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The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

Researchers created five new human scalp cell lines that could be useful for hair growth and loss research.

Variants in the CCDC47 gene are linked to trichohepatoneurodevelopmental syndrome.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

Human hair proteins vary by individual, body site, and ethnicity, useful for forensics.

Dermal papilla cells help skin stem cells grow into hair.

KLHL24-mutant stem cells help understand skin and heart disease.

Nonimmunogenic forms of keratins K71 and K31 can delay and prevent alopecia areata.

A new rat strain with a specific gene mutation causes hair loss and kidney issues.

Kremen is crucial for proper development and preventing tumors by regulating Wnt signaling.

CircAGK affects cell death in hair cells by controlling the miR-3180-5p/BAX pathway, which can lead to hair loss.

A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

Lipin-1 is important for skin cell differentiation and skin barrier function.

Hsc70 protein may influence hair growth by responding to androgens.

A specific gene mutation causes complete hair loss without other health issues.

The gene for Marie Unna hereditary hypotrichosis is located on chromosome 8p21, near the hairless gene.

AIRE protein, defective in APECED patients, is found in skin and hair cells and interacts with cytokeratin 17.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

Akt2 and SGK3 are both important for normal hair growth and development.

A new tool helps study hair follicle cells to develop better treatments for hair disorders.

7DHC and BM15766 damage hair follicle structure and reduce key gene expression.

Overexpressing PKCepsilon in mice reduces papillomas but increases carcinomas.

Nexin 1 helps control hair growth in young rats.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

Hair and nail cells share similar proteins, indicating a common differentiation pathway.

A 14-year-old boy was diagnosed with a rare hair condition that may lead to hair thinning and has no known effective treatments.