BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

126 related articles for article (PubMed ID: 15911376)

  • 1. Conformational analysis of the C-terminal Gly-Leu-Met-NH2 tripeptide of substance P bound to the NK-1 receptor.
    Sagan S; Quancard J; Lequin O; Karoyan P; Chassaing G; Lavielle S
    Chem Biol; 2005 May; 12(5):555-65. PubMed ID: 15911376
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Incorporation of vinylogous scaffolds in the C-terminal tripeptide of substance P.
    Claudel S; Tasseau O; Sagan S; Grison C; Coutrot P; Lavielle S
    J Pept Res; 2004 Nov; 64(5):186-93. PubMed ID: 15485556
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Characterization of the bioactive conformation of the C-terminal tripeptide Gly-Leu-Met-NH2 of substance P using [3-prolinoleucine10]SP analogues.
    Quancard J; Karoyan P; Sagan S; Convert O; Lavielle S; Chassaing G; Lequin O
    Eur J Biochem; 2003 Jul; 270(13):2869-78. PubMed ID: 12823557
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Point mutation increases a form of the NK1 receptor with high affinity for neurokinin A and B and septide.
    Ciucci A; Palma C; Manzini S; Werge TM
    Br J Pharmacol; 1998 Sep; 125(2):393-401. PubMed ID: 9786514
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Characterization of a conformationally sensitive TOAC spin-labeled substance P.
    Shafer AM; Nakaie CR; Deupi X; Bennett VJ; Voss JC
    Peptides; 2008 Nov; 29(11):1919-29. PubMed ID: 18775458
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The N-terminal domain of substance P is required for complete homologous desensitization but not phosphorylation of the rat neurokinin-1 receptor.
    Vigna SR
    Neuropeptides; 2001 Feb; 35(1):24-31. PubMed ID: 11346307
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The role of the N-terminal and mid-region residues of substance P in regulating functional selectivity at the tachykinin NK1 receptor.
    Perrine SA; Beard DJ; Young JK; Simmons MA
    Eur J Pharmacol; 2008 Sep; 592(1-3):1-6. PubMed ID: 18634782
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Synthesis and biological activity of NK-1 selective, N-backbone cyclic analogs of the C-terminal hexapeptide of substance P.
    Byk G; Halle D; Zeltser I; Bitan G; Selinger Z; Gilon C
    J Med Chem; 1996 Aug; 39(16):3174-8. PubMed ID: 8759639
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Internalization of [3H]substance P analogues in NK-1 receptor transfected CHO cells.
    Sagan S; Lavielle S
    Biochem Biophys Res Commun; 2001 Apr; 282(4):958-64. PubMed ID: 11352645
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Systematic study of substance P analogs. II. Rapid screening of 512 substance P stereoisomers for binding to NK1 receptor.
    Wang JX; Dipasquale AJ; Bray AM; Maeji NJ; Spellmeyer DC; Geysen HM
    Int J Pept Protein Res; 1993 Oct; 42(4):392-9. PubMed ID: 7503964
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Construction of covalently coupled, concatameric dimers of 7TM receptors.
    Terpager M; Scholl DJ; Kubale V; Martini L; Elling CE; Schwartz TW
    J Recept Signal Transduct Res; 2009; 29(5):235-45. PubMed ID: 19747085
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Interaction of substance P and its N- and C-terminal fragments with Ca2+: implications for hormone action.
    Ananthanarayanan VS; Orlicky S
    Biopolymers; 1992 Dec; 32(12):1765-73. PubMed ID: 1282041
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Extracellular domains of the neurokinin-1 receptor: structural characterization and interactions with substance P.
    Ulfers AL; Piserchio A; Mierke DF
    Biopolymers; 2002; 66(5):339-49. PubMed ID: 12539262
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The use of photolabelled peptides to localize the substance-P-binding site in the human neurokinin-1 tachykinin receptor.
    Girault S; Sagan S; Bolbach G; Lavielle S; Chassaing G
    Eur J Biochem; 1996 Aug; 240(1):215-22. PubMed ID: 8797856
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Discovery of dipeptides with high affinity to the specific binding site for substance P1-7.
    Fransson R; Botros M; Sköld C; Nyberg F; Lindeberg G; Hallberg M; Sandström A
    J Med Chem; 2010 Mar; 53(6):2383-9. PubMed ID: 20178322
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Backbone cyclization of the C-terminal part of substance P. Part 1: The important role of the sulphur in position 11.
    Bitan G; Zeltser I; Byk G; Halle D; Mashriki Y; Gluhov EV; Sukhotinsky I; Hanani M; Selinger Z; Gilon C
    J Pept Sci; 1996; 2(4):261-9. PubMed ID: 9231334
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Calpha methylation in molecular recognition. Application to substance P and the two neurokinin-1 receptor binding sites.
    Sagan S; Lequin O; Frank F; Convert O; Ayoub M; Lavielle S; Chassaing G
    Eur J Biochem; 2001 May; 268(10):2997-3005. PubMed ID: 11358518
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The common C-terminal sequences of substance P and neurokinin A contact the same region of the NK-1 receptor.
    Bremer AA; Leeman SE; Boyd ND
    FEBS Lett; 2000 Dec; 486(1):43-8. PubMed ID: 11108840
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Senktide-induced gerbil foot tapping behaviour is blocked by selective tachykinin NK1 and NK3 receptor antagonists.
    Sundqvist M; Kristensson E; Adolfsson R; Leffler A; Ahlstedt I; Engberg S; Drmota T; Sigfridsson K; Jussila R; de Verdier J; Novén A; Johansson A; Påhlman I; von Mentzer B; Lindström E
    Eur J Pharmacol; 2007 Dec; 577(1-3):78-86. PubMed ID: 17920583
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Restriction of a peptide turn conformation and conformational analysis of guanidino group using arginine-proline fused amino acids: application to mini atrial natriuretic peptide on binding to the receptor.
    Sugase K; Horikawa M; Sugiyama M; Ishiguro M
    J Med Chem; 2004 Jan; 47(2):489-92. PubMed ID: 14711318
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.