| pubmed-article:8805278 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:8805278 | lifeskim:mentions | umls-concept:C0085103 | lld:lifeskim |
| pubmed-article:8805278 | lifeskim:mentions | umls-concept:C0020291 | lld:lifeskim |
| pubmed-article:8805278 | lifeskim:mentions | umls-concept:C0031621 | lld:lifeskim |
| pubmed-article:8805278 | lifeskim:mentions | umls-concept:C0031684 | lld:lifeskim |
| pubmed-article:8805278 | lifeskim:mentions | umls-concept:C0021467 | lld:lifeskim |
| pubmed-article:8805278 | lifeskim:mentions | umls-concept:C0021469 | lld:lifeskim |
| pubmed-article:8805278 | pubmed:issue | 5 | lld:pubmed |
| pubmed-article:8805278 | pubmed:dateCreated | 1997-3-10 | lld:pubmed |
| pubmed-article:8805278 | pubmed:abstractText | Activated receptor tyrosine kinases bind downstream effector molecules with high affinity. Provided that they can be introduced into cells, peptides corresponding to these high-affinity sites should be able to compete for the interaction and thereby inhibit specific signal transduction cascades. The high-affinity binding site for phospholipase C gamma (PLCgamma) on the activated fibroblast growth factor receptor (FGFR) is centred around the tyrosine at position 766 (766Tyr), and peptides corresponding to this site inhibit PLCgamma binding to the receptor in vitro. A 16 amino-acid peptide from the third helix of the Antennapedia homeodomain protein has recently been shown to be able to act as an internalization vector that can deliver other peptides into cells. Here, we have designed a peptide that contains both the internalization sequence and the FGFR high-affinity binding site for PLCgamma, and tested it in cultures of cerebellar neurons for its ability to inhibit the activation of PLCgamma by basic FGF. | lld:pubmed |
| pubmed-article:8805278 | pubmed:language | eng | lld:pubmed |
| pubmed-article:8805278 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8805278 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:8805278 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8805278 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8805278 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8805278 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8805278 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8805278 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8805278 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8805278 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:8805278 | pubmed:month | May | lld:pubmed |
| pubmed-article:8805278 | pubmed:issn | 0960-9822 | lld:pubmed |
| pubmed-article:8805278 | pubmed:author | pubmed-author:HallHH | lld:pubmed |
| pubmed-article:8805278 | pubmed:author | pubmed-author:WalshF SFS | lld:pubmed |
| pubmed-article:8805278 | pubmed:author | pubmed-author:ProchiantzAA | lld:pubmed |
| pubmed-article:8805278 | pubmed:author | pubmed-author:DohertyPP | lld:pubmed |
| pubmed-article:8805278 | pubmed:author | pubmed-author:WilliamsE JEJ | lld:pubmed |
| pubmed-article:8805278 | pubmed:author | pubmed-author:MooreS ESE | lld:pubmed |
| pubmed-article:8805278 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:8805278 | pubmed:day | 1 | lld:pubmed |
| pubmed-article:8805278 | pubmed:volume | 6 | lld:pubmed |
| pubmed-article:8805278 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:8805278 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:8805278 | pubmed:pagination | 580-7 | lld:pubmed |
| pubmed-article:8805278 | pubmed:dateRevised | 2010-3-24 | lld:pubmed |
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| pubmed-article:8805278 | pubmed:meshHeading | pubmed-meshheading:8805278-... | lld:pubmed |
| pubmed-article:8805278 | pubmed:meshHeading | pubmed-meshheading:8805278-... | lld:pubmed |
| pubmed-article:8805278 | pubmed:meshHeading | pubmed-meshheading:8805278-... | lld:pubmed |
| pubmed-article:8805278 | pubmed:meshHeading | pubmed-meshheading:8805278-... | lld:pubmed |
| pubmed-article:8805278 | pubmed:meshHeading | pubmed-meshheading:8805278-... | lld:pubmed |
| pubmed-article:8805278 | pubmed:year | 1996 | lld:pubmed |
| pubmed-article:8805278 | pubmed:articleTitle | Inhibition of FGF-stimulated phosphatidylinositol hydrolysis and neurite outgrowth by a cell-membrane permeable phosphopeptide. | lld:pubmed |
| pubmed-article:8805278 | pubmed:affiliation | Department of Experimental Pathology, UMDS, Guy's Hospital, London Bridge, London SE1 9RT, UK. | lld:pubmed |
| pubmed-article:8805278 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:8805278 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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