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Neuropharmacology|November 3, 2024
Microglia phagocytosis of PNNs mediates PV-positive interneuron dysfunction and associated gamma oscillations in neuroinflammation-induced cognitive impairment in miceKai Liu, Yu-Zhu Gao, Xin-Miao Wu, et al.Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|August 4, 2020
Longitudinal Dynamics of the Neutralizing Antibody Response to Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) InfectionKai Wang, Quan-Xin Long, Hai-Jun Deng, et al.Journal of Environmental Sciences (China)|December 29, 2025
Dietary metal(loid)s exposure and their health risks to patients with gastric precancerous lesions and gastric cancer in Anhui Province, Eastern ChinaMengran Ke, Qingsong Jiang, Yan Zhu, et al.Plos One|August 6, 2015
Diagnostic Accuracy of Natriuretic Peptides for Heart Failure in Patients with Pleural Effusion: A Systematic Review and Updated Meta-AnalysisZhi-Jun Han, Xiao-Dan Wu, Juan-Juan Cheng, et al.Urology|September 7, 2012
Activation of VEGF and ERK1/2 and improvement of urethral function by adipose-derived stem cells in a rat stress urinary incontinence modelGuang-Yong Li, Feng Zhou, Yan-Qing Gong, et al.Zhongguo Zhong Yao Za Zhi = Zhongguo Zhongyao Zazhi = China Journal of Chinese Materia Medica|February 28, 2006
[Effect of glucocorticoid with traditional Chinese medicine in severe acute aespiratory syndrome (SARS)]Bao-yan Liu, Li-yun He, Zhi-wei Liang, et al.Frontiers in Genetics|April 3, 2025
Clinical genetic analysis of an adult polyglucosan body disease (APBD) family caused by the compound heterozygous variant of GBE1 p.R156C and deletion exon 3-7Juan Zhu, Hong-Ping Yu, Jing Zou, et al.Scientific Reports|July 9, 2025
Genetic analysis of a novel TSC1 splice mutation causing tuberous sclerosis without neurological phenotypesXiu-Juan Yao, Ying Lin, Jing Zou, et al.Journal of the American Heart Association|July 29, 2020
Macrophage NCOR1 Deficiency Ameliorates Myocardial Infarction and Neointimal Hyperplasia in MiceLin-Juan Du, Jian-Yong Sun, Wu-Chang Zhang, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|August 18, 2024
A novel stoploss mutation CYB5R3 c.906A>G(p.*302Trpext*42) involved in the pathogenesis of hereditary methemoglobinemiaKai-Ying He, Hong-Ping Yu, Jing Zou, et al.Pageof 13