-
1
-
-
0024292694
-
The molecular basis of blood coagulation
-
Furie B., and Furie B.C. The molecular basis of blood coagulation. Cell 53 4 (1988) 505-518
-
(1988)
Cell
, vol.53
, Issue.4
, pp. 505-518
-
-
Furie, B.1
Furie, B.C.2
-
2
-
-
0000476042
-
Role of high-molecular-weight kininogen in surface-binding and activation of coagulation Factor XI and prekallikrein
-
Wiggins R.C., Bouma B.N., Cochrane C.G., and Griffin J.H. Role of high-molecular-weight kininogen in surface-binding and activation of coagulation Factor XI and prekallikrein. Proc Natl Acad Sci U S A 74 10 (1977) 4636-4640
-
(1977)
Proc Natl Acad Sci U S A
, vol.74
, Issue.10
, pp. 4636-4640
-
-
Wiggins, R.C.1
Bouma, B.N.2
Cochrane, C.G.3
Griffin, J.H.4
-
3
-
-
0001525663
-
Role of surface in surface-dependent activation of Hageman factor (blood coagulation factor XII)
-
Griffin J.H. Role of surface in surface-dependent activation of Hageman factor (blood coagulation factor XII). Proc Natl Acad Sci U S A 75 4 (1978) 1998-2002
-
(1978)
Proc Natl Acad Sci U S A
, vol.75
, Issue.4
, pp. 1998-2002
-
-
Griffin, J.H.1
-
4
-
-
0026803207
-
The prevalence of factor XII deficiency in 103 orally anticoagulated outpatients suffering from recurrent venous and/or arterial thromboembolism
-
Halbmayer W.M., Mannhalter C., Feichtinger C., Rubi K., and Fischer M. The prevalence of factor XII deficiency in 103 orally anticoagulated outpatients suffering from recurrent venous and/or arterial thromboembolism. Thromb Haemost 68 3 (1992) 285-290
-
(1992)
Thromb Haemost
, vol.68
, Issue.3
, pp. 285-290
-
-
Halbmayer, W.M.1
Mannhalter, C.2
Feichtinger, C.3
Rubi, K.4
Fischer, M.5
-
5
-
-
33845497457
-
Levels of intrinsic coagulation factors and the risk of myocardial infarction among men: Opposite and synergistic effects of factors XI and XII
-
Doggen C.J., Rosendaal F.R., and Meijers J.C. Levels of intrinsic coagulation factors and the risk of myocardial infarction among men: Opposite and synergistic effects of factors XI and XII. Blood 108 13 (2006) 4045-4051
-
(2006)
Blood
, vol.108
, Issue.13
, pp. 4045-4051
-
-
Doggen, C.J.1
Rosendaal, F.R.2
Meijers, J.C.3
-
6
-
-
3242748377
-
Homozygosity of the T allele of the 46 C->T polymorphism in the F12 gene is a risk factor for ischemic stroke in the Spanish population
-
Santamaria A., Mateo J., Tirado I., Oliver A., Belvis R., Marti-Fabregas J., et al. Homozygosity of the T allele of the 46 C->T polymorphism in the F12 gene is a risk factor for ischemic stroke in the Spanish population. Stroke 35 8 (2004) 1795-1799
-
(2004)
Stroke
, vol.35
, Issue.8
, pp. 1795-1799
-
-
Santamaria, A.1
Mateo, J.2
Tirado, I.3
Oliver, A.4
Belvis, R.5
Marti-Fabregas, J.6
-
7
-
-
0032825571
-
Reevaluation of the incidence of thromboembolic complications in congenital factor XII deficiency-a study on 73 subjects from 14 Swiss families
-
Zeerleder S., Schloesser M., Redondo M., Wuillemin W.A., Engel W., Furlan M., et al. Reevaluation of the incidence of thromboembolic complications in congenital factor XII deficiency-a study on 73 subjects from 14 Swiss families. Thromb Haemost 82 4 (1999) 1240-1246
-
(1999)
Thromb Haemost
, vol.82
, Issue.4
, pp. 1240-1246
-
-
Zeerleder, S.1
Schloesser, M.2
Redondo, M.3
Wuillemin, W.A.4
Engel, W.5
Furlan, M.6
-
8
-
-
36349012420
-
