(Q34562397)

3 August 2017

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title

Renal hypoplasia: lessons from Pax2. (English)

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3 August 2017

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3

Paul Goodyer

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3 August 2017

Alison Dziarmaga

1

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3 August 2017

Jacklyn Quinlan

series ordinal

2

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3 August 2017

publication date

5 November 2005

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3 August 2017

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3 August 2017

volume

21

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3 August 2017

issue

1

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3 August 2017

page(s)

26-31

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Prenatal diagnosis of severe structural congenital malformations in Europe

3 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS00467-005-2039-X

Epidemiology of chronic renal failure in children: data from the ItalKid project

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00467-005-2039-X

Glomerular number and size in autopsy kidneys: the relationship to birth weight

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00467-005-2039-X

Nephron number in patients with primary hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-005-2039-X

Birth weight and renal function

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-005-2039-X

Nephric lineage specification by Pax2 and Pax8

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-005-2039-X

GATA3 haplo-insufficiency causes human HDR syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-005-2039-X

WT-1 is required for early kidney development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-005-2039-X

SLIT2-mediated ROBO2 signaling restricts kidney induction to a single site

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-005-2039-X

Eya protein phosphatase activity regulates Six1-Dach-Eya transcriptional effects in mammalian organogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-005-2039-X

Hox11 paralogous genes are essential for metanephric kidney induction

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-005-2039-X

Defects in enteric innervation and kidney development in mice lacking GDNF

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-005-2039-X

Renal agenesis and the absence of enteric neurons in mice lacking GDNF

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-005-2039-X

Clustering of mutations responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous region (eyaHR) of EYA1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-005-2039-X

A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-005-2039-X

SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-005-2039-X

Expression of a truncated Sall1 transcriptional repressor is responsible for Townes-Brocks syndrome birth defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-005-2039-X

Nephron number, renal function, and arterial pressure in aged GDNF heterozygous mice.

21 January 2018

1 reference

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Distal ureter morphogenesis depends on epithelial cell remodeling mediated by vitamin A and Ret

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-005-2039-X

Primary, nonsyndromic vesicoureteric reflux and its nephropathy is genetically heterogeneous, with a locus on chromosome 1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-005-2039-X

Genetic evidence for a novel gene(s) involved in urogenital development on 10q26.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-005-2039-X

Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux.

21 January 2018

1 reference

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Roles of uroplakins in plaque formation, umbrella cell enlargement, and urinary tract diseases.

21 January 2018

1 reference

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Mutation of PAX2 in two siblings with renal-coloboma syndrome

21 January 2018

1 reference

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PAX2 mutations in oligomeganephronia.

21 January 2018

1 reference

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The mouse Pax2(1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-005-2039-X

Primary renal hypoplasia in humans and mice with PAX2 mutations: evidence of increased apoptosis in fetal kidneys of Pax2(1Neu) +/- mutant mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-005-2039-X

Ureteric Bud Apoptosis and Renal Hypoplasia in Transgenic PAX2-Bax Fetal Mice Mimics the Renal-Coloboma Syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-005-2039-X

Rescue of defective branching nephrogenesis in renal-coloboma syndrome by the caspase inhibitor, Z-VAD-fmk

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-005-2039-X

Epithelial transformation of metanephric mesenchyme in the developing kidney regulated by Wnt-4

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-005-2039-X

Fraser syndrome and mouse blebbed phenotype caused by mutations in FRAS1/Fras1 encoding a putative extracellular matrix protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-005-2039-X

Fras1 deficiency results in cryptophthalmos, renal agenesis and blebbed phenotype in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-005-2039-X

Renal agenesis and hypodysplasia in ret-k- mutant mice result from defects in ureteric bud development

21 January 2018

1 reference

12 December 2020

Mild vitamin A deficiency leads to inborn nephron deficit in the rat

1 reference

12 December 2020

Renal aplasia is the predominant cause of congenital solitary kidneys

1 reference

12 December 2020

Regulation of ureteric bud outgrowth by Pax2-dependent activation of the glial derived neurotrophic factor gene

1 reference

12 December 2020

Murine forkhead/winged helix genes Foxc1 (Mf1) and Foxc2 (Mfh1) are required for the early organogenesis of the kidney and urinary tract

1 reference

12 December 2020

Duplex Kidneys: A Correlation of Renal Dysplasia with Position of the Ureteral Orifice

1 reference

12 December 2020

Pediatric renal transplantation--the NAPRTCS experience.

1 reference

12 December 2020

Molecular regulation of nephron endowment

1 reference

12 December 2020

The paired-box transcription factor, PAX2, positively modulates expression of the Wilms' tumor suppressor gene (WT1)

1 reference

12 December 2020

Wnt-4 is a mesenchymal signal for epithelial transformation of metanephric mesenchyme in the developing kidney

1 reference

12 December 2020

De Novo Uroplakin IIIa Heterozygous Mutations Cause Human Renal Adysplasia Leading to Severe Kidney Failure

1 reference

12 December 2020

10.1007/S00467-005-2039-X

Identifiers

DOI

1 reference

Dimensions Publication ID

3 August 2017

1018267198

0 references

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