A. Wacey

发表

Disentangling the perturbational effects of amino acid substitutions in the DNA-binding domain of p53

E. Hovig, D. Cooper, M. Krawczak, 1999, Human Genetics.

Inherited Factor VII Deficiency: Molecular Genetics and Pathophysiology

D. Cooper, D. Banner, A. Wacey, 1997, Thrombosis and Haemostasis.

Inherited Factor X Deficiency: Molecular Genetics and Pathophysiology

D. Cooper, D. Banner, A. Wacey, 1997, Thrombosis and Haemostasis.

Three novel PROC gene lesions causing protein C deficiency

A. Wacey, D. Bevan, L. Tengborn, 1998, Clinical genetics.

The factor VIII Structure and Mutation Resource Site: HAMSTeRS version 4

Adam I. Wacey, Geoffrey Kemball-Cook, Edward G. D. Tuddenham, 1998, Nucleic Acids Res..

Homology modelling of the catalytic domain of early mammalian protein C: evolution of structural features

D. Cooper, M. Krawczak, A. Wacey, 1997, Human Genetics.

A molecular model of the serine protease domain of activated protein C: application to the study of missense mutations causing protein C deficiency

A. Wacey, S. Pemberton, E. Tuddenham, 1993, British journal of haematology.

Molecular reconstruction and homology modelling of the catalytic domain of the common ancestor of the haemostatic vitamin-K-dependent serine proteinases

D. Cooper, M. Krawczak, A. Wacey, 1996, Human Genetics.

Detection and characterization of seven novel protein S (PROS) gene lesions: evaluation of reverse transcript-polymerase chain reaction as a mutation screening strategy

M. Rowley, A. Wacey, F. Bernardi, 1995 .

Molecular analysis of the genotype-phenotype relationship in factor X deficiency

D. Cooper, M. Krawczak, A. Wacey, 2000, Human Genetics.

Molecular defects in CRM+ factor VII deficiencies: modelling of missense mutations in the catalytic domain of FVII

A. Wacey, D. Liney, M. Pinotti, 1994, British journal of haematology.

Determinants of the factor IX mutational spectrum in haemophilia B: an analysis of missense mutations using a multi-domain molecular model of the activated protein

D. Cooper, M. Krawczak, V. Kakkar, 1994, Human Genetics.

Detection and characterization of seven novel protein S (PROS) gene lesions: evaluation of reverse transcript-polymerase chain reaction as a mutation screening strategy.

D. Cooper, V. Kakkar, M. Rowley, 1995, Blood.

Corrigendum: The haemophilia A mutation search test and resource site, home page of the factor VIII mutation database: HAMSTeRS (Nucleic Acids Research (1996) 24 (100-102))

S. Antonarakis, H. Kazazian, A. Wacey, 1996 .

The haemophilia A mutation search test and resource site, home page of the factor VIII mutation database: HAMSTeRS

Stylianos E. Antonarakis, Rainer Schwaab, Adam I. Wacey, 1996, Nucleic Acids Res..

Symptomatic type II protein C deficiency caused by a missense mutation (Gly 381 → Ser) in the substrate‐binding pocket

A. Wacey, F. Bernardi, G. Marchetti, 1993, British journal of haematology.

Three novel missense mutations in the antithrombin III (AT3) gene causing recurrent venous thrombosis

D. Cooper, V. Kakkar, A. Wacey, 1994, Human Genetics.