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Journal Abstract Search


595 related items for PubMed ID: 8690787

  • 21. Expression of proopiomelanocortin and prohormone convertase-1 and -2 in the late gestation fetal sheep pituitary.
    Bell ME, Myers TR, Myers DA.
    Endocrinology; 1998 Dec; 139(12):5135-43. PubMed ID: 9832453
    [Abstract] [Full Text] [Related]

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

  • 23. Biological processing of the cocaine and amphetamine-regulated transcript precursors by prohormone convertases, PC2 and PC1/3.
    Dey A, Xhu X, Carroll R, Turck CW, Stein J, Steiner DF.
    J Biol Chem; 2003 Apr 25; 278(17):15007-14. PubMed ID: 12584191
    [Abstract] [Full Text] [Related]

  • 24. Post-translational processing of proopiomelanocortin (POMC) in mouse pituitary melanotroph tumors induced by a POMC-simian virus 40 large T antigen transgene.
    Low MJ, Liu B, Hammer GD, Rubinstein M, Allen RG.
    J Biol Chem; 1993 Nov 25; 268(33):24967-75. PubMed ID: 8227058
    [Abstract] [Full Text] [Related]

  • 25. Defective prodynorphin processing in mice lacking prohormone convertase PC2.
    Berman Y, Mzhavia N, Polonskaia A, Furuta M, Steiner DF, Pintar JE, Devi LA.
    J Neurochem; 2000 Oct 25; 75(4):1763-70. PubMed ID: 10987860
    [Abstract] [Full Text] [Related]

  • 26. 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]

  • 27. Differential processing of proenkephalin by prohormone convertases 1(3) and 2 and furin.
    Breslin MB, Lindberg I, Benjannet S, Mathis JP, Lazure C, Seidah NG.
    J Biol Chem; 1993 Dec 25; 268(36):27084-93. PubMed ID: 8262946
    [Abstract] [Full Text] [Related]

  • 28. Structure and function of eukaryotic proprotein processing enzymes of the subtilisin family of serine proteases.
    Van de Ven WJ, Roebroek AJ, Van Duijnhoven HL.
    Crit Rev Oncog; 1993 Dec 25; 4(2):115-36. PubMed ID: 8420571
    [Abstract] [Full Text] [Related]

  • 29. Structural elements that direct specific processing of different mammalian subtilisin-like prohormone convertases.
    Zhou A, Paquet L, Mains RE.
    J Biol Chem; 1995 Sep 15; 270(37):21509-16. PubMed ID: 7665562
    [Abstract] [Full Text] [Related]

  • 30. Human lactase-phlorizin hydrolase is not processed by furin, PC1/PC3, PC2, PACE4 and PC5/PC6A of the family of subtilisin-like proprotein processing proteases.
    Wüthrich M, Creemers JW, van de Ven WJ, Sterchi EE.
    Biochim Biophys Acta; 1996 May 28; 1311(3):199-203. PubMed ID: 8664347
    [Abstract] [Full Text] [Related]

  • 31. 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 28; 46(1):101-8. PubMed ID: 9405499
    [Abstract] [Full Text] [Related]

  • 32. 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 28; 137(12):5651-61. PubMed ID: 8940396
    [Abstract] [Full Text] [Related]

  • 33. Furin and prohormone convertase 1/3 are major convertases in the processing of mouse pro-growth hormone-releasing hormone.
    Dey A, Norrbom C, Zhu X, Stein J, Zhang C, Ueda K, Steiner DF.
    Endocrinology; 2004 Apr 28; 145(4):1961-71. PubMed ID: 14684599
    [Abstract] [Full Text] [Related]

  • 34. The post-translational processing of chromogranin A in the pancreatic islet: involvement of the eukaryote subtilisin PC2.
    Arden SD, Rutherford NG, Guest PC, Curry WJ, Bailyes EM, Johnston CF, Hutton JC.
    Biochem J; 1994 Mar 15; 298 Pt 3(Pt 3):521-8. PubMed ID: 8141763
    [Abstract] [Full Text] [Related]

  • 35. Different degrees of processing of secretogranin II in large dense core vesicles of bovine adrenal medulla and sympathetic axons correlate with their content of soluble PC1 and PC2.
    Egger C, Kirchmair R, Hogue-Angeletti R, Fischer-Colbrie R, Winkler H.
    Neurosci Lett; 1993 Sep 03; 159(1-2):199-201. PubMed ID: 8264966
    [Abstract] [Full Text] [Related]

  • 36. The family of subtilisin/kexin like pro-protein and pro-hormone convertases: divergent or shared functions.
    Seidah NG, Chrétien M, Day R.
    Biochimie; 1994 Sep 03; 76(3-4):197-209. PubMed ID: 7819324
    [Abstract] [Full Text] [Related]

  • 37. The prohormone convertases PC1 and PC2 mediate distinct endoproteolytic cleavages in a strict temporal order during proopiomelanocortin biosynthetic processing.
    Zhou A, Bloomquist BT, Mains RE.
    J Biol Chem; 1993 Jan 25; 268(3):1763-9. PubMed ID: 8380577
    [Abstract] [Full Text] [Related]

  • 38. 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 25; 81(3):565-74. PubMed ID: 12065665
    [Abstract] [Full Text] [Related]

  • 39. Processing of prothyrotropin-releasing hormone (Pro-TRH) by bovine intermediate lobe secretory vesicle membrane PC1 and PC2 enzymes.
    Friedman TC, Loh YP, Cawley NX, Birch NP, Huang SS, Jackson IM, Nillni EA.
    Endocrinology; 1995 Oct 25; 136(10):4462-72. PubMed ID: 7664666
    [Abstract] [Full Text] [Related]

  • 40. The role of prohormone convertases PC1 (PC3) and PC2 in the cell-specific processing of proglucagon.
    Mineo I, Matsumura T, Shingu R, Namba M, Kuwajima M, Matsuzawa Y.
    Biochem Biophys Res Commun; 1995 Feb 15; 207(2):646-51. PubMed ID: 7864855
    [Abstract] [Full Text] [Related]


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