| pubmed-article:1659003 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:1659003 | lifeskim:mentions | umls-concept:C1521991 | lld:lifeskim |
| pubmed-article:1659003 | lifeskim:mentions | umls-concept:C0596235 | lld:lifeskim |
| pubmed-article:1659003 | lifeskim:mentions | umls-concept:C0439799 | lld:lifeskim |
| pubmed-article:1659003 | lifeskim:mentions | umls-concept:C1880371 | lld:lifeskim |
| pubmed-article:1659003 | pubmed:issue | 9 | lld:pubmed |
| pubmed-article:1659003 | pubmed:dateCreated | 1991-11-27 | lld:pubmed |
| pubmed-article:1659003 | pubmed:abstractText | Voltage-dependent Ca2+ channels regulate Ca2+ entry and thereby contribute to Ca2+ signalling in many cells. Functional studies have uncovered several types of Ca2+ channel, distinguished by pharmacology, electrophysiology and tissue localization. More recently, molecular cloning has revealed an even greater diversity among Ca2+ channels, arising from multiple genes and alternative splicing. L-type, dihydropyridine-sensitive Ca2+ channels have been the most extensively characterized to date. Recently, Numa's group has reported the cloning and expression of a dihydropyridine-insensitive Ca2+ channel from brain that most closely resembles the P-type channel described by Llinas and colleagues. These results contribute to rapidly growing knowledge about molecular determinants of Ca2+ channel diversity. | lld:pubmed |
| pubmed-article:1659003 | pubmed:language | eng | lld:pubmed |
| pubmed-article:1659003 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1659003 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:1659003 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1659003 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:1659003 | pubmed:month | Sep | lld:pubmed |
| pubmed-article:1659003 | pubmed:issn | 0165-6147 | lld:pubmed |
| pubmed-article:1659003 | pubmed:author | pubmed-author:TsienR WRW | lld:pubmed |
| pubmed-article:1659003 | pubmed:author | pubmed-author:EllinorP TPT | lld:pubmed |
| pubmed-article:1659003 | pubmed:author | pubmed-author:HorneW AWA | lld:pubmed |
| pubmed-article:1659003 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:1659003 | pubmed:volume | 12 | lld:pubmed |
| pubmed-article:1659003 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:1659003 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:1659003 | pubmed:pagination | 349-54 | lld:pubmed |
| pubmed-article:1659003 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
| pubmed-article:1659003 | pubmed:meshHeading | pubmed-meshheading:1659003-... | lld:pubmed |
| pubmed-article:1659003 | pubmed:meshHeading | pubmed-meshheading:1659003-... | lld:pubmed |
| pubmed-article:1659003 | pubmed:meshHeading | pubmed-meshheading:1659003-... | lld:pubmed |
| pubmed-article:1659003 | pubmed:meshHeading | pubmed-meshheading:1659003-... | lld:pubmed |
| pubmed-article:1659003 | pubmed:meshHeading | pubmed-meshheading:1659003-... | lld:pubmed |
| pubmed-article:1659003 | pubmed:year | 1991 | lld:pubmed |
| pubmed-article:1659003 | pubmed:articleTitle | Molecular diversity of voltage-dependent Ca2+ channels. | lld:pubmed |
| pubmed-article:1659003 | pubmed:affiliation | Department of Molecular and Cellular Physiology, Beckman Center, Stanford University Medical Center, CA 94305. | lld:pubmed |
| pubmed-article:1659003 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:1659003 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:1659003 | pubmed:publicationType | Review | lld:pubmed |
| pubmed-article:1659003 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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