SMNΔ7 S270A mutation stabilizes the SMN protein by blocking degron-mediated degradation pathways.
Modified AAV2 capsid proteins with inserted amino acid sections target cardiomyocytes while reducing liver transduction.
Non-ionic lipid nanoparticle formulations prevent aggregation by removing negative counter-ions, preserving siRNA delivery efficiency.
Multispecific antibodies bind distinct Zika virus epitopes to neutralize infection while preventing antibody-dependent enhancement and escape mutants.
Concatemeric DNA with phosphorothioated nucleotides boosts protein yield and stability, reducing production costs compared to traditional plasmid methods.
A bidirectional PGK-EF1a promoter co-expresses FOXP3 and ΔLNGFR in lentiviral vectors.
Plasmid segmentation using site-specific recombinase separates minicircle DNA from the replicative backbone.
ERbeta agonists overcome drug resistance in squamous cell carcinomas by activating Notch1 expression and inducing cellular differentiation.
Amphoteric lipid assemblies modulate surface charge via pH-responsive protonation to enhance cellular uptake while reducing systemic toxicity.
Engineered adipose pericytes secrete soluble TRAIL continuously, overcoming short half-life and reducing systemic toxicity.
Barcoding and sequencing quantify clonal populations, resolving precision versus complexity trade-offs.
Mutated Survivin antigens boost interferon gamma levels to reduce tumor mass despite poor expression.
Feeder cells expressing costimulatory molecules stimulate gamma delta T cell proliferation without T cell receptor activation.
Merging attachment and entry domains into a single chimeric protein reduces device complexity while improving transgene delivery efficiency.
Computational algorithms reconstruct T cell regulatory networks from transcriptomic data to identify therapeutic targets.