-
1
-
-
0026337077
-
The coagulation cascade: Initiation, maintenance and regulation
-
Davie EW, Fujikawa K, Kisiel W: The coagulation cascade: Initiation, maintenance and regulation. Biochemistry 30:10363, 1991
-
(1991)
Biochemistry
, vol.30
, pp. 10363
-
-
Davie, E.W.1
Fujikawa, K.2
Kisiel, W.3
-
2
-
-
0025815673
-
Factor XI deficiency in Ashkenazi Jews in Israel
-
Asakai R, Chung DW, Davie EW, Seligsohn U: Factor XI deficiency in Ashkenazi Jews in Israel. N Engl J Med 325:153, 1991
-
(1991)
N Engl J Med
, vol.325
, pp. 153
-
-
Asakai, R.1
Chung, D.W.2
Davie, E.W.3
Seligsohn, U.4
-
3
-
-
0004460795
-
The frequency of the type II and type III mutations causing factor XI deficiency in the general Jewish population
-
abstr
-
Seligsohn U, Weiss E, Kulka T, Eichel R, Zwang E, Peretz H: The frequency of the type II and type III mutations causing factor XI deficiency in the general Jewish population. Thromb Haemost 69:1297, 1993 (abstr)
-
(1993)
Thromb Haemost
, vol.69
, pp. 1297
-
-
Seligsohn, U.1
Weiss, E.2
Kulka, T.3
Eichel, R.4
Zwang, E.5
Peretz, H.6
-
4
-
-
0025817821
-
Factor XI: A review of its biochemistry and deficiency
-
Kitchens CS: Factor XI: A review of its biochemistry and deficiency. Semin Thromb Hemost 17:55, 1991
-
(1991)
Semin Thromb Hemost
, vol.17
, pp. 55
-
-
Kitchens, C.S.1
-
5
-
-
0027216858
-
Factor XI deficiency
-
Seligsohn U: Factor XI deficiency. Thromb Haemost 70:68, 1993
-
(1993)
Thromb Haemost
, vol.70
, pp. 68
-
-
Seligsohn, U.1
-
6
-
-
0028505156
-
Advances and dilemmas in factor XI
-
Gailani D: Advances and dilemmas in factor XI. Curr Opin Hematol 1:347, 1994
-
(1994)
Curr Opin Hematol
, vol.1
, pp. 347
-
-
Gailani, D.1
-
7
-
-
0013815101
-
Heredity and coagulation studies in ten families with factor XI (plasma thromboplastin antecedent) deficiency
-
Leiba H, Ramot B, Many R: Heredity and coagulation studies in ten families with factor XI (plasma thromboplastin antecedent) deficiency. Br J Haematol 11:654, 1965
-
(1965)
Br J Haematol
, vol.11
, pp. 654
-
-
Leiba, H.1
Ramot, B.2
Many, R.3
-
8
-
-
0021987658
-
Comparison of bleeding tendency, factor XI coagulant activity, and factor XI antigen in 25 factor XI-deficient kindreds
-
Ragni MV, Sinha D, Seaman F, Lewis JH, Spero JA, Walsh PN: Comparison of bleeding tendency, factor XI coagulant activity, and factor XI antigen in 25 factor XI-deficient kindreds. Blood 65:719, 1985
-
(1985)
Blood
, vol.65
, pp. 719
-
-
Ragni, M.V.1
Sinha, D.2
Seaman, F.3
Lewis, J.H.4
Spero, J.A.5
Walsh, P.N.6
-
9
-
-
0023731215
-
Inheritance and bleeding in factor XI deficiency
-
Bolton-Maggs PHB, Wan-Yin BY, McCraw AH, Slack J, Kernoff PBA: Inheritance and bleeding in factor XI deficiency. Br J Haematol 69:521, 1988
-
(1988)
Br J Haematol
, vol.69
, pp. 521
-
-
Bolton-Maggs, P.H.B.1
Wan-Yin, B.Y.2
McCraw, A.H.3
Slack, J.4
Kernoff, P.B.A.5
-
10
-
-
0000126344
-
The mode of inheritance of PTA deficiency: Evidence for the existence of major PTA deficiency and minor PTA deficiency
-
Rappaport SI, Proctor RR, Patch MJ, Yettra M: The mode of inheritance of PTA deficiency: Evidence for the existence of major PTA deficiency and minor PTA deficiency. Blood 18:149, 1961
-
(1961)
Blood
, vol.18
, pp. 149
-
-
Rappaport, S.I.1
Proctor, R.R.2
Patch, M.J.3
Yettra, M.4
-
11
-
-
0018105016
-
Factor XI deficiency: Detection and management during urologic surgery
-
Sidi A, Seligsohn U, Jonas P, Many M: Factor XI deficiency: Detection and management during urologic surgery. J Urol 119:528, 1978
