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Results: 1-18 |
Results: 18
INTERPARENTAL CONFLICT STYLES AND YOUTH PROBLEM BEHAVIORS - A 2-SAMPLE REPLICATION STUDY
Authors: BUEHLER C KRISHNAKUMAR A STONE G ANTHONY C PEMBERTON S GERARD J BARBER BK
Citation: C. Buehler et al., INTERPARENTAL CONFLICT STYLES AND YOUTH PROBLEM BEHAVIORS - A 2-SAMPLE REPLICATION STUDY, Journal of marriage and the family, 60(1), 1998, pp. 119-132
THE MOLECULAR-BASIS FOR CROSS-REACTING MATERIAL-POSITIVE HEMOPHILIA-ADUE TO MISSENSE MUTATIONS WITHIN THE A2-DOMAIN OF FACTOR-VIII
Authors: AMANO K SARKAR R PEMBERTON S KEMBALLCOOK G KAZAZIAN HH KAUFMAN RJ
Citation: K. Amano et al., THE MOLECULAR-BASIS FOR CROSS-REACTING MATERIAL-POSITIVE HEMOPHILIA-ADUE TO MISSENSE MUTATIONS WITHIN THE A2-DOMAIN OF FACTOR-VIII, Blood, 91(2), 1998, pp. 538-548
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
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
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
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
A NATIONAL-HEALTH-SERVICE - THE RESTRUCTURING OF HEALTH-CARE IN BRITAIN SINCE 1979 - MOHAN,J
Authors: PEMBERTON S
Citation: S. Pemberton, A NATIONAL-HEALTH-SERVICE - THE RESTRUCTURING OF HEALTH-CARE IN BRITAIN SINCE 1979 - MOHAN,J, Service industries journal, 17(4), 1997, pp. 690-691
FACTOR-VIII GENE ANALYSIS IN JAPANESE CRM-POSITIVE AND CRM-REDUCED HEMOPHILIA-A PATIENTS BY SINGLE-STRAND CONFORMATION POLYMORPHISM
Authors: MORICHIKA S SHIMA M KAMISUE S TANAKA I IMANAKA Y SUZUKI H SHIBATA H PEMBERTON S GALE K MCVEY J TUDDENHAM EGD YOSHIOKA A
Citation: S. Morichika et al., FACTOR-VIII GENE ANALYSIS IN JAPANESE CRM-POSITIVE AND CRM-REDUCED HEMOPHILIA-A PATIENTS BY SINGLE-STRAND CONFORMATION POLYMORPHISM, British Journal of Haematology, 98(4), 1997, pp. 901-906
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, Blood, 89(7), 1997, pp. 2413-2421
US AND THEM
Authors: PEMBERTON S
Citation: S. Pemberton, US AND THEM, Communications of the ACM, 40(3), 1997, pp. 28-28
INHERITED FACTOR-VII DEFICIENCY - GENETICS AND MOLECULAR PATHOLOGY
Authors: TUDDENHAM EGD PEMBERTON S COOPER DN
Citation: Egd. Tuddenham et al., INHERITED FACTOR-VII DEFICIENCY - GENETICS AND MOLECULAR PATHOLOGY, Thrombosis and haemostasis, 74(1), 1995, pp. 313-321
INCREASE OF ACTIVATED FACTOR VIIA AND HEMOSTATIC MOLECULAR MARKERS INJUVENILE CHRONIC ARTHRITIS
Authors: INAMO Y PEMBERTON S TUDDENHAM EGD WOO P
Citation: Y. Inamo et al., INCREASE OF ACTIVATED FACTOR VIIA AND HEMOSTATIC MOLECULAR MARKERS INJUVENILE CHRONIC ARTHRITIS, British journal of rheumatology, 34(5), 1995, pp. 466-469
FACTOR-VIII S373L - MUTATION AT P1' SITE CONFERS THROMBIN CLEAVAGE RESISTANCE, CAUSING MILD HEMOPHILIA-A
Authors: JOHNSON DJD PEMBERTON S ACQUILA M MORI PG TUDDENHAM EGD OBRIEN DP
Citation: Djd. Johnson et al., FACTOR-VIII S373L - MUTATION AT P1' SITE CONFERS THROMBIN CLEAVAGE RESISTANCE, CAUSING MILD HEMOPHILIA-A, Thrombosis and haemostasis, 71(4), 1994, pp. 428-433
ELECTRONIC PUBLISHING - A WORKSHOP AT THE 1ST INTERNATIONAL WWW CONFERENCE, GENEVA, MAY 1994
Authors: PEMBERTON S
Citation: S. Pemberton, ELECTRONIC PUBLISHING - A WORKSHOP AT THE 1ST INTERNATIONAL WWW CONFERENCE, GENEVA, MAY 1994, Computer networks and ISDN systems, 27(2), 1994, pp. 319-321
MOLECULAR DEFECTS IN CRM-VII DEFICIENCIES - MODELING OF MISSENSE MUTATIONS IN THE CATALYTIC DOMAIN OF FVII( FACTOR)
Authors: BERNARDI F LINEY DL PATRACCHINI P GEMMATI D LEGNANI C ARCIERI P PINOTTI M REDAELLI R BALLERINI G PEMBERTON S WACEY AI MARIANI G TUDDENHAM EGD MARCHETTI G
Citation: F. Bernardi et al., MOLECULAR DEFECTS IN CRM-VII DEFICIENCIES - MODELING OF MISSENSE MUTATIONS IN THE CATALYTIC DOMAIN OF FVII( FACTOR), British Journal of Haematology, 86(3), 1994, pp. 610-618
SINGLE-STRAND CONFORMATION POLYMORPHISM (SSCP) ANALYSIS OF THE MOLECULAR PATHOLOGY OF HEMOPHILIA-B
Authors: DAVID D ROSA HAV PEMBERTON S DINIZ MJ CAMPOS M LAVINHA J
Citation: D. David et al., SINGLE-STRAND CONFORMATION POLYMORPHISM (SSCP) ANALYSIS OF THE MOLECULAR PATHOLOGY OF HEMOPHILIA-B, Human mutation, 2(5), 1993, pp. 355-361
A MOLECULAR-MODEL OF THE SERINE-PROTEASE DOMAIN OF ACTIVATED PROTEIN-C - APPLICATION TO THE STUDY OF MISSENSE MUTATIONS CAUSING PROTEIN-C DEFICIENCY
Authors: WACEY A PEMBERTON S COOPER DN KAKKAR VV TUDDENHAM EGD
Citation: A. Wacey et al., A MOLECULAR-MODEL OF THE SERINE-PROTEASE DOMAIN OF ACTIVATED PROTEIN-C - APPLICATION TO THE STUDY OF MISSENSE MUTATIONS CAUSING PROTEIN-C DEFICIENCY, Thrombosis and haemostasis, 69(6), 1993, pp. 724-724
A MOLECULAR-MODEL OF THE SERINE-PROTEASE DOMAIN OF ACTIVATED PROTEIN-C - APPLICATION TO THE STUDY OF MISSENSE MUTATIONS CAUSING PROTEIN-C DEFICIENCY
Authors: WACEY AI PEMBERTON S COOPER DN KAKKAR VV TUDDENHAM EGD
Citation: Ai. Wacey et al., A MOLECULAR-MODEL OF THE SERINE-PROTEASE DOMAIN OF ACTIVATED PROTEIN-C - APPLICATION TO THE STUDY OF MISSENSE MUTATIONS CAUSING PROTEIN-C DEFICIENCY, British Journal of Haematology, 84(2), 1993, pp. 290-300
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