-
1
-
-
0018868033
-
Purification and properties of human coagulation factor VII
-
Broze GJ Jr, Majerus PW. Purification and properties of human coagulation factor VII. J Biol Chem 1980; 255: 1242-7.
-
(1980)
J Biol Chem
, vol.255
, pp. 1242-1247
-
-
Broze Jr., G.J.1
Majerus, P.W.2
-
2
-
-
0017639138
-
Activation of factor IX by the reaction product of tissue factor and factor VII: Additional pathway for initiating blood coagulation
-
Østerud B, Rapaport SI. Activation of factor IX by the reaction product of tissue factor and factor VII: Additional pathway for initiating blood coagulation. Proc Natl Acad Sci USA 1977; 74: 5260-4.
-
(1977)
Proc Natl Acad Sci USA
, vol.74
, pp. 5260-5264
-
-
Østerud, B.1
Rapaport, S.I.2
-
3
-
-
0027123107
-
Molecular and cellular biology of blood coagulation
-
Furie B, Furie BC. Molecular and cellular biology of blood coagulation. N Engl J Med 1992; 326: 800-6.
-
(1992)
N Engl J Med
, vol.326
, pp. 800-806
-
-
Furie, B.1
Furie, B.C.2
-
4
-
-
0018731365
-
Activation of human factor VII in plasma and in purified systems; roles of activated factor IX, kallikrein and activated factor XII
-
Seligsohn U, Østerud B, Brown SF, Griffin JH, Rapaport SI. Activation of human factor VII in plasma and in purified systems; roles of activated factor IX, kallikrein and activated factor XII. J Clin Invest 1979; 64: 1056-65.
-
(1979)
J Clin Invest
, vol.64
, pp. 1056-1065
-
-
Seligsohn, U.1
Østerud, B.2
Brown, S.F.3
Griffin, J.H.4
Rapaport, S.I.5
-
5
-
-
0026355315
-
Initiation of the extrinsic pathway of blood coagulation: Evidence for the tissue factor dependent autoactivation of human coagulation factor VII
-
Nakagaki T, Foster DC, Berkner KL, Kisiel W. Initiation of the extrinsic pathway of blood coagulation: evidence for the tissue factor dependent autoactivation of human coagulation factor VII. Biochemistry 1991; 30: 10819-24.
-
(1991)
Biochemistry
, vol.30
, pp. 10819-10824
-
-
Nakagaki, T.1
Foster, D.C.2
Berkner, K.L.3
Kisiel, W.4
-
6
-
-
0021342225
-
Regional mapping of clotting factors VII and X to 13q34. Expression of factor VII through chromosome 8
-
de Grouchy J, Dautzenberg MD, Turleau C, Béguin S, Chavin-Colin F. Regional mapping of clotting factors VII and X to 13q34. Expression of factor VII through chromosome 8. Hum Genet 1984; 66: 230-3.
-
(1984)
Hum Genet
, vol.66
, pp. 230-233
-
-
De Grouchy, J.1
Dautzenberg, M.D.2
Turleau, C.3
Béguin, S.4
Chavin-Colin, F.5
-
7
-
-
0004330552
-
Nucleotide sequence of the gene coding for human factor VII, a vitamin K-dependent protein participating in blood coagulation
-
O'Hara PJ, Grant FJ, Haldeman BA, Gray CL, Insley MY, Hagen FS, Murray MJ. Nucleotide sequence of the gene coding for human factor VII, a vitamin K-dependent protein participating in blood coagulation. Proc Natl Acad Sci USA 1987; 84: 5158-62.
-
(1987)
Proc Natl Acad Sci USA
, vol.84
, pp. 5158-5162
-
-
O'Hara, P.J.1
Grant, F.J.2
Haldeman, B.A.3
Gray, C.L.4
Insley, M.Y.5
Hagen, F.S.6
Murray, M.J.7
-
8
-
-
0022257323
-
Nucleotide sequence of the gene for human factor IX (antihemophilic factor B)
-
Yoshitake S, Schach BG, Foster DC, Davie EW, Kurachi K. Nucleotide sequence of the gene for human factor IX (antihemophilic factor B). Biochemistry 1985; 24: 3736-50.
