Literature DB >> 26891727

Renal failure from birth-AKI or CKD? Answers.

Sean Carter1, Abhijit Dixit2, Andrew Lunn2, Anjum Deorukhkar2, Martin Christian3.   

Abstract

Entities:  

Keywords:  Denys–Drash syndrome; Diffuse mesangial sclerosis; Neonatal nephrotic syndrome; WT1; Wilms tumour; c.1097G>A; p.(Arg366His)

Mesh：

Substances：

Year:  2016        PMID： 26891727     DOI： 10.1007/s00467-016-3332-6

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN： 0931-041X            Impact factor:   3.714


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  26 in total

1.  Pulmonary dysplasia, Denys-Drash syndrome and Wilms tumor 1 gene mutation in twins.

Authors:  V R Dharnidharka; E C Ruteshouser; S Rosen; H Kozakewich; H W Harris; J T Herrin; V Huff
Journal:  Pediatr Nephrol       Date:  2001-03       Impact factor: 3.714

2.  A syndrome of pseudohermaphroditism, Wilms' tumor, hypertension, and degenerative renal disease.

Authors:  A Drash; F Sherman; W H Hartmann; R M Blizzard
Journal:  J Pediatr       Date:  1970-04       Impact factor: 4.406

Review 3.  The Denys-Drash syndrome.

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

4.  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

5.  Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus.

Authors:  K M Call; T Glaser; C Y Ito; A J Buckler; J Pelletier; D A Haber; E A Rose; A Kral; H Yeger; W H Lewis
Journal:  Cell       Date:  1990-02-09       Impact factor: 41.582

6.  Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database.

Authors:  C Jeanpierre; E Denamur; I Henry; M O Cabanis; S Luce; A Cécille; J Elion; M Peuchmaur; C Loirat; P Niaudet; M C Gubler; C Junien
Journal:  Am J Hum Genet       Date:  1998-04       Impact factor: 11.025

7.  Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome.

Authors:  Rainer G Ruf; Michael Schultheiss; Anne Lichtenberger; Stephanie M Karle; Isabella Zalewski; Bettina Mucha; Anne Schulze Everding; Thomas Neuhaus; Ludwig Patzer; Christian Plank; Johannes P Haas; Fatih Ozaltin; Anita Imm; Arno Fuchshuber; Aysin Bakkaloglu; Friedhelm Hildebrandt
Journal:  Kidney Int       Date:  2004-08       Impact factor: 10.612

8.  Constitutional mutations in the WT1 gene in patients with Denys-Drash syndrome.

Authors:  P N Baird; A Santos; N Groves; L Jadresic; J K Cowell
Journal:  Hum Mol Genet       Date:  1992-08       Impact factor: 6.150

9.  Denys-Drash syndrome.

Authors:  Hsiao-Chen Lin; Shen-Kai Lin; Mei-Ching Wen; Chung-Fang Tseng; Lin-Shein Fu; Ching-Shiang Chi
Journal:  J Formos Med Assoc       Date:  2004-01       Impact factor: 3.282

10.  WT1 mutations in Meacham syndrome suggest a coelomic mesothelial origin of the cardiac and diaphragmatic malformations.

Authors:  Mohnish Suri; Peter Kelehan; David O'neill; Shantala Vadeyar; Judith Grant; S Faisal Ahmed; John Tolmie; Emma McCann; Wayne Lam; Shirley Smith; David Fitzpatrick; Nicholas D Hastie; William Reardon
Journal:  Am J Med Genet A       Date:  2007-10-01       Impact factor: 2.802
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