Mitochondrial cytochrome B gene mutation promotes tumor growth in bladder cancer
… role of a bonafide mitochondrial gene mutation in cancer. [Cancer Res 2008;68(3):700–06] …
the role of mitochondrial gene mutation in tumor development. Mitochondria are the key …
the role of mitochondrial gene mutation in tumor development. Mitochondria are the key …
Mitochondrial cytochrome c oxidase deficiency
M Rak, P Bénit, D Chrétien, J Bouchereau… - Clinical …, 2016 - portlandpress.com
… and nuclear gene mutations has been partially responsible for the steady increase in the
number of identified mutations in patients suspected to have dysfunctional mitochondria (see …
number of identified mutations in patients suspected to have dysfunctional mitochondria (see …
Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA
AL Andreu, MG Hanna, H Reichmann… - … England Journal of …, 1999 - Mass Medical Soc
… to the possibility of a cytochrome b gene mutation. Confirmation of the … cytochrome b
gene mutations in seven patients, we believe that somatic mutations in this mitochondrial gene …
gene mutations in seven patients, we believe that somatic mutations in this mitochondrial gene …
Mutations in mitochondrial cytochrome c oxidase genes segregate with late-onset Alzheimer disease
RE Davis, S Miller, C Herrnstadt… - Proceedings of the …, 1997 - National Acad Sciences
… We searched these genes, as well as other mitochondrial genes, for mutations that might …
missense mutations in the mitochondrial CO1 and CO2 genes but not the CO3 gene were …
missense mutations in the mitochondrial CO1 and CO2 genes but not the CO3 gene were …
Increased incidence of mitochondrial cytochrome c‐oxidase gene mutations in patients with myelodysplastic syndromes
PL Reddy, VT Shetty, D Dutt, A York… - British journal of …, 2002 - Wiley Online Library
… of DNA mutations in the mitochondrial encoded cytochrome c-oxidase I and II genes in 16/…
Gatterman et al (1997) described mitochondrial DNA mutations in cytochrome c-oxidase I in …
Gatterman et al (1997) described mitochondrial DNA mutations in cytochrome c-oxidase I in …
[HTML][HTML] Nuclear gene mutations as the cause of mitochondrial complex III deficiency
E Fernández-Vizarra, M Zeviani - Frontiers in genetics, 2015 - frontiersin.org
… Furthermore, the amount of cytochrome b was greatly reduced in mitochondria isolated
from fibroblasts. The child was reported to have undergone good clinical recovery, with neither …
from fibroblasts. The child was reported to have undergone good clinical recovery, with neither …
[HTML][HTML] Mutations of the SCO1 gene in mitochondrial cytochrome c oxidase deficiency with neonatal-onset hepatic failure and encephalopathy
I Valnot, S Osmond, N Gigarel, B Mehaye… - The American Journal of …, 2000 - cell.com
… Mutation screening revealed compound heterozygosity for SCO1 gene mutations in the
patients. The mutated allele, inherited from the father, harbored a 2-bp frameshift deletion (ΔGA; …
patients. The mutated allele, inherited from the father, harbored a 2-bp frameshift deletion (ΔGA; …
A mitochondrial cytochrome b mutation causing severe respiratory chain enzyme deficiency in humans and yeast
EL Blakely, AL Mitchell, N Fisher, B Meunier… - The FEBS …, 2005 - Wiley Online Library
… We describe a novel MTCYB gene mutation in a patient with muscle weakness and muscle
… III of the mitochondrial respiratory chain. A pathogenic role for the 15 699 G→C mutation is …
… III of the mitochondrial respiratory chain. A pathogenic role for the 15 699 G→C mutation is …
Mutational analysis of the mouse mitochondrial cytochrome b gene
N Howell, K Gilbert - Journal of molecular biology, 1988 - Elsevier
… ,ic cell genetic and biochemical studies indicated t)hat the resistance phenotypes were encoded
by mutations within the mitochondrial cytochrome b gene:. … t>he Gly23I residue of the cyt,…
by mutations within the mitochondrial cytochrome b gene:. … t>he Gly23I residue of the cyt,…
[PDF][PDF] Genetic defects of cytochrome c oxidase assembly
P Pecina, H Houst kova, J Zeman… - Physiological Research, 2004 - biomed.cas.cz
… hyperventilation and hypocapnia of patients with Leigh syndrome associated with SURF1
gene mutations as a cause of low serum bicarbonates. J Inherit Metab Dis 24: 707-714, 2001. …
gene mutations as a cause of low serum bicarbonates. J Inherit Metab Dis 24: 707-714, 2001. …
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