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 smart cell-targeting approach for potential use in specific cell ablation.
A 3D imaging approach that enables prolonged functional assessment of the mouse oviduct (or fallopian tube) in vivo.
Discussing the historical roots of the stem cell concept and the definition generally adopted today.
Ribosome production is a considerable energy investment for the cell—rRNAs and ribosomal proteins (RPs) are among the most abundant classes of RNAs and proteins—and their production must, therefore, be synchronized temporally and stoichiometrically to ensure efficient ribosome assembly.
Intercellular communication may provide a mechanism to exploit and buffer cell-to-cell variability.
In his review published in BioEssays, James Haber takes a look at how the ends of a broken chromosome find a template with which to repair such a double-strand break.
In their “Hypothesis” article published in BioEssays, Nirmalya Chatterjee and Dirk Bohmann discuss the interplay between Nrf2 and BET proteins and the resultant implications for therapies targeting these proteins.
Analyses representing the state-of-the-art in our understanding of the complex host–microbiome relationship are presented.
Protein immobilization directly from cell lysates is demonstrated in a new process that avoids expensive purification steps but expertly maintains target protein selectivity.