Exome sequencing identified NRG3 as a novel susceptible gene of Hirschsprung's disease in a Chinese population (Q34322326)

1 August 2017

title

Exome sequencing identified NRG3 as a novel susceptible gene of Hirschsprung's disease in a Chinese population (English)

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1 August 2017

main subject

Hirschsprung's disease

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Jun Yang

1

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1 August 2017

Shengyu Duan

2

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1 August 2017

Rong Zhong

3

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1 August 2017

Jieyun Yin

4

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1 August 2017

Jiarui Pu

5

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1 August 2017

Juntao Ke

6

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1 August 2017

Xuzai Lu

7

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1 August 2017

Li Zou

8

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1 August 2017

Hongmei Zhang

9

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1 August 2017

Zhidong Zhu

10

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1 August 2017

Depeng Wang

11

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1 August 2017

Huasheng Xiao

12

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1 August 2017

Anyuan Guo

13

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1 August 2017

Jiahong Xia

14

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1 August 2017

Xiaoping Miao

15

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1 August 2017

Shaotao Tang

16

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1 August 2017

Guobin Wang

17

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1 August 2017

publication date

12 January 2013

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1 August 2017

published in

Molecular Neurobiology

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1 August 2017

volume

47

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1 August 2017

issue

3

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1 August 2017

page(s)

957-966

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Hirschsprung disease is linked to defects in neural crest stem cell function

1 August 2017

cites work

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Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease

21 January 2018

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21 January 2018

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Mutations in SIP1, encoding Smad interacting protein-1, cause a form of Hirschsprung disease

21 January 2018

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A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease

21 January 2018

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A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome)

21 January 2018

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Mutations of the RET proto-oncogene in Hirschsprung's disease

21 January 2018

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Correlation between genetic variations in Hox clusters and Hirschsprung's disease.

21 January 2018

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Role of RET and PHOX2B gene polymorphisms in risk of Hirschsprung's disease in Chinese population

21 January 2018

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Reduced RET expression in gut tissue of individuals carrying risk alleles of Hirschsprung's disease

21 January 2018

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A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk.

21 January 2018

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Fine mapping of the 9q31 Hirschsprung's disease locus.

21 January 2018

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Differential contributions of rare and common, coding and noncoding Ret mutations to multifactorial Hirschsprung disease liability

21 January 2018

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What can exome sequencing do for you?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-012-8392-4

21 January 2018

Whole genome sequencing

1 reference

https://api.crossref.org/works/10.1007%2FS12035-012-8392-4

Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome

21 January 2018

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Speeding disease gene discovery by sequence based candidate prioritization

21 January 2018

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ToppGene Suite for gene list enrichment analysis and candidate gene prioritization

21 January 2018

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Gene prioritization through genomic data fusion

21 January 2018

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GenMAPP, a new tool for viewing and analyzing microarray data on biological pathways

21 January 2018

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KEGG: kyoto encyclopedia of genes and genomes

21 January 2018

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A method and server for predicting damaging missense mutations

21 January 2018

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The transcription factor Sox10 is a key regulator of peripheral glial development.

21 January 2018

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Genetic mapping in human disease

21 January 2018

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Global variation in copy number in the human genome

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12035-012-8392-4

Development of the enteric nervous system: bringing together cells, signals and genes

21 January 2018

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Neuregulins in development

21 January 2018

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Identification of the scaramanga gene implicates Neuregulin3 in mammary gland specification

21 January 2018

1 reference

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The role of NRG3 in mammary development

21 January 2018

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Human NRG3 gene Map position 10q22-q23.

21 January 2018

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The neuregulin-I/ErbB signaling system in development and disease

21 January 2018

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Untangling the ErbB signalling network

21 January 2018

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Neuregulin-3 (NRG3): a novel neural tissue-enriched protein that binds and activates ErbB4

21 January 2018

1 reference

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Genome-wide copy number analysis uncovers a new HSCR gene: NRG3

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-012-8392-4

Exome sequencing and disease-network analysis of a single family implicate a mutation in KIF1A in hereditary spastic paraparesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-012-8392-4

Colonic Epithelial Expression of ErbB2 Is Required for Postnatal Maintenance of the Enteric Nervous System

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12035-012-8392-4

Requirement of signalling by receptor tyrosine kinase RET for the directed migration of enteric nervous system progenitor cells during mammalian embryogenesis.

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23315268

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S12035-012-8392-4

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Dimensions Publication ID

1 August 2017

1000798859

0 references

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