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Results: 1-25/112
THE GENETIC-BASIS OF INHIBITOR DEVELOPMENT IN HEMOPHILIA-A
Authors: TUDDENHAM EGD MCVEY JH
Citation: Egd. Tuddenham et Jh. Mcvey, THE GENETIC-BASIS OF INHIBITOR DEVELOPMENT IN HEMOPHILIA-A, Haemophilia, 4(4), 1998, pp. 543-545
MUTATION ANALYSIS OF THE ERGIC53 GENE IN 39 FAMILIES WITH COMBINED DEFICIENCY OF COAGULATION-FACTOR-V AND COAGULATION-FACTOR-VIII (F5F8D)
Authors: NEERMANARBEZ M MORRIS MA NICHOLS WC GINSBURG D TUDDENHAM EGD ANTONARAKIS SE
Citation: M. Neermanarbez et al., MUTATION ANALYSIS OF THE ERGIC53 GENE IN 39 FAMILIES WITH COMBINED DEFICIENCY OF COAGULATION-FACTOR-V AND COAGULATION-FACTOR-VIII (F5F8D), European journal of human genetics, 6, 1998, pp. 201-201
IMPACT OF PREMATURE STOP CODONS ON FACTOR-VIII AND RECOMBINANT RE-FVIIISQ PRE-MESSENGER-RNA PROCESSING, CORRELATION WITH INHIBITOR FORMATION
Authors: DAVID D SCHWAAB R SANTOS AIM MCVEY J TUDDENHAM EGD
Citation: D. David et al., IMPACT OF PREMATURE STOP CODONS ON FACTOR-VIII AND RECOMBINANT RE-FVIIISQ PRE-MESSENGER-RNA PROCESSING, CORRELATION WITH INHIBITOR FORMATION, European journal of human genetics, 6, 1998, pp. 4055-4055
ANALYSIS OF THE F8 GENE IN INDIVIDUALS WITH HIGH PLASMA FACTOR VIII-CLEVELS AND ASSOCIATED VENOUS THROMBOSIS
Authors: MANSVELT EPG LAFFAN M MCVEY JH TUDDENHAM EGD
Citation: Epg. Mansvelt et al., ANALYSIS OF THE F8 GENE IN INDIVIDUALS WITH HIGH PLASMA FACTOR VIII-CLEVELS AND ASSOCIATED VENOUS THROMBOSIS, Thrombosis and haemostasis, 80(4), 1998, pp. 561-565
THE FACTOR-VIII STRUCTURE AND MUTATION RESOURCE SITE - HAMSTERS-VERSION-4
Authors: KEMBALLCOOK G TUDDENHAM EGD WACEY AI
Citation: G. Kemballcook et al., THE FACTOR-VIII STRUCTURE AND MUTATION RESOURCE SITE - HAMSTERS-VERSION-4, Nucleic acids research, 26(1), 1998, pp. 216-219
MUTATION DATABASES ON THE WEB
Authors: WACEY AI TUDDENHAM EGD
Citation: Ai. Wacey et Egd. Tuddenham, MUTATION DATABASES ON THE WEB, Journal of Medical Genetics, 35(7), 1998, pp. 529-533
COAGULATION-FACTOR-VII GLN(100)-]ARG - AMINO-ACID SUBSTITUTION AT THEEPIDERMAL GROWTH-FACTOR-2-PROTEASE DOMAIN INTERFACE RESULTS IN SEVERELY REDUCED TISSUE FACTOR-BINDING AND PROCOAGULANT FUNCTION
Authors: KEMBALLCOOK G JOHNSON DJD TAKAMIYA O BANNER DW MCVEY JH TUDDENHAM EGD
