-
1
-
-
0030199185
-
Fibrinogen and fibrin-proteins with complex roles in haemostasis and thrombosis
-
Blombäck B. Fibrinogen and fibrin-proteins with complex roles in haemostasis and thrombosis. Thromb Res 1996; 83: 1-75.
-
(1996)
Thromb Res
, vol.83
, pp. 1-75
-
-
Blombäck, B.1
-
2
-
-
0034089644
-
Fibrinogen functions and fibrin assembly
-
Mosesson M. Fibrinogen functions and fibrin assembly. Fibrinol Proteol 2000; 14: 182-6.
-
(2000)
Fibrinol Proteol
, vol.14
, pp. 182-186
-
-
Mosesson, M.1
-
5
-
-
0028877613
-
Familial dysfibrinogenemia and thrombophilia: report on a study of the SSC subcommittee on fibrinogen
-
Haverkate F, Samama M. Familial dysfibrinogenemia and thrombophilia: report on a study of the SSC subcommittee on fibrinogen. Thromb Haemost 1995; 73: 151-61.
-
(1995)
Thromb Haemost
, vol.73
, pp. 151-161
-
-
Haverkate, F.1
Samama, M.2
-
6
-
-
0032765219
-
Dysfibrinogenemia and thrombosis
-
Mosesson MW. Dysfibrinogenemia and thrombosis. Sem Thromb Hemost 1999; 3: 311-9.
-
(1999)
Sem Thromb Hemost
, vol.3
, pp. 311-319
-
-
Mosesson, M.W.1
-
7
-
-
0032723366
-
Structure and functions of fibrinogen: insights from dysfibrinogens
-
Matsuda M, Sugo T, Yoshida N, Terukina S, Yamazumi K, Niwa K, Maekawa H. Structure and functions of fibrinogen: insights from dysfibrinogens. Thromb Haemost 1999; 82: 283-90.
-
(1999)
Thromb Haemost
, vol.82
, pp. 283-290
-
-
Matsuda, M.1
Sugo, T.2
Yoshida, N.3
Terukina, S.4
Yamazumi, K.5
Niwa, K.6
Maekawa, H.7
-
8
-
-
0032697618
-
Biochemistry and physiology of blood coagulation
-
Mann KG. Biochemistry and physiology of blood coagulation. Thromb Haemost 1999; 82: 165-74.
-
(1999)
Thromb Haemost
, vol.82
, pp. 165-174
-
-
Mann, K.G.1
-
9
-
-
0020972653
-
The structure and evolution of vertebrate fibrinogen
-
Doolittle RF. The structure and evolution of vertebrate fibrinogen. Ann NY Acad Sci 1983; 408: 13-27.
-
(1983)
Ann NY Acad Sci
, vol.408
, pp. 13-27
-
-
Doolittle, R.F.1
-
10
-
-
0033519051
-
Venous thrombosis: a multicausal disease
-
Rosendaal FR. Venous thrombosis: a multicausal disease. Lancet 1999; 353: 1167-73.
-
(1999)
Lancet
, vol.353
, pp. 1167-1173
-
-
Rosendaal, F.R.1
-
11
-
-
0035912152
-
Genetic susceptibility to venous thrombosis
-
Seligsohn U, Lubetsky A. Genetic susceptibility to venous thrombosis. N Engl J Med 2001; 16: 1231-22.
-
(2001)
N Engl J Med
, vol.16
, pp. 1231-1322
-
-
Seligsohn, U.1
Lubetsky, A.2
-
12
-
-
62549105252
-
Bal dit Sollier C Drouet L. Environmental and genetic influences on fibrinogen level differently evidenced according to the technique of fibrinogen measurement: FITE-NAT multicenter study
-
(Abstract)
-
Mazoyer E, Ripoll L, Gueguen R, Bessie're C, Thomas S, Bal dit Sollier C, Drouet L. Environmental and genetic influences on fibrinogen level differently evidenced according to the technique of fibrinogen measurement: FITE-NAT multicenter study. Thromb Haemost 2001; Suppl.: P2197(Abstract).
