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Hoxc13 is important for hair and tongue development by controlling hair keratin genes.

Corneodesmosin is essential for skin and hair health, and its dysfunction can lead to skin and hair disorders.

Nε-(carboxymethyl) lysine delays hair growth by blocking a key protein.

Pannexin 3 helps skin and hair growth by controlling a protein called Epiprofin.

Different zinc compounds cause varying levels of skin irritation in animals.

Zinc deficiency disrupts hair growth and cycle, but zinc supplements can fix this.

Disrupting Bcl-xL in mice reduces skin cancer risk.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

SCUBE3 is a potential target for cancer and alopecia treatment but is challenging to target due to its varied roles.

MYC protooncogenes may be important for hair growth, but more research is needed.

The Celsr1 gene is crucial for normal hair patterning in mice.

A protein made in a plant stopped hair growth in mice.

Tabby mutations in mice affect hair follicle development and help study genetic mapping and certain medical conditions.

Loss of Msx2 function causes eye development issues similar to Peters anomaly.

Zinc deficiency in alcoholic cirrhosis patients causes skin issues, and zinc treatment improves symptoms.

NcoA4 may have roles beyond helping control gene activity, possibly affecting cell behavior and stability.

Zinc therapy improved hair health in a girl with acrodermatitis enteropathica.

Distinct β-catenin patterns are linked to cell growth, not cell death, in lung cancer.

The conclusion is that a new test was created to find substances that affect specific ion channels, and it works well for drug discovery.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

aPKCλ is crucial for keeping hair follicle stem cells inactive and maintaining normal hair growth.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Lack of TG2 increases fat storage and lowers cell cleanup in skin oil cells.

A boy with a rare form of early puberty caused by a new gene mutation responded well to treatment aimed at reducing testosterone and preserving adult height.

Pygo2 is important for early growth and progression of intestinal tumors, and could be a target for treating cancers with certain mutations.

A new genetic mutation was found causing hair and eye issues in a boy.

Runx1 controls fat-related genes important for normal and cancer cell growth, affecting skin and hair cell behavior.

Cathepsin L deficiency causes hair and skin issues in mice.