Genetic and epigenetic alterations on the short arm of chromosome 11 are involved in a majority of sporadic Wilms' tumours

Wilms' tumour is one of the most common solid tumours of childhood. 11p13 (WT1 locus) and 11p15.5 (WT2 locus) are known to have genetic or epigenetic aberrations in these tumours. In Wilms' tumours, mutation of the Wilms tumour 1 (WT1) gene at the WT1 locus has been reported, and the WT2 l...

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Detalles Bibliográficos
Autores principales: Satoh, Y, Nakadate, H, Nakagawachi, T, Higashimoto, K, Joh, K, Masaki, Z, Uozumi, J, Kaneko, Y, Mukai, T, Soejima, H
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2006
Materias:
Genetics and Genomics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2360663/
https://www.ncbi.nlm.nih.gov/pubmed/16909133
http://dx.doi.org/10.1038/sj.bjc.6603302

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2360663/
https://www.ncbi.nlm.nih.gov/pubmed/16909133
http://dx.doi.org/10.1038/sj.bjc.6603302

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