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The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

A new compound slows cancer cell growth and causes cell death by blocking cell cycle progression and increasing cell-damaging molecules.

Erlotinib causes skin inflammation through IL-1, which can be reduced by anakinra.

Basonuclin 2 is vital for the development of facial bones, hair follicles, and male germ cells in adult mice, and its absence can lead to dwarfism and abnormal follicles.

Mouse hair keratins mHa1 and mHb4 can't form a strong network on their own in cells.

A new microneedle patch significantly improves melanoma treatment by using a special material to activate cancer-fighting drugs and disrupt cancer cells.

CCCA may involve the PD1/PDL1 pathway and increased caspase 3, leading to permanent hair loss.

MPZL3 protein affects hair growth cycles and could help manage hair loss.

Removing GRK2 in skin cells causes hair loss similar to immune-related alopecia.

ZPK helps skin cells mature and may affect skin health.

ETS2 is crucial in squamous cell carcinoma development and could be a therapeutic target.

c-kit affects hair growth and color in alopecia areata and androgenetic alopecia.

Ca²⁺-mediated protein citrullination controls cell growth in the CNS and may help treat brain tumors.

Specific mutations in a receptor cause facial abnormalities and hair loss.

DNA methylation of miR-365-1 causes hair follicle stem cell death by affecting DAP3.

Ritlecitinib is being tested for safety and effectiveness in young children with severe alopecia areata.

Metformin, a diabetes drug, may also help fight cancer, but more research is needed to understand how.

High TSPEAR levels in colorectal cancer predict worse outcomes.

KAP8.1 protein is crucial for hair structure and interacts with keratin 85.

Activating certain hair follicle cells could prevent hair loss from cancer treatments.

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 new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

An allele of the KRTAP13-2 gene may improve wool quality in sheep.

ATP-dependent chromatin remodeling is crucial for skin development and stem cell function.

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

Arabidopsis Formin 2 stabilizes actin filaments to aid cell-to-cell trafficking.

Mirex seems to promote a unique group of skin cells different from those affected by another tumor promoter, TPA.

Vitamin C derivative reduces hair loss-related protein in cells.

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