Wacey AI - Search Results

1

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

Millar DS, Wacey AI, Ribando J, Melissari E, Laursen B, Woods P, Kakkar VV, Cooper DN. Millar DS, et al. Among authors: wacey ai. Hum Genet. 1994 Nov;94(5):509-12. doi: 10.1007/BF00211016. Hum Genet. 1994. PMID: 7959685

2

Three novel PROC gene lesions causing protein C deficiency.

Hallam PJ, Mannucci P, Tripodi A, Bevan D, Laursen B, Tengborn L, Wacey A, Cooper DN. Hallam PJ, et al. Clin Genet. 1998 Sep;54(3):231-3. doi: 10.1111/j.1399-0004.1998.tb04290.x. Clin Genet. 1998. PMID: 9788727

3

A novel missense mutation (Thr176-->Ile) at the putative hinge of the neo N-terminus of activated protein C.

Hallam PJ, Wacey AI, Mannucci PM, Legnani C, Kühnau W, Krawczak M, Kakkar VV, Cooper DN. Hallam PJ, et al. Among authors: wacey ai. Hum Genet. 1995 Apr;95(4):447-50. doi: 10.1007/BF00208974. Hum Genet. 1995. PMID: 7705844

4

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.

Wacey AI, Krawczak M, Kakkar VV, Cooper DN. Wacey AI, et al. Hum Genet. 1994 Dec;94(6):594-608. doi: 10.1007/BF00206951. Hum Genet. 1994. PMID: 7989034

5

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

Wacey AI, Pemberton S, Cooper DN, Kakkar VV, Tuddenham EG. Wacey AI, et al. Br J Haematol. 1993 Jun;84(2):290-300. doi: 10.1111/j.1365-2141.1993.tb03067.x. Br J Haematol. 1993. PMID: 8398833

6

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

Millar DS, Elliston L, Deex P, Krawczak M, Wacey AI, Reynaud J, Nieuwenhuis HK, Bolton-Maggs P, Mannucci PM, Reverter JC, Cachia P, Pasi KJ, Layton DM, Cooper DN. Millar DS, et al. Among authors: wacey ai. Hum Genet. 2000 Feb;106(2):249-57. doi: 10.1007/s004390051035. Hum Genet. 2000. PMID: 10746568

7

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

Wacey AI, Cooper DN, Liney D, Hovig E, Krawczak M. Wacey AI, et al. Hum Genet. 1999 Jan;104(1):15-22. doi: 10.1007/s004390050904. Hum Genet. 1999. PMID: 10071187

8

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

Krawczak M, Wacey A, Cooper DN. Krawczak M, et al. Hum Genet. 1996 Sep;98(3):351-70. doi: 10.1007/s004390050222. Hum Genet. 1996. PMID: 8707309

9

Inherited factor X deficiency: molecular genetics and pathophysiology.

Cooper DN, Millar DS, Wacey A, Pemberton S, Tuddenham EG. Cooper DN, et al. Thromb Haemost. 1997 Jul;78(1):161-72. Thromb Haemost. 1997. PMID: 9198147 Review. No abstract available.

10

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

Formstone CJ, Wacey AI, Berg LP, Rahman S, Bevan D, Rowley M, Voke J, Bernardi F, Legnani C, Simioni P, Girolami A, Tuddenham EG, Kakkar VV, Cooper DN. Formstone CJ, et al. Among authors: wacey ai. Blood. 1995 Oct 1;86(7):2632-41. Blood. 1995. PMID: 7545463 Free article.

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