These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

296 related articles for article (PubMed ID: 11487042)

  • 1. Physiopathology and regulation of factor XIII.
    Ichinose A
    Thromb Haemost; 2001 Jul; 86(1):57-65. PubMed ID: 11487042
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Gene defects in congenital factor XIII deficiency.
    Mikkola H; Palotie A
    Semin Thromb Hemost; 1996; 22(5):393-8. PubMed ID: 8989822
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular and genetic mechanisms of factor XIII A subunit deficiency.
    Ichinose A; Souri M; Izumi T; Takahashi N
    Semin Thromb Hemost; 2000; 26(1):5-10. PubMed ID: 10805274
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The normal and abnormal genes of the a and b subunits in coagulation factor XIII.
    Ichinose A; Izumi T; Hashiguchi T
    Semin Thromb Hemost; 1996; 22(5):385-91. PubMed ID: 8989821
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular modeling predicts structural changes in the A subunit of factor XIII caused by two novel mutations identified in a neonate with severe congenital factor XIII deficiency.
    Souri M; Yee VC; Fujii N; Ichinose A
    Thromb Res; 2012 Sep; 130(3):506-10. PubMed ID: 22633530
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Factor XIII deficiency: new nonsense and deletion mutations in the human factor XIIIA gene.
    Anwar R; Gallivan L; Richards M; Khair K; Wright M; Minford A
    Haematologica; 2005 Dec; 90(12):1718-20. PubMed ID: 16330458
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Characterization of a large deletion that leads to congenital factor XIII deficiency].
    Otaki M; Inaba H; Shinozawa K; Fujita S; Amano K; Fukutake K
    Rinsho Byori; 2008 Mar; 56(3):187-94. PubMed ID: 18411802
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Deficiency of A or B subunit for coagulation factor XIII].
    Souri M; Ichinose A
    Ryoikibetsu Shokogun Shirizu; 1998; (21 Pt 2):464-7. PubMed ID: 9833543
    [No Abstract]   [Full Text] [Related]  

  • 9. Molecular mechanisms of mutations in factor XIII A-subunit deficiency: in vitro expression in COS-cells demonstrates intracellular degradation of the mutant proteins.
    Mikkola H; Muszbek L; Haramura G; Hämäläinen E; Jalanko A; Palotie A
    Thromb Haemost; 1997 Jun; 77(6):1068-72. PubMed ID: 9241733
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Effect of four missense mutations in the factor XIII A-subunit gene on protein stability: studies with recombinant proteins.
    Vysokovsky A; Rosenberg N; Dardik R; Seligsohn U; Inbal A
    Blood Coagul Fibrinolysis; 2006 Mar; 17(2):125-30. PubMed ID: 16479194
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Molecular mechanisms of two novel mutations of factor XIII gene resulting in hereditary coagulation deficiency].
    Duan BH; Wang HL; Wang XF; Hu YQ; Chu HY; Wang H; Yin J; Guo XM; Fu QH; Wu WM; Ding QL; Fang Y; Wang WB; Zhou RF; Kang WY; Xie S; Wang ZY
    Zhonghua Yi Xue Za Zhi; 2003 Dec; 83(24):2158-61. PubMed ID: 14720426
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Phenotype-genotype characterization of 10 families with severe a subunit factor XIII deficiency.
    Peyvandi F; Tagliabue L; Menegatti M; Karimi M; Komáromi I; Katona E; Muszbek L; Mannucci PM
    Hum Mutat; 2004 Jan; 23(1):98. PubMed ID: 14695539
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Factor XIII deficiency due to a Leu660Pro mutation in the factor XIII subunit-a gene in three unrelated Palestinian Arab families.
    Inbal A; Yee VC; Kornbrot N; Zivelin A; Brenner B; Seligsohn U
    Thromb Haemost; 1997 Jun; 77(6):1062-7. PubMed ID: 9241732
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A point mutation in an invariant splice acceptor site results in a decreased mRNA level in a patient with severe coagulation factor XIII subunit A deficiency.
    Vreken P; Niessen RW; Peters M; Schaap MC; Zuithoff-Rijntjes JG; Sturk A
    Thromb Haemost; 1995 Aug; 74(2):584-9. PubMed ID: 8584988
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Factor XIII deficiency causing mutation, Ser295Arg, in exon 7 of the factor XIIIA gene.
    Anwar R; Gallivan L; Miloszewski KJ; Markham AF
    Thromb Haemost; 2000 Oct; 84(4):591-4. PubMed ID: 11057855
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel deletion and insertion mutations cause splicing defects, leading to severe reduction in mRNA levels of the A subunit in severe factor XIII deficiency.
    Izumi T; Nagaoka U; Saito T; Takamatsu J; Saito H; Ichinose A
    Thromb Haemost; 1998 Mar; 79(3):479-85. PubMed ID: 9531026
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Application of HUMF13A01 (AAAG)n STR polymorphism to the genetic diagnosis of coagulation factor XIII deficiency.
    Kangsadalampai S; Coggan M; Caglayan SH; Aktuglu G; Board PG
    Thromb Haemost; 1996 Dec; 76(6):879-82. PubMed ID: 8972004
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Male-specific cardiac pathologies in mice lacking either the A or B subunit of factor XIII.
    Souri M; Koseki-Kuno S; Takeda N; Yamakawa M; Takeishi Y; Degen JL; Ichinose A
    Thromb Haemost; 2008 Feb; 99(2):401-8. PubMed ID: 18278192
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Deficiency of coagulation factor XIII A subunit caused by the dinucleotide deletion at the 5' end of exon III.
    Kamura T; Okamura T; Murakawa M; Tsuda H; Teshima T; Shibuya T; Harada M; Niho Y
    J Clin Invest; 1992 Aug; 90(2):315-9. PubMed ID: 1644910
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A new family with congenital factor XIII deficiency showing a deficit of both subunit A and B. Type I factor XIII deficiency.
    Capellato MG; Lazzaro AR; Marafioti F; Polato G; Girolami A
    Haematologia (Budap); 1987; 20(3):179-87. PubMed ID: 2891592
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.