pubmed-article:1497801 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:1497801 | lifeskim:mentions | umls-concept:C0018561 | lld:lifeskim |
pubmed-article:1497801 | lifeskim:mentions | umls-concept:C0079058 | lld:lifeskim |
pubmed-article:1497801 | lifeskim:mentions | umls-concept:C1880022 | lld:lifeskim |
pubmed-article:1497801 | lifeskim:mentions | umls-concept:C1519595 | lld:lifeskim |
pubmed-article:1497801 | pubmed:issue | 4 | lld:pubmed |
pubmed-article:1497801 | pubmed:dateCreated | 1992-9-11 | lld:pubmed |
pubmed-article:1497801 | pubmed:databankReference | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1497801 | pubmed:databankReference | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1497801 | pubmed:abstractText | The coding sequences as well as 5'- and 3'-flanking sequences of the Syrian hamster c-Ha-ras gene were deduced from cDNA clones derived from embryo fibroblast cell lines. Sequences of introns B, C, and D were obtained from genomic DNA after amplification by the polymerase chain reaction. Sequence comparisons with rat, mouse, and human c-Ha-ras genes revealed a high degree of homology. One of 12 cDNA clones contained intron-D-exon (IDX) sequences due to alternative splicing that would encode a p19 Ha-ras gene product. Conservation between species suggests a functional role for the IDX, possibly as a negative control of p21 Ha-ras expression. | lld:pubmed |
pubmed-article:1497801 | pubmed:language | eng | lld:pubmed |
pubmed-article:1497801 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1497801 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:1497801 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1497801 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1497801 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1497801 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:1497801 | pubmed:issn | 0899-1987 | lld:pubmed |
pubmed-article:1497801 | pubmed:author | pubmed-author:EbertRR | lld:pubmed |
pubmed-article:1497801 | pubmed:author | pubmed-author:BarrettJ CJC | lld:pubmed |
pubmed-article:1497801 | pubmed:author | pubmed-author:ReissEE | lld:pubmed |
pubmed-article:1497801 | pubmed:author | pubmed-author:SchiffmannDD | lld:pubmed |
pubmed-article:1497801 | pubmed:author | pubmed-author:WisemanR WRW | lld:pubmed |
pubmed-article:1497801 | pubmed:author | pubmed-author:RollichGG | lld:pubmed |
pubmed-article:1497801 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:1497801 | pubmed:volume | 5 | lld:pubmed |
pubmed-article:1497801 | pubmed:geneSymbol | c-Ha-ras | lld:pubmed |
pubmed-article:1497801 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:1497801 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:1497801 | pubmed:pagination | 254-8 | lld:pubmed |
pubmed-article:1497801 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
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pubmed-article:1497801 | pubmed:year | 1992 | lld:pubmed |
pubmed-article:1497801 | pubmed:articleTitle | Characterization of the Syrian hamster c-Ha-ras gene and intron-D-exon transcript. | lld:pubmed |
pubmed-article:1497801 | pubmed:affiliation | Laboratory of Molecular Carcinogenesis, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, North Carolina 27709. | lld:pubmed |
pubmed-article:1497801 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:1497801 | pubmed:publicationType | Comparative Study | lld:pubmed |
pubmed-article:1497801 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
pubmed-article:1497801 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:1497801 | lld:pubmed |