ROBO2 gene variants are associated with familial vesicoureteral reflux. - Wikidata - awgldk - TriplyDB

ROBO2 gene variants are associated with familial vesicoureteral reflux.

ROBO2 gene variants are associated with familial vesicoureteral reflux.

http://www.wikidata.org/entity/Q36666892

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Lower urinary tract development and disease Noninvasive assessment of antenatal hydronephrosis in mice reveals a critical role for Robo2 in maintaining anti-reflux mechanism Gata3 acts downstream of beta-catenin signaling to prevent ectopic metanephric kidney induction Genes in the ureteric budding pathway: association study on vesico-ureteral reflux patients.Mutations of the SLIT2-ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tract.Congenital anomalies of the kidney and urinary tract: a genetic disorder?New congenital anomalies of the kidney and urinary tract and outcomes in Robo2 mutant mice with the inserted piggyBac transposon.Rare variants in tenascin genes in a cohort of children with primary vesicoureteric reflux Genetics of Vesicoureteral Reflux.A recessive gene for primary vesicoureteral reflux maps to chromosome 12p11-q13.Genetic and developmental basis for urinary tract obstruction.A new genome scan for primary nonsyndromic vesicoureteric reflux emphasizes high genetic heterogeneity and shows linkage and association with various genes already implicated in urinary tract development.Cell and molecular biology of kidney development.Genetics of congenital anomalies of the kidney and urinary tract.A single-center cohort of Canadian children with VUR reveals renal phenotypes important for genetic studies.Vesicoureteric reflux and reflux nephropathy: from mouse models to childhood disease.Slit2-Robo signaling in inflammation and kidney injury.Genetic, environmental, and epigenetic factors involved in CAKUT.Developmental Genetics and Congenital Anomalies of the Kidney and Urinary Tract.Nephron number, hypertension, and CKD: physiological and genetic insight from humans and animal models.Renal development in the fetus and premature infant.Genetics of vesicoureteral reflux.Genetics of kidney development: pathogenesis of renal anomalies.SLIT2/ROBO2 signaling pathway inhibits nonmuscle myosin IIA activity and destabilizes kidney podocyte adhesion.Identification of direct negative crosstalk between the SLIT2 and Bone Morphogenetic Protein-Gremlin signaling pathways.A homozygous missense variant in VWA2, encoding an interactor of the Fraser-complex, in a patient with vesicoureteral reflux.Mutation screening of BMP4 and Id2 genes in Chinese patients with congenital ureteropelvic junction obstruction.ROBO2 gene variants in children with primary nonsyndromic vesicoureteral reflux with or without renal hypoplasia/dysplasia.

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P2860

ROBO2 gene variants are associated with familial vesicoureteral reflux.

http://www.wikidata.org/entity/Q36666892

description

2008 nî lūn-bûn

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2008年の論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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2008年论文

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2008年论文

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name

ROBO2 gene variants are associated with familial vesicoureteral reflux.

@ast

ROBO2 gene variants are associated with familial vesicoureteral reflux.

@en

type

label

ROBO2 gene variants are associated with familial vesicoureteral reflux.

@ast

ROBO2 gene variants are associated with familial vesicoureteral reflux.

@en

prefLabel

ROBO2 gene variants are associated with familial vesicoureteral reflux.

@ast

ROBO2 gene variants are associated with familial vesicoureteral reflux.

@en

P1433

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P1433

Journal of the American Society of Nephrology

P1476

ROBO2 gene variants are associated with familial vesicoureteral reflux.

@en

P2093

Aida M Bertoli-Avella

http://www.w3.org/2001/XMLSchema#string

Angela La Manna

http://www.w3.org/2001/XMLSchema#string

Ben A Oostra

http://www.w3.org/2001/XMLSchema#string

Bianca M de Graaf

http://www.w3.org/2001/XMLSchema#string

Bruno Nobili

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Carolina Grassia

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Cesare Polito

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Francesca Punzo

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Giuliana Lama

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Maria Luisa Conte

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P2860

Extracellular Ig domains 1 and 2 of Robo are important for ligand (Slit) binding

Disruption of ROBO2 is associated with urinary tract anomalies and confers risk of vesicoureteral reflux

The DUTT1 gene, a novel NCAM family member is expressed in developing murine neural tissues and has an unusually broad pattern of expression

Roundabout controls axon crossing of the CNS midline and defines a novel subfamily of evolutionarily conserved guidance receptors

Robo1 and Robo2 are homophilic binding molecules that promote axonal growth

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

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

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

Permanent renal parenchymal defects after febrile UTI are closely associated with vesicoureteric reflux.

Vesico-ureteral reflux: a genetic condition?

P304

825-831

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scholarly article

P356

10.1681/ASN.2007060692

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4

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19

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2008-01-30T00:00:00Z

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18235093

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2390967

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