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Volumn 411, Issue 7-8, 2010, Pages 607-609

VWF pseudogene: Mimics, masks and spoils

Author keywords

[No Author keywords available]

Indexed keywords

VON WILLEBRAND FACTOR;

EID: 77649181621     PISSN: 00098981     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cca.2009.12.024     Document Type: Letter
Times cited : (5)

References (12)
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    • Human von Willebrand factor gene and pseudogene: structural analysis and differentiation by polymerase chain reaction
    • Mancuso D.J., Tuley E.A., Westfield L.A., Teresa L., Mancuso L., Michelle M., et al. Human von Willebrand factor gene and pseudogene: structural analysis and differentiation by polymerase chain reaction. Biochemistry 1991, 30:253-269.
    • (1991) Biochemistry , vol.30 , pp. 253-269
    • Mancuso, D.J.1    Tuley, E.A.2    Westfield, L.A.3    Teresa, L.4    Mancuso, L.5    Michelle, M.6
  • 3
    • 77649182633 scopus 로고    scopus 로고
    • http://www.vwf.group.shef.ac.uk.
  • 4
    • 0027472182 scopus 로고
    • A database of polymorphisms in the von Willebrand factor gene and pseudogene. For the Consortium on von Willebrand Factor Mutations and Polymorphisms and the Subcommittee on von Willebrand Factor of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis
    • Sadler J.E., Ginsburg D. A database of polymorphisms in the von Willebrand factor gene and pseudogene. For the Consortium on von Willebrand Factor Mutations and Polymorphisms and the Subcommittee on von Willebrand Factor of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis. Thromb Haemost 1993, 69:185-191.
    • (1993) Thromb Haemost , vol.69 , pp. 185-191
    • Sadler, J.E.1    Ginsburg, D.2
  • 5
    • 77649190868 scopus 로고    scopus 로고
    • NW_001838735.2|Hs22_WGA1294_36 (based on HuRef SCAF_1103279180335).
    • NW_001838735.2|Hs22_WGA1294_36 (based on HuRef SCAF_1103279180335). http://blast.ncbi.nlm.nih.gov/Blast.cgi.
  • 6
    • 0026640029 scopus 로고
    • Nonsense mutations of the von Willebrand factor gene in patients with von Willebrand disease type III and type I
    • Zhang Z.P., Lindstedt M., Falk G., Blomback M., Egberg M.N., Anvret M. Nonsense mutations of the von Willebrand factor gene in patients with von Willebrand disease type III and type I. Am J Hum Genet 1992, 51:850-858.
    • (1992) Am J Hum Genet , vol.51 , pp. 850-858
    • Zhang, Z.P.1    Lindstedt, M.2    Falk, G.3    Blomback, M.4    Egberg, M.N.5    Anvret, M.6
  • 7
    • 0028321794 scopus 로고
    • Characterization of the von Willebrand factor gene (VWF) in von Willebrand disease type III patients from 24 families of Swedish and Finnish origin
    • Zhang Z.P., Blomback M., Egberg N., Falk G., Anvret M. Characterization of the von Willebrand factor gene (VWF) in von Willebrand disease type III patients from 24 families of Swedish and Finnish origin. Genomics 1994, 21:188-193.
    • (1994) Genomics , vol.21 , pp. 188-193
    • Zhang, Z.P.1    Blomback, M.2    Egberg, N.3    Falk, G.4    Anvret, M.5
  • 8
  • 9
    • 0033782679 scopus 로고    scopus 로고
    • Molecular characterization of a multiethnic group of 21 patients with type 3 von Willebrand disease
    • Baronciani L., Cozzi G., Canciani M.T., Peyvandi F., Srivastava A., Federici A.B., et al. Molecular characterization of a multiethnic group of 21 patients with type 3 von Willebrand disease. Thromb Haemost 2000, 84:536-540.
    • (2000) Thromb Haemost , vol.84 , pp. 536-540
    • Baronciani, L.1    Cozzi, G.2    Canciani, M.T.3    Peyvandi, F.4    Srivastava, A.5    Federici, A.B.6
  • 10
    • 62549143505 scopus 로고    scopus 로고
    • Rapid molecular diagnosis of von Willebrand disease by direct sequencing. Detection of 12 novel putative mutations in VWF gene
    • Corrales I., Ramirez L., Altisent C., Parra R., Vidal F. Rapid molecular diagnosis of von Willebrand disease by direct sequencing. Detection of 12 novel putative mutations in VWF gene. Thromb Haemost 2009, 101:570-576.
    • (2009) Thromb Haemost , vol.101 , pp. 570-576
    • Corrales, I.1    Ramirez, L.2    Altisent, C.3    Parra, R.4    Vidal, F.5
  • 11
    • 0031957351 scopus 로고    scopus 로고
    • Characterization of the genetic defects in recessive type 1 and type 3 von Willebrand disease patients of Italian origin
    • Eikenboom J.C., Castaman G., Vos H.L., Bertina R.M., Rodeghiero F. Characterization of the genetic defects in recessive type 1 and type 3 von Willebrand disease patients of Italian origin. Thromb Haemost 1998, 79:709-717.
    • (1998) Thromb Haemost , vol.79 , pp. 709-717
    • Eikenboom, J.C.1    Castaman, G.2    Vos, H.L.3    Bertina, R.M.4    Rodeghiero, F.5
  • 12
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    • A novel mutation Gly?1672 Arg in type 2A and a homozygous mutation in type 2B von Willebrand Disease
    • Hagiwara T., Inaba H., Yoshida S., Nagaizumi K., Arai M., Hanabusa H., et al. A novel mutation Gly?1672 Arg in type 2A and a homozygous mutation in type 2B von Willebrand Disease. Thromb Haemost 1996, 76:253-257.
    • (1996) Thromb Haemost , vol.76 , pp. 253-257
    • Hagiwara, T.1    Inaba, H.2    Yoshida, S.3    Nagaizumi, K.4    Arai, M.5    Hanabusa, H.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.