pubmed-article:20591187 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:20591187 | lifeskim:mentions | umls-concept:C0262950 | lld:lifeskim |
pubmed-article:20591187 | lifeskim:mentions | umls-concept:C0024880 | lld:lifeskim |
pubmed-article:20591187 | lifeskim:mentions | umls-concept:C0699040 | lld:lifeskim |
pubmed-article:20591187 | lifeskim:mentions | umls-concept:C0206431 | lld:lifeskim |
pubmed-article:20591187 | lifeskim:mentions | umls-concept:C0024518 | lld:lifeskim |
pubmed-article:20591187 | lifeskim:mentions | umls-concept:C0542341 | lld:lifeskim |
pubmed-article:20591187 | lifeskim:mentions | umls-concept:C0441889 | lld:lifeskim |
pubmed-article:20591187 | lifeskim:mentions | umls-concept:C0443288 | lld:lifeskim |
pubmed-article:20591187 | lifeskim:mentions | umls-concept:C1515021 | lld:lifeskim |
pubmed-article:20591187 | pubmed:dateCreated | 2010-7-15 | lld:pubmed |
pubmed-article:20591187 | pubmed:abstractText | At present, it is highly controversial whether pure mast cells can serve as antigen presenting cells, and it is not known whether the capacity of antigen presenting function is temporally restricted to a particular subset of differentiated mast cells. Evidence is presented for a novel surface FcepsilonRIhi , MHC II +, and c-kit + pure mast cell subset, temporally restricted as antigen-presenting cells in the immune axis of T-cell activation. | lld:pubmed |
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pubmed-article:20591187 | pubmed:language | eng | lld:pubmed |
pubmed-article:20591187 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20591187 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:20591187 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:20591187 | pubmed:issn | 1471-2172 | lld:pubmed |
pubmed-article:20591187 | pubmed:author | pubmed-author:LiuFu-TongFT | lld:pubmed |
pubmed-article:20591187 | pubmed:author | pubmed-author:CroftMichaelM | lld:pubmed |
pubmed-article:20591187 | pubmed:author | pubmed-author:YangNing-SunN... | lld:pubmed |
pubmed-article:20591187 | pubmed:author | pubmed-author:SunLiangwuL | lld:pubmed |
pubmed-article:20591187 | pubmed:author | pubmed-author:GongJianJ | lld:pubmed |
pubmed-article:20591187 | pubmed:author | pubmed-author:ChenSwey-Shen... | lld:pubmed |
pubmed-article:20591187 | pubmed:author | pubmed-author:WengI-ChunIC | lld:pubmed |
pubmed-article:20591187 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:20591187 | pubmed:volume | 11 | lld:pubmed |
pubmed-article:20591187 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:20591187 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:20591187 | pubmed:pagination | 34 | lld:pubmed |
pubmed-article:20591187 | pubmed:dateRevised | 2010-9-28 | lld:pubmed |
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pubmed-article:20591187 | pubmed:year | 2010 | lld:pubmed |
pubmed-article:20591187 | pubmed:articleTitle | The antigen presentation function of bone marrow-derived mast cells is spatiotemporally restricted to a subset expressing high levels of cell surface FcepsilonRI and MHC II. | lld:pubmed |
pubmed-article:20591187 | pubmed:affiliation | Department of Allergy and Immunology, IgE Therapeutics, Inc., San Diego, CA, USA. | lld:pubmed |
pubmed-article:20591187 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:20591187 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
entrez-gene:14125 | entrezgene:pubmed | pubmed-article:20591187 | lld:entrezgene |
http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:20591187 | lld:entrezgene |