This non-viral CRISPR-Cas9 delivery vector is ten times as effective at genome modification as the standard plasmid transfection techniques, down-regulating Plk1 expression over 70% to inhibit tumor growth.

This non-viral CRISPR-Cas9 delivery vector is ten times as effective at genome modification as the standard plasmid transfection techniques, down-regulating Plk1 expression over 70% to inhibit tumor growth.
A technique using gold nanoparticles and laser pulses can successfully destroy retinoblastoma cells.
Intercellular communication may provide a mechanism to exploit and buffer cell-to-cell variability.
A new design approach for the fabrication of scaffolds for biomedical applications.
Complex, aqueous-stable, hydrogel ionic circuits towards transparent, flexible, biocompatible bioelectronic devices.
Drug eluting elastomers could potentially control tumor growth using long-term targeted release of tumor fighting drugs.
A team of researchers from the UK present the application of wavelength modulated Raman spectroscopy for the automated label‐ and fluorescence‐free classification of fixed squamous epithelial cells in suspension, such as those produced during a cervical smear test.
Green fluorescent protein (GFP) expression in HeLa EGFP cells is significantly downregulated by Hsp-R9/siRNA complexes
Imaging and analysis of Autophagic Lysosome Reformation.
Throughout development and into adulthood, Wnt proteins ensure embryonic patterning, cellular proliferation, cellular identity, and organization of tissues.