Reducing ABCA1 expression or function with miR-3202 or antibodies boosts cell-derived extracellular vesicle secretion for therapeutic carriers.
Pluripotent cells are induced into steroidogenic cells to address slow differentiation while enabling circadian hormone production.
SV40 T antigen with Bcl-2, Myc, and cyclin D genes supports cell immortalization without losing antibody-producing ability.
YAP overexpression and LATS inhibition differentiate AT2 cells into AT1 cells, avoiding difficult tissue isolation for lung models.
This case targets MUC16’s retained extracellular domain with antibody constructs for cancer diagnosis and therapy.
This culture approach uses transformed CD4+ T cells and costimulatory factors to expand cord blood NK cells for cell therapy.
A defined growth medium and enhancer composition reduce clumping while supporting up to 4 g/L recombinant protein expression in 14 days.
This case uses temporal plasmid expression to generate clonal iPSCs while reducing genomic changes and reversion risks.
This case uses TGFBR2 and CISH loss-of-function edits with CD16 variants to improve NK-cell survival, recognition, and ADCC.
Correct GBA1 variants before differentiation to produce consistent therapeutic neurons.
Pre-bound competitor antibodies separate non-competitive and blocking cells for more specific enrichment and isolation.
Iterative single-cell TF screening enables rapid iPSC differentiation into microglia-like cells resembling primary microglia.
This case uses c-Myc and BCL-XL control in erythroid progenitors to combine sustained expansion with efficient enucleation.
This case combines high-affinity PD1 binding with lower-affinity TIM3 binding to restore T-cell function while limiting off-target effects.
Stro-1+ cells enable efficient iPS reprogramming with lower oncogene risk.
This case addresses DLL3's Golgi localization with antibodies that promote tumor-cell lysis and macrophage phagocytosis.
This culture approach combines IL-4 and a TGF-βR agonist to expand pluripotent stem-derived Tregs without losing suppressive function.
This case uses antibodies against HLA-A2-presented TdT peptides for targeted cancer detection and treatment with fewer off-target effects.
Selecting CD34+CD45RA−CD90+ HSCs creates a more homogeneous population for predictable engraftment and lower cell doses.
Modular eRBC sensors reconstitute fluorescent or enzymatic signals upon ligand binding.
A defined naïve-like CD4+ to CD8+ ratio guides receptor engineering for more predictable, lower-toxicity T cell products.