(Q24307950)

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

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2243141%20AND%20SRC:MED&resulttype=core&format=json

25 September 2019

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

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2243141%20AND%20SRC:MED&resulttype=core&format=json

25 September 2019

cytochrome b-245 alpha chain

1 reference

GOA release 2020-03-11

human neutrophil

1 reference

based on heuristic

inferred from title

chronic granulomatous disease

1 reference

based on heuristic

inferred from title

2

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2243141%20AND%20SRC:MED&resulttype=core&format=json

25 September 2019

author name string

M C Dinauer

1

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2243141%20AND%20SRC:MED&resulttype=core&format=json

25 September 2019

G A Bruns

3

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2243141%20AND%20SRC:MED&resulttype=core&format=json

25 September 2019

J T Curnutte

4

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2243141%20AND%20SRC:MED&resulttype=core&format=json

25 September 2019

S H Orkin

5

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2243141%20AND%20SRC:MED&resulttype=core&format=json

25 September 2019

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publication date

1 November 1990

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2243141%20AND%20SRC:MED&resulttype=core&format=json

25 September 2019

Journal of Clinical Investigation

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2243141%20AND%20SRC:MED&resulttype=core&format=json

25 September 2019

86

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2243141%20AND%20SRC:MED&resulttype=core&format=json

25 September 2019

5

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2243141%20AND%20SRC:MED&resulttype=core&format=json

25 September 2019

1729-1737

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2243141%20AND%20SRC:MED&resulttype=core&format=json

25 September 2019

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296926

19 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296926

19 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296926

19 March 2017

Two cytosolic neutrophil oxidase components absent in autosomal chronic granulomatous disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296926

19 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296926

19 March 2017

Organization and expression of eucaryotic split genes coding for proteins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296926

19 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296926

19 March 2017

The X-linked chronic granulomatous disease gene codes for the beta-chain of cytochrome b-245

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296926

19 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296926

19 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296926

19 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296926

19 March 2017

Cloning the gene for an inherited human disorder--chronic granulomatous disease--on the basis of its chromosomal location

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296926

19 March 2017

Polymorphic DNA region adjacent to the 5' end of the human insulin gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296926

7 April 2017

Chronic granulomatous disease: a syndrome of phagocyte oxidase deficiencies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296926

27 September 2017

Quantitative nitroblue tetrazolium test in chronic granulomatous disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296926

27 September 2017

Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296926

27 September 2017

Building a multichain receptor: synthesis, degradation, and assembly of the T-cell antigen receptor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296926

27 September 2017

Chronic granulomatous disease due to a defect in the cytosolic factor required for nicotinamide adenine dinucleotide phosphate oxidase activation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296926

27 September 2017

Structure-independent DNA amplification by PCR using 7-deaza-2'-deoxyguanosine

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296926

27 September 2017

DNA linkage analysis of X chromosome-linked chronic granulomatous disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296926

27 September 2017

Cytosolic components of the respiratory burst oxidase: resolution of four components, two of which are missing in complementing types of chronic granulomatous disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296926

27 September 2017

Report of the committee on the genetic constitution of chromosome 16.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296926

27 September 2017

The electron transport chain of the microbicidal oxidase of phagocytic cells and its involvement in the molecular pathology of chronic granulomatous disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296926

27 September 2017

A phosphoprotein of Mr 47,000, defective in autosomal chronic granulomatous disease, copurifies with one of two soluble components required for NADPH:O2 oxidoreductase activity in human neutrophils

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296926

27 September 2017

Isolation of a cDNA clone encoding subunit IV of human cytochrome c oxidase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296926

27 September 2017

Human lysosomal genes: Arylsulfatase A and ?-Galactosidase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296926

27 September 2017

Human von Willebrand factor (vWF): isolation of complementary DNA (cDNA) clones and chromosomal localization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296926

30 May 2018

Two forms of autosomal chronic granulomatous disease lack distinct neutrophil cytosol factors.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296926

30 May 2018

Identification of the haem-binding subunit of cytochrome b-245.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296926

30 May 2018

Genetic variants of chronic granulomatous disease: prevalence of deficiencies of two cytosolic components of the NADPH oxidase system

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296926

29 November 2018

Phosphorylation of the oxidase-related 48K phosphoprotein family in the unusual autosomal cytochrome-negative and X-linked cytochrome-positive types of chronic granulomatous disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/2243141

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Purification and some properties of the small subunit of cytochrome b558 from human neutrophils

1 reference

https://pubmed.ncbi.nlm.nih.gov/2243141

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Defective Polymorphonuclear-Leukocyte Function and Chronic Granulomatous Disease in Two Female Children

1 reference

https://pubmed.ncbi.nlm.nih.gov/2243141

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Absence of cytochrome b-245 in chronic granulomatous disease. A multicenter European evaluation of its incidence and relevance

1 reference

https://pubmed.ncbi.nlm.nih.gov/2243141

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biogenesis of the acetylcholine receptor, a multisubunit integral membrane protein

1 reference

https://pubmed.ncbi.nlm.nih.gov/2243141

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Absence of both cytochrome b−245 subunits from neutrophils in X-linked chronic granulomatous disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/2243141

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chronic granulomatous disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/2243141

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The 35 kd pulmonary surfactant-associated protein is encoded on chromosome 10

1 reference

https://pubmed.ncbi.nlm.nih.gov/2243141

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Activation of neutrophil NADPH oxidase in a cell-free system. Partial purification of components and characterization of the activation process

1 reference

https://pubmed.ncbi.nlm.nih.gov/2243141

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1172/JCI114898

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2243141%20AND%20SRC:MED&resulttype=core&format=json

25 September 2019

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2243141%20AND%20SRC:MED&resulttype=core&format=json

25 September 2019

PubMed publication ID

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2243141%20AND%20SRC:MED&resulttype=core&format=json

25 September 2019

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