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Items: 8

1.

WTX inactivation is a frequent, but late event in Wilms tumors without apparent clinical impact.

Wegert J, Wittmann S, Leuschner I, Geissinger E, Graf N, Gessler M.

Genes Chromosomes Cancer. 2009 Dec;48(12):1102-11. doi: 10.1002/gcc.20712.

PMID:
19760609
2.

Pathology, genetics and cytogenetics of Wilms' tumour.

Md Zin R, Murch A, Charles A.

Pathology. 2011 Jun;43(4):302-12. doi: 10.1097/PAT.0b013e3283463575. Review.

PMID:
21516053
3.

Wilms' tumours: about tumour suppressor genes, an oncogene and a chameleon gene.

Huff V.

Nat Rev Cancer. 2011 Feb;11(2):111-21. doi: 10.1038/nrc3002. Epub 2011 Jan 20. Review.

4.

Genetics of pediatric renal tumors.

Royer-Pokora B.

Pediatr Nephrol. 2013 Jan;28(1):13-23. doi: 10.1007/s00467-012-2146-4. Epub 2012 Mar 30. Review.

PMID:
22461142
5.

The development of Wilms tumor: from WT1 and microRNA to animal models.

Tian F, Yourek G, Shi X, Yang Y.

Biochim Biophys Acta. 2014 Aug;1846(1):180-7. doi: 10.1016/j.bbcan.2014.07.003. Epub 2014 Jul 11. Review.

PMID:
25018051
6.

Two novel WTX mutations underscore the unpredictability of male survival in osteopathia striata with cranial sclerosis.

Perdu B, Lakeman P, Mortier G, Koenig R, Lachmeijer AM, Van Hul W.

Clin Genet. 2011 Oct;80(4):383-8. doi: 10.1111/j.1399-0004.2010.01553.x. Epub 2010 Oct 18. Review.

PMID:
20950377
7.

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.

Perotti D, Hohenstein P, Bongarzone I, Maschietto M, Weeks M, Radice P, Pritchard-Jones K.

Mol Cancer Ther. 2013 Dec;12(12):2619-27. doi: 10.1158/1535-7163.MCT-13-0335. Epub 2013 Nov 20. Review.

8.

WTX R353X mutation in a family with osteopathia striata and cranial sclerosis (OS-CS): case report and literature review of the disease clinical, genetic and radiological features.

Zicari AM, Tarani L, Perotti D, Papetti L, Nicita F, Liberati N, Spalice A, Salvatori G, Guaraldi F, Duse M.

Ital J Pediatr. 2012 Jun 20;38:27. doi: 10.1186/1824-7288-38-27. Review.

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