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Journal Abstract Search

145 related items for PubMed ID: 8165644

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  • 2. 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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  • 7. 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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  • 9. Abnormal propeptide processing resulting in the presence of two abnormal species of protein C in plasma: characterization of the dysfunctional protein C Padua3 (protein C(R-1L/propeptide)).
    Simioni P, Kalafatis M, Tormene D, Luni S, Zerbinati P, Barzon L, Palù G, Girolami A.
    Thromb Haemost; 2001 Oct; 86(4):1017-22. PubMed ID: 11686318
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  • 10. Genetic characterization of protein C deficiency in Japanese subjects using a rapid and nonradioactive method for single-stand conformational polymorphism analysis and a model building.
    Miyata T, Sakata T, Zheng YZ, Tsukamoto H, Umeyama H, Uchiyama S, Ikusaka M, Yoshioka A, Imanaka Y, Fujimura H, Kambayashi J, Kato H.
    Thromb Haemost; 1996 Sep; 76(3):302-11. PubMed ID: 8883262
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  • 11. 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. Scanning method to establish the molecular basis of protein C deficiencies.
    Gandrille S, Goossens M, Aiach M.
    Hum Mutat; 1994 Jun; 4(1):20-30. PubMed ID: 7951255
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  • 15. [A point mutation of protein C gene in a congenital protein C deficiency pedigree].
    Liu L, Guo WR, He LS, Mu H, Jiang Y, Huang FQ, Li JZ.
    Zhonghua Xue Ye Xue Za Zhi; 2003 Mar; 24(3):115-8. PubMed ID: 12697119
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  • 16. Genetic mutations in ten unrelated American patients with symptomatic type 1 protein C deficiency.
    Tsay W, Greengard JS, Montgomery RR, McPherson RA, Fucci JC, Koerper MA, Coughlin J, Griffin JH.
    Blood Coagul Fibrinolysis; 1993 Oct; 4(5):791-6. PubMed ID: 8292730
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  • 18. Compound heterozygosity in a family with protein C deficiency illustrating the complexity of the underlying molecular mechanism.
    Gandrille S, Jude B, Alhenc-Gelas M, Millaire A, Aiach M.
    Thromb Haemost; 1993 Nov 15; 70(5):747-52. PubMed ID: 8128429
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  • 19. [Screening methods in genetic diagnosis of hereditary protein C deficiency].
    Dávid M, Losonczy H, Nagy A, Kutscher G, Meyer M.
    Orv Hetil; 1999 Jan 17; 140(3):125-32. PubMed ID: 9990817
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