pubmed-article:18085230 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:18085230 | lifeskim:mentions | umls-concept:C0026339 | lld:lifeskim |
pubmed-article:18085230 | lifeskim:mentions | umls-concept:C0043240 | lld:lifeskim |
pubmed-article:18085230 | lifeskim:mentions | umls-concept:C0597694 | lld:lifeskim |
pubmed-article:18085230 | lifeskim:mentions | umls-concept:C1704675 | lld:lifeskim |
pubmed-article:18085230 | lifeskim:mentions | umls-concept:C0936012 | lld:lifeskim |
pubmed-article:18085230 | pubmed:dateCreated | 2007-12-18 | lld:pubmed |
pubmed-article:18085230 | pubmed:abstractText | Microtubule-actin interactions are fundamental to many cellular processes such as cytokinesis and cellular locomotion. Investigating the mechanism of microtubule-actin interactions is the key to understand the cellular morphogenesis and related pathological processes. The abundance and highly dynamic nature of microtubules and F-actin raise a serious challenge when trying to distinguish between the real and fortuitous interactions within a cell. Xenopus oocyte wound model represents an ideal system to study microtubule-actin interactions as well as microtubule-dependent control of the actin polymerization. Here, we describe a series of cytoskeleton specific treatments in Xenopus oocyte wound healing experiments and use confocal fluorescence microscopy to analyze fixed oocytes to examine microtubule-actin interactions. | lld:pubmed |
pubmed-article:18085230 | pubmed:language | eng | lld:pubmed |
pubmed-article:18085230 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18085230 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:18085230 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18085230 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18085230 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:18085230 | pubmed:issn | 1543-1894 | lld:pubmed |
pubmed-article:18085230 | pubmed:author | pubmed-author:ZhangTongT | lld:pubmed |
pubmed-article:18085230 | pubmed:author | pubmed-author:MandatoCraig... | lld:pubmed |
pubmed-article:18085230 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:18085230 | pubmed:volume | 137 | lld:pubmed |
pubmed-article:18085230 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:18085230 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:18085230 | pubmed:pagination | 181-8 | lld:pubmed |
pubmed-article:18085230 | pubmed:meshHeading | pubmed-meshheading:18085230... | lld:pubmed |
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pubmed-article:18085230 | pubmed:meshHeading | pubmed-meshheading:18085230... | lld:pubmed |
pubmed-article:18085230 | pubmed:year | 2007 | lld:pubmed |
pubmed-article:18085230 | pubmed:articleTitle | Xenopus oocyte wound healing as a model system for analysis of microtubule-actin interactions. | lld:pubmed |
pubmed-article:18085230 | pubmed:affiliation | McGill University, Montreal, Canada. | lld:pubmed |
pubmed-article:18085230 | pubmed:publicationType | Journal Article | lld:pubmed |