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Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

CRET therapy affects inflammation in skin cells by changing cytokine levels and activating certain proteins.

The dog's health improved after treatment with antibiotics and other medications.

Keratin mutations cause skin diseases and could lead to new treatments.

The PP2A-B55α protein is essential for brain and skin development in embryos.

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

Certain proteins, caspases-1 and -11, are important in the early development of skin inflammation in mice.

TRPA1 is crucial for mechanical sensitivity in skin sensory neurons.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

Stress keratins are expressed less in diseased skin and are linked to differentiation, inflammation, and immunity.

Deleting Twist1 in skin cells reduces UVB-induced skin cancer risk.

Cathepsin E is crucial for normal skin cell differentiation and development.

CK7 and CK20 help identify and classify tumors for accurate cancer diagnosis.

ACKR2 helps prevent skin scarring and hair loss by controlling inflammation.

Different bovine tissues show varying types of cytokeratins.

Calreticulin has roles in healing, immune response, and disease beyond its known functions in the endoplasmic reticulum.

CYP11A1 is crucial for skin health and disease by producing important steroids.

Dickkopf-related Protein 2 can help hair grow by activating a specific cell pathway.

Activating cannabinoid receptor 1 may help manage psoriasis by reducing certain keratins.

The gene therapy showed significant wound healing and was safe for treating severe RDEB.

Grasp protein helps maintain skin health after UVB exposure.

Lack of TrkC receptor delays hair follicle development.

Two siblings with tinea capitis improved after treatment with ketoconazole.

Retinoic acid-binding proteins in skin are regulated by β-catenin and Notch signalling.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

Human hair keratin genes have unique simple sequence repeats that may help track genetic variations.