| pubmed-article:2476050 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:2476050 | lifeskim:mentions | umls-concept:C0085512 | lld:lifeskim |
| pubmed-article:2476050 | lifeskim:mentions | umls-concept:C0085883 | lld:lifeskim |
| pubmed-article:2476050 | lifeskim:mentions | umls-concept:C0003250 | lld:lifeskim |
| pubmed-article:2476050 | lifeskim:mentions | umls-concept:C0871161 | lld:lifeskim |
| pubmed-article:2476050 | pubmed:issue | 7 | lld:pubmed |
| pubmed-article:2476050 | pubmed:dateCreated | 1989-10-5 | lld:pubmed |
| pubmed-article:2476050 | pubmed:abstractText | Seven hybridomas that secreted monoclonal antibodies (MAB) against the peplomer protein and one that secreted MAB against the nucleocapsid protein of Berne virus (proposed family Toroviridae) were isolated. All MAB directed against the peplomer protein neutralized virus infectivity and, with the exception of MAB 6A7, inhibited each other's binding in competition assays. Neutralization of Berne virus infectivity was potentiated when some MAB were used in pairs. The antibodies have been used to localize toroviral proteins in infected cells; use of antipeplomer MAB 6B10 yielded a diffuse intracytoplasmic immunofluorescence, whereas the antinucleocapsid MAB 1F1 detected antigen in the intra- and perinuclear compartments. By use of radioimmune precipitation, protein A of Staphylococcus aureus was found to bind directly to the nucleocapsid polypeptide, without the requirement for specific antibody. Using fluorescein isothiocyanate-conjugated protein A, the intranuclear accumulation of the nucleoprotein of Berne virus was confirmed by results of immunofluorescence. | lld:pubmed |
| pubmed-article:2476050 | pubmed:language | eng | lld:pubmed |
| pubmed-article:2476050 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2476050 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:2476050 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2476050 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2476050 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2476050 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2476050 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2476050 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2476050 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:2476050 | pubmed:month | Jul | lld:pubmed |
| pubmed-article:2476050 | pubmed:issn | 0002-9645 | lld:pubmed |
| pubmed-article:2476050 | pubmed:author | pubmed-author:HorzinekM CMC | lld:pubmed |
| pubmed-article:2476050 | pubmed:author | pubmed-author:van EdenWW | lld:pubmed |
| pubmed-article:2476050 | pubmed:author | pubmed-author:KaefferBB | lld:pubmed |
| pubmed-article:2476050 | pubmed:author | pubmed-author:EderveenJJ | lld:pubmed |
| pubmed-article:2476050 | pubmed:author | pubmed-author:van KootenPP | lld:pubmed |
| pubmed-article:2476050 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:2476050 | pubmed:volume | 50 | lld:pubmed |
| pubmed-article:2476050 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:2476050 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:2476050 | pubmed:pagination | 1131-7 | lld:pubmed |
| pubmed-article:2476050 | pubmed:dateRevised | 2003-11-14 | lld:pubmed |
| pubmed-article:2476050 | pubmed:meshHeading | pubmed-meshheading:2476050-... | lld:pubmed |
| pubmed-article:2476050 | pubmed:meshHeading | pubmed-meshheading:2476050-... | lld:pubmed |
| pubmed-article:2476050 | pubmed:meshHeading | pubmed-meshheading:2476050-... | lld:pubmed |
| pubmed-article:2476050 | pubmed:meshHeading | pubmed-meshheading:2476050-... | lld:pubmed |
| pubmed-article:2476050 | pubmed:meshHeading | pubmed-meshheading:2476050-... | lld:pubmed |
| pubmed-article:2476050 | pubmed:meshHeading | pubmed-meshheading:2476050-... | lld:pubmed |
| pubmed-article:2476050 | pubmed:meshHeading | pubmed-meshheading:2476050-... | lld:pubmed |
| pubmed-article:2476050 | pubmed:meshHeading | pubmed-meshheading:2476050-... | lld:pubmed |
| pubmed-article:2476050 | pubmed:meshHeading | pubmed-meshheading:2476050-... | lld:pubmed |
| pubmed-article:2476050 | pubmed:meshHeading | pubmed-meshheading:2476050-... | lld:pubmed |
| pubmed-article:2476050 | pubmed:meshHeading | pubmed-meshheading:2476050-... | lld:pubmed |
| pubmed-article:2476050 | pubmed:meshHeading | pubmed-meshheading:2476050-... | lld:pubmed |
| pubmed-article:2476050 | pubmed:meshHeading | pubmed-meshheading:2476050-... | lld:pubmed |
| pubmed-article:2476050 | pubmed:year | 1989 | lld:pubmed |
| pubmed-article:2476050 | pubmed:articleTitle | Properties of monoclonal antibodies against Berne virus (Toroviridae). | lld:pubmed |
| pubmed-article:2476050 | pubmed:affiliation | Department of Infectious Diseases and Immunology, Veterinary Faculty, State University of Utrecht, the Netherlands. | lld:pubmed |
| pubmed-article:2476050 | pubmed:publicationType | Journal Article | lld:pubmed |
