pubmed-article:21346176 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:21346176 | lifeskim:mentions | umls-concept:C0085243 | lld:lifeskim |
pubmed-article:21346176 | lifeskim:mentions | umls-concept:C1332717 | lld:lifeskim |
pubmed-article:21346176 | lifeskim:mentions | umls-concept:C1706438 | lld:lifeskim |
pubmed-article:21346176 | lifeskim:mentions | umls-concept:C0085358 | lld:lifeskim |
pubmed-article:21346176 | lifeskim:mentions | umls-concept:C1704632 | lld:lifeskim |
pubmed-article:21346176 | lifeskim:mentions | umls-concept:C0871261 | lld:lifeskim |
pubmed-article:21346176 | lifeskim:mentions | umls-concept:C1413244 | lld:lifeskim |
pubmed-article:21346176 | lifeskim:mentions | umls-concept:C2698600 | lld:lifeskim |
pubmed-article:21346176 | lifeskim:mentions | umls-concept:C2911692 | lld:lifeskim |
pubmed-article:21346176 | lifeskim:mentions | umls-concept:C1706817 | lld:lifeskim |
pubmed-article:21346176 | lifeskim:mentions | umls-concept:C1708528 | lld:lifeskim |
pubmed-article:21346176 | lifeskim:mentions | umls-concept:C0449445 | lld:lifeskim |
pubmed-article:21346176 | pubmed:issue | 4 | lld:pubmed |
pubmed-article:21346176 | pubmed:dateCreated | 2011-3-30 | lld:pubmed |
pubmed-article:21346176 | pubmed:abstractText | Type 1 diabetes can be inhibited in standard NOD mice by autoantigen-specific immunotherapy targeting pathogenic CD8+ T-cells. NOD.?2m(null).HHD mice expressing human HLA-A2.1 but lacking murine major histocompatibility complex class I molecules develop diabetes characterized by CD8 T-cells recognizing certain autoantigenic peptides also targeted in human patients. These include peptides derived from the pancreatic ?-cell proteins insulin (INS1/2 A(2-10) and INS1 B(5-14)) and islet-specific glucose-6-phosphatase catalytic subunit-related protein (IGRP(265-273) and IGRP(228-236)). Hence, NOD.?2m(null).HHD mice represent a model system for developing potentially clinically translatable interventions for suppressing diabetogenic HLA-A2.1-restricted T-cell responses. | lld:pubmed |
pubmed-article:21346176 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21346176 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21346176 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21346176 | pubmed:language | eng | lld:pubmed |
pubmed-article:21346176 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21346176 | pubmed:citationSubset | AIM | lld:pubmed |
pubmed-article:21346176 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21346176 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21346176 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21346176 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21346176 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:21346176 | pubmed:month | Apr | lld:pubmed |
pubmed-article:21346176 | pubmed:issn | 1939-327X | lld:pubmed |
pubmed-article:21346176 | pubmed:author | pubmed-author:KayThomas W... | lld:pubmed |
pubmed-article:21346176 | pubmed:author | pubmed-author:GreinerDale... | lld:pubmed |
pubmed-article:21346176 | pubmed:author | pubmed-author:SerrezeDavid... | lld:pubmed |
pubmed-article:21346176 | pubmed:author | pubmed-author:NiensMarijkeM | lld:pubmed |
pubmed-article:21346176 | pubmed:author | pubmed-author:GrierAlexandr... | lld:pubmed |
pubmed-article:21346176 | pubmed:author | pubmed-author:MarronMichele... | lld:pubmed |
pubmed-article:21346176 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:21346176 | pubmed:volume | 60 | lld:pubmed |
pubmed-article:21346176 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:21346176 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:21346176 | pubmed:pagination | 1229-36 | lld:pubmed |
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pubmed-article:21346176 | pubmed:meshHeading | pubmed-meshheading:21346176... | lld:pubmed |
pubmed-article:21346176 | pubmed:year | 2011 | lld:pubmed |
pubmed-article:21346176 | pubmed:articleTitle | Prevention of "Humanized" diabetogenic CD8 T-cell responses in HLA-transgenic NOD mice by a multipeptide coupled-cell approach. | lld:pubmed |
pubmed-article:21346176 | pubmed:affiliation | Jackson Laboratory, Bar Harbor, Maine, USA. | lld:pubmed |
pubmed-article:21346176 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:21346176 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
pubmed-article:21346176 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
entrez-gene:12010 | entrezgene:pubmed | pubmed-article:21346176 | lld:entrezgene |