-
1
-
-
0022624812
-
Biosynthesis and secretion of factor VII, protein C, protein S, and the Protein C inhibitor from a human hepatoma cell line
-
Fair DS, Marlar RA. Biosynthesis and secretion of factor VII, protein C, protein S, and the Protein C inhibitor from a human hepatoma cell line. Blood. 1986;67(1):64-70.
-
(1986)
Blood.
, vol.67
, Issue.1
, pp. 64-70
-
-
Fair, D.S.1
Marlar, R.A.2
-
2
-
-
34447540033
-
The tale of protein S and C4b-binding protein, a story of affection
-
Dahlbäck B. The tale of protein S and C4b-binding protein, a story of affection. Thromb Haemost. 2007;98(1):90-96.
-
(2007)
Thromb Haemost.
, vol.98
, Issue.1
, pp. 90-96
-
-
Dahlbäck, B.1
-
3
-
-
0021225618
-
Protein S and the regulation of activated protein C
-
Walker FJ. Protein S and the regulation of activated protein C. Semin Thromb Hemost. 1984;10(2):131-138.
-
(1984)
Semin Thromb Hemost.
, vol.10
, Issue.2
, pp. 131-138
-
-
Walker, F.J.1
-
4
-
-
33644772164
-
Protein S stimulates inhibition of the tissue factor pathway by tissue factor pathway inhibitor
-
Hackeng TM, Seré KM, Tans G, Rosing J. Protein S stimulates inhibition of the tissue factor pathway by tissue factor pathway inhibitor. Proc Natl Acad Sci USA. 2006;103(9):3106-3111.
-
(2006)
Proc Natl Acad Sci USA.
, vol.103
, Issue.9
, pp. 3106-3111
-
-
Hackeng, T.M.1
Seré, K.M.2
Tans, G.3
Rosing, J.4
-
5
-
-
84866282733
-
Similar hypercoagulable state and thrombosis risk in type I and type III protein S-deficient individuals from families with mixed type I/III protein S deficiency
-
Castoldi E, Maurissen LF, Tormene D, et al. Similar hypercoagulable state and thrombosis risk in type I and type III protein S-deficient individuals from families with mixed type I/III protein S deficiency. Haematologica. 2010;95(9):1563-1571.
-
(2010)
Haematologica.
, vol.95
, Issue.9
, pp. 1563-1571
-
-
Castoldi, E.1
Maurissen, L.F.2
Tormene, D.3
-
6
-
-
0027761414
-
Comparison of functional assays for protein S: European collaborative study of patients with congenital and acquired deficiency
-
Boyer-Neumann C, Bertina RM, Tripodi A, et al. Comparison of functional assays for protein S: European collaborative study of patients with congenital and acquired deficiency. Thromb Haemost. 1993;70(6):946-950.
-
(1993)
Thromb Haemost.
, vol.70
, Issue.6
, pp. 946-950
-
-
Boyer-Neumann, C.1
Bertina, R.M.2
Tripodi, A.3
-
7
-
-
0033678567
-
Protein S deficiency: A database of mutations-summary of the first update
-
Plasma Coagulation Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis
-
Gandrille S, Borgel D, Sala N, et al; Plasma Coagulation Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis. Protein S deficiency: a database of mutations-summary of the first update. Thromb Haemost. 2000;84(5):918.
-
(2000)
Thromb Haemost.
, vol.84
, Issue.5
, pp. 918
-
-
Gandrille, S.1
Borgel, D.2
Sala, N.3
-
8
-
-
34548692763
-
Molecular basis of protein S deficiency
-
García De Frutos P, Fuentes-Prior P, Hurtado B, Sala N. Molecular basis of protein S deficiency. Thromb Haemost. 2007;98(3):543-556.
-
(2007)
Thromb Haemost.
, vol.98
, Issue.3
, pp. 543-556
-
-
García De Frutos, P.1
Fuentes-Prior, P.2
Hurtado, B.3
Sala, N.4
-
9
-
-
77953446523
-
The Human Gene Mutation Database: 2008 update
-
Stenson PD, Mort M, Ball EV, et al. The Human Gene Mutation Database: 2008 update. Genome Med. 2009;1(1):13.
