Genetics of congenital anomalies of the kidney and urinary tract (Q37783542)

23 August 2017

title

Genetics of congenital anomalies of the kidney and urinary tract (English)

1 reference

developmental gene expression regulation

23 August 2017

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20798957

2 July 2024

author name string

Renfang Song

series ordinal

1

1 reference

23 August 2017

Ihor V. Yosypiv

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20798957

2 July 2024

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=20798957

2 July 2024

publication date

27 August 2010

1 reference

full work available at URL

23 August 2017

http://link.springer.com/content/pdf/10.1007/s00467-010-1629-4.pdf

file format

Portable Document Format

1 reference

https://api.crossref.org/works/10.1007/S00467-010-1629-4

http://link.springer.com/article/10.1007/s00467-010-1629-4/fulltext.html

2 July 2024

1 reference

https://api.crossref.org/works/10.1007/S00467-010-1629-4

http://link.springer.com/content/pdf/10.1007/s00467-010-1629-4

2 July 2024

1 reference

https://api.crossref.org/works/10.1007/S00467-010-1629-4

2 July 2024

1 reference

23 August 2017

volume

26

1 reference

23 August 2017

issue

3

1 reference

23 August 2017

page(s)

353-364

1 reference

Renal branching morphogenesis: concepts, questions, and recent advances

23 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Advances in early kidney specification, development and patterning

21 January 2018

1 reference

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Cell and molecular biology of kidney development

21 January 2018

1 reference

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Renin-angiotensin system-growth factor cross-talk: a novel mechanism for ureteric bud morphogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Architectural patterns in branching morphogenesis in the kidney.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Using mouse models to understand normal and abnormal urogenital tract development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Ret-dependent cell rearrangements in the Wolffian duct epithelium initiate ureteric bud morphogenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Branching morphogenesis of the ureteric epithelium during kidney development is coordinated by the opposing functions of GDNF and Sprouty1.

21 January 2018

1 reference

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Regulation of c-Ret in the developing kidney is responsive to Pax2 gene dosage

21 January 2018

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Kidney development in the absence of Gdnf and Spry1 requires Fgf10.

21 January 2018

1 reference

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Essential role of stromal mesenchyme in kidney morphogenesis revealed by targeted disruption of Winged Helix transcription factor BF-2

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

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%2FS00467-010-1629-4

Wnt9b plays a central role in the regulation of mesenchymal to epithelial transitions underlying organogenesis of the mammalian urogenital system

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Canonical WNT signaling during kidney development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

vHNF1 functions in distinct regulatory circuits to control ureteric bud branching and early nephrogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Wnt9b signaling regulates planar cell polarity and kidney tubule morphogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Six2 defines and regulates a multipotent self-renewing nephron progenitor population throughout mammalian kidney development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

The prepattern transcription factor Irx3 directs nephron segment identity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Notch2, but not Notch1, is required for proximal fate acquisition in the mammalian nephron.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Notch2 activation in the embryonic kidney depletes nephron progenitors

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

The podocyte-specific inactivation of Lmx1b, Ldb1 and E2a yields new insight into a transcriptional network in podocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Semaphorin3a regulates endothelial cell number and podocyte differentiation during glomerular development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

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%2FS00467-010-1629-4

Bone morphogenetic protein 4 regulates the budding site and elongation of the mouse ureter

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Congenital hydronephrosis: prenatal diagnosis and epidemiology in Europe.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Tbx18 regulates the development of the ureteral mesenchyme

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

SIX1 acts synergistically with TBX18 in mediating ureteral smooth muscle formation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Glomeruli and blood pressure. Less of one, more the other?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Determining the incidence of horseshoe kidney from radiographic data at a single institution

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Foxd1-dependent signals control cellularity in the renal capsule, a structure required for normal renal development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Loss of oriented cell division does not initiate cyst formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

GUDMAP: the genitourinary developmental molecular anatomy project

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Developmental biology of the human kidney

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Genotype-phenotype correlations in autosomal dominant and autosomal recessive polycystic kidney disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

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%2FS00467-010-1629-4

A transcriptional network in polycystic kidney disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

