Functional analysis of two-amino acid substitutions in gp91 phox in a patient with X-linked flavocytochrome b558-positive chronic granulomatous disease by means of transgenic PLB-985 cells (Q40520761)

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scientific article published on 24 August 2004

Language	Label	Description	Also known as
English	Functional analysis of two-amino acid substitutions in gp91 phox in a patient with X-linked flavocytochrome b558-positive chronic granulomatous disease by means of transgenic PLB-985 cells	scientific article published on 24 August 2004

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

Functional analysis of two-amino acid substitutions in gp91 phox in a patient with X-linked flavocytochrome b558-positive chronic granulomatous disease by means of transgenic PLB-985 cells (English)

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

chronic granulomatous disease

1 reference

based on heuristic

inferred from title

author name string

Clara Bionda

1

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Europe PubMed Central

PubMed publication ID

21 September 2017

Xing Jun Li

2

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Europe PubMed Central

PubMed publication ID

21 September 2017

Robin van Bruggen

3

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

Michel Eppink

4

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

Dirk Roos

5

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Europe PubMed Central

PubMed publication ID

21 September 2017

Françoise Morel

6

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Europe PubMed Central

PubMed publication ID

21 September 2017

Marie-José Stasia

7

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

publication date

24 August 2004

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Europe PubMed Central

PubMed publication ID

21 September 2017

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Europe PubMed Central

PubMed publication ID

21 September 2017

115

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Europe PubMed Central

PubMed publication ID

21 September 2017

5

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Europe PubMed Central

PubMed publication ID

21 September 2017

418-427

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Europe PubMed Central

PubMed publication ID

21 September 2017

A novel polymorphism in the coding region of CYBB, the human gp91-phox gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene targeting of X chromosome-linked chronic granulomatous disease locus in a human myeloid leukemia cell line and rescue by expression of recombinant gp91phox

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular and functional characterization of a new X-linked chronic granulomatous disease variant (X91+) case with a double missense mutation in the cytosolic gp91phox C-terminal tail.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

P67-phox-mediated NADPH oxidase assembly: imaging of cytochrome b558 liposomes by atomic force microscopy

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional analysis of NADPH oxidase in granulocytic cells expressing a delta488-497 gp91(phox) deletion mutant.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CCAAT displacement protein as a repressor of the myelomonocytic-specific gp91-phox gene promoter.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Processing and Maturation of Flavocytochromeb558Include Incorporation of Heme as a Prerequisite for Heterodimer Assembly

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Activation of O2(-)-generating oxidase in an heterologous cell-free system derived from Epstein-Barr-virus-transformed human B lymphocytes and bovine neutrophils. Application to the study of defects in cytosolic factors in chronic granulomatous dise

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Measurement of protein using bicinchoninic acid

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

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/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A point mutation in gp91-phox of cytochrome b558 of the human NADPH oxidase leading to defective translocation of the cytosolic proteins p47-phox and p67-phox

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a double mutation (D160V-K161E) in the p67phox gene of a chronic granulomatous disease patient

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

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/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A double missense mutation in the ATM gene of a Dutch family with ataxia telangiectasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of a new human diploid myeloid leukemia cell line (PLB-985) with granulocytic and monocytic differentiating capacity.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Contribution of two missense mutations (G71R and Y486D) of the bilirubin UDP glycosyltransferase (UGT1A1) gene to phenotypes of Gilbert's syndrome and Crigler-Najjar syndrome type II

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The mutational spectrum of single base-pair substitutions causing human genetic disease: patterns and predictions

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biochemical and immunochemical properties of B lymphocyte cytochrome b558

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Severe Clinical Forms of Cytochromeb–Negative Chronic Granulomatous Disease (X91−) in 3 Brothers with a Point Mutation in the Promoter Region ofCYBB

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The HUGO Gene Nomenclature Committee (HGNC).

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Respiratory burst in human neutrophils

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chronic granulomatous disease. Report on a national registry of 368 patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic, biochemical, and clinical features of chronic granulomatous disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homologs of gp91phox: cloning and tissue expression of Nox3, Nox4, and Nox5

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Location of the epitope for 7D5, a monoclonal antibody raised against human flavocytochrome b558, to the extracellular peptide portion of primate gp91phox

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the X-linked and autosomal recessive forms of chronic granulomatous disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

SWISS-MODEL and the Swiss-PdbViewer: an environment for comparative protein modeling

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA linkage analysis of X chromosome-linked chronic granulomatous disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chronic granulomatous disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Double missense mutation in exon 41 of the human dystrophin gene detected by double strand conformation analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Four novel mutations in the gene encoding gp91-phox of human NADPH oxidase: consequences for oxidase assembly

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human Gene Mutation Database (HGMD): 2003 update

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

NADPH oxidase: an enzyme for multicellularity?

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The superoxide-generating NADPH oxidase: structural aspects and activation mechanism

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Six Arabidopsis thaliana homologues of the human respiratory burst oxidase (gp91phox).

1 reference

https://pubmed.ncbi.nlm.nih.gov/15338276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00439-004-1173-Z

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

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0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

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