-
(1985)
Biochemistry
, vol.24
, pp. 3736-3750
-
-
Yoshitake, S.1
Schach, B.G.2
Foster, D.C.3
Davie, E.W.4
Kurachi, K.5
-
9
-
-
0022871419
-
Gene for human factor X: A blood coagulation factor whose gene organization is essentially identical with that of factor IX and protein C
-
Leytus SP, Foster DC, Kurachi K, Davie EW. Gene for human factor X: A blood coagulation factor whose gene organization is essentially identical with that of factor IX and protein C. Biochemistry 1986; 25: 5098-102.
-
(1986)
Biochemistry
, vol.25
, pp. 5098-5102
-
-
Leytus, S.P.1
Foster, D.C.2
Kurachi, K.3
Davie, E.W.4
-
10
-
-
0005882312
-
Congenital SPCA deficiency: A hitherto unrecognized coagulation defect with hemorrhage rectified by serum and serum reactions
-
Alexander B, Goldstein R, Landwehr G, Cook CD. Congenital SPCA deficiency: A hitherto unrecognized coagulation defect with hemorrhage rectified by serum and serum reactions. J Clin Invest 1951; 30: 237-46.
-
(1951)
J Clin Invest
, vol.30
, pp. 237-246
-
-
Alexander, B.1
Goldstein, R.2
Landwehr, G.3
Cook, C.D.4
-
11
-
-
0019465270
-
Factor VII deficiency
-
Ragni MV, Lewis JH, Spero JA, Hasiba U, Factor VII deficiency. Am J Hematol 1981; 10: 79-88.
-
(1981)
Am J Hematol
, vol.10
, pp. 79-88
-
-
Ragni, M.V.1
Lewis, J.H.2
Spero, J.A.3
Hasiba, U.4
-
12
-
-
0020552654
-
Factor VII congenital deficiency. Clinical picture and classification of the variants
-
Mariani G, Mazzucconi MG. Factor VII congenital deficiency. Clinical picture and classification of the variants. Haemostatis 1983; 13: 169-77.
-
(1983)
Haemostatis
, vol.13
, pp. 169-177
-
-
Mariani, G.1
Mazzucconi, M.G.2
-
14
-
-
0022410305
-
Hereditary factor VII deficiency: Heterogeneity defined by combined functional and immunochemical analysis
-
Triplett DA, Brandt JT, McGann Batard MA, Schaeffer Dixon JL, Fair DS. Hereditary factor VII deficiency: heterogeneity defined by combined functional and immunochemical analysis. Blood 1985; 66: 1284-7.
-
(1985)
Blood
, vol.66
, pp. 1284-1287
-
-
Triplett, D.A.1
Brandt, J.T.2
McGann Batard, M.A.3
Schaeffer Dixon, J.L.4
Fair, D.S.5
-
15
-
-
0017706908
-
Factor VII Verona coagulation disorder: Double heterozygosis with an abnormal factor VII and heterozygous factor VII deficiency
-
Girolami A, Falezza G, Patrassi G, Stenico M, Vettore L. Factor VII Verona coagulation disorder: double heterozygosis with an abnormal factor VII and heterozygous factor VII deficiency. Blood 1977; 50: 603-10.
-
(1977)
Blood
, vol.50
, pp. 603-610
-
-
Girolami, A.1
Falezza, G.2
Patrassi, G.3
Stenico, M.4
Vettore, L.5
-
16
-
-
0018779271
-
Factor VII Padua 2: Another factor VII abnormality with defective ox brain thromboplastin activation and complex hereditary pattern
-
Girolami A, Cattarozzi G, Dal Bo Zanon R, Cella G, Toffanin F. Factor VII Padua 2: another factor VII abnormality with defective ox brain thromboplastin activation and complex hereditary pattern. Blood 1979; 54: 46-53.
