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Journal of Hepatology
Volumn 53, Issue 6, 2010, Pages 1151-1153
Molecular pathology of Wilson's disease: A brief
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COPPER ION;
EID: 78049481012     PISSN: 01688278     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jhep.2010.07.008     Document Type: Note
Times cited : (36)
References (10)
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  • 2
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    • Lutsenko, S.E.1    Leshane, S.2    Shinde, U.3
  • 4
    • 0031730641 scopus 로고    scopus 로고
    • A C-terminal di-leucine is required for localization of the Menkes protein in the trans-Golgi network
    • M.J. Petris, J. Camakaris, M. Greenough, S. LaFontaine, and J.F. Mercer A C-terminal di-leucine is required for localization of the Menkes protein in the trans-Golgi network Hum Mol Genet 7 1998 2063 2071
    • (1998) Hum Mol Genet , vol.7 , pp. 2063-2071
    • Petris, M.J.1    Camakaris, J.2    Greenough, M.3    Lafontaine, S.4    Mercer, J.F.5
  • 5
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    • Regional distribution of mutations of the ATP7B gene in patients with Wilson disease: Impact on genetic testing
    • P. Ferenci Regional distribution of mutations of the ATP7B gene in patients with Wilson disease: impact on genetic testing Hum Genet 120 2006 151 159
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    • Ferenci, P.1
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    • 0034641603 scopus 로고    scopus 로고
    • Copper-dependent trafficking of Wilson disease mutant ATP7B proteins
    • J.R. Forbes, and D.W. Cox Copper-dependent trafficking of Wilson disease mutant ATP7B proteins Hum Mol Genet 9 2000 1927 1935
    • (2000) Hum Mol Genet , vol.9 , pp. 1927-1935
    • Forbes, J.R.1    Cox, D.W.2
  • 8
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    • Relationship between oxidative stress and antioxidant systems in the liver of patients with Wilson's disease: Hepatic manifestation in Wilson disease as a consequence of augmented oxidative stress
    • H. Nagasaka, I. Inoue, A. Inui, H. Komatsu, T. Sogo, and K. Murayama Relationship between oxidative stress and antioxidant systems in the liver of patients with Wilson's disease: hepatic manifestation in Wilson disease as a consequence of augmented oxidative stress Pediatr Res 60 2006 472 477
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    • Distinct Wilson's disease mutations in ATP7B are associated with enhanced binding to COMMD1 and reduced stability of ATP7B
    • P. de Bie, B. van de Sluis, E. Burstein, P.V. van de Berghe, P. Muller, and R. Berger Distinct Wilson's disease mutations in ATP7B are associated with enhanced binding to COMMD1 and reduced stability of ATP7B Gastroenterology 133 2007 1316 1326
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.