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Items: 1 to 20 of 159

1.

Single-nucleotide variations defining previously unreported ADAMTS13 haplotypes are associated with differential expression and activity of the VWF-cleaving protease in a Salvadoran congenital thrombotic thrombocytopenic purpura family.

Kim B, Hing ZA, Wu A, Schiller T, Struble EB, Liuwantara D, Kempert PH, Broxham EJ, Edwards NC, Marder VJ, Simhadri VL, Sauna ZE, Howard TE, Kimchi-Sarfaty C.

Br J Haematol. 2014 Apr;165(1):154-8. doi: 10.1111/bjh.12713. Epub 2014 Jan 16. No abstract available.

PMID:
24433405
2.

In-vitro and in-vivo consequences of mutations in the von Willebrand factor cleaving protease ADAMTS13 in thrombotic thrombocytopenic purpura.

Donadelli R, Banterla F, Galbusera M, Capoferri C, Bucchioni S, Gastoldi S, Nosari S, Monteferrante G, Ruggeri ZM, Bresin E, Scheiflinger F, Rossi E, Martinez C, Coppo R, Remuzzi G, Noris M; International Registry of Recurrent and Familial HUS/TTP.

Thromb Haemost. 2006 Oct;96(4):454-64.

PMID:
17003922
3.

Keeping von Willebrand Factor under Control: Alternatives for ADAMTS13.

Tersteeg C, Fijnheer R, Pasterkamp G, de Groot PG, Vanhoorelbeke K, de Maat S, Maas C.

Semin Thromb Hemost. 2016 Feb;42(1):9-17. doi: 10.1055/s-0035-1564838. Epub 2015 Nov 23. Review.

PMID:
26595154
4.

Genetic defects leading to hereditary thrombotic thrombocytopenic purpura.

Kokame K, Miyata T.

Semin Hematol. 2004 Jan;41(1):34-40. Review.

PMID:
14727257
5.

von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome.

Furlan M, Robles R, Galbusera M, Remuzzi G, Kyrle PA, Brenner B, Krause M, Scharrer I, Aumann V, Mittler U, Solenthaler M, Lämmle B.

N Engl J Med. 1998 Nov 26;339(22):1578-84.

6.

Congenital thrombotic thrombocytopenic purpura caused by new compound heterozygous mutations of the ADAMTS13 gene.

Rank CU, Kremer Hovinga J, Taleghani MM, Lämmle B, Gøtze JP, Nielsen OJ.

Eur J Haematol. 2014 Feb;92(2):168-71. doi: 10.1111/ejh.12197. Epub 2013 Dec 10.

PMID:
24033710
7.

[ADAMTS13, von Willebrand factor specific cleaving protease].

Veyradier A, Coppo P.

Med Sci (Paris). 2011 Dec;27(12):1097-105. doi: 10.1051/medsci/20112712016. Epub 2011 Dec 23. Review. French.

8.

[From gene to disease; congenital thrombotic thrombocytopenic purpura due to mutations in the ADAMTS13 gene].

Schiphorst RH, van de Kar NC, van den Heuvel LP.

Ned Tijdschr Geneeskd. 2003 Dec 6;147(49):2422-4. Review. Dutch.

PMID:
14694551
9.

Von Willebrand factor, ADAMTS13, and thrombotic thrombocytopenic purpura.

Tsai HM.

J Mol Med (Berl). 2002 Oct;80(10):639-47. Epub 2002 Sep 5. Review.

PMID:
12395148
10.

Plasmin cleavage of von Willebrand factor as an emergency bypass for ADAMTS13 deficiency in thrombotic microangiopathy.

Tersteeg C, de Maat S, De Meyer SF, Smeets MW, Barendrecht AD, Roest M, Pasterkamp G, Fijnheer R, Vanhoorelbeke K, de Groot PG, Maas C.

Circulation. 2014 Mar 25;129(12):1320-31. doi: 10.1161/CIRCULATIONAHA.113.006727. Epub 2014 Jan 21.

PMID:
24449821
11.

[Genetic polymorphism of von Willebrand factor (VWF)-cleaving protease, ADAMTS13].

Kokame K.

Brain Nerve. 2008 Nov;60(11):1325-32. Review. Japanese.

PMID:
19069166
12.

Congenital thrombotic thrombocytopenic purpura in association with a mutation in the second CUB domain of ADAMTS13.

Pimanda JE, Maekawa A, Wind T, Paxton J, Chesterman CN, Hogg PJ.

Blood. 2004 Jan 15;103(2):627-9. Epub 2003 Sep 25.

PMID:
14512317
13.
14.

Pathogenesis of thrombotic thrombocytopenic purpura: ADAMTS13 deficiency and beyond.

Lian EC.

Semin Thromb Hemost. 2005 Dec;31(6):625-32. Review.

PMID:
16388413
15.
16.

Molecular characterization of four ADAMTS13 mutations responsible for congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome).

Hommais A, Rayes J, Houllier A, Obert B, Legendre P, Veyradier A, Girma JP, Ribba AS.

Thromb Haemost. 2007 Sep;98(3):593-9.

PMID:
17849048
17.

Von Willebrand factor, ADAMTS-13, and thrombotic thrombocytopenic purpura.

Zhou Z, Nguyen TC, Guchhait P, Dong JF.

Semin Thromb Hemost. 2010 Feb;36(1):71-81. doi: 10.1055/s-0030-1248726. Epub 2010 Apr 13. Review.

PMID:
20391298
18.

[Hereditary form of thrombotic thrombocytopenic purpura].

Hrachovinová I, Rittich S, Salaj P, Suttnar J, Dyr JE, Suláková T, Pták J, Dulícek P, Seeman T.

Cas Lek Cesk. 2006;145(5):390-2. Czech.

PMID:
16755777
19.

Platelet activation and the formation of the platelet plug: deficiency of ADAMTS13 causes thrombotic thrombocytopenic purpura.

Tsai HM.

Arterioscler Thromb Vasc Biol. 2003 Mar 1;23(3):388-96. Epub 2003 Jan 30. Review.

PMID:
12615692
20.

An autoantibody epitope comprising residues R660, Y661, and Y665 in the ADAMTS13 spacer domain identifies a binding site for the A2 domain of VWF.

Pos W, Crawley JT, Fijnheer R, Voorberg J, Lane DA, Luken BM.

Blood. 2010 Feb 25;115(8):1640-9. doi: 10.1182/blood-2009-06-229203. Epub 2009 Dec 23.

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