Citation: G. Kemballcook et al., COAGULATION-FACTOR-VII GLN(100)-]ARG - AMINO-ACID SUBSTITUTION AT THEEPIDERMAL GROWTH-FACTOR-2-PROTEASE DOMAIN INTERFACE RESULTS IN SEVERELY REDUCED TISSUE FACTOR-BINDING AND PROCOAGULANT FUNCTION, The Journal of biological chemistry, 273(14), 1998, pp. 8516-8521
ENHANCED EXPRESSION OF UROKINASE RECEPTOR-INDUCED THROUGH THE TISSUE FACTOR-FACTOR VIIA PATHWAY IN HUMAN PANCREATIC-CANCER
Authors: TANIGUCHI T KAKKAR AK TUDDENHAM EGD WILLIAMSON RCN LEMOINE NR
Citation: T. Taniguchi et al., ENHANCED EXPRESSION OF UROKINASE RECEPTOR-INDUCED THROUGH THE TISSUE FACTOR-FACTOR VIIA PATHWAY IN HUMAN PANCREATIC-CANCER, Cancer research, 58(19), 1998, pp. 4461-4467
CORRELATION OF FVII LEVELS WITH PROTHROMBIN FRAGMENTS(1+2) AND THROMBIN ANTITHROMBIN COMPLEXES IN 44 PATIENTS WITH VENOUS THROMBOEMBOLISM
Authors: MURPHY KM TUDDENHAM EGD MANNING R LAFFAN M
Citation: Km. Murphy et al., CORRELATION OF FVII LEVELS WITH PROTHROMBIN FRAGMENTS(1+2) AND THROMBIN ANTITHROMBIN COMPLEXES IN 44 PATIENTS WITH VENOUS THROMBOEMBOLISM, British Journal of Haematology, 101, 1998, pp. 238-238
TOWARDS GENE-THERAPY FOR HEMOPHILIA-B - 2 SENSITIVE ELISAS FOR MOUSE FIX ANTIGEN
Authors: SALOOJA N MCVEY J TUDDENHAM EGD
Citation: N. Salooja et al., TOWARDS GENE-THERAPY FOR HEMOPHILIA-B - 2 SENSITIVE ELISAS FOR MOUSE FIX ANTIGEN, British Journal of Haematology, 101, 1998, pp. 241-241
BLEEDING SYMPTOMS IN 27 IRANIAN PATIENTS WITH THE COMBINED DEFICIENCYOF FACTOR-V AND FACTOR-VIII
Authors: PEYVANDI F TUDDENHAM EGD AKHTARI AM LAK M MANNUCCI PM
Citation: F. Peyvandi et al., BLEEDING SYMPTOMS IN 27 IRANIAN PATIENTS WITH THE COMBINED DEFICIENCYOF FACTOR-V AND FACTOR-VIII, British Journal of Haematology, 100(4), 1998, pp. 773-776
EXCLUSION OF THE FIRST EGF DOMAIN OF FACTOR-VII BY A SPLICE-SITE MUTATION CAUSES LETHAL FACTOR-VII DEFICIENCY
Authors: MCVEY JH BOSWELL EJ TAKAMIYA O TAMAGNINI G VALENTE V FIDALGO T LAYTON M TUDDENHAM EGD
Citation: Jh. Mcvey et al., EXCLUSION OF THE FIRST EGF DOMAIN OF FACTOR-VII BY A SPLICE-SITE MUTATION CAUSES LETHAL FACTOR-VII DEFICIENCY, Blood, 92(3), 1998, pp. 920-926
INHERITED THROMBOPHILIAS
Authors: LAFFAN MA TUDDENHAM EGD
Citation: Ma. Laffan et Egd. Tuddenham, INHERITED THROMBOPHILIAS, Quarterly Journal of Medicine, 90(6), 1997, pp. 375-378
FACTOR-VIII GENE-MUTATIONS FOUND BY A COMPARATIVE-STUDY OF SSCP, DGGEAND CMC AND THEIR ANALYSIS ON A MOLECULAR-MODEL OF FACTOR-VIII PROTEIN
