-
1
-
-
0029153854
-
Inherited FVII deficiency: Genetics and molecular pathology
-
Tuddenham EGD, Pemberton S, Cooper DN. Inherited FVII deficiency: genetics and molecular pathology. Thromb Haemost 1995; 74:313-321.
-
(1995)
Thromb Haemost
, vol.74
, pp. 313-321
-
-
Tuddenham, E.G.D.1
Pemberton, S.2
Cooper, D.N.3
-
2
-
-
0035165403
-
FVII deficiency and the FVII mutation database
-
McVey JH, Boswell E, Mumford AD, Kemball-Cook G, Tuddenham EG. FVII deficiency and the FVII mutation database. Hum Murat 2001; 17:3-17.
-
(2001)
Hum Murat
, vol.17
, pp. 3-17
-
-
McVey, J.H.1
Boswell, E.2
Mumford, A.D.3
Kemball-Cook, G.4
Tuddenham, E.G.5
-
3
-
-
0022410305
-
Hereditary FVII deficiency heterogeneity defined by combined functional and immuno-chemical analysis
-
Triplet DA, Brandt JT, Batard MA, Dixon JS, Fair DS. Hereditary FVII deficiency heterogeneity defined by combined functional and immuno-chemical analysis. Blood 1985; 66:1284-1287.
-
(1985)
Blood
, vol.66
, pp. 1284-1287
-
-
Triplet, D.A.1
Brandt, J.T.2
Batard, M.A.3
Dixon, J.S.4
Fair, D.S.5
-
4
-
-
0028305158
-
Molecular defects in CRM+ FVII deficiencies: Modelling of missense mutations in the catalytic domain of FVII
-
Bernardi F, Liney DL, Patracchini P, Gemmati D, Legnani C, Arcieri P, et al. Molecular defects in CRM+ FVII deficiencies: modelling of missense mutations in the catalytic domain of FVII. Br J Haematol 1994; 86:610-618.
-
(1994)
Br J Haematol
, vol.86
, pp. 610-618
-
-
Bernardi, F.1
Liney, D.L.2
Patracchini, P.3
Gemmati, D.4
Legnani, C.5
Arcieri, P.6
-
5
-
-
0024595101
-
Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms
-
Orita M, Iwahana H, Kanazawa H, Hayashi K, Sekiya T. Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms. Proc Natl Acad Sci USA 1989; 86:2766-2770.
-
(1989)
Proc Natl Acad Sci USA
, vol.86
, pp. 2766-2770
-
-
Orita, M.1
Iwahana, H.2
Kanazawa, H.3
Hayashi, K.4
Sekiya, T.5
-
6
-
-
0027433113
-
Conformation-sensitive gel electrophoresis for detection of single-base differences in double-strand PCR products and DNA fragments: Evidence for solvent-induced bends in DNA heteroduplexes
-
Ganguly A, Rock MJ, Prockkop DJ. Conformation-sensitive gel electrophoresis for detection of single-base differences in double-strand PCR products and DNA fragments: evidence for solvent-induced bends in DNA heteroduplexes. Proc Natl Acad Sci USA 1993; 90:10325-10329.
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 10325-10329
-
-
Ganguly, A.1
Rock, M.J.2
Prockkop, D.J.3
-
7
-
-
0026730351
-
Detection of two missense mutations and characterization of a repeat polymorphism in the F VII gene (F7)
-
Marchetti G, Patracchini P, Gemmati D, DeRosa V, Pinotti M, Casonato A, et al. Detection of two missense mutations and characterization of a repeat polymorphism in the F VII gene (F7). Hum Genet 1992; 89:497-502.
-
(1992)
Hum Genet
, vol.89
, pp. 497-502
-
-
Marchetti, G.1
Patracchini, P.2
Gemmati, D.3
DeRosa, V.4
Pinotti, M.5
Casonato, A.6
-
8
-
-
0025784472
-
PCR detection of repeat polymorphism within the F7 gene
-
Marchetti G, Gemmati D, Patracchini P, Pinotti M, Bernardi F. PCR detection of repeat polymorphism within the F7 gene [Letter]. Nucl Acids Res 1991; 19:4570.
-
(1991)
Nucl Acids Res
, vol.19
, pp. 4570
-
-
Marchetti, G.1
Gemmati, D.2
Patracchini, P.3
Pinotti, M.4
Bernardi, F.5
-
9
-
-
0025860324
-
A common genetic polymorphism associated with lower coagulation F 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 F VII levels in healthy individuals. Arterioscler Thromb 1991; 11:540-546.
-
(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
-
10
-
-
0006369656
-
Two common functional polymorphisms in the promoter region of the coagulation F7 gene determining plasma F VII activity and mass concentration
-
Van't Hooft FM, Silveira A, Tornvall P, Iliadou A, Ehrenborg E, Eriksson P, Hamsten A. Two common functional polymorphisms in the promoter region of the coagulation F7 gene determining plasma F VII activity and mass concentration. Blood 1999; 93:3432-3441.
-
(1999)
Blood
, vol.93
, pp. 3432-3441
-
-
Van't Hooft, F.M.1
Silveira, A.2
Tornvall, P.3
Iliadou, A.4
Ehrenborg, E.5
Eriksson, P.6
Hamsten, A.7
-
11
-
-
0028332374
-
F VII antigen levels in a healthy blood donor population
-
Howard PR, Bovill EG, Pike J, Church WR, Tracy RP. F VII antigen levels in a healthy blood donor population. Thromb Haemost 1994; 72:21-27.
-
(1994)
Thromb Haemost
, vol.72
, pp. 21-27
-
-
Howard, P.R.1
Bovill, E.G.2
Pike, J.3
Church, W.R.4
Tracy, R.P.5
-
12
-
-
0026583358
-
Haemophilia B: Database of point mutations and short additions and deletions, third edition
-
Giannelli F, Green PM, High KA, Sommer S, Lillicrap DP, LudwigM, et al. Haemophilia B: database of point mutations and short additions and deletions, third edition. Nucl Acids Res 1992; 20:2027-2063.
-
(1992)
Nucl Acids Res
, vol.20
, pp. 2027-2063
-
-
Giannelli, F.1
Green, P.M.2
High, K.A.3
Sommer, S.4
Lillicrap, D.P.5
Ludwig, M.6
-
13
-
-
17344368674
-
Contribution of F VII genotype to activated FVII levels
-
Bernardi F, Arcieri P, Bertina RM, Chiarotti F, Corral J, Pinotti M, et al. Contribution of F VII genotype to activated FVII levels. Arterioscler Thromb Vasc Biol 1997; 17:2548-2553.
-
(1997)
Arterioscler Thromb Vasc Biol
, vol.17
, pp. 2548-2553
-
-
Bernardi, F.1
Arcieri, P.2
Bertina, R.M.3
Chiarotti, F.4
Corral, J.5
Pinotti, M.6
-
14
-
-
0033757946
-
Molecular analysis of the genotype-phenotype relationship in F VII deficiency
-
Millar DS, Kemball-Cook G, McVey JH, Tuddenham EG, Mumford AD, Attock GB, et al. Molecular analysis of the genotype-phenotype relationship in F VII deficiency. Hum Genet 2000; 107:S327-S342.
-
(2000)
Hum Genet
, vol.107
-
-
Millar, D.S.1
Kemball-Cook, G.2
McVey, J.H.3
Tuddenham, E.G.4
Mumford, A.D.5
Attock, G.B.6
|