A mitochondrial cytochrome b mutation causing severe respiratory chain enzyme deficiency in humans and yeast - Wikidata - wikimedia - TriplyDB

A mitochondrial cytochrome b mutation causing severe respiratory chain enzyme deficiency in humans and yeast

A mitochondrial cytochrome b mutation causing severe respiratory chain enzyme deficiency in humans and yeast

http://www.wikidata.org/entity/Q28260897

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Significant modulation of mitochondrial electron transport system by nicotine in various rat brain regions Mitochondrial DNA polymerase editing mutation, PolgD257A, reduces the diabetic phenotype of Akita male mice by suppressing appetite.A novel mutation in the mitochondrial DNA cytochrome b gene (MTCYB) in a patient with mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes syndrome.Adult-onset leukodystrophies from respiratory chain disorders: do they exist?Supramolecular organization of the respiratory chain in Neurospora crassa mitochondria De novo mtDNA point mutations are common and have a low recurrence risk.Coexpression within Integrated Mitochondrial Pathways Reveals Different Networks in Normal and Chemically Treated Transcriptomes.Forced cytochrome B gene mutation expression induces mitochondrial proliferation and prevents apoptosis in human uroepithelial SV-HUC-1 cells.Mitochondrial complex III deficiency associated with a homozygous mutation in UQCRQ Stairway to heaven: evaluating levels of biological organization correlated with the successful ascent of natural waterfalls in the Hawaiian stream goby Sicyopterus stimpsoni.Relevance of mitochondrial genetics and metabolism in cancer development.The cytochrome b p.278Y>C mutation causative of a multisystem disorder enhances superoxide production and alters supramolecular interactions of respiratory chain complexes.Association of the level of heteroplasmy of the 15059G>A mutation in the MT-CYB mitochondrial gene with essential hypertension.The power of yeast to model diseases of the powerhouse of the cell.MT-CYB mutations in hypertrophic cardiomyopathy.Pseudo-obstruction, stroke, and mitochondrial dysfunction: A lethal combination.Genomics and genetics in the biology of adaptation to exercise.Polymorphisms of the murine mitochondrial ND4, CYTB and COX3 genes impact hematopoiesis during aging.Mitochondrial disorders caused by mutations in respiratory chain assembly factors.New developments on the functions of coenzyme Q in mitochondria.Application of 16s rDNA and cytochrome b ribosomal markers in studies of lineage and fish populations structure of aquatic species.Cyclophilin D over-expression increases mitochondrial complex III activity and accelerates supercomplex formation.Lifetime imaging of GFP at CoxVIIIa reports respiratory supercomplex assembly in live cells.Respiratory chain supercomplexes set the threshold for respiration defects in human mtDNA mutant cybrids.Mutations in mitochondrial complex III uniquely affect complex I in Caenorhabditis elegans.Investigation of the association between mitochondrial DNA and p53 gene mutations in transitional cell carcinoma of the bladder.Combined Respiratory Chain Deficiency and UQCC2 Mutations in Neonatal Encephalomyopathy: Defective Supercomplex Assembly in Complex III Deficiencies Nonsense mutations in the COX1 subunit impair the stability of respiratory chain complexes rather than their assembly Phosphocreatine protects against LPS-induced human umbilical vein endothelial cell apoptosis by regulating mitochondrial oxidative phosphorylation.Complex III staining in blue native polyacrylamide gels.A novel in-frame 18-bp microdeletion in MT-CYB causes a multisystem disorder with prominent exercise intolerance.Reconstruction of a human mitochondrial complex I mutation in the unicellular green alga Chlamydomonas.

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A mitochondrial cytochrome b mutation causing severe respiratory chain enzyme deficiency in humans and yeast

http://www.wikidata.org/entity/Q28260897

description

2005 nî lūn-bûn

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2005 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2005 թվականի հուլիսին հրատարակված գիտական հոդված

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2005年の論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年论文

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name

A mitochondrial cytochrome b m ...... deficiency in humans and yeast

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A mitochondrial cytochrome b m ...... deficiency in humans and yeast

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A mitochondrial cytochrome b m ...... deficiency in humans and yeast

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type

label

A mitochondrial cytochrome b m ...... deficiency in humans and yeast

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A mitochondrial cytochrome b m ...... deficiency in humans and yeast

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A mitochondrial cytochrome b m ...... deficiency in humans and yeast

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A mitochondrial cytochrome b m ...... deficiency in humans and yeast

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A mitochondrial cytochrome b m ...... deficiency in humans and yeast

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A mitochondrial cytochrome b m ...... deficiency in humans and yeast

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A mitochondrial cytochrome b m ...... deficiency in humans and yeast

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Douglass M Turnbull

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Emma L Blakely

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Leo G Nijtmans

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Margaret J Jackson

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Nicholas Fisher

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Robert W Taylor

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P2860

Supercomplexes in the respiratory chains of yeast and mammalian mitochondria

Sequence and organization of the human mitochondrial genome

Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA

A mitochondrial cytochrome b mutation but no mutations of nuclearly encoded subunits in ubiquinol cytochrome c reductase (complex III) deficiency

Mitochondrial respiratory-chain diseases

SOSUI: classification and secondary structure prediction system for membrane proteins

Mitochondrial encephalomyopathy and complex III deficiency associated with a stop-codon mutation in the cytochrome b gene.

Recapitulation in Saccharomyces cerevisiae of cytochrome b mutations conferring resistance to atovaquone in Pneumocystis jiroveci.

Disruption of the interaction between the Rieske iron-sulfur protein and cytochrome b in the yeast bc1 complex owing to a human disease-associated mutation within cytochrome b.

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14

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Anna L Mitchell

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Andrew M Schaefer

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2005-07-01T00:00:00Z

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7735182

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