| pubmed-article:7559858 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:7559858 | lifeskim:mentions | umls-concept:C0007634 | lld:lifeskim |
| pubmed-article:7559858 | lifeskim:mentions | umls-concept:C0035668 | lld:lifeskim |
| pubmed-article:7559858 | lifeskim:mentions | umls-concept:C0012893 | lld:lifeskim |
| pubmed-article:7559858 | lifeskim:mentions | umls-concept:C1511790 | lld:lifeskim |
| pubmed-article:7559858 | lifeskim:mentions | umls-concept:C0220781 | lld:lifeskim |
| pubmed-article:7559858 | lifeskim:mentions | umls-concept:C1883254 | lld:lifeskim |
| pubmed-article:7559858 | lifeskim:mentions | umls-concept:C0444498 | lld:lifeskim |
| pubmed-article:7559858 | pubmed:issue | 1 | lld:pubmed |
| pubmed-article:7559858 | pubmed:dateCreated | 1995-11-9 | lld:pubmed |
| pubmed-article:7559858 | pubmed:abstractText | A PCR-derived digoxigenin-labeled DNA probe was used for for Epstein-Barr early RNA (EBER) in situ hybridization in formalin-fixed paraffin-embedded tissues. The results showed that the hybridization signal was morphologically distinct and the intensity of signal was comparable with those by RNA riboprobe. The advantages of using PCR-derived DNA probes for EBER in situ hybridization include: (1) the synthesis of digoxigenin-labeled DNA probes is easy and simple by PCR; (2) the labeled amplification product can be used as a probe without further purification; (3) DNA probes are potentially more stable than RNA probes; and (4) the preparation of DNA probes is relatively efficient and rapid. It is concluded that this technique is an ideal candidate for detection of EBER expression in clinical specimens. | lld:pubmed |
| pubmed-article:7559858 | pubmed:language | eng | lld:pubmed |
| pubmed-article:7559858 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:7559858 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:7559858 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:7559858 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:7559858 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:7559858 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:7559858 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:7559858 | pubmed:month | Jul | lld:pubmed |
| pubmed-article:7559858 | pubmed:issn | 0166-0934 | lld:pubmed |
| pubmed-article:7559858 | pubmed:author | pubmed-author:TsaiS TST | lld:pubmed |
| pubmed-article:7559858 | pubmed:author | pubmed-author:WuT CTC | lld:pubmed |
| pubmed-article:7559858 | pubmed:author | pubmed-author:KimZ SZS | lld:pubmed |
| pubmed-article:7559858 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:7559858 | pubmed:volume | 54 | lld:pubmed |
| pubmed-article:7559858 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:7559858 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:7559858 | pubmed:pagination | 67-74 | lld:pubmed |
| pubmed-article:7559858 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
| pubmed-article:7559858 | pubmed:meshHeading | pubmed-meshheading:7559858-... | lld:pubmed |
| pubmed-article:7559858 | pubmed:meshHeading | pubmed-meshheading:7559858-... | lld:pubmed |
| pubmed-article:7559858 | pubmed:meshHeading | pubmed-meshheading:7559858-... | lld:pubmed |
| pubmed-article:7559858 | pubmed:meshHeading | pubmed-meshheading:7559858-... | lld:pubmed |
| pubmed-article:7559858 | pubmed:meshHeading | pubmed-meshheading:7559858-... | lld:pubmed |
| pubmed-article:7559858 | pubmed:meshHeading | pubmed-meshheading:7559858-... | lld:pubmed |
| pubmed-article:7559858 | pubmed:meshHeading | pubmed-meshheading:7559858-... | lld:pubmed |
| pubmed-article:7559858 | pubmed:meshHeading | pubmed-meshheading:7559858-... | lld:pubmed |
| pubmed-article:7559858 | pubmed:meshHeading | pubmed-meshheading:7559858-... | lld:pubmed |
| pubmed-article:7559858 | pubmed:meshHeading | pubmed-meshheading:7559858-... | lld:pubmed |
| pubmed-article:7559858 | pubmed:meshHeading | pubmed-meshheading:7559858-... | lld:pubmed |
| pubmed-article:7559858 | pubmed:year | 1995 | lld:pubmed |
| pubmed-article:7559858 | pubmed:articleTitle | Synthesis of PCR-derived, digoxigenin-labeled DNA probes for in situ detection of Epstein-Barr early RNAs in Epstein-Barr virus-infected cells. | lld:pubmed |
| pubmed-article:7559858 | pubmed:affiliation | Department of Otolaryngology, National Cheng Kung University Medical College, Taipan, Taiwan. | lld:pubmed |
| pubmed-article:7559858 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:7559858 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
