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Keratosis pilaris is common in young females, and dermoscopy helps diagnose it accurately.

The structure of SRD5A reveals how it reduces steroids, aiding drug design for related health conditions.

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

PAON shows skin patterns due to genetic mosaicism.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

WWP2 is crucial for tooth development in mice.

GPRC5D is linked to the formation of hair, nails, and certain tongue areas.

Overexpression of PKCepsilon leads to increased TNFalpha, promoting metastatic squamous cell carcinoma in mice.

Human tissue kallikreins help regulate skin barrier functions and affect skin health.

Recognizing keratosis pilaris in all skin tones helps diagnose related skin issues and reduce distress.

Keratins are crucial for tissue strength, and mutations in keratin genes can lead to various diseases, highlighting the need for targeted therapies.

Keratin proteins are increasingly recognized as important for cell health and are linked to many diseases.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

A specific gene mutation causes woolly hair and hair loss.

Long-term oral and topical treatments improved skin condition in a goldendoodle with a genetic disorder.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

The study found nine new hair protein genes in human hair follicles.

Enzymes called PADIs play a key role in hair growth and loss.

Diphencyprone initially increases mouse hair growth, then slows it, possibly due to changes in specific protein levels.

Keratin-associated proteins are crucial for hair strength and structure.

Electrostatic interactions mainly stabilize the binding of peptides to hair keratin.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

ALP and ACP have different roles in dog skin, with ALP aiding growth and maintenance, and ACP involved in breakdown processes.

CD18-deficient mice developed psoriasis-like skin disease, useful for studying inflammatory skin disorders.

Mutations in the desmoplakin gene can cause hair problems and deadly heart disease.

The study mapped keratin 15 and 19 genes, aiding future genetic disorder research.

Two peptides, RMYYY and VMYMI, may be effective anti-inflammatory drugs.