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Acta Pharmacologica Sinica|June 7, 2018
Identification of predominant GNPTAB gene mutations in Eastern Chinese patients with mucolipidosis II/III and a prenatal diagnosis of mucolipidosis IIYu Wang, Jun Ye, Wen-Juan Qiu, et al.
World Journal of Pediatrics : WJP|May 8, 2014
Clinical features and mutations in seven Chinese patients with very long chain acyl-CoA dehydrogenase deficiencyRui-Nan Zhang, Yi-Fan Li, Wen-Juan Qiu, et al.
Oncotarget|November 5, 2017
Up-regulation of IRF-3 expression through GATA-1 acetylation by histone deacetylase inhibitor in lung adenocarcinoma A549 cellsLu-Lu Wang, Lan-Bo Zhou, Jin Shu, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 6, 2023
Low-density lipoprotein triglyceride predicts outcomes in patients with chronic coronary syndrome following percutaneous coronary intervention according to inflammatory statusHui-Wen Zhang, Yuan-Lin Guo, Na-Qiong Wu, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|October 15, 2013
[Analysis of GALNS gene mutation in thirty-eight Chinese patients with mucopolysaccharidosis type IVA]Jun Ye, Hong-lin Lei, Hui-wen Zhang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 7, 2011
[Application of enzyme assay and gene analysis in the prenatal diagnosis for a family with glycogen storage disease type II]Min-hui Zeng, Wen-juan Qiu, Xue-fan Gu, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|April 30, 2010
[Clinical diagnosis and WISP3 gene mutation analysis for progressive pseudorheumatoid dysplasia]Jun Ye, Hui-wen Zhang, Tong Wang, et al.
Personalized Medicine|October 27, 2018
Oxidized-LDL is a useful marker for predicting the very early coronary artery disease and cardiovascular outcomesXi Zhao, Hui-Wen Zhang, Rui-Xia Xu, et al.
World Neurosurgery|April 7, 2023
Posterior Atlantoaxial Fusion With C1-2 Pedicle Screw Fixation for Atlantoaxial Dislocation in Pediatric Patients With Mucopolysaccharidosis IVA (Morquio a Syndrome): A Case SeriesHai-Tao Liu, Zhi-Hui Liang, Jia Song, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|December 23, 2008
[Diagnosis, treatment and gene mutation analysis of the first case with dihydropteridine reductase deficiency in the mainland of China]Jun Ye, Wen-juan Qiu, Lian-shu Han, et al.
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