Gong Chen

ORCID: 0000-0002-1857-3670
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About
Contact & Profiles
Research Areas
  • Neuroscience and Neuropharmacology Research
  • Neurogenesis and neuroplasticity mechanisms
  • Parallel Computing and Optimization Techniques
  • Colorectal Cancer Treatments and Studies
  • Pluripotent Stem Cells Research
  • Cancer Immunotherapy and Biomarkers
  • Genetic factors in colorectal cancer
  • Colorectal Cancer Surgical Treatments
  • Neuroinflammation and Neurodegeneration Mechanisms
  • Neuroscience and Neural Engineering
  • Colorectal and Anal Carcinomas
  • Nerve injury and regeneration
  • MicroRNA in disease regulation
  • RNA Research and Splicing
  • Cancer Genomics and Diagnostics
  • Photoreceptor and optogenetics research
  • Embedded Systems Design Techniques
  • Ion channel regulation and function
  • Gastric Cancer Management and Outcomes
  • RNA Interference and Gene Delivery
  • RNA modifications and cancer
  • CRISPR and Genetic Engineering
  • Drug Transport and Resistance Mechanisms
  • Pregnancy and preeclampsia studies
  • Advanced Data Storage Technologies

Beijing Jiaotong University
2023-2025

Sun Yat-sen University Cancer Center
2016-2025

Hunan Provincial Maternal and Child Health Hospital
2025

Sun Yat-sen University
2016-2025

Anhui Medical University
2020-2025

Chongqing Medical University
2024-2025

Second Affiliated Hospital of Chongqing Medical University
2024-2025

Beijing Anzhen Hospital
2025

Capital Medical University
2025

Dalian Medical University
2024-2025

Migration on sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) that does not correlate with formula molecular weights, termed "gel shifting," appears to be common for membrane proteins but has yet conclusively explained. In the present work, we investigate anomalous mobility of helical using a library wild-type and mutant helix-loop-helix ("hairpin") sequences derived from transmembrane segments 3 4 human cystic fibrosis conductance regulator (CFTR), including...

10.1073/pnas.0813167106 article EN Proceedings of the National Academy of Sciences 2009-01-31

Atrial fibrillation (AF) is frequently associated with enhanced inflammatory response. The NLRP3 (NACHT, LRR, and PYD domain containing protein 3) inflammasome mediates caspase-1 activation interleukin-1β release in immune cells but not known to play a role cardiomyocytes (CMs). Here, we assessed the of CM AF.

10.1161/circulationaha.118.035202 article EN Circulation 2018-05-25

Adult mammalian brains have largely lost neuroregeneration capability except for a few niches. Previous studies converted glial cells into neurons, but the total number of neurons generated is limited and therapeutic potential unclear. Here, we demonstrate that NeuroD1-mediated in situ astrocyte-to-neuron conversion can regenerate large functional new after ischemic injury. Specifically, using NeuroD1 adeno-associated virus (AAV)-based gene therapy, were able to one third caused by injury...

10.1016/j.ymthe.2019.09.003 article EN cc-by-nc-nd Molecular Therapy 2019-09-06

Significance Rett syndrome is a devastating neurodevelopmental disorder that currently has no cure. In this work, we demonstrate human neurons derived from patients with show significant deficit in neuron-specific K + -Cl − cotransporter2 (KCC2) expression, resulting delayed GABA functional switch. Restoring KCC2 level rescues deficits neurons. We further methyl CpG binding protein 2 regulates expression through inhibiting RE1-silencing transcriptional factor. Our data suggest potential...

10.1073/pnas.1524013113 article EN cc-by Proceedings of the National Academy of Sciences 2016-01-05

Abstract Huntington’s disease (HD) is caused by Huntingtin (Htt) gene mutation resulting in the loss of striatal GABAergic neurons and motor functional deficits. We report here an vivo cell conversion technology to reprogram astrocytes into both R6/2 YAC128 HD mouse models through AAV-mediated ectopic expression NeuroD1 Dlx2 transcription factors. found that astrocyte-to-neuron (AtN) rate reached 80% striatum >50% converted were DARPP32 + medium spiny neurons. The astrocyte-converted...

