Mycn regulates intestinal development through ribosomal biogenesis in a zebrafish model of Feingold syndrome 1.
Feingold syndrome type 1, caused by loss-of-function of MYCN, is characterized by varied phenotypes including esophageal and duodenal atresia. However, no adequate model exists for studying the syndrome's pathological or molecular mechanisms, nor is there a treatment strategy. Here, we develope...
Main Authors: | Yun-Fei Li, Tao Cheng, Ying-Jie Zhang, Xin-Xin Fu, Jing Mo, Guo-Qin Zhao, Mao-Guang Xue, Ding-Hao Zhuo, Yan-Yi Xing, Ying Huang, Xiao-Zhi Sun, Dan Wang, Xiang Liu, Yang Dong, Xiao-Sheng Zhu, Feng He, Jun Ma, Dong Chen, Xi Jin, Peng-Fei Xu |
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Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2022-11-01
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Series: | PLoS Biology |
Online Access: | https://doi.org/10.1371/journal.pbio.3001856 |
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