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Gene|December 28, 2024
Loss-of-function SLC25A20 variant causes carnitine-acylcarnitine translocase deficiency by reducing SLC25A20 protein stabilityZhongzhi Gan, Xiaofeng Wei, Yingchun Zheng, et al.
Biomarkers in Medicine|September 24, 2020
Prognostic value of endogenous and exogenous metabolites in liver transplantationXiao-Fu Xiong, Ding-Ding Chen, Huai-Jun Zhu, et al.
Infection and Drug Resistance|July 11, 2019
Rapid simultaneous detection of <i>bla</i> <sub>oxa-23</sub>, <i>Ade-B, int-1,</i> and <i>ISCR-1</i> in multidrug-resistant <i>Acinetobacter baumannii</i> using single-tube multiplex PCR and high resolution melting assayHengbiao Sun, Gang Xiao, Jing Zhang, et al.
AI Zheng = Aizheng = Chinese Journal of Cancer|November 30, 2004
[Clinical featares and treatment principles of appendix carcinoid tumor: a report of 13 cases]Qing-An Zeng, Hai-Yan Pan, Da-Fu Xiong, et al.
Anti-Cancer Drugs|June 13, 2025
Progression of drug resistance or multiple primary lung cancer: a case report and literature review of a patient with mesenchymal-epithelial transition factor exon 14 skipping alterations lung adenocarcinomaLiang Gong, Lihang Zhou, Pan Yang, et al.
BMC Medical Genetics|February 9, 2017
A novel, complex RUNX2 gene mutation causes cleidocranial dysplasiaWen'an Xu, Qiuyue Chen, Cuixian Liu, et al.
Frontiers in Pediatrics|February 13, 2023
The molecular mechanism of Gaucher disease caused by compound heterozygous mutations in <i>GBA1</i> geneQi Liu, Zongrui Shen, Hong Pan, et al.
European Radiology|June 21, 2024
Longitudinal investigation of undergraduates' radiation anxiety, interest, and career intention in interventional radiologyYanyan Cao, Li Yu, Fu Xiong, et al.
Human Mutation|April 20, 2026
A De Novo Mutation (c.2423A>G) in <i>SAMD9</i> Causing MIRAGE Syndrome With Intrauterine Growth Retardation and Renal Hypoplasia in a Chinese FamilyYuxin Huang, Jiahui Fu, Zhongzhi Gan, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 10, 2016
[Screening of CTSC gene mutations in a Chinese pedigree affected with Papillon-Lefevre syndrome]Cuixian Liu, Zhihui Tian, Qi Yang, et al.
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