Otolaryngology, The Second Affiliated Hospital, Wenzhou Medical College, Wenzhou, Zhejiang, China; Zhejiang Provincial Key Laboratory of Medical Genetics, School of Life Sciences, Wenzhou Medical College, Wenzhou, Zhejiang, China; Zhejiang Provincial Key Laboratory of Medical Genetics, School of Life Sciences, Wenzhou Medical College, Wenzhou, Zhejiang, China; Zhejiang Provincial Key Laboratory of Medical Genetics, School of Life Sciences, Wenzhou Medical College, Wenzhou, Zhejiang, China; Department of Otolaryngology, The Second Affiliated Hospital, Wenzhou Medical College, Wenzhou, Zheji; (American Journal of Medical Genetics. Part A, v.a146, 2008, pp.1248-1258)
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202
- Variants in mitochondrial tRNA<sup>Glu</sup>, tRNA<sup>Arg</sup>, and tRNA<sup>Thr</sup> may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese families with hearing loss
- Young, Wie-Yen; Zhao, Lidong; Qian, Yaping; Li, Ronghua; Chen, Jing; Yuan, Huijun; Dai, Pu; Zhai, Suoqiang; Han, Dongyi; Guan, 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 and Center for Hearing and Deafness Research, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio; Division and Program in Human Genetics and Center for Hearing and Deafness Research, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio; Institute of Otolaryngology, Chinese PLA General Hospital, Beijing, China; Institute of Otolaryngology, Chinese PLA General Hospital, Beijing, China; Institute of Otolaryngology, Chinese PLA General Hospital, Beijing, China; Institute of Otolaryngology, Chinese PLA General Hospital, Beijing, China; Institute of Otolaryngology, Chinese PLA General Hospital, Beijing, China; Division and Program in Human Genetics and Center for Hearing and Deafness Research, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio; (American Journal of Medical Genetics. Part A, v.a140, 2006, pp.2188-2197)
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203
- In-situ temperature measurements for aluminum etching
- Castricher, G.; Banks, P.M.; Pang, T-M.; Baumann, P.; Grü nwald, H.; Hussla, I.; Lorenz, G.; Stoll, H.; Ramisch, H.; Leybold AG, P.O. Box 1555, 6450 Hanau 1, F.R.G.; UKAEA Harwell Laboratory, Oxon, OX11 0RA, U.K.; Authors for correspondence.; Leybold AG, P.O. Box 1555, 6450 Hanau 1, F.R.G.; Leybold AG, P.O. Box 1555, 6450 Hanau 1, F.R.G.; Authors for correspondence.; Leybold AG, P.O. Box 1555, 6450 Hanau 1, F.R.G.; Leybold AG, P.O. Box 1555, 6450 Hanau 1, F.R.G.; Leybold AG, P.O. Box 1555, 6450 Hanau 1, F.R.G.; (Microelectronic engineering, v.6, 1987, pp.559-563)
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204
- Cosegregation of C-insertion at position 961 with the A1555G mutation of the mitochondrial 12S rRNA gene in a large Chinese family with maternally inherited hearing loss
- Li, Ronghua; Xing, Guangqian; Yan, Ming; Cao, Xing; Liu, Xue-Zhong; Bu, Xingkuan; Guan, Min-Xin; ; (American Journal of Medical Genetics. Part A, v.a124, 2004, pp.113-117)
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205
- 88 Variants in mitochondrial tRNAs may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G and C1494T mutations in Chinese families with hearing loss
- Guan, M.X.; Young, W.Y.; Zhao, L.; Qian, Y.; Li, R.; Chen, J.; Dai, P.; Han, D.; Young, W.Y.; ; (Mitochondrion, v.7, 2007, pp.430)
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206
- The coexistence of mitochondrial ND6 T14484C and 12S rRNA A1555G mutations in a Chinese family with Leber’s hereditary optic neuropathy and hearing loss
- Wei, Qi-Ping; Zhou, Xiangtian; Yang, Li; Sun, Yan-Hong; Zhou, Jian; Li, Guang; Jiang, Robert; Lu, Fan; Qu, Jia; Guan, Min-Xin; ; (Biochemical and biophysical research communications, v.357, 2007, pp.910-916)
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207
- Prevalence and Clinical Features of the Mitochondrial m.1555A>G Mutation in Taiwanese Patients with Idiopathic Sensorineural Hearing Loss and Association of Haplogroup F with Low Penetrance in Three Families
- Wu, Chen-Chi; Chiu, Yu-Hsun; Chen, Pei-Jer; Hsu, Chuan-Jen; ; (Ear and hearing, v.28, 2007, pp.332-342)
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208
- Incidencia de las mutaciones a1555g en el adn mitocondrial y 35delg en el gen gjb2 (conexina 26) en familias con hipoacusia neurosensorial postlocutiva no sindrómica en cantabria
- Gallo-Terá n, J.; Morales-Angulo, C.; Del Castillo, I.; Villamar, M.; Moreno-Pelayo, M.Á .; Garcí a-Mantilla, J.; Moreno, F.; ; (Acta otorrinolaringológica española, v.53, 2002, pp.563-571)
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210
- Correspondence re: Feyler et al., Point: Myeloperoxidase <sup>-463</sup>G → A Polymorphism and Lung Cancer Risk. 11: 1550-1554, 2002, and Xu et al., Counterpoint: The Myeloperoxidase <sup>-463</sup>G → A Polymorphism Does Not Decrease Lung Cancer Susceptibility in Caucasians. 11: 1555-1559, 2002
- Dally, H.; Bartsch, H.; Risch, A.; ; (Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, v.12, 2003, pp.683)
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