Warfarin resistance due to a Val29Leu mutation in the VKORC1 protein.

被引:0
|
作者
Huff, JD [1 ]
Lawson, HL [1 ]
Harish, VC [1 ]
Zhang, L [1 ]
Owen, J [1 ]
机构
[1] Wake Forest Univ, Bowman Gray Sch Med, Sect Hematol & Oncol, Winston Salem, NC USA
关键词
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
4146
引用
收藏
页码:117B / 117B
页数:1
相关论文
共 48 条
  • [31] Human VKORC1 mutations (His28Gln, Trp59Leu, Val66Met) investigated by the new cell-based assay exhibit warfarin resistance phenotypes not detected by the 'classical' DTT-driven VKOR assay
    Czogalla, K. J.
    Watzka, M.
    Wendeln, A. C.
    Bevans, C.
    Liphardt, K.
    Westhofen, P.
    Oldenburg, J.
    JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2013, 11 : 129 - 129
  • [32] Defective ER retention signal due to mutation VKORC1:p.Arg98Trp results in VKCFD2
    Czogalla, Katrin Jeannette
    Biswas, Arijit
    Watzka, Matthias
    Oldenburg, Johannes
    HAEMOPHILIA, 2014, 20 : 106 - 106
  • [33] Warfarin pharmacogenetics:: CYP2C9 and VKORC1 genotypes predict different sensitivity and resistance frequencies in the Ashkenazi and Sephardi Jewish populations
    Scott, Stuart A.
    Edelmann, Lisa
    Kornreich, Ruth
    Desnick, Robert J.
    AMERICAN JOURNAL OF HUMAN GENETICS, 2008, 82 (02) : 495 - 500
  • [34] Evaluation of the warfarin-resistance polymorphism, VKORC1 Asp36Tyr, and its effect on dosage algorithms in a genetically heterogeneous anticoagulant clinic
    Shuen, Andrew Y.
    Wong, Betty Y. L.
    Fu, Lei
    Selby, Rita
    Cole, David E. C.
    CLINICAL BIOCHEMISTRY, 2012, 45 (06) : 397 - 401
  • [35] Genetic causes of resistance to vitamin K antagonists in Polish patients: a novel p.Ile123Met mutation in VKORC1 gene
    Wzorek, Joanna
    Wypasek, Ewa
    Awsiuk, Magdalena
    Potaczek, Daniel P.
    Undas, Anetta
    BLOOD COAGULATION & FIBRINOLYSIS, 2018, 29 (05) : 429 - 434
  • [36] More on: endoplasmic reticulum loop VKORC1 substitutions cause warfarin resistance but do not diminish gamma-carboxylation of the vitamin K-dependent coagulation factors
    Harrington, D. J.
    Siddiq, S.
    Allford, S. L.
    Shearer, M. J.
    Mumford, A. D.
    JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2011, 9 (05) : 1093 - 1095
  • [37] Biochemical and pathological characterization of frontotemporal dementia due to a Leu266Val mutation in microtubule-associated protein tau in an African American individual
    Van Deerlin, Vivianna M.
    Forman, Mark S.
    Farmer, Jennifer M.
    Grossman, Murray
    Joyce, Sonali
    Crowe, Alex
    Trojanowski, John Q.
    Lee, Virginia M. -Y.
    Chatterjee, Anjan
    ACTA NEUROPATHOLOGICA, 2007, 113 (04) : 471 - 479
  • [38] Biochemical and pathological characterization of frontotemporal dementia due to a Leu266Val mutation in microtubule-associated protein tau in an African American individual
    Vivianna M. Van Deerlin
    Mark S. Forman
    Jennifer M. Farmer
    Murray Grossman
    Sonali Joyce
    Alex Crowe
    John Q. Trojanowski
    Virginia M.-Y. Lee
    Anjan Chatterjee
    Acta Neuropathologica, 2007, 113 : 471 - 479
  • [39] A fatal turkish case of CINCA-NOMID syndrome due to the novel Val-351-Leu CIAS1 gene mutation
    Gunduz, Zubeyde
    Dursun, Ismail
    Arostegui, Juan I.
    Yaguee, Jordi
    Dusunsel, Ruhan
    Poyrazoglu, Hakan M.
    Gurgoze, Metin Kaya
    Yikilmaz, Ali
    RHEUMATOLOGY INTERNATIONAL, 2008, 28 (04) : 379 - 383
  • [40] A fatal turkish case of CINCA-NOMID syndrome due to the novel Val-351-Leu CIAS1 gene mutation
    Zubeyde Gunduz
    Ismail Dursun
    Juan I. Aróstegui
    Jordi Yagüe
    Ruhan Dusunsel
    Hakan M. Poyrazoglu
    Metin Kaya Gurgoze
    Ali Yıkılmaz
    Rheumatology International, 2008, 28 : 379 - 383