Results 101 to 110 of about 1,300,680 (334)
Targeting DNA‐LNPs to Endothelial Cells Improves Expression Magnitude, Duration, and Specificity
Attaching antibodies against endothelial cell surface proteins redirects the delivery and expression of DNA‐lipid nanoparticles to organs of interest. Our targeted nanoparticles enable organ‐selective DNA expression in the endothelium of the lungs, brain, or spleen, providing a therapeutic platform for dozens of endothelial‐centric diseases.
Nicolas Marzolini +24 more
wiley +1 more source
A genre-based study of biomedical editorials and letters to the editor: a contrastive analysis [PDF]
This paper reports on a genre-based contrastive analysis of the textual organization of biomedical texts. In order to provide the maximum educational value to our research, our corpus is made up of 100 biomedical texts divided as follows: 25 Letters to ...
Esther Vázquez y del Árbol
doaj
Volume 10, Number 6 – March 1930 [PDF]
Volume 10, Number 6 – March 1930. 42 pages including covers and advertisements. Lillie, Edward C., On the Prairie Hickey, Carroll, Little Galahads (verse) Carlson, Edward C., Zeb, the Aesthete Schneider, Francis C., His Brother\u27s Inspiration
core +1 more source
Guest Editorial: Advanced Technologies and Services for Multimedia Big Data Processing [PDF]
Young‐Sik Jeong +3 more
openalex +1 more source
A miniaturized deaminase SsdAtox was scanned with AlphaFold to identify DNA binding pocket hot spots. Site‐saturation mutagenesis at gatekeeper residue K31 yielded ten‐fold activity enhancement. Trinity Screen, an E. coli‐based three‐in‐one platform selecting for high activity and reduced double‐strand breaks, enabled combinatorial evolution at DNA ...
Ryeo Gang Son +2 more
wiley +1 more source
Wayne L. Miller
doaj +1 more source
Editorial: What is this cleavage of mitral valve – Commissure, indentation, cleft, or cleft-like indentation? [PDF]
Masaki Nii
openalex +1 more source
Structure‐Guided Engineering of a Cas12i Nuclease Unlocks Near‐PAMless Genome Editing
CRISPR‐Cas nucleases are limited by PAM requirements, restricting genome accessibility. Structure‐guided engineering of the compact Cas12i nuclease SF01 produced three variants with near‐PAMless, enabling efficient editing at diverse 5'‐NNTN‐3' sites. These nucleases expand the editable portion of the human genome more than fourfold, enabling efficient
Qitong Chen +15 more
wiley +1 more source

