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Ren X
Chinese, English
Hubei
Huazhong University of Science and Technology
Life Sciences
  • 1997 Bachelor of Biology: Wuhan University
  • 2003 PhD in Genetics: Wuhan University
  • 2003-2005 Postdoctoral Researcher: Human Genome Research Center, Huazhong University of Science and Technology
  • 2006- Associate Professor: College of Life Science and Technology, Huazhong University of Science and Technology
Genetic diseases
Gene function in development and disease
  • Mutation in NPPA causes atrial fibrillation by activating inflammation and cardiac fibrosis in a knock-in rat model, Ren X et al., 2019
  • Knockout of mafba Causes Inner-Ear Developmental Defects in Zebrafish via the Impairment of Proliferation and Differentiation of Ionocyte Progenitor Cells, Ren X et al., 2021
  • Tulp1 deficiency causes early-onset retinal degeneration through affecting ciliogenesis and activating ferroptosis in zebrafish, Ren X et al., 2022
  • IFT27 regulates the long-term maintenance of photoreceptor outer segments in zebrafish, Ren X et al., 2024
  • The splicing factor Prpf31 is required for hematopoietic stem and progenitor cell expansion during zebrafish embryogenesis, Ren X et al., 2024
Genetics Diseases Gene Function Development Pathogenesis Muscular Dystrophy Atrial Fibrillation Cardiac Fibrosis Zebrafish Ciliogenesis

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