185 related articles for article (PubMed ID: 19343278)
21. Unique biological function of cathepsin L in secretory vesicles for biosynthesis of neuropeptides.
Funkelstein L; Beinfeld M; Minokadeh A; Zadina J; Hook V
Neuropeptides; 2010 Dec; 44(6):457-66. PubMed ID: 21047684
[TBL] [Abstract][Full Text] [Related]
22. Processing of high-molecular-weight form adrenocorticotropin in human adrenocorticotropin-secreting tumor cell line (DMS-79) after transfection of prohormone convertase 1/3 gene.
Tateno T; Kato M; Tani Y; Yoshimoto T; Oki Y; Hirata Y
J Endocrinol Invest; 2010 Feb; 33(2):113-7. PubMed ID: 19786827
[TBL] [Abstract][Full Text] [Related]
23. Prohormone-converting enzymes: regulation and evaluation of function using antisense RNA.
Bloomquist BT; Eipper BA; Mains RE
Mol Endocrinol; 1991 Dec; 5(12):2014-24. PubMed ID: 1791845
[TBL] [Abstract][Full Text] [Related]
24. Differential effects of fasting and leptin on proopiomelanocortin peptides in the arcuate nucleus and in the nucleus of the solitary tract.
Perello M; Stuart RC; Nillni EA
Am J Physiol Endocrinol Metab; 2007 May; 292(5):E1348-57. PubMed ID: 17227963
[TBL] [Abstract][Full Text] [Related]
25. Post-translational processing of pro-opiomelanocortin (POMC)-derived peptides during fetal monkey pituitary development. I. Adrenocorticotropin (ACTH) and alpha-melanotropins (alpha-MSHs).
Allen RG; Hatfield JM; Stack J
Dev Biol; 1988 Mar; 126(1):156-63. PubMed ID: 2830157
[TBL] [Abstract][Full Text] [Related]
26. Kex2-like endoproteases PC2 and PC3 accurately cleave a model prohormone in mammalian cells: evidence for a common core of neuroendocrine processing enzymes.
Thomas L; Leduc R; Thorne BA; Smeekens SP; Steiner DF; Thomas G
Proc Natl Acad Sci U S A; 1991 Jun; 88(12):5297-301. PubMed ID: 1647029
[TBL] [Abstract][Full Text] [Related]
27. The subtilisin/kexin family of precursor convertases. Emphasis on PC1, PC2/7B2, POMC and the novel enzyme SKI-1.
Seidah NG; Benjannet S; Hamelin J; Mamarbachi AM; Basak A; Marcinkiewicz J; Mbikay M; Chrétien M; Marcinkiewicz M
Ann N Y Acad Sci; 1999 Oct; 885():57-74. PubMed ID: 10816641
[TBL] [Abstract][Full Text] [Related]
28. Cathepsin L plays a major role in cholecystokinin production in mouse brain cortex and in pituitary AtT-20 cells: protease gene knockout and inhibitor studies.
Beinfeld MC; Funkelstein L; Foulon T; Cadel S; Kitagawa K; Toneff T; Reinheckel T; Peters C; Hook V
Peptides; 2009 Oct; 30(10):1882-91. PubMed ID: 19589362
[TBL] [Abstract][Full Text] [Related]
29. Cathepsin L and Arg/Lys aminopeptidase: a distinct prohormone processing pathway for the biosynthesis of peptide neurotransmitters and hormones.
Hook V; Yasothornsrikul S; Greenbaum D; Medzihradszky KF; Troutner K; Toneff T; Bundey R; Logrinova A; Reinheckel T; Peters C; Bogyo M
Biol Chem; 2004 Jun; 385(6):473-80. PubMed ID: 15255178
[TBL] [Abstract][Full Text] [Related]
30. POMC-related products in the intermediate pituitary of the amphibian, Bufo marinus: differential subcellular processing in the Golgi and secretory granules.
Steveson TC; Dores RM
Peptides; 1996; 17(3):425-34. PubMed ID: 8735969
[TBL] [Abstract][Full Text] [Related]
31. 60 YEARS OF POMC: Biosynthesis, trafficking, and secretion of pro-opiomelanocortin-derived peptides.
Cawley NX; Li Z; Loh YP
J Mol Endocrinol; 2016 May; 56(4):T77-97. PubMed ID: 26880796
[TBL] [Abstract][Full Text] [Related]
32. Evaluation of posttranslational processing of proopiomelanocortin in the banded houndshark pituitary by combined cDNA cloning and mass spectrometry.
Takahashi A; Kobayashi Y; Moriyama S; Hyodo S
Gen Comp Endocrinol; 2008 May; 157(1):41-8. PubMed ID: 18396285
[TBL] [Abstract][Full Text] [Related]
33. 60 YEARS OF POMC: From the prohormone theory to pro-opiomelanocortin and to proprotein convertases (PCSK1 to PCSK9).
Chrétien M; Mbikay M
J Mol Endocrinol; 2016 May; 56(4):T49-62. PubMed ID: 26762158
[TBL] [Abstract][Full Text] [Related]
34. [Corticotrope].
Tanaka K
Nihon Rinsho; 1993 Oct; 51(10):2606-10. PubMed ID: 8254928
[TBL] [Abstract][Full Text] [Related]
35. Proteases for processing proneuropeptides into peptide neurotransmitters and hormones.
Hook V; Funkelstein L; Lu D; Bark S; Wegrzyn J; Hwang SR
Annu Rev Pharmacol Toxicol; 2008; 48():393-423. PubMed ID: 18184105
[TBL] [Abstract][Full Text] [Related]
36. Immunocytochemical localization of POMC-derived peptides (adrenocorticotropic hormone, alpha-melanocyte-stimulating hormone and beta-endorphin) in the pituitary, brain and olfactory epithelium of the frog, Rana esculenta, during development.
D'Aniello B; Imperatore C; Fiorentino M; Vallarino M; Rastogi RK
Cell Tissue Res; 1994 Dec; 278(3):509-16. PubMed ID: 7850861
[TBL] [Abstract][Full Text] [Related]
37. Detection of N-acetylated forms of alpha-MSH and beta-endorphin in the intermediate pituitary of the holostean fishes, Lepisosteus spatula, Lepisosteus osseus, and Amia calva.
Dores RM; Keller H; White Y; Marra LE; Youson JH
Peptides; 1994; 15(3):483-7. PubMed ID: 7937324
[TBL] [Abstract][Full Text] [Related]
38. A slow and a fast secretory compartment of POMC-derived peptides in the neurointermediate lobe of the amphibian Xenopus laevis.
Van Zoest ID; Leenders HJ; Jenks BG; Roubos EW
Comp Biochem Physiol C Comp Pharmacol Toxicol; 1990; 96(1):199-203. PubMed ID: 1980877
[TBL] [Abstract][Full Text] [Related]
39. Impaired prohormone convertases in Cpe(fat)/Cpe(fat) mice.
Berman Y; Mzhavia N; Polonskaia A; Devi LA
J Biol Chem; 2001 Jan; 276(2):1466-73. PubMed ID: 11038363
[TBL] [Abstract][Full Text] [Related]
40. An analysis of the proopiomelanocortin systems in the pituitary of the squamate reptile Lacerta galloti.
Lancha A; Batista MA; Dores RM
Gen Comp Endocrinol; 1994 Mar; 93(3):438-47. PubMed ID: 8194743
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]