메뉴 건너뛰기




Volumn 14, Issue SUPPL. 3, 2008, Pages 113-118

Genetic aspects and research development in haemostasis

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CLOTTING FACTOR 10; BLOOD CLOTTING FACTOR 11; BLOOD CLOTTING FACTOR 13; BLOOD CLOTTING FACTOR 5; BLOOD CLOTTING FACTOR 7; BLOOD CLOTTING FACTOR 8; CYTOTOXIC T LYMPHOCYTE ANTIGEN 4; FIBRINOGEN; INTERLEUKIN 10; PROTHROMBIN;

EID: 44249105414     PISSN: 13518216     EISSN: 13652516     Source Type: Journal    
DOI: 10.1111/j.1365-2516.2008.01740.x     Document Type: Article
Times cited : (3)

References (19)
  • 1
    • 20144382370 scopus 로고    scopus 로고
    • Clinical phenotypes and factor VII genotype in congenital factor VII deficiency
    • Mariani G, Herrmann F, Dolce A, Batorova A, Etro D et al. Clinical phenotypes and factor VII genotype in congenital factor VII deficiency. Thromb Haemost 2005; 93: 481-7.
    • (2005) Thromb Haemost , vol.93 , pp. 481-487
    • Mariani, G.1    Herrmann, F.2    Dolce, A.3    Batorova, A.4    Etro, D.5
  • 3
    • 20544448426 scopus 로고    scopus 로고
    • Inhibitor to factor VII in severe factor VII deficiency: Detection and course of the inhibitory response
    • Ingerslev J, Christiansen K, Sørensen B. Inhibitor to factor VII in severe factor VII deficiency: Detection and course of the inhibitory response. J Thromb Haemost 2005; 3: 799-800.
    • (2005) J Thromb Haemost , vol.3 , pp. 799-800
    • Ingerslev, J.1    Christiansen, K.2    Sørensen, B.3
  • 7
    • 4444269047 scopus 로고    scopus 로고
    • Recessively inherited coagulation disorders
    • Mannucci PM, Duga S, Peyvandi F. Recessively inherited coagulation disorders. Blood 2004; 104: 1243-52.
    • (2004) Blood , vol.104 , pp. 1243-1252
    • Mannucci, P.M.1    Duga, S.2    Peyvandi, F.3
  • 8
    • 0038278822 scopus 로고    scopus 로고
    • Bleeding due to disruption of a cargo-specific ER-to-Golgi transport complex
    • Zhang B, Cunningham MA, Nichols WC, et al. Bleeding due to disruption of a cargo-specific ER-to-Golgi transport complex. Nat Genet. 2003; 34: 220-5.
    • (2003) Nat Genet. , vol.34 , pp. 220-225
    • Zhang, B.1    Cunningham, M.A.2    Nichols, W.C.3
  • 9
    • 1142298871 scopus 로고    scopus 로고
    • Medicine: K for koagulation
    • Sadler JE. Medicine: K for koagulation. Nature 2004; 427: 493-4.
    • (2004) Nature , vol.427 , pp. 493-494
    • Sadler, J.E.1
  • 12
    • 5444227748 scopus 로고    scopus 로고
    • Permanent phenotypic correction of Haemophilia B in immunocompetent mice by prenatal gene therapy
    • Waddington SN, Nivsarkar M, et al. Permanent phenotypic correction of Haemophilia B in immunocompetent mice by prenatal gene therapy. Blood 2004; 104: 2714-21.
    • (2004) Blood , vol.104 , pp. 2714-2721
    • Waddington, S.N.1    Nivsarkar, M.2
  • 13
    • 0033539486 scopus 로고    scopus 로고
    • Short-term correction of factor VIII deficiency in a murine model of hemophilia A after delivery of adenovirus murine factor VIII in utero
    • Lipshutz GS, Sarkar R, et al. Short-term correction of factor VIII deficiency in a murine model of hemophilia A after delivery of adenovirus murine factor VIII in utero. Proc Natl Acad Sci USA 1999; 96: 13324-9.
    • (1999) Proc Natl Acad Sci USA , vol.96 , pp. 13324-13329
    • Lipshutz, G.S.1    Sarkar, R.2
