| pubmed-article:14576439 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:14576439 | lifeskim:mentions | umls-concept:C0043457 | lld:lifeskim |
| pubmed-article:14576439 | lifeskim:mentions | umls-concept:C0178539 | lld:lifeskim |
| pubmed-article:14576439 | lifeskim:mentions | umls-concept:C0026559 | lld:lifeskim |
| pubmed-article:14576439 | pubmed:issue | 5645 | lld:pubmed |
| pubmed-article:14576439 | pubmed:dateCreated | 2003-10-24 | lld:pubmed |
| pubmed-article:14576439 | pubmed:abstractText | Many vertebrate organs adopt asymmetric positions with respect to the midline, but little is known about the cellular changes and tissue movements that occur downstream of left-right gene expression to produce this asymmetry. Here, we provide evidence that the looping of the zebrafish gut results from the asymmetric migration of the neighboring lateral plate mesoderm (LPM). Mutations that disrupt the epithelial structure of the LPM perturb this asymmetric migration and inhibit gut looping. Asymmetric LPM migration still occurs when the endoderm is ablated from the gut-looping region, suggesting that the LPM can autonomously provide a motive force for gut displacement. Finally, reducing left-sided Nodal activity randomizes the pattern of LPM migration and gut looping. These results reveal a cellular framework for the regulation of organ laterality by asymmetrically expressed genes. | lld:pubmed |
| pubmed-article:14576439 | pubmed:language | eng | lld:pubmed |
| pubmed-article:14576439 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:14576439 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:14576439 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:14576439 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:14576439 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:14576439 | pubmed:month | Oct | lld:pubmed |
| pubmed-article:14576439 | pubmed:issn | 1095-9203 | lld:pubmed |
| pubmed-article:14576439 | pubmed:author | pubmed-author:CantenotAA | lld:pubmed |
| pubmed-article:14576439 | pubmed:author | pubmed-author:RebagliatiMic... | lld:pubmed |
| pubmed-article:14576439 | pubmed:author | pubmed-author:Horne-Badovin... | lld:pubmed |
| pubmed-article:14576439 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:14576439 | pubmed:day | 24 | lld:pubmed |
| pubmed-article:14576439 | pubmed:volume | 302 | lld:pubmed |
| pubmed-article:14576439 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:14576439 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:14576439 | pubmed:pagination | 662-5 | lld:pubmed |
| pubmed-article:14576439 | pubmed:dateRevised | 2007-11-15 | lld:pubmed |
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| pubmed-article:14576439 | pubmed:year | 2003 | lld:pubmed |
| pubmed-article:14576439 | pubmed:articleTitle | A cellular framework for gut-looping morphogenesis in zebrafish. | lld:pubmed |
| pubmed-article:14576439 | pubmed:affiliation | Department of Biochemistry and Biophysics, Programs in Developmental Biology, Genetics, and Human Genetics, University of California, San Francisco, CA 94143, USA. | lld:pubmed |
| pubmed-article:14576439 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:14576439 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:14576439 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |
| pubmed-article:14576439 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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