Intrinsic pathway of coagulation and arterial thrombosis
-
Gailani D., and Renne T. Intrinsic pathway of coagulation and arterial thrombosis. Arterioscler Thromb Vasc Biol 27 12 (2007) 2507-2513
-
(2007)
Arterioscler Thromb Vasc Biol
, vol.27
, Issue.12
, pp. 2507-2513
-
-
Gailani, D.1
Renne, T.2
-
9
-
-
34250191847
-
Evidence of a U-shaped association between factor XII activity and overall survival
-
Endler G., Marsik C., Jilma B., Schickbauer T., Quehenberger P., and Mannhalter C. Evidence of a U-shaped association between factor XII activity and overall survival. J Thromb Haemost 5 6 (2007) 1143-1148
-
(2007)
J Thromb Haemost
, vol.5
, Issue.6
, pp. 1143-1148
-
-
Endler, G.1
Marsik, C.2
Jilma, B.3
Schickbauer, T.4
Quehenberger, P.5
Mannhalter, C.6
-
10
-
-
10544253846
-
Inherited thrombophilia: Part 1
-
Lane D.A., Mannucci P.M., Bauer K.A., Bertina R.M., Bochkov N.P., Boulyjenkov V., et al. Inherited thrombophilia: Part 1. Thromb Haemost 76 5 (1996) 651-662
-
(1996)
Thromb Haemost
, vol.76
, Issue.5
, pp. 651-662
-
-
Lane, D.A.1
Mannucci, P.M.2
Bauer, K.A.3
Bertina, R.M.4
Bochkov, N.P.5
Boulyjenkov, V.6
-
11
-
-
0347516652
-
Inherited thrombophilia: Part 2
-
Lane D.A., Mannucci P.M., Bauer K.A., Bertina R.M., Bochkov N.P., Boulyjenkov V., et al. Inherited thrombophilia: Part 2. Thromb Haemost 76 6 (1996) 824-834
-
(1996)
Thromb Haemost
, vol.76
, Issue.6
, pp. 824-834
-
-
Lane, D.A.1
Mannucci, P.M.2
Bauer, K.A.3
Bertina, R.M.4
Bochkov, N.P.5
Boulyjenkov, V.6
-
12
-
-
18244384262
-
A quantitative-trait locus in the human factor XII gene influences both plasma factor XII levels and susceptibility to thrombotic disease
-
Soria J.M., Almasy L., Souto J.C., Bacq D., Buil A., Faure A., et al. A quantitative-trait locus in the human factor XII gene influences both plasma factor XII levels and susceptibility to thrombotic disease. Am J Hum Genet 70 3 (2002) 567-574
-
(2002)
Am J Hum Genet
, vol.70
, Issue.3
, pp. 567-574
-
-
Soria, J.M.1
Almasy, L.2
Souto, J.C.3
Bacq, D.4
Buil, A.5
Faure, A.6
-
13
-
-
36348949734
-
Molecular analysis of multiple genetic variants in Spanish FXII-deficient families
-
Mordillo C., Martinez-Marchan E., Fontcuberta J., and Soria J.M. Molecular analysis of multiple genetic variants in Spanish FXII-deficient families. Haematologica 92 11 (2007) 1569-1572
-
(2007)
Haematologica
, vol.92
, Issue.11
, pp. 1569-1572
-
-
Mordillo, C.1
Martinez-Marchan, E.2
Fontcuberta, J.3
Soria, J.M.4
-
14
-
-
55049089726
-
Genetic study in patients with factor XII deficiency: a report of three new mutations exon 13 (Q501STOP), exon 14 (P547L) and -13C>T promoter region in three compound heterozygotes
-
Lombardi A.M., Bortoletto E., Scarparo P., Scapin M., Santarossa L., and Girolami A. Genetic study in patients with factor XII deficiency: a report of three new mutations exon 13 (Q501STOP), exon 14 (P547L) and -13C>T promoter region in three compound heterozygotes. Blood Coagul Fibrinolysis 19 7 (2008) 639-643
-
(2008)
Blood Coagul Fibrinolysis
, vol.19
, Issue.7
, pp. 639-643
-
-
Lombardi, A.M.1
Bortoletto, E.2
Scarparo, P.3
Scapin, M.4
Santarossa, L.5
Girolami, A.6
-
15
-
-
0024284028
-
A simple salting out procedure for extracting DNA from human nucleated cells
-
Miller S.A., Dykes D.D., and Polesky H.F. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 16 3 (1988) 1215
