387 related articles for article (PubMed ID: 2023902)
21. 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; 268(8):6041-9. PubMed ID: 8095501
[TBL] [Abstract][Full Text] [Related]
22. 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; 278(17):15007-14. PubMed ID: 12584191
[TBL] [Abstract][Full Text] [Related]
23. Comparative aspects of intracellular proteolytic processing of peptide hormone precursors: studies of proopiomelanocortin processing.
Tanaka S
Zoolog Sci; 2003 Oct; 20(10):1183-98. PubMed ID: 14569141
[TBL] [Abstract][Full Text] [Related]
24. Tissue distribution and processing of proSAAS by proprotein convertases.
Sayah M; Fortenberry Y; Cameron A; Lindberg I
J Neurochem; 2001 Mar; 76(6):1833-41. PubMed ID: 11259501
[TBL] [Abstract][Full Text] [Related]
25. Peptide biosynthetic processing: distinguishing prohormone convertases PC1 and PC2.
Paquet L; Zhou A; Chang EY; Mains RE
Mol Cell Endocrinol; 1996 Jul; 120(2):161-8. PubMed ID: 8832576
[TBL] [Abstract][Full Text] [Related]
26. Cleavage of recombinant proenkephalin and blockade mutants by prohormone convertases 1 and 2: an in vitro specificity study.
Peinado JR; Li H; Johanning K; Lindberg I
J Neurochem; 2003 Nov; 87(4):868-78. PubMed ID: 14622118
[TBL] [Abstract][Full Text] [Related]
27. Lipopolysaccharide mediated regulation of neuroendocrine associated proprotein convertases and neuropeptide precursor processing in the rat spleen.
Lansac G; Dong W; Dubois CM; Benlarbi N; Afonso C; Fournier I; Salzet M; Day R
J Neuroimmunol; 2006 Feb; 171(1-2):57-71. PubMed ID: 16337011
[TBL] [Abstract][Full Text] [Related]
28. 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; 98(1):148-56. PubMed ID: 8690787
[TBL] [Abstract][Full Text] [Related]
29. The processing proteases prohormone thiol protease, PC1/3 and PC2, and 70-kDa aspartic proteinase show preferences among proenkephalin, proneuropeptide Y, and proopiomelanocortin substrates.
Hook VY; Schiller MR; Azaryan AV
Arch Biochem Biophys; 1996 Apr; 328(1):107-14. PubMed ID: 8638918
[TBL] [Abstract][Full Text] [Related]
30. Processing of pro-opiomelanocortin in GH3 cells: inhibition by prohormone convertase 2 (PC2) antisense mRNA.
Friedman TC; Cool DR; Jayasvasti V; Louie D; Loh YP
Mol Cell Endocrinol; 1996 Jan; 116(1):89-96. PubMed ID: 8822269
[TBL] [Abstract][Full Text] [Related]
31. Structural elements that direct specific processing of different mammalian subtilisin-like prohormone convertases.
Zhou A; Paquet L; Mains RE
J Biol Chem; 1995 Sep; 270(37):21509-16. PubMed ID: 7665562
[TBL] [Abstract][Full Text] [Related]
32. Structure and expression of Xenopus prohormone convertase PC2.
Braks JA; Guldemond KC; van Riel MC; Coenen AJ; Martens GJ
FEBS Lett; 1992 Jun; 305(1):45-50. PubMed ID: 1633858
[TBL] [Abstract][Full Text] [Related]
33. 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; 75(4):1763-70. PubMed ID: 10987860
[TBL] [Abstract][Full Text] [Related]
34. Loss of hypothalamic Furin affects POMC to proACTH cleavage and feeding behavior in high-fat diet-fed mice.
Coppola I; Brouwers B; Walker L; Alar C; Meulemans S; White A; Ramos-Molina B; Creemers JWM
Mol Metab; 2022 Dec; 66():101627. PubMed ID: 36374777
[TBL] [Abstract][Full Text] [Related]
35. Age-related alterations in the expression of prohormone convertase messenger ribonucleic acid (mRNA) levels in hypothalamic proopiomelanocortin mRNA neurons in the female C57BL/6J mouse.
Joshi D; Miller MM; Seidah NG; Day R
Endocrinology; 1995 Jun; 136(6):2721-9. PubMed ID: 7750497
[TBL] [Abstract][Full Text] [Related]
36. N-glycosylation controls trafficking, zymogen activation and substrate processing of proprotein convertases PC1/3 and subtilisin kexin isozyme-1.
Zandberg WF; Benjannet S; Hamelin J; Pinto BM; Seidah NG
Glycobiology; 2011 Oct; 21(10):1290-300. PubMed ID: 21527438
[TBL] [Abstract][Full Text] [Related]
37. Processing of mouse proglucagon by recombinant prohormone convertase 1 and immunopurified prohormone convertase 2 in vitro.
Rothenberg ME; Eilertson CD; Klein K; Zhou Y; Lindberg I; McDonald JK; Mackin RB; Noe BD
J Biol Chem; 1995 Apr; 270(17):10136-46. PubMed ID: 7730317
[TBL] [Abstract][Full Text] [Related]
38. Up-regulation of splenic prohormone convertases PC1 and PC2 in diabetic rats.
Nakashima M; Nie Y; Li QL; Friedman TC
Regul Pept; 2001 Dec; 102(2-3):135-45. PubMed ID: 11730986
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. Prohormone convertases (PC1/3 and PC2) in rat and human pancreas and islet cell tumors: subcellular immunohistochemical analysis.
Itoh Y; Tanaka S; Takekoshi S; Itoh J; Osamura RY
Pathol Int; 1996 Oct; 46(10):726-37. PubMed ID: 8916141
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
