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 *

160 related articles for article (PubMed ID: 32920809)

  • 1. 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]  

  • 2. 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]  

  • 3. New genetic variant in the SERPINC1 gene: hereditary Antithrombin deficiency case report, familial thrombosis and considerations on genetic counseling.
    Polyak ME; Zaklyazminskaya EV
    BMC Med Genet; 2020 Apr; 21(1):73. PubMed ID: 32252658
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Antithrombin III deficiency in Indian patients with deep vein thrombosis: identification of first India based AT variants including a novel point mutation (T280A) that leads to aggregation.
    Bhakuni T; Sharma A; Rashid Q; Kapil C; Saxena R; Mahapatra M; Jairajpuri MA
    PLoS One; 2015; 10(3):e0121889. PubMed ID: 25811371
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular basis and thrombotic manifestations of antithrombin deficiency in 15 unrelated Chinese patients.
    Ding Q; Wang M; Xu G; Ye X; Xi X; Yu T; Wang X; Wang H
    Thromb Res; 2013 Sep; 132(3):367-73. PubMed ID: 23932013
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. Molecular basis of SERPINC1 mutations in Japanese patients with antithrombin deficiency.
    Tamura S; Hashimoto E; Suzuki N; Kakihara M; Odaira K; Hattori Y; Tokoro M; Suzuki S; Takagi A; Katsumi A; Hayakawa F; Suzuki A; Okamoto S; Kanematsu T; Matsushita T; Kojima T
    Thromb Res; 2019 Jun; 178():159-170. PubMed ID: 31030036
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Founder effect is responsible for the p.Leu131Phe heparin-binding-site antithrombin mutation common in Hungary: phenotype analysis in a large cohort.
    Gindele R; Oláh Z; Ilonczai P; Speker M; Udvari Á; Selmeczi A; Pfliegler G; Marján E; Kovács B; Boda Z; Muszbek L; Bereczky Z
    J Thromb Haemost; 2016 Apr; 14(4):704-15. PubMed ID: 26748602
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Antithrombin Dublin (p.Val30Glu): a relatively common variant with moderate thrombosis risk of causing transient antithrombin deficiency.
    Navarro-Fernández J; de la Morena-Barrio ME; Padilla J; Miñano A; Bohdan N; Águila S; Martínez-Martínez I; Sevivas TS; de Cos C; Fernández-Mosteirín N; Llamas P; Asenjo S; Medina P; Souto JC; Overvad K; Kristensen SR; Corral J; Vicente V
    Thromb Haemost; 2016 Jul; 116(1):146-54. PubMed ID: 27098529
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Antithrombin deficiency and decreased protein C activity in a young man with venous thromboembolism: a case report.
    Wang D; Tian M; Cui G; Wang DW
    Front Med; 2018 Jun; 12(3):319-323. PubMed ID: 28861852
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A heparin binding site Arg79Cys missense mutation in the SERPINC1 gene in a Korean patient with hereditary antithrombin deficiency.
    Yoo JH; Maeng HY; Kim HJ; Lee KA; Choi JR; Song J
    Ann Clin Lab Sci; 2011; 41(1):89-92. PubMed ID: 21325262
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Phenotypic and Genotypic Analysis of a Hereditary Antithrombin Deficiency Pedigree Due to a Novel SERPINC1 Mutation (p.Met281Thr).
    Liu S; Luo S; Yang L; Wang M; Jin Y; Li X; Xu Q
    Hamostaseologie; 2020 Dec; 40(5):687-690. PubMed ID: 32450575
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Subtypes of SERPINC1 mutations and the thrombotic phenotype of inherited antithrombin deficient individuals in Chinese Han population.
    Wang D; Cui G; Hu S; Wang DW
    Blood Cells Mol Dis; 2016 Nov; 62():38-41. PubMed ID: 27863268
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Atypical pulmonary thromboembolism caused by the mutation site SERPINC1 of the antithrombin III gene: A case report.
    Lin M; Sun X; Wu J
    Medicine (Baltimore); 2024 Aug; 103(31):e39175. PubMed ID: 39093784
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.