Identification of domain A7 of collagen type VI α3 chain as a von Willebrand factor binding site.

被引：0

作者：

Mazzucato, M ^{[1
]}

Spessotto, P ^{[1
]}

De Appollonia, L ^{[1
]}

Cozzi, MR ^{[1
]}

Pradella, P ^{[1
]}

Perris, R ^{[1
]}

Colombatti, A ^{[1
]}

De Marco, L ^{[1
]}

机构：

[1] IRCCS, Ctr Riferimento Oncol, Aviano, PN, Italy

来源：

BLOOD | 1998年 / 92卷 / 10期

关键词：

D O I：

暂无

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

1418

引用

页码：345A / 345A

页数：1

共 50 条

[41] Identification of a binding site for integrin αIIbβ3 in the von Willebrand factor (VWF) A1 domain:: Dual roles for the A1 domain in platelet thrombus formation.
Chen, JM
Cruz, MA
López, JA
BLOOD, 2004, 104 (11) : 995A - 995A
[42] The D' domain of von Willebrand factor requires the presence of the D3 domain for optimal factor VIII binding
Przeradzka, Malgorzata A.
Meems, Henriet
van der Zwaan, Carmen
Ebberink, Eduard H. T. M.
van den Biggelaar, Maartje
Mertens, Koen
Meijer, Alexander B.
BIOCHEMICAL JOURNAL, 2018, 475 : 2819 - 2830
[43] Molecular assessment of FVIII binding site in von Willebrand factor gene in suspects patients of von Willebrand disease type 2N
Damian, G. B.
Santos, A.
Di Migueli, Oliveira C.
Siqueira, L.
Prezoti, A.
Di Paula, E.
Bizzacchi, J.
Ozelo, M.
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2009, 7 : 840 - 840
[44] Desmopressin enhances the binding of plasma von Willebrand factor to collagen in plasmas from normal dogs and dogs with Type I von Willebrand's disease
Johnstone, IB
CANADIAN VETERINARY JOURNAL-REVUE VETERINAIRE CANADIENNE, 1999, 40 (09): : 645 - 648
[45] The acidic region of the factor VIII light chain and the C2 domain together form a high affinity binding site for von Willebrand factor.
Saenko, EL
Scandella, D
BLOOD, 1996, 88 (10) : 1287 - 1287
[46] Case report of two siblings with type 2A von Willebrand disease involving a novel mutation within the calcium-binding site of the A2 domain of von Willebrand factor
Igid, Henry P.
Thein, Kyaw Z.
Castine, Michael
Quick, Donald P.
BLOOD COAGULATION & FIBRINOLYSIS, 2019, 30 (04) : 161 - 167
[47] Type 2M von Willebrand disease caused by a novel Q1402P substitution in the botrocetin binding site of the von Willebrand factor A1 domain.
Kroner, PA
Gill, JC
Haberichter, SL
Bellissimo, DB
Buchholz, N
Desai, DL
Montgomery, RR
BLOOD, 2003, 102 (11) : 543A - 544A
[48] Dominant type 1 von Willebrand disease caused by mutated cysteine residues in the D3 domain of von Willebrand factor
Eikenboom, JCJ
Matsushita, T
Reitsma, PH
Tuley, EA
Castaman, G
Briet, E
Sadler, JE
BLOOD, 1996, 88 (07) : 2433 - 2441
[49] LOCALIZATION OF BINDING-SITES WITHIN HUMAN VON WILLEBRAND FACTOR FOR MONOMERIC TYPE-III COLLAGEN
ROTH, GJ
TITANI, K
HOYER, LW
HICKEY, MJ
BIOCHEMISTRY, 1986, 25 (26) : 8357 - 8361
[50] Identification of a missense mutation (p.Leu1733Pro) in the A3 domain of von Willebrand factor in a family with type 2M von Willebrand disease
Toshio Shigekiyo
Hikaru Yagi
Etsuko Sekimoto
Hironobu Shibata
Shuji Ozaki
Masanori Matsumoto
International Journal of Hematology, 2020, 111 : 467 - 470

← 1 2 3 4 5 →