(Q51853674)

14 April 2018

title

Mutation screening of BMP4 and Id2 genes in Chinese patients with congenital ureteropelvic junction obstruction. (English)

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14 April 2018

author name string

Jun Li He

1

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14 April 2018

Jun Hong Liu

2

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14 April 2018

Feng Liu

3

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14 April 2018

Ping Tan

4

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14 April 2018

Tao Lin

5

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14 April 2018

Xu Liang Li

6

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14 April 2018

publication date

17 September 2011

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14 April 2018

European Journal of Pediatrics

published in

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14 April 2018

volume

171

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14 April 2018

issue

3

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14 April 2018

page(s)

451-456

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14 April 2018

https://scigraph.springernature.com/pub.10.1007/s00431-011-1561-z

exact match

0 references

cites work

Id2 haploinsufficiency in mice leads to congenital hydronephrosis resembling that in humans

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1561-Z

Mutations in BMP4 cause eye, brain, and digit developmental anomalies: overlap between the BMP4 and hedgehog signaling pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1561-Z

ROBO2 gene variants are associated with familial vesicoureteral reflux

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1561-Z

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%2FS00431-011-1561-Z

Tailbud-derived mesenchyme promotes urinary tract segmentation via BMP4 signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1561-Z

Genetic analysis of the mammalian transforming growth factor-beta superfamily

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1561-Z

Cleavages within the prodomain direct intracellular trafficking and degradation of mature bone morphogenetic protein-4.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1561-Z

Hypergonadotropic ovarian failure associated with an inherited mutation of human bone morphogenetic protein-15 (BMP15) gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1561-Z

The family of bone morphogenetic proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1561-Z

Clinical relevance and implications of antenatal hydronephrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1561-Z

Mutations in SOX17 are associated with congenital anomalies of the kidney and the urinary tract

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1561-Z

A cohort study of recurrence patterns among more than 54,000 relatives of oral cleft cases in Denmark: support for the multifactorial threshold model of inheritance

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1561-Z

No evidence for AT2R gene derangement in human urinary tract anomalies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1561-Z

Bone morphogenetic proteins: multifunctional regulators of vertebrate development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1561-Z

Bone morphogenetic proteins in development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1561-Z

Smooth muscle cell apoptosis and defective neural development in congenital ureteropelvic junction obstruction.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1561-Z

Domain-specific mutations in TGFB1 result in Camurati-Engelmann disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1561-Z

Antenatal ultrasonography to detect fetal renal abnormalities: a prospective screening programme

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1561-Z

Computational approaches for predicting the biological effect of p53 missense mutations: a comparison of three sequence analysis based methods

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1561-Z

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%2FS00431-011-1561-Z

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1561-Z

SIFT: Predicting amino acid changes that affect protein function

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1561-Z

Bone morphogenetic protein 2 transiently enhances expression of a gene, Id (inhibitor of differentiation), encoding a helix-loop-helix molecule in osteoblast-like cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1561-Z

Nonsyndromic cleft lip and palate: complex genetics and environmental effects

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1561-Z

Id proteins Id1 and Id2 selectively inhibit DNA binding by one class of helix-loop-helix proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1561-Z

Mutations in BMP4 are associated with subepithelial, microform, and overt cleft lip.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1561-Z

Functional analysis of BMP4 mutations identified in pediatric CAKUT patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1561-Z

Antagonism of BMP4 signaling disrupts smooth muscle investment of the ureter and ureteropelvic junction

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1561-Z

SIX2 and BMP4 mutations associate with anomalous kidney development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1561-Z

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%2FS00431-011-1561-Z

Postnatal management of antenatal hydronephrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1561-Z

A molecular and genetic view of human renal and urinary tract malformations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1561-Z

Molecular mechanisms of human embryogenesis: developmental pathogenesis of renal tract malformations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1561-Z

Role of Id family proteins in growth control

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1561-Z

The activity and signaling range of mature BMP-4 is regulated by sequential cleavage at two sites within the prodomain of the precursor

21 January 2018

1 reference

12 December 2020

1 reference

12 December 2020

Ureteropelvic junction obstruction: morphological and clinical studies

1 reference

12 December 2020

Mutation screening of BMP4, BMP7, HOXA4 and HOXB6 genes in Chinese patients with hypospadias

1 reference

12 December 2020

Ureteral structure and ultrastructure. Part II. Congenital ureteropelvic junction obstruction and primary obstructive megaureter

1 reference

12 December 2020

Abnormal innervation and altered nerve growth factor messenger ribonucleic acid expression in ureteropelvic junction obstruction

1 reference

12 December 2020

Electrical characterization of interstitial cells of Cajal-like cells and smooth muscle cells isolated from the mouse ureteropelvic junction

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

Structural changes of collagen components and diminution of nerves in congenital ureteropelvic junction obstruction

1 reference

12 December 2020

Increased prevalence of renal and urinary tract anomalies in children with Down syndrome

1 reference

12 December 2020

10.1007/S00431-011-1561-Z

Identifiers

DOI

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14 April 2018

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14 April 2018