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Nutrients|October 16, 2024
Houttuynia cordata Thunb. Extracts Alleviate Atherosclerosis and Modulate Gut Microbiota in Male Hypercholesterolemic HamstersYuhong Lin, Chufeng He, Jianhui Liu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 5, 2017
[Study of gene mutation and pathogenetic mechanism for a family with Waardenburg syndrome]Hongsheng Chen, Xinbin Liao, Yalan Liu, et al.
Biochemical and Biophysical Research Communications|May 19, 2010
Novel mutations of PAX3, MITF, and SOX10 genes in Chinese patients with type I or type II Waardenburg syndromeHongsheng Chen, Lu Jiang, Zhiguo Xie, et al.
European Journal of Pharmacology|April 4, 2025
FKBP5 mediates glucocorticoid signaling in estrogen deficiency-associated endothelial dysfunctionRuiwen Zhu, Yiyue Xu, Huixian Li, et al.
BMC Medical Genomics|November 4, 2022
A comprehensive genotype-phenotype evaluation of eight Chinese probands with Waardenburg syndromeSijun Li, Mengyao Qin, Shuang Mao, et al.
Nutrients|September 9, 2023
Nutritional Assessment of Plant-Based Meat Products Available on Hong Kong Market: A Cross-Sectional SurveyQile Zhang, Yilin Liu, Chufeng He, et al.
Clinical Genetics|February 24, 2021
Otological manifestations in branchiootorenal spectrum disorder: A systematic review and meta-analysisAnhai Chen, Jian Song, Frederic R E Acke, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|May 25, 2020
Next-generation sequencing-based mutation analysis of genes associated with enlarged vestibular aqueduct in Chinese familiesYalan Liu, Jie Wen, Shushan Sang, et al.
FEBS Letters|October 27, 2012
Functional analysis of MITF gene mutations associated with Waardenburg syndrome type 2Hua Zhang, Hunjin Luo, Hongsheng Chen, et al.
Human Cell|February 21, 2024
Identification of a family with van der Hoeve's syndrome harboring a novel COL1A1 mutation and generation of patient-derived iPSC lines and CRISPR/Cas9-corrected isogenic iPSCsSiJun Li, Lingyun Mei, Chufeng He, et al.
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