نتایج جستجو برای: ژن nd5

تعداد نتایج: 16037  

2017
Wei Li Qiang Li Aiqin Nie Li Jiang

Mutations in mitochondrial genome are the important causes of Leber’s Hereditary Optic Neuropathy (LHON). To investigate the pathophysiology of LHON, we recently initiated a systematic mutational screening for the candidate pathogenic mutations in mitochondrial genome. In this study, we described a Chinese family with LHON. Four of nine matrilineal relatives exhibited variable degree of vision ...

Journal: :Microscopy and microanalysis : the official journal of Microscopy Society of America, Microbeam Analysis Society, Microscopical Society of Canada 2011
M Radermacher T Ruiz D J Fowler L Yu S Dröse S Krack S Kerscher V Zickermann U Brandt

Complex I is the first and largest enzyme in the respiratory chain located in the inner mitochondrial membrane and in the membrane of many bacteria [1]. In the process of oxidizing NADH, Complex I translocates 4 protons across the membrane. This is followed by additional proton translocation by complexes III and IV. The resulting membrane potential powers ATP production by the F-ATPase. The min...

Journal: :Biochemical and biophysical research communications 2010
Yang Zou Xiaoyun Jia A-Mei Zhang Wen-Zhi Wang Shiqiang Li Xiangming Guo Qing-Peng Kong Qingjiong Zhang Yong-Gang Yao

LHON is one of the most common and primary causes of acute blindness in young male adults. Over 95% of LHON cases are caused by one of the three primary mutations (m.11778G>A, m.14484T>C, and m.3460G>A). In contrast to these genetically diagnosed LHON patients, there are many patients with clinical features of LHON but without the three primary mutations, and these patients have been insufficie...

Journal: :Journal of immunology 2015
Stefano Pierini Chongyun Fang Stavros Rafail John G Facciponte Jialing Huang Francesco De Sanctis Mark A Morgan Mireia Uribe-Herranz Janos L Tanyi Andrea Facciabene

Mitochondria provide energy for cells via oxidative phosphorylation. Reactive oxygen species, a byproduct of this mitochondrial respiration, can damage mitochondrial DNA (mtDNA), and somatic mtDNA mutations have been found in all colorectal, ovarian, breast, urinary bladder, kidney, lung, and pancreatic tumors studied. The resulting altered mitochondrial proteins or tumor-associated mitochondri...

Journal: :Molecular biology and evolution 2000
C G Kim H Z Zhou Y Imura O Tominaga Z H Su S Osawa

Most of the mitochondrial NADH dehydrogenase subunit 5 (ND5) gene and a part of nuclear 28S ribosomal RNA gene were sequenced for 14 species of ground beetles belonging to the genus Leptocarabus. In both the ND5 and the 28S rDNA phylogenetic trees of Leptocarabus, three major lineages were recognized: (1) L. marcilhaci/L. yokoael/Leptocarabus sp. from China, (2) L. koreanus/L. truncaticollis/L....

2018
Ying Wang Jin-Jun Cao Wei-Hai Li

Stoneflies comprise an ancient group of insects, but the phylogenetic position of Plecoptera and phylogenetic relations within Plecoptera have long been controversial, and more molecular data is required to reconstruct precise phylogeny. Herein, we present the complete mitogenome of a stonefly, Suwallia teleckojensis, which is 16146 bp in length and consists of 13 protein-coding genes (PCGs), 2...

Journal: :Genetics and molecular research : GMR 2014
J S B Ferreira S R Paiva E C Silva C M McManus A R Caetano D A E Façanha M A N de Sousa

The aim of this study was to analyze genetic diversity and population structure among varieties of White (N = 40), Red (N = 32), and Black (N = 31) Morada Nova hair sheep from flocks in the northeastern Brazilian semiarid region. Fifteen nuclear microsatellite markers and two regions of mitochondrial DNA were used. The intra-population analysis demonstrated that the White variety had higher div...

Journal: :Molecular and cellular biology 2006
Jian-Hong Deng Youfen Li Jeong Soon Park Jun Wu Peiqing Hu James Lechleiter Yidong Bai

Previously, we characterized a mouse cell line, 4A, carrying a mitochondrial DNA mutation in the subunit for respiratory complex I, NADH dehydrogenase, in the ND6 gene. This mutation abolished the complex I assembly and disrupted the respiratory function of complex I. We now report here that a galactose-resistant clone, 4AR, was isolated from the cells carrying the ND6 mutation. 4AR still conta...

Journal: :Biochimica et biophysica acta 1995
H A Bentlage A J Janssen A Chomyn G Attardi J E Walker H Schägger R C Sengers F J Trijbels

Antibodies have been raised against synthetic peptides corresponding to several computer-predicted epitopes of three mtDNA-encoded subunits, ND4, ND5 and ND6, of the human respiratory chain NADH dehydrogenase (Complex I). Antibodies were characterized by a sensitive immunoblotting assay using proteins from human skeletal muscle mitochondria and by immunoprecipitation of radio-labeled HeLa cell ...

Journal: :Genetics 1998
C T Beagley R Okimoto D R Wolstenholme

The circular, 17,443 nucleotide-pair mitochondrial (mt) DNA molecule of the sea anemone, Metridium senile (class Anthozoa, phylum Cnidaria) is presented. This molecule contains genes for 13 energy pathway proteins and two ribosomal (r) RNAs but, relative to other metazoan mtDNAs, has two unique features: only two transfer RNAs (tRNA(f-Met) and tRNA(Trp)) are encoded, and the cytochrome c oxidas...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید