Works by Yu, Hong‐Ping

Results: 18

Genetic and clinical insights into acute kidney injury in maturity-onset diabetes of the young caused by the ABCC8 c.2500C>T mutation: Potential risk factors associated with SGLT2 inhibitors.

Published in:

Experimental & Therapeutic Medicine, 2025, v. 30, n. 2, p. N.PAG, doi. 10.3892/etm.2025.12914

By:

Zou, Jing;
Chen, Xiang;
Yu, Hong-Ping;
Chen, Ying;
He, Kai-Ying;
Ruan, Dan-Dan;
Zhu, Juan;
Chen, Qian;
Zhang, Jian-Hui;
Zhang, Li;
Gan, Yu-Mian;
Gao, Mei-Zhu;
Chen, Li;
Liang, Ji-Xing;
Wu, Tian-Min;
Liao, Li-Sheng;
Luo, Jie-Wei

Publication type:

Article

Genetic analysis of a novel TSC1 splice mutation causing tuberous sclerosis without neurological phenotypes.

Published in:

Scientific Reports, 2025, v. 15, n. 1, p. 1, doi. 10.1038/s41598-025-07906-6

By:

Yao, Xiu-juan;
Lin, Ying;
Zou, Jing;
Cai, Zun-lin;
Xu, Zi-Yan;
Li, Xiao-qin;
Chen, Qian;
Yu, Hong-ping;
Zhang, Jian-hui;
Ruan, Dan-dan;
Gao, Mei-zhu;
Zhang, Li;
Luo, Jie-wei;
Xie, Bao-song

Publication type:

Article

Association between polymorphisms in MicroRNA target sites of RAD51D genes and risk of hepatocellular carcinoma.

Published in:

Cancer Medicine, 2019, v. 8, n. 5, p. 2545, doi. 10.1002/cam4.2068

By:

Jiang, Yan‐Ji;
Zhong, Jian‐Hong;
Zhou, Zi‐Han;
Qiu, Mo‐Qin;
Zhou, Xian‐Guo;
Liu, Ying‐Chun;
Huo, Rong‐Rui;
Liang, Xiu‐Mei;
Chen, Zhu;
Lin, Qiu‐Ling;
Yu, Xiang‐Yuan;
Yu, Hong‐Ping

Publication type:

Article

Clinical genetic analysis of an adult polyglucosan body disease (APBD) family caused by the compound heterozygous variant of GBE1 p.R156C and deletion exon 3-7.

Published in:

Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1514610

By:

Zhu, Juan;
Yu, Hong-Ping;
Zou, Jing;
Zhang, Yi-Wu;
Han, Xin-Qi;
Xu, Zi-Yan;
Chen, Li;
Chen, Qian;
Gao, Mei-Zhu;
Xie, Li-Jun;
Zhang, Xi-Kui;
Luo, Jie-Wei;
Li, Yun-Fei;
Zhang, Li

Publication type:

Article

Expression of cyclooxygenase-2 (COX-2) in human esophageal cancer and in vitro inhibition by a specific COX-2 inhibitor, NS-398.

Published in:

Journal of Gastroenterology & Hepatology, 2004, v. 19, n. 6, p. 638, doi. 10.1111/j.1440-1746.2004.03345.x

By:

Yu, Hong-ping;
Shi, Lu-Yuan;
Lu, Wen-Hong;
Su, Yan-Hua;
Li, Yuan-Yuan;
Xu, Shun-Qing

Publication type:

Article

Dural sac cross-sectional area is a highly effective parameter for spinal anesthesia in geriatric patients undergoing transurethral resection of the prostate: a prospective, double blinded, randomized study.

Published in:

BMC Anesthesiology, 2020, v. 20, n. 1, p. 1, doi. 10.1186/s12871-020-01059-x

By:

Wang, Wei Bing;
Sun, Ai Jiao;
Yu, Hong Ping;
Dong, Jing Chun;
Xu, Huang

Publication type:

Article

Analysis of low-density lipoprotein receptor gene mutations in a family with familial hypercholesterolemia.

