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...

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Hauptverfasser: 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
Sprache:Inglês
Veröffentlicht: Neoplasia Press Inc. 2008
Schlagworte:
Research Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2213901/
https://ncbi.nlm.nih.gov/pubmed/18231640
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