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112 related items for PubMed ID: 12392171

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Polymorphism of the A subunit of coagulation factor XIII: evidence for subtypes of the FXIIIA*1 and FXIIIA*2 alleles.
    Suzuki K, Matsui K, Ito S, Fujita K, Matsumoto H.
    Am J Hum Genet; 1988 Aug; 43(2):170-4. PubMed ID: 3400643
    [Abstract] [Full Text] [Related]

  • 3. Genetic polymorphism of coagulation factor XIII B subunit in the Japanese population: description of three new rare alleles.
    Nakamura S, Ohue O, Abe K.
    Hum Genet; 1986 Jun; 73(2):183-5. PubMed ID: 3721505
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  • 4. Genotype/phenotype correlations for coagulation factor XIII: specific normal polymorphisms are associated with high or low factor XIII specific activity.
    Anwar R, Gallivan L, Edmonds SD, Markham AF.
    Blood; 1999 Feb 01; 93(3):897-905. PubMed ID: 9920838
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  • 5. Genetic polymorphisms of the A and B subunits of coagulation factor XIII in the Chinese population.
    Zhang L, Stradmann-Bellinghausen B, Schneider PM, Rittner C.
    Exp Clin Immunogenet; 1993 Feb 01; 10(3):137-40. PubMed ID: 8286125
    [Abstract] [Full Text] [Related]

  • 6. Factor XIII deficiency: complete phenotypic characterization of two cases with novel causative mutations.
    Katona É, Muszbek L, Devreese K, Kovács KB, Bereczky Z, Jonkers M, Shemirani AH, Mondelaers V, Ermens AA.
    Haemophilia; 2014 Jan 01; 20(1):114-20. PubMed ID: 24118344
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  • 7. [Identification of two novel mutation in two Chinese hereditary coagulation factor XIII deficiency families].
    Duan B, Wang H, Chu H, Wang X, Qu B, Li D, Wang H, Yin J, Kang W, Wang Z.
    Zhonghua Xue Ye Xue Za Zhi; 2002 Mar 01; 23(3):117-20. PubMed ID: 12015062
    [Abstract] [Full Text] [Related]

  • 8. Distinct C-terminus of the B subunit of factor XIII in a population-associated major phenotype: the first case of complete allele-specific alternative splicing products in the coagulation and fibrinolytic systems.
    Iwata H, Kitano T, Umetsu K, Yuasa I, Yamazaki K, Kemkes-Matthes B, Ichinose A.
    J Thromb Haemost; 2009 Jul 01; 7(7):1084-91. PubMed ID: 19422463
    [Abstract] [Full Text] [Related]

  • 9. Factor XIII V34L polymorphism modulates the risk of chronic venous leg ulcer progression and extension.
    Gemmati D, Tognazzo S, Serino ML, Fogato L, Carandina S, De Palma M, Izzo M, De Mattei M, Ongaro A, Scapoli GL, Caruso A, Liboni A, Zamboni P.
    Wound Repair Regen; 2004 Jul 01; 12(5):512-7. PubMed ID: 15453833
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  • 11. Genetic polymorphism of coagulation factor XIIIB subunit in Japanese.
    Nakamura S, Abe K.
    Ann Hum Genet; 1982 Jul 01; 46(3):203-7. PubMed ID: 7125593
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  • 13. Coagulation factor XIII Val34Leu gene polymorphism and Alzheimer's disease.
    Gerardino L, Papaleo P, Flex A, Gaetani E, Fioroni G, Pola P, Pola R.
    Neurol Res; 2006 Dec 01; 28(8):807-9. PubMed ID: 17288735
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  • 14. Alternative method of subtyping the A subunit of coagulation factor XIII (FXIIIA).
    Kido A, Oya M, Jin Z.
    Electrophoresis; 1997 May 01; 18(5):790-1. PubMed ID: 9194608
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  • 16. Factor XIII levels and factor XIII B subunit polymorphisms in patients with venous thromboembolism.
    Mezei ZA, Katona É, Kállai J, Bereczky Z, Somodi L, Molnár É, Kovács B, Miklós T, Ajzner É, Muszbek L.
    Thromb Res; 2017 Oct 01; 158():93-97. PubMed ID: 28865246
    [Abstract] [Full Text] [Related]

  • 17. Polymorphism of coagulation factor XIII B subunit: further occurrence of FXIIIB*15 in Japanese and phenotyping in bloodstains.
    Komatsu N, Kido A, Kimura Y, Oya M, Dobashi Y, Hashimoto K.
    Int J Legal Med; 1992 Oct 01; 104(6):317-9. PubMed ID: 1515357
    [Abstract] [Full Text] [Related]

  • 18. Factor XIII(A) subunit deficiency due to a homozygous 13-base pair deletion in exon 3 of the A subunit gene.
    Aslam S, Bowen DJ, Mandalaki T, Gialeraki R, Standen GR.
    Am J Hematol; 1996 Oct 01; 53(2):77-80. PubMed ID: 8892731
    [Abstract] [Full Text] [Related]

  • 19. The combined effect of fibrin formation and factor XIII A subunit Val34Leu polymorphism on the activation of factor XIII in whole plasma.
    Shemirani AH, Haramura G, Bagoly Z, Muszbek L.
    Biochim Biophys Acta; 2006 Aug 01; 1764(8):1420-3. PubMed ID: 16920044
    [Abstract] [Full Text] [Related]

  • 20. Prevalence of three common polymorphisms in the A-subunit gene of factor XIII in patients with coronary artery disease.
    Kohler HP, Futers TS, Grant PJ.
    Thromb Haemost; 1999 Apr 01; 81(4):511-5. PubMed ID: 10235430
    [Abstract] [Full Text] [Related]

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