| pubmed-article:8066463 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:8066463 | lifeskim:mentions | umls-concept:C0026809 | lld:lifeskim |
| pubmed-article:8066463 | lifeskim:mentions | umls-concept:C0017355 | lld:lifeskim |
| pubmed-article:8066463 | lifeskim:mentions | umls-concept:C0208355 | lld:lifeskim |
| pubmed-article:8066463 | lifeskim:mentions | umls-concept:C0017262 | lld:lifeskim |
| pubmed-article:8066463 | lifeskim:mentions | umls-concept:C1711351 | lld:lifeskim |
| pubmed-article:8066463 | lifeskim:mentions | umls-concept:C2911684 | lld:lifeskim |
| pubmed-article:8066463 | lifeskim:mentions | umls-concept:C0185117 | lld:lifeskim |
| pubmed-article:8066463 | pubmed:issue | 5176 | lld:pubmed |
| pubmed-article:8066463 | pubmed:dateCreated | 1994-9-19 | lld:pubmed |
| pubmed-article:8066463 | pubmed:abstractText | Proteasomes degrade endogenous proteins. Two subunits, LMP-2 and LMP-7, are encoded in a region of the major histocompatibility complex (MHC) that is critical for class I-restricted antigen presentation. Mice with a targeted deletion of the gene encoding LMP-7 have reduced levels of MHC class I cell-surface expression and present the endogenous antigen HY inefficiently; addition of peptides to splenocytes deficient in LMP-7 restores wild-type class I expression levels. This demonstrates the involvement of LMP-7 in the MHC class I presentation pathway and suggests that LMP-7 functions as an integral part of the peptide supply machinery. | lld:pubmed |
| pubmed-article:8066463 | pubmed:language | eng | lld:pubmed |
| pubmed-article:8066463 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8066463 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:8066463 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:8066463 | pubmed:month | Aug | lld:pubmed |
| pubmed-article:8066463 | pubmed:issn | 0036-8075 | lld:pubmed |
| pubmed-article:8066463 | pubmed:author | pubmed-author:MüllerUU | lld:pubmed |
| pubmed-article:8066463 | pubmed:author | pubmed-author:von BoehmerHH | lld:pubmed |
| pubmed-article:8066463 | pubmed:author | pubmed-author:RajewskyKK | lld:pubmed |
| pubmed-article:8066463 | pubmed:author | pubmed-author:KühnRR | lld:pubmed |
| pubmed-article:8066463 | pubmed:author | pubmed-author:SwapSS | lld:pubmed |
| pubmed-article:8066463 | pubmed:author | pubmed-author:FehlingH JHJ | lld:pubmed |
| pubmed-article:8066463 | pubmed:author | pubmed-author:LaplaceCC | lld:pubmed |
| pubmed-article:8066463 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:8066463 | pubmed:day | 26 | lld:pubmed |
| pubmed-article:8066463 | pubmed:volume | 265 | lld:pubmed |
| pubmed-article:8066463 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:8066463 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:8066463 | pubmed:pagination | 1234-7 | lld:pubmed |
| pubmed-article:8066463 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
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| pubmed-article:8066463 | pubmed:year | 1994 | lld:pubmed |
| pubmed-article:8066463 | pubmed:articleTitle | MHC class I expression in mice lacking the proteasome subunit LMP-7. | lld:pubmed |
| pubmed-article:8066463 | pubmed:affiliation | Basel Institute for Immunology, Switzerland. | lld:pubmed |
| pubmed-article:8066463 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:8066463 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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