-
(1979)
Blood
, vol.54
, pp. 46-53
-
-
Girolami, A.1
Cattarozzi, G.2
Dal Bo Zanon, R.3
Cella, G.4
Toffanin, F.5
-
17
-
-
0019447693
-
Factor VII deficiency: Immunological characterization of genetic variants and detection of carriers
-
Mariani G, Mazzucconi MG, Hermans J, Ciavarella N, Faiella A, Hassan HJ, Mannucci PM, Nenci GG, Orlando M, Romoli D, Mandelli F. Factor VII deficiency: immunological characterization of genetic variants and detection of carriers. Br J Haematol 1981; 48: 7-14.
-
(1981)
Br J Haematol
, vol.48
, pp. 7-14
-
-
Mariani, G.1
Mazzucconi, M.G.2
Hermans, J.3
Ciavarella, N.4
Faiella, A.5
Hassan, H.J.6
Mannucci, P.M.7
Nenci, G.G.8
Orlando, M.9
Romoli, D.10
Mandelli, F.11
-
18
-
-
0025871447
-
Purification and characterization of factor VII 304-Gln: A variant molecule with reduced activity isolated from a clinically unaffected male
-
O'Brien DP, Gale KM, Anderson JS, McVey JH, Miller GJ, Meade TW, Tuddenham EGD. Purification and characterization of factor VII 304-Gln: a variant molecule with reduced activity isolated from a clinically unaffected male. Blood 1991; 78: 132-40.
-
(1991)
Blood
, vol.78
, pp. 132-140
-
-
O'Brien, D.P.1
Gale, K.M.2
Anderson, J.S.3
McVey, J.H.4
Miller, G.J.5
Meade, T.W.6
Tuddenham, E.G.D.7
-
19
-
-
0026579362
-
Prenatal exclusion of severe factor VII deficiency by DNA sequencing
-
Millar DS, Cooper DN, Kakkar W, Schwartz M, Scheibel E. Prenatal exclusion of severe factor VII deficiency by DNA sequencing. Lancet 1992; 339: 1359.
-
(1992)
Lancet
, vol.339
, pp. 1359
-
-
Millar, D.S.1
Cooper, D.N.2
Kakkar, W.3
Schwartz, M.4
Scheibel, E.5
-
20
-
-
0027505065
-
Molecular analysis of factor VII deficiency in Italy: A frequent mutation (FVII Lazio) in a repeated intronic region
-
Bernardi F, Patracchini P, Gemmati D, Ferrati M, Arcieri P, Papacchini M, Redaelli R, Baudo F, Mariani G, Marchetti G. Molecular analysis of factor VII deficiency in Italy: a frequent mutation (FVII Lazio) in a repeated intronic region. Human Genet 1993; 92: 446-50.
-
(1993)
Human Genet
, vol.92
, pp. 446-450
-
-
Bernardi, F.1
Patracchini, P.2
Gemmati, D.3
Ferrati, M.4
Arcieri, P.5
Papacchini, M.6
Redaelli, R.7
Baudo, F.8
Mariani, G.9
Marchetti, G.10
-
21
-
-
0027171293
-
Detection of missense mutations by single-strand conformational polymorphism (SSCP) analysis in five dysfunctional variants of coagulation factor VII
-
Takamiya O, Kemball-Cook G, Martin DMA, Cooper DN, Von Felten A, Meili E, Hann I, Prangnell DR, Lumiey H, Tuddenham EGD, McVey JH. Detection of missense mutations by single-strand conformational polymorphism (SSCP) analysis in five dysfunctional variants of coagulation factor VII. Hum Mol Genet 1993; 2: 1355-9.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 1355-1359
-
-
Takamiya, O.1
Kemball-Cook, G.2
Martin, D.M.A.3
Cooper, D.N.4
Von Felten, A.5
Meili, E.6
Hann, I.7
Prangnell, D.R.8
Lumiey, H.9
Tuddenham, E.G.D.10
McVey, J.H.11
-
23
-
-
0028305158
-
Molecular defects in CRM+factor VII deficiencies: Modelling of missense mutations in catalytic domain of FVII
-
Bernardi F, Liney DL, Patracchini PP, Gemmati D, Legnani C, Arcieri P, Pinotti M, Redaelli R, Ballerini G, Pemberton S, Wacey AI, Mariani G, Tuddenham EGD, Marchetti G. Molecular defects in CRM+factor VII deficiencies: modelling of missense mutations in catalytic domain of FVII. Br J Haematol 1994; 86: 610-8.
