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Results: 1 to 20 of 172

Similar articles for PubMed (Select 10766790)

1.
2.

Molecular exploration of the α(1A)-adrenoceptor orthosteric site: binding site definition for epinephrine, HEAT and prazosin.

Maïga A, Dupont M, Blanchet G, Marcon E, Gilquin B, Servent D, Gilles N.

FEBS Lett. 2014 Dec 20;588(24):4613-9. doi: 10.1016/j.febslet.2014.10.033. Epub 2014 Nov 4.

PMID:
25447534
3.

Extracellular surface residues of the α1B-adrenoceptor critical for G protein-coupled receptor function.

Ragnarsson L, Andersson Å, Thomas WG, Lewis RJ.

Mol Pharmacol. 2015 Jan;87(1):121-9. doi: 10.1124/mol.114.094557. Epub 2014 Oct 28.

PMID:
25352041
4.

An aspartate in the second extracellular loop of the α(1B) adrenoceptor regulates agonist binding.

Campbell AP, MacDougall IJ, Griffith R, Finch AM.

Eur J Pharmacol. 2014 Jun 15;733:90-6. doi: 10.1016/j.ejphar.2014.03.034. Epub 2014 Mar 29.

PMID:
24690260
5.

Conopeptide ρ-TIA defines a new allosteric site on the extracellular surface of the α1B-adrenoceptor.

Ragnarsson L, Wang CI, Andersson Å, Fajarningsih D, Monks T, Brust A, Rosengren KJ, Lewis RJ.

J Biol Chem. 2013 Jan 18;288(3):1814-27. doi: 10.1074/jbc.M112.430785. Epub 2012 Nov 26.

6.

Identification and profiling of novel α1A-adrenoceptor-CXC chemokine receptor 2 heteromer.

Mustafa S, See HB, Seeber RM, Armstrong SP, White CW, Ventura S, Ayoub MA, Pfleger KD.

J Biol Chem. 2012 Apr 13;287(16):12952-65. doi: 10.1074/jbc.M111.322834. Epub 2012 Feb 27.

7.

A novel structural framework for α(1A/D)-adrenoceptor selective antagonists identified using subtype selective pharmacophores.

Stoddart ES, Senadheera S, MacDougall IJ, Griffith R, Finch AM.

PLoS One. 2011 May 10;6(5):e19695. doi: 10.1371/journal.pone.0019695.

8.

Pharmacological characterization of zinc and copper interaction with the human alpha(1A)-adrenoceptor.

Ciolek J, Maïga A, Marcon E, Servent D, Gilles N.

Eur J Pharmacol. 2011 Mar 25;655(1-3):1-8. doi: 10.1016/j.ejphar.2010.12.042. Epub 2011 Jan 22.

PMID:
21262225
9.

Constitutive activity and inverse agonism at the α(₁a) and α(₁b) adrenergic receptor subtypes.

Cotecchia S.

Methods Enzymol. 2010;485:123-38. doi: 10.1016/B978-0-12-381296-4.00007-5.

PMID:
21050914
10.

[A method for improving the accuracy and sensitivity of cell membrane chromatography].

Wang Y, Wang Y, Deng XL, Yuan BX, He LC.

Nan Fang Yi Ke Da Xue Xue Bao. 2009 Dec;29(12):2362-6. Chinese.

11.

A combined cell membrane chromatography and online HPLC/MS method for screening compounds from Radix Caulophylli acting on the human alpha(1A)-adrenoceptor.

Wang L, Ren J, Sun M, Wang S.

J Pharm Biomed Anal. 2010 Apr 6;51(5):1032-6. doi: 10.1016/j.jpba.2009.11.007. Epub 2009 Nov 13.

PMID:
20004544
12.

A conserved aromatic lock for the tryptophan rotameric switch in TM-VI of seven-transmembrane receptors.

Holst B, Nygaard R, Valentin-Hansen L, Bach A, Engelstoft MS, Petersen PS, Frimurer TM, Schwartz TW.

J Biol Chem. 2010 Feb 5;285(6):3973-85. doi: 10.1074/jbc.M109.064725. Epub 2009 Nov 17.

13.

Lipid rafts constrain basal alpha(1A)-adrenergic receptor signaling by maintaining receptor in an inactive conformation.

Lei B, Morris DP, Smith MP, Schwinn DA.

Cell Signal. 2009 Oct;21(10):1532-9. doi: 10.1016/j.cellsig.2009.06.001. Epub 2009 Jun 9.

PMID:
19520158
14.

Facilitatory interplay in alpha 1a and beta 2 adrenoceptor function reveals a non-Gq signaling mode: implications for diversification of intracellular signal transduction.

Copik AJ, Ma C, Kosaka A, Sahdeo S, Trane A, Ho H, Dietrich PS, Yu H, Ford AP, Button D, Milla ME.

Mol Pharmacol. 2009 Mar;75(3):713-28. doi: 10.1124/mol.108.050765. Epub 2008 Dec 24.

15.

The role of aromatic phenylalanine residues in binding carotenoid to light-harvesting model and wild-type complexes.

García-Martín A, Pazur A, Wilhelm B, Silber M, Robert B, Braun P.

J Mol Biol. 2008 Sep 26;382(1):154-66. doi: 10.1016/j.jmb.2008.07.002. Epub 2008 Jul 9.

PMID:
18640123
16.

Mutational analysis of the alpha 1a-adrenergic receptor binding pocket of antagonists by radioligand binding assay.

Ahmed M, Hossain M, Bhuiyan MA, Ishiguro M, Tanaka T, Muramatsu I, Nagatomo T.

Biol Pharm Bull. 2008 Apr;31(4):598-601.

17.

Me-talnetant and osanetant interact within overlapping but not identical binding pockets in the human tachykinin neurokinin 3 receptor transmembrane domains.

Malherbe P, Bissantz C, Marcuz A, Kratzeisen C, Zenner MT, Wettstein JG, Ratni H, Riemer C, Spooren W.

Mol Pharmacol. 2008 Jun;73(6):1736-50. doi: 10.1124/mol.107.042754. Epub 2008 Feb 28.

18.

Amino acids of the human alpha1d-adrenergic receptor involved in antagonist binding.

Nagaoka Y, Ahmed M, Hossain M, Bhuiyan MA, Ishiguro M, Nakamura T, Watanabe M, Nagatomo T.

J Pharmacol Sci. 2008 Jan;106(1):114-20. Epub 2008 Jan 11.

19.

Asp125 and Thr130 in transmembrane domain 3 are major sites of alpha1b-adrenergic receptor antagonist binding.

Takahashi K, Hossain M, Ahmed M, Bhuiyan MA, Ohnuki T, Nagatomo T.

Biol Pharm Bull. 2007 Oct;30(10):1891-4.

20.

Systematic analysis of the entire second extracellular loop of the V(1a) vasopressin receptor: key residues, conserved throughout a G-protein-coupled receptor family, identified.

Conner M, Hawtin SR, Simms J, Wootten D, Lawson Z, Conner AC, Parslow RA, Wheatley M.

J Biol Chem. 2007 Jun 15;282(24):17405-12. Epub 2007 Apr 2.

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