| pubmed-article:7680768 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:7680768 | lifeskim:mentions | umls-concept:C1522424 | lld:lifeskim |
| pubmed-article:7680768 | lifeskim:mentions | umls-concept:C0214230 | lld:lifeskim |
| pubmed-article:7680768 | lifeskim:mentions | umls-concept:C0205245 | lld:lifeskim |
| pubmed-article:7680768 | lifeskim:mentions | umls-concept:C0017262 | lld:lifeskim |
| pubmed-article:7680768 | lifeskim:mentions | umls-concept:C0678594 | lld:lifeskim |
| pubmed-article:7680768 | lifeskim:mentions | umls-concept:C0205225 | lld:lifeskim |
| pubmed-article:7680768 | lifeskim:mentions | umls-concept:C2911684 | lld:lifeskim |
| pubmed-article:7680768 | lifeskim:mentions | umls-concept:C0185117 | lld:lifeskim |
| pubmed-article:7680768 | pubmed:issue | 6416 | lld:pubmed |
| pubmed-article:7680768 | pubmed:dateCreated | 1993-4-13 | lld:pubmed |
| pubmed-article:7680768 | pubmed:abstractText | A complementary DNA encoding an inward rectifier K+ channel (IRK1) was isolated from a mouse macrophage cell line by expression cloning. This channel conducts inward K+ current below the K+ equilibrium potential but passes little outward K+ current. The IRK1 channel contains only two putative transmembrane segments per subunit and corresponds to the inner core structure of voltage-gated K+ channels. The IRK1 channel and an ATP-regulated K+ channel show extensive sequence similarity and constitute a new superfamily. | lld:pubmed |
| pubmed-article:7680768 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:7680768 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:7680768 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:7680768 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:7680768 | pubmed:month | Mar | lld:pubmed |
| pubmed-article:7680768 | pubmed:issn | 0028-0836 | lld:pubmed |
| pubmed-article:7680768 | pubmed:author | pubmed-author:TeeQ SQS | lld:pubmed |
| pubmed-article:7680768 | pubmed:author | pubmed-author:JanL YLY | lld:pubmed |
| pubmed-article:7680768 | pubmed:author | pubmed-author:KuboYY | lld:pubmed |
| pubmed-article:7680768 | pubmed:author | pubmed-author:BaldwinT JTJ | lld:pubmed |
| pubmed-article:7680768 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:7680768 | pubmed:day | 11 | lld:pubmed |
| pubmed-article:7680768 | pubmed:volume | 362 | lld:pubmed |
| pubmed-article:7680768 | pubmed:geneSymbol | IRK1 | lld:pubmed |
| pubmed-article:7680768 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:7680768 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:7680768 | pubmed:pagination | 127-33 | lld:pubmed |
| pubmed-article:7680768 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
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| pubmed-article:7680768 | pubmed:year | 1993 | lld:pubmed |
| pubmed-article:7680768 | pubmed:articleTitle | Primary structure and functional expression of a mouse inward rectifier potassium channel. | lld:pubmed |
| pubmed-article:7680768 | pubmed:affiliation | Howard Hughes Medical Institute, University of California, San Francisco 94143-0724. | lld:pubmed |
| pubmed-article:7680768 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:7680768 | pubmed:publicationType | Comparative Study | lld:pubmed |
| pubmed-article:7680768 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:7680768 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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