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 *

166 related articles for article (PubMed ID: 38474138)

  • 1. Clinical and Molecular Characterization of Nine Novel Antithrombin Mutations.
    Kállai J; Gindele R; Pénzes-Daku K; Balogh G; Bogáti R; Bécsi B; Katona É; Oláh Z; Ilonczai P; Boda Z; Róna-Tas Á; Nemes L; Marton I; Bereczky Z
    Int J Mol Sci; 2024 Mar; 25(5):. PubMed ID: 38474138
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Role of the C-sheet in the maturation of N-glycans on antithrombin: functional relevance of pleiotropic mutations.
    Aguila S; Navarro-Fernández J; Bohdan N; Gutiérrez-Gallego R; de la Morena-Barrio ME; Vicente V; Corral J; Martínez-Martínez I
    J Thromb Haemost; 2014 Jul; 12(7):1131-40. PubMed ID: 24824609
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. The superiority of anti-FXa assay over anti-FIIa assay in detecting heparin-binding site antithrombin deficiency.
    Kovács B; Bereczky Z; Oláh Z; Gindele R; Kerényi A; Selmeczi A; Boda Z; Muszbek L
    Am J Clin Pathol; 2013 Nov; 140(5):675-9. PubMed ID: 24124146
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [The functional study of antithrombin L99 mutation].
    Yu T; Dai J; Ding Q; Fu Q; Wang X
    Zhonghua Xue Ye Xue Za Zhi; 2014 Mar; 35(3):191-6. PubMed ID: 24666482
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Clinical and functional characterization of rare compound heterozygous mutations in the SERPINC1 gene causing severe thrombophilia.
    Zhang K; Zhang H; Yu D; Pan J; Wang M; Xie H
    Gene; 2024 Mar; 897():148085. PubMed ID: 38104950
    [TBL] [Abstract][Full Text] [Related]  

  • 8. SERPINC1 gene mutations in antithrombin deficiency.
    Mulder R; Croles FN; Mulder AB; Huntington JA; Meijer K; Lukens MV
    Br J Haematol; 2017 Jul; 178(2):279-285. PubMed ID: 28317092
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular basis of antithrombin deficiency.
    Luxembourg B; Delev D; Geisen C; Spannagl M; Krause M; Miesbach W; Heller C; Bergmann F; Schmeink U; Grossmann R; Lindhoff-Last E; Seifried E; Oldenburg J; Pavlova A
    Thromb Haemost; 2011 Apr; 105(4):635-46. PubMed ID: 21264449
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Antithrombin heparin binding site deficiency: A challenging diagnosis of a not so benign thrombophilia.
    Orlando C; Heylen O; Lissens W; Jochmans K
    Thromb Res; 2015 Jun; 135(6):1179-85. PubMed ID: 25837307
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Development of a novel, rapid assay for detection of heparin-binding defect antithrombin deficiencies: the heparin-antithrombin binding (HAB) ratio.
    Moore GW; de Jager N; Cutler JA
    Thromb Res; 2015 Jan; 135(1):161-6. PubMed ID: 25466846
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Activated Factor X-Based versus Thrombin-Based Antithrombin Testing in Thrombophilia Workup in the DOAC Era.
    Rühl H; Reda S; Müller J; Oldenburg J; Pötzsch B
    Thromb Haemost; 2018 Feb; 118(2):381-387. PubMed ID: 29378360
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Antithrombin Murcia (K241E) causing antithrombin deficiency: a possible role for altered glycosylation.
    Martínez-Martínez I; Ordóñez A; Navarro-Fernández J; Pérez-Lara A; Gutiérrez-Gallego R; Giraldo R; Martínez C; Llop E; Vicente V; Corral J
    Haematologica; 2010 Aug; 95(8):1358-65. PubMed ID: 20435622
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Inherited antithrombin deficiency caused by a mutation in the SERPINC1 gene: A case report.
    Hou X; Zhang K; Wu Q; Zhang M; Li L; Li H
    Medicine (Baltimore); 2022 Nov; 101(44):e31240. PubMed ID: 36343066
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Analysis of phenotype and gene mutation in three pedigrees with inherited antithrombin deficiency.
    Li M; Jiang S; Liu S; Jin Y; Wang M
    J Clin Lab Anal; 2022 Nov; 36(11):e24732. PubMed ID: 36268972
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Two SERPINC1 variants affecting N-glycosylation of Asn224 cause severe thrombophilia not detected by functional assays.
    de la Morena-Barrio ME; Suchon P; Jacobsen EM; Iversen N; Miñano A; de la Morena-Barrio B; Bravo-Pérez C; Padilla J; Cifuentes R; Asenjo S; Deleuze JF; Trégouët DA; Lozano ML; Vicente V; Sandset PM; Morange PE; Corral J
    Blood; 2022 Jul; 140(2):140-151. PubMed ID: 35486842
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cellular and functional characterization of three recombinant antithrombin mutants that caused pleiotropic effect-type deficiency.
    Shirotani H; Tokunaga F; Koide T
    J Biochem; 1999 Feb; 125(2):253-62. PubMed ID: 9990121
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hypoglycosylation is a common finding in antithrombin deficiency in the absence of a SERPINC1 gene defect.
    de la Morena-Barrio ME; Martínez-Martínez I; de Cos C; Wypasek E; Roldán V; Undas A; van Scherpenzeel M; Lefeber DJ; Toderici M; Sevivas T; España F; Jaeken J; Corral J; Vicente V
    J Thromb Haemost; 2016 Aug; 14(8):1549-60. PubMed ID: 27214821
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Antithrombin and its deficiency states.
    Lane DA; Olds RR; Thein SL
    Blood Coagul Fibrinolysis; 1992 Jun; 3(3):315-41. PubMed ID: 1643210
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Antithrombin Deficiency in Trauma and Surgical Critical Care.
    Ehrhardt JD; Boneva D; McKenney M; Elkbuli A
    J Surg Res; 2020 Dec; 256():536-542. PubMed ID: 32799002
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.