-
(2009)
Genome Med.
, vol.1
, Issue.1
, pp. 13
-
-
Stenson, P.D.1
Mort, M.2
Ball, E.V.3
-
10
-
-
27844561552
-
Large deletions of the PROS1 gene in a large fraction of mutationnegative patients with protein S deficiency
-
Johansson AM, Hillarp A, Säll T, Zöller B, Dahlbäck B, Halldén C. Large deletions of the PROS1 gene in a large fraction of mutationnegative patients with protein S deficiency. Thromb Haemost. 2005;94(5):951-957.
-
(2005)
Thromb Haemost.
, vol.94
, Issue.5
, pp. 951-957
-
-
Johansson, A.M.1
Hillarp, A.2
Säll, T.3
Zöller, B.4
Dahlbäck, B.5
Halldén, C.6
-
11
-
-
70349338885
-
Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiency
-
Pintao MC, Garcia AA, Borgel D, et al. Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiency. Hum Genet. 2009;126(3):449-456.
-
(2009)
Hum Genet.
, vol.126
, Issue.3
, pp. 449-456
-
-
Pintao, M.C.1
Garcia, A.A.2
Borgel, D.3
-
12
-
-
0034653996
-
Genetic analysis, phenotypic diagnosis, and risk of venous thrombosis in families with inherited deficiencies of protein S
-
Makris M, Leach M, Beauchamp NJ, et al. Genetic analysis, phenotypic diagnosis, and risk of venous thrombosis in families with inherited deficiencies of protein S. Blood. 2000;95(6):1935-1941.
-
(2000)
Blood.
, vol.95
, Issue.6
, pp. 1935-1941
-
-
Makris, M.1
Leach, M.2
Beauchamp, N.J.3
-
13
-
-
46749102183
-
PROS1 analysis in 87 pedigrees with hereditary protein S deficiency demonstrates striking genotypephenotype associations
-
Ten Kate MK, Platteel M, Mulder R, et al. PROS1 analysis in 87 pedigrees with hereditary protein S deficiency demonstrates striking genotypephenotype associations. Hum Mutat. 2008;29(7):939-947.
-
(2008)
Hum Mutat.
, vol.29
, Issue.7
, pp. 939-947
-
-
Ten Kate, M.K.1
Platteel, M.2
Mulder, R.3
-
14
-
-
60849127266
-
Clinical relevance of decreased free protein S levels: Results from a retrospective family cohort study involving 1143 relatives
-
Lijfering WM, Mulder R, Ten Kate MK, Veeger NJ, Mulder AB, Van Der Meer J. Clinical relevance of decreased free protein S levels: results from a retrospective family cohort study involving 1143 relatives. Blood. 2009;113(6):1225-1230.
-
(2009)
Blood.
, vol.113
, Issue.6
, pp. 1225-1230
-
-
Lijfering, W.M.1
Mulder, R.2
Ten Kate, M.K.3
Veeger, N.J.4
Mulder, A.B.5
Van Der Meer, J.6
-
15
-
-
23944444384
-
Risk of a first venous thrombotic event in carriers of a familial thrombophilic defect. The European Prospective Cohort on Thrombophilia (EPCOT)
-
Vossen CY, Conard J, Fontcuberta J, et al. Risk of a first venous thrombotic event in carriers of a familial thrombophilic defect. The European Prospective Cohort on Thrombophilia (EPCOT). J Thromb Haemost. 2005;3(3):459-464.
-
(2005)
J Thromb Haemost.
, vol.3
, Issue.3
, pp. 459-464
-
-
Vossen, C.Y.1
Conard, J.2
Fontcuberta, J.3
-
16
-
-
24144492688
-
Recurrence rate after a first venous thrombosis in patients with familial thrombophilia
-
Vossen CY, Walker ID, Svensson P, et al. Recurrence rate after a first venous thrombosis in patients with familial thrombophilia. Arterioscler Thromb Vasc Biol. 2005;25(9):1992-1997.
-
(2005)
Arterioscler Thromb Vasc Biol.