De novo HNF-1 beta gene mutation in familial hypoplastic glomerulocystic kidney disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Mutations in hepatocyte nuclear factor-1beta and their related phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Renal phenotypes related to hepatocyte nuclear factor-1beta (TCF2) mutations in a pediatric cohort

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

HNF1B alterations associated with congenital anomalies of the kidney and urinary tract.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Mutation analysis of the Uromodulin gene in 96 individuals with urinary tract anomalies (CAKUT)

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

A common variant of the PAX2 gene is associated with reduced newborn kidney size

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Common variants of the glial cell-derived neurotrophic factor gene do not influence kidney size of the healthy newborn

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Prevalence of mutations in renal developmental genes in children with renal hypodysplasia: results of the ESCAPE study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Whole-genome linkage and association scan in primary, nonsyndromic vesicoureteric reflux

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

ROBO2 gene variants are associated with familial vesicoureteral reflux

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Mutations in the ROBO2 and SLIT2 genes are rare causes of familial vesico-ureteral reflux.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Absence of mutations in the HOXA11 and HOXD11 genes in children with congenital renal malformations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Uroplakins in urothelial biology, function, and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Mutation analyses of Uroplakin II in children with renal tract malformations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Mutational analyses of UPIIIA, SHH, EFNB2 and HNF1beta in persistent cloaca and associated kidney malformations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Mutations in Uroplakin IIIA are a rare cause of renal hypodysplasia in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

SIX2 and BMP4 mutations associate with anomalous kidney development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Functional analysis of BMP4 mutations identified in pediatric CAKUT patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Interaction of the LMX1B and PAX2 gene products suggests possible molecular basis of differential phenotypes in Nail-Patella syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Modifier genes play a significant role in the phenotypic expression of PKD1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

The BRCT-domain containing protein PTIP links PAX2 to a histone H3, lysine 4 methyltransferase complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

DNA hypomethylation in the origin and pathogenesis of human diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Independent two-photon measurements of albumin GSC give low values

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Maternal diet programs embryonic kidney gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

High NPHP1 and NPHP6 mutation rate in patients with Joubert syndrome and nephronophthisis: potential epistatic effect of NPHP6 and AHI1 mutations in patients with NPHP1 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Congenital genitourinary tract abnormalities following cocaine exposure in utero

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

A shifting paradigm: histone deacetylases and transcriptional activation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Developmental roles of the histone lysine demethylases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Genetic analyses reveal a requirement for Dicer1 in the mouse urogenital tract.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Angiotensin induces the urinary peristaltic machinery during the perinatal period

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Deficiency of intrarenal angiotensin II type 2 receptor impairs paired homeo box-2 and N-myc expression during nephrogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Downregulation of Spry-1, an inhibitor of GDNF/Ret, causes angiotensin II-induced ureteric bud branching

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Angiotensin II-induced activation of c-Ret signaling is critical in ureteric bud branching morphogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Angiotensin II type 1 receptor-EGF receptor cross-talk regulates ureteric bud branching morphogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Angiotensin II AT2 receptor regulates ureteric bud morphogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Gene targeting in mice reveals a requirement for angiotensin in the development and maintenance of kidney morphology and growth factor regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

The microRNA-processing enzyme dicer maintains juxtaglomerular cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Angiotensin II-receptor-antagonists: further evidence of fetotoxicity but not teratogenicity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Adverse pregnancy outcomes associated with maternal enalapril antihypertensive treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Mutations in genes in the renin-angiotensin system are associated with autosomal recessive renal tubular dysgenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Renal tubular dysgenesis, a not uncommon autosomal recessive disorder leading to oligohydramnios: Role of the Renin-Angiotensin system

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Implication of genetic variations in congenital obstructive nephropathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Expression profiling of the AT2R mRNA in affected tissue from children with CAKUT.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Low renin-angiotensin system activity gene polymorphism and dysplasia associated with posterior urethral valves.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Renal aplasia in humans is associated with RET mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

