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Journal Abstract Search

91 related items for PubMed ID: 9576175

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  • 6. A mutation of the active protein S gene leading to an EGF1-lacking protein in a family with qualitative (type II) deficiency.
    Leroy-Matheron C, Gouault-Heilmann M, Aiach M, Gandrille S.
    Blood; 1998 Jun 15; 91(12):4608-15. PubMed ID: 9616157
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  • 7. Identification of protein Salpha gene mutations including four novel mutations in eight unrelated patients with protein S deficiency.
    Okada H, Takagi A, Murate T, Adachi T, Yamamoto K, Matsushita T, Takamatsu J, Sugita K, Sugimoto M, Yoshioka A, Yamazaki T, Saito H, Kojima T.
    Br J Haematol; 2004 Jul 15; 126(2):219-25. PubMed ID: 15238143
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  • 8. An evaluation of association between common variants in C4BPB/C4BPA genes and schizophrenia.
    Wang S, Lu H, Ni J, Zhang J, Tang W, Lu W, Cai J, Zhang C.
    Neurosci Lett; 2015 Mar 17; 590():189-92. PubMed ID: 25660618
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  • 9. Evaluation of the relationship between protein S and C4b-binding protein isoforms in hereditary protein S deficiency demonstrating type I and type III deficiencies to be phenotypic variants of the same genetic disease.
    Zöller B, García de Frutos P, Dahlbäck B.
    Blood; 1995 Jun 15; 85(12):3524-31. PubMed ID: 7780139
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  • 11. [A novel gene mutation in a congenital protein S deficiency pedigree].
    Liu L, He L, Yang S.
    Zhonghua Xue Ye Xue Za Zhi; 2001 Sep 15; 22(9):457-60. PubMed ID: 11758223
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  • 15. Poor relationship between phenotypes of protein S deficiency and mutations in the protein S alpha gene.
    Hermida J, Faioni EM, Mannucci PM.
    Thromb Haemost; 1999 Dec 15; 82(6):1634-8. PubMed ID: 10613647
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  • 18. Differences in protein S and C4b-binding protein levels in different groups of patients with antiphospholipid antibodies.
    Forastiero RR, Kordich L, Basilotta E, Carreras LO.
    Blood Coagul Fibrinolysis; 1994 Aug 15; 5(4):609-16. PubMed ID: 7841319
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  • 19. Promoter region of the human gene coding for beta-chain of C4b binding protein. Hepatocyte nuclear factor-3 and nuclear factor-I/CTF transcription factors are required for efficient expression of C4BPB in HepG2 cells.
    Arenzana N, Rodríguez de Córdoba S.
    J Immunol; 1996 Jan 01; 156(1):168-75. PubMed ID: 8598458
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  • 20. The molecular basis of complete complement C4A and C4B deficiencies in a systemic lupus erythematosus patient with homozygous C4A and C4B mutant genes.
    Rupert KL, Moulds JM, Yang Y, Arnett FC, Warren RW, Reveille JD, Myones BL, Blanchong CA, Yu CY.
    J Immunol; 2002 Aug 01; 169(3):1570-8. PubMed ID: 12133986
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