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PUBMED FOR HANDHELDS

Journal Abstract Search


135 related items for PubMed ID: 1515357

  • 21.
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  • 22. [Application of ORM1 phenotyping in forensic science].
    Tan M, Gou Q, Hou Y, Wu M.
    Hua Xi Yi Ke Da Xue Xue Bao; 1994 Mar; 25(1):105-7. PubMed ID: 8070760
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  • 23. Polymorphisms of serum proteins in Japanese patients with vascular diseases. I. Factor XIIIB, plasminogen and complement types in primary varicose veins.
    Mizutani K, Nishimukai H, Yasugi T, Iwahashi K, Tsunekawa K, Shinomiya T.
    Hum Hered; 1991 Mar; 41(4):270-5. PubMed ID: 1783414
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  • 24. Double replica electroblotting for the simultaneous phenotyping of C6 and C7, and its application to the examination of bloodstains.
    Komatsu N, Kido A, Kimura Y, Oya M.
    Forensic Sci Int; 1989 Mar; 41(1-2):3-9. PubMed ID: 2767577
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  • 26. Genetic polymorphism of the B subunit of human coagulation factor XIII: another classification.
    Kera Y, Nishimukai H, Yamasawa K.
    Hum Genet; 1981 Mar; 59(4):360-4. PubMed ID: 6949857
    [No Abstract] [Full Text] [Related]

  • 27. Genetic studies of low-abundance human plasma proteins. X. Coagulation factor XIIIB variants in blacks.
    Kamboh MI, Ferrell RE.
    Electrophoresis; 1989 Jan; 10(1):53-7. PubMed ID: 2714240
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  • 31. Plasminogen (PLG) polymorphism in northern Japanese: confirmation of PLG*M6 allele.
    Sebetan IM, Aoki Y, Funayama M.
    Z Rechtsmed; 1989 Jan; 103(1):43-5. PubMed ID: 2588818
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  • 32. Genetic Factors Influencing Coagulation Factor XIII B-Subunit Contribute to Risk of Ischemic Stroke.
    Hanscombe KB, Traylor M, Hysi PG, Bevan S, Dichgans M, Rothwell PM, Worrall BB, Seshadri S, Sudlow C, METASTROKE Consortium, Wellcome Trust Case Control Consortium 2, Williams FM, Markus HS, Lewis CM.
    Stroke; 2015 Aug; 46(8):2069-74. PubMed ID: 26159793
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  • 33.
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  • 35. Genetic and phenotypic polymorphisms of the A subunit of Coagulation factor XIII in Japanese population.
    Taniguchi M, Ayabe T, Ashida T, Fujimoto Y, Kohgo Y.
    Biochem Genet; 2002 Oct; 40(9-10):339-49. PubMed ID: 12392171
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  • 38. Genetic polymorphism of the B subunit of human coagulation factor XIII in Japanese.
    Nishigaki T, Omoto K.
    Jinrui Idengaku Zasshi; 1982 Sep; 27(3):265-70. PubMed ID: 7161935
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  • 39. In vitro secretion deficits are common among human coagulation factor XIII subunit B missense mutants: correlations with patient phenotypes and molecular models.
    Biswas A, Thomas A, Bevans CG, Ivaskevicius V, Oldenburg J.
    Hum Mutat; 2013 Nov; 34(11):1490-500. PubMed ID: 23913518
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  • 40.
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