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Journal Abstract Search

257 related items for PubMed ID: 7883050

  • 21. In vitro processing of anthrax toxin protective antigen by recombinant PC1 (SPC3) and bovine intermediate lobe secretory vesicle membranes.
    Friedman TC, Gordon VM, Leppla SH, Klimpel KR, Birch NP, Loh YP.
    Arch Biochem Biophys; 1995 Jan 10; 316(1):5-13. PubMed ID: 7840657
    [Abstract] [Full Text] [Related]

  • 22. Isolation and characterization of VGF peptides in rat brain. Role of PC1/3 and PC2 in the maturation of VGF precursor.
    Trani E, Giorgi A, Canu N, Amadoro G, Rinaldi AM, Halban PA, Ferri GL, Possenti R, Schininà ME, Levi A.
    J Neurochem; 2002 May 10; 81(3):565-74. PubMed ID: 12065665
    [Abstract] [Full Text] [Related]

  • 23. Secretoneurin--a neuropeptide generated in brain, adrenal medulla and other endocrine tissues by proteolytic processing of secretogranin II (chromogranin C).
    Kirchmair R, Hogue-Angeletti R, Gutierrez J, Fischer-Colbrie R, Winkler H.
    Neuroscience; 1993 Mar 10; 53(2):359-65. PubMed ID: 8492910
    [Abstract] [Full Text] [Related]

  • 24. The SAAS granin exhibits structural and functional homology to 7B2 and contains a highly potent hexapeptide inhibitor of PC1.
    Cameron A, Fortenberry Y, Lindberg I.
    FEBS Lett; 2000 May 12; 473(2):135-8. PubMed ID: 10812060
    [Abstract] [Full Text] [Related]

  • 25. Identification of the thyrotropin-releasing hormone precursor, its processing products, and its coexpression with convertase 1 in primary cultures of hypothalamic neurons: anatomic distribution of PC1 and PC2.
    Nillni EA, Luo LG, Jackson IM, McMillan P.
    Endocrinology; 1996 Dec 12; 137(12):5651-61. PubMed ID: 8940396
    [Abstract] [Full Text] [Related]

  • 26. Processing of prothyrotropin-releasing hormone by the family of prohormone convertases.
    Schaner P, Todd RB, Seidah NG, Nillni EA.
    J Biol Chem; 1997 Aug 08; 272(32):19958-68. PubMed ID: 9242664
    [Abstract] [Full Text] [Related]

  • 27. PC1 and PC2 are proprotein convertases capable of cleaving proopiomelanocortin at distinct pairs of basic residues.
    Benjannet S, Rondeau N, Day R, Chrétien M, Seidah NG.
    Proc Natl Acad Sci U S A; 1991 May 01; 88(9):3564-8. PubMed ID: 2023902
    [Abstract] [Full Text] [Related]

  • 28. Cleavage of recombinant proenkephalin and blockade mutants by prohormone convertases 1 and 2: an in vitro specificity study.
    Peinado JR, Li H, Johanning K, Lindberg I.
    J Neurochem; 2003 Nov 01; 87(4):868-78. PubMed ID: 14622118
    [Abstract] [Full Text] [Related]

  • 29. Proglucagon processing profile in canine L cells expressing endogenous prohormone convertase 1/3 and prohormone convertase 2.
    Damholt AB, Buchan AM, Holst JJ, Kofod H.
    Endocrinology; 1999 Oct 01; 140(10):4800-8. PubMed ID: 10499540
    [Abstract] [Full Text] [Related]

  • 30. Immunocytochemical localization of the prohormone convertases PC1 and PC2 in rat prolactin cells.
    Muller L, Picart R, Barret A, Seidah NG, Tougard C.
    J Histochem Cytochem; 1998 Jan 01; 46(1):101-8. PubMed ID: 9405499
    [Abstract] [Full Text] [Related]

  • 31. Processing of prodynorphin by the prohormone convertase PC1 results in high molecular weight intermediate forms. Cleavage at a single arginine residue.
    Dupuy A, Lindberg I, Zhou Y, Akil H, Lazure C, Chrétien M, Seidah NG, Day R.
    FEBS Lett; 1994 Jan 03; 337(1):60-5. PubMed ID: 8276115
    [Abstract] [Full Text] [Related]

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  • 33. Bovine posterior pituitary: presence of p65 (synaptotagmin), PC1, PC2 and secretoneurin in large dense core vesicles.
    Egger C, Kirchmair R, Kapelari S, Fischer-Colbrie R, Hogue-Angeletti R, Winkler H.
    Neuroendocrinology; 1994 Feb 03; 59(2):169-75. PubMed ID: 8127407
    [Abstract] [Full Text] [Related]

  • 34. Cellular processing of the nerve growth factor precursor by the mammalian pro-protein convertases.
    Seidah NG, Benjannet S, Pareek S, Savaria D, Hamelin J, Goulet B, Laliberte J, Lazure C, Chrétien M, Murphy RA.
    Biochem J; 1996 Mar 15; 314 ( Pt 3)(Pt 3):951-60. PubMed ID: 8615794
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  • 36. The processing proteases prohormone thiol protease, PC1/3 and PC2, and 70-kDa aspartic proteinase show preferences among proenkephalin, proneuropeptide Y, and proopiomelanocortin substrates.
    Hook VY, Schiller MR, Azaryan AV.
    Arch Biochem Biophys; 1996 Apr 01; 328(1):107-14. PubMed ID: 8638918
    [Abstract] [Full Text] [Related]

  • 37. Cellular distributions of the prohormone processing enzymes PC1 and PC2.
    Lindberg I, Ahn SC, Breslin MB.
    Mol Cell Neurosci; 1994 Dec 01; 5(6):614-22. PubMed ID: 7704436
    [Abstract] [Full Text] [Related]

  • 38. Prohormone convertases 1 and 2 process ProPACAP and generate matured, bioactive PACAP38 and PACAP27 in transfected rat pituitary GH4C1 cells.
    Li M, Shuto Y, Somogyvári-Vigh A, Arimura A.
    Neuroendocrinology; 1999 Mar 01; 69(3):217-26. PubMed ID: 10087454
    [Abstract] [Full Text] [Related]

  • 39. Lipopolysaccharide mediated regulation of neuroendocrine associated proprotein convertases and neuropeptide precursor processing in the rat spleen.
    Lansac G, Dong W, Dubois CM, Benlarbi N, Afonso C, Fournier I, Salzet M, Day R.
    J Neuroimmunol; 2006 Feb 01; 171(1-2):57-71. PubMed ID: 16337011
    [Abstract] [Full Text] [Related]

  • 40. Proglucagon processing in an islet cell line: effects of PC1 overexpression and PC2 depletion.
    Dhanvantari S, Brubaker PL.
    Endocrinology; 1998 Apr 01; 139(4):1630-7. PubMed ID: 9528943
    [Abstract] [Full Text] [Related]

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