(Q33745374)

29 July 2017

title

Expression of the Wilm's tumor gene WT1 during diaphragmatic development in the nitrofen model for congenital diaphragmatic hernia (English)

1 reference

congenital diaphragmatic hernia

29 July 2017

0 references

1 reference

4

Prem Puri

1 reference

29 July 2017

Jens Dingemann

1

1 reference

29 July 2017

Takashi Doi

series ordinal

2

1 reference

29 July 2017

Elke Ruttenstock

series ordinal

3

1 reference

29 July 2017

publication date

1 February 2011

1 reference

Pediatric Surgery International

29 July 2017

published in

1 reference

29 July 2017

volume

27

1 reference

29 July 2017

issue

2

1 reference

29 July 2017

page(s)

159-163

1 reference

https://scigraph.springernature.com/pub.10.1007/s00383-010-2795-y

29 July 2017

exact match

0 references

cites work

Congenital diaphragmatic hernia: an overview of the etiology and current management

1 reference

https://api.crossref.org/works/10.1007%2FS00383-010-2795-Y

Follow up of infants with congenital diaphragmatic hernia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00383-010-2795-Y

Evidence-based management of infants with congenital diaphragmatic hernia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00383-010-2795-Y

Diaphragm development and congenital diaphragmatic hernia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00383-010-2795-Y

Animal models in pediatric surgery

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00383-010-2795-Y

WT-1 is required for early kidney development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00383-010-2795-Y

YAC transgenic analysis reveals Wilms' tumour 1 gene activity in the proliferating coelomic epithelium, developing diaphragm and limb.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00383-010-2795-Y

Teratogen-induced, dietary and genetic models of congenital diaphragmatic hernia share a common mechanism of pathogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00383-010-2795-Y

Genetic factors in congenital diaphragmatic hernia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00383-010-2795-Y

WT1 splice-site mutations are rarely associated with primary steroid-resistant focal and segmental glomerulosclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00383-010-2795-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00383-010-2795-Y

The expression of the Wilms' tumour gene, WT1, in the developing mammalian embryo.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00383-010-2795-Y

Early development of the primordial mammalian diaphragm and cellular mechanisms of nitrofen-induced congenital diaphragmatic hernia

21 January 2018

1 reference

12 December 2020

Gene expression in the developing diaphragm: significance for congenital diaphragmatic hernia

1 reference

12 December 2020

Hydrothorax in a patient with Denys-Drash syndrome associated with a diaphragmatic defect

1 reference

12 December 2020

Diaphragmatic hernia in Denys-Drash syndrome

1 reference

12 December 2020

Downregulation of FGFRL1 contributes to the development of the diaphragmatic defect in the nitrofen model of congenital diaphragmatic hernia

1 reference

12 December 2020

10.1007/S00383-010-2795-Y

Identifiers

DOI

1 reference

Dimensions Publication ID

29 July 2017

1031270688

0 references

1 reference