Literature DB >> 11241056

Isolated diffuse mesangial sclerosis and Wilms tumor suppressor gene.

S Ito 1, A Takata, H Hataya, M Ikeda, H Kikuchi, J Hata , M Honda.   

Abstract

Diffuse mesangial sclerosis is a rare renal disease, occurring either in isolation or as part of Denys-Drash syndrome. Denys-Drash syndrome originates from mutations of the Wilms tumor suppressor gene (WT1 ). We describe the presence of WT1 mutations in 7 Japanese children with isolated diffuse mesangial sclerosis.

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Year:  2001        PMID： 11241056     DOI： 10.1067/mpd.2001.111317

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


  10 in total

1.  Broad and unexpected phenotypic expression in Greek children with steroid-resistant nephrotic syndrome due to mutations in the Wilms' tumor 1 (WT1) gene.

Authors:  Spyridon Megremis; Andromachi Mitsioni; Irene Fylaktou; Sofia Kitsiou Tzeli; Filadelfia Komianou; Constantinos J Stefanidis; Emmanuel Kanavakis; Joanne Traeger-Synodinos
Journal:  Eur J Pediatr       Date:  2011-04-16       Impact factor: 3.183

Review 2.  WT1 and glomerular diseases.

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

Review 3.  Hereditary nephrotic syndrome: a systematic approach for genetic testing and a review of associated podocyte gene mutations.

Authors:  Geneviève Benoit; Eduardo Machuca; Corinne Antignac
Journal:  Pediatr Nephrol       Date:  2010-03-24       Impact factor: 3.714

4.  A case of atypical congenital nephrotic syndrome.

Authors:  Janusz Swietliński; Iwona Maruniak-Chudek; Zofia I Niemir; Aldona Woźniak; Maria Wilińska; Joanna Zacharzewska
Journal:  Pediatr Nephrol       Date:  2004-01-09       Impact factor: 3.714

5.  Evolutive study of children with diffuse mesangial sclerosis.

Authors:  Ana Pilar Nso Roca; Antonia Peña Carrión; Marta Benito Gutiérrez; Carmen García Meseguer; Araceli García Pose; Mercedes Navarro
Journal:  Pediatr Nephrol       Date:  2008-12-10       Impact factor: 3.714

6.  Gonadal Function in 15 Patients Associated with WT1 Gene Mutations.

Authors:  Akiko Maesaka; Asako Higuchi; Shinobu Kotoh; Yukihiro Hasegawa; Masahiro Ikeda; Seiichirou Shishido; Masataka Honda
Journal:  Clin Pediatr Endocrinol       Date:  2006-11-03

7.  Spectrum of Clinical Manifestations in Children With WT1 Mutation: Case Series and Literature Review.

Authors:  Patricia Arroyo-Parejo Drayer; Wacharee Seeherunvong; Chryso P Katsoufis; Marissa J DeFreitas; Tossaporn Seeherunvong; Jayanthi Chandar; Carolyn L Abitbol
Journal:  Front Pediatr       Date:  2022-04-15       Impact factor: 3.418

8.  Two cases of isolated diffuse mesangial sclerosis with WT1 mutations.

Authors:  Hyewon Hahn; Young Mi Cho; Young Seo Park; Han Wook You; Hae Il Cheong
Journal:  J Korean Med Sci       Date:  2006-02       Impact factor: 2.153

9.  Epigenetic transcriptional reprogramming by WT1 mediates a repair response during podocyte injury.

Authors:  Sandrine Ettou; Youngsook L Jung; Tomoya Miyoshi; Dhawal Jain; Ken Hiratsuka; Valerie Schumacher; Mary E Taglienti; Ryuji Morizane; Peter J Park; Jordan A Kreidberg
Journal:  Sci Adv       Date:  2020-07-24       Impact factor: 14.136

10.  Clinical utility of ultra-rapid whole-genome sequencing in an infant with atypical presentation of WT1-associated nephrotic syndrome type 4.

Authors:  Erica Sanford; Terence Wong; Katarzyna A Ellsworth; Elizabeth Ingulli; Stephen F Kingsmore
Journal:  Cold Spring Harb Mol Case Stud       Date:  2020-08-25
  10 in total

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