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Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

Ribonucleotide excision repair is crucial to prevent skin cancer.

Calcifying epithelioma cells can differentiate into hair cortex and outer root sheath.

Two new gene clusters important for hair formation were found on human chromosome 11.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

Lysine carboxymethyl cysteinate (LCC) protects skin from UVB damage by activating autophagy.

Recent findings in cell biology help understand cell roles in health and disease.

Topical IKKα inhibitors may help prevent CCS tumours.

Follicular structures help differentiate keratoacanthoma from squamous cell carcinoma.

A dog had a rare skin cyst, known as a dilated pore of Winer, surgically removed from its neck.

Near-infrared probes can safely and effectively image cysteine protease activity for disease diagnosis.

Ribonucleotide excision repair is crucial to prevent skin cancer.

Rathke’s cleft cysts can rarely cause Cushing disease, and surgery can improve symptoms.

Punctate follicular porokeratosis is a skin condition with specific features seen in hair follicles.

Two new gene clusters important for hair formation were found on human chromosome 11.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

CDK4/6 inhibitors can protect hair cells from chemotherapy damage.

Hair proteins change location and structure as hair cells mature.

Newly designed proteins can effectively degrade specific proteins in cells, offering a promising alternative for targeted protein degradation.

aPKCλ is essential for hair follicle stem cell maintenance and wound healing.

A painless cheek lump was misdiagnosed but found to be a rare, benign skin lesion called pilomatrixoma, treatable by surgery.

Kerion is a severe scalp infection that needs quick treatment to avoid permanent hair loss in children.

KIF18B is important for correctly positioning cell division machinery in skin cells, affecting hair follicle development.

Activating PKM2 and Wnt/β-catenin signaling together can potentially enhance hair growth and could be a treatment for hair loss.

Hereditary elliptocytosis causes elongated red blood cells and can lead to mild or no symptoms.

Hair cells lose their nucleus and mitochondria in a specific order as they fill with keratin, which could help develop treatments for hair issues.

The lump on a woman's scalp was a rare, potentially cancerous tumor from the hair follicle, not a common cyst.