Yuting Fu

ORCID: 0009-0007-7585-1239
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About
Contact & Profiles
Research Areas
  • RNA Interference and Gene Delivery
  • Autophagy in Disease and Therapy
  • Nanoplatforms for cancer theranostics
  • Pancreatic function and diabetes
  • Immunotherapy and Immune Responses

Peking University
2024

Beijing Tian Tan Hospital
2016

Capital Medical University
2016

Scale drop disease virus (SDDV) is a distinct member in genus Megalocytivirus of family Iridoviridae, garnering increasing attention due to its significant threat teleost. Ferroptosis new type cell death discovered recently and involved various viral infections. Knowledges on SDDV induced ferroptosis remains unclear. Here, we demonstrated that infection triggers ferroptosis, as evidenced by hallmark features such iron overload, massive lipid peroxides accumulation, glutathione depletion...

10.1101/2025.03.18.643978 preprint EN cc-by-nc bioRxiv (Cold Spring Harbor Laboratory) 2025-03-18

Tumor vaccine therapy offers significant advantages over conventional treatments, including reduced toxic side effects. However, it currently functions primarily as an adjuvant treatment modality in clinical oncology due to limitations tumor antigen selection and delivery methods. vaccines often fail elicit a sufficiently robust immune response against progressive tumors, thereby limiting their efficacy. In this study, we developed nanoparticle-based vaccine, OVA@HA-PEI, utilizing ovalbumin...

10.1142/s1793545824500172 article EN cc-by Journal of Innovative Optical Health Sciences 2024-07-19

Deoxyribonuclease I (DNase I) is an endonuclease responsible for the destruction of chromatin during apoptosis. However, its role in diabetes remains unclear. The aim current study was to investigate DNase combined with high glucose levels β‑cell Human samples were collected and activity examined. High glucose‑cultured INS‑1 cells transfected small interfering RNA (siRNA) cell apoptosis examined by western blotting flow cytometry. Cell viability analyzed Counting Kit‑8 assay. resulting from...

10.3892/mmr.2016.5102 article EN cc-by-nc-nd Molecular Medicine Reports 2016-04-11
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