Area of research
Molecular Biology · Genetics
Research interest
Research interests include Epigenetics and DNA Methylation, Pluripotent Stem Cells Research, Genetics and Neurodevelopmental Disorders, and CRISPR and Genetic Engineering.
DNA methyltransferase 1 modulates mitochondrial function through bridging m5C RNA methylation
DNA methyltransferase 1 modulates mitochondrial function through bridging m5C RNA methylation
Tuning up gene transcription via direct crosstalk of DNA and RNA methylation.
Perioperative Oral decontamination and ImmunoNuTrition (POINT) to prevent postoperative pulmonary complications in elderly patients scheduled for elective non-cardiac surgeries: protocol for a multicentre, randomised controlled trial
Simultaneous profiling of RNA isoforms and chromatin accessibility of single cells of human retinal organoids.
Mechanistic basis of lineage restriction
Asc-2P Sustains Mitochondrial Glycolysis and Promotes Neural Progenitor Cell Activation via Metabotropic Glutamate Receptor 7
Targeting Metabotropic Glutamate Receptor 7 Promotes Neurogenesis
Single‐Cell RNA‐Sequencing Provides Insight into Skeletal Muscle Evolution during the Selection of Muscle Characteristics
Comparison of retinal degeneration treatment with four types of different mesenchymal stem cells, human induced pluripotent stem cells and RPE cells in a rat retinal degeneration model
Chemical-induced phase transition and global conformational reorganization of chromatin.
Distinct patterns of responses in endothelial cells and smooth muscle cells following vascular injury.
Single-cell RNA sequencing reveals heterogeneous tumor and immune cell populations in early-stage lung adenocarcinomas harboring EGFR mutations.
Loss of KDM4B exacerbates bone-fat imbalance and mesenchymal stromal cell exhaustion in skeletal aging
Single Molecule RNA Localization and Translation in the Mammalian Oocyte and Embryo.
Single-cell analysis of nonhuman primate preimplantation development in comparison to humans and mice.
Characterizing disease progression of nonalcoholic steatohepatitis in <i>Leptin</i>-deficient rats by integrated transcriptome analysis.
Reversing neural circuit and behavior deficit in mice exposed to maternal inflammation by Zika virus.
Capacity to erase gene occlusion is a defining feature distinguishing naive from primed pluripotency
Single-cell RNA sequencing reveals heterogeneous tumor and immune cell populations in early-stage lung adenocarcinomas harboring EGFR mutations
Stem cell-based treatment of kidney diseases.
X-chromosome dosage compensation dynamics in human early embryos
Single-cell RNA sequencing reveals regulatory mechanism for trophoblast cell-fate divergence in human peri-implantation conceptuses
Single-Cell RNA Sequencing of hESC-Derived 3D Retinal Organoids Reveals Novel Genes Regulating RPC Commitment in Early Human Retinogenesis
Single-cell RNA sequencing reveals regulatory mechanism for trophoblast cell-fate divergence in human peri-implantation conceptuses.
Stella safeguards the oocyte methylome by preventing de novo methylation mediated by DNMT1
Generation and characterization of a hypothyroidism rat model with truncated thyroid stimulating hormone receptor
Challenges and emerging directions in single-cell analysis
DNA methylation protects against cisplatin-induced kidney injury by regulating specific genes, including interferon regulatory factor 8
Simultaneous profiling of transcriptome and DNA methylome from a single cell