-
1
-
-
0037158606
-
Thrombotic microangiopathies
-
Moake JL. Thrombotic microangiopathies. N Engl J Med 2002;347:589-600.
-
(2002)
N Engl J Med
, vol.347
, pp. 589-600
-
-
Moake, J.L.1
-
2
-
-
0029925856
-
Partial purification and characterization of a protease from human plasma cleaving von Willebrand factor to fragments produced by in vivo proteolysis
-
Furlan M, Robles R, Läemmle B. Partial purification and characterization of a protease from human plasma cleaving von Willebrand factor to fragments produced by in vivo proteolysis. Blood 1996;87:4223-34.
-
(1996)
Blood
, vol.87
, pp. 4223-4234
-
-
Furlan, M.1
Robles, R.2
Läemmle, B.3
-
3
-
-
0030973267
-
Deficient activity of von Willebrand factor-cleaving protease in chronic relapsing thrombotic thrombocytopenic purpura
-
Furlan M, Robles R, Solenthaler M, Wassmer M, Sandoz P, Lämmle B. Deficient activity of von Willebrand factor-cleaving protease in chronic relapsing thrombotic thrombocytopenic purpura. Blood 1997;89:3097-103.
-
(1997)
Blood
, vol.89
, pp. 3097-3103
-
-
Furlan, M.1
Robles, R.2
Solenthaler, M.3
Wassmer, M.4
Sandoz, P.5
Lämmle, B.6
-
4
-
-
0032569884
-
von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolyticuremic syndrome
-
Furlan M, Robles R, Galbusera M, Remuzzi G, Kyrle PA, Brenner B, et al. von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolyticuremic syndrome. N Engl J Med 1998;339:1578-84.
-
(1998)
N Engl J Med
, vol.339
, pp. 1578-1584
-
-
Furlan, M.1
Robles, R.2
Galbusera, M.3
Remuzzi, G.4
Kyrle, P.A.5
Brenner, B.6
-
5
-
-
0025044664
-
Identification of a cleavage site directing the immunochemical detection of molecular abnormalities in type IIA von Willebrand factor
-
Dent JA, Berkowitz SD, Ware J, Kasper CK, Ruggeri ZM. Identification of a cleavage site directing the immunochemical detection of molecular abnormalities in type IIA von Willebrand factor. Proc Natl Acad Sci USA 1990;87: 6306-10.
-
(1990)
Proc Natl Acad Sci USA
, vol.87
, pp. 6306-6310
-
-
Dent, J.A.1
Berkowitz, S.D.2
Ware, J.3
Kasper, C.K.4
Ruggeri, Z.M.5
-
6
-
-
0035885972
-
Purification of human von Willebrand factor-cleaving protease and its identification as a new member of the metalloproteinase family
-
Fujikawa K, Suzuki H, McMullen B, Chung D. Purification of human von Willebrand factor-cleaving protease and its identification as a new member of the metalloproteinase family. Blood 2001;98:1662-6.
-
(2001)
Blood
, vol.98
, pp. 1662-1666
-
-
Fujikawa, K.1
Suzuki, H.2
McMullen, B.3
Chung, D.4
-
7
-
-
0029878123
-
Physiologic cleavage of von Willebrand factor by a plasma protease is dependent on its conformation and requires calcium ion
-
Tsai HM. Physiologic cleavage of von Willebrand factor by a plasma protease is dependent on its conformation and requires calcium ion. Blood 1996;87:4235-44.
-
(1996)
Blood
, vol.87
, pp. 4235-4244
-
-
Tsai, H.M.1
-
8
-
-
0035807348
-
Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura
-
Levy GG, Nichols WC, Lian EC, Foroud T, McClintick JN, McGee BM, et al. Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura. Nature 2001;413:488-94.
-
(2001)
Nature
, vol.413
, pp. 488-494
-
-
Levy, G.G.1
Nichols, W.C.2
Lian, E.C.3
Foroud, T.4
McClintick, J.N.5
McGee, B.M.6
-
9
-
-
0035885962
-
Partial amino acid sequence of purified von Willebrand factor-cleaving protease
-
Gerritsen HE, Robles R, Lämmle B, Furlan M. Partial amino acid sequence of purified von Willebrand factor-cleaving protease. Blood 2001;98:1654-61.