-
(2001)
Thromb Haemost
, Issue.SUPPL.
, pp. 2197
-
-
Mazoyer, E.1
Ripoll, L.2
Gueguen, R.3
Bessie're, C.4
Thomas, S.5
-
13
-
-
0021070892
-
Fibrinogen Tokyo II: an abnormal fibrinogen with an impaired polymerization site on the aligned DD domain of fibrin molecules
-
Matsuda M, Baba M, Morimoto K, Nakamikawa C. Fibrinogen Tokyo II: an abnormal fibrinogen with an impaired polymerization site on the aligned DD domain of fibrin molecules. J Clin Invest 1983; 72: 1034-41.
-
(1983)
J Clin Invest
, vol.72
, pp. 1034-1041
-
-
Matsuda, M.1
Baba, M.2
Morimoto, K.3
Nakamikawa, C.4
-
14
-
-
0001408345
-
The preparation and some properties of fibrinogen precipitated from human plasma by glycine
-
Kazal LA, Amsel S, Miller OP, Tocantins LM. The preparation and some properties of fibrinogen precipitated from human plasma by glycine. Proc Soc Exp Biol Med 1963; 113: 989-94.
-
(1963)
Proc Soc Exp Biol Med
, vol.113
, pp. 989-994
-
-
Kazal, L.A.1
Amsel, S.2
Miller, O.P.3
Tocantins, L.M.4
-
15
-
-
0000163138
-
-
Nolan C, Ford N, Ferguson M (eds), New York: Cold Spring Harbour Laboratory Press, Vol. 2
-
Sambrook J, Fritsch EF, Maniatis T. In: Nolan C, Ford N, Ferguson M (eds) Molecular Cloning, Vol. 2. New York: Cold Spring Harbour Laboratory Press, 1989: 9.16-9.
-
(1989)
Molecular Cloning
, vol.9
, pp. 16-19
-
-
Sambrook, J.1
Fritsch, E.F.2
Maniatis, T.3
-
16
-
-
0014219240
-
Inherited fibrinogen abnormality causing thrombophilia
-
Egeberg O. Inherited fibrinogen abnormality causing thrombophilia. Thromb Diath Haemorrh 1967; 17: 176-87.
-
(1967)
Thromb Diath Haemorrh
, vol.17
, pp. 176-187
-
-
Egeberg, O.1
-
17
-
-
0037030659
-
Misdiagnosis of hereditary amyloidosis as AL (primary) amyloidosis
-
Lachmann HJ, Booth DR, Booth SE, Bybee A, Gilbertson JA, Gillmore JD, Pepys MB, Hawkins PN. Misdiagnosis of hereditary amyloidosis as AL (primary) amyloidosis. N Engl J Med 2002; 346: 1786-91.
-
(2002)
N Engl J Med
, vol.346
, pp. 1786-1791
-
-
Lachmann, H.J.1
Booth, D.R.2
Booth, S.E.3
Bybee, A.4
Gilbertson, J.A.5
Gillmore, J.D.6
Pepys, M.B.7
Hawkins, P.N.8
-
18
-
-
0034975060
-
A database for human fibrinogen variants
-
Hanss M, Biot F. A database for human fibrinogen variants. Ann NY Acad Sci 2001; 936: 89-90.
-
(2001)
Ann NY Acad Sci
, vol.936
, pp. 89-90
-
-
Hanss, M.1
Biot, F.2
-
19
-
-
0033997107
-
Fibrinogen Longmont: a dysfibrinogenemia that causes prolonged clot based test results only when using an optical detection method
-
Lefkowitz JB, DeBoom T, Weller A, Clarke S, Lavrinets D. Fibrinogen Longmont: a dysfibrinogenemia that causes prolonged clot based test results only when using an optical detection method. Am J Hematol 2000; 63: 149-55.
