Separation and reformation of cell surface dopamine receptor oligomers visualized in cells

European Journal of Pharmacology

Volumn 658, Issue 2-3, 2011, Pages 74-83

  O'Dowd, Brian F ^a,b   Ji, Xiaodong ^a,b   Alijaniaram, Mohammad ^a,b   Nguyen, Tuan ^a,b   George, Susan R ^a,b  

^a UNIVERSITY OF TORONTO   (Canada)

^b UNIVERSITY OF TORONTO   (Canada)

Author keywords

Dopamine receptor; G protein coupled receptor; Nuclear localization; Oligomer; Protein structure

Indexed keywords

BUTACLAMOL; DOPAMINE 1 RECEPTOR; DOPAMINE 2 RECEPTOR; G PROTEIN COUPLED RECEPTOR; OLIGOMER;

ANALYTIC METHOD; ARTICLE; BINDING SITE; CELL NUCLEUS; CELL SURFACE; CELLULAR DISTRIBUTION; CONCENTRATION (PARAMETERS); CONTROLLED STUDY; MOLECULAR IMAGING; NUCLEAR LOCALIZATION SIGNAL; OLIGOMERIZATION; PRIORITY JOURNAL; PROCESS DESIGN; PROTEIN ANALYSIS; PROTEIN BINDING; PROTEIN CONFORMATION; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN LOCALIZATION; PROTEIN TRANSPORT; WILD TYPE;

DOPAMINE; DOPAMINE AGONISTS; HEK293 CELLS; HUMANS; MOLECULAR IMAGING; NUCLEAR LOCALIZATION SIGNALS; PROTEIN MULTIMERIZATION; PROTEIN STRUCTURE, QUATERNARY; RECEPTORS, DOPAMINE D1; RECEPTORS, DOPAMINE D2; RECEPTORS, G-PROTEIN-COUPLED;

EID: 79953802623     PISSN: 00142999     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejphar.2011.02.030     Document Type: Article

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