Common genetic variants in GAL , GAP 43 and NRSN 1 and interaction networks confer susceptibility to Hirschsprung disease-Reference-Cited by-同舟云学术

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Common genetic variants in GAL , GAP 43 and NRSN 1 and interaction networks confer susceptibility to Hirschsprung disease

Published:2018-04-14 Issue:7 Volume:22 Page:3377-3387
ISSN:1582-1838
Container-title:Journal of Cellular and Molecular Medicine
language:en
Short-container-title:J. Cell. Mol. Med.

Author:

Wang Yang¹²³^ORCID,Yan Weihui¹²³,Wang Jun¹²³,Zhou Ying¹²³,Chen Jie¹²³,Gu Beilin¹²³,Cai Wei¹²³

Affiliation:

1. Department of Pediatric Surgery Xinhua Hospital School of Medicine Shanghai Jiao Tong University Shanghai China

2. Shanghai Key Laboratory of Pediatric Gastroenterology and Nutrition Shanghai China

3. Shanghai Institute for Pediatric Research Shanghai China

Funder

Shanghai Jiao Tong University

Science and Technology Commission of Shanghai Municipality

National Natural Science Foundation of China

Publisher

Wiley

Subject

Cell Biology,Molecular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/jcmm.13612

Reference40 articles.

1. Hirschsprung disease, associated syndromes and genetics: a review

2. Genome-Wide Copy Number Analysis Uncovers a New HSCR Gene: NRG3

3. Genetic Background Strongly Modifies the Severity of Symptoms of Hirschsprung Disease, but Not Hearing Loss in Rats Carrying Ednrbsl Mutations

4. Genetic basis of Hirschsprung’s disease

5. Contribution of rare and common variants determine complex diseases—Hirschsprung disease as a model

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1. Dl-3-n-butylphthalide promotes neurite outgrowth of primary cortical neurons by Sonic Hedgehog signaling via upregulating Gap43;Experimental Cell Research;2021-01

2. Genetic variants in RET, ARHGEF3 and CTNNAL1, and relevant interaction networks, contribute to the risk of Hirschsprung disease;Aging;2020-03-06

3. MicroRNA-4516-mediated regulation of MAPK10 relies on 3′ UTR cis-acting variants and contributes to the altered risk of Hirschsprung disease;Journal of Medical Genetics;2020-02-17

4. Growth‐associated protein 43 promotes thyroid cancer cell lines progression via epithelial‐mesenchymal transition;Journal of Cellular and Molecular Medicine;2019-09-30

5. Integrative analysis identifies key molecular signatures underlying neurodevelopmental deficits in fragile X syndrome;2019-04-15

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