These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
438 related articles for article (PubMed ID: 8839848)
1. Type 2M:Milwaukee-1 von Willebrand disease: an in-frame deletion in the Cys509-Cys695 loop of the von Willebrand factor A1 domain causes deficient binding of von Willebrand factor to platelets. Mancuso DJ; Kroner PA; Christopherson PA; Vokac EA; Gill JC; Montgomery RR Blood; 1996 Oct; 88(7):2559-68. PubMed ID: 8839848 [TBL] [Abstract][Full Text] [Related]
2. Type 2M von Willebrand disease: F606I and I662F mutations in the glycoprotein Ib binding domain selectively impair ristocetin- but not botrocetin-mediated binding of von Willebrand factor to platelets. Hillery CA; Mancuso DJ; Evan Sadler J; Ponder JW; Jozwiak MA; Christopherson PA; Cox Gill J; Paul Scott J; Montgomery RR Blood; 1998 Mar; 91(5):1572-81. PubMed ID: 9473222 [TBL] [Abstract][Full Text] [Related]
3. Type 2M vWD resulting from a lysine deletion within a four lysine residue repeat in the A1 loop of von Willebrand factor. Hilbert L; Jenkins PV; Gaucher C; Meriane E; Collins PW; Pasi KJ; Mazurier C Thromb Haemost; 2000 Aug; 84(2):188-94. PubMed ID: 10959688 [TBL] [Abstract][Full Text] [Related]
4. N1421K mutation in the glycoprotein Ib binding domain impairs ristocetin- and botrocetin-mediated binding of von Willebrand factor to platelets. Lanke E; Kristoffersson AC; Isaksson C; Holmberg L; Lethagen S Eur J Haematol; 2008 Nov; 81(5):384-90. PubMed ID: 18637125 [TBL] [Abstract][Full Text] [Related]
5. Type IIB mutation His-505-->Asp implicates a new segment in the control of von Willebrand factor binding to platelet glycoprotein Ib. Rabinowitz I; Randi AM; Shindler KS; Tuley EA; Rustagi PK; Sadler JE J Biol Chem; 1993 Sep; 268(27):20497-501. PubMed ID: 8376405 [TBL] [Abstract][Full Text] [Related]
6. A new mutation, S1285F, within the A1 loop of von Willebrand factor induces a conformational change in A1 loop with abnormal binding to platelet GPIb and botrocetin causing type 2M von Willebrand disease. Stepanian A; Ribba AS; Lavergne JM; Fressinaud E; Juhan-Vague I; Mazurier C; Girma JP; Meyer D Br J Haematol; 2003 Feb; 120(4):643-51. PubMed ID: 12588351 [TBL] [Abstract][Full Text] [Related]
7. Expressed full-length von Willebrand factor containing missense mutations linked to type IIB von Willebrand disease shows enhanced binding to platelets. Kroner PA; Kluessendorf ML; Scott JP; Montgomery RR Blood; 1992 Apr; 79(8):2048-55. PubMed ID: 1373334 [TBL] [Abstract][Full Text] [Related]
8. Comparative analysis of type 2b von Willebrand disease mutations: implications for the mechanism of von Willebrand factor binding to platelets. Cooney KA; Ginsburg D Blood; 1996 Mar; 87(6):2322-8. PubMed ID: 8630394 [TBL] [Abstract][Full Text] [Related]
9. von Willebrand disease type B: a missense mutation selectively abolishes ristocetin-induced von Willebrand factor binding to platelet glycoprotein Ib. Rabinowitz I; Tuley EA; Mancuso DJ; Randi AM; Firkin BG; Howard MA; Sadler JE Proc Natl Acad Sci U S A; 1992 Oct; 89(20):9846-9. PubMed ID: 1409710 [TBL] [Abstract][Full Text] [Related]
10. Molecular modeling of ligand and mutation sites of the type A domains of human von Willebrand factor and their relevance to von Willebrand's disease. Jenkins PV; Pasi KJ; Perkins SJ Blood; 1998 Mar; 91(6):2032-44. PubMed ID: 9490688 [TBL] [Abstract][Full Text] [Related]
11. Analysis of the structure and function of the von Willebrand factor A1 domain using targeted deletions and alanine-scanning mutagenesis. Kroner PA; Frey AB Biochemistry; 1996 Oct; 35(41):13460-8. PubMed ID: 8873615 [TBL] [Abstract][Full Text] [Related]
12. Dominant type 1 von Willebrand disease caused by mutated cysteine residues in the D3 domain of von Willebrand factor. Eikenboom JC; Matsushita T; Reitsma PH; Tuley EA; Castaman G; Briƫt E; Sadler JE Blood; 1996 Oct; 88(7):2433-41. PubMed ID: 8839833 [TBL] [Abstract][Full Text] [Related]
13. Molecular genetics of type 2 von Willebrand disease. Fressinaud E; Mazurier C; Meyer D Int J Hematol; 2002 Jan; 75(1):9-18. PubMed ID: 11843298 [TBL] [Abstract][Full Text] [Related]
14. Identification of a new type 2M von Willebrand disease mutation also at position 1324 of von Willebrand factor. Hilbert L; Fressinaud E; Ribba AS; Meyer D; Mazurier C; Thromb Haemost; 2002 Apr; 87(4):635-40. PubMed ID: 12008946 [TBL] [Abstract][Full Text] [Related]
15. The arginine-552-cysteine (R1315C) mutation within the A1 loop of von Willebrand factor induces an abnormal folding with a loss of function resulting in type 2A-like phenotype of von Willebrand disease: study of 10 patients and mutated recombinant von Willebrand factor. Ribba AN; Hilbert L; Lavergne JM; Fressinaud E; Boyer-Neumann C; Ternisien C; Juhan-Vague I; Goudemand J; Girma J; Mazurier C; Meyer D Blood; 2001 Feb; 97(4):952-9. PubMed ID: 11159522 [TBL] [Abstract][Full Text] [Related]
17. Laboratory diagnosis of von Willebrand disease type 1/2E (2A subtype IIE), type 1 Vicenza and mild type 1 caused by mutations in the D3, D4, B1-B3 and C1-C2 domains of the von Willebrand factor gene. Role of von Willebrand factor multimers and the von Willebrand factor propeptide/antigen ratio. Gadisseur A; Berneman Z; Schroyens W; Michiels JJ Acta Haematol; 2009; 121(2-3):128-38. PubMed ID: 19506359 [TBL] [Abstract][Full Text] [Related]
18. Identification of amino acid residues essential for von Willebrand factor binding to platelet glycoprotein Ib. Charged-to-alanine scanning mutagenesis of the A1 domain of human von Willebrand factor. Matsushita T; Sadler JE J Biol Chem; 1995 Jun; 270(22):13406-14. PubMed ID: 7539426 [TBL] [Abstract][Full Text] [Related]
19. A novel von Willebrand factor mutation (I1372S) associated with type 2B-like von Willebrand disease: an elusive phenotype and a difficult diagnosis. Casonato A; Sartorello F; Pontara E; Gallinaro L; Bertomoro A; Grazia Cattini M; Daidone V; Szukowska M; Pagnan A Thromb Haemost; 2007 Dec; 98(6):1182-7. PubMed ID: 18064311 [TBL] [Abstract][Full Text] [Related]