검색어 : 통합검색[G1555]
총 291건 중 291건 출력
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11
- Analysis of mitochondrial A1555G mutation in infants with hearing impairment
- Wu Lihua; Li Ruiyu; Chen Juan; Chen Yanping; Yang Meijun; Wu Qing; Department of Otolaryngology, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou, Fujian 350001, P.R. China; Department of Otolaryngology, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou, Fujian 350001, P.R. China; Department of Otolaryngology, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou, Fujian 350001, P.R. China; Department of Obstetrics, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou, Fujian 350001, P.R. China; Department of Neonatology, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou, Fujian 350001, P.R. China; Department of Neonatology, Fujian Provincial Maternal and Child Health Care Hospital, Fuzhou, Fujian 350001, P.R. China; (Experimental and Therapeutic Medicine, v., 2018, )
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12
- Prevalence of Mitochondrial 1555A→G Mutation in European Children
- Bitner-Glindzicz, Maria; Pembrey, Marcus; Duncan, Andrew; Heron, Jon; Ring, Susan M.; Hall, Amanda; Rahman, Shamima; ; (The New England journal of medicine, v.360, 2009, pp.640-642)
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13
- Aminoglycosides: ototoxicity more severe with m.1555A>G mutation :
- &NA; ,; ; (Reactions weekly, v.&, 2007, pp.1)
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14
- The A1555G mtDNA mutation in Danish hearing-impaired patients: frequency and clinical signs
- Østergaard, E; Montserrat-Sentis, B; Grønskov, K; Brøndum-Nielsen, K; ; (Clinical genetics, v.62, 2002, pp.303-305)
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15
- Aminoglycosides: ototoxicity more severe with m.1555A>G mutation :
- &NA; ,; ; (Inpharma weekly, v.&, 2007, pp.21)
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16
- Factors that affect hearing level in individuals with the mitochondrial 1555A>G mutation
- Lu, SY; Nishio, S; Tsukada, K; Oguchi, T; Kobayashi, K; Abe, S; Usami, S; 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; Division of Advanced Technology and Development, BML, Inc, Kawagoe-shi, Saitama, Japan; Department of Otorhinolaryngology, Shinshu University School of Medicine, Matsumoto, Japan; (Clinical genetics, v.75, 2009, pp.480-484)
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17
- Identification of a mitochondrial 12S rRNA A1555G mutation causing aminoglycoside-induced deafness in a large Thai family
- Chaiyasap, Pongsathorn; Srichomthong, Chalurmpon; Tongkobpetch, Siraprapa; Suphapeetiporn, Kanya; Shotelersuk, Vorasuk; Interdepartment of Biomedical Sciences , Faculty of Graduate School , Chulalongkorn University , Bangkok 10330 , Thailand; Center of Excellence for Medical Genetics , Department of Pediatrics, Faculty of Medicine , Chulalongkorn University , Bangkok 10330 , Thailand; Center of Excellence for Medical Genetics , Department of Pediatrics, Faculty of Medicine , Chulalongkorn University , Bangkok 10330 , Thailand; Center of Excellence for Medical Genetics , Department of Pediatrics, Faculty of Medicine , Chulalongkorn University , Bangkok 10330 , Thailand; (Asian biomedicine : research, reviews and news, v.9, 2015, pp.211-215)
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18
- Carrier frequency of the 35delG and A1555G deafness mutations in the Argentinean population
- Gravina, L.P.; Foncuberta, M.E.; Estrada, R.C.; Barreiro, C.; Chertkoff, L.; ; (International journal of pediatric otorhinolaryngology, v.71, 2007, pp.639-643)
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19
- Molecular Characterization of Putative Modulatory Factors in Two Spanish Families with A1555G Deafness
- Otaegui, D.; Irizar, H.; Goicoechea, M.; Pé rez-Tur, J.; Belar, M.; Ló pez de Munain, A.; Unidad Experimental,; Unidad Experimental,; Unidad Experimental,; Unitat de Genè tica Molecular, Institut Biomedicina de Valencia-CSIC, Valencia, Spain; Servicio de Ginecologí a and; Servicio de Neurologí a, Hospital Donostia, San Sebastiá n, and; (Audiology and neurotology, v.13, 2008, pp.320-327)
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20
- Frequency of mitochondrial m.1555A > G mutation in Syrian patients with non-syndromic hearing impairment
- Kaheel, Hazem; Breß, Andreas; Hassan, Mohamed A.; Shah, Aftab Ali; Amin, Mutaz; Bakhit, Yousuf H. Y.; Kniper, Marlies; University, HNO -universities Klink-Tubingen, Tubingen, Germany; University, HNO -universities Klink-Tubingen, Tubingen, Germany; University, HNO -universities Klink-Tubingen, Tubingen, Germany; Faculty of Biotechnology, University of Malakand, Khyber Pakhtunkhwa, Pakistan; Department of Biochemistry, Faculty of Medicine, University of Khartoum, P. O. Box 102, Khartoum, Sudan; Department of Basic Medical Sciences, Faculty of Dentistry-University of Khartoum, Khartoum, Sudan; University, HNO -universities Klink-Tubingen, Tubingen, Germany; (BMC ear, nose, and throat disorders, v.18, 2018, pp.7)
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