| pubmed-article:17030366 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:17030366 | lifeskim:mentions | umls-concept:C0006675 | lld:lifeskim |
| pubmed-article:17030366 | lifeskim:mentions | umls-concept:C0029246 | lld:lifeskim |
| pubmed-article:17030366 | lifeskim:mentions | umls-concept:C0542341 | lld:lifeskim |
| pubmed-article:17030366 | pubmed:issue | 5-6 | lld:pubmed |
| pubmed-article:17030366 | pubmed:dateCreated | 2006-11-7 | lld:pubmed |
| pubmed-article:17030366 | pubmed:abstractText | Microdomains of Ca(2+), which are formed at sites where Ca(2+) enters the cytoplasm either at the cell surface or at the internal stores, are a key element of Ca(2+) signalling. The term microdomain includes the elementary events that are the basic building blocks of Ca(2+) signals. As Ca(2+) enters the cytoplasm, it produces a local plume of Ca(2+) that has been given different names (sparks, puffs, sparklets and syntillas). These elementary events can combine to produce larger microdomains. The significance of these localized domains of Ca(2+) is that they can regulate specific cellular processes in different regions of the cell. Such microdomains are particularly evident in neurons where both pre- and postsynaptic events are controlled by highly localized pulses of Ca(2+). The ability of single neurons to process enormous amounts of information depends upon such miniaturization of the Ca(2+) signalling system. Control of cardiac cell contraction and gene transcription provides another example of how the parallel processing of Ca(2+) signalling can occur through microdomains of intracellular Ca(2+). | lld:pubmed |
| pubmed-article:17030366 | pubmed:language | eng | lld:pubmed |
| pubmed-article:17030366 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17030366 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:17030366 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:17030366 | pubmed:issn | 0143-4160 | lld:pubmed |
| pubmed-article:17030366 | pubmed:author | pubmed-author:BerridgeMicha... | lld:pubmed |
| pubmed-article:17030366 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:17030366 | pubmed:volume | 40 | lld:pubmed |
| pubmed-article:17030366 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:17030366 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:17030366 | pubmed:pagination | 405-12 | lld:pubmed |
| pubmed-article:17030366 | pubmed:dateRevised | 2009-11-19 | lld:pubmed |
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| pubmed-article:17030366 | pubmed:articleTitle | Calcium microdomains: organization and function. | lld:pubmed |
| pubmed-article:17030366 | pubmed:affiliation | Babraham Institute, Babraham, Cambridge, UK. michael.berridge@bbsrc.ac.uk | lld:pubmed |
| pubmed-article:17030366 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:17030366 | pubmed:publicationType | Review | lld:pubmed |
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