pubmed-article:2023923 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:2023923 | lifeskim:mentions | umls-concept:C0033684 | lld:lifeskim |
pubmed-article:2023923 | lifeskim:mentions | umls-concept:C0019652 | lld:lifeskim |
pubmed-article:2023923 | lifeskim:mentions | umls-concept:C0055062 | lld:lifeskim |
pubmed-article:2023923 | lifeskim:mentions | umls-concept:C1413338 | lld:lifeskim |
pubmed-article:2023923 | lifeskim:mentions | umls-concept:C1998793 | lld:lifeskim |
pubmed-article:2023923 | pubmed:issue | 9 | lld:pubmed |
pubmed-article:2023923 | pubmed:dateCreated | 1991-5-31 | lld:pubmed |
pubmed-article:2023923 | pubmed:abstractText | CENP-A, a centromere-specific 17-kDa protein, has histone-like properties. However, in contrast to the common somatic histones, CENP-A is quantitatively retained in bull spermatozoa, and we have exploited this fact to purify CENP-A to apparent homogeneity. Partial sequence analysis of the purified protein indicates that CENP-A is a distinctive gene product. Some CENP-A sequences are highly similar to regions of histone H3. Other segments of CENP-A are not related to H3 or any other histone. These unrelated segments are presumably involved in localizing CENP-A to centromeric DNA or in centromere-specific functions of CENP-A. | lld:pubmed |
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pubmed-article:2023923 | pubmed:language | eng | lld:pubmed |
pubmed-article:2023923 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2023923 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:2023923 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:2023923 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:2023923 | pubmed:month | May | lld:pubmed |
pubmed-article:2023923 | pubmed:issn | 0027-8424 | lld:pubmed |
pubmed-article:2023923 | pubmed:author | pubmed-author:CharbonneauHH | lld:pubmed |
pubmed-article:2023923 | pubmed:author | pubmed-author:MargolisR LRL | lld:pubmed |
pubmed-article:2023923 | pubmed:author | pubmed-author:O'DayKK | lld:pubmed |
pubmed-article:2023923 | pubmed:author | pubmed-author:PalmerD KDK | lld:pubmed |
pubmed-article:2023923 | pubmed:author | pubmed-author:TrongH LHL | lld:pubmed |
pubmed-article:2023923 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:2023923 | pubmed:day | 1 | lld:pubmed |
pubmed-article:2023923 | pubmed:volume | 88 | lld:pubmed |
pubmed-article:2023923 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:2023923 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:2023923 | pubmed:pagination | 3734-8 | lld:pubmed |
pubmed-article:2023923 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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pubmed-article:2023923 | pubmed:year | 1991 | lld:pubmed |
pubmed-article:2023923 | pubmed:articleTitle | Purification of the centromere-specific protein CENP-A and demonstration that it is a distinctive histone. | lld:pubmed |
pubmed-article:2023923 | pubmed:affiliation | Fred Hutchinson Cancer Research Center, Seattle, WA 98104. | lld:pubmed |
pubmed-article:2023923 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:2023923 | pubmed:publicationType | Comparative Study | lld:pubmed |
pubmed-article:2023923 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
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