-
1
-
-
0025833619
-
Protein S and C4b-binding protein: Components involved in the regulation of the protein C anticoagulant system
-
1. Dahlbäck B. Protein S and C4b-binding protein: Components involved in the regulation of the protein C anticoagulant system. Thromb Haemost 1991;66:49-61.
-
(1991)
Thromb Haemost
, vol.66
, pp. 49-61
-
-
Dahlbäck, B.1
-
2
-
-
0027404562
-
Binding of protein S to factor Va associated with inhibition of prothrombinase that is independent of activated protein C
-
2. Heeb MJ, Mesters RM, Tans G, Rosing J, Griffin JH. Binding of protein S to factor Va associated with inhibition of prothrombinase that is independent of activated protein C. J Biol Chem 1993;268:2872-7.
-
(1993)
J Biol Chem
, vol.268
, pp. 2872-2877
-
-
Heeb, M.J.1
Mesters, R.M.2
Tans, G.3
Rosing, J.4
Griffin, J.H.5
-
3
-
-
0040426308
-
High molecular weight complex in human plasma between vitamin K-dependent protein S and complement component C4b-binding protein
-
3. Dahlbäck B, Stenflo J. High molecular weight complex in human plasma between vitamin K-dependent protein S and complement component C4b-binding protein. Proc Natl Acad Sci USA 1981;78:2512-6.
-
(1981)
Proc Natl Acad Sci USA
, vol.78
, pp. 2512-2516
-
-
Dahlbäck, B.1
Stenflo, J.2
-
4
-
-
0022929854
-
a cofactor function of human and bovine protein S by C4b-binding protein
-
a cofactor function of human and bovine protein S by C4b-binding protein. J Biol Chem 1986;261: 12022-7.
-
(1986)
J Biol Chem
, vol.261
, pp. 12022-12027
-
-
Dahlbäck, B.1
-
5
-
-
0024343523
-
Plasma protein S in disseminated intravascular coagulation, liver disease, collagen disease, diabetes mellitus, and under oral anticoagulant therapy
-
5. Takahashi H, Tatewaki W, Wada K, Shibata A. Plasma protein S in disseminated intravascular coagulation, liver disease, collagen disease, diabetes mellitus, and under oral anticoagulant therapy. Clin Chem Acta 1989;182:195-208.
-
(1989)
Clin Chem Acta
, vol.182
, pp. 195-208
-
-
Takahashi, H.1
Tatewaki, W.2
Wada, K.3
Shibata, A.4
-
6
-
-
0028783339
-
Plasma levels of protein S, protein C, and factor X: Effects of sex, hormonal state and age
-
6. Henkens CMA, Bom VJJ, Schaaf W, Pelsma PM, Sibinga CTS, Kam PJ, Meer J. Plasma levels of protein S, protein C, and factor X: Effects of sex, hormonal state and age. Thromb Haemost 1995;74:1271-5.
-
(1995)
Thromb Haemost
, vol.74
, pp. 1271-1275
-
-
Henkens, C.M.A.1
Bom, V.J.J.2
Schaaf, W.3
Pelsma, P.M.4
Sibinga, C.T.S.5
Kam, P.J.6
Meer, J.7
-
7
-
-
0022357574
-
Hereditary protein S deficiency
-
7. Bertina RM. Hereditary protein S deficiency. Haemostasis 1985;15:241-4.
-
(1985)
Haemostasis
, vol.15
, pp. 241-244
-
-
Bertina, R.M.1
-
8
-
-
0023880718
-
Prevalence of hereditary thrombophilia and the identification of genetic risk factors
-
8. Bertina RM. Prevalence of hereditary thrombophilia and the identification of genetic risk factors. Fibrinolysis 1988;2(Suppl 2):7.
-
(1988)
Fibrinolysis
, vol.2
, Issue.SUPPL. 2
, pp. 7
-
-
Bertina, R.M.1
-
9
-
-
0029876985
-
Inherited thrombophilia: Pathogenesis, clinical syndromes, and management
-
9. De Stefano V, Finazzi G, Mannucci PM. Inherited thrombophilia: pathogenesis, clinical syndromes, and management. Blood 1996; 87:3531-44.
