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 *

248 related articles for article (PubMed ID: 7236530)

  • 1. Genetic heterogeneity of factor XIII deficiency: first description of unstable A subunits.
    Castle S; Board PG; Anderson RA
    Br J Haematol; 1981 Jun; 48(2):337-42. PubMed ID: 7236530
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. An electrophoretic and quantitative analysis of coagulation factor XIII in normal and deficient subjects.
    Board PG; Coggan M; Hamer JW
    Br J Haematol; 1980 Aug; 45(4):633-40. PubMed ID: 7426441
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 23(3):117-20. PubMed ID: 12015062
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Factor-XIII subunits-A and -S in congenital deficiency and in acute myeloblastic leukemia.
    Barbui T; Rodeghiero F; Dini E
    Haematologica; 1974 Dec; 59(4):458-66. PubMed ID: 4219003
    [No Abstract]   [Full Text] [Related]  

  • 9. 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]  

  • 10. Subunit A of factor XIII regulates subunit B plasma concentration.
    Rodeghiero F; Morbin M; Barbui T
    Thromb Haemost; 1981 Oct; 46(3):621-2. PubMed ID: 7314056
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Factor XIII deficiency due to lack of both the S and A subunits. (Classification of factor XIII deficiency in 2 groups)].
    Girolami A; Burul A; Cappellato MG; Betterle C; Casonato A; Dal Bo Zanon R
    Ric Clin Lab; 1979; 9(2 Suppl):35-49. PubMed ID: 395620
    [No Abstract]   [Full Text] [Related]  

  • 12. [A novel genetic defect in a Chinese family with inherited coagulation factor XIII deficiency].
    Wu SY; Wang ZY; Dong NZ; Zhang W; Bai X; Ruan CG
    Zhonghua Xue Ye Xue Za Zhi; 2006 Mar; 27(3):145-9. PubMed ID: 16792911
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Electroimmunoassay of plasma subunits-a and -s in a case of congenital fibrin stabilizing factor deficiency.
    Barbui T; Cartei G; Chisesi T; Dini E
    Thromb Diath Haemorrh; 1974 Sep; 32(1):124-31. PubMed ID: 4454035
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [An investigation of a family tree with congenital deficiency in coagulation factor XIII].
    Jia X; Zheng H; Chen S
    Zhonghua Nei Ke Za Zhi; 1996 Sep; 35(9):598-600. PubMed ID: 9592353
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Congenital deficiency of coagulation factor XIII].
    Hule V
    Vnitr Lek; 1979 May; 25(5):501-4. PubMed ID: 452434
    [No Abstract]   [Full Text] [Related]  

  • 16. An unusual clinical presentation of factor XIII deficiency and issues relating to the monitoring of factor XIII replacement therapy.
    Dargaud Y; de Mazancourt P; Rugeri L; Hanss M; Borg JY; Gaucherand P; Negrier C; Trzeciak C
    Blood Coagul Fibrinolysis; 2008 Jul; 19(5):447-52. PubMed ID: 18600098
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular characterization of five Italian families with inherited severe factor XIII deficiency.
    Castaman G; Giacomelli SH; Ivaskevicius V; Schroeder V; Kohler HP; Dragani A; Biasioli C; Oldenburg J; Madeo D; Rodeghiero F
    Haemophilia; 2008 Jan; 14(1):96-102. PubMed ID: 18028394
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Identification of a novel mutation of F (13) A gene in a pedigree with factor XIII deficiency].
    Jiao WY; Wu JS; Ding QL; Wang XF; Xu XC; Ding KY; Liu X
    Zhonghua Xue Ye Xue Za Zhi; 2007 Sep; 28(9):598-601. PubMed ID: 18246815
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Factor XIII deficiency: blood coagulation defect in pregnancy].
    Butterwegge M; von der Burg WW; Gethmann U
    Zentralbl Gynakol; 1992; 114(10):515-8. PubMed ID: 1414069
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Factor XIII deficiency. A family study by measurement of factor XIII subunits A and S.
    Francis JL; Todd PJ
    Acta Haematol; 1979; 62(3):167-72. PubMed ID: 118616
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.