| Inhibitors of TLR8 reduce TNF production from human rheumatoid synovial membrane cultures. Sacre S.M., Lo A., Gregory B., Simmonds R.E., Williams L., Feldmann M., Brennan F.M., Foxwell B.M.
J. Immunol. 181:8002-8009(2008) · Mapped (6) |
| Molecular diversity and thrombotic risk in protein S deficiency: the PROSIT study. Protein S Italian team (PROSIT)
Biguzzi E., Razzari C., Lane D.A., Castaman G., Cappellari A., Bucciarelli P., Fontana G., Margaglione M., D'Andrea G., Simmonds R.E. et al.
Hum. Mutat. 25:259-269(2005) · UniProtKB (1) |
| Coagulation, inflammation, and apoptosis: different roles for protein S and the protein S-C4b binding protein complex. Rezende S.M., Simmonds R.E., Lane D.A.
Blood 103:1192-1201(2004) · Mapped (48) |
| Regulation of the human endothelial cell protein C receptor gene promoter by multiple Sp1 binding sites. Rance J.B., Follows G.A., Cockerill P.N., Bonifer C., Lane D.A., Simmonds R.E.
Blood 101:4393-4401(2003) · Mapped (8) |
| Protein S Gla-domain mutations causing impaired Ca(2+)-induced phospholipid binding and severe functional protein S deficiency. Rezende S.M., Lane D.A., Mille-Baker B., Samama M.M., Conard J., Simmonds R.E.
Blood 100:2812-2819(2002) · UniProtKB (1) |
| Genetic and phenotypic variability between families with hereditary protein S deficiency. Rezende S.M., Lane D.A., Zoeller B., Mille-Baker B., Laffan M., Dalhbaeck B., Simmonds R.E.
Thromb. Haemost. 87:258-265(2002) · UniProtKB (1) · Mapped (27) |
| 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 domains. Simmonds R.E., Lane D.A.
Blood 94:632-641(1999) · UniProtKB (1) |
| Identification of 19 protein S gene mutations in patients with phenotypic protein S deficiency and thrombosis. Protein S study group
Simmonds R.E., Ireland H., Kunz G., Lane D.A.
Blood 88:4195-4204(1996) · UniProtKB (1) |
