BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

152 related articles for article (PubMed ID: 32151802)

  • 1. Seventeen novel SERPINC1 variants causing hereditary antithrombin deficiency in a Czech population.
    Provazníková D; Matýšková M; Čápová I; Grančarová D; Drbohlavová E; Šlechtová M; Hrachovinová I
    Thromb Res; 2020 May; 189():39-41. PubMed ID: 32151802
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. A novel mutation p.Met1Val in SERPINC1 gene causes hereditary antithrombin deficiency in a Chinese family with thrombotic disease.
    Zeng M; Jia K; Liu M; Wang M; Yang L; Xie H
    Thromb Res; 2023 Dec; 232():104-107. PubMed ID: 37976729
    [No Abstract]   [Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 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. 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]  

  • 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 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. 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]  

  • 11.
    Lu Z; Wang F; Liang M
    Clin Sci (Lond); 2017 May; 131(9):823-831. PubMed ID: 28424376
    [TBL] [Abstract][Full Text] [Related]  

  • 12. c.1058C>T variant in the SERPINC1 gene is pathogenic for antithrombin deficiency.
    Kumar R; Dawson JE; Chan AK; Forman-Kay JD; Kahr WH; Williams S
    Br J Haematol; 2015 Jul; 170(1):123-5. PubMed ID: 25522812
    [No Abstract]   [Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

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

  • 16. Genotype-phenotype gradient of SERPINC1 variants in a single family reveals a severe compound antithrombin deficiency in a dead embryo.
    Bravo-Pérez C; de la Morena-Barrio ME; Palomo A; Entrena L; de la Morena-Barrio B; Padilla J; Miñano A; Navarro E; Cifuentes R; Corral J; Vicente V
    Br J Haematol; 2020 Oct; 191(1):e32-e35. PubMed ID: 32686144
    [No Abstract]   [Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. Hereditary Antithrombin Deficiency Presenting with Deep Venous Thrombosis During the Second Pregnancy.
    Yamashita M; Komaki T; Tashiro K; Inada Y; Iwata A; Ogawa M; Morishita E; Miura SI
    Intern Med; 2020 Jan; 59(2):235-239. PubMed ID: 31554754
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Gene symbol: SERPINC1. Disease: Antithrombin deficiency. Accession #Hd0514.
    Schleithoff L; Seelig HP
    Hum Genet; 2006 Feb; 118(6):775. PubMed ID: 17297683
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.