Literature DB >> 8281164

A novel mutation of the WT1 gene (a tumor suppressor gene for Wilms' tumor) in a patient with Denys-Drash syndrome.

A Sakai1, K Tadokoro, H Yanagisawa, S Nagafuchi, N Hoshikawa, T Suzuki, T Kohsaka, T Hasegawa, Y Nakahori, M Yamada.   

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Year:  1993        PMID： 8281164     DOI： 10.1093/hmg/2.11.1969

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN： 0964-6906            Impact factor:   6.150


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  5 in total

1.  Rapid detection of monogenic causes of childhood-onset steroid-resistant nephrotic syndrome.

Authors:  Svjetlana Lovric; Humphrey Fang; Virginia Vega-Warner; Carolin E Sadowski; Heon Yung Gee; Jan Halbritter; Shazia Ashraf; Pawaree Saisawat; Neveen A Soliman; Jameela A Kari; Edgar A Otto; Friedhelm Hildebrandt
Journal:  Clin J Am Soc Nephrol       Date:  2014-04-17       Impact factor: 8.237

2.  Discordant expression of a new WT1 gene mutation in a family with monozygotic twins presenting with congenital nephrotic syndrome.

Authors:  Filip Fencl; Michal Malina; Veronika Stará; Jakub Zieg; Dana Mixová; Tomáš Seeman; Květa Bláhová
Journal:  Eur J Pediatr       Date:  2011-05-26       Impact factor: 3.183

Review 3.  The Denys-Drash syndrome.

Authors:  R F Mueller
Journal:  J Med Genet       Date:  1994-06       Impact factor: 6.318

4.  Software and database for the analysis of mutations in the human WT1 gene.

Authors:  C Jeanpierre; C Béroud; P Niaudet; C Junien
Journal:  Nucleic Acids Res       Date:  1998-01-01       Impact factor: 16.971

Review 5.  The role of WT1 in oncogenesis: tumor suppressor or oncogene?

Authors:  David M Loeb; Saraswati Sukumar
Journal:  Int J Hematol       Date:  2002-08       Impact factor: 2.490
  5 in total

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