-
(2001)
Blood
, vol.98
, pp. 1654-1661
-
-
Gerritsen, H.E.1
Robles, R.2
Lämmle, B.3
Furlan, M.4
-
10
-
-
0035798582
-
Structure of von Willebrand factor-cleaving protease (ADAMTS13), a metalloprotease involved in thrombotic thrombocytopenic purpura
-
Zheng X, Chung D, Takayama TK, Majerus EM, Sadler JE, Fujikawa K. Structure of von Willebrand factor-cleaving protease (ADAMTS13), a metalloprotease involved in thrombotic thrombocytopenic purpura. J Biol Chem 2001;276:41059-63.
-
(2001)
J Biol Chem
, vol.276
, pp. 41059-41063
-
-
Zheng, X.1
Chung, D.2
Takayama, T.K.3
Majerus, E.M.4
Sadler, J.E.5
Fujikawa, K.6
-
11
-
-
0346095394
-
Genetic defects leading to hereditary thrombotic thrombocytopenic purpura
-
Kokame K, Miyata T. Genetic defects leading to hereditary thrombotic thrombocytopenic purpura. Semin Hematol 2004;41:34-40.
-
(2004)
Semin Hematol
, vol.41
, pp. 34-40
-
-
Kokame, K.1
Miyata, T.2
-
12
-
-
0032522952
-
Acquired deficiency of von Willebrand factor-cleaving protease in a patient with thrombotic thrombocytopenic purpura
-
Furlan M, Robles R, Solenthaler M, Lämmle B. Acquired deficiency of von Willebrand factor-cleaving protease in a patient with thrombotic thrombocytopenic purpura. Blood 1998;91:2839-46.
-
(1998)
Blood
, vol.91
, pp. 2839-2846
-
-
Furlan, M.1
Robles, R.2
Solenthaler, M.3
Lämmle, B.4
-
13
-
-
0032569840
-
Antibodies to von Willebrand factor-cleaving protease in acute thrombotic thrombocytopenic purpura
-
Tsai HM, Lian EC. Antibodies to von Willebrand factor-cleaving protease in acute thrombotic thrombocytopenic purpura. N Engl J Med 1998;339:1585-94.
-
(1998)
N Engl J Med
, vol.339
, pp. 1585-1594
-
-
Tsai, H.M.1
Lian, E.C.2
-
14
-
-
32944456736
-
Current concepts in thrombotic thrombocytopenic purpura
-
Tsai HM. Current concepts in thrombotic thrombocytopenic purpura. Annu Rev Med 2006;57:419-36.
-
(2006)
Annu Rev Med
, vol.57
, pp. 419-436
-
-
Tsai, H.M.1
-
15
-
-
0037015057
-
Mutations and common polymorphisms in ADAMTS13 gene responsible for von Willebrand factor-cleaving protease activity
-
Kokame K, Matsumoto M, Soejima K, Yagi H, Ishizashi H, Funato M, et al. Mutations and common polymorphisms in ADAMTS13 gene responsible for von Willebrand factor-cleaving protease activity. Proc Natl Acad Sci USA 2002;99:11902-7.
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 11902-11907
-
-
Kokame, K.1
Matsumoto, M.2
Soejima, K.3
Yagi, H.4
Ishizashi, H.5
Funato, M.6
-
16
-
-
10744226155
-
Molecular characterization of ADAMTS13 gene mutations in Japanese patients with Upshaw-Schulman syndrome
-
Matsumoto M, Kokame K, Soejima K, Miura M, Hayashi S, Fujii Y, et al. Molecular characterization of ADAMTS13 gene mutations in Japanese patients with Upshaw-Schulman syndrome. Blood 2003;103:1305-10.