, vol.25
, Issue.9
, pp. 1992-1997
-
-
Vossen, C.Y.1
Walker, I.D.2
Svensson, P.3
-
17
-
-
67149089651
-
Selective testing for thrombophilia in patients with first venous thrombosis: Results from a retrospective family cohort study on absolute thrombotic risk for currently known thrombophilic defects in 2479 relatives
-
Lijfering WM, Brouwer JL, Veeger NJ, et al. Selective testing for thrombophilia in patients with first venous thrombosis: results from a retrospective family cohort study on absolute thrombotic risk for currently known thrombophilic defects in 2479 relatives. Blood. 2009;113(21):5314-5322.
-
(2009)
Blood.
, vol.113
, Issue.21
, pp. 5314-5322
-
-
Lijfering, W.M.1
Brouwer, J.L.2
Veeger, N.J.3
-
18
-
-
0029016883
-
Resistance to activated protein C as an additional genetic risk factor in hereditary deficiency of protein S
-
Zöller B, Berntsdotter A, García De Frutos P, Dahlbäck B. Resistance to activated protein C as an additional genetic risk factor in hereditary deficiency of protein S. Blood. 1995;85(12):3518-3523.
-
(1995)
Blood.
, vol.85
, Issue.12
, pp. 3518-3523
-
-
Zöller, B.1
Berntsdotter, A.2
García De Frutos, P.3
Dahlbäck, B.4
-
19
-
-
0030727792
-
Free protein S deficiency is a risk factor for venous thrombosis
-
Faioni EM, Valsecchi C, Palla A, Taioli E, Razzari C, Mannucci PM. Free protein S deficiency is a risk factor for venous thrombosis. Thromb Haemost. 1997;78(5):1343-1346.
-
(1997)
Thromb Haemost.
, vol.78
, Issue.5
, pp. 1343-1346
-
-
Faioni, E.M.1
Valsecchi, C.2
Palla, A.3
Taioli, E.4
Razzari, C.5
Mannucci, P.M.6
-
20
-
-
0029033740
-
Protein C deficiency in a controlled series of unselected outpatients: An infrequent but clear risk factor for venous thrombosis (Leiden Thrombophilia Study)
-
Koster T, Rosendaal FR, Briët E, et al. Protein C deficiency in a controlled series of unselected outpatients: an infrequent but clear risk factor for venous thrombosis (Leiden Thrombophilia Study). Blood. 1995;85(10):2756- 2761.
-
(1995)
Blood.
, vol.85
, Issue.10
, pp. 2756-2761
-
-
Koster, T.1
Rosendaal, F.R.2
Briët, E.3
-
21
-
-
0032849481
-
Hormonal state rather than age influences cut-off values of protein S: Reevaluation of the thrombotic risk associated with protein S deficiency
-
Liberti G, Bertina RM, Rosendaal FR. Hormonal state rather than age influences cut-off values of protein S: reevaluation of the thrombotic risk associated with protein S deficiency. Thromb Haemost. 1999;82(3):1093-1096.
-
(1999)
Thromb Haemost.
, vol.82
, Issue.3
, pp. 1093-1096
-
-
Liberti, G.1
Bertina, R.M.2
Rosendaal, F.R.3
-
22
-
-
13444256137
-
Malignancies, prothrombotic mutations, and the risk of venous thrombosis
-
Blom JW, Doggen CJ, Osanto S, Rosendaal FR. Malignancies, prothrombotic mutations, and the risk of venous thrombosis. JAMA. 2005;293(6):715-722.
-
(2005)
JAMA
, vol.293
, Issue.6
, pp. 715-722
-
-
Blom, J.W.1
Doggen, C.J.2
Osanto, S.3
Rosendaal, F.R.4
-
23
-
-
0030205254
-
Molecular basis for protein S hereditary deficiency: Genetic defects observed in 118 patients with type I and type IIa deficiencies
-
The French Network on Molecular Abnormalities Responsible for Protein C and Protein S Deficiencies
-
Borgel D, Duchemin J, Alhenc-Gelas M, Matheron C, Aiach M, Gandrille S; The French Network on Molecular Abnormalities Responsible for Protein C and Protein S Deficiencies. Molecular basis for protein S hereditary deficiency: genetic defects observed in 118 patients with type I and type IIa deficiencies. J Lab Clin Med. 1996;128(2):218-227.