Authors: SCHWAAB R OLDENBURG J LALLOZ MRA SCHWAAB U PEMBERTON S HANFLAND P BRACKMANN HH TUDDENHAM EGD MICHAELIDES K
Citation: R. Schwaab et al., FACTOR-VIII GENE-MUTATIONS FOUND BY A COMPARATIVE-STUDY OF SSCP, DGGEAND CMC AND THEIR ANALYSIS ON A MOLECULAR-MODEL OF FACTOR-VIII PROTEIN, Human genetics, 101(3), 1997, pp. 323-332
EXPRESSION AND CHARACTERIZATION OF SITE-DIRECTED VARIANTS OF THE EGF-1 DOMAIN OF HUMAN FACTOR-VII
Authors: BOSWELL EJ TUDDENHAM EGD MCVEY JH
Citation: Ej. Boswell et al., EXPRESSION AND CHARACTERIZATION OF SITE-DIRECTED VARIANTS OF THE EGF-1 DOMAIN OF HUMAN FACTOR-VII, Thrombosis and haemostasis, 1997, pp. 41-41
HOMOZYGOUS LEU-105 PRO MUTATION IN PLATELET MEMBRANE GP1B-ALPHA CAUSING BERNARD-SOULIER-SYNDROME AND ITS ANALYSIS ON A STRUCTURE MODEL OF THE LRG DOMAIN
Authors: MICHAELIDES K PEMBERTON S TUDDENHAM EGD
Citation: K. Michaelides et al., HOMOZYGOUS LEU-105 PRO MUTATION IN PLATELET MEMBRANE GP1B-ALPHA CAUSING BERNARD-SOULIER-SYNDROME AND ITS ANALYSIS ON A STRUCTURE MODEL OF THE LRG DOMAIN, Thrombosis and haemostasis, 1997, pp. 277-277
THE FACTOR-VIII MUTATION DATABASE ON THE WORLD-WIDE-WEB - THE HEMOPHILIA-A MUTATION, SEARCH, TEST AND RESOURCE SITE - HAMSTERS UPDATE (V3.0)
Authors: KEMBALLCOOK G TUDDENHAM EGD
Citation: G. Kemballcook et Egd. Tuddenham, THE FACTOR-VIII MUTATION DATABASE ON THE WORLD-WIDE-WEB - THE HEMOPHILIA-A MUTATION, SEARCH, TEST AND RESOURCE SITE - HAMSTERS UPDATE (V3.0), Thrombosis and haemostasis, 1997, pp. 924-924
AUTOMATED MODELING ANALYSIS OF THE HETERODIMERIC COMPLEX BETWEEN FACTOR VIIA AND THE EXTRACELLULAR DOMAINS OF HUMAN TISSUE FACTOR CONSTRAINED BY X-RAY AND NEUTRON-SCATTERING CURVES AND HOMOLOGY MODELS
Authors: ASHTON AW KEMBALLCOOK G JOHNSON DJD TUDDENHAM EGD PERKINS SJ
Citation: Aw. Ashton et al., AUTOMATED MODELING ANALYSIS OF THE HETERODIMERIC COMPLEX BETWEEN FACTOR VIIA AND THE EXTRACELLULAR DOMAINS OF HUMAN TISSUE FACTOR CONSTRAINED BY X-RAY AND NEUTRON-SCATTERING CURVES AND HOMOLOGY MODELS, Thrombosis and haemostasis, 1997, pp. 1650-1650
CHARACTERIZATION OF 2 NATURALLY-OCCURRING VARIANTS OF HUMAN FACTOR-VII
Authors: ALSHINAWI CR BOSWELL EJ FELICE AE TUDDENHAM EGD MCVEY JH
Citation: Cr. Alshinawi et al., CHARACTERIZATION OF 2 NATURALLY-OCCURRING VARIANTS OF HUMAN FACTOR-VII, Thrombosis and haemostasis, 1997, pp. 1689-1689
