J A Cutler

Summary

Affiliation: Guy's and St Thomas' NHS Foundation Trust
Country: UK

Publications

  1. ncbi request reprint The significance of published polymorphisms in 14 cases of mild factor VII deficiency
    Jacqueline A Cutler
    Centre for Haemostasis and Thrombosis Haemophilia Reference Centre, St Thomas Hospital, London, UK
    Blood Coagul Fibrinolysis 16:91-5. 2005
  2. doi request reprint Molecular characterization of 11 novel mutations in patients with heterozygous and homozygous FV deficiency
    J A Cutler
    Centre for Haemostasis and Thrombosis, St Thomas Hospital, London, UK
    Haemophilia 16:937-42. 2010
  3. ncbi request reprint A rapid and cost-effective method for analysis of three common genetic risk factors for thrombosis
    J A Cutler
    The Reference Centre for Haemostatic and Thrombotic Disorders, St Thomas Hospital, London, UK
    Blood Coagul Fibrinolysis 12:33-6. 2001
  4. ncbi request reprint Diagnostic and therapeutic difficulties in type 2A von Willebrand disease: resolution
    M R Thomas
    The Reference Centre for Haemostasis and Thrombosis, St Thomas Hospital, London, United Kingdom
    Clin Appl Thromb Hemost 12:237-9. 2006
  5. ncbi request reprint The identification and classification of 41 novel mutations in the factor VIII gene (F8C)
    J A Cutler
    The Haemophilia Reference Centre, Centre for Thrombosis and Haemostasis, St Thomas Hospital, Lambeth Palace Road, London, UK
    Hum Mutat 19:274-8. 2002

Collaborators

Detail Information

Publications5

  1. ncbi request reprint The significance of published polymorphisms in 14 cases of mild factor VII deficiency
    Jacqueline A Cutler
    Centre for Haemostasis and Thrombosis Haemophilia Reference Centre, St Thomas Hospital, London, UK
    Blood Coagul Fibrinolysis 16:91-5. 2005
    ..This study highlights the significance of mild FVII deficiency, and examines the importance of seven previously published polymorphisms in such patients...
  2. doi request reprint Molecular characterization of 11 novel mutations in patients with heterozygous and homozygous FV deficiency
    J A Cutler
    Centre for Haemostasis and Thrombosis, St Thomas Hospital, London, UK
    Haemophilia 16:937-42. 2010
    ..The addition of a significant number of previously unidentified mutations to the public domain will contribute to the knowledge and understanding of the molecular pathology of this rare disorder...
  3. ncbi request reprint A rapid and cost-effective method for analysis of three common genetic risk factors for thrombosis
    J A Cutler
    The Reference Centre for Haemostatic and Thrombotic Disorders, St Thomas Hospital, London, UK
    Blood Coagul Fibrinolysis 12:33-6. 2001
    ..This sensitive protocol obviates the need for endonuclease digestion and the associated gel running and documentation, and leads to a reduction in the recurrent costs of laboratory consumables...
  4. ncbi request reprint Diagnostic and therapeutic difficulties in type 2A von Willebrand disease: resolution
    M R Thomas
    The Reference Centre for Haemostasis and Thrombosis, St Thomas Hospital, London, United Kingdom
    Clin Appl Thromb Hemost 12:237-9. 2006
    ..Proactive management with definitive diagnosis of angiodysplasia and ablative treatment where feasible is recommended to stop bleeding symptoms and minimize exposure to blood products...
  5. ncbi request reprint The identification and classification of 41 novel mutations in the factor VIII gene (F8C)
    J A Cutler
    The Haemophilia Reference Centre, Centre for Thrombosis and Haemostasis, St Thomas Hospital, Lambeth Palace Road, London, UK
    Hum Mutat 19:274-8. 2002
    ..Our findings support the view that the phenotypic result of a mutation in the FVIII gene correlates more with the position of the amino acid change within the 3D structure of the protein than with the actual nature of the alteration...