-
(2000)
Am J Hematol
, vol.63
, pp. 149-155
-
-
Lefkowitz, J.B.1
DeBoom, T.2
Weller, A.3
Clarke, S.4
Lavrinets, D.5
-
20
-
-
0021961821
-
Characterization of fibrinogen New York I A dysfunctional fibrinogen with a deletion of B b (9-72) corresponding exactly to exon 2 of the gene
-
Liu CY, Koehn JA, Morgan FJ. Characterization of fibrinogen New York I. A dysfunctional fibrinogen with a deletion of B b (9-72) corresponding exactly to exon 2 of the gene. J Biol Chem 1985; 260: 4390-6.
-
(1985)
J Biol Chem
, vol.260
, pp. 4390-4396
-
-
Liu, C.Y.1
Koehn, J.A.2
Morgan, F.J.3
-
21
-
-
0027461540
-
Paris I dysfibrinogenemia: a point mutation in intron 8 results in insertion of a 15 amino acid sequence in the fibrinogen gamma-chain
-
Rosenberg JB, Newman PJ, Mosesson MW, Guillin MC, Amrani DL. Paris I dysfibrinogenemia: a point mutation in intron 8 results in insertion of a 15 amino acid sequence in the fibrinogen gamma-chain. Thromb Haemost 1993; 69: 217-20.
-
(1993)
Thromb Haemost
, vol.69
, pp. 217-220
-
-
Rosenberg, J.B.1
Newman, P.J.2
Mosesson, M.W.3
Guillin, M.C.4
Amrani, D.L.5
-
22
-
-
0023686606
-
Fibrinogen Baltimore III: congenital dysfibrinogenemia with a shortened gamma-subunit
-
Ebert RF, Bell WR. Fibrinogen Baltimore III: congenital dysfibrinogenemia with a shortened gamma-subunit. Thromb Res 1988; 51: 251-8.
-
(1988)
Thromb Res
, vol.51
, pp. 251-258
-
-
Ebert, R.F.1
Bell, W.R.2
-
23
-
-
0011945366
-
Fibrinogen Pontoise-a genetically abnormal fibrinogen with defective fibrin polymerization but normal fibrinopeptide release
-
Lane DA, Henschen A, Jasani MK, eds, Berlin: Walter de Gruyter
-
Kaudewitz H, Henschen A, Soria J, Soria C. Fibrinogen Pontoise-a genetically abnormal fibrinogen with defective fibrin polymerization but normal fibrinopeptide release. In: Lane DA, Henschen A, Jasani MK, eds. Fibrinogen-Fibrin Formation and Fibrinolysis. Berlin: Walter de Gruyter, 1986: 91-6.
-
(1986)
Fibrinogen-Fibrin Formation and Fibrinolysis
, pp. 91-96
-
-
Kaudewitz, H.1
Henschen, A.2
Soria, J.3
Soria, C.4
-
24
-
-
0027299807
-
Molecular basis for fibrinogen Dusard (Aa 554Arg!Cys) and its association with abnormal fibrin polymerization and thrombophilia
-
Koopman J, Haverkate F, Grimbergen J, Lord ST, Mosesson MW, DiOrio JP, Siebenlist KS, Legrand C, Soria J, Soria C, Caen JP. Molecular basis for fibrinogen Dusard (Aa 554Arg!Cys) and its association with abnormal fibrin polymerization and thrombophilia. J Clin Invest 1993; 91: 1637-43.
-
(1993)
J Clin Invest
, vol.91
, pp. 1637-1643
-
-
Koopman, J.1
Haverkate, F.2
Grimbergen, J.3
Lord, S.T.4
Mosesson, M.W.5
DiOrio, J.P.6
Siebenlist, K.S.7
Legrand, C.8
Soria, J.9
Soria, C.10
Caen, J.P.11
-
25
-
-
0037150105
-
Structural organization of the fibrin (ogen) alpha C-domain
-
Tsurupa G, Tsonev L, Medved L. Structural organization of the fibrin (ogen) alpha C-domain. Biochemistry 2002; 41: 6449-59.
