Biology Reference
In-Depth Information
23.
Costa T, Herz A. Antagonists with negative intrinsic activity at delta opioid receptors
coupled to GTP-binding proteins.
Proc Natl Acad Sci USA
. 1989;86(19):7321-
7325.
24.
Samama P, Cotecchia S, Costa T, Lefkowitz RJ. A mutation-induced activated state of
the beta 2-adrenergic receptor. Extending the ternary complex model.
J Biol Chem
.
1993;268:4625
-
4636.
25.
Weiss JM, Morgan PH, Lutz MW, Kenakin TP. The cubic ternary complex receptor-
occupancy model. III. Resurrecting efficacy.
J Theor Biol
. 1996;181:381
-
397.
26.
Maudsley S, Martin B, Luttrell LM. The origins of diversity and specificity in G protein-
coupled receptor signaling.
J Pharmacol Exp Ther
. 2005;314:485-
494.
27.
Laugwitz KL, Allgeier A, Offermanns S, et al. The human thyrotropin receptor: a hep-
tahelical receptor capable of stimulating members of all four G protein families.
Proc Natl
Acad Sci USA
. 1996;93:116
-
120.
28.
Angers S, Salahpour A, Joly E, et al. Detection of beta 2-adrenergic receptor dimeriza-
tion in living cells using bioluminescence resonance energy transfer (BRET).
Proc Natl
Acad Sci USA
. 2000;97:3684
-
3689.
29.
Hay DL, Poyner DR, Sexton PM. GPCR modulation by RAMPs.
Pharmacol Ther
.
2006;109:173-
197.
30.
Foord SM, Marshall FH. RAMPs: accessory proteins for seven transmembrane domain
receptors.
Trends Pharmacol Sci
. 1999;20:184
-
187.
31.
Brady AE, Limbird LE. G protein-coupled receptor interacting proteins: emerging roles
in localization and signal transduction.
Cell Signal
. 2002;14:297
-
309.
32.
Hall RA, Lefkowitz RJ. Regulation of G protein-coupled receptor signaling by scaffold
proteins.
Circ Res
. 2002;91:672
-
680.
33.
Bockaert J, Marin P, Dumuis A, Fagni L. The 'magic tail' of G protein-coupled recep-
tors: an anchorage for functional protein networks.
FEBS Lett
. 2003;546:65-
72.
34.
Luttrell LM, Gesty-Palmer D. Beyond desensitization: physiological relevance of
arrestin-dependent signaling.
Pharmacol Rev
. 2010;62:305
-
330.
35.
Galandrin S, Bouvier M. Distinct signaling profiles of beta1 and beta2 adrenergic recep-
tor ligands toward adenylyl cyclase and mitogen-activated protein kinase reveals the
pluridimensionality of efficacy.
Mol Pharmacol
. 2006;70:1575
-
1584.
36.
Kenakin T. Agonist-receptor efficacy II: agonist trafficking of receptor signals.
Trends
Pharmacol Sci
. 1995;16:232
-
238.
37.
Wisler JW, DeWire SM, Whalen EJ, et al. A unique mechanism of beta-blocker action:
carvedilol stimulates beta-arrestin signaling.
Proc Natl Acad Sci USA
. 2007;104:
16657
-
16662.
38.
Bisello A, Chorev M, Rosenblatt M, Monticelli L, Mierke DF, Ferrari SL. Selective
ligand-induced stabilization of active and desensitized parathyroid hormone type 1
receptor conformations.
J Biol Chem
. 2002;277:38524-
38530.
39.
Bisello A, Manen D, Pierroz DD, Usdin TB, Rizzoli R, Ferrari SL. Agonist-specific
regulation of parathyroid hormone (PTH) receptor type 2 activity: structural and func-
tional analysis of PTH- and tuberoinfundibular peptide (TIP) 39-stimulated desensitiza-
tion and internalization.
Mol Endocrinol
. 2004;18:1486
-
1498.
40.
Jouishomme H, Whitfield JF, Chakravarthy B, et al. The protein kinase-C activation
domain of the parathyroid hormone.
Endocrinology
. 1992;130:53
-
60.
41.
Azarani A, Goltzman D, Orlowski J. Structurally diverse N-terminal peptides of para-
thyroid hormone (PTH) and PTH-related peptide (PTHRP) inhibit the Na
þ
exchanger NHE3 isoform by binding to the PTH/PTHRP receptor type I and activat-
ing distinct signaling pathways.
J Biol Chem
. 1996;271:14931-
14936.
42.
Takasu H, Gardella TJ, Luck MD, Potts JT, Bringhurst FR. Amino-terminal modifica-
tions of human parathyroid hormone (PTH) selectively alter phospholipase C signaling
via the type 1 PTH receptor: implications for design of signal-specific PTH ligands.
Bio-
chemistry
. 1999;38:13453
-
13460.
þ
/H
Previous Page
Next Page
Progress in Molecular Biology and Translational Science
Search WWH ::
Custom Search
Home