-
(1996)
Blood
, vol.87
, pp. 3531-3544
-
-
Stefano D. V1
Finazzi, G.2
Mannucci, P.M.3
-
10
-
-
0028861951
-
Coagulation factor V Leiden mutation may have a racial background
-
10. Fujimura H, Kambayashi J, Monden M, Kato H, Miyata T. Coagulation factor V Leiden mutation may have a racial background. Thromb Haemost 1995;74:1381-2.
-
(1995)
Thromb Haemost
, vol.74
, pp. 1381-1382
-
-
Fujimura, H.1
Kambayashi, J.2
Monden, M.3
Kato, H.4
Miyata, T.5
-
11
-
-
0025064295
-
Neonatal purpura fulminans associated with homozygous protein S deficiency
-
11. Mahasandana C, Suvatte V, Marlar RA, Manco-Johnson MJ, Jacobson LJ, Hathaway WE. Neonatal purpura fulminans associated with homozygous protein S deficiency. Lancet 1990;335:61-2.
-
(1990)
Lancet
, vol.335
, pp. 61-62
-
-
Mahasandana, C.1
Suvatte, V.2
Marlar, R.A.3
Manco-Johnson, M.J.4
Jacobson, L.J.5
Hathaway, W.E.6
-
13
-
-
0023851558
-
The gene for protein S maps near the centromere of human chromosome 3
-
13. Watkins PC, Eddy R, Fukushima Y, et al. The gene for protein S maps near the centromere of human chromosome 3. Blood 1988;71:238-41.
-
(1988)
Blood
, vol.71
, pp. 238-241
-
-
Watkins, P.C.1
Eddy, R.2
Fukushima, Y.3
-
14
-
-
0025035552
-
Organization of the human protein S gene
-
14. Schmidel DK, Tatro AV, Phelps LG, Tomczak JA, Long GL. Organization of the human protein S gene. Biochemistry 1990;29:7845-52.
-
(1990)
Biochemistry
, vol.29
, pp. 7845-7852
-
-
Schmidel, D.K.1
Tatro, A.V.2
Phelps, L.G.3
Tomczak, J.A.4
Long, G.L.5
-
15
-
-
0025003450
-
Intron-exon organization of the active human protein S gene PSa and its pseudogene PSb: Duplication and silencing during primate evolution
-
15. Ploos van Amstel HK, Reitsma PH, van der Logt PE, Bertina RM. Intron-exon organization of the active human protein S gene PSa and its pseudogene PSb: Duplication and silencing during primate evolution. Biochemistry 1990;29:7853-61.
-
(1990)
Biochemistry
, vol.29
, pp. 7853-7861
-
-
Ploos Van Amstel, H.K.1
Reitsma, P.H.2
Van Der Logt, P.E.3
Bertina, R.M.4
-
16
-
-
0025182946
-
Molecular analysis of the gene for vitamin K dependent protein S and its pseudogene: Cloning and partial gene organization
-
16. Edenbrandt C-M, Lundwall A, Wydro R, Stenflo J. Molecular analysis of the gene for vitamin K dependent protein S and its pseudogene: Cloning and partial gene organization. Biochemistry 1990;29:7861-8.
-
(1990)
Biochemistry
, vol.29
, pp. 7861-7868
-
-
Edenbrandt, C.-M.1
Lundwall, A.2
Wydro, R.3
Stenflo, J.4
-
17
-
-
0028054971
-
Three missense mutations in the protein C heavy chain causing type I and type II protein C deficiency
-
17. Miyata T, Zheng YZ, Sakata T, Tsushima N, Kato H. Three missense mutations in the protein C heavy chain causing type I and type II protein C deficiency. Thromb Haemost 1994; 71:32-7.
-
(1994)
Thromb Haemost
, vol.71
, pp. 32-37
-
-
Miyata, T.1
Zheng, Y.Z.2
Sakata, T.3
Tsushima, N.4
Kato, H.5
-
18
-
-
0023850178
-
Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase
-
18. Saiki RK, Gelfand DH, Stoffel S, et al. Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase. Science 1988; 239:487-91.
