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 *

134 related articles for article (PubMed ID: 32810967)

  • 21. 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]  

  • 22. Evidence linking familial thrombosis with a defective antithrombin III gene in two British kindreds.
    Sacks SH; Old JM; Reeders ST; Weatherall DJ; Douglas AS; Winter JH; Rizza CR
    J Med Genet; 1988 Jan; 25(1):20-4. PubMed ID: 3162535
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [A novel mutation in antithrombin gene results in hereditary antithrombin deficiency].
    Zhang FH; Ding QL; Wu JS; Zhou RF; Wang XF; Xu XC
    Zhonghua Xue Ye Xue Za Zhi; 2006 Sep; 27(9):598-601. PubMed ID: 17278425
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [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]  

  • 25. Molecular heterogeneity of inherited antithrombin III deficiency.
    Prochownik EV; Antonarakis S; Bauer KA; Rosenberg RD; Fearon ER; Orkin SH
    N Engl J Med; 1983 Jun; 308(26):1549-52. PubMed ID: 6304514
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [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]  

  • 27. 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]  

  • 28. Antithrombin-p.Ala416Pro: the second reported case in Japan.
    Shigekiyo T; Sekimoto E; Shibata H; Ozaki S; Kurushima A; Aihara K
    Intern Med; 2014; 53(5):477-81. PubMed ID: 24583439
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. 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]  

  • 31. Genetic testing of hereditary antithrombin deficiency in a large US pedigree using saliva samples.
    Mulder R; Meijer K; Lukens MV
    Int J Lab Hematol; 2021 Jun; 43(3):e101-e103. PubMed ID: 33220012
    [No Abstract]   [Full Text] [Related]  

  • 32. 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]  

  • 33. The phenotypic and genetic assessment of antithrombin deficiency.
    Cooper PC; Coath F; Daly ME; Makris M
    Int J Lab Hematol; 2011 Jun; 33(3):227-37. PubMed ID: 21401902
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Antithrombin-III (AT-III) deficiency spanning four generations.
    Mazza JJ; Mueller-Rizner NJ; Roberts RC
    Thromb Haemost; 1991 Dec; 66(6):737-8. PubMed ID: 1796421
    [No Abstract]   [Full Text] [Related]  

  • 35. 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]  

  • 36. 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]  

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

  • 38. 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]  

  • 39. 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]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 7.