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

149 related items for PubMed ID: 10482305

  • 1. Quality control in the endoplasmic reticulum: lessons from hereditary myeloperoxidase deficiency.
    Nauseef WM.
    J Lab Clin Med; 1999 Sep; 134(3):215-21. PubMed ID: 10482305
    [Abstract] [Full Text] [Related]

  • 2. A novel form of hereditary myeloperoxidase deficiency linked to endoplasmic reticulum/proteasome degradation.
    DeLeo FR, Goedken M, McCormick SJ, Nauseef WM.
    J Clin Invest; 1998 Jun 15; 101(12):2900-9. PubMed ID: 9637725
    [Abstract] [Full Text] [Related]

  • 3. Impact of missense mutations on biosynthesis of myeloperoxidase.
    Nauseef WM, McCormick S, Goedken M.
    Redox Rep; 2000 Jun 15; 5(4):197-206. PubMed ID: 10994874
    [Abstract] [Full Text] [Related]

  • 4. Coordinated participation of calreticulin and calnexin in the biosynthesis of myeloperoxidase.
    Nauseef WM, McCormick SJ, Goedken M.
    J Biol Chem; 1998 Mar 20; 273(12):7107-11. PubMed ID: 9507022
    [Abstract] [Full Text] [Related]

  • 5. Calreticulin functions as a molecular chaperone in the biosynthesis of myeloperoxidase.
    Nauseef WM, McCormick SJ, Clark RA.
    J Biol Chem; 1995 Mar 03; 270(9):4741-7. PubMed ID: 7876246
    [Abstract] [Full Text] [Related]

  • 6. Roles of heme insertion and the mannose-6-phosphate receptor in processing of the human myeloid lysosomal enzyme, myeloperoxidase.
    Nauseef WM, McCormick S, Yi H.
    Blood; 1992 Nov 15; 80(10):2622-33. PubMed ID: 1330078
    [Abstract] [Full Text] [Related]

  • 7. Biosynthesis and processing of myeloperoxidase--a marker for myeloid cell differentiation.
    Nauseef WM, Olsson I, Arnljots K.
    Eur J Haematol; 1988 Feb 15; 40(2):97-110. PubMed ID: 2831080
    [Abstract] [Full Text] [Related]

  • 8. Impact of two novel mutations on the structure and function of human myeloperoxidase.
    Goedken M, McCormick S, Leidal KG, Suzuki K, Kameoka Y, Astern JM, Huang M, Cherkasov A, Nauseef WM.
    J Biol Chem; 2007 Sep 21; 282(38):27994-8003. PubMed ID: 17650507
    [Abstract] [Full Text] [Related]

  • 9. Insights into myeloperoxidase biosynthesis from its inherited deficiency.
    Nauseef WM.
    J Mol Med (Berl); 1998 Sep 21; 76(10):661-8. PubMed ID: 9766843
    [Abstract] [Full Text] [Related]

  • 10. Pattern of inheritance in hereditary myeloperoxidase deficiency associated with the R569W missense mutation.
    Nauseef WM, Cogley M, Bock S, Petrides PE.
    J Leukoc Biol; 1998 Feb 21; 63(2):264-9. PubMed ID: 9468285
    [Abstract] [Full Text] [Related]

  • 11. Effect of the R569W missense mutation on the biosynthesis of myeloperoxidase.
    Nauseef WM, Cogley M, McCormick S.
    J Biol Chem; 1996 Apr 19; 271(16):9546-9. PubMed ID: 8621627
    [Abstract] [Full Text] [Related]

  • 12. Biosynthesis of human myeloperoxidase.
    Nauseef WM.
    Arch Biochem Biophys; 2018 Mar 15; 642():1-9. PubMed ID: 29408362
    [Abstract] [Full Text] [Related]

  • 13. Hereditary myeloperoxidase deficiency due to a missense mutation of arginine 569 to tryptophan.
    Nauseef WM, Brigham S, Cogley M.
    J Biol Chem; 1994 Jan 14; 269(2):1212-6. PubMed ID: 7904599
    [Abstract] [Full Text] [Related]

  • 14. Glycoprotein degradation: do sugars hold the key?
    Frigerio L, Lord JM.
    Curr Biol; 2000 Sep 21; 10(18):R674-7. PubMed ID: 10996809
    [Abstract] [Full Text] [Related]

  • 15. Biochemical and molecular characterization of hereditary myeloperoxidase deficiency.
    Romano M, Dri P, Da Dalt L, Patriarca P, Baralle FE.
    Blood; 1997 Nov 15; 90(10):4126-34. PubMed ID: 9354683
    [Abstract] [Full Text] [Related]

  • 16. Lectins as chaperones in glycoprotein folding.
    Trombetta ES, Helenius A.
    Curr Opin Struct Biol; 1998 Oct 15; 8(5):587-92. PubMed ID: 9818262
    [Abstract] [Full Text] [Related]

  • 17. Distinct patterns of folding and interactions with calnexin and calreticulin in human class I MHC proteins with altered N-glycosylation.
    Zhang Q, Salter RD.
    J Immunol; 1998 Jan 15; 160(2):831-7. PubMed ID: 9551918
    [Abstract] [Full Text] [Related]

  • 18. Sorting for storage in myeloid cells of nonmyeloid proteins and chimeras with the propeptide of myeloperoxidase precursor.
    Bülow E, Nauseef WM, Goedken M, McCormick S, Calafat J, Gullberg U, Olsson I.
    J Leukoc Biol; 2002 Feb 15; 71(2):279-88. PubMed ID: 11818449
    [Abstract] [Full Text] [Related]

  • 19. Biochemical and immunologic analysis of hereditary myeloperoxidase deficiency.
    Nauseef WM, Root RK, Malech HL.
    J Clin Invest; 1983 May 15; 71(5):1297-307. PubMed ID: 6189859
    [Abstract] [Full Text] [Related]

  • 20. Biosynthesis, processing, and sorting of human myeloperoxidase.
    Hansson M, Olsson I, Nauseef WM.
    Arch Biochem Biophys; 2006 Jan 15; 445(2):214-24. PubMed ID: 16183032
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.