446 related articles for article (PubMed ID: 18664504)
41. Liver-Specific Inactivation of the Proprotein Convertase FURIN Leads to Increased Hepatocellular Carcinoma Growth.
Declercq J; Brouwers B; Pruniau VP; Stijnen P; Tuand K; Meulemans S; Prat A; Seidah NG; Khatib AM; Creemers JW
Biomed Res Int; 2015; 2015():148651. PubMed ID: 26167473
[TBL] [Abstract][Full Text] [Related]
42. 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; 362(2):143-6. PubMed ID: 7720860
[TBL] [Abstract][Full Text] [Related]
43. How Do Enveloped Viruses Exploit the Secretory Proprotein Convertases to Regulate Infectivity and Spread?
Seidah NG; Pasquato A; Andréo U
Viruses; 2021 Jun; 13(7):. PubMed ID: 34202098
[TBL] [Abstract][Full Text] [Related]
44. Cellular processing of the neurotrophin precursors of NT3 and BDNF by the mammalian proprotein convertases.
Seidah NG; Benjannet S; Pareek S; Chrétien M; Murphy RA
FEBS Lett; 1996 Feb; 379(3):247-50. PubMed ID: 8603699
[TBL] [Abstract][Full Text] [Related]
45. Subtilisin-like proprotein convertases, PACE4 and PC8, as well as furin, are endogenous proalbumin convertases in HepG2 cells.
Mori K; Imamaki A; Nagata K; Yonetomi Y; Kiyokage-Yoshimoto R; Martin TJ; Gillespie MT; Nagahama M; Tsuji A; Matsuda Y
J Biochem; 1999 Mar; 125(3):627-33. PubMed ID: 10050053
[TBL] [Abstract][Full Text] [Related]
46. Correlation of proteolytic cleavage of F protein precursors in paramyxoviruses with expression of the fur, PACE4 and PC6 genes in mammalian cells.
Sakaguchi T; Fujii Y; Kiyotani K; Yoshida T
J Gen Virol; 1994 Oct; 75 ( Pt 10)():2821-7. PubMed ID: 7931173
[TBL] [Abstract][Full Text] [Related]
47. 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; 4(2):115-36. PubMed ID: 8420571
[TBL] [Abstract][Full Text] [Related]
48. Inhibition of furin/proprotein convertase-catalyzed surface and intracellular processing by small molecules.
Komiyama T; Coppola JM; Larsen MJ; van Dort ME; Ross BD; Day R; Rehemtulla A; Fuller RS
J Biol Chem; 2009 Jun; 284(23):15729-38. PubMed ID: 19332539
[TBL] [Abstract][Full Text] [Related]
49. The paired basic amino acid-cleaving enzyme 4 (PACE4) is involved in the maturation of insulin receptor isoform B: an opportunity to reduce the specific insulin receptor-dependent effects of insulin-like growth factor 2 (IGF2).
Kara I; Poggi M; Bonardo B; Govers R; Landrier JF; Tian S; Leibiger I; Day R; Creemers JW; Peiretti F
J Biol Chem; 2015 Jan; 290(5):2812-21. PubMed ID: 25527501
[TBL] [Abstract][Full Text] [Related]
50. Identification of the paired basic convertases implicated in HIV gp160 processing based on in vitro assays and expression in CD4(+) cell lines.
Decroly E; Wouters S; Di Bello C; Lazure C; Ruysschaert JM; Seidah NG
J Biol Chem; 1996 Nov; 271(48):30442-50. PubMed ID: 8940009
[TBL] [Abstract][Full Text] [Related]
51. The Role of Proprotein Convertases in the Regulation of the Function of Immune Cells in the Oncoimmune Response.
Rose M; Duhamel M; Rodet F; Salzet M
Front Immunol; 2021; 12():667850. PubMed ID: 33995401
[TBL] [Abstract][Full Text] [Related]
52. The proprotein convertases and their implication in sterol and/or lipid metabolism.
Seidah NG; Khatib AM; Prat A
Biol Chem; 2006 Jul; 387(7):871-7. PubMed ID: 16913836
[TBL] [Abstract][Full Text] [Related]
53. Proprotein convertase activity contributes to the processing of the Alzheimer's beta-amyloid precursor protein in human cells: evidence for a role of the prohormone convertase PC7 in the constitutive alpha-secretase pathway.
Lopez-Perez E; Seidah NG; Checler F
J Neurochem; 1999 Nov; 73(5):2056-62. PubMed ID: 10537065
[TBL] [Abstract][Full Text] [Related]
54. Furin is the primary in vivo convertase of angiopoietin-like 3 and endothelial lipase in hepatocytes.
Essalmani R; Susan-Resiga D; Chamberland A; Asselin MC; Canuel M; Constam D; Creemers JW; Day R; Gauthier D; Prat A; Seidah NG
J Biol Chem; 2013 Sep; 288(37):26410-8. PubMed ID: 23918928
[TBL] [Abstract][Full Text] [Related]
55. Role of PCSK5 expression in mouse ovarian follicle development: identification of the inhibin α- and β-subunits as candidate substrates.
Antenos M; Lei L; Xu M; Malipatil A; Kiesewetter S; Woodruff TK
PLoS One; 2011 Mar; 6(3):e17348. PubMed ID: 21408162
[TBL] [Abstract][Full Text] [Related]
56. The proprotein convertases are potential targets in the treatment of dyslipidemia.
Seidah NG; Prat A
J Mol Med (Berl); 2007 Jul; 85(7):685-96. PubMed ID: 17351764
[TBL] [Abstract][Full Text] [Related]
57. Structure-function analysis of the prosegment of the proprotein convertase PC5A.
Nour N; Basak A; Chrétien M; Seidah NG
J Biol Chem; 2003 Jan; 278(5):2886-95. PubMed ID: 12414802
[TBL] [Abstract][Full Text] [Related]
58. 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; 36(51):16309-20. PubMed ID: 9405066
[TBL] [Abstract][Full Text] [Related]
59. cDNA structure of the mouse and rat subtilisin/kexin-like PC5: a candidate proprotein convertase expressed in endocrine and nonendocrine cells.
Lusson J; Vieau D; Hamelin J; Day R; Chrétien M; Seidah NG
Proc Natl Acad Sci U S A; 1993 Jul; 90(14):6691-5. PubMed ID: 8341687
[TBL] [Abstract][Full Text] [Related]
60. Proprotein processing activity and cleavage site selectivity of the Kex2-like endoprotease PACE4.
Creemers JW; Groot Kormelink PJ; Roebroek AJ; Nakayama K; Van de Ven WJ
FEBS Lett; 1993 Dec; 336(1):65-9. PubMed ID: 8262218
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
