Magnetic nanoparticles (MNPs) offer tremendous potentialities in biomedical applications for
a long while. Since these materials' interactions in biological media largely rely on their …

The successful transplantation of stem cells has the potential to transform regenerative
medicine approaches and open promising avenues to repair, replace, and regenerate …

Gene editing is a versatile technique in biomedicine that promotes fundamental research as
well as clinical therapy. The development of Clustered Regularly Interspaced Short …

RISPR-Cas9 has exhibited enormous potential in gene therapy. It can perform genome
editing with single-nucleotide precision in various types of cell and tissue, providing a …

Biomedical researchers have subsequently been inspired the development of new
approaches for precisely changing an organism's genomic DNA in order to investigate …

With the development of genome editing techniques, gene therapy is becoming a viable
option for the treatment of a variety of human diseases. Genome editing techniques mainly …

Clustered regularly interspaced short palindromic repeats-associated protein
(CRISPR/Cas9) system has become a revolutionary tool for gene editing. Since viral …

Antibiotic resistance is a significant crisis that threatens human health and safety worldwide.
There is an urgent need for new strategies to control multidrug-resistant (MDR) bacterial …

Rapid developments in the field of plant genome editing using clustered regularly
interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein (Cas) systems …

Liposomes are one of the most widely investigated carriers for CRISPR/Cas9 delivery. The
surface properties of liposomal carriers, including the surface charge, PEGylation, and …