Allosteric interactions between the oxytocin receptor and the β2-adrenergic receptor in the modulation of ERK1/2 activation are mediated by heterodimerization-Reference-Cited by-同舟云学术

Allosteric interactions between the oxytocin receptor and the β2-adrenergic receptor in the modulation of ERK1/2 activation are mediated by heterodimerization

Published:2012-01 Issue:1 Volume:24 Page:342-350
ISSN:0898-6568
Container-title:Cellular Signalling
language:en
Short-container-title:Cellular Signalling

Author:

Wrzal Paulina K.,Devost Dominic,Pétrin Darlaine,Goupil Eugénie,Iorio-Morin Christian,Laporte Stéphane A.,Zingg Hans H.,Hébert Terence E.

Funder

Canadian Institutes of Health Research (CIHR)

CIHR Research Team Grant in GPCR Allosteric Regulation

Publisher

Elsevier BV

Subject

Cell Biology

Reference43 articles.

1. Structural diversity of G protein-coupled receptors and significance for drug discovery

2. How many drug targets are there?

3. Oligomeric forms of G protein-coupled receptors (GPCRs)

4. Allosteric modulation of heterodimeric G-protein-coupled receptors

5. Prevention of Preterm Delivery

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