| pubmed-article:2419164 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:2419164 | lifeskim:mentions | umls-concept:C0150369 | lld:lifeskim |
| pubmed-article:2419164 | lifeskim:mentions | umls-concept:C1622418 | lld:lifeskim |
| pubmed-article:2419164 | lifeskim:mentions | umls-concept:C0682529 | lld:lifeskim |
| pubmed-article:2419164 | lifeskim:mentions | umls-concept:C0332466 | lld:lifeskim |
| pubmed-article:2419164 | lifeskim:mentions | umls-concept:C0016315 | lld:lifeskim |
| pubmed-article:2419164 | lifeskim:mentions | umls-concept:C1533691 | lld:lifeskim |
| pubmed-article:2419164 | lifeskim:mentions | umls-concept:C1510438 | lld:lifeskim |
| pubmed-article:2419164 | pubmed:issue | 1-2 | lld:pubmed |
| pubmed-article:2419164 | pubmed:dateCreated | 1986-4-24 | lld:pubmed |
| pubmed-article:2419164 | pubmed:abstractText | A new technique has been developed to study fusion of biological membrane vesicles. Bovine chromaffin granule ghosts (CGG) were loaded with fluorescein isothiocyanate-dextran (FITC-dextran) at self-quenching concentrations. Loaded ghosts were then made to fuse with empty CGG. Fusion was induced by synexin, a protein previously proposed to be involved in exocytosis. The fusion process was monitored by measuring the dequenching of the fluorescence. Dequenching occurred as FITC-dextran was diluted into the increased volume due to fusion with empty ghosts. Spurious signals from leakage or breakage of vesicles were removed by including a specific anti-fluorescein antibody in the reaction medium. This new technique may prove to be of more general use for studying membrane fusion processes in other systems. | lld:pubmed |
| pubmed-article:2419164 | pubmed:language | eng | lld:pubmed |
| pubmed-article:2419164 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2419164 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:2419164 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2419164 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2419164 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2419164 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2419164 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2419164 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2419164 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2419164 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2419164 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2419164 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:2419164 | pubmed:month | Mar | lld:pubmed |
| pubmed-article:2419164 | pubmed:issn | 0014-5793 | lld:pubmed |
| pubmed-article:2419164 | pubmed:author | pubmed-author:StutzinAA | lld:pubmed |
| pubmed-article:2419164 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:2419164 | pubmed:day | 3 | lld:pubmed |
| pubmed-article:2419164 | pubmed:volume | 197 | lld:pubmed |
| pubmed-article:2419164 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:2419164 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:2419164 | pubmed:pagination | 274-80 | lld:pubmed |
| pubmed-article:2419164 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
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| pubmed-article:2419164 | pubmed:meshHeading | pubmed-meshheading:2419164-... | lld:pubmed |
| pubmed-article:2419164 | pubmed:meshHeading | pubmed-meshheading:2419164-... | lld:pubmed |
| pubmed-article:2419164 | pubmed:year | 1986 | lld:pubmed |
| pubmed-article:2419164 | pubmed:articleTitle | A fluorescence assay for monitoring and analyzing fusion biological membrane vesicles in vitro. | lld:pubmed |
| pubmed-article:2419164 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:2419164 | pubmed:publicationType | Comparative Study | lld:pubmed |
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