Neutrophil membrane-camouflaged SiRNA nanoplatform targeting IL-33 attenuates osteoarthritis through autophagy-dependent senescence regulation. [PDF]
Fu Z, Chen J, Sun D, Zhang S, Chen J.
europepmc +1 more source
Chondrocyte‐targeted CS‐NAC nanoparticles restore redox balance, inhibit ferroptosis, and protect cartilage under mechanical stress. This nanoplatform enhances joint retention, elevates GPX4 activity, and attenuates osteoarthritis progression, offering a promising disease‐modifying therapeutic strategy.
Shaoyi Wang +8 more
wiley +1 more source
Activating Endogenous Condylar Stem Cells to Enhance TMJ Repair. [PDF]
Tuwatnawanit T, Anthwal N, Tucker AS.
europepmc +1 more source
Role of Pyroptosis in the Pathogenesis of Osteoarthritis: An Updated Review. [PDF]
Yang F, Li D, Long W, Li E, Wei B.
europepmc +1 more source
Integration of Network Pharmacology, Molecular Docking, and Experimental Validation to Identify the Effect of EGCG on Alleviating Chondrocyte Inflammatory Damage by Targeting ER Stress-STAT3 Crosstalk. [PDF]
Zhao MJ +11 more
europepmc +1 more source
Three-dimensional human mucopolysaccharidosis IVA chondrocyte culture reveals significant impairments in the lysosomal-mitochondrial crosstalk. [PDF]
Leal AF, Saikia S, Khan SA, Tomatsu S.
europepmc +1 more source
Conjoint analysis of single-cell sequencing and high-throughput virtual screening regarding DDR2 in osteoarthritis disease models. [PDF]
Mei H +7 more
europepmc +1 more source
Microenvironmental response-based treatment of osteoarthritis is a highly effective and durable program: a review. [PDF]
Meng Y, Wu S, Liu S, Yang Y.
europepmc +1 more source
The Role of Chondrocyte Hypertrophy and Senescence in Osteoarthritis Initiation and Progression
Osteoarthritis (OA) is the most common joint disease that causes pain and disability in the adult population. OA is primarily caused by trauma induced by an external force or by age-related cartilage damage.
Yeri Alice Rim, Yoojun Nam, Ji Hyeon Ju
exaly +2 more sources

