Literature DB >> 11182928

Constitutional WT1 correlate with clinical features in children with progressive nephropathy.

A Takata, H Kikuchi, R Fukuzawa, S Ito, M Honda, J Hata.   

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Year:  2000        PMID： 11182928      PMCID： PMC1734675          DOI： 10.1136/jmg.37.9.698

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  9 in total

1.  Patients with different or identical genotypes of the WT1 gene present different phenotypes.

Authors:  Yonghui Yang; Feng Zhao; Jun Huang; Xiaojing Nie; Zihua Yu
Journal:  Eur J Pediatr       Date:  2013-07-09       Impact factor: 3.183

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

Authors:  Katsuyoshi Kanemoto; Kenji Ishikura; Daisuke Ariyasu; Yuko Hamasaki; Hiroshi Hataya; Yukihiro Hasegawa; Masahiro Ikeda
Journal:  Pediatr Nephrol       Date:  2006-10-24       Impact factor: 3.714

3.  A child with isolated nephrotic syndrome and WT1 mutation presenting as a 46, XY phenotypic male.

Authors:  Yonghui Yang; Dongning Feng; Jun Huang; Xiaojing Nie; Zihua Yu
Journal:  Eur J Pediatr       Date:  2012-07-05       Impact factor: 3.183

4.  Discordant phenotypes in monozygotic twins with identical de novo WT1 mutation.

Authors:  Zihua Yu; Yonghui Yang; Dongning Feng
Journal:  Clin Kidney J       Date:  2012-04-02

5.  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

6.  Role for first zinc finger of WT1 in DNA sequence specificity: Denys-Drash syndrome-associated WT1 mutant in ZF1 enhances affinity for a subset of WT1 binding sites.

Authors:  Dongxue Wang; John R Horton; Yu Zheng; Robert M Blumenthal; Xing Zhang; Xiaodong Cheng
Journal:  Nucleic Acids Res       Date:  2018-05-04       Impact factor: 16.971

7.  New mutation in WT1 gene in a boy with an incomplete form of Denys-Drash syndrome: A CARE-compliant case report.

Authors:  Nail R Akramov; Rafael F Shavaliev; Ilsiya V Osipova
Journal:  Medicine (Baltimore)       Date:  2021-05-14       Impact factor: 1.889

8.  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

9.  Denys-Drash syndrome, septated vagina and low level of anti-Mullerian hormone in male neonate.

Authors:  Hong Jun Lee; Jung-Sook Yeom; Ji Sook Park; Eun Sil Park; Ji-Hyun Seo; Jae Young Lim; Chan-Hoo Park; Hyang-Ok Woo; Hee-Shang Youn
Journal:  Ann Pediatr Endocrinol Metab       Date:  2014-06-30
  9 in total

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