Wacey AI[au] - Search Results

Year	Number of Results
1993	2
1994	2
1995	2
1996	1
1997	1
1998	2
1999	1
2000	1
2024	0

1

Wacey AI, Tuddenham EG. Wacey AI, et al. J Med Genet. 1998 Jul;35(7):529-33. doi: 10.1136/jmg.35.7.529. J Med Genet. 1998. PMID: 9678695 Free PMC article. No abstract available.

2

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

3

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

Kemball-Cook G, Tuddenham EG, Wacey AI. Kemball-Cook G, et al. Among authors: wacey ai. Nucleic Acids Res. 1998 Jan 1;26(1):216-9. doi: 10.1093/nar/26.1.216. Nucleic Acids Res. 1998. PMID: 9399839 Free PMC article.

4

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

5

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

Wacey AI, Kemball-Cook G, Kazazian HH, Antonarakis SE, Schwaab R, Lindley P, Tuddenham EG. Wacey AI, et al. Nucleic Acids Res. 1996 Jan 1;24(1):100-2. doi: 10.1093/nar/24.1.100. Nucleic Acids Res. 1996. PMID: 8594555 Free PMC article.

6

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

7

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.

8

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

9

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

10

A novel point mutation (Val 297-->Met) in the serine proteinase domain of protein C in a patient with both venous and arterial thromboembolic disease.

Millar DS, Wacey AI, Voke J, Kakkar VV, Cooper DN. Millar DS, et al. Among authors: wacey ai. Blood Coagul Fibrinolysis. 1993 Aug;4(4):631-3. doi: 10.1097/00001721-199308000-00015. Blood Coagul Fibrinolysis. 1993. PMID: 8218861

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