pubmed-article:3422464 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:3422464 | lifeskim:mentions | umls-concept:C0699040 | lld:lifeskim |
pubmed-article:3422464 | lifeskim:mentions | umls-concept:C0028959 | lld:lifeskim |
pubmed-article:3422464 | lifeskim:mentions | umls-concept:C0332621 | lld:lifeskim |
pubmed-article:3422464 | lifeskim:mentions | umls-concept:C0597767 | lld:lifeskim |
pubmed-article:3422464 | lifeskim:mentions | umls-concept:C0086149 | lld:lifeskim |
pubmed-article:3422464 | pubmed:issue | 3 | lld:pubmed |
pubmed-article:3422464 | pubmed:dateCreated | 1988-3-11 | lld:pubmed |
pubmed-article:3422464 | pubmed:abstractText | Plasma membrane glycoproteins from Dictyostelium discoideum amoebae at three stages of early development were digested with Pronase and endoglycosidase H and fractionated by gel filtration. This gave three classes of glycans (polysaccharides, endoglycosidase H-resistant glycopeptides, and endoglycosidase H-released oligosaccharides), which were tested for their ability to block agglutination of amoebae from vegetative, aggregation (8-hr), and late-aggregation (13-hr) stages of development. The endoglycosidase H-resistant glycopeptides from 8-hr cells inhibited agglutination of disaggregated 8-hr cells but not vegetative or 13-hr cells. The 8-hr polysaccharide and endo H-sensitive oligosaccharides did not inhibit. The glycopeptides from 8-hr cells were resolved into five species by electrophoresis in borate-containing buffer. Two of these had agglutination-inhibiting activity, and three did not. None of the glycan fractions from vegetative or 13-hr cells inhibited agglutination of vegetative, 8-, or 13-hr cells. These data implicate specific cell surface glycans in aggregation-stage intercellular cohesion and suggest that both these glycans and receptors for them are developmentally regulated. | lld:pubmed |
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pubmed-article:3422464 | pubmed:language | eng | lld:pubmed |
pubmed-article:3422464 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:3422464 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:3422464 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:3422464 | pubmed:month | Feb | lld:pubmed |
pubmed-article:3422464 | pubmed:issn | 0027-8424 | lld:pubmed |
pubmed-article:3422464 | pubmed:author | pubmed-author:HendersonE... | lld:pubmed |
pubmed-article:3422464 | pubmed:author | pubmed-author:ZiskaS ESE | lld:pubmed |
pubmed-article:3422464 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:3422464 | pubmed:volume | 85 | lld:pubmed |
pubmed-article:3422464 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:3422464 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:3422464 | pubmed:pagination | 817-21 | lld:pubmed |
pubmed-article:3422464 | pubmed:dateRevised | 2010-9-10 | lld:pubmed |
pubmed-article:3422464 | pubmed:meshHeading | pubmed-meshheading:3422464-... | lld:pubmed |
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pubmed-article:3422464 | pubmed:meshHeading | pubmed-meshheading:3422464-... | lld:pubmed |
pubmed-article:3422464 | pubmed:year | 1988 | lld:pubmed |
pubmed-article:3422464 | pubmed:articleTitle | Cell surface oligosaccharides participate in cohesion during aggregation of Dictyostelium discoideum. | lld:pubmed |
pubmed-article:3422464 | pubmed:affiliation | Department of Biology, Georgetown University, Washington, DC 20057. | lld:pubmed |
pubmed-article:3422464 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:3422464 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
pubmed-article:3422464 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |
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