Similar articles for PMID: 23618379

Year	Number of Results
1985	2
1987	1
1989	1
1991	1
1992	4
1993	13
1994	5
1995	5
1996	6
1997	6
1998	4
1999	8
2000	4
2001	6
2002	2
2003	2
2004	3
2005	3
2006	2
2007	4
2008	4
2009	3
2010	5
2011	3
2012	3
2013	4
2014	1
2015	3
2016	3
2017	2
2018	1
2019	1
2020	1
2021	4
2022	7
2023	5
2024	0

1

WT1 microdeletion and slowly progressing focal glomerulosclerosis in a patient with male pseudohermaphroditism, childhood leukemia, Wilms tumor and cerebellar angioblastoma.

Buglyó G, Méhes G, Vargha G, Biró S, Mátyus J. Buglyó G, et al. Clin Nephrol. 2013 May;79(5):414-8. doi: 10.5414/cn107276. Clin Nephrol. 2013. PMID: 23618379

2

[Glomerulopathy in Denys-Drash syndrome. Case report of a model disease].

Stallmach T, Neuhaus TJ, Kösters R, Hailemariam S. Stallmach T, et al. Pathologe. 1998 May;19(3):230-4. doi: 10.1007/s002920050279. Pathologe. 1998. PMID: 9648150 German.

3

A novel WT1 gene mutation in a three-generation family with progressive isolated focal segmental glomerulosclerosis.

Benetti E, Caridi G, Malaventura C, Dagnino M, Leonardi E, Artifoni L, Ghiggeri GM, Tosatto SC, Murer L. Benetti E, et al. Clin J Am Soc Nephrol. 2010 Apr;5(4):698-702. doi: 10.2215/CJN.05670809. Epub 2010 Feb 11. Clin J Am Soc Nephrol. 2010. PMID: 20150449 Free PMC article.

4

Effects of Denys-Drash syndrome point mutations on the DNA binding activity of the Wilms' tumor suppressor protein WT1.

Borel F, Barilla KC, Hamilton TB, Iskandar M, Romaniuk PJ. Borel F, et al. Biochemistry. 1996 Sep 17;35(37):12070-6. doi: 10.1021/bi960758o. Biochemistry. 1996. PMID: 8810912

5

Bilateral Wilms tumor in a boy with severe hypospadias and cryptochidism due to a heterozygous mutation in the WT1 gene.

Köhler B, Schumacher V, Schulte-Overberg U, Biewald W, Lennert T, l'Allemand D, Royer-Pokora B, Grüters A. Köhler B, et al. Pediatr Res. 1999 Feb;45(2):187-90. doi: 10.1203/00006450-199902000-00005. Pediatr Res. 1999. PMID: 10022588

6

WT1 and glomerular diseases.

Niaudet P, Gubler MC. Niaudet P, et al. Pediatr Nephrol. 2006 Nov;21(11):1653-60. doi: 10.1007/s00467-006-0208-1. Epub 2006 Aug 23. Pediatr Nephrol. 2006. PMID: 16927106 Review.

7

Mother-to-child transmitted WT1 splice-site mutation is responsible for distinct glomerular diseases.

Denamur E, Bocquet N, Mougenot B, Da Silva F, Martinat L, Loirat C, Elion J, Bensman A, Ronco PM. Denamur E, et al. J Am Soc Nephrol. 1999 Oct;10(10):2219-23. doi: 10.1681/ASN.V10102219. J Am Soc Nephrol. 1999. PMID: 10505700

8

Identical genetic changes in different histologic components of Wilms' tumors.

Zhuang Z, Merino MJ, Vortmeyer AO, Bryant B, Lash AE, Wang C, Deavers MT, Shelton WF, Kapur S, Chandra RS. Zhuang Z, et al. J Natl Cancer Inst. 1997 Aug 6;89(15):1148-52. doi: 10.1093/jnci/89.15.1148. J Natl Cancer Inst. 1997. PMID: 9262253

9

WT1 intron 9 splice acceptor site mutation in a 46,XY male with focal segmental glomerulosclerosis.

Kanemoto K, Ishikura K, Ariyasu D, Hamasaki Y, Hataya H, Hasegawa Y, Ikeda M. Kanemoto K, et al. Pediatr Nephrol. 2007 Mar;22(3):454-8. doi: 10.1007/s00467-006-0333-x. Epub 2006 Oct 24. Pediatr Nephrol. 2007. PMID: 17061122

10

The role of Wilms' tumor genes.

Hirose M. Hirose M. J Med Invest. 1999 Aug;46(3-4):130-40. J Med Invest. 1999. PMID: 10687307 Review.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

124 results

Results by year