M. Begbie

发表

Directional Next-Generation RNA Sequencing and Examination of Premature Termination Codon Mutations in Endoglin/Hereditary Haemorrhagic Telangiectasia

L. Game, C. Shovlin, A. Giess, 2013, Molecular Syndromology.

Role of the liver-enriched transcription factor hepatocyte nuclear factor 1 in transcriptional regulation of the factor V111 gene

D. Lillicrap, C. Mueller, C. Notley, 1996, Molecular and cellular biology.

Enhanced binding of HLF/DBP heterodimers represents one mechanism of PAR protein transactivation of the factor VIII and factor IX genes.

D. Lillicrap, C. Mueller, M. Begbie, 1999, DNA and cell biology.

The Factor VIII Acute Phase Response Requires the Participation of NFκB and C/EBP

D. Lillicrap, S. Tinlin, C. Notley, 2000, Thrombosis and Haemostasis.

An important role for the activation peptide domain in controlling factor IX levels in the blood of haemophilia B mice

G. Hortelano, V. Bhakta, W. Sheffield, 2005, Thrombosis and Haemostasis.

Effects of genetic fusion of factor IX to albumin on in vivo clearance in mice and rabbits

G. Hortelano, F. Ofosu, W. Sheffield, 2004, British journal of haematology.

A new locus for hereditary haemorrhagic telangiectasia (HHT3) maps to chromosome 5

C. Shovlin, M. Begbie, S. Cole, 2005, Journal of Medical Genetics.

Hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): a view from the 21st century

C. Shovlin, M. Begbie, G. M. Wallace, 2003, Postgraduate medical journal.

Redefining Disease? The Nosologic Implications of Molecular Genetic Knowledge

M. Giacomini, M. Begbie, Catherine Ahern, 2006, Perspectives in biology and medicine.

Elevated factor VIII in hereditary haemorrhagic telangiectasia (HHT): Association with venous thromboembolism

C. Shovlin, F. Govani, M. Begbie, 2007, Thrombosis and Haemostasis.

A new locus for hereditary haemorrhagic telangiectasia (HHT3) maps to chromosome 5

C. Shovlin, M. Begbie, S. Cole, 2005, Journal of Medical Genetics.