-
(1978)
J Urol
, vol.119
, pp. 528
-
-
Sidi, A.1
Seligsohn, U.2
Jonas, P.3
Many, M.4
-
13
-
-
3042761915
-
Clinical and laboratory studies of plasma thromboplastin antecedent deficiency (PTA)
-
Cavins JA, Wall RL: Clinical and laboratory studies of plasma thromboplastin antecedent deficiency (PTA). Am J Med 29:444, 1960
-
(1960)
Am J Med
, vol.29
, pp. 444
-
-
Cavins, J.A.1
Wall, R.L.2
-
14
-
-
0023906675
-
Factor XI deficiency: Genetic and clinical studies of a single kindred
-
Litz CE, Swaim WR, Dalmasso AP: Factor XI deficiency: Genetic and clinical studies of a single kindred. Am J Hematol 28:8, 1988
-
(1988)
Am J Hematol
, vol.28
, pp. 8
-
-
Litz, C.E.1
Swaim, W.R.2
Dalmasso, A.P.3
-
15
-
-
0017740353
-
Human blood coagulation factor XI, purification, properties, and mechanism of activation by activated factor XII
-
Bouma BN, Griffin JH: Human blood coagulation factor XI, purification, properties, and mechanism of activation by activated factor XII. J Biol Chem 252:6432, 1977
-
(1977)
J Biol Chem
, vol.252
, pp. 6432
-
-
Bouma, B.N.1
Griffin, J.H.2
-
16
-
-
0027500241
-
Von Willebrand disease: A database of point mutations, insertions, and deletions
-
Ginsburg D, Sadler JE: von Willebrand disease: A database of point mutations, insertions, and deletions. Thromb Haemost 69:177, 1993
-
(1993)
Thromb Haemost
, vol.69
, pp. 177
-
-
Ginsburg, D.1
Sadler, J.E.2
-
17
-
-
0022252887
-
Failure to detect variant (CRM+) plasma thromboplastin antecedent (factor XI) molecules in hereditary plasma thromboplastin antecedent deficiency: A study of 125 patients of several ethnic backgrounds
-
Saito H, Ratnoff OD, Bouma BN, Seligsohn U: Failure to detect variant (CRM+) plasma thromboplastin antecedent (factor XI) molecules in hereditary plasma thromboplastin antecedent deficiency: A study of 125 patients of several ethnic backgrounds. J Lab Clin Med 106:718, 1985
-
(1985)
J Lab Clin Med
, vol.106
, pp. 718
-
-
Saito, H.1
Ratnoff, O.D.2
Bouma, B.N.3
Seligsohn, U.4
-
18
-
-
0012992989
-
Factor XI (plasma thromboplastin antecedent) deficiency in Ashkenazi Jews is a bleeding disorder that can result from three types of point mutations
-
Asaki R, Chung DW, Ratnoff OD, Davie EW: Factor XI (plasma thromboplastin antecedent) deficiency in Ashkenazi Jews is a bleeding disorder that can result from three types of point mutations. Proc Natl Acad Sci USA 86:7667, 1989
-
(1989)
Proc Natl Acad Sci USA
, vol.86
, pp. 7667
-
-
Asaki, R.1
Chung, D.W.2
Ratnoff, O.D.3
Davie, E.W.4
-
19
-
-
0026606348
-
Expression of human blood coagulation factor XI: Characterization of the defect in factor XI type III deficiency
-
Meijers JCM, Davie EW, Chung DW: Expression of human blood coagulation factor XI: Characterization of the defect in factor XI type III deficiency. Blood 79:1435, 1992
-
(1992)
Blood
, vol.79
, pp. 1435
-
-
Meijers, J.C.M.1
Davie, E.W.2
Chung, D.W.3
-
20
-
-
0028965129
-
Six point mutations that cause factor XI deficiency
-
Pugh RE, McVey JH, Tuddenham EGD, Hancock JF: Six point mutations that cause factor XI deficiency. Blood 85:1509, 1995
-
(1995)
Blood
, vol.85
, pp. 1509
-
-
Pugh, R.E.1
McVey, J.H.2
Tuddenham, E.G.D.3
Hancock, J.F.4
-
21
-
-
0026611384
-
Dideoxy fingerprinting (ddF): A rapid and efficient screen for the presence of mutations
-
Arkar G, Yoon H, Sommer SS: Dideoxy fingerprinting (ddF): A rapid and efficient screen for the presence of mutations. Genomics 13:441, 1992
-
(1992)
Genomics
, vol.13
