C. Cameron

发表

Aberrant Splicing and Premature Termination of Transcription of the FVIII Gene as a Cause of Severe Canine Hemophilia A: Similarities with the Intron 22 Inversion Mutation in Human Hemophilia

A. Giles, D. Lillicrap, C. Hough, 2002, Thrombosis and Haemostasis.

The −1185 A/G and −1051 G/A dimorphisms in the von Willebrand factor gene promoter and risk of myocardial infarction

N. Samani, R. Steeds, D. Lillicrap, 2001, British journal of haematology.

The Canine Factor VIII cDNA and 5’ Flanking Sequence

A. Giles, D. Lillicrap, C. Hough, 1998, Thrombosis and Haemostasis.

Systemic delivery of an adenoviral vector encoding canine factor VIII results in short-term phenotypic correction, inhibitor development, and biphasic liver toxicity in hemophilia A dogs.

M. Kaleko, S. Connelly, D. Lillicrap, 2001, Blood.

Androgen effects on factor IX expression: in‐vitro and in‐vivo studies in mice

D. Lillicrap, C. Cameron, C. Notley, 1998, British journal of haematology.

Absence of allelic loss on chromosome 5q by RFLP analysis in preleukemia.

D. Lillicrap, C. Cameron, S. Windsor, 1991, Leukemia research.

Founder von Willebrand factor haplotype associated with type 1 von Willebrand disease.

J. Sutherland, L. O'Brien, M. Othman, 2003, Blood.

The canine factor VIII 3'-untranslated region and a concatemeric hepatocyte nuclear factor 1 regulatory element enhance factor VIII transgene expression in vivo.

D. Lillicrap, C. Hough, A. Killoran, 2002, Human gene therapy.

Genetic linkage and association analysis in type 1 von Willebrand disease: results from the Canadian Type 1 VWD Study

A. Paterson, L. O'Brien, J. Leggo, 2006, Journal of thrombosis and haemostasis : JTH.

In vivo evaluation of an adenoviral vector encoding canine factor VIII: high-level, sustained expression in hemophiliac mice.

D. Kayda, M. Kaleko, S. Connelly, 1999, Human gene therapy.

Characterization of the Original Christmas Disease Mutation (Cysteine 206 → Serine): From Clinical Recognition to Molecular Pathogenesis

J. Teitel, D. Lillicrap, B. Garvey, 1992, Thrombosis and Haemostasis.

Influence of a GT repeat element on shear stress responsiveness of the VWF gene promoter

L. O'Brien, D. Lillicrap, C. Hough, 2008, Journal of thrombosis and haemostasis : JTH.

A single nucleotide polymorphism at nucleotide −1793 in the von Willebrand factor (VWF) regulatory region is associated with plasma VWF:Ag levels

P. Harvey, D. Lillicrap, C. Cameron, 2000, British journal of haematology.

Variation at the von Willebrand factor (vWF) gene locus is associated with plasma vWF :Ag levels : Identification of three novel single nucleotide polymorphisms in the vWF gene promoter

D. Lillicrap, C. Cameron, A. Keightley, 1999 .

Variation at the von Willebrand factor (vWF) gene locus is associated with plasma vWF:Ag levels: identification of three novel single nucleotide polymorphisms in the vWF gene promoter.

D. Lillicrap, C. Cameron, A. Keightley, 1999, Blood.

Differential termination of primer extension: a novel, quantifiable method for detection of point mutations

D. Lillicrap, S. Taylor, C. Cameron, 1992, Human Genetics.