A Pathologic Link between Wilms Tumor Suppressor Gene, WT1, and IFI16

The Wilms tumor gene (WT1) is mutated or deleted in patients with heredofamilial syndromes associated with the development of Wilms tumors, but is infrequently mutated in sporadic Wilms tumors. By comparing the microarray profiles of syndromic versus sporadic Wilms tumors and WT1-inducible Saos-2 os...

Full description

Saved in:
Bibliographic Details
Main Authors: Kim, Marianne K-H, Mason, Jacqueline M, Li, Chi-Ming, Berkofsky-Fessler, Windy, Jiang, Le, Choubey, Divaker, Grundy, Paul E, Tycko, Benjamin, Licht, Jonathan D
Format: Artigo
Language:Inglês
Published: Neoplasia Press Inc. 2008
Subjects:
Research Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC2213901/
https://ncbi.nlm.nih.gov/pubmed/18231640
Tags: Add Tag
No Tags, Be the first to tag this record!

Similar Items