Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Alain Boudreault"'
Publikováno v:
The Prostate. 77:866-877
Background Castration-resistant prostate cancer (CRPC) remains incurable and identifying effective treatments continues to present a clinical challenge. Although treatment with enzalutamide, a second generation androgen receptor (AR) antagonist, prol
Publikováno v:
The Prostate. 77(8)
Castration-resistant prostate cancer (CRPC) remains incurable and identifying effective treatments continues to present a clinical challenge. Although treatment with enzalutamide, a second generation androgen receptor (AR) antagonist, prolongs surviv
Autor:
Wai Chi Ho, Alain Boudreault, Snezana Milutinovic, Kathleen M. Dickson, Philip A. Barker, John W. Gillard, James B. Jaquith, Stephen Morris, Jon P. Durkin, Mathieu J.M. Bertrand
Publikováno v:
Molecular Cell. 30(6):689-700
Summary The inhibitor of apoptosis (IAP) family of proteins enhances cell survival through mechanisms that remain uncertain. In this report, we show that cIAP1 and cIAP2 promote cancer cell survival by functioning as E3 ubiquitin ligases that maintai
Publikováno v:
Journal of Neurochemistry. 66:2596-2605
Peptidylglycine alpha-amidating enzyme (PAM; EC 1.14.17.3) is responsible for the conversion of peptides with a COOH-terminal glycine into alpha-amidated peptides, a posttranslational modification often required for biological activity and/or increas
Autor:
Diane Savaria, Alain Boudreault, Claude Lazure, Nabil G. Seidah, Normand Rondeau, Michel Chrétien, Dany Gauthier
Publikováno v:
Protein Expression and Purification. 14:353-366
A cDNA coding for the murine proprotein convertase-1 (mPC1 also known as mPC3 or mSPC3) was inserted into the Autographa californica nuclear polyhedrosis virus. Following infection of Spodoptera frugiperda cells, the recombinant N-glycosylated protei
Autor:
Alain Boudreault, Geoffrey N. Hendy, François Jean, Dany Gauthier, Hugh P.J. Bennett, Claude Lazure, Nabil G. Seidah
Publikováno v:
Journal of Biological Chemistry. 273:8572-8580
The cleavage of parathyroid hormone (PTH) from its precursor proparathyroid hormone (pro-PTH) is accomplished efficiently by the proprotein convertase furin (Hendy, G. N., Bennett, H. P. J., Gibbs, B. F., Lazure, C., Day, R., and Seidah, N. G. (1995)
Autor:
Alain Boudreault, R Day, Iris Lindberg, Weijia Dong, Paul Limperis, Ajoy Basak, Claude Lazure
Publikováno v:
Journal of Biological Chemistry. 273:829-836
Endoproteolytic processing of the 26-kDa protein precursor prodynorphin (proDyn) at paired and single basic residues is most likely carried out by the proprotein convertases (PCs); however, the role of PCs at single basic residues is unclear. In prev
Publikováno v:
Journal of Peptide Science. 1:385-395
Antiserum against an N-terminal sequence of murine prohormone convertase-1 (mPC1) incorporating the sequence immediately following the junction between the putative pro-region and the active enzyme was obtained. This was accomplished using the multip
Publikováno v:
Journal of Biological Chemistry. 270:19225-19231
The substrate specificities of two human prohormone convertases, furin and PC1, were examined with a series of 7-amino-4-methylcoumarinamide (MCA) containing peptidyl substrates. Using acetyl-Arg-Ser-Lys-Arg-MCA as model, P4 Arg substitution by Lys o
Autor:
Julie M. Rumble, Clara Hwang, Colin S. Duckett, Stephen Morris, Jon P. Durkin, Alain Boudreault, Karolyn A. Oetjen, Stefanie Galbán, John W. Gillard, James B. Jaquith, Casey W. Wright
Publikováno v:
The Biochemical journal. 417(3)
Deregulated expression of members of the IAP (inhibitor of apoptosis) family has been identified in a wide variety of neoplastic cells, and synthetic IAP antagonists represent a promising novel class of chemotherapeutic agents. Early work focused on