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Journal Abstract Search

105 related items for PubMed ID: 8822580

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  • 23. The Ser 460 to Pro substitution of the protein S alpha (PROS1) gene is a frequent mutation associated with free protein S (type IIa) deficiency.
    Duchemin J, Gandrille S, Borgel D, Feurgard P, Alhenc-Gelas M, Matheron C, Dreyfus M, Dupuy E, Juhan-Vague I, Aiach M.
    Blood; 1995 Nov 01; 86(9):3436-43. PubMed ID: 7579448
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  • 27. Familial thrombophilia is an oligogenetic disease: involvement of the prothrombin G20210A, PROC and PROS gene mutations.
    Boinot C, Borgel D, Kitzis A, Guicheteau M, Aiach M, Alhenc-Gelas M.
    Blood Coagul Fibrinolysis; 2003 Feb 01; 14(2):191-6. PubMed ID: 12632031
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  • 28. Protein S Thr103Asn mutation associated with type II deficiency reproduced in vitro and functionally characterised.
    Giri TK, García de Frutos P, Dahlbäck B.
    Thromb Haemost; 2000 Sep 01; 84(3):413-9. PubMed ID: 11019964
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  • 30. Genetic modulation of plasma protein S levels by two frequent dimorphisms in the PROS1 gene.
    Leroy-Matheron C, Duchemin J, Levent M, Gouault-Heilmann M.
    Thromb Haemost; 1999 Sep 01; 82(3):1088-92. PubMed ID: 10494768
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  • 31. Large deletions of the PROS1 gene in a large fraction of mutation-negative patients with protein S deficiency.
    Johansson AM, Hillarp A, Säll T, Zöller B, Dahlbäck B, Halldén C.
    Thromb Haemost; 2005 Nov 01; 94(5):951-7. PubMed ID: 16363235
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  • 35. A novel splice acceptor site mutation which produces multiple splicing abnormalities resulting in protein S deficiency type I.
    Tatewaki H, Iida H, Nakahara M, Tsuda H, Kinoshita S, Kanaji T, Yoshida N, Miyazaki S, Hamasaki N.
    Thromb Haemost; 1999 Jul 01; 82(1):65-71. PubMed ID: 10456456
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  • 36. Gene symbol: PROS1. Disease: Protein S deficiency.
    Steidle M, Pfanner G, Haug B.
    Hum Genet; 2008 Oct 01; 124(3):313. PubMed ID: 18846658
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  • 38. A novel mutation in intron K of the PROS1 gene causes aberrant RNA splicing and is a common cause of protein S deficiency in a UK thrombophilia cohort.
    Beauchamp NJ, Daly ME, Makris M, Preston FE, Peake IR.
    Thromb Haemost; 1998 Jun 01; 79(6):1086-91. PubMed ID: 9657428
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  • 39. [Type I protein C deficiency caused by a novel protein C gene mutation].
    Zheng Y, Zhu D, Zhou B.
    Zhonghua Xue Ye Xue Za Zhi; 1998 Mar 01; 19(3):138-42. PubMed ID: 11243145
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  • 40. Biochemical activity and gene analysis of inherited protein C and antithrombin deficiency in two Chinese pedigrees.
    Zhou RF, Fu QH, Wang WB, Xie S, Hu YQ, Wang XF, Wang ZY, Wang HL.
    Chin Med J (Engl); 2004 Jun 01; 117(6):813-7. PubMed ID: 15198878
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