Pages that link to "Q28301419"
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The following pages link to The X-linked chronic granulomatous disease gene codes for the beta-chain of cytochrome b-245 (Q28301419):
Displaying 50 items.
- Purified cytochrome b from human granulocyte plasma membrane is comprised of two polypeptides with relative molecular weights of 91,000 and 22,000 (Q24297934) (← links)
- Localization of Nox2 N-terminus using polyclonal antipeptide antibodies (Q24298524) (← links)
- Isolation and characterization of grancalcin, a novel 28 kDa EF-hand calcium-binding protein from human neutrophils (Q24301048) (← links)
- Human neutrophil cytochrome b light chain (p22-phox). Gene structure, chromosomal location, and mutations in cytochrome-negative autosomal recessive chronic granulomatous disease (Q24307950) (← links)
- Point mutation in the cytoplasmic domain of the neutrophil p22-phox cytochrome b subunit is associated with a nonfunctional NADPH oxidase and chronic granulomatous disease (Q24319232) (← links)
- Autosomal recessive chronic granulomatous disease caused by deletion at a dinucleotide repeat (Q24563767) (← links)
- Characterization of the 47-kilodalton autosomal chronic granulomatous disease protein: tissue-specific expression and transcriptional control by retinoic acid (Q24597756) (← links)
- 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 (Q24603771) (← links)
- A missense mutation in the neutrophil cytochrome b heavy chain in cytochrome-positive X-linked chronic granulomatous disease (Q24620524) (← links)
- Primary structure and unique expression of the 22-kilodalton light chain of human neutrophil cytochrome b (Q24650898) (← links)
- PU.1 as an essential activator for the expression of gp91(phox) gene in human peripheral neutrophils, monocytes, and B lymphocytes (Q24655677) (← links)
- Cytochrome b558-negative, autosomal recessive chronic granulomatous disease: two new mutations in the cytochrome b558 light chain of the NADPH oxidase (p22-phox) (Q24669611) (← links)
- Genes for two autosomal recessive forms of chronic granulomatous disease assigned to 1q25 (NCF2) and 7q11.23 (NCF1) (Q24676461) (← links)
- Role of oxidants in microbial pathophysiology (Q24683780) (← links)
- Mouse model of X-linked chronic granulomatous disease, an inherited defect in phagocyte superoxide production (Q28114945) (← links)
- Deletion mutagenesis of p22phox subunit of flavocytochrome b558: identification of regions critical for gp91phox maturation and NADPH oxidase activity (Q28256579) (← links)
- Topology of cytochrome b558 in neutrophil membrane analyzed by anti-peptide antibodies and proteolysis (Q28288636) (← links)
- The glycoprotein encoded by the X-linked chronic granulomatous disease locus is a component of the neutrophil cytochrome b complex (Q28301409) (← links)
- Oxidases and peroxidases in cardiovascular and lung disease: new concepts in reactive oxygen species signaling (Q28393242) (← links)
- Granulocyte function in grancalcin-deficient mice (Q28513571) (← links)
- Assembly and activation of the phagocyte NADPH oxidase. Specific interaction of the N-terminal Src homology 3 domain of p47phox with p22phox is required for activation of the NADPH oxidase (Q30176829) (← links)
- SH3-dependent assembly of the phagocyte NADPH oxidase (Q30193848) (← links)
- Role of Src homology 3 domains in assembly and activation of the phagocyte NADPH oxidase (Q30194274) (← links)
- Assembly of the neutrophil respiratory burst oxidase. Protein kinase C promotes cytoskeletal and membrane association of cytosolic oxidase components (Q30195706) (← links)
- Molecular cloning and characterization of grancalcin, a novel EF-hand calcium-binding protein abundant in neutrophils and monocytes (Q33279621) (← links)
- Complement-independent Ab-induced peroxide lysis of platelets requires 12-lipoxygenase and a platelet NADPH oxidase pathway (Q33360225) (← links)
- Platelet particle formation by anti GPIIIa49-66 Ab, Ca2 ionophore A23187, and phorbol myristate acetate is induced by reactive oxygen species and inhibited by dexamethasone blockade of platelet phospholipase A2, 12-lipoxygenase, and NADPH oxidase (Q33375459) (← links)
- Two cytosolic components of the human neutrophil respiratory burst oxidase translocate to the plasma membrane during cell activation (Q34244747) (← links)
- Ultrastructural localization of cytochrome b in the membranes of resting and phagocytosing human granulocytes (Q34245500) (← links)
- NADPH oxidase and the respiratory burst (Q34391668) (← links)
- Higher-plant plasma membrane cytochrome b561: a protein in search of a function (Q34458636) (← links)
- The electron transport chain of the microbicidal oxidase of phagocytic cells and its involvement in the molecular pathology of chronic granulomatous disease (Q34573983) (← links)
- Immune consequences of mutations in the human common gamma-chain gene (Q34749470) (← links)
- Regulation of Monocyte Adhesion and Migration by Nox4 (Q34794515) (← links)
- Coregulation of NADPH oxidase activation and phosphorylation of a 48-kD protein(s) by a cytosolic factor defective in autosomal recessive chronic granulomatous disease (Q35588081) (← links)
- Genetic study of a new X-linked recessive immunodeficiency syndrome (Q35599142) (← links)
- Identification of a thermolabile component of the human neutrophil NADPH oxidase. A model for chronic granulomatous disease caused by deficiency of the p67-phox cytosolic component (Q35602381) (← links)
- Prognosis of chronic granulomatous disease (Q35624817) (← links)
- Reduction in superoxide anion secretion and bactericidal activity of neutrophils from aged rats: reversal by the combination of gamma interferon and growth hormone (Q35770863) (← links)
- The NADPH oxidase of professional phagocytes--prototype of the NOX electron transport chain systems (Q35828194) (← links)
- The molecular basis of X-linked immunodeficiency disease (Q35848833) (← links)
- Biochemistry and molecular biology of chronic granulomatous disease. (Q35848838) (← links)
- Genetic lessons learned from X-linked Mendelian susceptibility to mycobacterial diseases (Q35860015) (← links)
- NOX2 As a Target for Drug Development: Indications, Possible Complications, and Progress (Q35985407) (← links)
- Chronic granulomatous disease: diagnosis and classification at the molecular level. (Q36239002) (← links)
- NADPH oxidases: an overview from structure to innate immunity-associated pathologies (Q36302873) (← links)
- Activation of the human neutrophil superoxide-generating oxidase: studies in a reconstituted subcellular system (Q36646969) (← links)
- Expression of the X-CGD gene during induced differentiation of myeloid leukemia cell line HL-60. (Q36791771) (← links)
- The involvement of oxygen radicals in microbicidal mechanisms of leukocytes and macrophages (Q36993226) (← links)
- Genetics and immunopathology of chronic granulomatous disease (Q37176109) (← links)