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HuGE Navigator|HuGE Literature Finder|PHGKB

HuGE Literature Finder

Records 1-10

Query Trace: Neurodegenerative Diseases and ATP6[orginal query]

Mitochondrial DNA haplogroup B5 confers genetic susceptibility to Alzheimer's disease in Han Chinese. Neurobiology of aging 2015 Mar 36 (3): 1604.e7-16. Bi Rui, Zhang Wen, Yu Dandan, Li Xiao, Wang Hui-Zhen, Hu Qiu-Xiang, Zhang Chen, Lu Weihong, Ni Jianliang, Fang Yiru, Li Tao, Yao Yong-Ga Similar articles in PubMed
Role of dynamic and mitochondrial mutations in neurodegenerative diseases with ataxia: lower repeats and LNAs at multiple loci as alternative pathogenesis. Journal of molecular neuroscience : MN 2014 Dec 54 (4): 837-47. Gul Lone Waseem, Poornima Subhadra, Meena Angmuthu Kanikannan, Rao Kaipa Prabhakar, Hasan Qurratula Similar articles in PubMed
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 Similar articles in PubMed
Mitochondrial DNA polymorphisms/haplogroups in hereditary spastic paraplegia. Journal of neurology 2012 Feb 259 (2): 246-50. Sánchez-Ferrero Elena, Coto Eliecer, Corao Ana I, Díaz Marta, Gámez Josep, Esteban Jesús, Gonzalo Juan F, Pascual-Pascual Samuel I, López De Munaín Adolfo, Morís Germán, Infante Jon, Del Castillo Emilia, Márquez Celedonio, Alvarez Victor Similar articles in PubMed
Mitochondrial tRNALeu/Lys and ATPase 6/8 gene variations in spinocerebellar ataxias. Neuro-degenerative diseases 2009 6 (1-2): 16-22. Safaei Sepideh, Houshmand Massoud, Banoei Mohammad Mehdi, Panahi Mehdi Shafa Shariat, Nafisi Shahriar, Parivar Kazem, Rostami Maryam, Shariati Parv Similar articles in PubMed
MtSNPscore: a combined evidence approach for assessing cumulative impact of mitochondrial variations in disease. BMC bioinformatics 2009 10 Suppl 8 S7. Bhardwaj Anshu, Mukerji Mitali, Sharma Shipra, Paul Jinny, Gokhale Chaitanya S, Srivastava Achal K, Tiwari Shri Similar articles in PubMed
Mitochondrial DNA haplogroups M7b1'2 and M8a affect clinical expression of leber hereditary optic neuropathy in Chinese families with the m.11778G-->a mutation. American journal of human genetics 2008 Dec 83 (6): 760-8. Ji Yanli, Zhang A-Mei, Jia Xiaoyun, Zhang Ya-Ping, Xiao Xueshan, Li Shiqiang, Guo Xiangming, Bandelt Hans-Jürgen, Zhang Qingjiong, Yao Yong-Ga Similar articles in PubMed
Common mitochondrial DNA and POLG1 mutations are rare in the Chinese patients with adult-onset ataxia on Taiwan. Journal of the neurological sciences 2007 Mar 254 (1-2): 65-8. Lee Yi-Chung, Lu Yi-Chun, Chang Ming-Hon, Soong Bing-W Similar articles in PubMed
Genotyping Parkinson disease-associated mitochondrial polymorphisms. Clinical medicine & research 2004 May 2 (2): 99-106. Jiang Yiguo, Ellis Tammy, Greenlee Anne Similar articles in PubMed
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, Similar articles in PubMed

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