-
(1988)
Science
, vol.239
, pp. 487-491
-
-
Saiki, R.K.1
Gelfand, D.H.2
Stoffel, S.3
-
19
-
-
0024756969
-
Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction
-
19. Orita M, Suzuki Y, Sekiya T, Hayashi K. Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction. Genomics 1989;5:874-9.
-
(1989)
Genomics
, vol.5
, pp. 874-879
-
-
Orita, M.1
Suzuki, Y.2
Sekiya, T.3
Hayashi, K.4
-
20
-
-
10344257566
-
Gene characterization of protein C deficiency in Japanese subjects using a rapid and nonradioactive method for single-strand conformational polymorphism analysis and a model building
-
20. Miyata T, Sakata T, Zheng YZ, et al. Gene characterization of protein C deficiency in Japanese subjects using a rapid and nonradioactive method for single-strand conformational polymorphism analysis and a model building. Thromb Haemost 1996;76:302-11.
-
(1996)
Thromb Haemost
, vol.76
, pp. 302-311
-
-
Miyata, T.1
Sakata, T.2
Zheng, Y.Z.3
-
21
-
-
0021720421
-
Recurrent venous thromboembolism in patients with a partial deficiency of protein S
-
21. Comp P, Esmon C. Recurrent venous thromboembolism in patients with a partial deficiency of protein S. N Engl J Med 1984;311:1525-8.
-
(1984)
N Engl J Med
, vol.311
, pp. 1525-1528
-
-
Comp, P.1
Esmon, C.2
-
22
-
-
0010662163
-
Primary structure of bovine vitamin K-dependent protein S
-
22. Dahlbäck B, Lundwall A, Stenflo J. Primary structure of bovine vitamin K-dependent protein S. Proc Natl Acad Sci USA 1986;83: 4199-203.
-
(1986)
Proc Natl Acad Sci USA
, vol.83
, pp. 4199-4203
-
-
Dahlbäck, B.1
Lundwall, A.2
Stenflo, J.3
-
23
-
-
0027431508
-
Molecular cloning, expression and functional characterization of rabbit anticoagulant vitamin-K-dependent protein S
-
23. He X, Dahlbäck B. Molecular cloning, expression and functional characterization of rabbit anticoagulant vitamin-K-dependent protein S. Eur J Biochem 1993;217:857-65.
-
(1993)
Eur J Biochem
, vol.217
, pp. 857-865
-
-
He, X.1
Dahlbäck, B.2
-
24
-
-
0028021343
-
Structure of mouse protein S as determined by PCR amplification and DNA sequencing of cDNA
-
24. Deshun L, Schmidel DK, Long GL. Structure of mouse protein S as determined by PCR amplification and DNA sequencing of cDNA. Thromb Res 1994;74:135-42.
-
(1994)
Thromb Res
, vol.74
, pp. 135-142
-
-
Deshun, L.1
Schmidel, D.K.2
Long, G.L.3
-
25
-
-
0028949435
-
Molecular cloning and functional characterization of rat plasma protein S
-
25. Yasuda F, Hayashi T, Tanitame K, Nishioka J, Suzuki K. Molecular cloning and functional characterization of rat plasma protein S. J Biochem 1995;117:374-83.
-
(1995)
J Biochem
, vol.117
, pp. 374-383
-
-
Yasuda, F.1
Hayashi, T.2
Tanitame, K.3
Nishioka, J.4
Suzuki, K.5
-
26
-
-
0023651307
-
RNA splice junctions of different classes of eukaryotes: Sequence statistics and functional implications in gene expression
-
26. Shapiro MB, Senapathy P. RNA splice junctions of different classes of eukaryotes: Sequence statistics and functional implications in gene expression. Nucleic Acids Res 1987;15: 7155-74.
-
(1987)
Nucleic Acids Res
, vol.15
, pp. 7155-7174
-
-
Shapiro, M.B.1
Senapathy, P.2
-
29
-
-
0027953010
-
Protein S Tokushima: Abnormal molecule with a substitution of Glu for Lys-155 in the second epidermal growth factor-like domain of protein S
-
29. Hayashi T, Nishioka J, Shigekiyo T, Saito S, Suzuki K. Protein S Tokushima: Abnormal molecule with a substitution of Glu for Lys-155 in the second epidermal growth factor-like domain of protein S. Blood 1994;83:683-90.
