Results 91 to 100 of about 12,888 (214)

Bioinformatics Study of m.9053G>A Mutation at the Gene in Relation to Type 2 Diabetes Mellitus and Cataract Diseases

Bioinformatics and Biology Insights, 2017
The mitochondrial disease often associated with various illnesses in relation to the activity of cells metabolites and the synthesis of adenosine triphosphate (ATP), including alteration in the mitochondrial DNA.
*Iman Permana Maksum, Sandy Risfi Saputra, Nenden Indrayati, *Muhammad Yusuf, Toto Subroto   +4 more
doaj   +1 more source

Plants for planting; indirect evidence for the movement of a serious forest pathogen, Teratosphaeria destructans, in Asia [PDF]

, 2011
Fungal diseases caused by native pathogens and pathogens introduced with planting stock have a significant impact on exotic plantation forestry in the tropics.
Wingfield, Michael J., Treena Burgess, Burgess, Treena I., Vera Andjic, Giles Hardy, Bernard Dell, Wingfield, M., Hardy, G., Paul Barber, Andjic, V., Barber, Paul A., Hardy, Giles E. St. J., Dell, Bernard (Bernie), Barber, P., Andjic, Vera, Dell, B., Michael Wingfield, Burgess, T.   +17 more
core   +1 more source

The mitochondrial genome analysis of Trypetoptera punctulata (Diptera: Sciomyzidae)

Mitochondrial DNA. Part B. Resources, 2019
The mitochondrial genome of Trypetoptera punctulate Scopoli, 1763, the first representative of Sciomyzidae, was sequenced and annotated. And we used this new nucleotide information under Maximum Likelihood analyses to explore the superfamilies ...
Qicheng Yang, Xin Li, Zhu Li, Zhaohui Pan, Ding Yang   +4 more
doaj   +1 more source

The clinical features and genetic characteristics of MT-ATP6-related mitochondrial disease: a national, observational study [PDF]

, 2019
Importance: Mutations in the mitochondrial MT-ATP6 gene are an important cause of mitochondrial disease. Phenotypes related to these mutations include Leigh syndrome (LS), and the syndrome of neuropathy, ataxia, and retinitis pigmentosa (NARP); however ...
Alston, Cl, Fratter, C, Blakely, El, Degoede, C, Horvath, R, Pitceathly, R, Taylor, Rw, Gorman, G, Bunting, A, Nesbitt, V, McEntagart, M, Horrocks, I, Ng, Ys, Blain, A, Hughes, I, Bugiardini, E, Turnbull, D, Schaefer, A, Spinty, S, Martikainen, M, Hanna, M, Poulton, J, Lim, A, Chinnery, P, McFarland, R   +24 more
core   +1 more source

Hereditary spastic paraplegia-like disorder due to a mitochondrial ATP6 gene point mutation [PDF]

, 2010
Hereditary spastic paraplegia refers to a genetically heterogeneous syndrome. We identified five members of a family suffering from a late-onset spastic paraplegia-like disorder, carrying the homoplasmic m.9176 T>C mutation in the mitochondrial ATP6 ...
Cassereau, Julien, A. Prundean, Verny, Christophe, Ferré, Marc, Desquiret-Dumas, Valérie, F. Dubas, V. Procaccio, Vincent Procaccio, Prundean, Adriana, A. Chevrollier, Adriana Prundean, Marc Ferre, Procaccio, Vincent, Naig Guegen, Pascal Reynier, Gueguen, Naïg, Chevrollier, Arnaud, Frederic Dubas, Dubas, Frédéric, Amati-Bonneau, Patrizia, Arnaud Chevrollier, D. Bonneau, Julien Cassereau, C. Verny, Dominique Bonneau, Bonneau, Dominique, Patrizia Amati-Bonneau, Valerie Desquiret, M. Ferré, P. Reynier, Christophe Verny, P. Amati-Bonneau, Reynier, Pascal, J. Cassereau, N. Gueguen, V. Desquiret-Dumas   +35 more
core   +1 more source

Mitochondrial DNA Missense Mutations ChrMT: 8981A > G and ChrMT: 6268C > T Identified in a Caucasian Female with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) Triggered by the Epstein–Barr Virus

Case Reports in Genetics
Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a multisystem disabling disease with unclear etiology and pathophysiology, whose typical symptoms include prolonged debilitating recovery from fatigue or postexertional malaise (PEM ...
Gaoyan G. Tang-Siegel, David W. Maughan, Milah B. Frownfelter, Alan R. Light   +3 more
doaj   +1 more source

Comparison of efficiency in different types of SNPs in accD and atp6 gene detected by ORG-EcoTILLING and DNA sequencing.

, 2012
*indicated that the reference sample was A64 and A24 in accD gene and atp6 gene, respectively. “+” indicated that there was an intense band visualized by ORG-EcoTIILLING. “−” indicated that there was no intense band detected by ORG-EcoTIILLING.
Guang-Yong Wang (116870), Bo Zhao (13553), Jun Li (6494), Kun Xu (116877), Chang-Li Zeng (116868), Bi-Yun Chen (116876), Gui-Zhen Gao (116879), Gui-Xin Yan (116875), Xiao-Ming Wu (116881), Jian-Bo Wang (116873), Lei Liu (5074)   +10 more
core   +1 more source

利用酵母双杂交系统筛选甘蓝型油菜ATP6的相互作用蛋白质

四川大学学报. 自然科学版, 2010
通过酵母双杂交系统,以ATP6作为诱饵蛋白筛选与ATP6有相互作用的蛋白质.通过筛选和鉴定,获得了5个与ATP6有相互作用的蛋白质.其中一个与拟南芥中内质网膜上的蛋白转运复合体中的α亚基(Sec61α)有很高的相似性.通过TAIL PCR和设计简并引物扩增初步得到了甘蓝型油菜Sec61α全长基因组序列和cDNA序列.并利用生物信息学分析手段对甘蓝型油菜Sec61α进行了比对和分析,推测该蛋白质可能参与了花粉的发育过程.
孙力, 李娜娜, 余渝, 柴靓, 王健美, 杨毅, 李旭峰   +6 more
doaj  

Complete mitochondrial genome sequence of the broad-winged damselfly, Mnais pruinosa Selys, 1853 (Odonata: Calopterygidae)

Mitochondrial DNA. Part B. Resources, 2019
In this study, we analyzed the complete mitochondrial genome of the Mnais pruinosa Selys, 1853 from Saga Prefecture, Japan. The mitochondrial genome of M. pruinosa was identified as a circular molecule of 15,494 bp, and was found to be similar to that of
Hisashi Okuyama, Takuya Kiyoshi, Jun-Ichi Takahashi, Yoshitaka Tsubaki   +3 more
doaj   +1 more source

Mitochondrial genome in sporadic breast cancer: A case control study and a proteomic analysis in a Sinhalese cohort from Sri Lanka

PLoS ONE, 2023
Breast cancer is the commonest malignancy in women and the majority occurs sporadically with no hereditary predisposition. However, sporadic breast cancer has been studied less intensively than the hereditary form and to date hardly any predictive ...
Lakshika P. Jayasekera, Ruwandi Ranasinghe, Kanishka S. Senathilake, Joanne T. Kotelawala, Kanishka de Silva, Priyanka H. Abeygunasekara, Renuka Goonesinghe, Kamani H. Tennekoon   +7 more
doaj