-
(2003)
Blood
, vol.103
, pp. 1305-1310
-
-
Matsumoto, M.1
Kokame, K.2
Soejima, K.3
Miura, M.4
Hayashi, S.5
Fujii, Y.6
-
17
-
-
33645774439
-
Mechanisms of the interaction between two ADAMTS13 gene mutations leading to severe deficiency of enzymatic activity
-
Peyvandi F, Lavoretano S, Palla R, Valsecchi C, Merati G, De Cristofaro R, et al. Mechanisms of the interaction between two ADAMTS13 gene mutations leading to severe deficiency of enzymatic activity. Hum Mutat 2006;27:330-6.
-
(2006)
Hum Mutat
, vol.27
, pp. 330-336
-
-
Peyvandi, F.1
Lavoretano, S.2
Palla, R.3
Valsecchi, C.4
Merati, G.5
De Cristofaro, R.6
-
18
-
-
0942287728
-
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. Congenital thrombotic thrombocytopenic purpura in association with a mutation in the second CUB domain of ADAMTS13. Blood 2004;103:627-9.
-
(2004)
Blood
, vol.103
, pp. 627-629
-
-
Pimanda, J.E.1
Maekawa, A.2
Wind, T.3
Paxton, J.4
Chesterman, C.N.5
Hogg, P.J.6
-
19
-
-
4644271599
-
Identification of novel mutations in ADAMTS13 in an adult patient with congenital thrombotic thrombocytopenic purpura
-
Uchida T, Wada H, Mizutani M, Iwashita M, Ishihara H, Shibano T, et al. Identification of novel mutations in ADAMTS13 in an adult patient with congenital thrombotic thrombocytopenic purpura. Blood 2004;104:2081-3.
-
(2004)
Blood
, vol.104
, pp. 2081-2083
-
-
Uchida, T.1
Wada, H.2
Mizutani, M.3
Iwashita, M.4
Ishihara, H.5
Shibano, T.6
-
20
-
-
0037372508
-
von Willebrand factor cleaving protease and ADAMTS13 mutations in childhood TTP
-
Schneppenheim R, Budde U, Oyen F, Angerhaus D, Aumann V, Drewke E, et al. von Willebrand factor cleaving protease and ADAMTS13 mutations in childhood TTP. Blood 2003;101:1845-50.
-
(2003)
Blood
, vol.101
, pp. 1845-1850
-
-
Schneppenheim, R.1
Budde, U.2
Oyen, F.3
Angerhaus, D.4
Aumann, V.5
Drewke, E.6
-
21
-
-
8844286829
-
von Willebrand factor cleaving protease (ADAMTS-13) and ADAMTS-13 neutralizing autoantibodies in 100 patients with thrombotic thrombocytopenic purpura
-
Peyvandi F, Ferrari S, Lavoretano S, Canciani MT, Mannucci PM. von Willebrand factor cleaving protease (ADAMTS-13) and ADAMTS-13 neutralizing autoantibodies in 100 patients with thrombotic thrombocytopenic purpura. Br J Haematol 2004;27:433-9.
-
(2004)
Br J Haematol
, vol.27
, pp. 433-439
-
-
Peyvandi, F.1
Ferrari, S.2
Lavoretano, S.3
Canciani, M.T.4
Mannucci, P.M.5
-
22
-
-
0004423852
-
Assay of von Willebrand factor (vWF)-cleaving protease based on decreased collagen binding affinity of degraded vWF: A tool for the diagnosis of thrombotic thrombocytopenic purpura (TTP)
-
Gerritsen HE, Turecek PL, Schwarz HP, Lämmle B, Furlan M. Assay of von Willebrand factor (vWF)-cleaving protease based on decreased collagen binding affinity of degraded vWF: a tool for the diagnosis of thrombotic thrombocytopenic purpura (TTP). Thromb Haemost 1999;82:1386-9.
