pubmed-article:8348149 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:8348149 | lifeskim:mentions | umls-concept:C0026809 | lld:lifeskim |
pubmed-article:8348149 | lifeskim:mentions | umls-concept:C0017337 | lld:lifeskim |
pubmed-article:8348149 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
pubmed-article:8348149 | lifeskim:mentions | umls-concept:C0214604 | lld:lifeskim |
pubmed-article:8348149 | lifeskim:mentions | umls-concept:C0443348 | lld:lifeskim |
pubmed-article:8348149 | pubmed:issue | 2 | lld:pubmed |
pubmed-article:8348149 | pubmed:dateCreated | 1993-9-16 | lld:pubmed |
pubmed-article:8348149 | pubmed:abstractText | Mice with the recessive motheaten (me) or the allelic viable motheaten (mev) mutations express a severe autoimmune and immunodeficiency syndrome. We have shown that the basic defect in these mice involves lesions in the gene which encodes haematopoietic cell phosphatase (HCP). These mice thus provide excellent models for investigating the roles of phosphatases in haematopoiesis and the nature of the genetic and cellular events linking impaired haematopoiesis to severe immunodeficiency and expression of systemic autoimmunity. | lld:pubmed |
pubmed-article:8348149 | pubmed:language | eng | lld:pubmed |
pubmed-article:8348149 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8348149 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:8348149 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8348149 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8348149 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8348149 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8348149 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8348149 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:8348149 | pubmed:month | Jun | lld:pubmed |
pubmed-article:8348149 | pubmed:issn | 1061-4036 | lld:pubmed |
pubmed-article:8348149 | pubmed:author | pubmed-author:TsuiH WHW | lld:pubmed |
pubmed-article:8348149 | pubmed:author | pubmed-author:SiminovitchK... | lld:pubmed |
pubmed-article:8348149 | pubmed:author | pubmed-author:de SouzaLL | lld:pubmed |
pubmed-article:8348149 | pubmed:author | pubmed-author:TangX PXP | lld:pubmed |
pubmed-article:8348149 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:8348149 | pubmed:volume | 4 | lld:pubmed |
pubmed-article:8348149 | pubmed:geneSymbol | me<up>v</up> | lld:pubmed |
pubmed-article:8348149 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:8348149 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:8348149 | pubmed:pagination | 124-9 | lld:pubmed |
pubmed-article:8348149 | pubmed:dateRevised | 2007-11-15 | lld:pubmed |
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pubmed-article:8348149 | pubmed:year | 1993 | lld:pubmed |
pubmed-article:8348149 | pubmed:articleTitle | Motheaten and viable motheaten mice have mutations in the haematopoietic cell phosphatase gene. | lld:pubmed |
pubmed-article:8348149 | pubmed:affiliation | Toronto Hospital, Ontario, Canada. | lld:pubmed |
pubmed-article:8348149 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:8348149 | pubmed:publicationType | Comparative Study | lld:pubmed |
pubmed-article:8348149 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
pubmed-article:8348149 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
entrez-gene:15170 | entrezgene:pubmed | pubmed-article:8348149 | lld:entrezgene |
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