-
(1994)
Br J Haematol
, vol.86
, pp. 610-618
-
-
Bernardi, F.1
Liney, D.L.2
Patracchini, P.P.3
Gemmati, D.4
Legnani, C.5
Arcieri, P.6
Pinotti, M.7
Redaelli, R.8
Ballerini, G.9
Pemberton, S.10
Wacey, A.I.11
Mariani, G.12
Tuddenham, E.G.D.13
Marchetti, G.14
-
24
-
-
0028175691
-
Factor VII Mie: Homozygous asymptomatic type I deficiency caused by an amino acid substitution of His (CAC) for Arg (247) (CGC) in the catalytic domain
-
Ohiwa M, Hayashi T, Wada H, Minamikawa K, Shirakawa S, Suzuki K. Factor VII Mie: Homozygous asymptomatic type I deficiency caused by an amino acid substitution of His (CAC) for Arg (247) (CGC) in the catalytic domain. Thromb Haemost 1994; 71: 773-7.
-
(1994)
Thromb Haemost
, vol.71
, pp. 773-777
-
-
Ohiwa, M.1
Hayashi, T.2
Wada, H.3
Minamikawa, K.4
Shirakawa, S.5
Suzuki, K.6
-
25
-
-
0028263506
-
Severe factor VII deficiency caused by mutations abolishing the cleavage site for activation and altering binding to tissue factor
-
Chaing S, Clarke B, Sridhara S, Chu K, Friedman P, VanDusen W, Roberts HR, Blajchman M, Monroe DM, High KA. Severe factor VII deficiency caused by mutations abolishing the cleavage site for activation and altering binding to tissue factor. Blood 1994; 83: 3524-35.
-
(1994)
Blood
, vol.83
, pp. 3524-3535
-
-
Chaing, S.1
Clarke, B.2
Sridhara, S.3
Chu, K.4
Friedman, P.5
VanDusen, W.6
Roberts, H.R.7
Blajchman, M.8
Monroe, D.M.9
High, K.A.10
-
26
-
-
0028059812
-
Molecular analysis of Polish patients with factor VII deficiency
-
Arbini AA, Bodkin D, Lopaciuk S, Bauer KA. Molecular analysis of Polish patients with factor VII deficiency. Blood 1994; 84: 2214-20.
-
(1994)
Blood
, vol.84
, pp. 2214-2220
-
-
Arbini, A.A.1
Bodkin, D.2
Lopaciuk, S.3
Bauer, K.A.4
-
27
-
-
0029153854
-
Inherited factor VII deficiency: Genetic and molecular pathology
-
Tuddenham EGD, Pemberton S, Cooper DN. Inherited factor VII deficiency: genetic and molecular pathology. Thromb Haemost 1995; 74: 313-21.
-
(1995)
Thromb Haemost
, vol.74
, pp. 313-321
-
-
Tuddenham, E.G.D.1
Pemberton, S.2
Cooper, D.N.3
-
28
-
-
0014858462
-
Dubin-Johnson syndrome in Israel. II. Association with Factor-VII deficiency
-
Seligsohn U, Shani M, Ramot B, Adam A, Sheba C. Dubin-Johnson syndrome in Israel. II. Association with Factor-VII deficiency. Quart J Med 1970; 39: 569-84.
-
(1970)
Quart J Med
, vol.39
, pp. 569-584
-
-
Seligsohn, U.1
Shani, M.2
Ramot, B.3
Adam, A.4
Sheba, C.5
-
29
-
-
0003010558
-
A perspective on genetic diseases among the Jewish people
-
Goodman RM, Motulsky AG, eds. New York: Raven Press
-
Goodman RM. A perspective on genetic diseases among the Jewish people. In: Genetic diseases among Ashkenazic Jews. Goodman RM, Motulsky AG, eds. New York: Raven Press, 1979, pp 1-17.
