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Volumn 44, Issue 6, 2007, Pages 393-396

Different CTNNB1 mutations as molecular genetic proof for the independent origin of four Wilms tumours in a patient with a novel germ line WT1 mutation

Author keywords

[No Author keywords available]

Indexed keywords

BETA CATENIN; CATENIN BETA 1; DACTINOMYCIN; UNCLASSIFIED DRUG; VINCRISTINE; WT1 PROTEIN;

EID: 34250738407     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.2006.047530     Document Type: Article
Times cited : (25)

References (11)
  • 1
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    • A clinical overview of WT1 gene mutations
    • Little M, Wells C. A clinical overview of WT1 gene mutations. Hum Mutat 1997;9:209-25.
    • (1997) Hum Mutat , vol.9 , pp. 209-225
    • Little, M.1    Wells, C.2
  • 3
    • 17544395621 scopus 로고    scopus 로고
    • Correlation between a specific Wilms tumours suppressor gene (WT1) mutation and the histological findings in Wilms tumour (WT)
    • Shibata R, Hashigushi A, Sakamoto J, Yamada T, Umezawa A, Hata J. Correlation between a specific Wilms tumours suppressor gene (WT1) mutation and the histological findings in Wilms tumour (WT). J Med Genet 2002;39:e83.
    • (2002) J Med Genet , vol.39
    • Shibata, R.1    Hashigushi, A.2    Sakamoto, J.3    Yamada, T.4    Umezawa, A.5    Hata, J.6
  • 4
    • 2542462400 scopus 로고    scopus 로고
    • Twenty-four new cases of WT1 germline mutations and review of the literature: Genotype/phenotype correlations for Wilms tumor development
    • Royer-Pokora B, Beier M, Henzler M, Alam R, Schumacher V, Weirich A, Huff V. Twenty-four new cases of WT1 germline mutations and review of the literature: genotype/phenotype correlations for Wilms tumor development. Am J Med Genet 2004;127:249-57.
    • (2004) Am J Med Genet , vol.127 , pp. 249-257
    • Royer-Pokora, B.1    Beier, M.2    Henzler, M.3    Alam, R.4    Schumacher, V.5    Weirich, A.6    Huff, V.7
  • 6
    • 0033677022 scopus 로고    scopus 로고
    • Frequent association of β-catenin and WT1 mutations in Wilms tumors
    • Maiti S, Alam R, Amos CI, Huff V. Frequent association of β-catenin and WT1 mutations in Wilms tumors. Cancer Res 2000;60:6288-92.
    • (2000) Cancer Res , vol.60 , pp. 6288-6292
    • Maiti, S.1    Alam, R.2    Amos, C.I.3    Huff, V.4
  • 7
    • 0036781630 scopus 로고    scopus 로고
    • Codon 45 of the β-catenin gene, a specific mutational target site of Wilms' tumor
    • Kusafuka T, Miao J, Kuroda S, Udatsu Y, Yoneda A. Codon 45 of the β-catenin gene, a specific mutational target site of Wilms' tumor. Int J Mol Med 2002;10:395-9.
    • (2002) Int J Mol Med , vol.10 , pp. 395-399
    • Kusafuka, T.1    Miao, J.2    Kuroda, S.3    Udatsu, Y.4    Yoneda, A.5
  • 8
    • 2642552403 scopus 로고    scopus 로고
    • Myogenesis in Wilms' tumors is associated with mutations of the WT1 gene and activation of Bcl-2 and the Wnt signaling pathway
    • Fukuzawa R, Heathcott RW, Sano M, Morison IM, Yun K, Reeve AE. Myogenesis in Wilms' tumors is associated with mutations of the WT1 gene and activation of Bcl-2 and the Wnt signaling pathway. Pediatr Dev Pathol 2004;7:125-37.
    • (2004) Pediatr Dev Pathol , vol.7 , pp. 125-137
    • Fukuzawa, R.1    Heathcott, R.W.2    Sano, M.3    Morison, I.M.4    Yun, K.5    Reeve, A.E.6
  • 10
    • 11244305880 scopus 로고    scopus 로고
    • Little S, Hanks S, King-Underwood L, Picton S, Cullinane C, Rapley E, Rahman N, Pritchard-Jones K. A WT1 exon 1 mutation in a child diagnosed with Denys-Drash syndrome. Pediatr Nephrol 2005;20:81-5.
    • Little S, Hanks S, King-Underwood L, Picton S, Cullinane C, Rapley E, Rahman N, Pritchard-Jones K. A WT1 exon 1 mutation in a child diagnosed with Denys-Drash syndrome. Pediatr Nephrol 2005;20:81-5.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.