Literature DB >> 8281163

Further evidence that imbalance of WT1 isoforms may be involved in Denys-Drash syndrome.

A König1, S Jakubiczka, P Wieacker, H W Schlösser, M Gessler.   

Abstract

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Year:  1993        PMID： 8281163     DOI： 10.1093/hmg/2.11.1967

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


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  5 in total

Review 1.  The Denys-Drash syndrome.

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

2.  Do intronic mutations affecting splicing of WT1 exon 9 cause Frasier syndrome?

Authors:  H Kikuchi; A Takata; Y Akasaka; R Fukuzawa; H Yoneyama; Y Kurosawa; M Honda; Y Kamiyama; J Hata
Journal:  J Med Genet       Date:  1998-01       Impact factor: 6.318

Review 3.  WT1 and glomerular diseases.

Authors:  Patrick Niaudet; Marie-Claire Gubler
Journal:  Pediatr Nephrol       Date:  2006-08-23       Impact factor: 3.714

4.  Frasier syndrome, a potential cause of end-stage renal failure in childhood.

Authors:  Manon Bache; Céline Dheu; Bérénice Doray; Hélène Fothergill; Sylvie Soskin; Françoise Paris; Charles Sultan; Michel Fischbach
Journal:  Pediatr Nephrol       Date:  2010-03       Impact factor: 3.714

5.  Refining transcriptional programs in kidney development by integration of deep RNA-sequencing and array-based spatial profiling.

Authors:  Rathi D Thiagarajan; Nicole Cloonan; Brooke B Gardiner; Tim R Mercer; Gabriel Kolle; Ehsan Nourbakhsh; Shivangi Wani; Dave Tang; Keerthana Krishnan; Kylie M Georgas; Bree A Rumballe; Han S Chiu; Jason A Steen; John S Mattick; Melissa H Little; Sean M Grimmond
Journal:  BMC Genomics       Date:  2011-09-05       Impact factor: 3.969
  5 in total

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