A phenotypically neutral dimorphism of protein S: the substitution of Lys155 by Glu in the second EGF domain predicted by an A to G base exchange in the gene.
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J. Takamatsu | T. Matsushita | I. Sugiura | H. Saito | T. Yamazaki | T. Kojima | K. Kagami
[1] H. Saito,et al. Three Distinct Candidate Point Mutations of the von Willebrand Factor Gene in Four Patients with Type IIA von Willebrand Disease , 1992, Thrombosis and Haemostasis.
[2] C. Esmon. The protein C anticoagulant pathway. , 1992, Arteriosclerosis and thrombosis : a journal of vascular biology.
[3] J. Stenflo,et al. Structure-function relationships of epidermal growth factor modules in vitamin K-dependent clotting factors. , 1991, Blood.
[4] P. Reitsma,et al. A CCA/CCG neutral dimorphism in the codon for Pro 626 of the human protein S gene PSα (PROS1) , 1991 .
[5] B. Dahlbäck. Protein S and C4b-Binding Protein: Components Involved in the Regulation of the Protein C Anticoagulant System , 1991, Thrombosis and Haemostasis.
[6] M. Tanimoto,et al. Genotype establishments for protein C deficiency by use of a DNA polymorphism in the gene. , 1991, Blood.
[7] R. Marlar,et al. A 5.3-kb deletion including exon XIII of the protein S alpha gene occurs in two protein S-deficient families. , 1991, Blood.
[8] G. Long,et al. Organization of the human protein S genes. , 1990, Biochemistry.
[9] P. Reitsma,et al. Heerlen polymorphism of protein S, an immunologic polymorphism due to dimorphism of residue 460. , 1990, Blood.
[10] B. Dahlbäck,et al. Characterization of functionally important domains in human vitamin K-dependent protein S using monoclonal antibodies. , 1990, The Journal of biological chemistry.
[11] C. Levenson,et al. Effects of primer-template mismatches on the polymerase chain reaction: human immunodeficiency virus type 1 model studies. , 1990, Nucleic acids research.
[12] P. Mannucci,et al. Familial Dysfunction of Protein S , 1989, Thrombosis and Haemostasis.
[13] S. Kume,et al. Functional activity of protein S determined with use of protein C activated by venom activator. , 1989, Clinical chemistry.
[14] J. Griffin,et al. FAMILIAL PROTEIN S DEFICIENCY WITH A VARIANT PROTEIN S MOLECULE IN PLASMA AND PLATELETS , 1989, Thrombosis and Haemostasis.
[15] P. Reitsma,et al. Partial protein S gene deletion in a family with hereditary thrombophilia , 1989 .
[16] K. Kurachi,et al. DNA analysis of seven patients with hemophilia B who have anti-factor IX antibodies: relationship to clinical manifestations and evidence that the abnormal gene was inherited. , 1988, The Journal of laboratory and clinical medicine.
[17] J. Gorski,et al. Enzymatic amplification of platelet-specific messenger RNA using the polymerase chain reaction. , 1988, The Journal of clinical investigation.
[18] M. Ogura,et al. Biosynthesis and secretion of functional protein S by a human megakaryoblastic cell line (MEG-01) , 1987 .
[19] C. Esmon,et al. An abnormal plasma distribution of protein S occurs in functional protein S deficiency. , 1986, Blood.
[20] J. Nishioka,et al. Inherited deficiency of protein S in a Japanese family with recurrent venous thrombosis: a study of three generations. , 1986, Blood.
[21] C. Esmon,et al. Recurrent venous thromboembolism in patients with a partial deficiency of protein S. , 1984, The New England journal of medicine.
[22] C. Esmon,et al. Familial protein S deficiency is associated with recurrent thrombosis. , 1984, The Journal of clinical investigation.
[23] B. Dahlbäck. Purification of human vitamin K-dependent protein S and its limited proteolysis by thrombin. , 1983, The Biochemical journal.
[24] E. H. Cohen,et al. The gene for protein S maps near the centromere of human chromosome 3. , 1988, Blood.
[25] G. Long,et al. Cloning and characterization of human liver cDNA encoding a protein S precursor. , 1987, Proceedings of the National Academy of Sciences of the United States of America.