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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2001 | 1 |
2009 | 1 |
2010 | 1 |
2014 | 1 |
2015 | 1 |
2016 | 1 |
2024 | 0 |
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6 results
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Page 1
Characterization of W1745C and S1783A: 2 novel mutations causing defective collagen binding in the A3 domain of von Willebrand factor.
Blood. 2009 Oct 15;114(16):3489-96. doi: 10.1182/blood-2008-10-184317. Epub 2009 Aug 17.
Blood. 2009.
PMID: 19687512
Free article.
Absent collagen binding in a VWF A3 domain mutant: utility of the VWF:CB in diagnosis of VWD.
Flood VH, Lederman CA, Wren JS, Christopherson PA, Friedman KD, Hoffmann RG, Montgomery RR.
Flood VH, et al.
J Thromb Haemost. 2010 Jun;8(6):1431-3. doi: 10.1111/j.1538-7836.2010.03869.x. Epub 2010 Mar 23.
J Thromb Haemost. 2010.
PMID: 20345715
Free PMC article.
No abstract available.
Item in Clipboard
Analysis of the role of von Willebrand factor, platelet glycoprotein VI-, and α2β1-mediated collagen binding in thrombus formation.
Shida Y, Rydz N, Stegner D, Brown C, Mewburn J, Sponagle K, Danisment O, Crawford B, Vidal B, Hegadorn CA, Pruss CM, Nieswandt B, Lillicrap D.
Shida Y, et al.
Blood. 2014 Sep 11;124(11):1799-807. doi: 10.1182/blood-2013-09-521484. Epub 2014 Jul 22.
Blood. 2014.
PMID: 25051961
Free PMC article.
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Crucial role for the VWF A1 domain in binding to type IV collagen.
Flood VH, Schlauderaff AC, Haberichter SL, Slobodianuk TL, Jacobi PM, Bellissimo DB, Christopherson PA, Friedman KD, Gill JC, Hoffmann RG, Montgomery RR; Zimmerman Program Investigators.
Flood VH, et al.
Blood. 2015 Apr 2;125(14):2297-304. doi: 10.1182/blood-2014-11-610824. Epub 2015 Feb 6.
Blood. 2015.
PMID: 25662333
Free PMC article.
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A Laboratory Phenotype/Genotype Correlation of 1167 French Patients From 670 Families With von Willebrand Disease: A New Epidemiologic Picture.
Veyradier A, Boisseau P, Fressinaud E, Caron C, Ternisien C, Giraud M, Zawadzki C, Trossaert M, Itzhar-Baïkian N, Dreyfus M, d'Oiron R, Borel-Derlon A, Susen S, Bezieau S, Denis CV, Goudemand J; French Reference Center for von Willebrand disease.
Veyradier A, et al.
Medicine (Baltimore). 2016 Mar;95(11):e3038. doi: 10.1097/MD.0000000000003038.
Medicine (Baltimore). 2016.
PMID: 26986123
Free PMC article.
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Ser968Thr mutation within the A3 domain of von Willebrand factor (VWF) in two related patients leads to a defective binding of VWF to collagen.
Ribba AS, Loisel I, Lavergne JM, Juhan-Vague I, Obert B, Cherel G, Meyer D, Girma JP.
Ribba AS, et al.
Thromb Haemost. 2001 Sep;86(3):848-54.
Thromb Haemost. 2001.
PMID: 11583318
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