BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

189 related articles for article (PubMed ID: 3162535)

  • 21. Confirmation of linkage between antithrombin III and Duffy blood group and assignment of AT3 to 1q22 lead to q25.
    Winter JH; Bennett B; Watt JL; Brown T; San Román C; Schinzel A; King J; Cook PJ
    Ann Hum Genet; 1982 Jan; 46(1):29-34. PubMed ID: 7103410
    [No Abstract]   [Full Text] [Related]  

  • 22. Identification of Regulatory Mutations in SERPINC1 Affecting Vitamin D Response Elements Associated with Antithrombin Deficiency.
    Toderici M; de la Morena-Barrio ME; Padilla J; Miñano A; Antón AI; Iniesta JA; Herranz MT; Fernández N; Vicente V; Corral J
    PLoS One; 2016; 11(3):e0152159. PubMed ID: 27003919
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A novel mutation of antithrombin deficiency in six family siblings and the clinical combat.
    Nadir Y; Hoffman R; Corral J; Barak Y; Hasin T; Keren-Politansky A; Brenner B
    Thromb Haemost; 2015 Oct; 114(4):859-61. PubMed ID: 26177694
    [No Abstract]   [Full Text] [Related]  

  • 24. Familial thrombophilia: a complex genetic disorder.
    Koeleman BP; Reitsma PH; Bertina RM
    Semin Hematol; 1997 Jul; 34(3):256-64. PubMed ID: 9241710
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Conformational Asn187Asp/Lys antithrombin variants and thrombosis. Clinical and biological features in 13 new heterozygotes.
    Picard V; Bauters A; Khairy M; Ochat N; Jude B; Aiach M; Alhenc-Gelas M
    Thromb Haemost; 2005 Jan; 93(1):57-62. PubMed ID: 15630491
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Antithrombin-Gly 424 Arg: a novel point mutation responsible for type 1 antithrombin deficiency and neonatal thrombosis.
    Jochmans K; Lissens W; Vervoort R; Peeters S; De Waele M; Liebaers I
    Blood; 1994 Jan; 83(1):146-51. PubMed ID: 8274732
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Genetic analysis should be included in clinical practice when screening for antithrombin deficiency.
    Zeng W; Tang L; Jian XR; Li YQ; Guo T; Wang QY; Liu H; Wu YY; Cheng ZP; Hu B; Lu X; Yu JM; Deng J; Wang HF; Sun CY; Yang Y; Hu Y
    Thromb Haemost; 2015 Feb; 113(2):262-71. PubMed ID: 25298121
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [A family with an estrogen-related thrombotic tendency and hereditary deficiency on antithrombin].
    Brandt P
    Ugeskr Laeger; 1981; 143(34):2141-5. PubMed ID: 7281334
    [No Abstract]   [Full Text] [Related]  

  • 29. Familial antithrombin III deficiency.
    Winter JH; Fenech A; Ridley W; Bennett B; Cumming AM; Mackie M; Douglas AS
    Q J Med; 1982; 51(204):373-95. PubMed ID: 7156320
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Familial antithrombin III deficiency].
    Velasco F; Torres A; Andrés P; Echeverría P; Durán MI
    Sangre (Barc); 1982; 27(4A):564-71. PubMed ID: 7157147
    [No Abstract]   [Full Text] [Related]  

  • 31. Central retinal vein occlusion in a patient with familial antithrombin III deficiency: case report.
    Ririe DG; Cosgriff TM; Martin B
    Ann Ophthalmol; 1979 Dec; 11(12):1841-5. PubMed ID: 576075
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Major structural defects in the antithrombin gene in four families with type I antithrombin deficiency--partial/complete deletions and rearrangement of the antithrombin gene.
    Beauchamp NJ; Makris M; Preston FE; Peake IR; Daly ME
    Thromb Haemost; 2000 May; 83(5):715-21. PubMed ID: 10823268
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Familial functional antithrombin III deficiency.
    Sørensen PJ; Dyerberg J; Stoffersen E; Jensen MK
    Scand J Haematol; 1980 Feb; 24(2):105-9. PubMed ID: 7375809
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [The diagnosis of congenital antithrombin III deficiency and abnormality].
    Takahashi K; Yamagishi R; Sakuragawa N
    Rinsho Byori; 1987 May; 35(5):505-10. PubMed ID: 3302410
    [No Abstract]   [Full Text] [Related]  

  • 35. Linkage relationships of dominant antithrombin III deficiency and the heterochromatic region of chromosome 1.
    Magenis RE; Donlon T; Parks M; Rivas ML; Lovrien EW
    Cytogenet Cell Genet; 1978; 22(1-6):327-9. PubMed ID: 752496
    [No Abstract]   [Full Text] [Related]  

  • 36. Analysis for antithrombin gene polymorphisms in Japanese subjects and cosegregation studies in families with hereditary antithrombin deficiency.
    Yamazaki T; Katsumi A; Tsuzuki S; Sugiura I; Kojima T; Takamatsu J; Saito H
    Thromb Res; 1996 May; 82(3):275-80. PubMed ID: 8732631
    [No Abstract]   [Full Text] [Related]  

  • 37. Familial antithrombin III deficiency: its natural history, genetics, diagnosis and treatment.
    Cosgriff TM; Bishop DT; Hershgold EJ; Skolnick MH; Martin BA; Baty BJ; Carlson KS
    Medicine (Baltimore); 1983 Jul; 62(4):209-20. PubMed ID: 6877092
    [No Abstract]   [Full Text] [Related]  

  • 38. Familial deficiency of antithrombin III: evidence for heterogeneity existing within the family.
    d'Souza S; Ekert H
    Aust N Z J Med; 1984 Dec; 14(6):835-40. PubMed ID: 6598052
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Pst I polymorphism of the antithrombin III gene in a French population.
    Le Paslier D; Rochu D; Lucotte G
    Vox Sang; 1985; 49(2):168-70. PubMed ID: 3862280
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Effect of danazol on the biochemical abnormality of inherited antithrombin III deficiency.
    Fairfax AJ; Ibbotson RM
    Thorax; 1985 Sep; 40(9):646-50. PubMed ID: 4060104
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.