Published in:

PLoS ONE, 2024, v. 19, n. 10, p. 1, doi. 10.1371/journal.pone.0310547

By:

Hu, Ya-nan;
Wu, Min;
Yu, Hong-ping;
Wu, Qiu-yan;
Chen, Ying;
Zhang, Jian-Hui;
Ruan, Dan-dan;
Zhang, Yan-ping;
Zou, Jing;
Zhang, Li;
Lin, Xin-fu;
Fang, Zhu-ting;
Liao, Li-Sheng;
Lin, Fan;
Li, Hong;
Luo, Jie-Wei

Publication type:

Article

Adult type I Gaucher disease with splenectomy caused by a compound heterozygous GBA1 mutation in a Chinese patient: a case report.

Published in:

Annals of Hematology, 2024, v. 103, n. 5, p. 1765, doi. 10.1007/s00277-024-05710-2

By:

Zhang, Jian-hui;
Chen, Hui;
Ruan, Dan-dan;
Chen, Ying;
Zhang, Li;
Gao, Mei-zhu;
Chen, Qian;
Yu, Hong-ping;
Wu, Jia-yi;
Lin, Xin-fu;
Fang, Zhu-ting;
Zheng, Xiao-ling;
Luo, Jie-wei;
Liao, Li-sheng;
Li, Hong

Publication type:

Article

Correction to: Pedigree Analysis of Nonclassical Cholesteryl Ester Storage Disease with Dominant Inheritance in a LIPA I378T Heterozygous Carrier.

Published in:

2025

By:

Zhang, Jian-hui;
Lin, Ai-ping;
Zhang, Li;
Ruan, Dan-dan;
Gao, Mei-zhu;
Chen, Qian;
Yu, Hong-ping;
Liao, Li-sheng;
Lin, Xin-fu;
Fang, Zhu-ting;
Lin, Fan;
Lu, Shi-yun;
Luo, Jie-wei;
Zheng, Xiao-ling;
Chen, Meng-shi

Publication type:

Correction Notice

Pedigree Analysis of Nonclassical Cholesteryl Ester Storage Disease with Dominant Inheritance in a LIPA I378T Heterozygous Carrier.

Published in:

Digestive Diseases & Sciences, 2024, v. 69, n. 6, p. 2109, doi. 10.1007/s10620-024-08395-9

By:

Zhang, Jian-hui;
Lin, Ai-ping;
Zhang, Li;
Ruan, Dan-dan;
Gao, Mei-zhu;
Chen, Qian;
Yu, Hong-ping;
Liao, Li-sheng;
Lin, Xin-fu;
Fang, Zhu-ting;
Lin, Fan;
Lu, Shi-yun;
Luo, Jie-wei;
Zheng, Xiao-ling;
Chen, Meng-shi

Publication type:

Article

A novel splicing mutation DNAH5 c.13,338 + 5G > C is involved in the pathogenesis of primary ciliary dyskinesia in a family with primary familial brain calcification.

Published in:

BMC Pulmonary Medicine, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12890-024-03164-w

By:

Yao, Xiu-juan;
Chen, Qian;
Yu, Hong-ping;
Ruan, Dan-dan;
Li, Shi-jie;
Wu, Min;
Liao, Li-sheng;
Lin, Xin-fu;
Fang, Zhu-ting;
Luo, Jie-wei;
Xie, Bao-song

Publication type:

Article

Case report: a rare concurrence of dense deposit disease in an adolescent patient with IgA nephropathy.

Published in:

BMC Pediatrics, 2025, v. 25, n. 1, p. 1, doi. 10.1186/s12887-025-05415-z

By:

Zhang, Jian-Hui;
Yu, Hong-Ping;
Chen, Ying;
Chen, Qian;
Zheng, Xiao-Ling;
Luo, Jie-Wei;
Zhang, Li

Publication type:

Article

Diagnostic journey and genetic analysis of a novel homozygous CYP2U1 mutation causing autosomal recessive spastic paraplegia type 56 (SPG56) in a consanguineous family.

