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Journal Abstract Search

149 related items for PubMed ID: 7792728

  • 1. Six different point mutations in seven Danish families with symptomatic protein C deficiency.
    Lind B, Schwartz M, Thorsen S.
    Thromb Haemost; 1995 Feb; 73(2):186-93. PubMed ID: 7792728
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  • 2. 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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  • 4. 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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  • 6. 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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  • 10. Influence of six mutations of the protein C gene on the Gla domain conformation and calcium affinity.
    Gaussem P, Gandrille S, Duchemin J, Emmerich J, Alhenc-Gelas M, Aillaud MF, Aiach M.
    Thromb Haemost; 1994 Jun; 71(6):748-54. PubMed ID: 7974343
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  • 12. 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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  • 17. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
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  • 18. [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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