HuGE Literature Finder
Records 1-19
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Mitochondrial ND1 Variants in 1281 Chinese Subjects With Leber's Hereditary Optic Neuropathy.
Investigative ophthalmology & visual science 2016 May 57 (6): 2377-89. Ji Yanchun, Liang Min, Zhang Juanjuan, Zhu Ling, Zhang Zengjun, Fu Runing, Liu Xiaoling, Zhang Minglian, Fu Qun, Zhao Fuxin, Tong Yi, Sun Yanhong, Jiang Pingping, Guan Min-X |
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Genetic aetiology of ophthalmological manifestations in children - a focus on mitochondrial disease-related symptoms.
Acta ophthalmologica 2015 Oct . Widgren Paula, Hurme Anri, Falck Aura, Keski-Filppula Riikka, Remes Anne M, Moilanen Jukka, Majamaa Kari, Kervinen Marko, Uusimaa Johan |
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Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated ND1 G3460A mutation in Chinese families.
Journal of human genetics 2014 Mar 59 (3): 134-40. Ji Yanchun, Liang Min, Zhang Juanjuan, Zhang Minglian, Zhu Jinping, Meng Xiangjuan, Zhang Sai, Gao Min, Zhao Fuxin, Wei Qi-Ping, Jiang Pingping, Tong Yi, Liu Xiaoling, Qin Mo Jun, Guan Min-X |
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Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated m.14484T>C (MT-ND6) mutation in Chinese families.
Mitochondrion 2013 Nov 13 (6): 772-81. Zhang Juanjuan, Zhao Fuxin, Fu Qun, Liang Min, Tong Yi, Liu Xiaoling, Lin Bei, Mi Hui, Zhang Minglian, Wei Qi-Ping, Xue Ling, Jiang Pingping, Zhou Xiangtian, Mo Jun Qin, Huang Taosheng, Qu Jia, Guan Min-X |
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Prevalence of the primary LHON mutations in Northern Finland associated with bilateral optic atrophy and tobacco-alcohol amblyopia.
Acta ophthalmologica 2013 Nov 91 (7): 630-4. Korkiamäki Paula, Kervinen Marko, Karjalainen Karoliina, Majamaa Kari, Uusimaa Johanna, Remes Anne |
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Applications of the method of high resolution melting analysis for diagnosis of Leber's disease and the three primary mutation spectrum of LHON in the Han Chinese population.
Gene 2013 Jan 512 (1): 108-12. Cui Guanglin, Ding Hu, Xu Yujun, Li Bin, Wang Dao W |
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[A clinical study of Leber hereditary optic neuropathy].
[Zhonghua yan ke za zhi] Chinese journal of ophthalmology 2012 Dec 48 (12): 1065-8. Wei Qi-Ping, Sun Yan-Hong, Zhou Xiang-tian, Zhou Jian, Gong Xiao-hong, Jia Xiao-y |
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[Study on three common mitochondrial DNA mutations in Leber's hereditary optic neuropathy].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2012 Oct 29 (5): 519-23. Ma Yun-xia, Zhou Yon-gan, Zhang Jing-ping, Zhang Quan-bin, Liu Wei-la, Ren Cai-fen, Li Xiao- |
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Mitochondrial DNA variant associated with Leber hereditary optic neuropathy and high-altitude Tibetans.
Proceedings of the National Academy of Sciences of the United States of America 2012 May 109 (19): 7391-6. Ji Fuyun, Sharpley Mark S, Derbeneva Olga, Alves Leonardo Scherer, Qian Pin, Wang Yaoli, Chalkia Dimitra, Lvova Maria, Xu Jiancheng, Yao Wei, Simon Mariella, Platt Julia, Xu Shiqin, Angelin Alessia, Davila Antonio, Huang Taosheng, Wang Ping H, Chuang Lee-Ming, Moore Lorna G, Qian Guisheng, Wallace Douglas |
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Screening the three LHON primary mutations in the general Chinese population by using an optimized multiplex allele-specific PCR.
Clinica chimica acta; international journal of clinical chemistry 2010 Nov 411 (21-22): 1671-4. Bi Rui, Zhang A-Mei, Yu Dandan, Chen Diana, Yao Yong-Ga |
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Extensive screening system using suspension array technology to detect mitochondrial DNA point mutations.
Mitochondrion 2010 Apr 10 (3): 300-8. Nishigaki Yutaka, Ueno Hitomi, Coku Jorida, Koga Yasutoshi, Fujii Tatsuya, Sahashi Ko, Nakano Kazutoshi, Yoneda Makoto, Nonaka Michiko, Tang Linya, Liou Chia-Wei, Paquis-Flucklinger Veronique, Harigaya Yasuo, Ibi Tohru, Goto Yu-ichi, Hosoya Hiroko, DiMauro Salvatore, Hirano Michio, Tanaka Masas |
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Gene-environment interactions in Leber hereditary optic neuropathy.
Brain : a journal of neurology 2009 Sep 132 (Pt 9): 2317-26. Kirkman Matthew Anthony, Yu-Wai-Man Patrick, Korsten Alex, Leonhardt Miriam, Dimitriadis Konstantin, De Coo Ireneaus F, Klopstock Thomas, Chinnery Patrick Franc |
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Mutational analysis of the mitochondrial tRNALeu(UUR) gene in Tunisian patients with mitochondrial diseases.
Biochemical and biophysical research communications 2007 Apr 355 (4): 1031-7. Mkaouar-Rebai Emna, Tlili Abdelaziz, Masmoudi Saber, Belguith Neila, Charfeddine Ilhem, Mnif Mouna, Triki Chahnez, Fakhfakh Fai |
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Mitochondrial D-loop variation in leber hereditary neuropathy patients harboring primary G11778A, G3460A, T14484C mutations: J and W haplogroups as high-risk factors.
Archives of medical research 2006 Nov 37 (8): 1028-33. Shafa Shariat Panahi Mehdi, Houshmand Massoud, Tabassi Abdol Re |
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[Clinical features and the mutation of Leber's hereditary optic neuropathy in Chinese patients].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2005 Jun 22 (3): 334-6. Wang Yan, Guo Xiang-ming, Jia Xiao-yun, Li Shi-qiang, Xiao Xue-shan, Guo Li, Zhang Qing-jio |
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Lack of association between Leber's hereditary optic neuropathy primary point mutations and multiple sclerosis in Iran.
European neurology 2004 51 (2): 68-71. Houshmand M, Sanati M-H, Rashedi I, Sharifpanah F, Asghari E, Lotfi |
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Accumulation of mitochondrial genome variations in Persian LQTS patients: a possible risk factor?
Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology 0 19 (2): e21-7. Khatami Mehri, Houshmand Massoud, Sadeghizadeh Majid, Eftekharzadeh Mahmood, Heidari Mohammad Mehdi, Saber Siamak, Banihashemi Kambiz, Scheiber-Mojdehkar Barba |
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Meta-analysis of the prevalence of Leber hereditary optic neuropathy mtDNA mutations in Europe.
European journal of ophthalmology 0 22 (3): 461-5. Mascialino Barbara, Leinonen Mika, Meier Thom |
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Mitochondrial DNA mutations with Leber's hereditary optic neuropathy in Japanese patients with open-angle glaucoma.
Japanese journal of ophthalmology 0 50 (2): 128-34. Inagaki Yoko, Mashima Yukihiko, Fuse Nobuo, Ohtake Yuichiro, Fujimaki Takuro, Fukuchi Takeo, |
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- Page last updated:Jan 23, 2020
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