Yongxin Ma
6PUBLICATIONS
0CO-AUTHORS
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Publications (6)
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|Jan 31, 2022
A novel NPHS2 mutation (c.865A > G) identified in a Chinese family with steroid-resistant nephrotic syndrome alters subcellular localization of nephrin.Na Wu, Yingchuan Zhu, Wenhao Jiang
|Sep 18, 2021
Compound heterozygous KCNV2 variants contribute to cone dystrophy with supernormal rod responses in a Chinese family.Man Liu, Yingchuan Zhu, Lian Huang
|Jan 20, 2021
PIWIL2 interacting with IKK to regulate autophagy and apoptosis in esophageal squamous cell carcinoma.Xu Zhao, Lian Huang, Yilu Lu
|Jul 30, 2020
Identification of two rare mutations c.1318G>A and c.6438+2T>G in a Chinese DMD family as genetic markers.Yingchuan Zhu, Lijun Yang, Tengjiao Ma
|May 18, 2019
PIWIL1 suppresses circadian rhythms through GSK3β-induced phosphorylation and degradation of CLOCK and BMAL1 in cancer cells.Hao Tan, Yingchuan Zhu, Xulei Zheng
|Nov 07, 2017
Decreased Plasma COMP and Increased Plasma CTX-II Levels in a Chinese Pseudoachondroplasia Family with Novel COMP Mutation.Chongjuan Gu, Zhao Yang, Hao Tan
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