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Articles of Interest

• Lvova, Maria A.; Derbeneva, Olga A.; Chalkia, Dimitra; Chuang, Lee-Ming; Wang, Ping H.; Chang, Yi-Cheng; Mishmar, Dan & Wallace, Douglas (2010). 117 Asian mitochondrial DNA (mtDNA) lineage F4 is associated with increased risk of developing metabolic syndrome. Mitochondrion, 10(2), 233.
• Williams, Si^on; Urnov, Fyodor; Zhang, Lei & Moraes, Carlos (2010). 34 Zinc finger nucleases targeted to the m3243A>G mutation in mitochondrial encephalomyopathy (MELAS). Mitochondrion, 10(2), 209.
• Rani, Deepa S.; Dhandapany, Perundurai S.; Nallari, Pratibha; Govindaraj, Periyasamy; Singh, Lalji & Thangaraj, Kumarasamy (2010). Mitochondrial DNA haplogroup ‘R' is associated with Noonan syndrome of South India. Mitochondrion, 10(2), 166-173.
• Lu, Jianxin; Qian, Yaping; Li, Zhiyuan; Yang, Aifen; Zhu, Yi; Li, Ronghua; Yang, Li; Tang, Xiaowen; Chen, Bobei & Ding, Yu (2010). Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation. Mitochondrion, 10(1), 69-81.
• Lupi, Renato; de Meo, Paolo DOnorio D.; Picardi, Ernesto; DAntonio, Mattia; Paoletti, Daniele; Castrignano, Tiziana; Pesole, Graziano & Gissi, Carmela (2010). MitoZoa: a curated mitochondrial genome database of metazoans for comparative genomics studies. Mitochondrion, 10(2), 192-199.
• Elango, S., Govindaraj, P., Vishwanadha, V.P., Reddy, A.G., Tamang, R., Muthusami, U., Kunnoth, S., Koyilil, V.K., Lakshman, M., Shanmugasundharam, N. and Singh, L. (2011). Analysis of mitochondrial genome revealed a rare 50 bp deletion and substitutions in a family with hypertension. Mitochondrion, 11(6), 878-885.
• Fan, L., & Yao, Y. G. (2011). MitoTool: a web server for the analysis and retrieval of human mitochondrial DNA sequence variations. Mitochondrion, 11(2), 351-356.
• Fan, L., & Yao, Y. G. (2013). An update to MitoTool: using a new scoring system for faster mtDNA haplogroup determination. Mitochondrion, 13(4), 360-363.
• Govindaraj, P., Khan, N.A., Gopalakrishna, P., Chandra, R.V., Vanniarajan, A., Reddy, A.A., Singh, S., Kumaresan, R., Srinivas, G., Singh, L. and Thangaraj, K. (2011). Mitochondrial dysfunction and genetic heterogeneity in chronic periodontitis. Mitochondrion, 11(3), 504-512.
• Guillet, V., Chevrollier, A., Cassereau, J., Letournel, F., Gueguen, N., Richard, L., Desquiret, V., Verny, C., Procaccio, V., Amati-Bonneau, P. and Reynier, P. (2010). Ethambutol-induced optic neuropathy linked to OPA1 mutation and mitochondrial toxicity. Mitochondrion, 10(2), 115-124.
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