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This method is effective for needle-free HIV-1 vaccination by activating immune responses in the skin.

Nonionic liposomes are the best for delivering genes to skin cells.

Non-viral delivery systems and stimuli-responsive nanoformulations can improve CRISPR-Cas9 gene therapy.

Gene therapy, especially using atoh1, shows promise for creating functional sensory hair cells in the inner ear, but dosing and side effects need to be managed for clinical application.

The assay effectively identifies compounds that affect immune cell activation.

A new lab-grown lung model helps study adenoviruses and test antiviral drugs.

INTASYL is a promising, adaptable RNAi technology for treating skin cancers.

Intranasal delivery of gene therapy shows promise for treating ischemic stroke.

Sheep cells were successfully modified to include a spider silk protein gene.

The new particle system could be a promising treatment for diseases related to the 5-α reductase enzyme.

The LTF gene may help predict and manage nonspecific orbital inflammation.

Injecting recipient splenocytes into donors' thymus can prevent graft-versus-host disease.

The method successfully created stable transfection donor cells for goat hair follicle research.

Mouse models help target specific genes in lymphatic cells for research.

Modified liposomes with exosomes effectively deliver RNA to stem cells.

RNA delivery is best for in-body use, while RNP delivery is good for outside-body use. Both methods are expected to greatly impact future treatments.

Transgenic sheep cells with spider silk gene were successfully created for future sheep hair expression.

NSC167409 can effectively inhibit the virus causing hand, foot, and mouth disease.

Stem cell-derived vesicles improve blood vessel growth in limbs.

Engineered extracellular vesicles show promise for targeted therapy but need more research for clinical use.

Live vaccines can be safely given to infants with a FOXN1 variant if their immune function improves over time.

Low power red laser with efavirenz can reduce HIV-1 infection to undetectable levels and improve diagnosis.

A new method using gold nanoshells and infrared light effectively delivers siRNA to cancer and stem cells with precision and minimal damage.

Amotosalen-treated donor T-cells can prevent late CMV infection after bone marrow transplants.

Lecithin-encapsulated resveratrol nanoparticles could be a safe and effective anti-cancer treatment.

An HIV patient's complete hair loss was reversed after switching from lopinavir/ritonavir to nelfinavir.

Entospletinib effectively prevents eye and skin GVHD in mice.

EV-based drug delivery shows promise but faces challenges in standardization and scalability.

Engineered vesicles with EGF mRNA improve skin wound healing and reduce scarring.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.