BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

149 related articles for article (PubMed ID: 27863268)

  • 21. 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]  

  • 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. Influence of natural SERPINC1 mutations on ex vivo thrombin generation.
    Alhenc-Gelas M; Canonico M; Picard V
    J Thromb Haemost; 2010 Apr; 8(4):845-8. PubMed ID: 20088933
    [No Abstract]   [Full Text] [Related]  

  • 24. A novel splice-site mutation c.42-2A>T (IVS1-2A>T) of SERPINC1 in a Korean family with inherited antithrombin deficiency.
    Jang MJ; Lee JG; Chong SY; Huh JY; Jang MA; Kim HJ; Oh D
    Blood Coagul Fibrinolysis; 2011 Dec; 22(8):742-5. PubMed ID: 21885952
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Antithrombin Debrecen (p.Leu205Pro) - Clinical and molecular characterization of a novel mutation associated with severe thrombotic tendency.
    Selmeczi A; Gindele R; Ilonczai P; Fekete A; Komáromi I; Schlammadinger Á; Rázsó K; Kovács KB; Bárdos H; Ádány R; Muszbek L; Bereczky Z; Boda Z; Oláh Z
    Thromb Res; 2017 Oct; 158():1-7. PubMed ID: 28783511
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Novel Mutation p.Asp374Val of
    Aslan D
    Turk J Haematol; 2021 Jun; 38(2):161-163. PubMed ID: 33401890
    [No Abstract]   [Full Text] [Related]  

  • 27. Three case reports of inherited antithrombin deficiency in China: double novel missense mutations, a nonsense mutation and a frameshift mutation.
    Deng H; Shen W; Gu Y; Ma X; Zhang J; Zhang L
    J Thromb Thrombolysis; 2012 Aug; 34(2):244-50. PubMed ID: 22535529
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Two Novel Mutations Cause Hereditary Antithrombin Deficiency in a Chinese Family.
    Zhang H; Liu S; Luo S; Jin Y; Yang L; Xie H; Pan J; Wang M
    Acta Haematol; 2020; 143(3):260-265. PubMed ID: 31480053
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Genetic characterization of antithrombin, protein C, and protein S deficiencies in Polish patients.
    Wypasek E; Corral J; Alhenc-Gelas M; Sydor W; Iwaniec T; Celińska-Lowenhoff M; Potaczek DP; Blecharczyk A; Zawilska K; Musiał J; Undas A
    Pol Arch Intern Med; 2017 Aug; 127(7-8):512-523. PubMed ID: 28607330
    [TBL] [Abstract][Full Text] [Related]  

  • 30. High levels of latent antithrombin in plasma from patients with antithrombin deficiency.
    de la Morena-Barrio M; Sandoval E; Llamas P; Wypasek E; Toderici M; Navarro-Fernández J; Rodríguez-Alen A; Revilla N; López-Gálvez R; Miñano A; Padilla J; de la Morena-Barrio B; Cuesta J; Corral J; Vicente V
    Thromb Haemost; 2017 May; 117(5):880-888. PubMed ID: 28229161
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Antithrombin p.Thr147Ala: The First Founder Mutation in People of African Origin Responsible for Inherited Antithrombin Deficiency.
    Orlando C; de la Morena-Barrio B; Pareyn I; Vanhoorelbeke K; Martínez-Martínez I; Vicente V; Corral J; Jochmans K; de la Morena-Barrio ME
    Thromb Haemost; 2021 Feb; 121(2):182-191. PubMed ID: 32920809
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. The influence of specific mutations in the AT gene (SERPINC1) on the type of pregnancy related complications.
    Kovac M; Mitic G; Mikovic Z; Mandic V; Miljic P; Mitrovic M; Tomic B; Bereczky Z
    Thromb Res; 2019 Jan; 173():12-19. PubMed ID: 30458337
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Molecular analysis and genotype-phenotype correlation in patients with antithrombin deficiency from Southern Italy.
    Castaldo G; Cerbone AM; Guida A; Tandurella I; Ingino R; Tufano A; Ceglia C; Di Minno MN; Ruocco AL; Di Minno G
    Thromb Haemost; 2012 Apr; 107(4):673-80. PubMed ID: 22398878
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Recurrent mutations in a
    Zeng W; Hu B; Tang L; You YY; Toderici M; de la Morena-Barrio ME; Corral J; Hu Y
    Oncotarget; 2017 Oct; 8(48):84417-84425. PubMed ID: 29137435
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Pulmonary thromboembolism associated with hereditary antithrombin III deficiency: A case report.
    Liu J; Wang Y; Rong C; Wang B; Liu X; Zhang W
    Medicine (Baltimore); 2024 Mar; 103(10):e37429. PubMed ID: 38457560
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Antithrombin deficiency in three Japanese families: one novel and two reported point mutations in the antithrombin gene.
    Maruyama K; Morishita E; Karato M; Kadono T; Sekiya A; Goto Y; Sato T; Nomoto H; Omi W; Tsuzura S; Imai H; Asakura H; Ohtake S; Nakao S
    Thromb Res; 2013 Aug; 132(2):e118-23. PubMed ID: 23809926
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Mutations in the shutter region of antithrombin result in formation of disulfide-linked dimers and severe venous thrombosis.
    Corral J; Huntington JA; González-Conejero R; Mushunje A; Navarro M; Marco P; Vicente V; Carrell RW
    J Thromb Haemost; 2004 Jun; 2(6):931-9. PubMed ID: 15140129
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Prevalence of hereditary antithrombin mutations is higher than estimated in patients with thrombotic events.
    Fischer R; Sachs UJ; Heidinger KS; Eisenburger D; Kemkes-Matthes B
    Blood Coagul Fibrinolysis; 2013 Jun; 24(4):444-8. PubMed ID: 23429250
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Gene analysis of inherited antithrombin deficiency and functional analysis of abnormal antithrombin protein (N87D).
    Kamijima S; Sekiya A; Takata M; Nakano H; Murakami M; Nakazato T; Asakura H; Morishita E
    Int J Hematol; 2018 Apr; 107(4):490-494. PubMed ID: 29071478
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.