Publications by authors named "Rongyu Chen"

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Auricular acupressure combined with auricular acupoint massage enhances cognitive function in night shift nurses: a P300 wave analysis.
Xiaoqin Li, Zhun Zhang, Litian Xiao, Xuan Zhang, Huiqi Yao, Rongyu Chen

Front Hum Neurosci· October 2025

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Alpha-lipoamide prevents acute kidney injury in mouse by inhibiting renal tubular epithelial cell pyroptosis.
Wan-Lin Tan, Xiong Yu, Jing Jia, Rong-Yu Chen, Xiao-Xiao Xu, Yu-Ting Chen

Biochem Pharmacol· July 2025

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Study on Freeze-Thaw Cycle Performance and Regional Service Life Prediction of Hydrophobic Aerogel-Modified ACEPS Boards.
Lu Lu, Rongyu Chen, Mingming Wang, Wenjia Xi, Shan Yun

Materials (Basel)· June 2025

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Alpha lipoamide inhibits diabetic kidney fibrosis via improving mitochondrial function and regulating RXRα expression and activation.
Hui-Fang Zhang, Hui-Ming Liu, Jia-Yi Xiang, Xing-Cheng Zhou, Dan Wang, Rong-Yu Chen

Acta Pharmacol Sin· May 2023

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miR-124-3p improves mitochondrial function of renal tubular epithelial cells in db/db mice.
Luqun Liang, Chunxin Wo, Yao Yuan, Hongjuan Cao, Wanlin Tan, Xingcheng Zhou, Rongyu Chen

FASEB J· March 2023

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Senescent renal tubular epithelial cells activate fibroblasts by secreting Shh to promote the progression of diabetic kidney disease.
Dan Wang, Ling Yin, Rongyu Chen, Wanlin Tan, Luqun Liang, Xingcheng Zhou

Front Med (Lausanne)· January 2023

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Atorvastatin Restores PPARα Inhibition of Lipid Metabolism Disorders by Downregulating miR-21 Expression to Improve Mitochondrial Function and Alleviate Diabetic Nephropathy Progression.
Jiayi Xiang, Huifang Zhang, Xingcheng Zhou, Dan Wang, Rongyu Chen

Front Pharmacol· February 2022

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[Application of SNP-array technology in the genetic analysis of pediatric patients with growth retardation].
Shiyu Luo, Chunyun Fu, Shujie Zhang, Jin Wang, Xin Fan, Rongyu Chen, Shaoke Chen

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· June 2017

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Next-generation sequencing analysis of twelve known causative genes in congenital hypothyroidism.
Xin Fan, Chunyun Fu, Yiping Shen, Chuan Li, Shiyu Luo, Rongyu Chen, Shaoke Chen

Clin Chim Acta· May 2017

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A rare occurrence of two large de novo duplications on 1q42-q44 and 9q21.12-q21.33.
Jin Wang, Chunyun Fu, Shujie Zhang, Jingsi Luo, Luping Ouyang, Rongyu Chen, Shaoke Chen

Gene· December 2016

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Next-generation sequencing analysis of TSHR in 384 Chinese subclinical congenital hypothyroidism (CH) and CH patients.
Chunyun Fu, Jin Wang, Shiyu Luo, Qi Yang, Qifei Li, Rongyu Chen, Shaoke Chen

Clin Chim Acta· November 2016

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[A novel compound heterozygous mutation causing 3-methylcrotonyl-CoA carboxylase deficiency].
Bobo Xie, Jingsi Luo, Yaqin Lei, Rongyu Chen, Jin Wang, Shaoke Chen

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· October 2016

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Mutation screening of the SLC26A4 gene in a cohort of 192 Chinese patients with congenital hypothyroidism.
Chunyun Fu, Haiyang Zheng, Shujie Zhang, Yun Chen, Jiasun Su, Rongyu Chen, Shaoke Chen

Arch Endocrinol Metab· August 2016

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Maternal uniparental disomy 14 and mosaic trisomy 14 in a Chinese boy with moderate to severe intellectual disability.
Shujie Zhang, Haisong Qin, Jin Wang, Luping OuYang, Shiyu Luo, Rongyu Chen, Shaoke Chen

Mol Cytogenet· August 2016

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Next-generation sequencing analysis of DUOX2 in 192 Chinese subclinical congenital hypothyroidism (SCH) and CH patients.
Chunyun Fu, Shiyu Luo, Shujie Zhang, Jin Wang, Haiyang Zheng, Rongyu Chen, Shaoke Chen

Clin Chim Acta· July 2016

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A novel de novo microdeletion at 17q11.2 adjacent to NF1 gene associated with developmental delay, short stature, microcephaly and dysmorphic features.
Bobo Xie, Xin Fan, Yaqin Lei, Rongyu Chen, Jin Wang, Shaoke Chen

Mol Cytogenet· June 2016

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de novo interstitial deletions at the 11q23.3-q24.2 region.
Jiasun Su, Rongyu Chen, Jingsi Luo, Xin Fan, Chunyun Fu, Shaoke Chen

Mol Cytogenet· May 2016

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Mutation screening of the TPO gene in a cohort of 192 Chinese patients with congenital hypothyroidism.
Chunyun Fu, Bobo Xie, Shujie Zhang, Jin Wang, Shiyu Luo, Rongyu Chen, Shaoke Chen

BMJ Open· May 2016

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[Identification of two novel mutations of MUT gene in a Chinese family affected with isolated methylmalonic acidemia].
Bobo Xie, Jingsi Luo, Xin Fan, Rongyu Chen, Jin Wang, Shaoke Chen

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· April 2016

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Persistent and energetic bottom-trapped topographic Rossby waves observed in the southern South China Sea.
Yeqiang Shu, Huijie Xue, Dongxiao Wang, Fei Chai, Qiang Xie, Rongyu Chen, Ju Chen

Sci Rep· April 2016

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SCSPOD14, a South China Sea physical oceanographic dataset derived from in situ measurements during 1919-2014.
Lili Zeng, Dongxiao Wang, Ju Chen, Weiqiang Wang, Rongyu Chen

Sci Data· April 2016

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Hb H Hydrops Fetalis Syndrome Caused by Association of the - -(SEA) Deletion and Hb Constant Spring (HBA2: c.427T > C) Mutation in a Chinese Family.
Sheng He, Chenguang Zheng, Dahua Meng, Rongyu Chen, Qiang Zhang, Shaoke Chen

Hemoglobin· March 2016

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Thyroglobulin gene mutations in Chinese patients with congenital hypothyroidism.
Xuyun Hu, Rongyu Chen, Chunyun Fu, Xin Fan, Jin Wang, Yun Chen, Shaoke Chen

Mol Cell Endocrinol· March 2016

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PAX8 pathogenic variants in Chinese patients with congenital hypothyroidism.
Chunyun Fu, Rongyu Chen, Shujie Zhang, Shiyu Luo, Jin Wang, Yun Chen, Shaoke Chen

Clin Chim Acta· October 2015

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EPHA4 haploinsufficiency is responsible for the short stature of a patient with 2q35-q36.2 deletion and Waardenburg syndrome.
Chuan Li, Rongyu Chen, Xin Fan, Jingsi Luo, Jiale Qian, Shaoke Chen

BMC Med Genet· April 2015

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