| pubmed-article:9287222 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:9287222 | lifeskim:mentions | umls-concept:C0043342 | lld:lifeskim |
| pubmed-article:9287222 | lifeskim:mentions | umls-concept:C0029974 | lld:lifeskim |
| pubmed-article:9287222 | lifeskim:mentions | umls-concept:C0007586 | lld:lifeskim |
| pubmed-article:9287222 | lifeskim:mentions | umls-concept:C0598312 | lld:lifeskim |
| pubmed-article:9287222 | lifeskim:mentions | umls-concept:C0597304 | lld:lifeskim |
| pubmed-article:9287222 | lifeskim:mentions | umls-concept:C1413263 | lld:lifeskim |
| pubmed-article:9287222 | lifeskim:mentions | umls-concept:C1514873 | lld:lifeskim |
| pubmed-article:9287222 | pubmed:issue | 5332 | lld:pubmed |
| pubmed-article:9287222 | pubmed:dateCreated | 1997-9-29 | lld:pubmed |
| pubmed-article:9287222 | pubmed:abstractText | The cell division cycle gene, CDC34, is required for ubiquitin-mediated degradation of G1 regulators and cell cycle progression through the transition from G1 to S phase in budding yeast. A CDC34 requirement for S phase onset in higher eukaryotes has not been established. Studies of the simple embryonic cell cycle of Xenopus laevis eggs demonstrated that Cdc34p in a large molecular size complex was required in the initiation of DNA replication. Cdc34p appears to regulate the initiation function of Cdk2-cyclin E, perhaps through the degradation of the Xenopus cdk inhibitor, Xic1. | lld:pubmed |
| pubmed-article:9287222 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:9287222 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:9287222 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:9287222 | pubmed:month | Sep | lld:pubmed |
| pubmed-article:9287222 | pubmed:issn | 0036-8075 | lld:pubmed |
| pubmed-article:9287222 | pubmed:author | pubmed-author:KirschnerM... | lld:pubmed |
| pubmed-article:9287222 | pubmed:author | pubmed-author:YewP RPR | lld:pubmed |
| pubmed-article:9287222 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:9287222 | pubmed:day | 12 | lld:pubmed |
| pubmed-article:9287222 | pubmed:volume | 277 | lld:pubmed |
| pubmed-article:9287222 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:9287222 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:9287222 | pubmed:pagination | 1672-6 | lld:pubmed |
| pubmed-article:9287222 | pubmed:dateRevised | 2009-11-19 | lld:pubmed |
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| pubmed-article:9287222 | pubmed:year | 1997 | lld:pubmed |
| pubmed-article:9287222 | pubmed:articleTitle | Proteolysis and DNA replication: the CDC34 requirement in the Xenopus egg cell cycle. | lld:pubmed |
| pubmed-article:9287222 | pubmed:affiliation | Department of Cell Biology, Harvard Medical School, 25 Shattuck Street, Boston, MA 02115, USA. | lld:pubmed |
| pubmed-article:9287222 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:9287222 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:9287222 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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