BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

268 related articles for article (PubMed ID: 15309521)

  • 1. Antithrombin gene mutation 5356-5364*delCTT with type I deficiency and early-onset thrombophilia and a brief review of the antithrombin alpha-helix D molecular pathology.
    Steiner M; Steiner B; Rolfs A; Wangnick M; Burstein C; Freund M; Schuff-Werner P
    Ann Hematol; 2005 Jan; 84(1):56-8. PubMed ID: 15309521
    [No Abstract]   [Full Text] [Related]  

  • 2. Homozygous antithrombin deficiency type II (99 Leu to Phe mutation) and childhood thromboembolism.
    Kuhle S; Lane DA; Jochmanns K; Male C; Quehenberger P; Lechner K; Pabinger I
    Thromb Haemost; 2001 Oct; 86(4):1007-11. PubMed ID: 11686316
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Molecular structural analysis of a novel and de-novo mutation in the SERPINC1 gene associated with type 1 antithrombin deficiency.
    Wang TF; Dawson JE; Forman-Kay JD; Kahr WHA; Williams S; Chan AK; Kumar R
    Br J Haematol; 2017 May; 177(4):654-656. PubMed ID: 27098850
    [No Abstract]   [Full Text] [Related]  

  • 5. Report of a novel kindred with antithrombin heparin-binding site variant (47 Arg to His): demand for an automated progressive antithrombin assay to detect molecular variants with low thrombotic risk.
    Rossi E; Chiusolo P; Za T; Marietti S; Ciminello A; Leone G; De Stefano V
    Thromb Haemost; 2007 Sep; 98(3):695-7. PubMed ID: 17849067
    [No Abstract]   [Full Text] [Related]  

  • 6. Antithrombin--early prophecies and present challenges.
    Abildgaard U
    Thromb Haemost; 2007 Jul; 98(1):97-104. PubMed ID: 17597998
    [No Abstract]   [Full Text] [Related]  

  • 7. 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]  

  • 8. Molecular bases of antithrombin deficiency: twenty-two novel mutations in the antithrombin gene.
    Picard V; Nowak-Göttl U; Biron-Andreani C; Fouassier M; Frere C; Goualt-Heilman M; de Maistre E; Regina S; Rugeri L; Ternisien C; Trichet C; Vergnes C; Aiach M; Alhenc-Gelas M
    Hum Mutat; 2006 Jun; 27(6):600. PubMed ID: 16705712
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Creation of an additional glycosylation site as a mechanism for type I antithrombin deficiency.
    Fitches AC; Lewandowski K; Olds RJ
    Thromb Haemost; 2001 Oct; 86(4):1023-7. PubMed ID: 11686319
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Deficiencies of natural anticoagulants, protein C, protein S, and antithrombin.
    Lipe B; Ornstein DL
    Circulation; 2011 Oct; 124(14):e365-8. PubMed ID: 21969320
    [No Abstract]   [Full Text] [Related]  

  • 11. [Thrombophilia in a patient with congenital deficiency of AT III].
    Miljić P; Colović M; Stanojević M; Elezović I; Bosković D
    Srp Arh Celok Lek; 1994; 122(11-12):344-6. PubMed ID: 17974415
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Antithrombin III deficiency: when substitute, when heparin? Thrombosis ABC, 3: The role of antithrombin III].
    Stiefelhagen P
    MMW Fortschr Med; 1999 Sep; 141(37):41. PubMed ID: 10897973
    [No Abstract]   [Full Text] [Related]  

  • 13. [Antithrombin deficiency due to heterozygous antithrombin gene mutation and a pedigree study].
    Ye X; Feng Y; Jin PP; Zhou XH; Ding QL; Wang XF
    Zhonghua Xue Ye Xue Za Zhi; 2007 Sep; 28(9):587-9. PubMed ID: 18246812
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular basis of type I antithrombin deficiency in two women with recurrent venous thromboembolism in the first trimester of pregnancy.
    Xia Y; Lu QY; Lu YL; Dai J; Ding QL; Wang XF; Xi XD; Wang HL
    Blood Cells Mol Dis; 2012 Apr; 48(4):254-9. PubMed ID: 22424603
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Inherited antithrombin deficiency: a review.
    Patnaik MM; Moll S
    Haemophilia; 2008 Nov; 14(6):1229-39. PubMed ID: 19141163
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The prevalence and clinical manifestation of hereditary thrombophilia in Korean patients with unprovoked venous thromboembolisms.
    Lee SY; Kim EK; Kim MS; Shin SH; Chang H; Jang SY; Kim HJ; Kim DK
    PLoS One; 2017; 12(10):e0185785. PubMed ID: 29040284
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Puzzling questions on antithrombin: Diagnostic limitations and real incidence in venous and arterial thrombosis.
    Corral J; Vicente V
    Thromb Res; 2015 Jun; 135(6):1047-8. PubMed ID: 25910517
    [No Abstract]   [Full Text] [Related]  

  • 18. [Advances in the molecular biological study of hereditary antithrombin III deficiency].
    Chui H; Wang H
    Zhonghua Xue Ye Xue Za Zhi; 1998 Mar; 19(3):162-4. PubMed ID: 11243148
    [No Abstract]   [Full Text] [Related]  

  • 19. Regulatory regions of SERPINC1 gene: identification of the first mutation associated with antithrombin deficiency.
    de la Morena-Barrio ME; Antón AI; Martínez-Martínez I; Padilla J; Miñano A; Navarro-Fernández J; Águila S; López MF; Fontcuberta J; Vicente V; Corral J
    Thromb Haemost; 2012 Mar; 107(3):430-7. PubMed ID: 22234719
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Arterial and venous thrombosis and prothrombotic fibrin clot phenotype in a Polish family with type 1 antithrombin deficiency (antithrombin Krakow).
    Celinska-Lowenhoff M; Iwaniec T; Alhenc-Gelas M; Musial J; Undas A
    Thromb Haemost; 2011 Aug; 106(2):379-81. PubMed ID: 21655678
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 14.