검색어 : 통합검색[G1555]
총 291건 중 291건 출력
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181
- Pilgrimage to Puritanism: History and Theology of the Marian Exiles at Geneva. 1555-1560. By Dan G. Danner. New York: Peter Lang, 1999. 168 pp. np.
- Johnson, G.; ; (A Journal of Church and State, v.41, 1999, pp.837-838)
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182
- Isolation and Characterization of the Putative Nuclear Modifier Gene MTO1 Involved in the Pathogenesis of Deafness-associated Mitochondrial 12 S rRNA A1555G Mutation
- Li, Xiaoming; Li, Ronghua; Lin, Xinhua; Guan, Min-Xin; ; (The Journal of biological chemistry, v.277, 2002, pp.27256-27264)
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183
- Mitochondrial COX2 G7598A Mutation May Have a Modifying Role in the Phenotypic Manifestation of Aminoglycoside Antibiotic-Induced Deafness Associated with 12S rRNA A1555G Mutation in a Han Chinese Pedigree
- Chen, Tianbin; Liu, Qicai; Jiang, Ling; Liu, Can; Ou, Qishui; First Clinical College, Fujian Medical University, Fuzhou, China.; Department of Laboratory Medicine, The First Affiliated Hospital of Fujian Medical University, Fuzhou, China.; Department of Laboratory Medicine, The First Affiliated Hospital of Fujian Medical University, Fuzhou, China.; Department of Laboratory Medicine, The First Affiliated Hospital of Fujian Medical University, Fuzhou, China.; Department of Laboratory Medicine, The First Affiliated Hospital of Fujian Medical University, Fuzhou, China.; (Genetic testing and molecular biomarkers, v.17, 2013, pp.122-130)
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185
- Atypical muscle pathology and a survey of <I>cis</I>-mutations in deaf patients harboring a 1555 A-to-G point mutation in the mitochondrial ribosomal RNA gene
- Yamasoba, Tatsuya; Goto, Yu-ichi; Oka, Yoshitomo; Nishino, Ichizo; Tsukuda, Katsunori; Nonaka, Ikuya; ; (Neuromuscular disorders : NMD, v.12, 2002, pp.506-512)
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186
- [A novel method of detecting mitochondrial C1494T and A1555G mutations by using the base-quenched probe technique in a single PCR assay].
- ZHENG, Lu; LUO, Guang-hua; ZHANG, Jun; ZHANG, Xiao-ying; XU, Ning; ; (中華耳鼻咽喉頭頸外科雜誌 = Chinese journal of otorhinolaryngology head and neck surgery, v.47, 2012, pp.326-329)
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187
- The 12S rRNA A1555G mutation in the mitochondrial haplogroup D5a is responsible for maternally inherited hypertension and hearing loss in two Chinese pedigrees
- Chen, Hong; Zheng, Jing; Xue, Ling; Meng, Yanzi; Wang, Yan; Zheng, Bingjiao; Fang, Fang; Shi, Suxue; Qiu, Qiaomeng; Jiang, Pingping; Lu, Zhongqiu; Mo, Jun Qin; Lu, Jianxin; Guan, Min-Xin; 1] Attardi Institute of Mitochondrial Biomedicine and Zhejiang Provincial Key Laboratory of Medical Genetics, Wenzhou Medical College, Wenzhou, Zhejiang, China [2] Emergercy Medical Department, The First Affiliated Hospital, of Wenzhou Medical College, Wenzhou, Zhejiang, China; Attardi Institute of Mitochondrial Biomedicine and Zhejiang Provincial Key Laboratory of Medical Genetics, Wenzhou Medical College, Wenzhou, Zhejiang, China; Attardi Institute of Mitochondrial Biomedicine and Zhejiang Provincial Key Laboratory of Medical Genetics, Wenzhou Medical College, Wenzhou, Zhejiang, China; Attardi Institute of Mitochondrial Biomedicine and Zhejiang Provincial Key Laboratory of Medical Genetics, Wenzhou Medical College, Wenzhou, Zhejiang, China; Attardi Institute of Mitochondrial Biomedicine and Zhejiang Provincial Key Laboratory of Medical Genetics, Wenzhou Medical College, Wenzhou, Zhejiang, China; Attardi Institute of Mitochondrial Biomedicine and Zhejiang Provincial Key Laborator; (European journal of human genetics : EJHG, v.20, 2012, pp.607-612)
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188
- Co segregation of the m.1555A>G mutation in the MT-RNR1 gene and mutations in MT-ATP6 gene in a family with dilated mitochondrial cardiomyopathy and hearing loss: A whole mitochondrial genome screening
- Alila-Fersi, Olfa; Chamkha, Imen; Majdoub, Imen; Gargouri, Lamia; Mkaouar-Rebai, Emna; Tabebi, Mouna; Tlili, Abdelaziz; Keskes, Leila; Mahfoudh, Abdelmajid; Fakhfakh, Faiza; Laboratoire de Gé né tique Molé culaire et Fonctionnelle, Faculté des Sciences de Sfax, University of Sfax, Tunisia; Department of Mitochondrial Medicine, Lund University, Sweden; Service de Ré animation Pé diatrique, C.H.U. Hé di Chaker de Sfax, Tunisia; Service de Ré animation Pé diatrique, C.H.U. Hé di Chaker de Sfax, Tunisia; Laboratoire de Gé né tique Molé culaire et Fonctionnelle, Faculté des Sciences de Sfax, University of Sfax, Tunisia; Laboratoire de Gé né tique Molé culaire Humaine, Faculté de Mé decine de Sfax, University of Sfax, Tunisia; Department of Applied Biology, College of Sciences, University of Sharjah, Sharjah, United Arab Emirates; Laboratoire de Gé né tique Molé culaire Humaine, Faculté de Mé decine de Sfax, University of Sfax, Tunisia; Service de Ré animation Pé diatrique, C.H.U. Hé di Chak; (Biochemical and biophysical research communications, v.484, 2017, pp.71-78)
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189
- Corrigendum: Chikusetsusaponin IVa methyl ester induces G1 cell cycle arrest, triggers apoptosis and inhibits migration and invasion in ovarian cancer cells. Phytomedicine, 2016, 23(13): 1555-1565
- Chen, X.; Wu, Q.S.; Meng, F.C.; Tang, Z.H.; Chen, X.; Lin, L.G.; Chen, P.; Qiang, W.A.; Wang, Y.T.; Zhang, Q.W.; Lu, J.J.; ; (Phytomedicine : international journal of phytotherapy and phytopharmacology, v.29, 2017, pp.e1)
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190
- The use of a MITO-Porter to deliver exogenous therapeutic RNA to a mitochondrial disease’s cell with a A1555G mutation in the mitochondrial 12S rRNA gene results in an increase in mitochondrial respiratory activity
- Yamada, Yuma; Maruyama, Minako; Kita, Tomoko; Usami, Shin-ichi; Kitajiri, Shin-ichiro; Harashima, Hideyoshi; Faculty of Pharmaceutical Sciences, Hokkaido University; Faculty of Pharmaceutical Sciences, Hokkaido University; Center for iPS Research and Application, Kyoto University; School of Medicine, Shinshu University; School of Medicine, Shinshu University; Faculty of Pharmaceutical Sciences, Hokkaido University; (Mitochondrion, v.55, 2020, pp.134-144)
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