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Orphanet Journal of Rare Diseases|May 26, 2023
Clinical and genetic characteristics of 42 Chinese paediatric patients with X-linked adrenal hypoplasia congenitaWanqi Zheng, Ying Duan, Yu Xia, et al.
The Journal of Molecular Diagnostics : JMD|July 25, 2025
Additional Diagnostic Yield through the Analysis of Short Tandem Repeats Based on Exome Sequencing DataShiyi Xu, Xiaomei Luo, Bing Xiao, et al.
Nanoscale Research Letters|March 12, 2017
A Rapid Detection Method of Brucella with Quantum Dots and Magnetic Beads Conjugated with Different Polyclonal AntibodiesDandan Song, Xiaofeng Qu, Yushen Liu, et al.
Journal of Clinical Anesthesia|March 28, 2025
Effect of esketamine on postoperative depression in women with breast cancer and preoperative depressive symptoms: The EASE randomized trialQingfeng Wei, Mengmeng Li, Qiuling Du, et al.
Iscience|May 2, 2023
Lithium ameliorates Niemann-Pick C1 disease phenotypes by impeding STING/SREBP2 activationShiqian Han, Qijun Wang, Yongfeng Song, et al.
Gels (Basel, Switzerland)|May 27, 2026
Natural-Origin Bioadhesive Injectable Hydrogels Composed of Polyphenol and Chitosan with Antibacterial Activity for Wound HealingHongyu Zheng, Shikui Wu, Yujie Liu, et al.
Journal of Medical Genetics|August 16, 2023
Genetic and phenotypic spectrum of non-21-hydroxylase-deficiency primary adrenal insufficiency in childhood: data from 111 Chinese patientsYing Duan, Wanqi Zheng, Yu Xia, et al.
Prenatal Diagnosis|July 7, 2019
Prenatal diagnosis of methylmalonic aciduria from amniotic fluid using genetic and biochemical approachesXing Ji, Huanhuan Wang, Jun Ye, et al.
Anesthesiology|January 26, 2026
The role of preoptic area GABAergic neurons in distinctly regulating sleep and rousability under dexmedetomidine sedation in miceGaolin Qiu, Peng Wang, Zhilai Yang, et al.
Gene|May 19, 2019
In vitro residual activities in 20 variants of phenylalanine hydroxylase and genotype-phenotype correlation in phenylketonuria patientsXia Zhang, Jun Ye, Nan Shen, et al.
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