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| pubmed-article:20181261 | pubmed:dateCreated | 2010-3-19 | lld:pubmed |
| pubmed-article:20181261 | pubmed:abstractText | Tumor initiating cells (TICs) provide a new paradigm for developing original therapeutic strategies. | lld:pubmed |
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| pubmed-article:20181261 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:20181261 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:20181261 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:20181261 | pubmed:issn | 1471-2407 | lld:pubmed |
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| pubmed-article:20181261 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:20181261 | pubmed:volume | 10 | lld:pubmed |
| pubmed-article:20181261 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:20181261 | pubmed:authorsComplete | Y | lld:pubmed |
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| pubmed-article:20181261 | pubmed:year | 2010 | lld:pubmed |
| pubmed-article:20181261 | pubmed:articleTitle | CD133, CD15/SSEA-1, CD34 or side populations do not resume tumor-initiating properties of long-term cultured cancer stem cells from human malignant glio-neuronal tumors. | lld:pubmed |
| pubmed-article:20181261 | pubmed:affiliation | Glial Plasticity lab, Inserm UMR 894, University Paris Descartes, Paris, France. | lld:pubmed |
| pubmed-article:20181261 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:20181261 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
