pubmed-article:11842224 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:11842224 | lifeskim:mentions | umls-concept:C0037868 | lld:lifeskim |
pubmed-article:11842224 | lifeskim:mentions | umls-concept:C0037857 | lld:lifeskim |
pubmed-article:11842224 | lifeskim:mentions | umls-concept:C0033684 | lld:lifeskim |
pubmed-article:11842224 | lifeskim:mentions | umls-concept:C0205307 | lld:lifeskim |
pubmed-article:11842224 | lifeskim:mentions | umls-concept:C1420509 | lld:lifeskim |
pubmed-article:11842224 | lifeskim:mentions | umls-concept:C1704241 | lld:lifeskim |
pubmed-article:11842224 | lifeskim:mentions | umls-concept:C0033268 | lld:lifeskim |
pubmed-article:11842224 | lifeskim:mentions | umls-concept:C0205224 | lld:lifeskim |
pubmed-article:11842224 | lifeskim:mentions | umls-concept:C1633520 | lld:lifeskim |
pubmed-article:11842224 | pubmed:issue | 4 | lld:pubmed |
pubmed-article:11842224 | pubmed:dateCreated | 2002-2-20 | lld:pubmed |
pubmed-article:11842224 | pubmed:abstractText | Differentiation of spermatids into spermatozoa is regulated via phosphorylated RNA-binding proteins that modulate the expression of stage-specific mRNAs. We demonstrate that the phosphoserine, -threonine or -tyrosine, interaction protein, Styx, complexes with a testicular RNA-binding protein and is essential for normal spermiogenesis. Ablation of Styx expression in mouse disrupts round and elongating spermatid development, resulting in a >1,000-fold decrease in spermatozoa production. Moreover, Styx(-/-) males are infertile because of structural head abnormalities in residual epididymal sperm. Immunoprecipitation of Styx with Crhsp-24, a phosphorylated RNA-binding protein implicated in translational repression of histone mRNAs, provides a strategy for regulating posttranscriptional gene expression. | lld:pubmed |
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pubmed-article:11842224 | pubmed:language | eng | lld:pubmed |
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pubmed-article:11842224 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:11842224 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:11842224 | pubmed:month | Feb | lld:pubmed |
pubmed-article:11842224 | pubmed:issn | 0027-8424 | lld:pubmed |
pubmed-article:11842224 | pubmed:author | pubmed-author:DixonJack EJE | lld:pubmed |
pubmed-article:11842224 | pubmed:author | pubmed-author:WishartMatthe... | lld:pubmed |
pubmed-article:11842224 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:11842224 | pubmed:day | 19 | lld:pubmed |
pubmed-article:11842224 | pubmed:volume | 99 | lld:pubmed |
pubmed-article:11842224 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:11842224 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:11842224 | pubmed:pagination | 2112-7 | lld:pubmed |
pubmed-article:11842224 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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pubmed-article:11842224 | pubmed:year | 2002 | lld:pubmed |
pubmed-article:11842224 | pubmed:articleTitle | The archetype STYX/dead-phosphatase complexes with a spermatid mRNA-binding protein and is essential for normal sperm production. | lld:pubmed |
pubmed-article:11842224 | pubmed:affiliation | Life Sciences Institute and Department of Biological Chemistry, University of Michigan, Ann Arbor, MI 48109, USA. | lld:pubmed |
pubmed-article:11842224 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:11842224 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
pubmed-article:11842224 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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