^“Genes for human vitamin K-dependent plasma proteins C and S are located on chromosomes 2 and 3, respectively”. Somat. Cell Mol. Genet.14 (1): 93–8. (January 1988). doi:10.1007/BF01535052. PMID2829367.
^Stenflo J (1999). “Contributions of Gla and EGF-like domains to the function of vitamin K-dependent coagulation factors”. Critical Reviews in Eukaryotic Gene Expression9 (1): 59–88. doi:10.1615/CritRevEukaryotGeneExpr.v9.i1.50. PMID10200912.
^Kaushansky, K; Lichtman, M; Prchal, J; Levi, M; Press, O; Burns, L; Caligiuri, M (2015). Williams Hematology. McGraw-Hill. p. 1926
^“The prevalence of, and molecular defects underlying, inherited protein S deficiency in the general population”. Br. J. Haematol.125 (5): 647–54. (June 2004). doi:10.1111/j.1365-2141.2004.04961.x. PMID15147381.
^Heeb, M J; Kojima Y; Rosing J; Tans G; Griffin J H (Dec 1999). “C-terminal residues 621-635 of protein S are essential for binding to factor Va”. J. Biol. Chem. (UNITED STATES) 274 (51): 36187–92. doi:10.1074/jbc.274.51.36187. ISSN0021-9258. PMID10593904.
^Heeb, M J; Mesters R M; Tans G; Rosing J; Griffin J H (Feb 1993). “Binding of protein S to factor Va associated with inhibition of prothrombinase that is independent of activated protein C”. J. Biol. Chem. (UNITED STATES) 268 (4): 2872–7. doi:10.1016/S0021-9258(18)53854-0. ISSN0021-9258. PMID8428962.
参考資料
Dahlbäck B (1991). “Protein S and C4b-binding protein: components involved in the regulation of the protein C anticoagulant system”. Thromb. Haemost.66 (1): 49–61. doi:10.1055/s-0038-1646373. PMID1833851.
Witt, I (2002). “Molekularbiologische Grundlagen und Diagnostik der hereditären Defekte von Antithrombin III, Protein C und Protein S [Molecular biological basis and diagnosis of hereditary defect of antithrombin III, protein c and protein S]” (ドイツ語). Hamostaseologie22 (2): 57–66. doi:10.1055/s-0037-1619540. PMID12193972.
“Coagulation, inflammation, and apoptosis: different roles for protein S and the protein S-C4b binding protein complex”. Blood103 (4): 1192–201. (2004). doi:10.1182/blood-2003-05-1551. PMID12907438.
Dahlbäck B (2007). “The tale of protein S and C4b-binding protein, a story of affection”. Thromb. Haemost.98 (1): 90–6. doi:10.1160/th07-04-0269. PMID17597997.
“Protein-S, a vitamin K-dependent protein, is a bone matrix component synthesized and secreted by osteoblasts”. Endocrinology130 (3): 1599–604. (1992). doi:10.1210/endo.130.3.1531628. PMID1531628.
“A novel functional assay of protein C in human plasma and its comparison with amidolytic and anticoagulant assays”. Thromb. Haemost.67 (1): 46–9. (1992). doi:10.1055/s-0038-1648377. PMID1615482.
“Heerlen polymorphism of protein S, an immunologic polymorphism due to dimorphism of residue 460”. Blood76 (3): 538–48. (1990). doi:10.1182/blood.V76.3.538.538. PMID2143091.
“Intron-exon organization of the active human protein S gene PS alpha and its pseudogene PS beta: duplication and silencing during primate evolution”. Biochemistry29 (34): 7853–61. (1991). doi:10.1021/bi00486a011. PMID2148111.
“Hereditary protein S deficiency in young adults with arterial occlusive disease”. Thromb. Haemost.64 (2): 206–10. (1991). PMID2148653.
“Beta-hydroxyaspartic acid in the first epidermal growth factor-like domain of protein C. Its role in Ca2+ binding and biological activity”. J. Biol. Chem.263 (35): 19240–8. (1989). doi:10.1016/S0021-9258(18)37415-5. PMID2461936.
“Familial protein S deficiency with a variant protein S molecule in plasma and platelets”. Blood74 (1): 213–21. (1989). doi:10.1182/blood.V74.1.213.213. PMID2526663.
“Human protein S cDNA encodes Phe-16 and Tyr 222 in consensus sequences for the post-translational processing”. FEBS Lett.222 (1): 186–90. (1987). doi:10.1016/0014-5793(87)80217-X. PMID2820795.