These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

106 related articles for article (PubMed ID: 7643110)

  • 1. Functional importance of the carboxyl tail cysteine residues in the human D1 dopamine receptor.
    Jensen AA; Pedersen UB; Kiemer A; Din N; Andersen PH
    J Neurochem; 1995 Sep; 65(3):1325-31. PubMed ID: 7643110
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Chimeric D1/D2 dopamine receptors. Distinct determinants of selective efficacy, potency, and signal transduction.
    Kozell LB; Machida CA; Neve RL; Neve KA
    J Biol Chem; 1994 Dec; 269(48):30299-306. PubMed ID: 7982941
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The role of phosphorylation in D1 dopamine receptor desensitization: evidence for a novel mechanism of arrestin association.
    Kim OJ; Gardner BR; Williams DB; Marinec PS; Cabrera DM; Peters JD; Mak CC; Kim KM; Sibley DR
    J Biol Chem; 2004 Feb; 279(9):7999-8010. PubMed ID: 14660631
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A primordial dopamine D1-like adenylyl cyclase-linked receptor from Drosophila melanogaster displaying poor affinity for benzazepines.
    Sugamori KS; Demchyshyn LL; McConkey F; Forte MA; Niznik HB
    FEBS Lett; 1995 Apr; 362(2):131-8. PubMed ID: 7720859
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Elimination of palmitoylation sites in the human dopamine D1 receptor does not affect receptor-G protein interaction.
    Jin H; Zastawny R; George SR; O'Dowd BF
    Eur J Pharmacol; 1997 Apr; 324(1):109-16. PubMed ID: 9137920
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Distinct function of the cytoplasmic tail in human D1-like receptor ligand binding and coupling.
    Jackson A; Iwasiow RM; Tiberi M
    FEBS Lett; 2000 Mar; 470(2):183-8. PubMed ID: 10734231
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Dopamine D1B receptor chimeras reveal modulation of partial agonist activity by carboxyl-terminal tail sequences.
    Sugamori KS; Scheideler MA; Vernier P; Niznik HB
    J Neurochem; 1998 Dec; 71(6):2593-9. PubMed ID: 9832160
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Homologous regulation of the heptahelical D1A receptor responsiveness: specific cytoplasmic tail regions mediate dopamine-induced phosphorylation, desensitization and endocytosis.
    Jackson A; Iwasiow RM; Chaar ZY; Nantel MF; Tiberi M
    J Neurochem; 2002 Aug; 82(3):683-97. PubMed ID: 12153492
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Binding sites for [3H]SCH 23390 in retina: properties and possible relationship to dopamine D1-receptors mediating stimulation of adenylate cyclase.
    Makman MH; Dvorkin B
    Brain Res; 1986 Dec; 387(3):261-70. PubMed ID: 2950967
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Pharmacological characterization of behavioural responses to SK&F 83959 in relation to 'D1-like' dopamine receptors not linked to adenylyl cyclase.
    Deveney AM; Waddington JL
    Br J Pharmacol; 1995 Oct; 116(3):2120-6. PubMed ID: 8640354
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Agonist-induced desensitization of D1-dopamine receptors linked to adenylyl cyclase activity in cultured NS20Y neuroblastoma cells.
    Barton AC; Sibley DR
    Mol Pharmacol; 1990 Oct; 38(4):531-41. PubMed ID: 1978240
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Dopamine D5 receptor agonist high affinity and constitutive activity profile conferred by carboxyl-terminal tail sequence.
    Demchyshyn LL; McConkey F; Niznik HB
    J Biol Chem; 2000 Aug; 275(31):23446-55. PubMed ID: 10807903
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Functional differentiation of multiple dopamine D1-like receptors by NNC 01-0012.
    Sugamori KS; Hamadanizadeh SA; Scheideler MA; Hohlweg R; Vernier P; Niznik HB
    J Neurochem; 1998 Oct; 71(4):1685-93. PubMed ID: 9751203
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Sensitization of adenylate cyclase induced by a dopamine D2 receptor mutant: inverse agonism by D2 receptor antagonists.
    Bullock CM; Li C; Li M; Bermak JC; Zhou QY
    Prog Neuropsychopharmacol Biol Psychiatry; 2001 Oct; 25(7):1387-402. PubMed ID: 11513354
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Agonist-induced desensitization of dopamine D1 receptor-stimulated adenylyl cyclase activity is temporally and biochemically separated from D1 receptor internalization.
    Ng GY; Trogadis J; Stevens J; Bouvier M; O'Dowd BF; George SR
    Proc Natl Acad Sci U S A; 1995 Oct; 92(22):10157-61. PubMed ID: 7479745
    [TBL] [Abstract][Full Text] [Related]  

  • 16. (+/-)-3-[4'-(N,N-dimethylamino)cinnamyl]benzazepine analogs: novel dopamine D1 receptor antagonists.
    Shah JH; Kline RH; Geter-Douglass B; Izenwasser S; Witkin JM; Newman AH
    J Med Chem; 1996 Aug; 39(17):3423-8. PubMed ID: 8765528
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Beta 1-adrenergic and dopamine (D1)-receptors coupled to adenylyl cyclase activation in GT1 gonadotropin-releasing hormone neurosecretory cells.
    Findell PR; Wong KH; Jackman JK; Daniels DV
    Endocrinology; 1993 Feb; 132(2):682-8. PubMed ID: 8093877
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Functional analysis of the human D5 dopamine receptor missense and nonsense variants: differences in dopamine binding affinities.
    Cravchik A; Gejman PV
    Pharmacogenetics; 1999 Apr; 9(2):199-206. PubMed ID: 10376767
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Delineation of the structural basis for the activation properties of the dopamine D1 receptor subtypes.
    Iwasiow RM; Nantel MF; Tiberi M
    J Biol Chem; 1999 Nov; 274(45):31882-90. PubMed ID: 10542214
    [TBL] [Abstract][Full Text] [Related]  

  • 20. D1A, D1B, and D1C dopamine receptors from Xenopus laevis.
    Sugamori KS; Demchyshyn LL; Chung M; Niznik HB
    Proc Natl Acad Sci U S A; 1994 Oct; 91(22):10536-40. PubMed ID: 7937989
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.