A MOLECULAR-MODEL FOR THE TRIPLICATED A DOMAINS OF HUMAN FACTOR-VIII BASED ON THE CRYSTAL-STRUCTURE OF HUMAN CERULOPLASMIN
Authors: PEMBERTON S LINDLEY P ZAITSEV V CARD G TUDDENHAM EGD KEMBALLCOOK G
Citation: S. Pemberton et al., A MOLECULAR-MODEL FOR THE TRIPLICATED A DOMAINS OF HUMAN FACTOR-VIII BASED ON THE CRYSTAL-STRUCTURE OF HUMAN CERULOPLASMIN, Thrombosis and haemostasis, 1997, pp. 2558-2558
HUMAN TISSUE FACTOR PATHWAY INHIBITOR FUSED TO CD4 BINDS BOTH FXA ANDTF FVIIA AT THE CELL-SURFACE/
Authors: RIESBECK K DORLING A KEMBALLCOOK G MCVEY JH JONES M TUDDENHAM EGD LECHLER RI
Citation: K. Riesbeck et al., HUMAN TISSUE FACTOR PATHWAY INHIBITOR FUSED TO CD4 BINDS BOTH FXA ANDTF FVIIA AT THE CELL-SURFACE/, Thrombosis and haemostasis, 78(6), 1997, pp. 1488-1494
INHERITED FACTOR-VII DEFICIENCY - MOLECULAR-GENETICS AND PATHOPHYSIOLOGY
Authors: COOPER DN MILLAR DS WACEY A BANNER DW TUDDENHAM EGD
Citation: Dn. Cooper et al., INHERITED FACTOR-VII DEFICIENCY - MOLECULAR-GENETICS AND PATHOPHYSIOLOGY, Thrombosis and haemostasis, 78(1), 1997, pp. 151-160
INHERITED FACTOR-X DEFICIENCY - MOLECULAR-GENETICS AND PATHOPHYSIOLOGY
Authors: COOPER DN MILLAR DS WACEY A PEMBERTON S TUDDENHAM EGD
Citation: Dn. Cooper et al., INHERITED FACTOR-X DEFICIENCY - MOLECULAR-GENETICS AND PATHOPHYSIOLOGY, Thrombosis and haemostasis, 78(1), 1997, pp. 161-172
HIGH PREVALENCE OF ELEVATED FACTOR-VIII LEVELS IN PATIENTS REFERRED FOR THROMBOPHILIA SCREENING - ROLE OF INCREASED SYNTHESIS AND RELATIONSHIP TO THE ACUTE-PHASE REACTION
Authors: ODONNELL J TUDDENHAM EGD MANNING R KEMBALLCOOK G JOHNSON D LAFFAN M
Citation: J. Odonnell et al., HIGH PREVALENCE OF ELEVATED FACTOR-VIII LEVELS IN PATIENTS REFERRED FOR THROMBOPHILIA SCREENING - ROLE OF INCREASED SYNTHESIS AND RELATIONSHIP TO THE ACUTE-PHASE REACTION, Thrombosis and haemostasis, 77(5), 1997, pp. 825-828
FACTOR-VIII ISE (R2159C) IN A PATIENT WITH MILD HEMOPHILIA-A, AN ABNORMAL FACTOR-VIII WITH RETENTION OF FUNCTION BUT MODIFICATION OF C2 EPITOPES
Authors: SUZUKI H SHIMA M ARAI M KAGAWA K FUKUTAKE K KAMISUE S NAKAI H MORICHIKA S TANAKA I INOUE M GALE K TUDDENHAM EGD YOSHIOKA A
Citation: H. Suzuki et al., FACTOR-VIII ISE (R2159C) IN A PATIENT WITH MILD HEMOPHILIA-A, AN ABNORMAL FACTOR-VIII WITH RETENTION OF FUNCTION BUT MODIFICATION OF C2 EPITOPES, Thrombosis and haemostasis, 77(5), 1997, pp. 862-867
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