(Q28293120)

1

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Cécile Martel

2

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Azmi Mahafzah

4

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Mohammad S El-Khateeb

5

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Adel M Al-Wahadneh

6

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Wail A Hayajneh

7

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Hanan A Hamamy

8

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Elisabeth Maquet

9

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Michelle Molin

10

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Marie José Stasia

Journal of Clinical Immunology

11

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language of work or name

English

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publication date

March 2009

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published in

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volume

29

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issue

2

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page(s)

215-30

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exact match

https://scigraph.springernature.com/pub.10.1007/s10875-008-9243-y

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cites work

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

Crossref

https://api.crossref.org/works/10.1007%2FS10875-008-9243-Y

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

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10875-008-9243-Y

Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environment

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10875-008-9243-Y

Genetic and mutational heterogeneity of autosomal recessive chronic granulomatous disease in Tunisia

21 January 2018

1 reference

12 December 2020

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

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12 December 2020

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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12 December 2020

Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease (first update).

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12 December 2020

The respiratory burst of bovine neutrophils. Role of a b type cytochrome and coenzyme specificity.

1 reference

12 December 2020

NITROBLUE-TETRAZOLIUM TESTS

1 reference

12 December 2020

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

1 reference

12 December 2020

Isolation of mononuclear cells and granulocytes from human blood. Isolation of monuclear cells by one centrifugation, and of granulocytes by combining centrifugation and sedimentation at 1 g

1 reference

12 December 2020

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

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12 December 2020

Consanguinity and genetic disorders. Profile from Jordan

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12 December 2020

Clinical features, long-term follow-up and outcome of a large cohort of patients with Chronic Granulomatous Disease: an Italian multicenter study

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12 December 2020

Characterization of two monoclonal antibodies against cytochrome b558 of human neutrophils

1 reference

12 December 2020

A novel mutation at a probable heme-binding ligand in neutrophil cytochrome b558 in atypical X-linked chronic granulomatous disease

1 reference

12 December 2020

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

1 reference

12 December 2020

Jordan: communities and community genetics.

1 reference

12 December 2020

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

1 reference

12 December 2020

Hepatic abnormalities in patients with chronic granulomatous disease

1 reference

12 December 2020

Chronic granulomatous disease caused by mutations other than the common GT deletion in NCF1, the gene encoding the p47phox component of the phagocyte NADPH oxidase

1 reference

12 December 2020

Biochemical and immunochemical properties of B lymphocyte cytochrome b558

1 reference

12 December 2020

Statistical and mutational analysis of chronic granulomatous disease in Japan with special reference to gp91-phox and p22-phox deficiency

1 reference

12 December 2020

Autosomal recessive chronic granulomatous disease caused by deletion at a dinucleotide repeat

1 reference

12 December 2020

Prenatal diagnosis in two families with autosomal, p47(phox)-deficient chronic granulomatous disease due to a novel point mutation in NCF1.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Regulation of novel superoxide-producing NAD(P)H oxidases

1 reference

12 December 2020

Gene-scan method for the recognition of carriers and patients with p47(phox)-deficient autosomal recessive chronic granulomatous disease

1 reference

12 December 2020

156Pro-->Gln substitution in the light chain of cytochrome b558 of the human NADPH oxidase (p22-phox) leads to defective translocation of the cytosolic proteins p47-phox and p67-phox

1 reference

12 December 2020

Molecular characterization of autosomal recessive chronic granulomatous disease caused by a defect of the nicotinamide adenine dinucleotide phosphate (reduced form) oxidase component p67-phox

1 reference

12 December 2020

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

1 reference

12 December 2020

Complementation of NADPH oxidase in p67-phox-deficient CGD patients

1 reference

12 December 2020

Crucial role of two potential cytosolic regions of Nox2, 191TSSTKTIRRS200 and 484DESQANHFAVHHDEEKD500, on NADPH oxidase activation

1 reference

12 December 2020

Chronic granulomatous disease.

1 reference

12 December 2020

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

1 reference

12 December 2020

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

1 reference

12 December 2020

A new mutation in exon 12 of the gp91-phox gene leading to cytochrome b-positive X-linked chronic granulomatous disease

1 reference

12 December 2020

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

1 reference

12 December 2020

[The X+ chronic granulomatous disease as a fabulous model to study the NADPH oxidase complex activation]

1 reference

12 December 2020

X-Linked chronic granulomatous disease: mutations in the CYBB gene encoding the gp91-phox component of respiratory-burst oxidase.

1 reference

12 December 2020

Leu505 of Nox2 is crucial for optimal p67phox-dependent activation of the flavocytochrome b558 during phagocytic NADPH oxidase assembly.

1 reference

12 December 2020

Autosomal recessive chronic granulomatous disease caused by defects in NCF-1, the gene encoding the phagocyte p47-phox: mutations not arising in the NCF-1 pseudogenes

1 reference

12 December 2020

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

1 reference

12 December 2020

Genetics and immunopathology of chronic granulomatous disease

1 reference

12 December 2020

Complementation of NADPH oxidase in p67-phox-deficient CGD patients p67-phox/p40-phox interaction

1 reference

12 December 2020