-
(1979)
Genetic Diseases among Ashkenazic Jews
, pp. 1-17
-
-
Goodman, R.M.1
-
30
-
-
0014986702
-
Abnormal excretion of the isomers of urinary coproporphyrin by patients with Dubin-Johnson syndrome in Israel
-
Ben-Ezzer J, Rimington C, Shani M, Seligsohn U, Sheba C, Szeinberg A. Abnormal excretion of the isomers of urinary coproporphyrin by patients with Dubin-Johnson syndrome in Israel. Clin Sci 1971; 40: 17-30.
-
(1971)
Clin Sci
, vol.40
, pp. 17-30
-
-
Ben-Ezzer, J.1
Rimington, C.2
Shani, M.3
Seligsohn, U.4
Sheba, C.5
Szeinberg, A.6
-
31
-
-
0020049449
-
Construction of human gene libraries from small amounts of peripheral blood: Analysis of beta-like globin genes
-
Poncz M, Solowiejczyk D, Harpel B, Mory Y, Schwartz E, Surrey S. Construction of human gene libraries from small amounts of peripheral blood: analysis of beta-like globin genes. Hemoglobin 1982; 6: 27-36.
-
(1982)
Hemoglobin
, vol.6
, pp. 27-36
-
-
Poncz, M.1
Solowiejczyk, D.2
Harpel, B.3
Mory, Y.4
Schwartz, E.5
Surrey, S.6
-
32
-
-
0018237450
-
Coupled amidolytic assay for factor VII: Its use with a clotting assay to determine the activity state of factor VII
-
Seligsohn U, Østerud B, Rapaport SI. Coupled amidolytic assay for factor VII: its use with a clotting assay to determine the activity state of factor VII. Blood 1978; 52: 978-88.
-
(1978)
Blood
, vol.52
, pp. 978-988
-
-
Seligsohn, U.1
Østerud, B.2
Rapaport, S.I.3
-
33
-
-
0025993003
-
A simple and rapid method of direct sequencing using Dynabeads
-
Them SL, Hinton J. A simple and rapid method of direct sequencing using Dynabeads. Br J Haematol 1991; 79: 113-5.
-
(1991)
Br J Haematol
, vol.79
, pp. 113-115
-
-
Them, S.L.1
Hinton, J.2
-
34
-
-
0025860324
-
A common genetic polymorphism associated with lower coagulation factor VII levels in healthy individuals
-
Green F, Kelleher C, Wilkes H, Temple A, Meade T, Humphries S. A common genetic polymorphism associated with lower coagulation factor VII levels in healthy individuals. Arterioscler Thromb 1991; 11: 540-6.
-
(1991)
Arterioscler Thromb
, vol.11
, pp. 540-546
-
-
Green, F.1
Kelleher, C.2
Wilkes, H.3
Temple, A.4
Meade, T.5
Humphries, S.6
-
35
-
-
9044243754
-
Factor VII gene polymorphism contribute about one third of the factor VII level variation in plasma
-
Bernardi F, Marchetti G, Pinotti M, Baroncini C, Papcchini M, Zepponi E, Ursicino N, Chiarotti F, Mariani G. Factor VII gene polymorphism contribute about one third of the factor VII level variation in plasma. Arterioscier Thromb Vascular Biol 1996; 16: 72-6.
-
(1996)
Arterioscier Thromb Vascular Biol
, vol.16
, pp. 72-76
-
-
Bernardi, F.1
Marchetti, G.2
Pinotti, M.3
Baroncini, C.4
Papcchini, M.5
Zepponi, E.6
Ursicino, N.7
Chiarotti, F.8
Mariani, G.9
-
36
-
-
0004069901
-
-
W. H. Freeman and Company, San Francisco, CA, USA
-
Sneath PH, Sokal RR. Numerical Taxonomy. W. H. Freeman and Company, San Francisco, CA, USA, 1971.