-
(1996)
J Lab Clin Med.
, vol.128
, Issue.2
, pp. 218-227
-
-
Borgel, D.1
Duchemin, J.2
Alhenc-Gelas, M.3
Matheron, C.4
Aiach, M.5
Gandrille, S.6
-
24
-
-
3543023204
-
Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification
-
Schouten JP, McElgunn CJ, Waaijer R, Zwijnenburg D, Diepvens F, Pals G. Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification. Nucleic Acids Res. 2002;30(12):e57.
-
(2002)
Nucleic Acids Res.
, vol.30
, Issue.12
-
-
Schouten, J.P.1
McElgunn, C.J.2
Waaijer, R.3
Zwijnenburg, D.4
Diepvens, F.5
Pals, G.6
-
25
-
-
77957103178
-
Associations between high factor VIII and low free protein S levels with traditional arterial thrombotic risk factors and their risk on arterial thrombosis: Results from a retrospective family cohort study
-
Mulder R, Van Schouwenburg IM, Mahmoodi BK, et al. Associations between high factor VIII and low free protein S levels with traditional arterial thrombotic risk factors and their risk on arterial thrombosis: results from a retrospective family cohort study. Thromb Res. 2010;126(4):e249-e254.
-
(2010)
Thromb Res.
, vol.126
, Issue.4
-
-
Mulder, R.1
Van Schouwenburg, I.M.2
Mahmoodi, B.K.3
-
26
-
-
0028783339
-
Plasma levels of protein S, protein C, and factor X: Effects of sex, hormonal state and age
-
Henkens CM, Bom VJ, Van Der Schaaf W, Pelsma PM, Sibinga CT, De Kam PJ, Van Der Meer J. Plasma levels of protein S, protein C, and factor X: effects of sex, hormonal state and age. Thromb Haemost. 1995;74(5):1271-1275.
-
(1995)
Thromb Haemost.
, vol.74
, Issue.5
, pp. 1271-1275
-
-
Henkens, C.M.1
Bom, V.J.2
Van Der Schaaf, W.3
Pelsma, P.M.4
Sibinga, C.T.5
De Kam, P.J.6
Van Der Meer, J.7
-
27
-
-
54949134866
-
What do case-control studies estimate? Survey of methods and assumptions in published casecontrol research
-
Knol MJ, Vandenbroucke JP, Scott P, Egger M. What do case-control studies estimate? Survey of methods and assumptions in published casecontrol research. Am J Epidemiol. 2008;168(9):1073-1081.
-
(2008)
Am J Epidemiol.
, vol.168
, Issue.9
, pp. 1073-1081
-
-
Knol, M.J.1
Vandenbroucke, J.P.2
Scott, P.3
Egger, M.4
-
28
-
-
0033917642
-
Effects on coagulation of levonorgestreland desogestrel-containing low dose oral contraceptives: A cross-over study
-
Middeldorp S, Meijers JC, Van Den Ende AE, et al. Effects on coagulation of levonorgestreland desogestrel-containing low dose oral contraceptives: a cross-over study. Thromb Haemost. 2000;84(1):4-8.
-
(2000)
Thromb Haemost.
, vol.84
, Issue.1
, pp. 4-8
-
-
Middeldorp, S.1
Meijers, J.C.2
Van Den Ende, A.E.3
-
29
-
-
77952060000
-
Altered reference ranges for protein C and protein S during early pregnancy: Implications for the diagnosis of protein C and protein S deficiency during pregnancy
-
Said JM, Ignjatovic V, Monagle PT, Walker SP, Higgins JR, Brennecke SP. Altered reference ranges for protein C and protein S during early pregnancy: Implications for the diagnosis of protein C and protein S deficiency during pregnancy. Thromb Haemost. 2010;103(5):984-988.
-
(2010)
Thromb Haemost.
