Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2008-2-25
pubmed:abstractText
von Willebrand Factor (vWF) structure-function relationship has been studied only in vitro. To investigate the physiological importance of particular vWF domains, we have introduced mutations into murine vWF (mvWF) cDNA inhibiting vWF binding to glycoprotein (Gp) Ib, GpIIbIIIa, and to fibrillar collagen.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
1524-4636
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
28
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
419-24
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:18187670-Animals, pubmed-meshheading:18187670-Bleeding Time, pubmed-meshheading:18187670-Blood Coagulation Tests, pubmed-meshheading:18187670-DNA, Complementary, pubmed-meshheading:18187670-Disease Models, Animal, pubmed-meshheading:18187670-Enzyme-Linked Immunosorbent Assay, pubmed-meshheading:18187670-Female, pubmed-meshheading:18187670-Gene Expression Regulation, pubmed-meshheading:18187670-Gene Therapy, pubmed-meshheading:18187670-Gene Transfer Techniques, pubmed-meshheading:18187670-Male, pubmed-meshheading:18187670-Mice, pubmed-meshheading:18187670-Mice, Inbred C57BL, pubmed-meshheading:18187670-Mice, Mutant Strains, pubmed-meshheading:18187670-Reference Values, pubmed-meshheading:18187670-Sensitivity and Specificity, pubmed-meshheading:18187670-von Willebrand Diseases, pubmed-meshheading:18187670-von Willebrand Factor
pubmed:year
2008
pubmed:articleTitle
Correction of bleeding symptoms in von Willebrand factor-deficient mice by liver-expressed von Willebrand factor mutants.
pubmed:affiliation
INSERM U770, 80 rue du Général Leclerc, 94276 Le Kremlin-Bicêtre Cedex, France.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't