-
(1971)
Numerical Taxonomy
-
-
Sneath, P.H.1
Sokal, R.R.2
-
37
-
-
0014757386
-
A general method applicable to the search for similarities in the amino acid sequence of two proteins
-
Needleman SB, Wünsch CD. A general method applicable to the search for similarities in the amino acid sequence of two proteins. J Mol Biol 1970; 48: 443-53.
-
(1970)
J Mol Biol
, vol.48
, pp. 443-453
-
-
Needleman, S.B.1
Wünsch, C.D.2
-
38
-
-
0025287330
-
Comparative modeling methods: Application to the family of the mammalian serine proteases
-
Greer J. Comparative modeling methods: application to the family of the mammalian serine proteases. Proteins 1990; 7: 317-34.
-
(1990)
Proteins
, vol.7
, pp. 317-334
-
-
Greer, J.1
-
39
-
-
0017411710
-
The Protein Data Bank: A computer-based archival file for macromolecular structures
-
Bernstein FC, Koetzle TF, Williams GJ, Meyer EF Jr, Brice MD, Rodger JR, Kennard O, Shimanouchi T, Tasumi M. The Protein Data Bank: a computer-based archival file for macromolecular structures. J Mol Biol 1977; 112: 535-42.
-
(1977)
J Mol Biol
, vol.112
, pp. 535-542
-
-
Bernstein, F.C.1
Koetzle, T.F.2
Williams, G.J.3
Meyer Jr., E.F.4
Brice, M.D.5
Rodger, J.R.6
Kennard, O.7
Shimanouchi, T.8
Tasumi, M.9
-
40
-
-
0023632422
-
Determination of three-dimensional protein structure from nuclear magnetic resonance data using fragments of known structures
-
Kruiis PJ, Jones TA. Determination of three-dimensional protein structure from nuclear magnetic resonance data using fragments of known structures. Protein 1987; 2: 188-201.
-
(1987)
Protein
, vol.2
, pp. 188-201
-
-
Kruiis, P.J.1
Jones, T.A.2
-
41
-
-
0021366157
-
Restriction sites containing CpG show a higher frequency of polymorphism in human DNA
-
Barker D, Schafer M, White R. Restriction sites containing CpG show a higher frequency of polymorphism in human DNA. Cell 1984; 36: 131-8.
-
(1984)
Cell
, vol.36
, pp. 131-138
-
-
Barker, D.1
Schafer, M.2
White, R.3
-
42
-
-
0019888748
-
Comparative model-building of the mammalian serine proteases
-
Greer J. Comparative model-building of the mammalian serine proteases. J Mol Biol 1981; 153: 1027-42.
-
(1981)
J Mol Biol
, vol.153
, pp. 1027-1042
-
-
Greer, J.1
-
43
-
-
0021766631
-
Critical evaluation of comparative model building of Streptomyces griseus trypsin
-
Read RJ, Brayer GD, Jurasek L, James MN. Critical evaluation of comparative model building of Streptomyces griseus trypsin. Biochemistry 1984; 23: 6570-5.
-
(1984)
Biochemistry
, vol.23
, pp. 6570-6575
-
-
Read, R.J.1
Brayer, G.D.2
Jurasek, L.3
James, M.N.4
-
44
-
-
0026317115
-
Factor IX Amagasaki: A new mutation in the catalytic domain resulting in the loss of both coagulant and esterase activities
-
Miyata T, Sakai T, Sugimoto M, Naka H, Yamamoto K, Yoshioka A, Fukui H, Mitsui K, Kamiya K, Umeyama H, Iwangag S. Factor IX Amagasaki: a new mutation in the catalytic domain resulting in the loss of both coagulant and esterase activities. Biochemistry 1991; 30: 11286-91.
-
(1991)
Biochemistry
, vol.30
, pp. 11286-11291
-
-
Miyata, T.1
Sakai, T.2
Sugimoto, M.3
Naka, H.4
Yamamoto, K.5
Yoshioka, A.6
Fukui, H.7
Mitsui, K.8
Kamiya, K.9
Umeyama, H.10
Iwangag, S.11
-
46
-
-
0019809306
-
Model of a specific interaction. Salt bridges form between prothrombin and its activating enzyme blood clotting factor Xa
-
Greer J. Model of a specific interaction. Salt bridges form between prothrombin and its activating enzyme blood clotting factor Xa. J Mol Biol 1981; 153: 1043-53.
