These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

319 related items for PubMed ID: 8245781

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. CD34+ peripheral blood progenitors as a target for genetic correction of the two flavocytochrome b558 defective forms of chronic granulomatous disease.
    Li F, Linton GF, Sekhsaria S, Whiting-Theobald N, Katkin JP, Gallin JI, Malech HL.
    Blood; 1994 Jul 01; 84(1):53-8. PubMed ID: 7517218
    [Abstract] [Full Text] [Related]

  • 4. Hypoxic induction of gene expression in chronic granulomatous disease-derived B-cell lines: oxygen sensing is independent of the cytochrome b558-containing nicotinamide adenine dinucleotide phosphate oxidase.
    Wenger RH, Marti HH, Schuerer-Maly CC, Kvietikova I, Bauer C, Gassmann M, Maly FE.
    Blood; 1996 Jan 15; 87(2):756-61. PubMed ID: 8555500
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. High-level reconstitution of respiratory burst activity in a human X-linked chronic granulomatous disease (X-CGD) cell line and correction of murine X-CGD bone marrow cells by retroviral-mediated gene transfer of human gp91phox.
    Ding C, Kume A, Björgvinsdóttir H, Hawley RG, Pech N, Dinauer MC.
    Blood; 1996 Sep 01; 88(5):1834-40. PubMed ID: 8781441
    [Abstract] [Full Text] [Related]

  • 7. Cytochrome b558-negative, autosomal recessive chronic granulomatous disease: two new mutations in the cytochrome b558 light chain of the NADPH oxidase (p22-phox).
    de Boer M, de Klein A, Hossle JP, Seger R, Corbeel L, Weening RS, Roos D.
    Am J Hum Genet; 1992 Nov 01; 51(5):1127-35. PubMed ID: 1415254
    [Abstract] [Full Text] [Related]

  • 8. Intersecting Stories of the Phagocyte NADPH Oxidase and Chronic Granulomatous Disease.
    Nauseef WM, Clark RA.
    Methods Mol Biol; 2019 Nov 01; 1982():3-16. PubMed ID: 31172463
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. NADPH oxidase activity and cytochrome b558 content of human Epstein-Barr-virus-transformed B lymphocytes correlate with expression of genes encoding components of the oxidase system.
    Condino-Neto A, Newburger PE.
    Arch Biochem Biophys; 1998 Dec 15; 360(2):158-64. PubMed ID: 9851826
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. [Molecular aspects of chronic granulomatous disease. "the NADPH oxidase complex"].
    Morel F.
    Bull Acad Natl Med; 2007 Feb 15; 191(2):377-90; discussion 390-2. PubMed ID: 17969555
    [Abstract] [Full Text] [Related]

  • 16. The superoxide-generating NADPH oxidase: structural aspects and activation mechanism.
    Vignais PV.
    Cell Mol Life Sci; 2002 Sep 15; 59(9):1428-59. PubMed ID: 12440767
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Drug-selected complete restoration of superoxide generation in Epstein-Barr virus-transformed B cells from p47phox-deficient chronic granulomatous disease patients by using a bicistronic retrovirus vector encoding a human multi-drug resistance gene (MDR1) and the p47phox gene.
    Iwata M, Nunoi H, Matsuda I, Kanegasaki S, Tsuruo T, Sugimoto Y.
    Hum Genet; 1998 Oct 15; 103(4):419-23. PubMed ID: 9856484
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 16.