| pubmed-article:9891972 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:9891972 | lifeskim:mentions | umls-concept:C0034493 | lld:lifeskim |
| pubmed-article:9891972 | lifeskim:mentions | umls-concept:C0225336 | lld:lifeskim |
| pubmed-article:9891972 | lifeskim:mentions | umls-concept:C0003483 | lld:lifeskim |
| pubmed-article:9891972 | lifeskim:mentions | umls-concept:C2936792 | lld:lifeskim |
| pubmed-article:9891972 | lifeskim:mentions | umls-concept:C0441655 | lld:lifeskim |
| pubmed-article:9891972 | lifeskim:mentions | umls-concept:C1424497 | lld:lifeskim |
| pubmed-article:9891972 | lifeskim:mentions | umls-concept:C0675244 | lld:lifeskim |
| pubmed-article:9891972 | lifeskim:mentions | umls-concept:C0851285 | lld:lifeskim |
| pubmed-article:9891972 | pubmed:issue | 3 | lld:pubmed |
| pubmed-article:9891972 | pubmed:dateCreated | 1999-2-5 | lld:pubmed |
| pubmed-article:9891972 | pubmed:abstractText | In Xenopus oocytes with an endogenous calcitonin gene-related peptide (CGRP) receptor, a receptor activity modifying protein (RAMP1) enhancing CGRP stimulated chloride currents of the cystic fibrosis transmembrane regulator was recently cloned [McLatchie, L.M. et al. (1998) Nature 393, 333-339]. Here, transient expression of RAMP1 in rabbit aortic endothelial cells (RAEC) brought about stimulation of cAMP accumulation by human (h) alphaCGRP with an EC50 of 0.41 nM. This was antagonized by a CGRP receptor antagonist alphaCGRP(8-37). Co-expression of RAMP3 together with RAMP1 reduced the maximal cAMP response to h alphaCGRP by 47% (P < 0.05). The cells also express RAMP2 encoding mRNA and an adrenomedullin (ADM) receptor coupled to stimulation of cAMP formation by hADM (EC50 0.18 nM). The latter was antagonized by an ADM receptor antagonist hADM(22-52). In conclusion, expression of a CGRP receptor in RAEC requires RAMP1. The same receptor presumably recognizes ADM making use of endogenous RAMP2. The results reveal competition between the different RAMPs in the regulation of CGRP/ADM receptor activity. | lld:pubmed |
| pubmed-article:9891972 | pubmed:language | eng | lld:pubmed |
| pubmed-article:9891972 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9891972 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:9891972 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:9891972 | pubmed:month | Dec | lld:pubmed |
| pubmed-article:9891972 | pubmed:issn | 0014-5793 | lld:pubmed |
| pubmed-article:9891972 | pubmed:author | pubmed-author:FischerJ AJA | lld:pubmed |
| pubmed-article:9891972 | pubmed:author | pubmed-author:BoseAA | lld:pubmed |
| pubmed-article:9891972 | pubmed:author | pubmed-author:PageH MHM | lld:pubmed |
| pubmed-article:9891972 | pubmed:author | pubmed-author:FoordS MSM | lld:pubmed |
| pubmed-article:9891972 | pubmed:author | pubmed-author:LeuthäuserKK | lld:pubmed |
| pubmed-article:9891972 | pubmed:author | pubmed-author:BühlmannNN | lld:pubmed |
| pubmed-article:9891972 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:9891972 | pubmed:day | 28 | lld:pubmed |
| pubmed-article:9891972 | pubmed:volume | 441 | lld:pubmed |
| pubmed-article:9891972 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:9891972 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:9891972 | pubmed:pagination | 366-8 | lld:pubmed |
| pubmed-article:9891972 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
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| pubmed-article:9891972 | pubmed:meshHeading | pubmed-meshheading:9891972-... | lld:pubmed |
| pubmed-article:9891972 | pubmed:year | 1998 | lld:pubmed |
| pubmed-article:9891972 | pubmed:articleTitle | Receptor activity modifying proteins regulate the activity of a calcitonin gene-related peptide receptor in rabbit aortic endothelial cells. | lld:pubmed |
| pubmed-article:9891972 | pubmed:affiliation | Department of Orthopaedic Surgery, University of Zurich, Klinik Balgrist, Switzerland. ramuz@balgrist.unizh.ch | lld:pubmed |
| pubmed-article:9891972 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:9891972 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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