Identification of two novel PCDHA9 mutations associated with Hirschsprung's disease-Reference-Cited by-同舟云学术

Identification of two novel PCDHA9 mutations associated with Hirschsprung's disease

Published:2018-06 Issue: Volume:658 Page:96-104
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

Shen Qiyang,Zhang Hua,Su Yang,Wen Zechao,Zhu Zhongxian,Chen Guanglin,Peng Lei,Du Chunxia,Xie Hua,Li Hongxing,Lv Xiaofeng,Lu Changgui,Xia Yankai,Tang Weibing^ORCID

Funder

National Natural Science Foundation of China

Jiangsu Higher Education Institutions

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference62 articles.

1. A method and server for predicting damaging missense mutations;Adzhubei;Nat. Methods,2010

2. Protocadherin alpha (PCDHA) as a novel susceptibility gene for autism;Anitha;J. Psychiatry Neurosci.,2013

3. The SWISS-MODEL workspace: a web-based environment for protein structure homology modelling;Arnold;Bioinformatics,2006

4. The clustered protocadherins Pcdhalpha and Pcdhgamma form a heteromeric complex in zebrafish;Biswas;Neuroscience,2012

5. Neuron and glia generating progenitors of the mammalian enteric nervous system isolated from foetal and postnatal gut cultures;Bondurand;Development,2003

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Hypoplastic Left Heart Syndrome: Signaling & Molecular Perspectives, and the Road Ahead;International Journal of Molecular Sciences;2023-10-17

2. A Prognostic Model for Prostate Cancer Patients Based on Two DNA Damage Response Mutation-Related Immune Genes;Cancer Biotherapy and Radiopharmaceuticals;2023-08-22

3. Dielectric Spectroscopy Shows a Permittivity Contrast between Meningioma Tissue and Brain White and Gray Matter—A Potential Physical Biomarker for Meningioma Discrimination;Cancers;2023-08-17

4. Whole Exome Sequencing of Thymoma Patients Exhibiting Exceptional Responses to Pemetrexed Monotherapy;Cancers;2023-08-08

5. Comprehensive characterization of the genetic landscape of familial Hirschsprung’s disease;World Journal of Pediatrics;2023-03-01