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TCDD changes skin cell growth and keratin production in mice.

Targeting vitamin D and androgen receptors may effectively treat triple-negative breast cancer, especially with chemotherapy.

EGFR inhibitors can cause unusual localized hair growth.

Dupilumab improved hair and skin in a woman with Netherton syndrome.

Activating β-catenin in different skin stem cells causes various types of hair growth and skin tumors.

Twist2 is essential for scarless skin healing and hair growth in mouse fetuses.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

MAP-2 is crucial for the structure of hair follicles and nails.

Suppressing ODC activity reduces tumor growth in hair follicles.

Targeting EGFR may help reduce hair loss from chemotherapy.

A mutation in the Sgkl gene causes defective hair growth in mice.

The assay effectively identifies compounds that affect immune cell activation.

Sesn2 protects inner ear hair cells from damage by regulating certain cell survival pathways.

Delta-opioid receptors affect skin cell circadian rhythms, possibly impacting wound healing and cancer.

β-Catenin signaling is involved in brain cell growth after injury and could be a therapy target.

Fixing DNA errors is crucial to prevent skin cancer.

RhoA helps skin stem cells grow, aiding wound healing.

New treatments targeting specific genes show promise for treating keratin disorders.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

Patients on dabrafenib and trametinib for melanoma often experience skin side effects.

PH-762 shows promise in treating skin cancer by effectively targeting and silencing PD-1 in tumors with minimal side effects.

Pitx2 helps outer root sheath cells differentiate but can't start hair growth on its own.

Brg1 is crucial for hair growth and skin repair by maintaining stem cells and promoting regeneration.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

Lgr5 and the vitamin D receptor are key in controlling skin inflammation and tumor risk in mice.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

Transferrin receptor 1 is essential for normal function in the intestines, pancreas, and skin.