Associated Papers
Mutational scanning reveals substrate-assisted autoregulation of the WNT destruction complex.
Padmanarayana M et al.
Biorxiv : the Preprint Server for Biology, 2025
41278994 (PubMed )
Supplement: media-1.xlsx › WNT_DC_ABE_Screen
Dysfunction of protein C anticoagulant system, main genetic risk factor for venous thromboembolism in northeast Asians.
Yin T et al.
Journal of Thrombosis and Thrombolysis, 2014
Potentially functional SNPs (pfSNPs) as novel genomic predictors of 5-FU response in metastatic colorectal cancer patients.
Wang J et al.
Plos One, 2014
25372392 (PubMed )
Supplement: pone.0111694.s006.pdf
Activated protein C anticoagulant system dysfunction and thrombophilia in Asia.
Hamasaki N et al.
Annals of Laboratory Medicine, 2013
New quantitative total protein S-assay system for diagnosing protein S type II deficiency: clinical application of the screening system for protein S type II deficiency.
Tsuda T et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis, 2012
Protein S and protein C gene mutations in Japanese deep vein thrombosis patients.
Kinoshita S et al.
Clinical Biochemistry, 2005
Identification of protein Salpha gene mutations including four novel mutations in eight unrelated patients with protein S deficiency.
Okada H et al.
British Journal of Haematology, 2004
Deletion or replacement of the second EGF-like domain of protein S results in loss of APC cofactor activity.
Mille-Baker B et al.
Blood, 2003
Four missense mutations identified in the protein S gene of thrombosis patients with protein S deficiency: effects on secretion and anticoagulant activity of protein S.
Tsuda H et al.
Thrombosis Research, 2002
Kinetic characterization of the unisite catalytic pathway of seven beta-subunit mutant F1-ATPases from Escherichia coli.
al-Shawi MK et al.
The Journal of Biological Chemistry, 1989
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