Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Yingsi Li"'
Autor:
Meiting Huang, Xiaoming Yan, Yuan Gao, Wenjing Song, Yu Cheng, Luoying Xie, Yingsi Li, Xuecong Zhou, Songlin Yang
Publikováno v:
Heliyon, Vol 10, Iss 17, Pp e36912- (2024)
Introduction: This cross-sectional study was conducted to investigate the impact of type 2 diabetes mellitus(DM) and its duration on indicators such as lid wiper epitheliopathy(LWE), and to assess the significance of LWE for early diagnosis of dry ey
Externí odkaz:
https://doaj.org/article/14f03e0766924b05a10d2961048ec55f
Autor:
Fang Fu, Xin Yang, Ru Li, Yingsi Li, Hang Zhou, Ken Cheng, Ruibin Huang, You Wang, Fei Guo, Lina Zhang, Min Pan, Jin Han, Li Zhen, Lushan Li, Tingying Lei, Dongzhi Li, Can Liao
Publikováno v:
BMC Medical Genomics, Vol 17, Iss 1, Pp 1-10 (2024)
Abstract Background The molecular mechanism of fetal cystic hygroma (CH) is still unclear, and no study has previously reported the transcriptome changes of single cells in CH. In this study, single-cell transcriptome sequencing (scRNA-seq) was used
Externí odkaz:
https://doaj.org/article/9b455270797844668b3ce0cf8eaa49ad
Autor:
Shudi Chen, Yingsi Li, Wenjing Song, Yu Cheng, Yuan Gao, Luoying Xie, Meiting Huang, Xiaoming Yan
Publikováno v:
BMC Ophthalmology, Vol 24, Iss 1, Pp 1-10 (2024)
Abstract Introduction In recent years, insulin eye drops have attracted increasing attention from researchers and ophthalmologists. The aim of this study was to investigate the efficacy and possible mechanism of action of insulin eye drops in diabeti
Externí odkaz:
https://doaj.org/article/4c0e8cb507604b36b2f8a4bd0e05a0f1
Autor:
Yuan Gao, Yu Cheng, Yingsi Li, Luoying Xie, Wenjing Song, Shudi Chen, Meiting Huang, Xiaoming Yan, Songlin Yang
Publikováno v:
BMJ Open, Vol 13, Iss 11 (2023)
Purpose To report a systematic review and meta-analysis of the association between dry eye disease (DED) and dyslipidaemia.Methods PubMed, Embase, Web of Science and Cochrane Library were systematically searched from January 2000 to December 2021. We
Externí odkaz:
https://doaj.org/article/0593ba223d864ade8cc737491f38d3c2
Autor:
Fang Fu, Ru Li, Qiuxia Yu, Dan Wang, Qiong Deng, Lushan Li, Tingying Lei, Guilan Chen, Zhiqiang Nie, Xin Yang, Jin Han, Min Pan, Li Zhen, Yongling Zhang, Xiangyi Jing, Fucheng Li, Fatao Li, Lina Zhang, Cuixing Yi, Yingsi Li, Yan Lu, Hang Zhou, Ken Cheng, Jian Li, Lina Xiang, Jing Zhang, Sha Tang, Ping Fang, Dongzhi Li, Can Liao
Publikováno v:
Genome Medicine, Vol 14, Iss 1, Pp 1-20 (2022)
Abstract Background Exome sequencing (ES) is becoming more widely available in prenatal diagnosis. However, data on its clinical utility and integration into clinical management remain limited in practice. Herein, we report our experience implementin
Externí odkaz:
https://doaj.org/article/9017e03aca3941f79ba8d55459ae1e83
Autor:
Ruibin Huang, Hang Zhou, Fang Fu, Ru Li, Tingying Lei, Yingsi Li, Ken Cheng, You Wang, Xin Yang, Lushan Li, Xiangyi Jing, Yongling Zhang, Fucheng Li, Dongzhi Li, Can Liao
Publikováno v:
Molecular Cytogenetics, Vol 15, Iss 1, Pp 1-6 (2022)
Abstract Background There are a few literature reports of prenatal ultrasound manifestations of Williams-Beuren syndrome. We aimed to explore the prenatal diagnosis of Williams-Beuren syndrome by ultrasound and chromosomal microarray analysis and des
Externí odkaz:
https://doaj.org/article/fd6360d149a34d9ba2b2c451eebbd8f8
Autor:
Guilan Chen, Hang Zhou, Yan Lu, You Wang, Yingsi Li, Jiaxin Xue, Ken Cheng, Ruibin Huang, Jin Han
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
The clinical features of the PCDH19 gene mutation include febrile epilepsy ranging from mild to severe, with or without intellectual disability, cognitive impairment, and psych-behavioral disorders, but there has been little research on males with th
Externí odkaz:
https://doaj.org/article/c78bd5603ddf40ce980a814ba2c985dc
Autor:
Luoying Xie, Wenjing Song, Wenhui Dong, Yingsi Li, Shudi Chen, Xiaona Sun, Meiting Huang, Yu Cheng, Yuan Gao, Songlin Yang, Xiaoming Yan
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
PurposeTo investigate the indirect effects of intense pulsed light (IPL) on morphological and pathological changes of the meibomian glands (MGs) in apolipoprotein E knockout (ApoE–/–) mice and explore the underlying mechanisms.MethodsApoE–/–
Externí odkaz:
https://doaj.org/article/438938ec6b9342e8a975a6f0bae74bbd
Autor:
Hang Zhou, Ken Cheng, Yingsi Li, Fang Fu, Ru Li, Yongling Zhang, Xin Yang, Xiangyi Jing, Fucheng Li, Jin Han, Min Pan, Li Zhen, Dongzhi Li, Can Liao
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Objective: To evaluate the utility of a chromosomal microarray (CMA) in fetuses with isolated fetal growth restriction (FGR) and explore risk factors for the prediction of chromosomal aberration and perinatal adverse outcomes.Method: This study inclu
Externí odkaz:
https://doaj.org/article/a6df5a07d67b4701acb5718f1dad9633
Case Report: Two Novel L1CAM Mutations in Two Unrelated Chinese Families With X-Linked Hydrocephalus
Autor:
Hang Zhou, Qiuxia Yu, Yingsi Li, Fang Fu, Ru Li, Guilan Chen, Dan Wang, Yan Lu, Xin Yang, Dongzhi Li, Can Liao
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
L1 cell adhesion molecule is a type I transmembrane glycoprotein belonging to the immunoglobulin superfamily. Pathogenic mutations of L1CAM can cause L1 syndrome, referred to as a variety of disease spectrums characterized by hydrocephalus. In the pr
Externí odkaz:
https://doaj.org/article/11bc3b449958437082f0aaf510571cb3