10.1038/s41467-020-14855-3 article EN cc-by Nature Communications 2020-02-27

1. Gramicidin-perforated patch clamp recording was employed to study GABA-mediated responses in rat hypothalamic neurones (n = 102) with an intracellular Cl- concentration unaltered by the pipette solution. 2. In young cultures after 1-7 days vitro (DIV), GABA induced depolarizing membrane potentials (+16.5 +/- 1.3 mV) that often surpassed threshold for firing of action (-42 1 and resulted increase neuronal activity. The were dose dependent. necessary evoke half-maximal depolarization (EC50)...

10.1113/jphysiol.1996.sp021505 article EN The Journal of Physiology 1996-07-15

GABA is the dominant inhibitory neurotransmitter in CNS. By opening Cl − channels, generally hyperpolarizes membrane potential, decreases neuronal activity, and reduces intracellular Ca 2+ of mature neurons. In present experiment, we show that after trauma, GABA, both synaptically released exogenously applied, exerted a novel opposite effect, depolarizing neurons increasing . Different types trauma were effective included neurite transection, replating, osmotic imbalance, excess heat. The...

10.1523/jneurosci.16-13-04283.1996 article EN cc-by-nc-sa Journal of Neuroscience 1996-07-01

Golgi-specific DHHC (Asp-His-His-Cys) zinc finger protein (GODZ) is a family palmitoyl acyltransferase that implicated in palmitoylation and regulated trafficking of diverse substrates function either at inhibitory or excitatory synapses. Of particular interest the γ2 subunit GABA A receptors, which required for targeting these receptors to Here, we report GODZ and, lesser extent, its close paralog sertoli cell gene with domain-β (SERZ-β) are main members enzymes able palmitoylate...

10.1523/jneurosci.4214-06.2006 article EN cc-by-nc-sa Journal of Neuroscience 2006-12-06

MiR-637 (microRNA-637) is a primate-specific miRNA belonging to the small noncoding RNA family, which represses gene regulation at post-transcriptional expression level. Although it was discovered approximately 5 years ago, its biomedical significance and regulatory mechanism remain obscure. Our preliminary data showed that miR-637 significantly suppressed in four HCC cell lines and, also, most of hepatocellular carcinoma (HCC) specimens, thereby suggesting would be tumor suppressor HCC....

10.1002/hep.24595 article EN cc-by Hepatology 2010-12-01

Schizophrenia is a severe chronic mental disorder with high genetic component in its etiology.Several lines of study have suggested that synaptic dysfunction may underlie the pathogenesis schizophrenia.Neuroligin proteins function as cell-adhesion molecules at post-synaptic membrane and play critical roles synaptogenesis maturation.In this study, we systemically sequenced all exons promoter region neuroligin-2 (NLGN2) gene sample 584 schizophrenia patients 549 control subjects from Taiwan.In...

10.1093/hmg/ddr208 article EN Human Molecular Genetics 2011-05-06

ABSTRACT Colistin-induced nephrotoxicity is a dose-limiting adverse effect when colistin used against Gram-negative pathogens. This study examined the nephroprotective of melatonin in rats. Rats ( n = 7 per group) were treated intravenously twice daily with saline, (at increasing doses from 0.5 to 4.0 mg/kg), (5 or both and for days. The severity renal alteration was biochemically histologically. coadministration on pharmacokinetics investigated. Significantly lower urinary N -acetyl-β- d...

10.1128/aac.00328-11 article EN Antimicrobial Agents and Chemotherapy 2011-06-28

Abstract Surgical stress and inflammatory response induce the release of catecholamines PGs, which may be key factors in facilitating cancer recurrence through immunosuppression. Animal studies have suggested efficacy perioperative blockades PGs reducing In this study, to our knowledge, we present first report effects propranolol and/or parecoxib on peripheral regulatory T cells (Tregs) breast patients. Patients were randomly assigned control, propranolol, parecoxib, plus groups. We...

10.4049/jimmunol.1501677 article EN The Journal of Immunology 2016-03-12
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