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Journal Abstract Search

120 related items for PubMed ID: 20398916

  • 21. Functional characterization of twelve natural PROS1 mutations associated with anticoagulant protein S deficiency.
    Hurtado B, Muñoz X, Mulero MC, Navarro G, Domènech P, García de Frutos P, Pérez-Riba M, Sala N.
    Haematologica; 2008 Apr; 93(4):574-80. PubMed ID: 18322254
    [Abstract] [Full Text] [Related]

  • 22. Novel human pathological mutations. Gene symbol: PROS1. Disease: Protein S deficiency.
    Pintao M, Garcia AA, Borgel D, Alhenc-Gelas M, Spek CA, de Visser MC, Gandrille S, Reitsma PH.
    Hum Genet; 2010 Jan; 127(1):121. PubMed ID: 20108435
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  • 23. Compound heterozygous mutations in the PROS1 gene responsible for quantitative and qualitative protein S deficiency.
    Yamanouchi J, Hato T, Tamura T, Fujiwara H, Yakushijin Y, Yasukawa M.
    Int J Hematol; 2009 Nov; 90(4):537-539. PubMed ID: 19826897
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  • 24. A novel splicing mutation in the PROS1 gene causes hereditary protein S deficiency in a Chinese family with thrombotic disease.
    Tan Y, Yang K, Wang J, Sun X, Li R, Dong Z, Zhao N, Yan Y, Lin L.
    Thromb Res; 2020 May; 189():93-95. PubMed ID: 32192997
    [No Abstract] [Full Text] [Related]

  • 25. PROS1 mutations associated with protein S deficiency in Polish patients with residual vein obstruction on rivaroxaban therapy.
    Wypasek E, Potaczek DP, Alhenc-Gelas M, Undas A.
    Thromb Res; 2014 Jul; 134(1):199-201. PubMed ID: 24507871
    [No Abstract] [Full Text] [Related]

  • 26. Two mutations in exon XII of the protein S alpha gene in four thrombophilic families resulting in premature stop codons and depressed levels of mutated mRNA.
    Andersen BD, Lind B, Philips M, Hansen AB, Ingerslev J, Thorsen S.
    Thromb Haemost; 1996 Aug; 76(2):143-50. PubMed ID: 8865520
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  • 30. A common 4G allele in the promoter of the plasminogen activator inhibitor-1 (PAI-1) gene as a risk factor for pulmonary embolism and arterial thrombosis in hereditary protein S deficiency.
    Zöller B, García de Frutos P, Dahlbäck B.
    Thromb Haemost; 1998 Apr; 79(4):802-7. PubMed ID: 9569196
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  • 31. Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiency.
    Pintao MC, Garcia AA, Borgel D, Alhenc-Gelas M, Spek CA, de Visser MC, Gandrille S, Reitsma PH.
    Hum Genet; 2009 Sep; 126(3):449-56. PubMed ID: 19466456
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  • 32. PROS1 variant c.1574C>T p.Ala525Val causes portal vein thrombosis with protein S deficiency.
    Ye X, Mi X, Sun J, ShenTu Y, Fei Y, Tang D, Ye X, Ma X, Shi J, Chen G, Gong L.
    Clin Res Hepatol Gastroenterol; 2023 May; 47(6):102141. PubMed ID: 37207893
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  • 33. Molecular basis of protein S deficiency.
    García de Frutos P, Fuentes-Prior P, Hurtado B, Sala N.
    Thromb Haemost; 2007 Sep; 98(3):543-56. PubMed ID: 17849042
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  • 34. [Hereditary protein S deficiency and familial thrombosis. A review with description of a Danish family with protein S deficiency].
    Ingerslev J, Ingerslev J, Thelle T.
    Ugeskr Laeger; 1993 May 31; 155(22):1703-7. PubMed ID: 8317013
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  • 35. Venous thromboembolism associated with protein S deficiency due to Arg451* mutation in PROS1 gene: a case report and a literature review.
    Wypasek E, Karpinski M, Alhenc-Gelas M, Undas A.
    J Genet; 2017 Dec 31; 96(6):1047-1051. PubMed ID: 29321366
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  • 36. Severe protein S deficiency resulting from two novel mutations in PROS1 presenting with a relatively mild clinical phenotype.
    Carter IS, Hewitt J, Pu CH, Wu JK, Carter CJ, Macgillivray RT.
    J Thromb Haemost; 2008 Jul 31; 6(7):1237-9. PubMed ID: 18485091
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