| pubmed-article:4310667 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:4310667 | lifeskim:mentions | umls-concept:C0006675 | lld:lifeskim |
| pubmed-article:4310667 | lifeskim:mentions | umls-concept:C0032176 | lld:lifeskim |
| pubmed-article:4310667 | lifeskim:mentions | umls-concept:C0001492 | lld:lifeskim |
| pubmed-article:4310667 | lifeskim:mentions | umls-concept:C0002335 | lld:lifeskim |
| pubmed-article:4310667 | pubmed:issue | 3 | lld:pubmed |
| pubmed-article:4310667 | pubmed:dateCreated | 1969-12-22 | lld:pubmed |
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| pubmed-article:4310667 | pubmed:language | eng | lld:pubmed |
| pubmed-article:4310667 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:4310667 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:4310667 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:4310667 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:4310667 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:4310667 | pubmed:month | Oct | lld:pubmed |
| pubmed-article:4310667 | pubmed:issn | 0006-291X | lld:pubmed |
| pubmed-article:4310667 | pubmed:author | pubmed-author:VigdahlR LRL | lld:pubmed |
| pubmed-article:4310667 | pubmed:author | pubmed-author:TavorminaP... | lld:pubmed |
| pubmed-article:4310667 | pubmed:author | pubmed-author:MarquisN RNR | lld:pubmed |
| pubmed-article:4310667 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:4310667 | pubmed:day | 22 | lld:pubmed |
| pubmed-article:4310667 | pubmed:volume | 37 | lld:pubmed |
| pubmed-article:4310667 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:4310667 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:4310667 | pubmed:pagination | 409-15 | lld:pubmed |
| pubmed-article:4310667 | pubmed:dateRevised | 2009-10-27 | lld:pubmed |
| pubmed-article:4310667 | pubmed:otherAbstract | PIP: In exploration of the proposal that prostaglandin E1 (PGE1) inhibits platelet aggregation via stimulation of adenyl cyclase, the temporal relationship of adenosine cyclic 3',5' monophosphate (cyclic AMP) synthesis and inhibition of ADP-induced aggregation in response to PGE1 was studied. The requirement for calcium in aggregation led to the investigation of the effects of calcium ions on platelet adenyl cyclase activity. PGE1 stimulated the synthesis of cyclic AMP from adenosine-5'-triphosphate-8-14-C by platelet membrane fractions and also increased cyclic AMP synthesis in intact platelets previously incubated for 2 hours with adenosine-14-C. The accumulation of cyclic AMP increased signficiantly at low concentrations of PGE1 and reached a maximum at about 1 mug. Regardless of the inducing agent, calcium ions are an absolute requirement for the aggregation of platelets. | lld:pubmed |
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| pubmed-article:4310667 | pubmed:meshHeading | pubmed-meshheading:4310667-... | lld:pubmed |
| pubmed-article:4310667 | pubmed:year | 1969 | lld:pubmed |
| pubmed-article:4310667 | pubmed:articleTitle | Platelet aggregation. II. Adenyl cyclase, prostaglandin E1, and calcium. | lld:pubmed |
| pubmed-article:4310667 | pubmed:publicationType | Journal Article | lld:pubmed |
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