-
1
-
-
0026337077
-
The coagulation cascade: Initiation, maintenance, and regulation
-
Davie EW, Fujikawa K, Kisiel W. The coagulation cascade: initiation, maintenance, and regulation. Biochemistry. 1991 ;30:10,363-10,370.
-
(1991)
Biochemistry.
, vol.30
, pp. 10363-10370
-
-
Davie, E.W.1
Fujikawa, K.2
Kisiel, W.3
-
4
-
-
0032560553
-
Prothrombin deficiency results in embryonic and neonatal lethality in mice
-
Sun WY, Witte D, Degen JL, et al. Prothrombin deficiency results in embryonic and neonatal lethality in mice. Proc Natl Acad Sei U S A. 199895:7597-7602.
-
(1998)
Proc Natl Acad Sei U S A.
, vol.95
, pp. 7597-7602
-
-
Sun, W.Y.1
Witte, D.2
Degen, J.L.3
-
5
-
-
0032560579
-
Incomplete embry-onic lethality and fatal neonatal hemorrhage caused by prothrombin deficiency in mice
-
Xue J, Wu, Westfield LA, et al. Incomplete embry-onic lethality and fatal neonatal hemorrhage caused by prothrombin deficiency In mice. Proc Natl Acad Sei USA. 1998:95:7603-7607.
-
(1998)
Proc Natl Acad Sei USA.
, vol.95
, pp. 7603-7607
-
-
Xue, J.1
Wu2
Westfield, L.A.3
-
6
-
-
0012368975
-
A quantitative one-stage method for the assay of prothrombin
-
Owen PA. A quantitative one-stage method for the assay of prothrombin. Scan J Clin Lab Invest. 1949;1:81-89.
-
(1949)
Scan J Clin Lab Invest.
, vol.1
, pp. 81-89
-
-
Owen, P.A.1
-
7
-
-
0345128844
-
Polymorphic DMA region adjacent to the 5' end of the human insulin gene
-
Bell Gl, Karam JH, Rutter WJ. Polymorphic DMA region adjacent to the 5' end of the human insulin gene. Proc Natl Acad Sei U S A. 1981 ;78:57595763.
-
(1981)
Proc Natl Acad Sei U S A.
, vol.78
, pp. 57595763
-
-
Gl, B.1
Karam, J.H.2
Rutter, W.J.3
-
9
-
-
0031820586
-
The SSCP phenomenon: Addition of HEPES buffer dramatically affects electophoretic mobility
-
Liu Q, Sommer SS. The SSCP phenomenon: addition of HEPES buffer dramatically affects electophoretic mobility. Biotechniques. 1998:25:5056.
-
(1998)
Biotechniques.
, vol.25
, pp. 5056
-
-
Liu, Q.1
Sommer, S.S.2
-
10
-
-
0023230641
-
Nucleotide sequence of the gene for human prothrombin
-
Degen SJF, Davie EW. Nucleotide sequence of the gene for human prothrombin. Biochemistry. 1937:26:6165-6177.
-
(1937)
Biochemistry.
, vol.26
, pp. 6165-6177
-
-
Degen, S.J.F.1
Davie, E.W.2
-
11
-
-
0029035987
-
A point mutation (Arg271-Cys) of a homozygote for dysfunctional prothrombin, prothrombin Obihiro, which has a region of high sequence variability
-
iMyata, T, Zheng Y-Z, Kalo A, Kalo H. A point mutation (Arg271-Cys) of a homozygote for dysfunctional prothrombin, prothrombin Obihiro, which has a region of high sequence variability. Br J Haematol. 1995:90:688-692.
-
(1995)
Br J Haematol.
, vol.90
, pp. 688-692
-
-
Myata, T.1
Zheng, Y.-Z.2
Kalo, A.3
Kalo, H.4
-
12
-
-
0020584329
-
Characterization of the complementary deoxynucleic acid and gene coding for human prothrombin
-
Degen SJF, MacGillivrary RTA, Davie EW. Characterization of the complementary deoxynucleic acid and gene coding for human prothrombin. Biochemistry. 1983:22:2087-2097.