-
(2002)
Biochemistry
, vol.41
, pp. 6449-6459
-
-
Tsurupa, G.1
Tsonev, L.2
Medved, L.3
-
26
-
-
0029902174
-
Prediction of secondary structure content of proteins from their amino acid composition alone I. New analytic vector decomposition methods
-
Eisenhaber F, Imperiale F, Argos P, Froemmel C. Prediction of secondary structure content of proteins from their amino acid composition alone. I. New analytic vector decomposition methods. Proteins: Struct Funct Design 1996; 25: 169-79.
-
(1996)
Proteins: Struct Funct Design
, vol.25
, pp. 169-179
-
-
Eisenhaber, F.1
Imperiale, F.2
Argos, P.3
Froemmel, C.4
-
27
-
-
0027522533
-
Diversity of primary structures of the carboxy-terminal regions of mammalian fibrinogen Aa-chains
-
Murakawa M, Okamura T, Kamura T, Shibuya T, Harada M, Niho Y. Diversity of primary structures of the carboxy-terminal regions of mammalian fibrinogen Aa-chains. Thromb Haemost 1993; 69: 351-60.
-
(1993)
Thromb Haemost
, vol.69
, pp. 351-360
-
-
Murakawa, M.1
Okamura, T.2
Kamura, T.3
Shibuya, T.4
Harada, M.5
Niho, Y.6
-
28
-
-
0035936549
-
Identification and characterization of novel tPAand plasminogen-binding sites within fibrin(ogen) alpha C-domains
-
Tsurupa G, Medved L. Identification and characterization of novel tPAand plasminogen-binding sites within fibrin(ogen) alpha C-domains. Biochemistry 2001; 40: 801-8.
-
(2001)
Biochemistry
, vol.40
, pp. 801-808
-
-
Tsurupa, G.1
Medved, L.2
-
29
-
-
0018765359
-
The amino acid sequence of the alpha-chain of human fibrinogen
-
Doolittle RF, Watt KW, Cottrell BA, Strong DD, Riley M. The amino acid sequence of the alpha-chain of human fibrinogen. Nature 1979; 280: 464-8.
-
(1979)
Nature
, vol.280
, pp. 464-468
-
-
Doolittle, R.F.1
Watt, K.W.2
Cottrell, B.A.3
Strong, D.D.4
Riley, M.5
-
30
-
-
0023731893
-
Characterization of an apparently lower molecular weight gamma chain variant in fibrinogen Kyoto I The replacement of gamma asparagine 308 by lysine which causes accelerated cleavage of fragment D1 by plasmin and the generation of a new plasmin cleavage site
-
Yoshida N, Terukina S, Okuma M, Moroi M, Aoki N, Matsuda M. Characterization of an apparently lower molecular weight gamma chain variant in fibrinogen Kyoto I. The replacement of gamma asparagine 308 by lysine which causes accelerated cleavage of fragment D1 by plasmin and the generation of a new plasmin cleavage site. J Biol Chem 1988; 263: 13848-56.
-
(1988)
J Biol Chem
, vol.263
, pp. 13848-13856
-
-
Yoshida, N.1
Terukina, S.2
Okuma, M.3
Moroi, M.4
Aoki, N.5
Matsuda, M.6
-
31
-
-
0026507160
-
Abnormal fibrinogens Ijmuiden (Bβ Arg14→Cys) and Nijmegen (Bβ Arg44→Cys) form disulfide-linked fibrinogen-albumin complexes
-
Koopman J, Haverkate F, Grimbergen J, Engesser L, Novakova I, Kerst AF, Lord ST. Abnormal fibrinogens Ijmuiden (Bβ Arg14→Cys) and Nijmegen (Bβ Arg44→Cys) form disulfide-linked fibrinogen-albumin complexes. Proc Natl Acad Sci USA 1992; 89: 3478-82.
-
(1992)
Proc Natl Acad Sci USA
, vol.89
, pp. 3478-3482
-
-
Koopman, J.1
Haverkate, F.2
Grimbergen, J.3
Engesser, L.4
Novakova, I.5
Kerst, A.F.6
Lord, S.T.7
-
32
-
-
0028051450
-
A correlation between thrombotic disease and a specific fibrinogen abnormality (Aα 554 Arg→Cys) in two unrelated kindred Dusart and Chapel Hill III
-
Wada Y, Lord ST. A correlation between thrombotic disease and a specific fibrinogen abnormality (Aα 554 Arg→Cys) in two unrelated kindred, Dusart and Chapel Hill III. Blood 1994; 84: 3709-14.