The Uromodulin C744G mutation causes MCKD2 and FJHN in children and adults and may be due to a possible founder effect.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Dominantly inherited renal adysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Immature Renal Structures Associated With a Novel UMOD Sequence Variant

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Milder Presentation of Recessive Polycystic Kidney Disease Requires Presence of Amino Acid Substitution Mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-010-1629-4

Angiotensin type 2 receptor is important in the normal development of the ureter

21 January 2018

1 reference

12 December 2020

Angiotensin type II receptor expression and ureteral budding

1 reference

12 December 2020

Apoptosis induced by vitamin A signaling is crucial for connecting the ureters to the bladder

1 reference

12 December 2020

Ontogenesis of angiotensin-I converting enzyme in human Kidney

1 reference

12 December 2020

Hoxa11 and Hoxd11 regulate branching morphogenesis of the ureteric bud in the developing kidney

1 reference

12 December 2020

The where, what and why of the developing renal stroma

1 reference

12 December 2020

Genetic disorders of human congenital anomalies of the kidney and urinary tract (CAKUT)

1 reference

12 December 2020

Congenitally small kidneys with reflux as a common cause of nephropathy in boys

1 reference

12 December 2020

Paracrine PDGF-B/PDGF-Rbeta signaling controls mesangial cell development in kidney glomeruli

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

Analysis of hypertension in children post renal transplantation--a report of the North American Pediatric Renal Transplant Cooperative Study (NAPRTCS)

1 reference

12 December 2020

Regulation of c-ret expression by retinoic acid in rat metanephros: implication in nephron mass control

1 reference

12 December 2020

Effect of maternal iron restriction during pregnancy on renal morphology in the adult rat offspring

1 reference

12 December 2020

Bradykinin B2 null mice are prone to renal dysplasia: gene-environment interactions in kidney development.

1 reference

12 December 2020

Developmentally regulated conversion of mesenchyme to epithelium

1 reference

12 December 2020

Inductive epitheliomesenchymal interaction in cultured organ rudiments of the mouse

1 reference

12 December 2020

Renal anomalies in fetal alcohol syndrome

1 reference

12 December 2020

Early expression of all the components of the renin-angiotensin-system in human development

1 reference

12 December 2020

Stromal cells mediate retinoid-dependent functions essential for renal development.

1 reference

12 December 2020

Maturation of ureter-bladder connection in mice is controlled by LAR family receptor protein tyrosine phosphatases

1 reference

12 December 2020

Radiographic manifestations of renal anomalies

1 reference

12 December 2020

Prenatal detection of congenital renal malformations by fetal ultrasonographic examination: an analysis of 709,030 births in 12 European countries

1 reference

12 December 2020

Role of the Angiotensin Type 2 Receptor Gene in Congenital Anomalies of the Kidney and Urinary Tract, CAKUT, of Mice and Men

1 reference

12 December 2020

Screening for mutations in BMP4 and FOXC1 genes in congenital anomalies of the kidney and urinary tract in humans

1 reference

12 December 2020

Repression of Pax-2 by WT1 during normal kidney development

1 reference

12 December 2020

Vascular endothelial growth factor induces nephrogenesis and vasculogenesis

1 reference

12 December 2020

CBP and p300 are essential for renin cell identity and morphological integrity of the kidney

1 reference

12 December 2020

THE GROWTH AND MATURATION OF HUMAN GLOMERULI AND PROXIMAL CONVOLUTIONS FROM TERM TO ADULTHOOD: STUDIES BY MICRODISSECTION

1 reference

12 December 2020

Angiotensin-converting enzyme and angiotensin type 2 receptor gene genotype distributions in Italian children with congenital uropathies

1 reference

12 December 2020

Allelic variation in gene expression is common in the human genome

1 reference

12 December 2020

American Journal of Physiology

17

275

F938

E Moreau

1998

1 reference

https://api.crossref.org/works/10.1007/S00467-010-1629-4

Journal of Clinical Investigation

2 July 2024

40

119

924

N Uetani

2009

1 reference

https://api.crossref.org/works/10.1007/S00467-010-1629-4

2 July 2024

Identifiers

1 reference

23 August 2017

1 reference