-
(1999)
Thromb Haemost
, vol.82
, pp. 1386-1389
-
-
Gerritsen, H.E.1
Turecek, P.L.2
Schwarz, H.P.3
Lämmle, B.4
Furlan, M.5
-
23
-
-
33645642908
-
ADAMTS-13 plasma level determination uncovers antigen absence in acquired thrombotic thrombocytopenic purpura and ethnic differences
-
Feys HB, Liu F, Dong N, Pareyn I, Vauterin S, Vandeputte N, et al. ADAMTS-13 plasma level determination uncovers antigen absence in acquired thrombotic thrombocytopenic purpura and ethnic differences. J Thromb Haemost 2006;4:955-62.
-
(2006)
J Thromb Haemost
, vol.4
, pp. 955-962
-
-
Feys, H.B.1
Liu, F.2
Dong, N.3
Pareyn, I.4
Vauterin, S.5
Vandeputte, N.6
-
24
-
-
34447309717
-
ADAMTS13 activity to antigen ratio in physiological and pathological conditions associated with an increased risk of thrombosis
-
Feys HB, Canciani MT, Peyvandi F, Deckmyn H, Vanhoorelbeke K, Mannucci PM. ADAMTS13 activity to antigen ratio in physiological and pathological conditions associated with an increased risk of thrombosis. Br J Haematol 2007;138:534-40.
-
(2007)
Br J Haematol
, vol.138
, pp. 534-540
-
-
Feys, H.B.1
Canciani, M.T.2
Peyvandi, F.3
Deckmyn, H.4
Vanhoorelbeke, K.5
Mannucci, P.M.6
-
25
-
-
40849114959
-
ADAMTS13 and anti-ADAMTS13 antibodies as markers for recurrence of acquired thrombotic thrombocytopenic purpura during remission
-
Peyvandi F, Lavoretano S, Palla R, Feys HB, Vanhoorelbeke K, Battaglioli T, et al. ADAMTS13 and anti-ADAMTS13 antibodies as markers for recurrence of acquired thrombotic thrombocytopenic purpura during remission. Haematologica 2008;93:232-9.
-
(2008)
Haematologica
, vol.93
, pp. 232-239
-
-
Peyvandi, F.1
Lavoretano, S.2
Palla, R.3
Feys, H.B.4
Vanhoorelbeke, K.5
Battaglioli, T.6
-
26
-
-
0024284028
-
A simple salting out procedure for extracting DNA from human nucleated cells
-
Miller I, Djkes DD. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acid Res 1988;16:1215-20.
-
(1988)
Nucleic Acid Res
, vol.16
, pp. 1215-1220
-
-
Miller, I.1
Djkes, D.D.2
-
27
-
-
33746742947
-
A common origin of the 4143insA ADAMTS13 mutation
-
Schneppenheim R, Kremer Hovinga JA, Becker T, Budde U, Karpman D, Brockhaus W, et al. A common origin of the 4143insA ADAMTS13 mutation. Thromb Haemost 2006;96:3-6.
-
(2006)
Thromb Haemost
, vol.96
, pp. 3-6
-
-
Schneppenheim, R.1
Kremer Hovinga, J.A.2
Becker, T.3
Budde, U.4
Karpman, D.5
Brockhaus, W.6
-
28
-
-
27644516551
-
Role of the 2 adenine (g.11293_11294insAA) insertion polymorphism in the 3′ untranslated region of the factor VII (FVII) gene: Molecular characterization of a patient with severe FVII deficiency
-
Peyvandi F, Garagiola I, Palla R, Marziliano N, Mannucci PM. Role of the 2 adenine (g.11293_11294insAA) insertion polymorphism in the 3′ untranslated region of the factor VII (FVII) gene: molecular characterization of a patient with severe FVII deficiency. Hum Mutat 2005;26:455-61.
-
(2005)
Hum Mutat
, vol.26
, pp. 455-461
-
-
Peyvandi, F.1
Garagiola, I.2
Palla, R.3
Marziliano, N.4
Mannucci, P.M.5
-
29
-
-
0027536976
-
Nonsense codons can reduce the abundance of nuclear mRNA without affecting the abundance of pre-mRNA or the half-life of cytoplasmic mRNA
-
Cheng J, Maquat LE. Nonsense codons can reduce the abundance of nuclear mRNA without affecting the abundance of pre-mRNA or the half-life of cytoplasmic mRNA. Mol Cell Biol 1993;13:1892-902.
