Cooper DN - Search Results

1

Compound heterozygous protein C deficiency resulting in the presence of only the beta-form of protein C in plasma.

Simioni P, Kalafatis M, Millar DS, Henderson SC, Luni S, Cooper DN, Girolami A. Simioni P, et al. Among authors: cooper dn. Blood. 1996 Sep 15;88(6):2101-8. Blood. 1996. PMID: 8822929 Free article.

2

Three novel mutations in the protein C (PROC) gene causing venous thrombosis.

Millar DS, Bevan D, Chitolie A, Reynaud J, Chisholm M, Kakkar VV, Cooper DN. Millar DS, et al. Among authors: cooper dn. Blood Coagul Fibrinolysis. 1995 Apr;6(2):138-40. doi: 10.1097/00001721-199504000-00009. Blood Coagul Fibrinolysis. 1995. PMID: 7605880

3

A novel dysfunctional protein C (protein C Padua 2) associated with a thrombotic tendency: substitution of Cys for Arg-1 results in a strongly reduced affinity for binding of Ca++.

Girolami A, Simioni P, Girolami B, Marchiori A, Millar DS, Bignell P, Kakkar VV, Cooper DN. Girolami A, et al. Among authors: cooper dn. Br J Haematol. 1993 Nov;85(3):521-7. doi: 10.1111/j.1365-2141.1993.tb03342.x. Br J Haematol. 1993. PMID: 8136274

4

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: cooper dn. Blood. 1995 Oct 1;86(7):2632-41. Blood. 1995. PMID: 7545463 Free article.

5

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: cooper dn. Blood Coagul Fibrinolysis. 1993 Aug;4(4):631-3. doi: 10.1097/00001721-199308000-00015. Blood Coagul Fibrinolysis. 1993. PMID: 8218861

6

A Gla domain mutation (Arg 15-->Trp) in the protein C (PROC) gene causing type 2 protein C deficiency and recurrent venous thrombosis.

Millar DS, Grundy CB, Bignell P, Moffat EH, Martin R, Kakkar VV, Cooper DN. Millar DS, et al. Among authors: cooper dn. Blood Coagul Fibrinolysis. 1993 Apr;4(2):345-7. doi: 10.1097/00001721-199304000-00014. Blood Coagul Fibrinolysis. 1993. PMID: 8499568

7

Recurrent deletion in the human antithrombin III gene.

Grundy CB, Thomas F, Millar DS, Krawczak M, Melissari E, Lindo V, Moffat E, Kakkar VV, Cooper DN. Grundy CB, et al. Among authors: cooper dn. Blood. 1991 Aug 15;78(4):1027-32. Blood. 1991. PMID: 1868237 Free article.

8

A homozygous deletion/insertion mutation in the protein C (PROC) gene causing neonatal Purpura fulminans: prenatal diagnosis in an at-risk pregnancy.

Millar DS, Allgrove J, Rodeck C, Kakkar VV, Cooper DN. Millar DS, et al. Among authors: cooper dn. Blood Coagul Fibrinolysis. 1994 Aug;5(4):647-9. Blood Coagul Fibrinolysis. 1994. PMID: 7841323

9

Screening for inversions in the factor VIII (F8) gene causing severe haemophilia A.

Millar DS, Kakkar VV, Cooper DN. Millar DS, et al. Among authors: cooper dn. Blood Coagul Fibrinolysis. 1994 Apr;5(2):239-42. doi: 10.1097/00001721-199404000-00013. Blood Coagul Fibrinolysis. 1994. PMID: 8054456

10

A novel nonsense mutation in the protein C (PROC) gene (Trp-29-->term) causing recurrent venous thrombosis.

Millar DS, Grundy CB, Bignell P, Mitchell DC, Corden D, Woods P, Kakkar VV, Cooper DN. Millar DS, et al. Among authors: cooper dn. Hum Genet. 1993 Mar;91(2):196. doi: 10.1007/BF00222726. Hum Genet. 1993. PMID: 8462980

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