• >
  • >
  • >
  • >
  • >
Upload Avatar (500 x 500)
Jing Yang
Life Science
Tongji University
Shanghai
Language: Chinese, English
Contact
Leukemia Malignant Diseases Targeted Therapy Immunotherapy Protein Degradation Dub E3 Ligases Drug Discovery Resistance Mechanisms Clinical Development
Areas of Focus
  • Targeted and immunotherapy for malignant diseases such as leukemia
  • Discovery and development of first-in-class targeted degraders
Work Experience
  • 2015-2020 - Dana-Farber Cancer Institute, Harvard Medical School: Postdoctoral Training
  • 2021 Jan-Aug - Hefei Institutes of Physical Science, Chinese Academy of Sciences: Associate Researcher
  • 2022 Sep-Present - Tongji University, School of Life Sciences and Technology: Distinguished Researcher
Academic Background & Achievements
  • 2009 - Bachelor of Science: Shandong University
  • 2015 - Doctor of Science: Shanghai Pasteur Institute, Chinese Academy of Sciences
  • Identified several pathogenic protein degradation targets DUB/E3 during doctoral studies
Publications
  • Repurposing clinically available drugs and therapies for pathogenic targets to combat SARS-COV-2, Jing Yang et al., 2023
  • Gilteritinib: Repurposing of AXL-targeting kinase inhibitors against COVID-19, Jing Yang et al., 2023
  • Discovery of IHMT-337 as a potent irreversible inhibitor targeting novel noncanonical role of EZH2 for triple-negative breast cancer, Jing Yang et al., 2023
  • Inhibition of deubiquitinating enzyme USP47 as a novel targeted therapy for hematologic malignancies expressing mutant EZH2, Jing Yang et al., 2022
  • Small molecule inhibition of deubiquitinating enzyme JOSD1 as a novel targeted therapy for leukemias with mutant JAK2, Jing Yang et al., 2022
  • The deubiquitinase USP44 promotes Treg function during inflammation by preventing FOXP3 degradation, Jing Yang et al., 2020
  • Inhibition of the deubiquitinase USP10 induces degradation of SYK, Jing Yang et al., 2020
  • HSP70 and FLT3-ITD: targeting chaperone system to overcome drug resistance, Jing Yang et al., 2021
  • Ubiquitin-Specific Protease 4 Promotes Th17 Cell Function under Inflammation by Deubiquitinating and Stabilizing RORγt, Jing Yang et al., 2015
  • TRAF5 Mediated K63-linked Polyubiquitination Plays an Essential Role in the Positive regulation of RORγt on promoting IL-17A Expression, Jing Yang et al., 2015
  • The E3 deubiquitinase USP17 is a positive regulator of retinoic acid-related orphan nuclear receptor γt (RORγt) in Th17 cells, Jing Yang et al., 2014
Post a Project

Contact us

Let's talk!
* Required
* Required
* Required
* Invalid email address
By submitting this form, you agree that AGP may contact you with insights and marketing messaging.
No thanks, I don't want to receive any marketing emails from AGP.
Submit

Thank you for your message!
We will contact you soon.