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Journal Abstract Search

140 related items for PubMed ID: 1469096

  • 1. 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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  • 4. Hereditary protein C deficiency associated with mutations in exon IX of the protein C gene.
    Doig RG, Begley CG, McGrath KM.
    Thromb Haemost; 1994 Aug; 72(2):203-8. PubMed ID: 7831652
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  • 7. 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; 117(6):813-7. PubMed ID: 15198878
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  • 8. 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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  • 13. 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
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  • 14. Three missense mutations in the protein C heavy chain causing type I and type II protein C deficiency.
    Miyata T, Zheng YZ, Sakata T, Tsushima N, Kato H.
    Thromb Haemost; 1994 Jan; 71(1):32-7. PubMed ID: 8165644
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  • 15. Protein C deficiency Hong Kong 1 and 2: hereditary protein C deficiency caused by two mutant alleles, a 5-nucleotide deletion and a missense mutation.
    Sugahara Y, Miura O, Yuen P, Aoki N.
    Blood; 1992 Jul 01; 80(1):126-33. PubMed ID: 1611081
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  • 16. Gene mutations in 21 unrelated cases of phenotypic heterozygous protein C deficiency and thrombosis. Protein C Study Group.
    Ireland H, Thompson E, Lane DA.
    Thromb Haemost; 1996 Dec 01; 76(6):867-73. PubMed ID: 8972002
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  • 17. Gene analysis of heterozygous protein C deficiency in a patient with pulmonary arterial thromboembolism.
    Ohwada A, Takahashi H, Uchida K, Nukiwa T, Kira S.
    Am Rev Respir Dis; 1992 Jun 01; 145(6):1491-4. PubMed ID: 1596024
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  • 19. [Type I hereditary protein C deficiency due to C5498T mutation in protein C gene].
    Zhou RF, Wang HL, Fu QH, Wang WB, Wu WM, Ding QL, Xie S, Hu YQ, Wang XF, Wang ZY.
    Zhonghua Yi Xue Za Zhi; 2003 Oct 10; 83(19):1694-7. PubMed ID: 14642106
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  • 20. Ectopic transcript analysis indicates that allelic exclusion is an important cause of type I protein C deficiency in patients with nonsense and frameshift mutations in the PROC gene.
    Soria JM, Berg LP, Fontcuberta J, Kakkar VV, Estivill X, Cooper DN, Sala N.
    Thromb Haemost; 1996 Jun 10; 75(6):870-6. PubMed ID: 8822578
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