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Journal Abstract Search

103 related items for PubMed ID: 8560401

  • 1. Protein C Osaka 10 with aberrant propeptide processing: loss of anticoagulant activity due to an amino acid substitution in the protein C precursor.
    Miyata T, Zheng YZ, Sakata T, Kato H.
    Thromb Haemost; 1995 Oct; 74(4):1003-8. PubMed ID: 8560401
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  • 4. Homozygous protein C deficiency: identification of a novel missense mutation that causes impaired secretion of the mutant protein C.
    Yamamoto K, Matsushita T, Sugiura I, Takamatsu J, Iwasaki E, Wada H, Deguchi K, Shirakawa S, Saito H.
    J Lab Clin Med; 1992 Jun; 119(6):682-9. PubMed ID: 1593215
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  • 12. [A point mutation at Arg169 (CGG-->TGG) in hereditary protein C deficiency].
    Morishita E, Asakura H, Saito M, Yamazaki M, Ontachi Y, Mizutani T, Kato M, Nakao S.
    Rinsho Ketsueki; 2001 Feb; 42(2):104-9. PubMed ID: 11280915
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  • 13. Two novel mutations responsible for hereditary type I protein C deficiency: characterization by denaturing gradient gel electrophoresis.
    Gandrille S, Vidaud M, Aiach M, Alhenc-Gelas M, Fischer AM, Gouault-Heilman M, Toulon P, Fiessinger JN, Goossens M.
    Hum Mutat; 1992 Feb; 1(6):491-500. PubMed ID: 1301959
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  • 14. The protein C omega-loop substitution Asn2Ile is associated with reduced protein C anticoagulant activity.
    Preston RJ, Morse C, Murden SL, Brady SK, O'Donnell JS, Mumford AD.
    Br J Haematol; 2009 Mar; 144(6):946-53. PubMed ID: 19133979
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  • 16. Impaired secretion of the elongated mutant of protein C (protein C-Nagoya). Molecular and cellular basis for hereditary protein C deficiency.
    Yamamoto K, Tanimoto M, Emi N, Matsushita T, Takamatsu J, Saito H.
    J Clin Invest; 1992 Dec; 90(6):2439-46. PubMed ID: 1469096
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  • 17. Severe type I protein C deficiency in a compound heterozygote for Y124C and Q132X mutations in exon 6 of the PROC gene.
    Soria JM, Morell M, Jiménez-Astorga C, Estivill X, Sala N.
    Thromb Haemost; 1995 Nov; 74(5):1215-20. PubMed ID: 8607097
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