(Q41205789)

English

Detection of gp91-phox precursor protein in B-cell lines from patients with X-linked chronic granulomatous disease as an indicator for mutations impairing cytochrome b558 biosynthesis

scientific article published on April 1996

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scholarly article

1 reference

Europe PubMed Central

28 September 2017

Detection of gp91-phox precursor protein in B-cell lines from patients with X-linked chronic granulomatous disease as an indicator for mutations impairing cytochrome b558 biosynthesis (English)

1 reference

Europe PubMed Central

28 September 2017

X-linked chronic granulomatous disease

0 references

author name string

Porter CD

1

1 reference

Europe PubMed Central

28 September 2017

Kuribayashi F

2

1 reference

Europe PubMed Central

28 September 2017

Parkar MH

3

1 reference

Europe PubMed Central

28 September 2017

Roos D

4

1 reference

Europe PubMed Central

28 September 2017

Kinnon C

5

1 reference

Europe PubMed Central

28 September 2017

language of work or name

0 references

publication date

1 April 1996

1 reference

Europe PubMed Central

28 September 2017

number of pages

5

1 reference

based on heuristic

inferred from page(s)

Biochemical Journal

1 reference

Europe PubMed Central

28 September 2017

315 ( Pt 2)

1 reference

Europe PubMed Central

28 September 2017

571-575

1 reference

Europe PubMed Central

28 September 2017

A structural model for the nucleotide binding domains of the flavocytochrome b-245 beta-chain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1217234

28 September 2017

A newly recognized point mutation in the cytochrome b558 heavy chain gene replacing alanine57 by glutamic acid, in a patient with cytochrome b 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=1217234

28 September 2017

The genetic basis 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=1217234

28 September 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=1217234

28 September 2017

The structure of cytochrome b561, a secretory vesicle-specific electron transport protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1217234

28 September 2017

Site directed mutagenesis of the heme axial ligands of cytochrome b559 affects the stability of the photosystem II complex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1217234

28 September 2017

Topology of cytochrome b558 in neutrophil membrane analyzed by anti-peptide antibodies and proteolysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1217234

28 September 2017

Point mutations in the beta-subunit of cytochrome b558 leading to 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=1217234

28 September 2017

Cytochrome b558-negative, autosomal recessive chronic granulomatous disease: two new mutations in the cytochrome b558 light chain of the NADPH oxidase (p22-phox)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1217234

28 September 2017

p22-phox-deficient chronic granulomatous disease: reconstitution by retrovirus-mediated expression and identification of a biosynthetic intermediate of gp91-phox.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1217234

28 September 2017

X-linked chronic granulomatous disease: correction of NADPH oxidase defect by retrovirus-mediated expression of gp91-phox

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1217234

17 June 2018

Human neutrophil cytochrome b contains multiple hemes. Evidence for heme associated with both subunits

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1217234

17 June 2018

Superoxide production by normal and chronic granulomatous disease (CGD) patient-derived EBV-transformed B cell lines measured by chemiluminescence-based assays

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1217234

17 June 2018

Cytochrome b-245 is a flavocytochrome containing FAD and the NADPH-binding site of the microbicidal oxidase of phagocytes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1217234

17 June 2018

Cytochrome b558: the flavin-binding component of the phagocyte NADPH oxidase.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1217234

17 June 2018

Cytochrome b-245 of the neutrophil superoxide-generating system contains two nonidentical hemes. Potentiometric studies of a mutant form of gp91phox

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1217234

19 August 2018

B cell lines as models for inherited phagocytic diseases: abnormal superoxide generation in chronic granulomatous disease and giant granules in Chediak-Higashi syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8615831

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of two monoclonal antibodies against cytochrome b558 of human neutrophils

1 reference

https://pubmed.ncbi.nlm.nih.gov/8615831

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chronic granulomatous disease with partial deficiency of cytochrome b558 and incomplete respiratory burst: variants of the X-linked, cytochrome b558-negative form of the disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8615831

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chronic granulomatous disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8615831

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A variant X-linked chronic granulomatous disease patient (X91+) with partially functional cytochrome b

1 reference

https://pubmed.ncbi.nlm.nih.gov/8615831

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Splice site mutations are a common cause of X-linked chronic granulomatous disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8615831

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1042/BJ3150571

1 reference

Europe PubMed Central

28 September 2017

1 reference

Europe PubMed Central

28 September 2017

1 reference

Europe PubMed Central

28 September 2017

ResearchGate publication ID

0 references

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