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Journal Abstract Search

132 related items for PubMed ID: 22166512

  • 1. A rare splicing mutation in the PROS1 gene of a Korean patient with type I hereditary protein S deficiency.
    Choi J, Kim HJ, Chang MH, Choi JR, Yoo JH.
    Ann Clin Lab Sci; 2011; 41(4):397-400. PubMed ID: 22166512
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  • 2. One novel and one recurrent mutation in the PROS1 gene cause type I protein S deficiency in patients with pulmonary embolism associated with deep vein thrombosis.
    Mizukami K, Nakabayashi T, Naitoh S, Takeda M, Tarumi T, Mizoguchi I, Ieko M, Koike T.
    Am J Hematol; 2006 Oct; 81(10):787-97. PubMed ID: 16868938
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  • 4. 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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  • 5. 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; 96(6):1047-1051. PubMed ID: 29321366
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  • 6. Recurrent pulmonary embolism associated with deep venous thrombosis diagnosed as protein s deficiency owing to a novel mutation in PROS1: A case report.
    Huang X, Xu F, Assa CR, Shen L, Chen B, Liu Z.
    Medicine (Baltimore); 2018 May; 97(19):e0714. PubMed ID: 29742732
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  • 8. 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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  • 9. [A family of hereditary protein S deficiency with the onset of pulmonary embolism and literature review].
    Wei CJ, Guo CY, Li QR, Ye LP.
    Zhonghua Er Ke Za Zhi; 2022 Feb 02; 60(2):134-138. PubMed ID: 35090231
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  • 18. A large deletion of the PROS1 gene in a deep vein thrombosis patient with protein S deficiency.
    Yin T, Takeshita S, Sato Y, Sakata T, Shin Y, Honda S, Kawasaki T, Tsuji H, Kojima T, Madoiwa S, Sakata Y, Murata M, Ikeda Y, Miyata T.
    Thromb Haemost; 2007 Oct 02; 98(4):783-9. PubMed ID: 17938802
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  • 19. 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 02; 8(12):2718-26. PubMed ID: 20880255
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  • 20. Novel Splice Site Mutation in the PROS1 Gene in a Polish Patient with Venous Thromboembolism: c.602-2delA, Splice Acceptor Site of Exon 7.
    Mrożek M, Wypasek E, Alhenc-Gelas M, Potaczek DP, Undas A.
    Medicina (Kaunas); 2020 Sep 22; 56(9):. PubMed ID: 32971918
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