검색어 : 통합검색[G1555]
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31
- Clinical and molecular findings in a Chinese family with a de novo mitochondrial A1555G mutation
- Gu, Ping; Wang, Guojian; Gao, Xue; Kang, Dongyang; Dai, Pu; Huang, Shasha; College of Otolaryngology Head and Neck Surgery, Chinese PLA General Hospital, Chinese PLA Medical School, Do.28 Fuxing Road, Beijing, 100853 People’s Republic of China; College of Otolaryngology Head and Neck Surgery, Chinese PLA General Hospital, Chinese PLA Medical School, Do.28 Fuxing Road, Beijing, 100853 People’s Republic of China; College of Otolaryngology Head and Neck Surgery, Chinese PLA General Hospital, Chinese PLA Medical School, Do.28 Fuxing Road, Beijing, 100853 People’s Republic of China; College of Otolaryngology Head and Neck Surgery, Chinese PLA General Hospital, Chinese PLA Medical School, Do.28 Fuxing Road, Beijing, 100853 People’s Republic of China; College of Otolaryngology Head and Neck Surgery, Chinese PLA General Hospital, Chinese PLA Medical School, Do.28 Fuxing Road, Beijing, 100853 People’s Republic of China; College of Otolaryngology Head and Neck Surgery, Chinese PLA General Hospital, Chinese PLA Medical School, Do.28 Fuxing Road, Beijing,; (BMC medical genomics, v.15, 2022, pp.121)
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32
- Analysis of GJB2 gene and mtDNA A1555G mutation in non-syndromic hearing loss patients
- LU, Yajie; CHENG, Hongbo; XING, Guangqian; CAO, Xin; DAI, Dachun; CHEN, Zhibin; Ji, Qiang; WEI, Qingjun; BU, Xingkuan; Department of Biotechnology; NJMU; Department of Biotechnology; NJMU; Department of Otorhinolaryngology; the First Affiliated Hospital of NJMU; Department of Biotechnology; NJMU; Department of Otorhinolaryngology; the First Affiliated Hospital of NJMU; Department of Otorhinolaryngology; the First Affiliated Hospital of NJMU; Department of Forensic Medicine, NJMU; Department of Biotechnology; NJMU; Department of Otorhinolaryngology; the First Affiliated Hospital of NJMU; (南京醫科大學學報. Acta Universitatis Medicinalis Nanjing. 自然科學版, v.28, 2008, pp.855-860)
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33
- The A1555G mitochondrial DNA mutation in Greek patients with non-syndromic, sensorineural hearing loss
- Kokotas, Haris; Grigoriadou, Maria; Korres, George S.; Ferekidou, Elisabeth; Papadopoulou, Eleftheria; Neou, Polyxene; Giannoulia-Karantana, Aglaia; Kandiloros, Dimitrios; Korres, Stavros; Petersen, Michael B.; ; (Biochemical and biophysical research communications, v.390, 2009, pp.755-757)
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34
- Aminoglycoside-induced deafness associated with the mitochondrial DNA mutation A1555G
- Shohat, Mordechai; Fischel-Ghodsian, Nathan; Legum, Cyril; Halpern, Gabrielle J.; ; (American journal of otolaryngology, v.20, 1999, pp.64-67)
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35
- Hearing loss due to the mitochondrial A1555G mutation in Italian families
- Casano, Rosaria A.M.S.; Bykhovskaya, Yelena; Johnson, David F.; Hamon, Melanie; Torricelli, Francesca; Bigozzi, Minna; Fischel-Ghodsian, Nathan; Ahmanson Department of Pediatrics, Steven Spielberg Pediatric Research Center, Medical Genetics Birth Defects Center, Cedars-Sinai Medical Center and UCLA School of Medicine, Los Angeles, California; Ahmanson Department of Pediatrics, Steven Spielberg Pediatric Research Center, Medical Genetics Birth Defects Center, Cedars-Sinai Medical Center and UCLA School of Medicine, Los Angeles, California; Ahmanson Department of Pediatrics, Steven Spielberg Pediatric Research Center, Medical Genetics Birth Defects Center, Cedars-Sinai Medical Center and UCLA School of Medicine, Los Angeles, California; Ahmanson Department of Pediatrics, Steven Spielberg Pediatric Research Center, Medical Genetics Birth Defects Center, Cedars-Sinai Medical Center and UCLA School of Medicine, Los Angeles, California; Cytogenetic and Genetic O. Unity, Azienda Ospedaliera Careggi, Florence, Italy; Otolaryngology Clinic, Department of Audiology, University of Study, Florence, Italy; Ahmanson Department of Pedia; (American journal of medical genetics, v.79, 1998, pp.388-391)
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36
- Audio Profiles in Mitochondrial Deafness m.1555A>G and m.3243A>G Show Distinct Differences
- Iwanicka-Pronicka, Katarzyna; Pollak, Agnieszka; Skó rka, Agata; Lechowicz, Urszula; Korniszewski, Lech; Westfal, Przemysław; Skarż yń ski, Henryk; Płoski, Rafał; Department of Audiology Phoniatrics and Laryngology, Children’s Memorial Health Institute, Warsaw, Poland; Department of Genetics, Institut of Physiology and Pathology of Hearing, Kajetany/Warsaw, Poland; Department of Pediatrics, Medical University of Warsaw, Warsaw, Poland; Department of Genetics, Institut of Physiology and Pathology of Hearing, Kajetany/Warsaw, Poland; Department of Genetics, Institut of Physiology and Pathology of Hearing, Kajetany/Warsaw, Poland; Department of Administration, Children’s Memorial Health Institute, Warsaw, Poland; Department of Otorhinolaryngology, Institute of Physiology and Pathology of Hearing, Kajetany/Warsaw, Poland; Department of Medical Genetics, Medical University of Warsaw, Warsaw, Poland; (Medical science monitor : international medical journal of experimental and clinical research, v.21, 2015, pp.694-700)
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37
- Создание цибридных культур, содержащих мутацию митохондриального генома m.1555A>G (ген MT-RNR1), имеющую протективный эффект при атеросклерозе
- Сазонова, М.А.; Синёв, В.В.; Рыжкова, А.И.; Сазонова, М.Д.; Дорощук, Н.А.; Кириченко, Т.В.; Орехов, А.Н.; Собенин, И.А.; ; (Patologicheskaia fiziologiia i èksperimental'naia terapiia, v.65, 2021, pp.121-127)
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38
- A1555G Polymorphism and Aminoglycoside-induced Hearing Loss from Intratympanic Gentamicin Therapy
- Wan, Tan-Kuai; Huang, Chi-Jung; Wang, Pa-Chun; ; (Otolaryngology-head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery, v.149, 2013, pp.P148-P148)
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39
- Características audiométricas de la hipoacusia familiar transmitida por herencia mitocondrial (A1555G)
- Morales Angulo, C.; Gallo Terá n, J.; Garcí a-Mantilla, J.; Del Castillo, I.; Moreno Pelayo, M.Á .; Moreno Herrero, F.; ; (Acta otorrinolaringológica española, v.53, 2002, pp.641-648)
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40
- A South African family with the mitochondrial A1555G mutation on haplogroup L0d
- Human, H.; Lombard, D.; de Jong, G.; Bardien, S.; Division of Molecular Biology and Human Genetics, University of Stellenbosch, Cape Town, South Africa; (Biochemical and biophysical research communications, v.382, 2009, pp.390-394)
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