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 *

181 related articles for article (PubMed ID: 118616)

  • 1. 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]  

  • 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. [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]  

  • 4. Subunits A and S inheritance in four families with congenital factor XIII deficiency.
    Barbui T; Rodeghiero F; Dini E; Mariani G; Paa ML; De Biasi R; Murillo RC; Umana CM
    Br J Haematol; 1978 Feb; 38(2):267-71. PubMed ID: 638074
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. A familial factor XIII subunit B deficiency.
    Saito M; Asakura H; Yoshida T; Ito K; Okafuji K; Yoshida T; Matsuda T
    Br J Haematol; 1990 Mar; 74(3):290-4. PubMed ID: 2334637
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [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]  

  • 9. Segmental uniparental disomy as a rare cause of congenital severe factor XIII deficiency in a girl with only one heterozygous carrier parent.
    Shen MC; Chen M; Chang SP; Lin PT; Hsieh HN; Lin KH
    Pediatr Hematol Oncol; 2018; 35(7-8):442-446. PubMed ID: 30702381
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Type I factor XIII deficiency is caused by a genetic defect of its b subunit: insertion of triplet AAC in exon III leads to premature termination in the second Sushi domain.
    Izumi T; Hashiguchi T; Castaman G; Tosetto A; Rodeghiero F; Girolami A; Ichinose A
    Blood; 1996 Apr; 87(7):2769-74. PubMed ID: 8639893
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Congenital deficiency of factor XIII caused by two missense mutations in a Dutch family.
    Onland W; Böing AN; Meijer AB; Schaap MC; Nieuwland R; Haasnoot K; Sturk A; Peters M
    Haemophilia; 2005 Sep; 11(5):539-47. PubMed ID: 16128900
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Congenital deficiency of factor XIII with normal subunit S and lack of subunit A. Report of a new family.
    Girolami A; Burul A; Sticchi A
    Acta Haematol; 1977; 58(1):17-26. PubMed ID: 410213
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Mutations causing coagulation factor XIII subunit A deficiency: characterization of the mutant proteins after expression in yeast.
    Coggan M; Baker R; Miloszewski K; Woodfield G; Board P
    Blood; 1995 May; 85(9):2455-60. PubMed ID: 7727776
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Severe congenital factor XIII deficiency caused by novel W187X and G273V mutations in the F13A gene; diagnosis and classification according to the ISTH/SSC guidelines.
    Souri M; Biswas A; Misawa M; Omura H; Ichinose A
    Haemophilia; 2014 Mar; 20(2):255-62. PubMed ID: 24286209
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Identification of a new mutation (Gly420Ser), distal to the active site, that leads to factor XIII deficiency.
    Kangsadalampai S; Yenchitsomanus P; Chelvanayagam G; Sawasdee N; Laosombat V; Board P
    Eur J Haematol; 2000 Oct; 65(4):279-84. PubMed ID: 11073170
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.