Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Qiu-Xia Yu"'
Publikováno v:
Chinese Medicine, Vol 19, Iss 1, Pp 1-15 (2024)
Abstract Background Psoriasis is a long-term inflammatory skin disease. A novel herbal formula containing nine Chinese herbal medicines, named Inflammation Skin Disease Formula (ISDF), has been prescribed in clinics for decades. Aims To investigate t
Externí odkaz:
https://doaj.org/article/2479e25c1f204724a7411a589e581cb5
Autor:
Fang Fu, Ru Li, Qiu-Xia Yu, Xiao Dang, Shu-Juan Yan, Hang Zhou, Ken Cheng, Rui-Bin Huang, You Wang, Yong-Ling Zhang, Xiang-Yi Jing, Li-Na Zhang, Dong-Zhi Li, Can Liao
Publikováno v:
Genes, Vol 13, Iss 12, p 2365 (2022)
Currently, there are still many challenges in prenatal diagnosis, such as limited or uncertain fetal phenotyping, variant interpretation, and rapid turnaround times. The aim of this study was to illustrate the value of a comprehensive genomic evaluat
Externí odkaz:
https://doaj.org/article/83205c2e3ae2493eb76ddcb5e4865304
Autor:
Qiu-Xia Yu, Hong Zhang, Wen-Hui Xu, Fei Hao, Su-Lai Liu, Meng-Meng Bai, Jia-Wei Mu, Hui-Juan Zhang
Publikováno v:
Kidney & Blood Pressure Research, Vol 40, Iss 5, Pp 467-477 (2015)
Background/Aims: Chemerin was introduced as a novel adipokine that plays a crucial role in insulin signaling and diabetic nephropathy. Serum chemerin levels are significantly elevated in type 2 diabetes patients with macroalbuminuria. However, the un
Externí odkaz:
https://doaj.org/article/60680df0488946aaa055351c17f00aec
Publikováno v:
European Journal of Obstetrics & Gynecology and Reproductive Biology. 284:16-19
Autor:
Fang Fu, Chen Chen, Kun Du, Lu-shan Li, Ru Li, Ting-ying Lei, Qiong Deng, Dan Wang, Qiu-xia Yu, Xin Yang, Jin Han, Min Pan, Li Zhen, Li-na Zhang, Jian Li, Fa-tao Li, Yong-ling Zhang, Xiang-yi Jing, Fu-cheng Li, Dong-zhi Li, Can Liao
Publikováno v:
Molecular Neurobiology. 60:2986-3003
The Dandy–Walker malformation (DWM) is characterized by neuron dysregulation in embryonic development; however, the regulatory mechanisms associated with it are unclear. This study aimed to investigate the role of NADH dehydrogenase 1 alpha subcomp
Publikováno v:
Hemoglobin. 46:347-350
Publikováno v:
Molecular Syndromology. 14:59-64
Introduction: HNF1B-associated diseases are a group of genetic conditions that affect the kidney as well as other organ systems. Kidney anomalies are the most common symptoms. Other defects may include early-onset diabetes, genital abnormalities, and
Autor:
Ting‐ying Lei, Qin She, Fang Fu, Li Zhen, Ru Li, Qiu‐xia Yu, Dan Wang, Ying‐si Li, Ken Cheng, Hang Zhou, Xin Yang, Min Pan, Dong‐zhi Li, Can Liao
Publikováno v:
Prenatal Diagnosis. 42:744-752
We aimed to investigate the value of exome sequencing (ES) in fetuses with callosal anomalies (CA) with or without other structural anomalies, but with normal findings by karyotyping and chromosome microarray analysis (CMA).Cases with CA with or with
Publikováno v:
Prenatal diagnosisREFERENCES. 42(13)
To examine the diagnostic yield of exome sequencing (ES) in singleton pregnancies with isolated fetal clubfoot.Clinical data from singleton pregnancies with a sonographic diagnosis of isolated clubfoot and ES results between 2018 and 2021 were retros
Publikováno v:
European Journal of Obstetrics & Gynecology and Reproductive Biology. 282:170-171