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139 related items for PubMed ID: 9296377

  • 1. Somatostatin-14, somatostatin-28, and prosomatostatin[1-10] are independently and efficiently processed from prosomatostatin in the constitutive secretory pathway in islet somatostatin tumor cells (1027B2).
    Patel YC, Galanopoulou AS, Rabbani SN, Liu JL, Ravazzola M, Amherdt M.
    Mol Cell Endocrinol; 1997 Aug 08; 131(2):183-94. PubMed ID: 9296377
    [Abstract] [Full Text] [Related]

  • 2. Heterologous processing of prosomatostatin in constitutive and regulated secretory pathways. Putative role of the endoproteases furin, PC1, and PC2.
    Galanopoulou AS, Kent G, Rabbani SN, Seidah NG, Patel YC.
    J Biol Chem; 1993 Mar 15; 268(8):6041-9. PubMed ID: 8095501
    [Abstract] [Full Text] [Related]

  • 3. Heterologous processing of rat prosomatostatin to somatostatin-14 by PC2: requirement for secretory cell but not the secretion granule.
    Galanopoulou AS, Seidah NG, Patel YC.
    Biochem J; 1995 Oct 01; 311 ( Pt 1)(Pt 1):111-8. PubMed ID: 7575441
    [Abstract] [Full Text] [Related]

  • 4. Processing and intracellular targeting of prosomatostatin-derived peptides: the role of mammalian endoproteases.
    Patel YC, Galanopoulou A.
    Ciba Found Symp; 1995 Oct 01; 190():26-40; discussion 40-50. PubMed ID: 7587651
    [Abstract] [Full Text] [Related]

  • 5. Comparative proteolytic processing of rat prosomatostatin by the convertases PC1, PC2, furin, PACE4 and PC5 in constitutive and regulated secretory pathways.
    Brakch N, Galanopoulou AS, Patel YC, Boileau G, Seidah NG.
    FEBS Lett; 1995 Apr 03; 362(2):143-6. PubMed ID: 7720860
    [Abstract] [Full Text] [Related]

  • 6. Direct role of furin in mammalian prosomatostatin processing.
    Galanopoulou AS, Seidah NG, Patel YC.
    Biochem J; 1995 Jul 01; 309 ( Pt 1)(Pt 1):33-40. PubMed ID: 7619075
    [Abstract] [Full Text] [Related]

  • 7. Maintained PC1 and PC2 expression in the AtT-20 variant cell line 6T3 lacking regulated secretion and POMC: restored POMC expression and regulated secretion after cAMP treatment.
    Day R, Benjannet S, Matsuuchi L, Kelly RB, Marcinkiewicz M, Chrétien M, Seidah NG.
    DNA Cell Biol; 1995 Feb 01; 14(2):175-88. PubMed ID: 7865135
    [Abstract] [Full Text] [Related]

  • 8. Role of prohormone convertases in pro-neuropeptide Y processing: coexpression and in vitro kinetic investigations.
    Brakch N, Rist B, Beck-Sickinger AG, Goenaga J, Wittek R, Bürger E, Brunner HR, Grouzmann E.
    Biochemistry; 1997 Dec 23; 36(51):16309-20. PubMed ID: 9405066
    [Abstract] [Full Text] [Related]

  • 9. Comparative biosynthesis, covalent post-translational modifications and efficiency of prosegment cleavage of the prohormone convertases PC1 and PC2: glycosylation, sulphation and identification of the intracellular site of prosegment cleavage of PC1 and PC2.
    Benjannet S, Rondeau N, Paquet L, Boudreault A, Lazure C, Chrétien M, Seidah NG.
    Biochem J; 1993 Sep 15; 294 ( Pt 3)(Pt 3):735-43. PubMed ID: 8397508
    [Abstract] [Full Text] [Related]

  • 10. Chromogranin A processing and secretion: specific role of endogenous and exogenous prohormone convertases in the regulated secretory pathway.
    Eskeland NL, Zhou A, Dinh TQ, Wu H, Parmer RJ, Mains RE, O'Connor DT.
    J Clin Invest; 1996 Jul 01; 98(1):148-56. PubMed ID: 8690787
    [Abstract] [Full Text] [Related]

  • 11. Glucocorticoids regulate somatostatin peptide and steady state messenger ribonucleic acid levels in normal rat tissues and in a somatostatin-producing islet tumor cell line (1027B2).
    Papachristou DN, Liu JL, Patel YC.
    Endocrinology; 1994 May 01; 134(5):2259-66. PubMed ID: 7908873
    [Abstract] [Full Text] [Related]

  • 12. The developmental expression in rat of proteases furin, PC1, PC2, and carboxypeptidase E: implications for early maturation of proteolytic processing capacity.
    Zheng M, Streck RD, Scott RE, Seidah NG, Pintar JE.
    J Neurosci; 1994 Aug 01; 14(8):4656-73. PubMed ID: 8046441
    [Abstract] [Full Text] [Related]

  • 13. Processing of pro-islet amyloid polypeptide (proIAPP) by the prohormone convertase PC2.
    Badman MK, Shennan KI, Jermany JL, Docherty K, Clark A.
    FEBS Lett; 1996 Jan 15; 378(3):227-31. PubMed ID: 8557106
    [Abstract] [Full Text] [Related]

  • 14. 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 15; 137(12):5651-61. PubMed ID: 8940396
    [Abstract] [Full Text] [Related]

  • 15. Tissue distribution and processing of proSAAS by proprotein convertases.
    Sayah M, Fortenberry Y, Cameron A, Lindberg I.
    J Neurochem; 2001 Mar 15; 76(6):1833-41. PubMed ID: 11259501
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  • 19. The pro-protein convertase PC1 is induced in the transected sciatic nerve and is present in cultured Schwann cells: comparison with PC5, furin and PC7, implication in pro-BDNF processing.
    Marcinkiewicz M, Savaria D, Marcinkiewicz J.
    Brain Res Mol Brain Res; 1998 Aug 31; 59(2):229-46. PubMed ID: 9729404
    [Abstract] [Full Text] [Related]

  • 20. Endoproteolytic processing of integrin pro-alpha subunits involves the redundant function of furin and proprotein convertase (PC) 5A, but not paired basic amino acid converting enzyme (PACE) 4, PC5B or PC7.
    Lissitzky JC, Luis J, Munzer JS, Benjannet S, Parat F, Chrétien M, Marvaldi J, Seidah NG.
    Biochem J; 2000 Feb 15; 346 Pt 1(Pt 1):133-8. PubMed ID: 10657249
    [Abstract] [Full Text] [Related]

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