, vol.103
, Issue.5
, pp. 984-988
-
-
Said, J.M.1
Ignjatovic, V.2
Monagle, P.T.3
Walker, S.P.4
Higgins, J.R.5
Brennecke, S.P.6
-
30
-
-
63849314208
-
The value of family history as a risk indicator for venous thrombosis
-
Bezemer ID, Van Der Meer FJ, Eikenboom JC, Rosendaal FR, Doggen CJ. The value of family history as a risk indicator for venous thrombosis. Arch Intern Med. 2009;169(6):610-615.
-
(2009)
Arch Intern Med.
, vol.169
, Issue.6
, pp. 610-615
-
-
Bezemer, I.D.1
Van Der Meer, F.J.2
Eikenboom, J.C.3
Rosendaal, F.R.4
Doggen, C.J.5
-
31
-
-
77956640807
-
Low cut-off values increase diagnostic performance of protein S assays
-
Mulder R, Ten Kate MK, Kluin-Nelemans HC, Mulder AB. Low cut-off values increase diagnostic performance of protein S assays. Thromb Haemost. 2010;104(3):618-625.
-
(2010)
Thromb Haemost.
, vol.104
, Issue.3
, pp. 618-625
-
-
Mulder, R.1
Ten Kate, M.K.2
Kluin-Nelemans, H.C.3
Mulder, A.B.4
-
32
-
-
55949086628
-
Protein S deficiency: A clinical perspective
-
Ten Kate MK, Van Der Meer J. Protein S deficiency: a clinical perspective. Haemophilia. 2008;14(6):1222-1228.
-
(2008)
Haemophilia.
, vol.14
, Issue.6
, pp. 1222-1228
-
-
Ten Kate, M.K.1
Van Der Meer, J.2
-
33
-
-
60849133332
-
High long-term absolute risk of recurrent venous thromboembolism in patients with hereditary deficiencies of protein S, protein C or antithrombin
-
Brouwer JL, Lijfering WM, Ten Kate MK, Kluin-Nelemans HC, Veeger NJ, Van Der Meer J. High long-term absolute risk of recurrent venous thromboembolism in patients with hereditary deficiencies of protein S, protein C or antithrombin. Thromb Haemost. 2009;101(1):93-99.
-
(2009)
Thromb Haemost.
, vol.101
, Issue.1
, pp. 93-99
-
-
Brouwer, J.L.1
Lijfering, W.M.2
Ten Kate, M.K.3
Kluin-Nelemans, H.C.4
Veeger, N.J.5
Van Der Meer, J.6
-
34
-
-
0033933677
-
A randomized cross-over study on the effects of levonorgestrel- and desogestrel-containing oral contraceptives on the anticoagulant pathways
-
Tans G, Curvers J, Middeldorp S, et al. A randomized cross-over study on the effects of levonorgestrel- and desogestrel-containing oral contraceptives on the anticoagulant pathways. Thromb Haemost. 2000;84(1):15-21.
-
(2000)
Thromb Haemost.
, vol.84
, Issue.1
, pp. 15-21
-
-
Tans, G.1
Curvers, J.2
Middeldorp, S.3
-
35
-
-
79952391692
-
Changes in fibrin D-dimer, fibrinogen, and protein S during pregnancy
-
Hansen AT, Andreasen BH, Salvig JD, Hvas AM. Changes in fibrin D-dimer, fibrinogen, and protein S during pregnancy. Scand J Clin Lab Invest. 2011;71(2):173-176.
-
(2011)
Scand J Clin Lab Invest.
, vol.71
, Issue.2
, pp. 173-176
-
-
Hansen, A.T.1
Andreasen, B.H.2
Salvig, J.D.3
Hvas, A.M.4
-
36
-
-
80054086506
-
Free protein S level as a risk factor for coronary heart disease and stroke in a prospective cohort study of healthy United Kingdom men
-
Ken-Dror G, Cooper JA, Humphries SE, Drenos F, Ireland HA. Free protein S level as a risk factor for coronary heart disease and stroke in a prospective cohort study of healthy United Kingdom men. Am J Epidemiol. 2011;174(8):958-968.
-
(2011)
Am J Epidemiol.
