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Journal Abstract Search

179 related items for PubMed ID: 9756897

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  • 3. Design and synthesis of novel inhibitors of prohormone convertases.
    Basak A, Jean F, Seidah NG, Lazure C.
    Int J Pept Protein Res; 1994 Sep; 44(3):253-61. PubMed ID: 7822102
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  • 4. 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
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  • 8. Polyarginines are potent furin inhibitors.
    Cameron A, Appel J, Houghten RA, Lindberg I.
    J Biol Chem; 2000 Nov 24; 275(47):36741-9. PubMed ID: 10958789
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  • 12. Inhibitory specificity and potency of proSAAS-derived peptides toward proprotein convertase 1.
    Basak A, Koch P, Dupelle M, Fricker LD, Devi LA, Chrétien M, Seidah NG.
    J Biol Chem; 2001 Aug 31; 276(35):32720-8. PubMed ID: 11435430
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  • 14. An internally quenched fluorogenic substrate of prohormone convertase 1 and furin leads to a potent prohormone convertase inhibitor.
    Jean F, Basak A, DiMaio J, Seidah NG, Lazure C.
    Biochem J; 1995 May 01; 307 ( Pt 3)(Pt 3):689-95. PubMed ID: 7741698
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  • 15. The convertases furin and PC1 can both cleave the human immunodeficiency virus (HIV)-1 envelope glycoprotein gp160 into gp120 (HIV-1 SU) and gp41 (HIV-I TM).
    Decroly E, Vandenbranden M, Ruysschaert JM, Cogniaux J, Jacob GS, Howard SC, Marshall G, Kompelli A, Basak A, Jean F.
    J Biol Chem; 1994 Apr 22; 269(16):12240-7. PubMed ID: 8163529
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  • 16. 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
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  • 17. Synthetic peptides derived from the prosegments of proprotein convertase 1/3 and furin are potent inhibitors of both enzymes.
    Basak A, Lazure C.
    Biochem J; 2003 Jul 01; 373(Pt 1):231-9. PubMed ID: 12662153
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  • 18. 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
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  • 20. Fluorescent peptidyl substrates as an aid in studying the substrate specificity of human prohormone convertase PC1 and human furin and designing a potent irreversible inhibitor.
    Jean F, Boudreault A, Basak A, Seidah NG, Lazure C.
    J Biol Chem; 1995 Aug 18; 270(33):19225-31. PubMed ID: 7642593
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