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Items: 1 to 20 of 92

1.

The delta e13 isoform of the calcitonin receptor forms a six-transmembrane domain receptor with dominant-negative effects on receptor surface expression and signaling.

Seck T, Pellegrini M, Florea AM, Grignoux V, Baron R, Mierke DF, Horne WC.

Mol Endocrinol. 2005 Aug;19(8):2132-44. Epub 2005 Apr 28.

3.
4.

Calcitonin (CT) rapidly increases NA(+)/H(+) exchange and metabolic acid production: effects mediated selectively by the C1A CT receptor isoform.

Santhanagopal A, Chidiac P, Horne WC, Baron R, Dixon SJ.

Endocrinology. 2001 Oct;142(10):4401-13.

PMID:
11564704
5.

Truncation of the porcine calcitonin receptor cytoplasmic tail inhibits internalization and signal transduction but increases receptor affinity.

Findlay DM, Houssami S, Lin HY, Myers DE, Brady CL, Darcy PK, Ikeda K, Martin TJ, Sexton PM.

Mol Endocrinol. 1994 Dec;8(12):1691-700.

PMID:
7708057
6.

The extracellular domain of receptor activity-modifying protein 1 is sufficient for calcitonin receptor-like receptor function.

Fitzsimmons TJ, Zhao X, Wank SA.

J Biol Chem. 2003 Apr 18;278(16):14313-20. Epub 2003 Feb 6.

7.

Functions of the cytoplasmic tails of the human receptor activity-modifying protein components of calcitonin gene-related peptide and adrenomedullin receptors.

Kuwasako K, Cao YN, Chu CP, Iwatsubo S, Eto T, Kitamura K.

J Biol Chem. 2006 Mar 17;281(11):7205-13. Epub 2006 Jan 11.

9.

Distinct receptor activity-modifying protein domains differentially modulate interaction with calcitonin receptors.

Udawela M, Christopoulos G, Tilakaratne N, Christopoulos A, Albiston A, Sexton PM.

Mol Pharmacol. 2006 Jun;69(6):1984-9. Epub 2006 Mar 10.

10.

Truncation of the A1 adenosine receptor reveals distinct roles of the membrane-proximal carboxyl terminus in receptor folding and G protein coupling.

Pankevych H, Korkhov V, Freissmuth M, Nanoff C.

J Biol Chem. 2003 Aug 8;278(32):30283-93. Epub 2003 May 22.

11.

A critical role for the short intracellular C terminus in receptor activity-modifying protein function.

Udawela M, Christopoulos G, Morfis M, Christopoulos A, Ye S, Tilakaratne N, Sexton PM.

Mol Pharmacol. 2006 Nov;70(5):1750-60. Epub 2006 Aug 15.

12.

Isoforms of the rat calcitonin receptor: consequences for ligand binding and signal transduction.

Houssami S, Findlay DM, Brady CL, Myers DE, Martin TJ, Sexton PM.

Endocrinology. 1994 Jul;135(1):183-90.

PMID:
8013352
13.

Novel down-regulatory mechanism of the surface expression of the vasopressin V2 receptor by an alternative splice receptor variant.

Sarmiento JM, Añazco CC, Campos DM, Prado GN, Navarro J, González CB.

J Biol Chem. 2004 Nov 5;279(45):47017-23. Epub 2004 Sep 8.

15.

Recognition of double-stranded RNA by human toll-like receptor 3 and downstream receptor signaling requires multimerization and an acidic pH.

de Bouteiller O, Merck E, Hasan UA, Hubac S, Benguigui B, Trinchieri G, Bates EE, Caux C.

J Biol Chem. 2005 Nov 18;280(46):38133-45. Epub 2005 Sep 6.

16.

A naturally occurring isoform inhibits parathyroid hormone receptor trafficking and signaling.

Alonso V, Ardura JA, Wang B, Sneddon WB, Friedman PA.

J Bone Miner Res. 2011 Jan;26(1):143-55. doi: 10.1002/jbmr.167.

17.
18.

Transport of the IgE receptor alpha-chain is controlled by a multicomponent intracellular retention signal.

Cauvi DM, Tian X, von Loehneysen K, Robertson MW.

J Biol Chem. 2006 Apr 14;281(15):10448-60. Epub 2006 Feb 3.

19.

Divergent structural requirements exist for calcitonin receptor binding specificity and adenylate cyclase activation.

Houssami S, Findlay DM, Brady CL, Martin TJ, Epand RM, Moore EE, Murayama E, Tamura T, Orlowski RC, Sexton PM.

Mol Pharmacol. 1995 Apr;47(4):798-809.

PMID:
7723741
20.

A truncated isoform of c-Mpl with an essential C-terminal peptide targets the full-length receptor for degradation.

Coers J, Ranft C, Skoda RC.

J Biol Chem. 2004 Aug 27;279(35):36397-404. Epub 2004 Jun 21.

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