pubmed-article:10884060 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:10884060 | lifeskim:mentions | umls-concept:C0007634 | lld:lifeskim |
pubmed-article:10884060 | lifeskim:mentions | umls-concept:C0034721 | lld:lifeskim |
pubmed-article:10884060 | lifeskim:mentions | umls-concept:C0034693 | lld:lifeskim |
pubmed-article:10884060 | lifeskim:mentions | umls-concept:C0521390 | lld:lifeskim |
pubmed-article:10884060 | lifeskim:mentions | umls-concept:C0380603 | lld:lifeskim |
pubmed-article:10884060 | lifeskim:mentions | umls-concept:C0038952 | lld:lifeskim |
pubmed-article:10884060 | lifeskim:mentions | umls-concept:C0033414 | lld:lifeskim |
pubmed-article:10884060 | lifeskim:mentions | umls-concept:C1517499 | lld:lifeskim |
pubmed-article:10884060 | pubmed:issue | 9 | lld:pubmed |
pubmed-article:10884060 | pubmed:dateCreated | 2000-10-10 | lld:pubmed |
pubmed-article:10884060 | pubmed:abstractText | We constructed two replication-deficient recombinant adenovirus vectors coding human basic fibroblast growth factor (bFGF), one with and one without the interleukin-2 (IL-2) secretory signal sequence and examined their neurotrophic effects on primary neuronal cells in vitro. The primary neuronal cells were successfully infected at a high efficiency with the adenovirus vectors. bFGF protein was detected in the culture medium of the neurons infected with both these vectors. The cells infected with the bFGF-expressing adenovirus containing the IL-2 signal sequence showed 2- to 10-fold higher levels of secretion levels than cells infected with the native bFGF-expressing adenovirus alone. Both bFGF-expressing vectors augmented the survival of primary neuronal cells in an in vitro culture, compared with a mock infection or control virus infection. Notably, the cells infected with the bFGF-expressing adenovirus containing the IL-2 signal sequence were markedly enhanced cell survival in the early phase of the culture, compared with the control cells and even those infected with the bFGF-expressing adenovirus without the IL-2 signal sequence. However, in the late phase of neuronal culture, neither viral vector could support the cell survival. In contrast the co-infection of the bFGF-expressing vector with a Bcl-xL-expressing vector was extremely effective on neuronal survival. | lld:pubmed |
pubmed-article:10884060 | pubmed:language | eng | lld:pubmed |
pubmed-article:10884060 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10884060 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:10884060 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10884060 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10884060 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10884060 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10884060 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10884060 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10884060 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:10884060 | pubmed:month | Jun | lld:pubmed |
pubmed-article:10884060 | pubmed:issn | 0959-4965 | lld:pubmed |
pubmed-article:10884060 | pubmed:author | pubmed-author:MoriHH | lld:pubmed |
pubmed-article:10884060 | pubmed:author | pubmed-author:SaikiMM | lld:pubmed |
pubmed-article:10884060 | pubmed:author | pubmed-author:MatsuokaNN | lld:pubmed |
pubmed-article:10884060 | pubmed:author | pubmed-author:IshiiKK | lld:pubmed |
pubmed-article:10884060 | pubmed:author | pubmed-author:HashimotoNN | lld:pubmed |
pubmed-article:10884060 | pubmed:author | pubmed-author:HamadaHH | lld:pubmed |
pubmed-article:10884060 | pubmed:author | pubmed-author:YukawaHH | lld:pubmed |
pubmed-article:10884060 | pubmed:author | pubmed-author:AkimotoMM | lld:pubmed |
pubmed-article:10884060 | pubmed:author | pubmed-author:MiyatakeSS | lld:pubmed |
pubmed-article:10884060 | pubmed:author | pubmed-author:TakahashiJ... | lld:pubmed |
pubmed-article:10884060 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:10884060 | pubmed:day | 26 | lld:pubmed |
pubmed-article:10884060 | pubmed:volume | 11 | lld:pubmed |
pubmed-article:10884060 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:10884060 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:10884060 | pubmed:pagination | 2001-6 | lld:pubmed |
pubmed-article:10884060 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
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pubmed-article:10884060 | pubmed:year | 2000 | lld:pubmed |
pubmed-article:10884060 | pubmed:articleTitle | Adenovirus-mediated gene transfer of basic fibroblast growth factor promotes the survival of primary-cultured rat neuronal cells. | lld:pubmed |
pubmed-article:10884060 | pubmed:affiliation | Department of Neurosurgery and Clinical Neuroscience, Faculty of Medicine, Kyoto University, Japan. | lld:pubmed |
pubmed-article:10884060 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:10884060 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:10884060 | lld:pubmed |