| pubmed-article:8382477 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:8382477 | lifeskim:mentions | umls-concept:C0029246 | lld:lifeskim |
| pubmed-article:8382477 | lifeskim:mentions | umls-concept:C0031809 | lld:lifeskim |
| pubmed-article:8382477 | lifeskim:mentions | umls-concept:C0007603 | lld:lifeskim |
| pubmed-article:8382477 | lifeskim:mentions | umls-concept:C0021547 | lld:lifeskim |
| pubmed-article:8382477 | lifeskim:mentions | umls-concept:C0031621 | lld:lifeskim |
| pubmed-article:8382477 | lifeskim:mentions | umls-concept:C1151895 | lld:lifeskim |
| pubmed-article:8382477 | lifeskim:mentions | umls-concept:C1511572 | lld:lifeskim |
| pubmed-article:8382477 | lifeskim:mentions | umls-concept:C1998793 | lld:lifeskim |
| pubmed-article:8382477 | pubmed:dateCreated | 1993-3-23 | lld:pubmed |
| pubmed-article:8382477 | pubmed:abstractText | Experiments were carried out to determine whether or not CDP-diacylglycerol:myo-inositol 3-phosphatidyltransferase (IT) activity (EC 2.7.8.11) could be detected in purified plasma-membrane fractions from WRK-1 rat mammary tumour cells. These cells have previously been shown to have a very active phosphoinositide cycle. Sucrose-density-gradient-purified plasma membranes contained no IT activity that could not be accounted for by endoplasmic-reticulum contamination. However, we also determined that the relative amount of IT activity in endoplasmic reticulum and plasma-membrane fractions could be altered by changing the concentration of detergent in the assay system. | lld:pubmed |
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| pubmed-article:8382477 | pubmed:language | eng | lld:pubmed |
| pubmed-article:8382477 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8382477 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:8382477 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:8382477 | pubmed:month | Feb | lld:pubmed |
| pubmed-article:8382477 | pubmed:issn | 0264-6021 | lld:pubmed |
| pubmed-article:8382477 | pubmed:author | pubmed-author:MonacoM EME | lld:pubmed |
| pubmed-article:8382477 | pubmed:author | pubmed-author:RosenbergL... | lld:pubmed |
| pubmed-article:8382477 | pubmed:author | pubmed-author:SantiagoO MOM | lld:pubmed |
| pubmed-article:8382477 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:8382477 | pubmed:day | 15 | lld:pubmed |
| pubmed-article:8382477 | pubmed:volume | 290 ( Pt 1) | lld:pubmed |
| pubmed-article:8382477 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:8382477 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:8382477 | pubmed:pagination | 179-83 | lld:pubmed |
| pubmed-article:8382477 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:8382477 | pubmed:year | 1993 | lld:pubmed |
| pubmed-article:8382477 | pubmed:articleTitle | Organization of the phosphoinositide cycle. Assessment of inositol transferase activity in purified plasma membranes. | lld:pubmed |
| pubmed-article:8382477 | pubmed:affiliation | Department of Physiology & Biophysics, N.Y.U. Medical Center, New York. | lld:pubmed |
| pubmed-article:8382477 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:8382477 | pubmed:publicationType | Comparative Study | lld:pubmed |
| pubmed-article:8382477 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |
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