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Items: 1 to 20 of 89

1.

Mutation of a conserved serine in TM4 of opioid receptors confers full agonistic properties to classical antagonists.

Claude PA, Wotta DR, Zhang XH, Prather PL, McGinn TM, Erickson LJ, Loh HH, Law PY.

Proc Natl Acad Sci U S A. 1996 Jun 11;93(12):5715-9.

2.

Antagonist efficacy in MORS196L mutant is affected by the interaction between transmembrane domains of the opioid receptor.

Claude-Geppert PA, Liu J, Solberg J, Erickson-Herbrandson LJ, Loh HH, Law PY.

J Pharmacol Exp Ther. 2005 Apr;313(1):216-26.

4.
5.

Opioid receptors from a lower vertebrate (Catostomus commersoni): sequence, pharmacology, coupling to a G-protein-gated inward-rectifying potassium channel (GIRK1), and evolution.

Darlison MG, Greten FR, Harvey RJ, Kreienkamp HJ, Stühmer T, Zwiers H, Lederis K, Richter D.

Proc Natl Acad Sci U S A. 1997 Jul 22;94(15):8214-9.

6.

Functional selectivity of orphanin FQ for its receptor coexpressed with potassium channel subunits in Xenopus laevis oocytes.

Matthes H, Seward EP, Kieffer B, North RA.

Mol Pharmacol. 1996 Sep;50(3):447-50.

PMID:
8794880
8.

mu-opioid receptor regulates CFTR coexpressed in Xenopus oocytes in a cAMP independent manner.

Wotta DR, Birnbaum AK, Wilcox GL, Elde R, Law PY.

Brain Res Mol Brain Res. 1997 Feb;44(1):55-65.

PMID:
9030698
9.

Functional couplings of the delta- and the kappa-opioid receptors with the G-protein-activated K+ channel.

Ikeda K, Kobayashi T, Ichikawa T, Usui H, Kumanishi T.

Biochem Biophys Res Commun. 1995 Mar 8;208(1):302-8.

PMID:
7887943
10.

Effects of interferon-alpha on cloned opioid receptors expressed in Xenopus oocytes.

Kobayashi T, Washiyama K, Ikeda K.

Life Sci. 2004 Dec 10;76(4):407-15.

PMID:
15530503
11.

Mutation of human mu opioid receptor extracellular "disulfide cysteine" residues alters ligand binding but does not prevent receptor targeting to the cell plasma membrane.

Zhang P, Johnson PS, Zöllner C, Wang W, Wang Z, Montes AE, Seidleck BK, Blaschak CJ, Surratt CK.

Brain Res Mol Brain Res. 1999 Oct 1;72(2):195-204.

PMID:
10529478
12.

Coexpression of full-length gamma-aminobutyric acid(B) (GABA(B)) receptors with truncated receptors and metabotropic glutamate receptor 4 supports the GABA(B) heterodimer as the functional receptor.

Sullivan R, Chateauneuf A, Coulombe N, Kolakowski LF Jr, Johnson MP, Hebert TE, Ethier N, Belley M, Metters K, Abramovitz M, O'Neill GP, Ng GY.

J Pharmacol Exp Ther. 2000 May;293(2):460-7.

13.

A recombinant inwardly rectifying potassium channel coupled to GTP-binding proteins.

Chan KW, Langan MN, Sui JL, Kozak JA, Pabon A, Ladias JA, Logothetis DE.

J Gen Physiol. 1996 Mar;107(3):381-97.

16.

The weaver mutation changes the ion selectivity of the affected inwardly rectifying potassium channel GIRK2.

Tong Y, Wei J, Zhang S, Strong JA, Dlouhy SR, Hodes ME, Ghetti B, Yu L.

FEBS Lett. 1996 Jul 15;390(1):63-8.

17.

beta-Funaltrexamine, a gauge for the recognition site of wildtype and mutant H297Q mu-opioid receptors.

Spivak CE, Beglan CL, Zöllner C, Surratt CK.

Synapse. 2003 Jul;49(1):55-60.

PMID:
12710015
18.
19.

Serine 329 of the mu-opioid receptor interacts differently with agonists.

Pil J, Tytgat J.

J Pharmacol Exp Ther. 2003 Mar;304(3):924-30.

20.

Differential effects of general anesthetics on G protein-coupled inwardly rectifying and other potassium channels.

Yamakura T, Lewohl JM, Harris RA.

Anesthesiology. 2001 Jul;95(1):144-53.

PMID:
11465552
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