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COX3 cytochrome c oxidase III

COX3, cytochrome c oxidase subunit III, COIII, COX III, oxi2
Top mentioned proteins: ND4, ACID, ND5, CAN, DiI
Papers on COX3
Sperm mitochondrial DNA 15bp deletion of cytochrome c oxidase subunit III is significantly associated with human male infertility in Pakistan.
Jahan et al., Islamabad, Pakistan. In J Pak Med Assoc, Jan 2016
OBJECTIVE: To find genetic association of sperm mitochondrial deoxyribonucleic acid cytochrome c oxidase III subunit 15bp deletion with male infertility in Pakistan.
The complete mitochondrial genome of the fulvous parrotbill Paradoxornis fulvifrons (Passeriformes: Muscicapidae).
Dai et al., Leshan, China. In Mitochondrial Dna, Jan 2016
One PCG (COX1) is terminated with AGG, three PCGs (COX3, ND2 and ND4) with the incomplete stop codon T--/TA-, while all the others with TAA.
The complete mitochondrial genome of Acanthosaura lepidogaster (Squamata: Agamidae).
Lin et al., Hangzhou, China. In Mitochondrial Dna, Jan 2016
We constructed a phylogeny that included for 10 species of Leiolepidinae lizards and one outgroup Leiocephalus personatus constructed in BEAST, based on 15 mitochondrial genes (12S, 16S, ND1, ND2, COI, COII, ATP8, ATP6, COIII, ND3, ND4L, ND4, ND5, ND6, and cytochrome b).
[Determining mitochondrial molecular markers suitable for genetic diversity analysis of Cordyceps militaris].
Liu et al., In Wei Sheng Wu Xue Bao, Aug 2015
cox2-nad5, cox2, cox3, cob, and cox1 for future genetic diversity and population genetic studies of C. militaris.
Analysis of the mitochondrial maxicircle of Trypanosoma lewisi, a neglected human pathogen.
Lun et al., Guangzhou, China. In Parasit Vectors, 2014
The high GC content in at least 9 maxicircle genes of T. lewisi (ATPase6; NADH dehydrogenase subunits ND3, ND7, ND8 and ND9; G-rich regions GR3 and GR4; cytochrome oxidase subunit COIII and ribosomal protein RPS12) implies that their products may be extensively edited.
Screening of mitochondrial mutations in Tunisian patients with mitochondrial disorders: an overview study.
Fakhfakh et al., Sfax, Tunisia. In Mitochondrial Dna, 2013
Three cases with m.8993T>G mutation, two patients with the novel m.5523T>G and m.5559A>G mutations in the tRNA(Trp) gene, and two individuals with the undescribed m.9478T>C mutation in the cytochrome c oxidase subunit III (COXIII) gene were found with LS.
Novel single base pair COX III subunit deletion of mitochondrial DNA associated with rhabdomyolysis.
Collins et al., Melbourne, Australia. In J Clin Neurosci, 2011
A novel COX III subunit single base pair deletion is associated with a high number (45%) of COX-negative muscle fibers in a patient with severe rhabdomyolysis but no family history of neuromuscular disorder.
Molecular-clinical correlation in a family with a novel heteroplasmic Leigh syndrome missense mutation in the mitochondrial cytochrome c oxidase III gene.
Fakhfakh et al., Sfax, Tunisia. In J Child Neurol, 2011
a novel heteroplasmic missense mitochondrial mutation at nucleotide 9478 in COX3 gene in patients with Leigh syndrome
Major arc mitochondrial DNA deletions in cytochrome c oxidase-deficient human cochlear spiral ganglion cells.
Hinojosa et al., Chicago, United States. In Acta Otolaryngol, 2010
The total mtDNA major arc deletion level was greater than the common deletion level in COX 3-deficient spiral ganglion cells.
A MELAS syndrome family harboring two mutations in mitochondrial genome.
Chung et al., Seoul, South Korea. In Exp Mol Med, 2008
a MELAS syndrome Korean family harbor homoplasmic missense mutation in mitochondrial genom, which confers pathogenicity (Phe251Leu)
[Mitochondrial DNA mutations in the pathogenesis in the head and neck squamous cell carcinoma].
Czarnecka et al., Laizhou, China. In Otolaryngol Pol, 2007
Moreover mutations in genes encoding ND2, ND5, COIII, CYTB, and ATP6 were observed in 17% of patients.
Melatonin as antioxidant, geroprotector and anticarcinogen.
Vinogradova et al., Saint Petersburg, Russia. In Biochim Biophys Acta, 2006
Melatonin also increased the expression of some mitochondrial genes (16S, cytochrome c oxidases 1 and 3 (COX1 and COX3), and NADH dehydrogenases 1 and 4 (ND1 and ND4)), which agrees with its ability to inhibit free radical processes.
Mutations in mtDNA-encoded cytochrome c oxidase subunit genes causing isolated myopathy or severe encephalomyopathy.
Lochm├╝ller et al., M├╝nchen, Germany. In Neuromuscul Disord, 2005
Mutations in mtDNA-encoded cytochrome c oxidase subunit III genes causing isolated myopathy or severe encephalomyopathy.
Bilobalide and neuroprotection.
Defeudis, United States. In Pharmacol Res, 2002
In vitro and ex vivo studies indicate that bilobalide has multiple mechanisms of action that may be associated with neuroprotection, including its preservation of mitochondrial ATP synthesis, its inhibition of apoptotic damage induced by staurosporine or by serum-free medium, its suppression of hypoxia-induced membrane deterioration in the brain, and its actions of increasing the expression of the mitochondrial DNA-encoded COX III subunit of cytochrome c oxidase and the ND1 subunit of NADH dehydrogenase.
The beneficial effects of total cavopulmonary conversion and arrhythmia surgery for the failed Fontan.
Backer et al., Chicago, United States. In Semin Thorac Cardiovasc Surg Pediatr Card Surg Annu, 2001
Maze-Cox III was used for 14 patients with atrial fibrillation.
RNA editing as a source of genetic variation.
Gilbert et al., Cambridge, United States. In Nature, 1993
Although the COIII gene encoding cytochrome c oxidase subunit III in Trypanosoma brucei is edited along its entire length, the presumably homologous genes in two related trypanosomes, Leishmania tarentolae and Crithidia fasciculata, are only modestly edited at their 5' ends.
Characterization of cytochrome c oxidase III transcripts that are edited only in the 3' region.
Stuart et al., Seattle, United States. In Cell, 1988
The cytochrome c oxidase subunit III (COIII) transcript of T. brucei is extensively edited by the addition and deletion of uridines.
Editing of kinetoplastid mitochondrial mRNAs by uridine addition and deletion generates conserved amino acid sequences and AUG initiation codons.
Simpson et al., Los Angeles, United States. In Cell, 1988
Uridine additions and deletions in the 5' ends of the COIII, MURF2, and MURF3 transcripts create new N-terminal amino acid sequences that are conserved between species, and new AUG initiation codons in several cases.
Extensive editing of the cytochrome c oxidase III transcript in Trypanosoma brucei.
Stuart et al., Seattle, United States. In Cell, 1988
The gene for cytochrome oxidase subunit III (COIII) is not detected in T. brucei by nucleotide sequence analysis or by cross-hybridization studies.
Are mitochondrial structural genes selectively amplified during senescence in Podospora anserina?
Cummings et al., In Cell, 1982
We have unambiguously assigned the alpha-event senDNA (the 2.6 kb monomer) to the oxi3 gene locus and the beta-event senDNA to the oxi2 gene locus.
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