Related Articles
Wilms' tumor 1 gene (WT1) is overexpressed and provides an oncogenic function in pediatric nephroblastomas harboring the wild-type WT1
Histone deacetylase 5 promotes Wilms' tumor cell proliferation through the upregulation of c-Met
miR‑590‑5p suppresses osteosarcoma cell proliferation and invasion via targeting KLF5
Berberine inhibits Wilms' tumor cell progression through upregulation of Wilms' tumor gene on the X chromosome
Aberrant expression and mechanism of miR‑130b‑3p/phosphatase and tensin homolog in nephroblastoma in children