Pages that link to "Q45345263"

The following pages link to WTX inactivation is a frequent, but late event in Wilms tumors without apparent clinical impact (Q45345263):

Displaying 27 items.

• Is Wilms tumor a candidate neoplasia for treatment with WNT/β-catenin pathway modulators?--A report from the renal tumors biology-driven drug development workshop (Q26829595) (← links)
• Wilms' tumor: biology, diagnosis and treatment (Q26862181) (← links)
• Deducing the stage of origin of Wilms' tumours from a developmental series of Wt1-mutant mice (Q30660201) (← links)
• X-linked tumor suppressors: perplexing inheritance, a unique therapeutic opportunity. (Q33980087) (← links)
• Deletions of 16q in Wilms tumors localize to blastemal-anaplastic cells and are associated with reduced expression of the IRXB renal tubulogenesis gene cluster. (Q34254608) (← links)
• Wilms' tumours: about tumour suppressor genes, an oncogene and a chameleon gene (Q35095712) (← links)
• The yin and yang of kidney development and Wilms' tumors (Q35173260) (← links)
• Inactivation of X-Linked Tumor Suppressor Genes in Human Cancer (Q35206452) (← links)
• Stratification of Wilms tumor by genetic and epigenetic analysis (Q35987087) (← links)
• Genetic variation frequencies in Wilms' tumor: A meta-analysis and systematic review (Q37146691) (← links)
• Intra-Tumor Genetic Heterogeneity in Wilms Tumor: Clonal Evolution and Clinical Implications (Q37149909) (← links)
• Wilms tumor—a renal stem cell malignancy? (Q37866140) (← links)
• The genetic factors contributing to the development of Wilm's tumor and their clinical utility in its diagnosis and prognosis. (Q38764772) (← links)
• The WTX Tumor Suppressor Interacts with the Transcriptional Corepressor TRIM28. (Q38886016) (← links)
• Functional characterization of Wilms tumor-suppressor WTX and tumor-associated mutants (Q39642614) (← links)
• Different incidences of epigenetic but not genetic abnormalities between Wilms tumors in Japanese and Caucasian children. (Q43570166) (← links)
• Deletions in the AMER1 gene destabilize the destruction complex (Q45314416) (← links)
• Truncations of AMER1 destabilize the destruction complex (Q45314417) (← links)
• TP53 alterations in Wilms tumour represent progression events with strong intratumour heterogeneity that are closely linked but not limited to anaplasia (Q47141863) (← links)
• A knock-in mouse line conditionally expressing the tumor suppressor WTX/AMER1. (Q47726957) (← links)
• Deletions of the AMER1 gene prevent expression of AMER1 protein (Q50288861) (← links)
• Truncated AMER1 mutants destabilize the destruction complex (Q50288863) (← links)
• Characterization of primary Wilms tumor cultures as an in vitro model (Q51849264) (← links)
• Germline mutations and somatic inactivation of TRIM28 in Wilms tumour. (Q55262812) (← links)
• Mir20a/106a-WTX axis regulates RhoGDIa/CDC42 signaling and colon cancer progression (Q60912762) (← links)
• The genetic changes of Wilms tumour (Q91297749) (← links)
• Zebrafish Wtx is a negative regulator of Wnt signaling but is dispensable for embryonic development and organ homeostasis (Q91760244) (← links)