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 *

142 related articles for article (PubMed ID: 7631305)

  • 1. Nonsense mutation Arg197stop in a Dutch family with type 1 hereditary antithrombin (AT) deficiency causing thrombophilia.
    Michiels JJ; van der Luit L; van Vliet HH; Jochmans K; Lissens W
    Thromb Res; 1995 May; 78(3):251-4. PubMed ID: 7631305
    [No Abstract]   [Full Text] [Related]  

  • 2. A novel nonsense mutation in the antithrombin III gene (Cys-4-->stop) causing recurrent venous thrombosis.
    Saleun S; De Moerloose P; Bura A; Aiach M; Emmerich J
    Blood Coagul Fibrinolysis; 1996 Jul; 7(5):578-9. PubMed ID: 8874869
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Three novel missense mutations in the antithrombin III (AT3) gene causing recurrent venous thrombosis.
    Millar DS; Wacey AI; Ribando J; Melissari E; Laursen B; Woods P; Kakkar VV; Cooper DN
    Hum Genet; 1994 Nov; 94(5):509-12. PubMed ID: 7959685
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Identification of the antithrombin III Kyoto mutation by restriction fragment length polymorphism analysis.
    Masuda H; Tsuji H; Nakagawa K; Nakahara Y; Kitamura H; Ogasahara Y; Nakagawa M
    Int J Hematol; 1995 Jun; 61(4):197-204. PubMed ID: 8547608
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Hereditary abnormalities of antithrombin III in patients with recurrent thrombophlebitis].
    Bekić-Kaluza S; Rezaković D; Musa M
    Med Arh; 1986; 40(1-2):51-3. PubMed ID: 3272307
    [No Abstract]   [Full Text] [Related]  

  • 8. A novel missense mutation in the antithrombin III gene (Ser349----Pro) causing recurrent venous thrombosis.
    Grundy CB; Holding S; Millar DS; Kakkar VV; Cooper DN
    Hum Genet; 1992 Mar; 88(6):707-8. PubMed ID: 1551681
    [No Abstract]   [Full Text] [Related]  

  • 9. The prevalence of hereditary antithrombin-III deficiency in patients with a history of venous thromboembolism.
    Vikydal R; Korninger C; Kyrle PA; Niessner H; Pabinger I; Thaler E; Lechner K
    Thromb Haemost; 1985 Dec; 54(4):744-5. PubMed ID: 4089808
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel missense mutation in the antithrombin III gene (Ala387-->Val) causing recurrent venous thrombosis.
    White D; Abraham G; Carter C; Kakkar VV; Cooper DN
    Hum Genet; 1992 Dec; 90(4):472-3. PubMed ID: 1483709
    [No Abstract]   [Full Text] [Related]  

  • 11. Detection of large deletion mutations in the SERPINC1 gene causing hereditary antithrombin deficiency by multiplex ligation-dependent probe amplification (MLPA).
    Lee ST; Kim HJ; Kim DK; Schuit RJ; Kim SH
    J Thromb Haemost; 2008 Apr; 6(4):701-3. PubMed ID: 18208532
    [No Abstract]   [Full Text] [Related]  

  • 12. Novel SERPINC1 missense mutation (Cys462Tyr) causes disruption of the 279Cys-462Cys disulfide bond and leads to type Ⅰ hereditary antithrombin deficiency.
    Zhang F; Gui Y; Lu Y; Liu D; Chen H; Qin X; Li S
    Clin Biochem; 2020 Nov; 85():38-42. PubMed ID: 32745482
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Significance of hereditary thrombophilia for risk of thrombosis with oral contraceptives].
    Bauersachs R; Lindhoff-Last E; Ehrly AM; Kuhl H
    Zentralbl Gynakol; 1996; 118(5):262-70. PubMed ID: 8701622
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [A family with venous thrombosis and hereditary antithrombin III deficiency].
    Michiels JJ; van Vliet HD
    Ned Tijdschr Geneeskd; 1986 Jan; 130(1):28-31. PubMed ID: 3951576
    [No Abstract]   [Full Text] [Related]  

  • 15. Impact of the type of SERPINC1 mutation and subtype of antithrombin deficiency on the thrombotic phenotype in hereditary antithrombin deficiency.
    Luxembourg B; Pavlova A; Geisen C; Spannagl M; Bergmann F; Krause M; Alesci S; Seifried E; Lindhoff-Last E
    Thromb Haemost; 2014 Feb; 111(2):249-57. PubMed ID: 24196373
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Screening for mutations in the antithrombin III gene causing recurrent venous thrombosis by single-strand conformation polymorphism analysis.
    Millar DS; Lopez A; White D; Abraham G; Laursen B; Holding S; Reverter JC; Reynaud J; Martinowitz U; Hayes JP
    Hum Mutat; 1993; 2(4):324-6. PubMed ID: 8401542
    [No Abstract]   [Full Text] [Related]  

  • 17. [Diagnosis of thrombophilia - hereditary deficiency of antithrombin III].
    Al'pidovskiĭ VK; Lagutina NIa; Fedulova GA; Gerasimov AA
    Probl Gematol Pereliv Krovi; 1982 Mar; 27(3):51-5. PubMed ID: 6806802
    [No Abstract]   [Full Text] [Related]  

  • 18. The incidence of dysfunctional antithrombin variants: four cases in 210 patients with thromboembolic disease.
    Harper PL; Luddington RJ; Daly M; Bruce D; Williamson D; Edgar PF; Perry DJ; Carrell RW
    Br J Haematol; 1991 Mar; 77(3):360-4. PubMed ID: 2012760
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Pulmonary embolism and deep venous thrombosis during pregnancy or oral contraceptive use: prevalence of factor V Leiden.
    Hirsch DR; Mikkola KM; Marks PW; Fox EA; Dorfman DM; Ewenstein BM; Goldhaber SZ
    Am Heart J; 1996 Jun; 131(6):1145-8. PubMed ID: 8644593
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic analysis in Japanese kindreds of congenital type I antithrombin deficiency causing thrombosis.
    Nakahara Y; Tsuji H; Nakagawa K; Masuda H; Kitamura H; Nishimura H; Kasahara T; Sugano T; Sawada S; Nakagawa M
    Thromb Haemost; 1997 Apr; 77(4):616-9. PubMed ID: 9134630
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.