, pp. 441
-
-
Arkar, G.1
Yoon, H.2
Sommer, S.S.3
-
22
-
-
0029961247
-
Improved detection of p53 point mutations by dideoxyfingerprinting (ddF)
-
Martincic D, Whitlock J: Improved detection of p53 point mutations by dideoxyfingerprinting (ddF). Oncogene 13:2039, 1996
-
(1996)
Oncogene
, vol.13
, pp. 2039
-
-
Martincic, D.1
Whitlock, J.2
-
23
-
-
0030740013
-
A comparison of murine and human factor XI
-
Gailani D, Sun M, Sun Y: A comparison of murine and human factor XI. Blood 90:1055, 1997
-
(1997)
Blood
, vol.90
, pp. 1055
-
-
Gailani, D.1
Sun, M.2
Sun, Y.3
-
24
-
-
0026254627
-
OSP: A computer program for choosing PCR and DNA sequencing primers
-
Hillier L, Green P: OSP: A computer program for choosing PCR and DNA sequencing primers. PCR Methods and Applications 1:124, 1991
-
(1991)
PCR Methods and Applications
, vol.1
, pp. 124
-
-
Hillier, L.1
Green, P.2
-
25
-
-
0023515093
-
Organization of the gene for human factor XI
-
Asakai R, Davie EW, Chung DW: Organization of the gene for human factor XI. Biochemistry 26:7221, 1987
-
(1987)
Biochemistry
, vol.26
, pp. 7221
-
-
Asakai, R.1
Davie, E.W.2
Chung, D.W.3
-
26
-
-
0029826460
-
Identification of a factor IX binding site on the third apple domain of activated factor XI
-
Sun Y, Gailani D: Identification of a factor IX binding site on the third apple domain of activated factor XI. J Biol Chem 271:29023, 1996
-
(1996)
J Biol Chem
, vol.271
, pp. 29023
-
-
Sun, Y.1
Gailani, D.2
-
27
-
-
0023392945
-
High-efficiency transformation of mammalian cells by plasmid DNA
-
Chen C, Okayama H: High-efficiency transformation of mammalian cells by plasmid DNA. Mol Cell Biol 7:2745, 1987
-
(1987)
Mol Cell Biol
, vol.7
, pp. 2745
-
-
Chen, C.1
Okayama, H.2
-
28
-
-
0023043178
-
Amino acid sequence of human factor XI, a blood coagulation factor with four tandem repeats that are highly homologous with plasma prekallikrein
-
Fujikawa K, Chung DW, Hendrickson LE, Davie EW: Amino acid sequence of human factor XI, a blood coagulation factor with four tandem repeats that are highly homologous with plasma prekallikrein. Biochemistry 25:2417, 1986
-
(1986)
Biochemistry
, vol.25
, pp. 2417
-
-
Fujikawa, K.1
Chung, D.W.2
Hendrickson, L.E.3
Davie, E.W.4
-
29
-
-
77049137927
-
New hemophilia-like disease caused by deficiency of a third plasma thromboplastin factor
-
Rosenthal RL, Dreskin OH, Rosenthal N: New hemophilia-like disease caused by deficiency of a third plasma thromboplastin factor. Proc Soc Exp Biol Med 82:171, 1953
-
(1953)
Proc Soc Exp Biol Med
, vol.82
, pp. 171
-
-
Rosenthal, R.L.1
Dreskin, O.H.2
Rosenthal, N.3
-
30
-
-
0029083217
-
Identification of two novel mutations in non-Jewish factor XI deficiency
-
Imanaka Y, Lala K, Nishimura T, Bolton-Maggs PHB, Tuddenham EGD, McVey JH: Identification of two novel mutations in non-Jewish factor XI deficiency. Br J Haematol 90:916, 1995
-
(1995)
Br J Haematol
, vol.90
, pp. 916
-
-
Imanaka, Y.1
Lala, K.2
Nishimura, T.3
Bolton-Maggs, P.H.B.4
Tuddenham, E.G.D.5
McVey, J.H.6
-
31
-
-
0030006913
-
A 14-base pair-deletion (codon 554 del AAGgtaacagagtg) at the exon 14/intron N junction of the coagulation factor XI gene disrupts splicing and causes severe factor XI deficiency
-
Peretz H, Zivelin A, Usher S, Seligsohn U: A 14-base pair-deletion (codon 554 del AAGgtaacagagtg) at the exon 14/intron N junction of the coagulation factor XI gene disrupts splicing and causes severe factor XI deficiency. Hum Mutat 8:77, 1996
-
(1996)
Hum Mutat
, vol.8
