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Results: 1-12 |
Results: 12
Aberrant dimerization of von Willebrand factor as the result of mutations in the carboxy-terminal region: identification of 3 mutations in members of3 different families with type 2A (phenotype IID) von Willebrand disease
Authors: Enayat, MS Guilliatt, AM Surdhar, GK Jenkins, PV Pasi, KJ Toh, CH Williams, MD Hill, FGH
Citation: Ms. Enayat et al., Aberrant dimerization of von Willebrand factor as the result of mutations in the carboxy-terminal region: identification of 3 mutations in members of3 different families with type 2A (phenotype IID) von Willebrand disease, BLOOD, 98(3), 2001, pp. 674-680
Identification and three-dimensional structural analysis of nine novel mutations in patients with prothrombin deficiency
Authors: Akhavan, S Mannucci, PM Lak, M Mancuso, G Mazzucconi, MG Rocino, A Jenkins, PV Perkins, SJ
Citation: S. Akhavan et al., Identification and three-dimensional structural analysis of nine novel mutations in patients with prothrombin deficiency, THROMB HAEM, 84(6), 2000, pp. 989-997
Identification of type 2 von Willebrand disease in previously diagnosed type 1 patients. a reappraisal using phenotypes, genotypes and molecular modelling
Authors: Nitu-Whalley, IC Riddell, A Lee, CA Pasi, KJ Owens, D Enayat, MS Perkins, SJ Jenkins, PV
Citation: Ic. Nitu-whalley et al., Identification of type 2 von Willebrand disease in previously diagnosed type 1 patients. a reappraisal using phenotypes, genotypes and molecular modelling, THROMB HAEM, 84(6), 2000, pp. 998-1004
Homozygous 2bp deletion in the human factor VII gene: A non-lethal mutation that is associated with a complete absence of circulating factor VII
Authors: Peyvandi, F Mannucci, PM Jenkins, PV Lee, A Coppola, R Perry, DJ
Citation: F. Peyvandi et al., Homozygous 2bp deletion in the human factor VII gene: A non-lethal mutation that is associated with a complete absence of circulating factor VII, THROMB HAEM, 84(4), 2000, pp. 635-637
Type 2M vWD resulting from a lysine deletion within a four lysine residue repeat in the A1 loop of von Willebrand factor
Authors: Hilbert, L Jenkins, PV Gaucher, C Meriane, E Collins, PW Pasi, KJ Mazurier, C
Citation: L. Hilbert et al., Type 2M vWD resulting from a lysine deletion within a four lysine residue repeat in the A1 loop of von Willebrand factor, THROMB HAEM, 84(2), 2000, pp. 188-194
Molecular characterisation and three-dimensional structural analysis of mutations in 21 unrelated families with inherited factor VII deficiency
Authors: Peyvandi, F Jenkins, PV Mannucci, PM Billio, A Zeinali, S Perkins, SJ Perry, DJ
Citation: F. Peyvandi et al., Molecular characterisation and three-dimensional structural analysis of mutations in 21 unrelated families with inherited factor VII deficiency, THROMB HAEM, 84(2), 2000, pp. 250-257
The effects of the 32-bp CCR-5 deletion on HIV transmission and HIV disease progression in individuals with haemophilia
Authors: Pasi, KJ Sabin, CA Jenkins, PV Devereux, HL Ononye, C Lee, CA
Citation: Kj. Pasi et al., The effects of the 32-bp CCR-5 deletion on HIV transmission and HIV disease progression in individuals with haemophilia, BR J HAEM, 111(1), 2000, pp. 136-142
Type 1 von Willebrand disease - a clinical retrospective study of the diagnosis, the influence of the ABO blood group and the role of the bleeding history
Authors: Nitu-Whalley, IC Lee, CA Griffioen, A Jenkins, PV Pasi, KJ
Citation: Ic. Nitu-whalley et al., Type 1 von Willebrand disease - a clinical retrospective study of the diagnosis, the influence of the ABO blood group and the role of the bleeding history, BR J HAEM, 108(2), 2000, pp. 259-264
Structural and functional modelling of von Willebrand factor type A domains in complement and coagulation
Authors: Perkins, SJ Hinshelwood, J Edwards, YJK Jenkins, PV
Citation: Sj. Perkins et al., Structural and functional modelling of von Willebrand factor type A domains in complement and coagulation, BIOCH SOC T, 27, 1999, pp. 815-820
Detection of mutations causing Hemophilia A using an in vitro coupled transcription and translation system
Authors: Ononye, C Jenkins, PV
Citation: C. Ononye et Pv. Jenkins, Detection of mutations causing Hemophilia A using an in vitro coupled transcription and translation system, METH MOL M, 31, 1999, pp. 117-124
Inversion mutation analysis in hemophilia A by restriction enzyme analysisand Southern blotting
Authors: Ononye, C Jenkins, PV
Citation: C. Ononye et Pv. Jenkins, Inversion mutation analysis in hemophilia A by restriction enzyme analysisand Southern blotting, METH MOL M, 31, 1999, pp. 151-157
Screening for candidate mutations causing von Willebrand's disease (vWD)
Authors: Jenkins, PV
Citation: Pv. Jenkins, Screening for candidate mutations causing von Willebrand's disease (vWD), METH MOL M, 31, 1999, pp. 169-177
Risultati: 1-12 |