Nolasco JG - Search Results

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Complement Component C3 Binds to the A3 Domain of von Willebrand Factor.

Nolasco JG, Nolasco LH, Da Q, Cirlos S, Ruggeri ZM, Moake JL, Cruz MA. Nolasco JG, et al. TH Open. 2018;2(3):e338-e345. doi: 10.1055/s-0038-1672189. TH Open. 2018. PMID: 31080944 Free PMC article.

In vitro phosphorylation of von Willebrand factor by FAM20c enhances its ability to support platelet adhesion.

Da Q, Han H, Valladolid C, Fernández M, Khatlani T, Pradhan S, Nolasco J, Matsunami RK, Engler DA, Cruz MA, Vijayan KV. Da Q, et al. J Thromb Haemost. 2019 Jun;17(6):866-877. doi: 10.1111/jth.14426. Epub 2019 Apr 5. J Thromb Haemost. 2019. PMID: 30864273 Free PMC article.

Thrombotic microangiopathies and the linkage between von Willebrand factor and the alternative complement pathway.

Turner N, Nolasco L, Nolasco J, Sartain S, Moake J. Turner N, et al. Semin Thromb Hemost. 2014 Jul;40(5):544-50. doi: 10.1055/s-0034-1383547. Epub 2014 Jun 26. Semin Thromb Hemost. 2014. PMID: 24967890 Review.

Human complement factor H is a reductase for large soluble von Willebrand factor multimers--brief report.

Nolasco L, Nolasco J, Feng S, Afshar-Kharghan V, Moake J. Nolasco L, et al. Arterioscler Thromb Vasc Biol. 2013 Nov;33(11):2524-8. doi: 10.1161/ATVBAHA.113.302280. Epub 2013 Sep 5. Arterioscler Thromb Vasc Biol. 2013. PMID: 24008159

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