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Journal Abstract Search

209 related items for PubMed ID: 29321366

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  • 27. 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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  • 28. 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 01; 90(4):537-539. PubMed ID: 19826897
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  • 29. [PROSI Mutation With Clinical Heterogeneity in Protein S Deficiency:Report of One Case].
    Wei XY, Wang J, Tan BY, Li ZJ.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2023 Oct 01; 45(5):863-866. PubMed ID: 37621108
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  • 31. Clinical characteristics, genes identification and follow-up study of a patient with central venous thrombosis from a protein S deficiency pedigree.
    Wang T, Zhao XJ, Zhu HD, Lu M, Wen B, Ma L.
    Eur Rev Med Pharmacol Sci; 2021 Jan 01; 25(1):353-361. PubMed ID: 33506924
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  • 35. Protein S gene mutation in a young woman with type III protein S deficiency and venous thrombosis during pregnancy.
    Hirose M, Kimura F, Wang HQ, Takebayashi K, Kobayashi M, Nakanishi K, Akiyama M, Kimura T, Noda Y.
    J Thromb Thrombolysis; 2002 Apr 01; 13(2):85-8. PubMed ID: 12101385
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  • 36. Protein S inherited qualitative deficiency: novel mutations and phenotypic influence.
    Alhenc-Gelas M, Canonico M, Morange PE, Emmerich J, Geht Genetic Thrombophilia Group.
    J Thromb Haemost; 2010 Dec 01; 8(12):2718-26. PubMed ID: 20880255
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  • 37. [Recurrent deep vein thrombosis caused by heterozygous missense mutation of the protein S gene: genetic analysis of a case].
    Ye X, Liu XL, Feng Y, Zhou XH, Xing ZF.
    Nan Fang Yi Ke Da Xue Xue Bao; 2011 Jun 01; 31(7):1228-31. PubMed ID: 21764702
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  • 38. [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 01; 22(9):457-60. PubMed ID: 11758223
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  • 39. 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 01; 93(4):574-80. PubMed ID: 18322254
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  • 40. Genotype and laboratory and clinical phenotypes of protein s deficiency.
    Duebgen S, Kauke T, Marschall C, Giebl A, Lison S, Hart C, Dick A, Spannagl M.
    Am J Clin Pathol; 2012 Feb 01; 137(2):178-84. PubMed ID: 22261441
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