Published in:

2025

By:

Yu, Hong-ping;
Zou, Jing;
Chen, Xiang;
Chen, Ying;
Ruan, Dan-dan;
Chen, Qian;
Zhang, Jian-hui;
Cheng, Qiong;
Ruan, Xing-lin;
Wen, Wei;
Chen, Li;
Luo, Jie-wei;
Li, Yun-fei;
Jiang, Xiao-lin

Publication type:

Case Study

Clinical implications and biological features of a novel postoperative recurrent HCC classification: A multi‐centre study.

Published in:

Liver International, 2022, v. 42, n. 10, p. 2283, doi. 10.1111/liv.15363

By:

Qi, Lu‐Nan;
Ma, Liang;
Wu, Fei‐Xiang;
Chen, Yuan‐Yuan;
Xu, Jing‐Xuan;
Peng, Yu‐Chong;
Chen, Zu‐Shun;
Gong, Wen‐Feng;
Yang, Cheng‐Lei;
Wei, Hao‐Wen;
Qin, Shui‐Ling;
Shang, Jin‐Jie;
Wang, Qiu‐Yan;
Yu, Hong‐Ping;
Peng, Tao;
Huang, Ying‐Wu;
Ling, Yong‐Chi;
Tang, Wei‐Zhong;
Xiang, Bang‐De;
Li, Le‐Qun

Publication type:

Article

Polymorphisms in the XPG gene and risk of gastric cancer in Chinese populations.

Published in:

Human Genetics, 2012, v. 131, n. 7, p. 1235, doi. 10.1007/s00439-012-1152-8

By:

He, Jing;
Qiu, Li-Xin;
Wang, Meng-Yun;
Hua, Rui-Xi;
Zhang, Ruo-Xin;
Yu, Hong-Ping;
Wang, Ya-Nong;
Sun, Meng-Hong;
Zhou, Xiao-Yan;
Yang, Ya-Jun;
Wang, Jiu-Cun;
Jin, Li;
Wei, Qing-Yi;
Li, Jin

Publication type:

Article

Genetic variations of mTORC1 genes and risk of gastric cancer in an eastern chinese population.

Published in:

Molecular Carcinogenesis, 2013, v. 52, p. 70, doi. 10.1002/mc.22013

By:

He, Jing;
Wang, Meng‐Yun;
Qiu, Li‐Xin;
Zhu, Mei‐Ling;
Shi, Ting‐Yan;
Zhou, Xiao‐Yan;
Sun, Meng‐Hong;
Yang, Ya‐Jun;
Wang, Jiu‐Cun;
Jin, Li;
Wang, Ya‐Nong;
Li, Jin;
Yu, Hong‐Ping;
Wei, Qing‐Yi

Publication type:

Article

Transmission and evolution of OXA-48-producing Klebsiella pneumoniae ST11 in a single hospital in Taiwan.

Published in:

2020

By:

Lu, Min-Chi;
Chen, Ying-Tsong;
Tang, Hui-Ling;
Liu, Yen-Yi;
Chen, Bo-Han;
Wang, You-Wun;
Chen, Yi-Syong;
Teng, Ru-Hsiou;
Hong, Yu-Ping;
Chiou, Chien-Shun;
Chiang, Ming-Ko;
Lai, Yi-Chyi

Publication type:

journal article

Radiotherapy plus anti-PD1 versus radiotherapy for hepatic toxicity in patients with hepatocellular carcinoma.

Published in:

Radiation Oncology, 2023, v. 18, n. 1, p. 1, doi. 10.1186/s13014-023-02309-1

By:

Zhang, Rui-Jun;
Zhou, Hong-Mei;
Lu, Hai-Yan;
Yu, Hong-Ping;
Tang, Wei-Zhong;
Qiu, Mo-Qin;
Yan, Liu-Ying;
Long, Mei-Ying;
Su, Ting-Shi;
Xiang, Bang-De;
He, Mei-Ling;
Wang, Xiao-Ting;
Liang, Shi-Xiong;
Li, Jian-Xu

Publication type:

Article