검색어 : 통합검색[G1555]
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21
- Mutant A1555G Mitochondrial 12S rRNA and Aminoglycoside Susceptibility
- Bö ttger, Erik C.; Institut fü r Medizinische Mikrobiologie Universitä t Zü rich Gloriastrasse 30/32 8006 Zurich, Switzerland Phone: 41-44-6342660 Fax: 41-44-6344906; (Antimicrobial agents and chemotherapy, v.54, 2010, pp.3073-3075)
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22
- Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutation
- Giordano, Carla; Pallotti, Francesco; Walker, Winsome F; Checcarelli, Nicoletta; Musumeci, Olimpia; Santorelli, Filippo; d'Amati, Giulia; Schon, Eric A; DiMauro, Salvatore; Hirano, Michio; Davidson, Mercy M; ; (Biochemical and biophysical research communications, v.293, 2002, pp.521-529)
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23
- Co-occurrence of A1555G and G11778A in a Chinese family with high penetrance of Leber's hereditary optic neuropathy
- Zhang, A.M.; Jia, X.; Yao, Y.G.; Zhang, Q.; ; (Biochemical and biophysical research communications, v.376, 2008, pp.221-224)
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24
- Mitochondrial tRNAThr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese families
- Wang, Xinjian; Lu, Jianxin; Zhu, Yi; Yang, Aifen; Yang, Li; Li, Ronghua; Chen, Bobei; Qian, Yaping; Tang, Xiaowen; Wang, Jindan; Zhang, Xue; Guan, Min-Xin; aDivision of Human Genetics and Center for Hearing and Deafness Research, Cincinnati Children’s Hospital Medical Center bDepartment of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA cZhejiang Provincial Key Laboratory of Medical Genetics, School of Life Sciences dDepartment of Otolaryngology, the First Affiliated Hospital eDepartment of Otolaryngology, the Second Affiliated Hospital, Wenzhou Medical College, Wenzhou, Zhejiang fDepartment of Genetics, Peking Union Medical College, Beijing, China; (Pharmacogenetics and genomics, v.18, 2008, pp.1059-1070)
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25
- Prevalence of the A1555G MTDNA mutation in sporadic hearing-impaired patients without known history of aminoglycoside treatment
- Morales Angulo, C.; Gallo-Teran, J.; Senaris, B.; Fontalva, A.; Gonzalez-Aguado, R.; Luis Fernandez-Luna, J.; ; (Acta otorrinolaringologica, v.62, 2011, pp.83-86)
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26
- Prevalence of Mitochondrial 1555A→G Mutation in Adults of European Descent
- Vandebona, Himesha; Mitchell, Paul; Manwaring, Neil; Griffiths, Kate; Gopinath, Bamini; Wang, Jie Jin; Sue, Carolyn M.; ; (The New England journal of medicine, v.360, 2009, pp.642-644)
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27
- Noninvasive Test for Mitochondrial DNA A1555G Mutation Associated with Deafness
- Fan, Wenlu; Zhu, Yi; Tang, Xiaowen; Xue, Ling; ; (Clinical laboratory, v.63, 2017, pp.127-132)
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28
- Prevalence of the mitochondrial A 1555G mutation in Moroccan patients with non-syndromic hearing loss
- Nahili, H.; Charif, M.; Boulouiz, R.; bounaceur, S.; Benrahma, H.; Abidi, O.; Chafik, A.; Rouba, H.; Kandil, M.; Barakat, A.; Laboratoire de Genetique Moleculaire et Humaine, Departement de Recherche Scientifique, Institut Pasteur, Place Louis Pasteur, 20360 Casablanca, Morocco; (International journal of pediatric otorhinolaryngology, v.74, 2010, pp.1071-1074)
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29
- Relevance of the A1555G Mutation in the 12S rRNA Gene for Hearing Impairment in Austria
- Ramsebner, Reinhard; Lucas, Trevor; Schoefer, Christian; Ludwig, Martin; Baumgartner, Wolf-Dieter; Wachtler, Franz J.; Kirschhofer, Karin; Frei, Klemens; *Department of Otorhinolaryngology; †Center of Anatomy and Cell Biology, Department of Chromatin and Developmental Dynamics, Medical University of Vienna; and ‡Department of Otorhinolaryngology, Krankenhaus der Barmherzigen Brü der, Vienna, Austria; (Otology & neurotology, v.28, 2007, pp.884-886)
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30
- Noninvasive Test for Mitochondrial DNA A1555G Mutation Associated with Deafness
- Fan, Wenlu; Zhu, Yi; Tang, Xiaowen; Xue, Ling; ; (Clinical laboratory, v.63, 2017, )
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