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Frontiers in Physiology|April 23, 2026
Integration of neutrophil to high-density lipoprotein ratio for prognostic assessment of nasopharyngeal carcinoma: a large-scale long-term retrospective studyNan-Jun Chen, Xu-Xin Lin, Rui-Xin Cheng, et al.Frontiers in Nutrition|March 14, 2022
Multi-Omic Analysis in a Metabolic Syndrome Porcine Model Implicates Arachidonic Acid Metabolism Disorder as a Risk Factor for AtherosclerosisSong-Song Xu, Xiu-Ling Zhang, Sha-Sha Liu, et al.Brain, Behavior, and Immunity|November 14, 2025
SARS-CoV-2 spike protein induces depressive-like behaviors by disrupting astrocytic Cx43-mediated gap junction intercellular communicationRuo-Lan Yuan, Sha-Sha Wang, Pei-Yi Li, et al.Journal of Affective Disorders|May 16, 2026
Adverse childhood experiences and mental health symptoms among aviation shift workers in China: A national cohort studyRuihan Li, Ya Su, Lin Zhang, et al.Plos One|April 29, 2015
Identification of Two Novel Compound Heterozygous PTPRQ Mutations Associated with Autosomal Recessive Hearing Loss in a Chinese FamilyXue Gao, Yu Su, Yu-Lan Chen, et al.Vascular Pharmacology|July 19, 2015
Salidroside improves endothelial function and alleviates atherosclerosis by activating a mitochondria-related AMPK/PI3K/Akt/eNOS pathwaySha-Sha Xing, Xiao-Yan Yang, Tao Zheng, et al.Oncogene|January 16, 2019
Genome-wide screening identifies oncofetal lncRNA Ptn-dt promoting the proliferation of hepatocellular carcinoma cells by regulating the Ptn receptorJin-Feng Huang, Hong-Yue Jiang, Hui Cai, et al.JCI Insight|April 7, 2026
Norepinephrinergic projection from locus coeruleus to parafascicular nucleus promotes pain and anxiety-like behaviors in miceZhong-Yi Liu, Fei Li, Li-Ming Liu, et al.International Journal of Oncology|April 11, 2019
Cathepsin B defines leader cells during the collective invasion of salivary adenoid cystic carcinomaJia-Shun Wu, Zhu-Feng Li, Hao-Fan Wang, et al.BMC Medical Genomics|November 19, 2022
Addition of an affected family member to a previously ascertained autosomal recessive nonsyndromic hearing loss pedigree and systematic phenotype-genotype analysis of splice-site variants in MYO15AJin-Yuan Yang, Wei-Qian Wang, Ming-Yu Han, et al.Pageof 154