-
(1993)
Mol Cell Biol
, vol.13
, pp. 1892-1902
-
-
Cheng, J.1
Maquat, L.E.2
-
30
-
-
0029330286
-
When cells stop making sense: Effects of nonsense codons on RNA metabolism in vertebrate cells
-
Maquat LE. When cells stop making sense: effects of nonsense codons on RNA metabolism in vertebrate cells. RNA 1995;1:453-65.
-
(1995)
RNA
, vol.1
, pp. 453-465
-
-
Maquat, L.E.1
-
31
-
-
19444368979
-
Nonsense-mediated mRNA decay in mammals
-
Maquat LE. Nonsense-mediated mRNA decay in mammals. J Cell Sci 2005;118:1773-6.
-
(2005)
J Cell Sci
, vol.118
, pp. 1773-1776
-
-
Maquat, L.E.1
-
32
-
-
0036142862
-
Killing the messenger: New insights into nonsense-mediated mRNA decay
-
Byers PH. Killing the messenger: new insights into nonsense-mediated mRNA decay. J Clin Invest 2002;109:3-6.
-
(2002)
J Clin Invest
, vol.109
, pp. 3-6
-
-
Byers, P.H.1
-
33
-
-
0027993583
-
Introns are cis effectors of the nonsense-codon-mediated reduction in nuclear mRNA abundance
-
Cheng J, Belgrader P, Zhou X, Maquat LE. Introns are cis effectors of the nonsense-codon-mediated reduction in nuclear mRNA abundance. Mol Cell Biol 1994;14:6317-25.
-
(1994)
Mol Cell Biol
, vol.14
, pp. 6317-6325
-
-
Cheng, J.1
Belgrader, P.2
Zhou, X.3
Maquat, L.E.4
-
34
-
-
0031840487
-
At least one intron is required for the nonsense-mediated decay of triosephosphate isomerase mRNA: A possible link between nuclear splicing and cytoplasmic translation
-
Zhang J, Sun X, Qian Y, La Duca JP, Maquat LE. At least one intron is required for the nonsense-mediated decay of triosephosphate isomerase mRNA: a possible link between nuclear splicing and cytoplasmic translation. Mol Cell Biol 1998;18:5272-83.
-
(1998)
Mol Cell Biol
, vol.18
, pp. 5272-5283
-
-
Zhang, J.1
Sun, X.2
Qian, Y.3
La Duca, J.P.4
Maquat, L.E.5
-
35
-
-
0037335672
-
ADAMTS13 gene defects in two brothers with constitutional thrombotic thrombocytopenic purpura and normalization of von Willebrand factor-cleaving protease activity by recombinant human ADAMTS13
-
Antoine G, Zimmermann K, Plaimauer B, Grillowitzer M, Studt JD, Lämmle B, et al. ADAMTS13 gene defects in two brothers with constitutional thrombotic thrombocytopenic purpura and normalization of von Willebrand factor-cleaving protease activity by recombinant human ADAMTS13. Br J Haematol 2003;120:821-4.
-
(2003)
Br J Haematol
, vol.120
, pp. 821-824
-
-
Antoine, G.1
Zimmermann, K.2
Plaimauer, B.3
Grillowitzer, M.4
Studt, J.D.5
Lämmle, B.6
-
36
-
-
4344637504
-
Two novel ADAMTS13 gene mutations in thrombotic thrombocytopenic purpura/hemolytic-uremic syndrome (TTP/HUS)
-
Licht C, Stapenhorst L, Simon T, Budde U, Schneppenheim R, Hoppe B. Two novel ADAMTS13 gene mutations in thrombotic thrombocytopenic purpura/hemolytic-uremic syndrome (TTP/HUS). Kidney Int 2004;66:955-8.
-
(2004)
Kidney Int
, vol.66
, pp. 955-958
-
-
Licht, C.1
Stapenhorst, L.2
Simon, T.3
Budde, U.4
Schneppenheim, R.5
Hoppe, B.6
|