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Literature DB >> 18187945

Wilms' tumor in children: an overview.

Ali Varan¹.

Abstract

Entities: Disease Species

Mesh：

Substances：
Antineoplastic Agents

Year: 2008 PMID： 18187945 DOI： 10.1159/000113012

Source DB: PubMed Journal: Nephron Clin Pract ISSN： 1660-2110

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9 in total

1. β-Catenin and K-RAS synergize to form primitive renal epithelial tumors with features of epithelial Wilms' tumors.

Authors: Peter E Clark; Dina Polosukhina; Harold Love; Hernan Correa; Cheryl Coffin; Elizabeth J Perlman; Mark de Caestecker; Harold L Moses; Roy Zent
Journal: Am J Pathol Date: 2011-10-08 Impact factor: 4.307

Review 2. Inactivation of X-linked tumor suppressor genes in human cancer.

Authors: Runhua Liu; Mandy Kain; Lizhong Wang
Journal: Future Oncol Date: 2012-04 Impact factor: 3.404

3. MiR-200a with CDC7 as a direct target declines cell viability and promotes cell apoptosis in Wilm's tumor via Wnt/β-catenin signaling pathway.

Authors: Xiu-Ling Liang; Yu-Long Wang; Pei-Rong Wang
Journal: Mol Cell Biochem Date: 2021-02-18 Impact factor: 3.396

Review 4. Ultrasound in diagnosis of intrascrotal metastasis of Wilms' tumor: first case report of a Chinese boy and review of the literature.

Authors: Yu-Jia Yang; Bo Xiang; Ju-Xian Liu; Mei Yang; Hui-Zhu Chen
Journal: J Med Ultrason (2001) Date: 2015-06-07 Impact factor: 1.314

Wilms' tumor in children: an overview.

1. β-Catenin and K-RAS synergize to form primitive renal epithelial tumors with features of epithelial Wilms' tumors.

Review 2. Inactivation of X-linked tumor suppressor genes in human cancer.

3. MiR-200a with CDC7 as a direct target declines cell viability and promotes cell apoptosis in Wilm's tumor via Wnt/β-catenin signaling pathway.

Review 4. Ultrasound in diagnosis of intrascrotal metastasis of Wilms' tumor: first case report of a Chinese boy and review of the literature.

5. Wilms tumour in children: 18 years of experience at Vilnius University Hospital Santaros Klinikos, Lithuania.

6. Loss of heterozygosity and SOSTDC1 in adult and pediatric renal tumors.

7. Functional KRAS mutations and a potential role for PI3K/AKT activation in Wilms tumors.

8. Prognostic Factors and Nomograms to Predict Overall and Cancer-Specific Survival for Children with Wilms' Tumor.

9. Expression of PAX2 and PAX8 in Wilms Tumor: A Tissue Microarray-based Immunohistochemical Study.