, pp. 77
-
-
Peretz, H.1
Zivelin, A.2
Usher, S.3
Seligsohn, U.4
-
32
-
-
3643077899
-
Molecular pathology of factor XI deficiency in the Portuguese population
-
abstr
-
Ventura C, Santos AIM, Tavares A, de Deus G, Gago T, David D: Molecular pathology of factor XI deficiency in the Portuguese population. Thromb Haemost 87:PS859, 1997 (abstr)
-
(1997)
Thromb Haemost
, vol.87
-
-
Ventura, C.1
Santos, A.I.M.2
Tavares, A.3
De Deus, G.4
Gago, T.5
David, D.6
-
33
-
-
3643074789
-
Severe factor XI deficiency in an Arab family associated with a novel mutation in exon 11
-
abstr
-
Wistinghausen B, Reischer A, Nardi M, Karpatkin M: Severe factor XI deficiency in an Arab family associated with a novel mutation in exon 11. Thromb Haemost 78:PS857, 1997 (abstr)
-
(1997)
Thromb Haemost
, vol.78
-
-
Wistinghausen, B.1
Reischer, A.2
Nardi, M.3
Karpatkin, M.4
-
34
-
-
3643083098
-
Cross-reacting material positive (CRM+) factor XI deficiency, XI Yamagata, with a GT to at transition at donor splicing site in intron J of the factor XI gene
-
abstr
-
Hayashi T, Satoh S, Suzuki S, Yahagi A, Yoshino M, Sasaki H: Cross-reacting material positive (CRM+) factor XI deficiency, XI Yamagata, with a GT to AT transition at donor splicing site in intron J of the factor XI gene. Thromb Haemost 78:PS1883, 1997 (abstr)
-
(1997)
Thromb Haemost
, vol.78
-
-
Hayashi, T.1
Satoh, S.2
Suzuki, S.3
Yahagi, A.4
Yoshino, M.5
Sasaki, H.6
-
35
-
-
0028948754
-
Identification and characterization of a binding site for platelets in the apple 3 domain of coagulation factor XI
-
Baglia FA, Jameson BA, Walsh PN: Identification and characterization of a binding site for platelets in the apple 3 domain of coagulation factor XI. J Biol Chem 270:6734, 1995
-
(1995)
J Biol Chem
, vol.270
, pp. 6734
-
-
Baglia, F.A.1
Jameson, B.A.2
Walsh, P.N.3
-
36
-
-
0040884747
-
Identification of contiguous and distinct binding sites for platelets and heparin in the apple 3 domain of coagulation factor XI
-
abstr
-
Ho DH, Baglia FA, Walsh PN: Identification of contiguous and distinct binding sites for platelets and heparin in the apple 3 domain of coagulation factor XI. Blood 88:282a, 1996 (abstr)
-
(1996)
Blood
, vol.88
-
-
Ho, D.H.1
Baglia, F.A.2
Walsh, P.N.3
-
37
-
-
0006340485
-
Laboratory evaluation of hemostatic disorders
-
Hoffman R, Benz EJ, Shattil, SJ, Furie B, Cohen HJ, Silberstein LE (eds). New York, NY, Churchill Livingstone
-
Santoro SA, Eby CS: Laboratory evaluation of hemostatic disorders, in Hoffman R, Benz EJ, Shattil, SJ, Furie B, Cohen HJ, Silberstein LE (eds): Hematology: Basic Principles and Practice. New York, NY, Churchill Livingstone, 1995, pp 1622-1632
-
(1995)
Hematology: Basic Principles and Practice
, pp. 1622-1632
-
-
Santoro, S.A.1
Eby, C.S.2
-
38
-
-
0025874052
-
Factor XI activation in a revised model of blood coagulation
-
Gailani D, Broze GJ: Factor XI activation in a revised model of blood coagulation. Science 253:909, 1991
-
(1991)
Science
, vol.253
, pp. 909
-
-
Gailani, D.1
Broze, G.J.2
-
39
-
-
0028843737
-
Feedback activation of factor XI by thrombin in plasma results in additional formation of thrombin that protects fibrin clots from fibrinolysis
-
von dem Borne PA, Meijers JCM, Bouma, BN: Feedback activation of factor XI by thrombin in plasma results in additional formation of thrombin that protects fibrin clots from fibrinolysis. Blood 86:3035, 1995
-
(1995)
Blood
, vol.86
, pp. 3035
-
-
Von dem Borne, P.A.1
Meijers, J.C.M.2
Bouma, B.N.3
|