-
(1988)
Nucleic Acids Res
, vol.16
, Issue.3
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
16
-
-
0034603799
-
Genetic determinants of hemostasis phenotypes in Spanish families
-
Souto J.C., Almasy L., Borrell M., Gari M., Martinez E., Mateo J., et al. Genetic determinants of hemostasis phenotypes in Spanish families. Circulation 101 13 (2000) 1546-1551
-
(2000)
Circulation
, vol.101
, Issue.13
, pp. 1546-1551
-
-
Souto, J.C.1
Almasy, L.2
Borrell, M.3
Gari, M.4
Martinez, E.5
Mateo, J.6
-
17
-
-
0034908554
-
Nomenclature for the description of human sequence variations
-
den Dunnen J.T., and Antonarakis S.E. Nomenclature for the description of human sequence variations. Hum Genet 109 1 (2001) 121-124
-
(2001)
Hum Genet
, vol.109
, Issue.1
, pp. 121-124
-
-
den Dunnen, J.T.1
Antonarakis, S.E.2
-
18
-
-
0031860769
-
Size, diffusibility and transfection performance of linear PEI/DNA complexes in the mouse central nervous system
-
Goula D., Remy J.S., Erbacher P., Wasowicz M., Levi G., Abdallah B., et al. Size, diffusibility and transfection performance of linear PEI/DNA complexes in the mouse central nervous system. Gene Ther 5 5 (1998) 712-717
-
(1998)
Gene Ther
, vol.5
, Issue.5
, pp. 712-717
-
-
Goula, D.1
Remy, J.S.2
Erbacher, P.3
Wasowicz, M.4
Levi, G.5
Abdallah, B.6
-
19
-
-
0035480096
-
Functional quantification of cyclosporine A and FK506 in human whole blood by flow cytometry, using the green fluorescent protein as an interleukin-2 reporter gene
-
Taupin J.L., Merville P., McBride T., Potaux L., and Moreau J.F. Functional quantification of cyclosporine A and FK506 in human whole blood by flow cytometry, using the green fluorescent protein as an interleukin-2 reporter gene. J Immunol Methods 256 1-2 (2001) 77-87
-
(2001)
J Immunol Methods
, vol.256
, Issue.1-2
, pp. 77-87
-
-
Taupin, J.L.1
Merville, P.2
McBride, T.3
Potaux, L.4
Moreau, J.F.5
-
20
-
-
0028850321
-
Quantitative imaging of green fluorescent protein in cultured cells: comparison of microscopic techniques, use in fusion proteins and detection limits
-
Niswender K.D., Blackman S.M., Rohde L., Magnuson M.A., and Piston D.W. Quantitative imaging of green fluorescent protein in cultured cells: comparison of microscopic techniques, use in fusion proteins and detection limits. J Microsc 180 Pt 2 (1995) 109-116
-
(1995)
J Microsc
, vol.180
, Issue.PART 2
, pp. 109-116
-
-
Niswender, K.D.1
Blackman, S.M.2
Rohde, L.3
Magnuson, M.A.4
Piston, D.W.5
-
21
-
-
34250695026
-
Functional analysis of the genetic variability in the F7 gene promoter
-
Sabater-Lleal M., Chillon M., Howard T.E., Gil E., Almasy L., Blangero J., et al. Functional analysis of the genetic variability in the F7 gene promoter. Atherosclerosis 197 2 (2007) 262-268
-
(2007)
Atherosclerosis
, vol.197
, Issue.2
, pp. 262-268
-
-
Sabater-Lleal, M.1
Chillon, M.2
Howard, T.E.3
Gil, E.4
Almasy, L.5
Blangero, J.6
-
22
-
-
0032850195
-
Modulation of transcriptional activation and coactivator interaction by a splicing variation in the F domain of nuclear receptor hepatocyte nuclear factor 4alpha1
-
Sladek F.M., Ruse Jr. M.D., Nepomuceno L., Huang S.M., and Stallcup M.R. Modulation of transcriptional activation and coactivator interaction by a splicing variation in the F domain of nuclear receptor hepatocyte nuclear factor 4alpha1. Mol Cell Biol 19 10 (1999) 6509-6522