-
(1994)
Blood
, vol.83
, pp. 683-690
-
-
Hayashi, T.1
Nishioka, J.2
Shigekiyo, T.3
Saito, S.4
Suzuki, K.5
-
30
-
-
0029021380
-
A quantitative protein S deficiency associated with a novel nonsense mutation and markedly reduced levels of mutated mRNA
-
30. Yamazaki T, Hamaguchi M, Katsumi A, Kagami K, Kojima T, Takamatsu J, Saito, H. A quantitative protein S deficiency associated with a novel nonsense mutation and markedly reduced levels of mutated mRNA. Thromb Haemost 1995;74:590-5.
-
(1995)
Thromb Haemost
, vol.74
, pp. 590-595
-
-
Yamazaki, T.1
Hamaguchi, M.2
Katsumi, A.3
Kagami, K.4
Kojima, T.5
Takamatsu, J.6
Saito, H.7
-
31
-
-
0029956042
-
Molecular basis of a hereditary type I protein S deficiency caused by a substitution of Cys for Arg474
-
31. Yamazaki T, Katsumi A, Kagami K, et al. Molecular basis of a hereditary type I protein S deficiency caused by a substitution of Cys for Arg474. Blood 1996;87:4643-50.
-
(1996)
Blood
, vol.87
, pp. 4643-4650
-
-
Yamazaki, T.1
Katsumi, A.2
Kagami, K.3
-
32
-
-
0029855572
-
A novel nonsense mutation associated with an exon skipping in a patient with hereditary protein S deficiency type I
-
32. Okamoto Y, Yamazaki T, Katsumi A, Kojima T, Takamatsu J, Nishida M, Saito H. A novel nonsense mutation associated with an exon skipping in a patient with hereditary protein S deficiency type I. Thromb Haemost 1996;75: 877-82.
-
(1996)
Thromb Haemost
, vol.75
, pp. 877-882
-
-
Okamoto, Y.1
Yamazaki, T.2
Katsumi, A.3
Kojima, T.4
Takamatsu, J.5
Nishida, M.6
Saito, H.7
-
33
-
-
0021723531
-
Differences of frequency distribution of plasminogen phenotypes between Japanese and American population: New methods for the detection of plasminogen variants
-
33. Aoki N, Tateno K, Sakata Y. Differences of frequency distribution of plasminogen phenotypes between Japanese and American population: New methods for the detection of plasminogen variants. Biochem Genet 1984; 22:871-81.
-
(1984)
Biochem Genet
, vol.22
, pp. 871-881
-
-
Aoki, N.1
Tateno, K.2
Sakata, Y.3
-
34
-
-
0029794495
-
Genetic diagnosis of dysplasminogenemia: Detection of an Ala601-Thr mutation in 118 out of 125 families and identification of a new Asp676-Asn mutation
-
34. Tsutsumi S, Saito T, Sakata T, Miyata T, Ichinose A. Genetic diagnosis of dysplasminogenemia: Detection of an Ala601-Thr mutation in 118 out of 125 families and identification of a new Asp676-Asn mutation. Thromb Haemost 1996;76:135-8.
-
(1996)
Thromb Haemost
, vol.76
, pp. 135-138
-
-
Tsutsumi, S.1
Saito, T.2
Sakata, T.3
Miyata, T.4
Ichinose, A.5
-
35
-
-
0031042313
-
Two distinct novel splice site mutations in a compound heterozygous patient with protein S deficiency
-
35. Yamazaki T, Katsumi A, Okamoto Y, et al. Two distinct novel splice site mutations in a compound heterozygous patient with protein S deficiency. Thromb Haemost 1997;77:14-20.
-
(1997)
Thromb Haemost
, vol.77
, pp. 14-20
-
-
Yamazaki, T.1
Katsumi, A.2
Okamoto, Y.3
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