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The oncoprotein causes abnormal hair growth without increasing skin cancer risk.

Integrin α6 helps identify different neural crest cell types in the skin.

Rat hair follicle stem cells can be used to improve blood vessel growth in engineered skin.

Lrig1 could be a marker for advanced sebaceous carcinoma.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

The DMI3 gene is essential for nodule development and symbiosis in certain plants.

A unique gene mutation causes vitamin D-resistant rickets without causing hair loss.

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

Knocking out certain genes in mice helps understand skin and hair growth problems.

A chimeric keratin partially improved skin structure in mice lacking keratin 5, but didn't fully restore normal skin.

Keratin gene mutations cause various skin and hair disorders, but new research offers hope for future treatments.

Matriptase is highly active in hair follicles and sebaceous glands, especially during hair growth phases.

Skin plays a key role in managing iron levels, and inflammation can affect systemic iron, potentially causing anemia.

Higher CRHR1 levels in AA patients lead to increased inflammation.

MFN2 mutations cause mitochondrial problems, leading to more upper body fat and lower leptin levels.

HT-scCAT-seq helps understand gene regulation in embryonic skin development.

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

K42 and K124 keratins are only found in horse hoof lamellae.

Msx and Dlx genes are crucial for development, controlling cell behaviors like growth and differentiation through their roles as gene regulators.

A specific gene mutation causes complete hair loss in an Irish Traveller family.

Keratin 16 delays skin maturation and affects skin and hair development in mice.

The gene p53 is crucial for removing damaged cells to allow for healthy tissue renewal.

Fox genes are important for hair growth and development in cashmere goats.

The CUBIC protocol allows detailed 3D visualization of proteins in mouse skin biopsies.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

Progerin affects cell shape but not hair or skin in mice.

Monilethrix involves multiple genes affecting hair structure, including DSG4 mutations.

MsPG3 protein gathers at root hair tips, aiding growth.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.