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JAM-A modification speeds up skin wound healing by boosting fibroblast growth.

GATA6 is important for maintaining and differentiating cells in a key area of human skin.

Th22 cells are essential for Tβ15-induced hair growth in mice.

The PLP2 gene affects cashmere fiber quality in goats and is linked to hair growth and loss.

Increasing TSPO in the brain reduces anxiety and depression.

Hemidesmosomes and Notch signaling help skin cells mature by moving them to the outer layer.

Certain alkaloids could help create new coronavirus drugs.

The AVET system effectively delivers genes to human keratinocytes and may help treat skin diseases.

Effective delivery of gene editors is crucial for safe and successful gene editing in healthcare and agriculture.

The vector successfully directed specific gene expression in hair follicles.

Engineered extracellular vesicles could improve CRISPR/Cas delivery, making gene editing safer and more effective.

ELIP-based CRISPR delivery improves heart disease gene editing but needs more testing.

Genosomes are promising for safe and effective gene delivery in therapy.

Gene therapy in mice increased lifespan and improved health without causing cancer.

Modified HDL can better deliver drugs and genes, potentially improving treatments and reducing side effects.

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.