Human neutrophil cytochrome b light chain (p22-phox). Gene structure, chromosomal location, and mutations in cytochrome-negative autosomal recessive chronic granulomatous disease - sprookjes - yvandenbroek - TriplyDB

Human neutrophil cytochrome b light chain (p22-phox). Gene structure, chromosomal location, and mutations in cytochrome-negative autosomal recessive chronic granulomatous disease

Human neutrophil cytochrome b light chain (p22-phox). Gene structure, chromosomal location, and mutations in cytochrome-negative autosomal recessive chronic granulomatous disease

http://www.wikidata.org/entity/Q24307950

about

Chronic Granulomatous Disease; fundamental stages in our understanding of CGD Mutagenesis of p22(phox) histidine 94. A histidine in this position is not required for flavocytochrome b558 function Point mutation in the cytoplasmic domain of the neutrophil p22-phox cytochrome b subunit is associated with a nonfunctional NADPH oxidase and chronic granulomatous disease X-Linked chronic granulomatous disease: mutations in the CYBB gene encoding the gp91-phox component of respiratory-burst oxidase.A p47-phox pseudogene carries the most common mutation causing p47-phox- deficient chronic granulomatous disease Autosomal recessive chronic granulomatous disease caused by deletion at a dinucleotide repeat NADPH-oxidase and a hydrogen peroxide-sensitive K+ channel may function as an oxygen sensor complex in airway chemoreceptors and small cell lung carcinoma cell lines Inhibitory action of NoxA1 on dual oxidase activity in airway cells Cytochrome b558-negative, autosomal recessive chronic granulomatous disease: two new mutations in the cytochrome b558 light chain of the NADPH oxidase (p22-phox)The molecular pathology of primary immunodeficiencies NADPH oxidases as electrochemical generators to produce ion fluxes and turgor in fungi, plants and humans Redox balance dynamically regulates vascular growth and remodeling Preliminary characterisation of the promoter of the human p22(phox) gene: identification of a new polymorphism associated with hypertension Analysis of human phagocyte flavocytochrome b(558) by mass spectrometry Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease (second update)Relationship of the p22phox (CYBA) gene polymorphism C242T with risk of coronary artery disease: a meta-analysis The A930G polymorphism ofP22phox (CYBA) gene but not C242T variation is associated with hypertension: a meta-analysis Polymorphisms of C242T and A640G in CYBA gene and the risk of coronary artery disease: a meta-analysis The p47phox mouse knock-out model of chronic granulomatous disease INF-γ Enhances Nox2 Activity by Upregulating phox Proteins When Applied to Differentiating PLB-985 Cells but Does Not Induce Nox2 Activity by Itself Nox5 and the regulation of cellular function.NOX enzymes and pulmonary disease.Towards routine screening of rare genetic diseases: the example of chronic granulomatous disease Identification of a Novel Mutation in the CYBB Gene, p.Asp378Gly, in a Patient With X-linked Chronic Granulomatous Disease.Exercise training, NADPH oxidase p22phox gene polymorphisms, and hypertension.Invariant local conformation in p22phox p.Y72H polymorphisms suggested by mass spectral analysis of crosslinked human neutrophil flavocytochrome b.The C242T polymorphism of the p22-phox gene (CYBA) is associated with higher left ventricular mass in Brazilian hypertensive patients.Association between NADPH oxidase p22(phox) C242T polymorphism and ischemic cerebrovascular disease: a meta-analysis NADPH oxidase activation in pancreatic cancer cells is mediated through Akt-dependent up-regulation of p22phox Differential effect of p47phox and gp91phox deficiency on the course of Pneumococcal Meningitis Identification of a thermolabile component of the human neutrophil NADPH oxidase. A model for chronic granulomatous disease caused by deficiency of the p67-phox cytosolic component.CYBA Gene Polymorphisms and Adverse Outcomes in Acute Kidney Injury: A Prospective Cohort Study In vitro molecular reconstitution of the respiratory burst in B lymphoblasts from p47-phox-deficient chronic granulomatous disease The NADPH oxidase of professional phagocytes--prototype of the NOX electron transport chain systems.NOX2 As a Target for Drug Development: Indications, Possible Complications, and Progress.Association of the NAD(P)H oxidase p22 phox gene C242T polymorphism with type 2 diabetes mellitus, diabetic nephropathy, and carotid atherosclerosis with type 2 diabetes mellitus: A meta-analysis Gp91(phox) is the heme binding subunit of the superoxide-generating NADPH oxidase.Disturbed interaction of p21-rac with mutated p67-phox causes chronic granulomatous disease Animal models of human granulocyte diseases.Gene targeting of X chromosome-linked chronic granulomatous disease locus in a human myeloid leukemia cell line and rescue by expression of recombinant gp91phox

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P2860

Human neutrophil cytochrome b light chain (p22-phox). Gene structure, chromosomal location, and mutations in cytochrome-negative autosomal recessive chronic granulomatous disease

http://www.wikidata.org/entity/Q24307950

description

1990 nî lūn-bûn

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1990 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

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1990 թվականի նոյեմբերին հրատարակված գիտական հոդված

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1990年の論文

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1990年論文

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1990年論文

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1990年論文

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1990年論文

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1990年論文

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name

Human neutrophil cytochrome b ...... chronic granulomatous disease

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Human neutrophil cytochrome b ...... chronic granulomatous disease

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Human neutrophil cytochrome b ...... chronic granulomatous disease

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Human neutrophil cytochrome b ...... chronic granulomatous disease

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type

label

Human neutrophil cytochrome b ...... chronic granulomatous disease

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Human neutrophil cytochrome b ...... chronic granulomatous disease

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Human neutrophil cytochrome b ...... chronic granulomatous disease

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Human neutrophil cytochrome b ...... chronic granulomatous disease

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prefLabel

Human neutrophil cytochrome b ...... chronic granulomatous disease

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Human neutrophil cytochrome b ...... chronic granulomatous disease

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Human neutrophil cytochrome b ...... chronic granulomatous disease

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Human neutrophil cytochrome b ...... chronic granulomatous disease

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Journal of Clinical Investigation

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Human neutrophil cytochrome b ...... chronic granulomatous disease

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G A Bruns

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J T Curnutte

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M C Dinauer

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S H Orkin

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P2860

Two cytosolic neutrophil oxidase components absent in autosomal chronic granulomatous disease

Purified cytochrome b from human granulocyte plasma membrane is comprised of two polypeptides with relative molecular weights of 91,000 and 22,000

A missense mutation in the neutrophil cytochrome b heavy chain in cytochrome-positive X-linked chronic granulomatous disease

Primary structure and unique expression of the 22-kilodalton light chain of human neutrophil cytochrome b

Platelet-derived growth factor A chain: gene structure, chromosomal location, and basis for alternative mRNA splicing

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

Organization and expression of eucaryotic split genes coding for proteins

Absence of both the 91kD and 22kD subunits of human neutrophil cytochrome b in two genetic forms of chronic granulomatous disease

Heterogeneous mutations in the beta subunit common to the LFA-1, Mac-1, and p150,95 glycoproteins cause leukocyte adhesion deficiency

The glycoprotein encoded by the X-linked chronic granulomatous disease locus is a component of the neutrophil cytochrome b complex

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1729-1737

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1540123

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10.1172/JCI114898

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5

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86

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1990-11-01T00:00:00Z

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20913213

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2243141

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oxidation-reduction process

Cytochrome b-245 alpha chain

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296926

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