, vol.174
, Issue.8
, pp. 958-968
-
-
Ken-Dror, G.1
Cooper, J.A.2
Humphries, S.E.3
Drenos, F.4
Ireland, H.A.5
-
37
-
-
0025038379
-
High total and free protein S in patients with acute deep vein thrombosis
-
Toulon P, Gandrille S, Vitoux JF, Fiessinger JN, Sultan Y, Aiach M. High total and free protein S in patients with acute deep vein thrombosis. Thromb Res. 1990;59(1):213-217.
-
(1990)
Thromb Res.
, vol.59
, Issue.1
, pp. 213-217
-
-
Toulon, P.1
Gandrille, S.2
Vitoux, J.F.3
Fiessinger, J.N.4
Sultan, Y.5
Aiach, M.6
-
38
-
-
33846165762
-
Obesity and thrombosis
-
Darvall KA, Sam RC, Silverman SH, Bradbury AW, Adam DJ. Obesity and thrombosis. Eur J Endovasc Surg. 2007;33(2):223-233.
-
(2007)
Eur J Endovasc Surg.
, vol.33
, Issue.2
, pp. 223-233
-
-
Darvall, K.A.1
Sam, R.C.2
Silverman, S.H.3
Bradbury, A.W.4
Adam, D.J.5
-
39
-
-
0036881564
-
A review of the technical, diagnostic, and epidemiologic considerations for protein S assays
-
Goodwin AJ, Rosendaal FR, Kottke-Marchant K, Bovill EG. A review of the technical, diagnostic, and epidemiologic considerations for protein S assays. Arch Pathol Lab Med. 2002;126(11):1349-1366.
-
(2002)
Arch Pathol Lab Med.
, vol.126
, Issue.11
, pp. 1349-1366
-
-
Goodwin, A.J.1
Rosendaal, F.R.2
Kottke-Marchant, K.3
Bovill, E.G.4
-
40
-
-
0028871033
-
Identification of 15 different candidate causal point mutations and three polymorphisms in 19 patients with protein S deficiency using a scanning method for the analysis of the protein S active gene
-
Gandrille S, Borgel D, Eschwege-Gufflet V, et al. Identification of 15 different candidate causal point mutations and three polymorphisms in 19 patients with protein S deficiency using a scanning method for the analysis of the protein S active gene. Blood. 1995;85(1):130-138.
-
(1995)
Blood.
, vol.85
, Issue.1
, pp. 130-138
-
-
Gandrille, S.1
Borgel, D.2
Eschwege-Gufflet, V.3
-
41
-
-
0033981955
-
Protein S secretion differences of missense mutants account for phenotypic heterogeneity
-
Espinosa-Parrilla Y, Yamazaki T, Sala N, Dahlbäck B, De Frutos PG. Protein S secretion differences of missense mutants account for phenotypic heterogeneity. Blood. 2000;95(1):173-179.
-
(2000)
Blood.
, vol.95
, Issue.1
, pp. 173-179
-
-
Espinosa-Parrilla, Y.1
Yamazaki, T.2
Sala, N.3
Dahlbäck, B.4
De Frutos, P.G.5
-
42
-
-
0036166536
-
Genetic and phenotypic variability between families with hereditary protein S deficiency
-
Rezende SM, Lane DA, Zöller B, Mille-Baker B, Laffan M, Dalhbäck B, Simmonds RE. Genetic and phenotypic variability between families with hereditary protein S deficiency. Thromb Haemost. 2002;87(2):258-265.
-
(2002)
Thromb Haemost.
, vol.87
, Issue.2
, pp. 258-265
-
-
Rezende, S.M.1
Lane, D.A.2
Zöller, B.3
Mille-Baker, B.4
Laffan, M.5
Dalhbäck, B.6
Simmonds, R.E.7
-
43
-
-
0033987736
-
Mutation nomenclature extensions and suggestions to describe complex mutations: A discussion
-
Den Dunnen JT, Antonarakis SE. Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion. Hum Mutat. 2000;15(1):7-12.
-
(2000)
Hum Mutat.
, vol.15
, Issue.1
, pp. 7-12
-
-
Den Dunnen, J.T.1
Antonarakis, S.E.2
|