-
(1983)
Biochemistry.
, vol.22
, pp. 2087-2097
-
-
Degen, S.J.F.1
MacGillivrary, R.T.A.2
Davie, E.W.3
-
13
-
-
0026598028
-
Highly polymorphic region of the human prothrombin (F2) gene
-
Iwahana H, Yoshimoto K, Itakura M. Highly polymorphic region of the human prothrombin (F2) gene.. Human Genet. 1992;89:123-124.
-
(1992)
Human Genet.
, vol.89
, pp. 123-124
-
-
Iwahana, H.1
Yoshimoto, K.2
Itakura, M.3
-
14
-
-
0019908206
-
Cleavage and activation of human prothrombin by Echis carinatus venom
-
Briet MJ, Noyes CM, Roberts HR, Griffith MJ. Cleavage and activation of human prothrombin by Echis carinatus venom. Thromb Res. 1982;27: 591-600.
-
(1982)
Thromb Res.
, vol.27
, pp. 591-600
-
-
Briet, M.J.1
Noyes, C.M.2
Roberts, H.R.3
Griffith, M.J.4
-
15
-
-
0020322011
-
Role of meizothrombin and meizothrombin-(desF1) in the conversion of prothrombin to thrombin by Echis carinatus venom
-
Rhee MJ, Morris S, Kosow DP. Role of meizothrombin and meizothrombin-(desF1) in the conversion of prothrombin to thrombin by Echis carinatus venom. Biochemistry. 1982;21:3437-3443.
-
(1982)
Biochemistry.
, vol.21
, pp. 3437-3443
-
-
Rhee, M.J.1
Morris, S.2
Kosow, D.P.3
-
16
-
-
0022455302
-
Prothrombin Clamart: Prothrombin variant with defective Arg 320-lle cleavage by factor Xa
-
Huisse M-G, Dreyfus M, Guillin M-C. Prothrombin Clamart: prothrombin variant with defective Arg 320-lle cleavage by factor Xa. Thromb Res. 1986; 44:11-21.
-
(1986)
Thromb Res.
, vol.44
, pp. 11-21
-
-
Huisse, M.-G.1
Dreyfus, M.2
Guillin, M.-C.3
-
17
-
-
0028073896
-
Prothrombin Padua I: Incomplete activation due to anamino acid substitution at a factor Xa cleavage site
-
James HL, Kim DJ. Zheng D-Q, Girolami A. Prothrombin Padua I: incomplete activation due to anamino acid substitution at a factor Xa cleavage site. Blood Coagul Fibrinolysis. 1994:5:841-844.
-
(1994)
Blood Coagul Fibrinolysis.
, vol.5
, pp. 841-844
-
-
James, H.L.1
Kim, D.J.2
Zheng, D.-Q.3
Girolami, A.4
-
18
-
-
0029815902
-
Genetic analysis and functional characterization of prothrombins Corpus Christi (Arg 382-Cys), Dhahran (Arg271-His), and Hypoprothrombinemia
-
O'Marcaigh AS, Nichols WL, Hassinger NL, et al. Genetic analysis and functional characterization of prothrombins Corpus Christi (Arg 382-Cys), Dhahran (Arg271-His), and Hypoprothrombinemia. Blood. 1996:88:2611-2618.
-
(1996)
Blood.
, vol.88
, pp. 2611-2618
-
-
O'Marcaigh, A.S.1
Nichols, W.L.2
Hassinger, N.L.3
-
19
-
-
0022978454
-
Molecular defect of prothrombin Barcelona: Substitution of cysteine förarginine at residue 273
-
Rabiet M-J, Furie BC, Furie B. Molecular defect of prothrombin Barcelona: substitution of cysteine förarginine at residue 273. J Biol. Chem. 1986; 261:15,045-15,048.
-
(1986)
J Biol. Chem.
, vol.261
, pp. 15045-15048
-
-
Rabiet, M.-J.1
Furie, B.C.2
Furie, B.3
|