Jing Chen

发表

Genomic characterisation and epidemiology of 2019 novel coronavirus: implications for virus origins and receptor binding

E. Holmes, Honglong Wu, G. Gao, 2020, The Lancet.

C-terminus of OX2R significantly affects downstream signaling pathways

Jing Chen, Bo Bai, Chunmei Wang, 2017, Molecular medicine reports.

Roles for heterodimerization of APJ and B2R in promoting cell proliferation via ERK1/2-eNOS signaling pathway.

Jing Chen, L. Wan, Bao-hua Cheng, 2020, Cellular signalling.

Dual-agonist occupancy of orexin receptor 1 and cholecystokinin A receptor heterodimers decreases G-protein-dependent signaling and migration in the human colon cancer cell line HT-29.

Jing Chen, Bo Bai, Rumin Zhang, 2017, Biochimica et biophysica acta. Molecular cell research.

Novel signaling of dynorphin at κ-opioid receptor/bradykinin B2 receptor heterodimers.

Jing Chen, Bo Bai, Rumin Zhang, 2017, Cellular signalling.

Global gene expression profile of cerebral ischemia-reperfusion injury in rat MCAO model

Jing Chen, Bo Bai, Chunmei Wang, 2017, Oncotarget.

Studies of the interaction between Aloe-emodin and DNA and preparation of DNA biosensor for detection of PML-RARalpha fusion gene in acute promyelocytic leukemia.

Jing Chen, Xinhua Lin, H. Wan, 2008, Talanta.

Valosin-containing protein is associated with maintenance of meiotic arrest in mouse oocytes†.

Jing Chen, Yanyan Zhang, Jianchao Huo, 2018, Biology of reproduction.

A novel phosphorylation site on orexin receptor 1 regulating orexinA-induced GRK2-biased signaling.

Jing Chen, Zhen Zhang, Huannan Wang, 2020, Cellular signalling.

Orexin-A protects against cerebral ischemia-reperfusion injury by inhibiting excessive autophagy through OX1R-mediated MAPK/ERK/mTOR pathway.

Jing Chen, Bao-hua Cheng, Chunmei Wang, 2020, Cellular signalling.

Individual phosphorylation sites at the C-terminus of the apelin receptor play different roles in signal transduction

Jing Chen, Maocai Yan, Rumin Zhang, 2020, Redox biology.

(Pro)renin receptor involves in myocardial fibrosis and oxidative stress in diabetic cardiomyopathy via the PRR–YAP pathway

Jing Chen, Q. Su, Bo Dong, 2021, Scientific Reports.

Label-free electrochemical biosensor using home-made 10-methyl-3-nitro-acridone as indicator for picomolar detection of nuclear factor kappa B.

Jing Chen, Jing Zhang, Shuxian Cai, 2014, Biosensors & bioelectronics.

Orexin-A protects against oxygen-glucose deprivation/reoxygenation-induced cell damage by inhibiting endoplasmic reticulum stress-mediated apoptosis via the Gi and PI3K signaling pathways.

Jing Chen, Bao-hua Cheng, Chunmei Wang, 2019, Cellular signalling.

Orexin-A alleviates astrocytic apoptosis and inflammation via Inhibiting OX1R-mediated NF-κB and MAPK signaling pathways in cerebral ischemia/reperfusion injury.

Jing Chen, Rumin Zhang, Q. Kong, 2021, Biochimica et biophysica acta. Molecular basis of disease.

The transmembrane domains of GPCR dimers as targets for drug development.

Jing Chen, Rumin Zhang, Yanchun Chen, 2022, Drug discovery today.

Apelin-13 prevents the effects of oxygen–glucose deprivation/reperfusion on bEnd.3 cells by inhibiting AKT–mTOR signaling

Jing Chen, Rumin Zhang, Bao-hua Cheng, 2022, Experimental biology and medicine.

Neuroprotection of microRNA in neurological disorders (Review).

Jing Chen, Bo Bai, Bao-hua Cheng, 2014, Biomedical reports.

Orexin-A alleviates cerebral ischemia-reperfusion injury by inhibiting endoplasmic reticulum stress-mediated apoptosis

Jing Chen, Rumin Zhang, Bao-hua Cheng, 2021, Molecular medicine reports.

Endoplasmic reticulum stress in cerebral ischemia

Jing Chen, Bo Bai, Bao-hua Cheng, 2014, Neurochemistry International.

Neuroprotective effects of apelin-13 on experimental ischemic stroke through suppression of inflammation

Jing Chen, Bo Bai, Bao-hua Cheng, 2015, Peptides.

Identification of Serine 348 on the Apelin Receptor as a Novel Regulatory Phosphorylation Site in Apelin-13-induced G Protein-independent Biased Signaling*

Jing Chen, Bo Bai, Yanjun Tian, 2014, The Journal of Biological Chemistry.

Apelin receptor homodimer inhibits apoptosis in vascular dementia.

Jing Chen, Huannan Wang, Baoqi Sun, 2021, Experimental cell research.

Heterodimerization of the kappa opioid receptor and neurotensin receptor 1 contributes to a novel β-arrestin-2-biased pathway.

Jing Chen, Bo Bai, Yunlu Jiang, 2016, Biochimica et Biophysica Acta.

Edaravone protected PC12 cells against MPP(+)-cytoxicity via inhibiting oxidative stress and up-regulating heme oxygenase-1 expression

Bo Bai, Baohua Cheng, Jing Chen, 2014, Journal of the Neurological Sciences.

(-)-Clausenamide alleviated ER stress and apoptosis induced by OGD/R in primary neuron cultures

Jing Chen, Rumin Zhang, Fei Wu, 2020, Neurological research.

Heterodimerization of human orexin receptor 1 and kappa opioid receptor promotes protein kinase A/cAMP-response element binding protein signaling via a Gαs-mediated mechanism.

Jing Chen, Bo Bai, Rumin Zhang, 2015, Cellular signalling.

RNA-seq expression profiling of rat MCAO model following reperfusion Orexin-A

Jing Chen, Bo Bai, Bao-hua Cheng, 2017, Oncotarget.

Transmembrane peptide 4 and 5 of APJ are essential for its heterodimerization with OX1R.

Jing Chen, Peixiang Wang, L. Wan, 2020, Biochemical and biophysical research communications.

Dynamics of apelin receptor/G protein coupling in living cells.

Jing Chen, Bo Bai, Yunlu Jiang, 2014, Experimental cell research.

High-throughput sequencing analysis of differentially expressed miRNAs and target genes in ischemia/reperfusion injury and apelin-13 neuroprotection

Jing Chen, Bo Bai, Bao-hua Cheng, 2018, Neural regeneration research.

Disruption of 5-hydroxytryptamine 1A receptor and orexin receptor 1 heterodimer formation affects novel G protein-dependent signaling pathways and has antidepressant effects in vivo

H. Randeva, Jing Chen, Maocai Yan, 2022, Translational Psychiatry.

A method for identifying G protein-coupled receptor dimers and their interfaces.

Jing Chen, Maocai Yan, Chunmei Wang, 2020, Biochimica et biophysica acta. Molecular cell research.