Source:http://linkedlifedata.com/resource/pubmed/id/19548905
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2009-6-24
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pubmed:abstractText |
Functional deficiency of ADAMTS13 in thrombotic thrombocytopenic purpura (TTP) patients is associated with circulating ultralarge von Willebrand factor (VWF) molecules that display spontaneous platelet-binding capacities. Upon remission, however, ADAMTS13 activity does not always return to baseline.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1538-7836
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
7
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
962-9
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pubmed:meshHeading |
pubmed-meshheading:19548905-ADAM Proteins,
pubmed-meshheading:19548905-Cells, Cultured,
pubmed-meshheading:19548905-Enzyme-Linked Immunosorbent Assay,
pubmed-meshheading:19548905-Humans,
pubmed-meshheading:19548905-Immunoprecipitation,
pubmed-meshheading:19548905-Protein Conformation,
pubmed-meshheading:19548905-Purpura, Thrombotic Thrombocytopenic,
pubmed-meshheading:19548905-von Willebrand Factor
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pubmed:year |
2009
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pubmed:articleTitle |
The active conformation of von Willebrand factor in patients with thrombotic thrombocytopenic purpura in remission.
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pubmed:affiliation |
Department of Clinical Chemistry and Haematology, University Medical Centre Utrecht, Utrecht, the Netherlands.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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