-
(1999)
Mol Cell Biol
, vol.19
, Issue.10
, pp. 6509-6522
-
-
Sladek, F.M.1
Ruse Jr., M.D.2
Nepomuceno, L.3
Huang, S.M.4
Stallcup, M.R.5
-
23
-
-
33645416119
-
Role of hepatocyte nuclear factor 4alpha in control of blood coagulation factor gene expression
-
Inoue Y., Peters L.L., Yim S.H., Inoue J., and Gonzalez F.J. Role of hepatocyte nuclear factor 4alpha in control of blood coagulation factor gene expression. J Mol Med 84 4 (2006) 334-344
-
(2006)
J Mol Med
, vol.84
, Issue.4
, pp. 334-344
-
-
Inoue, Y.1
Peters, L.L.2
Yim, S.H.3
Inoue, J.4
Gonzalez, F.J.5
-
24
-
-
0032521229
-
A common genetic polymorphism (46 C to T substitution) in the 5'-untranslated region of the coagulation factor XII gene is associated with low translation efficiency and decrease in plasma factor XII level
-
Kanaji T., Okamura T., Osaki K., Kuroiwa M., Shimoda K., Hamasaki N., et al. A common genetic polymorphism (46 C to T substitution) in the 5'-untranslated region of the coagulation factor XII gene is associated with low translation efficiency and decrease in plasma factor XII level. Blood 91 6 (1998) 2010-2014
-
(1998)
Blood
, vol.91
, Issue.6
, pp. 2010-2014
-
-
Kanaji, T.1
Okamura, T.2
Osaki, K.3
Kuroiwa, M.4
Shimoda, K.5
Hamasaki, N.6
-
25
-
-
0035864343
-
A common C->T polymorphism at nt 46 in the promoter region of coagulation factor XII is associated with decreased factor XII activity
-
Endler G., Exner M., Mannhalter C., Meier S., Ruzicka K., Handler S., et al. A common C->T polymorphism at nt 46 in the promoter region of coagulation factor XII is associated with decreased factor XII activity. Thromb Res 101 4 (2001) 255-260
-
(2001)
Thromb Res
, vol.101
, Issue.4
, pp. 255-260
-
-
Endler, G.1
Exner, M.2
Mannhalter, C.3
Meier, S.4
Ruzicka, K.5
Handler, S.6
-
26
-
-
0038380256
-
The epidemiology of venous thromboembolism
-
White R.H. The epidemiology of venous thromboembolism. Circulation 107 23 Suppl 1 (2003) I4-I8
-
(2003)
Circulation
, vol.107
, Issue.23 SUPPL. 1
-
-
White, R.H.1
-
27
-
-
0038042011
-
Risk factors for venous thromboembolism
-
Anderson Jr. F.A., and Spencer F.A. Risk factors for venous thromboembolism. Circulation 107 23 Suppl 1 (2003) I9-I16
-
(2003)
Circulation
, vol.107
, Issue.23 SUPPL. 1
-
-
Anderson Jr., F.A.1
Spencer, F.A.2
-
28
-
-
36549036104
-
The genetic basis of complex traits: rare variants or "common gene, common disease"?
-
Iyengar S.K., and Elston R.C. The genetic basis of complex traits: rare variants or "common gene, common disease"?. Methods Mol Biol 376 (2007) 71-84
-
(2007)
Methods Mol Biol
, vol.376
, pp. 71-84
-
-
Iyengar, S.K.1
Elston, R.C.2
-
29
-
-
44349132708
-
Common and rare variants in multifactorial susceptibility to common diseases
-
Bodmer W., and Bonilla C. Common and rare variants in multifactorial susceptibility to common diseases. Nat Genet 40 6 (2008) 695-701
-
(2008)
Nat Genet
, vol.40
, Issue.6
, pp. 695-701
-
-
Bodmer, W.1
Bonilla, C.2
-
30
-
-
13144306071
-
Genome-wide association studies for common diseases and complex traits
-
Hirschhorn J.N., and Daly M.J. Genome-wide association studies for common diseases and complex traits. Nat Rev Genet 6 2 (2005) 95-108
-
(2005)
Nat Rev Genet
, vol.6
, Issue.2
, pp. 95-108
-
-
Hirschhorn, J.N.1
Daly, M.J.2
|