| pubmed-article:20696097 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:20696097 | lifeskim:mentions | umls-concept:C0017535 | lld:lifeskim |
| pubmed-article:20696097 | lifeskim:mentions | umls-concept:C0243192 | lld:lifeskim |
| pubmed-article:20696097 | lifeskim:mentions | umls-concept:C0220908 | lld:lifeskim |
| pubmed-article:20696097 | lifeskim:mentions | umls-concept:C0018270 | lld:lifeskim |
| pubmed-article:20696097 | lifeskim:mentions | umls-concept:C0348080 | lld:lifeskim |
| pubmed-article:20696097 | lifeskim:mentions | umls-concept:C1514485 | lld:lifeskim |
| pubmed-article:20696097 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:20696097 | pubmed:dateCreated | 2011-1-17 | lld:pubmed |
| pubmed-article:20696097 | pubmed:abstractText | Giardia lamblia is one of the most prevalent parasites of mankind and is estimated to cause over 200 million infections per year. To screen chemical libraries for compounds that perturb trophozoite proliferation we adapted a conventional culture method to 384-well plates and identified numerous inhibitors. Here we used a modified assay to screen for compounds that promote trophozoite multiplication. Trophozoite growth was reduced by dilution of the culture medium and the growth period was extended to screen 2 compound libraries comprising 1500 compounds. A total of 4 agonists of trophozoite multiplication were identified. In the presence of one of these compounds, strychnine, enhanced growth was accompanied by unusual trophozoite morphology characterized by dividing trophozoites displaying more than the 2 nuclei per cell which are normally observed. The other agonists, although belonging to 2 distinct chemical groups, are known to affect isoprenylation, indicating a link between protein or lipid isoprenylation and growth in culture. Although inhibitors of isoprenylation are known to antagonize proliferation of mammalian cells, an agonistic effect of isoprenylation modulators has to our knowledge not been described previously. These observations illustrate the power of chemical genetics for identifying pathways controlling specific traits in G. lamblia. | lld:pubmed |
| pubmed-article:20696097 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20696097 | pubmed:language | eng | lld:pubmed |
| pubmed-article:20696097 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20696097 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:20696097 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20696097 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20696097 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:20696097 | pubmed:month | Feb | lld:pubmed |
| pubmed-article:20696097 | pubmed:issn | 1469-8161 | lld:pubmed |
| pubmed-article:20696097 | pubmed:author | pubmed-author:WidmerGG | lld:pubmed |
| pubmed-article:20696097 | pubmed:author | pubmed-author:WuZZ | lld:pubmed |
| pubmed-article:20696097 | pubmed:author | pubmed-author:FaghiriZZ | lld:pubmed |
| pubmed-article:20696097 | pubmed:author | pubmed-author:SantiagoR... | lld:pubmed |
| pubmed-article:20696097 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:20696097 | pubmed:volume | 138 | lld:pubmed |
| pubmed-article:20696097 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:20696097 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:20696097 | pubmed:pagination | 194-200 | lld:pubmed |
| pubmed-article:20696097 | pubmed:meshHeading | pubmed-meshheading:20696097... | lld:pubmed |
| pubmed-article:20696097 | pubmed:meshHeading | pubmed-meshheading:20696097... | lld:pubmed |
| pubmed-article:20696097 | pubmed:meshHeading | pubmed-meshheading:20696097... | lld:pubmed |
| pubmed-article:20696097 | pubmed:meshHeading | pubmed-meshheading:20696097... | lld:pubmed |
| pubmed-article:20696097 | pubmed:meshHeading | pubmed-meshheading:20696097... | lld:pubmed |
| pubmed-article:20696097 | pubmed:meshHeading | pubmed-meshheading:20696097... | lld:pubmed |
| pubmed-article:20696097 | pubmed:meshHeading | pubmed-meshheading:20696097... | lld:pubmed |
| pubmed-article:20696097 | pubmed:meshHeading | pubmed-meshheading:20696097... | lld:pubmed |
| pubmed-article:20696097 | pubmed:meshHeading | pubmed-meshheading:20696097... | lld:pubmed |
| pubmed-article:20696097 | pubmed:meshHeading | pubmed-meshheading:20696097... | lld:pubmed |
| pubmed-article:20696097 | pubmed:meshHeading | pubmed-meshheading:20696097... | lld:pubmed |
| pubmed-article:20696097 | pubmed:meshHeading | pubmed-meshheading:20696097... | lld:pubmed |
| pubmed-article:20696097 | pubmed:year | 2011 | lld:pubmed |
| pubmed-article:20696097 | pubmed:articleTitle | High-throughput screening in suboptimal growth conditions identifies agonists of Giardia lamblia proliferation. | lld:pubmed |
| pubmed-article:20696097 | pubmed:affiliation | Tufts Cummings School of Veterinary Medicine, 200 Westboro Road, North Grafton, Massachusetts 01536, USA. | lld:pubmed |
| pubmed-article:20696097 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:20696097 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:20696097 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