  • 14
    • 85005688727 scopus 로고
    • Results in three Australian haemophilia B patients with high-responding inhibitors treated with the Malmömodel
    • Nilsson IM, Berntorp E, Rickard KA. Results in three Australian haemophilia B patients with high-responding inhibitors treated with the Malmömodel. Haemophilia 1995; 1: 59-66.
    • (1995) Haemophilia , vol.1 , pp. 59-66
    • Nilsson, I.M.1    Berntorp, E.2    Rickard, K.A.3
  • 15
    • 6644227418 scopus 로고    scopus 로고
    • The MalmöInternational Brother Study (MIBS): Further support for genetic predisposition to inhibitor development in hemophilia patients
    • the MIBS Study Group
    • Astermark J, Berntorp E, White GC, Kroner BL, the MIBS Study Group. The MalmöInternational Brother Study (MIBS): Further support for genetic predisposition to inhibitor development in hemophilia patients. Haemophilia 2001; 7: 267-72.
    • (2001) Haemophilia , vol.7 , pp. 267-272
    • Astermark, J.1    Berntorp, E.2    White, G.C.3    Kroner, B.L.4
  • 16
    • 22544473061 scopus 로고    scopus 로고
    • Genetic defects and inhibitor development in siblings with severe hemophilia A
    • the MalmöInternational Brother Study (MIBS)
    • Astermark J, Oldenburg J, Escobar M, White GC 2nd, Berntorp E, the MalmöInternational Brother Study (MIBS). Genetic defects and inhibitor development in siblings with severe hemophilia A. Haematologica 2005; 90: 924-31.
    • (2005) Haematologica , vol.90 , pp. 924-931
    • Astermark, J.1    Oldenburg, J.2    Escobar, M.3    White II, G.C.4    Berntorp, E.5
  • 17
    • 33645751563 scopus 로고    scopus 로고
    • Polymorphisms in the IL10 but not in the IL1beta and IL4 genes are associated with inhibitor development in patients with hemophilia A
    • the MIBS Study Group
    • Astermark J, Oldenburg J, Pavlova A, Berntorp E, Lefvert AK, the MIBS Study Group. Polymorphisms in the IL10 but not in the IL1beta and IL4 genes are associated with inhibitor development in patients with hemophilia A. Blood 2006a; 107: 3167-72.
    • (2006) Blood , vol.107 , pp. 3167-3172
    • Astermark, J.1    Oldenburg, J.2    Pavlova, A.3    Berntorp, E.4    Lefvert, A.K.5
  • 18
    • 33845239946 scopus 로고    scopus 로고
    • Polymorphisms in the TNFA gene and the risk of inhibitor development in patients with hemophilia A
    • Astermark J, Oldenburg J, Carlson J, Pavlova A, Kavakli K, Berntorp E, Lefvert AK. Polymorphisms in the TNFA gene and the risk of inhibitor development in patients with hemophilia A. Blood 2006b; 108: 3739-45.
    • (2006) Blood , vol.108 , pp. 3739-3745
    • Astermark, J.1    Oldenburg, J.2    Carlson, J.3    Pavlova, A.4    Kavakli, K.5    Berntorp, E.6    Lefvert, A.K.7
  • 19
    • 33846420672 scopus 로고    scopus 로고
    • Polymorphisms in the CTLA-4 gene and inhibitor development in patients with severe hemophilia A
    • for the MIBS Study Group
    • Astermark J, Wang X, Oldenburg J, Berntorp E, Lefvert AK for the MIBS Study Group. Polymorphisms in the CTLA-4 gene and inhibitor development in patients with severe hemophilia A. J Thromb Haemost 2007; 5: 263-5.
    • (2007) J Thromb Haemost , vol.5 , pp. 263-265
    • Astermark, J.1    Wang, X.2    Oldenburg, J.3    Berntorp, E.4    Lefvert, A.K.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.