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Neuroscience Letters|August 30, 2024
Single-nucleus RNA-sequencing of orbitofrontal cortex in rat model of methamphetamine-induced sensitizationQiong Li, Zhi-Peng Yu, Yan-Guo Li, et al.
Small (Weinheim an Der Bergstrasse, Germany)|November 24, 2025
Electronic Backflow Through Oxygen Bridge in RuO<sub>x</sub>-Graphdiyne for Stable Acidic Water OxidationYong Feng, Lisheng Qian, Kun Feng, et al.
Clinical and Vaccine Immunology : CVI|June 29, 2007
Type IVB pilus operon promoter controlling expression of the severe acute respiratory syndrome-associated coronavirus nucleocapsid gene in Salmonella enterica Serovar Typhi elicits full immune response by intranasal vaccinationFengling Luo, Yong Feng, Min Liu, et al.
Zhonghua Wai Ke Za Zhi [Chinese Journal of Surgery]|September 15, 2004
[Analysis of rejection after simultaneous pancreas-kidney transplantation]Lei Yang, Yong-Feng Liu, Shu-Rong Liu, et al.
Stem Cell Research|September 20, 2022
Establishment of two iPSC lines from healthy donor with heterozygous mutation in the SLC26A4 geneSiJun Li, Chufeng He, Qi Feng, et al.
Frontiers in Oncology|December 31, 2021
Modelled Economic Analysis for Dacomitinib-A Cost Effectiveness Analysis in Treating Patients With EGFR-Mutation-Positive Non-Small Cell Lung Cancer in ChinaYong-Feng Yu, Luan Luan, Fan-Fan Zhu, et al.
Analytical Chemistry|October 12, 2022
Novel <i>Meso</i>-Benzothiazole-Substituted BODIPY-Based AIE Fluorescent Rotor for Imaging Lysosomal Viscosity and Monitoring AutophagyWen-Jing Shi, Ru Chen, Jinrong Yang, et al.
Biochemical and Biophysical Research Communications|May 3, 2011
Novel mutations in the SOX10 gene in the first two Chinese cases of type IV Waardenburg syndromeLu Jiang, Hongsheng Chen, Wen Jiang, et al.
BMC Infectious Diseases|March 19, 2013
Cryptococcosis of lumbar vertebra in a patient with rheumatoid arthritis and scleroderma: case report and literature reviewHeng-Xing Zhou, Guang-Zhi Ning, Shi-Qing Feng, et al.
Plos One|April 12, 2019
A rapid improved multiplex ligation detection reaction method for the identification of gene mutations in hereditary hearing lossYalan Liu, Chang Hu, Chang Liu, et al.
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