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Blood|July 9, 1999
Structural and functional implications of the intron/exon organization of the human endothelial cell protein C/activated protein C receptor (EPCR) gene: comparison with the structure of CD1/major histocompatibility complex alpha1 and alpha2 domainsR E Simmonds, D A Lane
Rheumatology (Oxford, England)|February 1, 2008
Signalling, inflammation and arthritis: NF-kappaB and its relevance to arthritis and inflammationR E Simmonds, B M Foxwell
Blood|December 1, 1996
Identification of 19 protein S gene mutations in patients with phenotypic protein S deficiency and thrombosis. Protein S Study GroupR E Simmonds, H Ireland, G Kunz, et al.
Thrombosis and Haemostasis|August 7, 2001
Haemostatic genetic risk factors in arterial thrombosisR E Simmonds, J Hermida, S M Rezende, et al.
Scandinavian Journal of Immunology|June 14, 2012
TLR signalling and adapter utilization in primary human in vitro differentiated adipocytesC Brenner, R E Simmonds, S Wood, et al.
Annals of Internal Medicine|January 10, 1998
Clarification of the risk for venous thrombosis associated with hereditary protein S deficiency by investigation of a large kindred with a characterized gene defectR E Simmonds, H Ireland, D A Lane, et al.
Blood|June 15, 1997
Genetic and phenotypic analysis of a large (122-member) protein S-deficient kindred provides an explanation for the familial coexistence of type I and type III plasma phenotypesR E Simmonds, B Zöller, H Ireland, et al.
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