-
(1994)
Blood
, vol.84
, pp. 3709-3714
-
-
Wada, Y.1
Lord, S.T.2
-
33
-
-
0027932744
-
A new substitution, γ358 Ser→Cys, in fibrinogen Milano VII causes defective fibrin polymerization
-
Steinmann C, Bögli C, Jungo M, Lämmle B, Heinemann G,Wermuth B, Redaelli R, Baudo F, Furlan M. A new substitution, γ358 Ser→Cys, in fibrinogen Milano VII causes defective fibrin polymerization. Blood 1994; 84: 1874-80.
-
(1994)
Blood
, vol.84
, pp. 1874-1880
-
-
Steinmann, C.1
Bögli, C.2
Jungo, M.3
Lämmle, B.4
Heinemann, G.5
Wermuth, B.6
Redaelli, R.7
Baudo, F.8
Furlan, M.9
-
34
-
-
0034912425
-
The molecular basis of inherited afibrinogenaemia
-
Neerman-Arbez M. The molecular basis of inherited afibrinogenaemia. Thromb Haemost 2001; 86: 154-63.
-
(2001)
Thromb Haemost
, vol.86
, pp. 154-163
-
-
Neerman-Arbez, M.1
-
35
-
-
0034651759
-
Missense mutations in the human β fibrinogen gene cause congenital afibrinogenemia by impairing fibrinogen secretion
-
Duga S, Asselta R, Santagostino E, Zeinali S, Simonic T, Malcovati M, Mannucci PM, Tenchini ML. Missense mutations in the human β fibrinogen gene cause congenital afibrinogenemia by impairing fibrinogen secretion. Blood 2000; 95: 1336-41.
-
(2000)
Blood
, vol.95
, pp. 1336-1341
-
-
Duga, S.1
Asselta, R.2
Santagostino, E.3
Zeinali, S.4
Simonic, T.5
Malcovati, M.6
Mannucci, P.M.7
Tenchini, M.L.8
-
36
-
-
0035986777
-
Analysis of Iranian patients allowed the identification of the first truncating mutation in the fibrinogen Bβ-chain gene causing afibrinogenemia
-
Asselta R, Spena S, Duga S, Peyvandi F, Malcovati M, Mannucci PM, Tenchini ML. Analysis of Iranian patients allowed the identification of the first truncating mutation in the fibrinogen Bβ-chain gene causing afibrinogenemia. Haematologica 2002; 87: 855-9.
-
(2002)
Haematologica
, vol.87
, pp. 855-859
-
-
Asselta, R.1
Spena, S.2
Duga, S.3
Peyvandi, F.4
Malcovati, M.5
Mannucci, P.M.6
Tenchini, M.L.7
-
37
-
-
0037114754
-
Congenital afibrinogenemia: first identification of splicing mutations in the fibrinogen Bβ-chain gene causing activation of cryptic splice sites
-
Spena S, Duga S, Asselta R, Malcovati M, Peyvandi F, Tenchini ML. Congenital afibrinogenemia: first identification of splicing mutations in the fibrinogen Bβ-chain gene causing activation of cryptic splice sites. Blood 2002; 100: 4478-84.
-
(2002)
Blood
, vol.100
, pp. 4478-4484
-
-
Spena, S.1
Duga, S.2
Asselta, R.3
Malcovati, M.4
Peyvandi, F.5
Tenchini, M.L.6
-
38
-
-
0026801171
-
Identification of Bβ chain domains involved in human fibrinogen assembly
-
Zhang JZ, Redman CM. Identification of Bβ chain domains involved in human fibrinogen assembly. J Biol Chem 1992; 267: 21727-32.
-
(1992)
J Biol Chem
, vol.267
, pp. 21727-21732
-
-
Zhang, J.Z.1
Redman, C.M.2
|