-
(1981)
J Mol Biol
, vol.153
, pp. 1043-1053
-
-
Greer, J.1
-
47
-
-
0019957643
-
Computer-generated models of blood coagulation factor Xa, factor IXa, and thrombin based upon structural homology with other serine proteases
-
Furie B, Bing DH, Feldmann RJ, Robison DJ, Burnier JP, Furie BC. Computer-generated models of blood coagulation factor Xa, factor IXa, and thrombin based upon structural homology with other serine proteases. J Biol Chem 1982; 257: 3875-81.
-
(1982)
J Biol Chem
, vol.257
, pp. 3875-3881
-
-
Furie, B.1
Bing, D.H.2
Feldmann, R.J.3
Robison, D.J.4
Burnier, J.P.5
Furie, B.C.6
-
48
-
-
0022407061
-
A characterization of human blood coagulation factor XII cDNA. Prediction of the primary structure of factor XII and the tertiary structure of β-factor XIIa
-
Cool DE, Edgell SC, Louie GV, Zoller MJ, Brayer GD, MacGillivray RT. A characterization of human blood coagulation factor XII cDNA. Prediction of the primary structure of factor XII and the tertiary structure of β-factor XIIa. J Biol Chem 1985; 260: 13666-76.
-
(1985)
J Biol Chem
, vol.260
, pp. 13666-13676
-
-
Cool, D.E.1
Edgell, S.C.2
Louie, G.V.3
Zoller, M.J.4
Brayer, G.D.5
MacGillivray, R.T.6
-
49
-
-
0025125947
-
Mutations causing hemophilia B: Direct estimate of the underlying rates of spontaneous germ-line transitions, transversions and deletions in the human gene
-
Koeberl DD, Bottema CDK, Ketterling RP, Bridge PJ, Lillicrap DP, Somer SS. Mutations causing hemophilia B: direct estimate of the underlying rates of spontaneous germ-line transitions, transversions and deletions in the human gene. Am J Hum Genet 1990; 47: 202-17.
-
(1990)
Am J Hum Genet
, vol.47
, pp. 202-217
-
-
Koeberl, D.D.1
Bottema, C.D.K.2
Ketterling, R.P.3
Bridge, P.J.4
Lillicrap, D.P.5
Somer, S.S.6
-
50
-
-
0027311097
-
A molecular model of the serine protease domain of activated protein C: Application to the study of missense mutations causing protein C deficiency
-
Wacey AI, Pemberton S, Cooper DN, Kakkar VV, Tuddenham EGD. A molecular model of the serine protease domain of activated protein C: application to the study of missense mutations causing protein C deficiency. Br J Hematol 1993; 84: 290-300.
-
(1993)
Br J Hematol
, vol.84
, pp. 290-300
-
-
Wacey, A.I.1
Pemberton, S.2
Cooper, D.N.3
Kakkar, V.V.4
Tuddenham, E.G.D.5
-
51
-
-
0026498483
-
The study of gene-environment interactions that influence thrombosis and fibrinolysis
-
Humphries SE, Lane A, Dawson S, Green FR. The study of gene-environment interactions that influence thrombosis and fibrinolysis. Arch Pathol Lab Med 1992; 116: 1322-9.
-
(1992)
Arch Pathol Lab Med
, vol.116
, pp. 1322-1329
-
-
Humphries, S.E.1
Lane, A.2
Dawson, S.3
Green, F.R.4
-
52
-
-
0343213918
-
Reduced plasma factor VII coagulant activity due to the Arg 353 Gin polymorphism in the factor VII gene results from defective secretion
-
Arbini AA, Bauer KA. Reduced plasma factor VII coagulant activity due to the Arg 353 Gin polymorphism in the factor VII gene results from defective secretion. Blood (abstr) 1994; 84: 333a.
-
(1994)
Blood
, vol.84
, Issue.ABSTR
-
-
Arbini, A.A.1
Bauer, K.A.2
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