Page last updated: 2024-08-23

heme and Granulomatous Disease, Chronic

heme has been researched along with Granulomatous Disease, Chronic in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's6 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Kinnon, C; Kuribayashi, F; Parkar, MH; Porter, CD; Roos, D1
Gahr, M; Heyden, S; Jendrossek, V; Neubauer, B; Ritzel, A1
Dinauer, MC; Yu, L; Zhen, L1
Segal, AW; Shatwell, KP1
Saruta, F; Tatsuzawa, O; Tsunawaki, S; Yoshida, LS; Yoshikawa, K1
Inana, I; Kakinuma, K; Kaneda, M; Kiryu, C; Owada, M; Sakiyama, T; Shiraishi, T; Tsuda, M1

Reviews

1 review(s) available for heme and Granulomatous Disease, Chronic

ArticleYear
The NADPH oxidase of phagocytic leukocytes.
    Annals of the New York Academy of Sciences, 1997, Dec-15, Volume: 832

    Topics: Flavins; Granulomatous Disease, Chronic; Heme; Humans; Models, Biological; Models, Molecular; NADPH Oxidases; Phagocytes; Phagocytosis; Protein Conformation; Vacuoles

1997

Other Studies

5 other study(ies) available for heme and Granulomatous Disease, Chronic

ArticleYear
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.
    The Biochemical journal, 1996, Apr-15, Volume: 315 ( Pt 2)

    Topics: Amino Acid Sequence; B-Lymphocytes; Binding Sites; Cell Line; Cytochrome b Group; Genetic Linkage; Granulomatous Disease, Chronic; Heme; Humans; Membrane Glycoproteins; Membrane Transport Proteins; Molecular Sequence Data; Molecular Structure; Mutation; NADPH Dehydrogenase; NADPH Oxidase 2; NADPH Oxidases; Phosphoproteins; Protein Conformation; Protein Precursors; Sequence Homology, Amino Acid; X Chromosome

1996
An in-frame triplet deletion within the gp91-phox gene in an adult X-linked chronic granulomatous disease patient with residual NADPH-oxidase activity.
    European journal of haematology, 1997, Volume: 58, Issue:2

    Topics: Adult; Amino Acid Sequence; Antibodies; Bacterial Infections; Cytochrome b Group; Exons; Fatal Outcome; Female; Genetic Carrier Screening; Granulocytes; Granulomatous Disease, Chronic; Heme; Humans; Male; Membrane Glycoproteins; Models, Structural; Molecular Sequence Data; Monocytes; N-Formylmethionine Leucyl-Phenylalanine; NADPH Oxidase 2; NADPH Oxidases; Neutrophils; Pedigree; Peptide Fragments; Polymorphism, Genetic; Protein Conformation; Sequence Deletion; Superoxides; Tetradecanoylphorbol Acetate; X Chromosome; Zymosan

1997
Biosynthesis of the phagocyte NADPH oxidase cytochrome b558. Role of heme incorporation and heterodimer formation in maturation and stability of gp91phox and p22phox subunits.
    The Journal of biological chemistry, 1997, Oct-24, Volume: 272, Issue:43

    Topics: 3T3 Cells; Animals; Cell Differentiation; Cell Membrane; COS Cells; Cytochrome b Group; Dimerization; Enzyme Inhibitors; Enzyme Stability; Granulocytes; Granulomatous Disease, Chronic; Heme; Heptanoates; HL-60 Cells; Humans; Leukemia, Myeloid; Membrane Glycoproteins; Membrane Transport Proteins; Mice; NADPH Dehydrogenase; NADPH Oxidase 2; NADPH Oxidases; Phagocytes; Phosphoproteins; Recombinant Proteins; Superoxides; Transfection; Tumor Cells, Cultured

1997
Mutation at histidine 338 of gp91(phox) depletes FAD and affects expression of cytochrome b558 of the human NADPH oxidase.
    The Journal of biological chemistry, 1998, Oct-23, Volume: 273, Issue:43

    Topics: Amino Acid Sequence; Binding Sites; Biological Transport; Child, Preschool; Cytochrome b Group; Cytosol; Ferredoxin-NADP Reductase; Flavin-Adenine Dinucleotide; Genetic Linkage; Granulomatous Disease, Chronic; Heme; Histidine; Humans; Male; Membrane Glycoproteins; Membrane Transport Proteins; Molecular Sequence Data; Mutation; NADPH Dehydrogenase; NADPH Oxidase 2; NADPH Oxidases; Neutrophils; Phosphoproteins; Sequence Homology, Amino Acid; Sex Chromosome Aberrations; Superoxides; X Chromosome

1998
A novel mutation at a probable heme-binding ligand in neutrophil cytochrome b558 in atypical X-linked chronic granulomatous disease.
    Human genetics, 1998, Volume: 103, Issue:4

    Topics: Adolescent; Cytochrome b Group; Genetic Linkage; Granulomatous Disease, Chronic; Heme; Humans; Ligands; Male; Membrane Glycoproteins; Membrane Transport Proteins; Mutation; NADPH Dehydrogenase; NADPH Oxidase 2; NADPH Oxidases; Neutrophils; Phosphoproteins; X Chromosome

1998