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Protein kinase C epsilon may promote skin cancer development after UV exposure by affecting nearby cells.

PTCH gene mutations contribute to basal cell carcinoma development.

MCSP may help identify and regulate skin stem cells, affecting hair growth and regeneration.

Different hair types in mammals are linked to variations in specific protein genes, with changes influenced by their living environments.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

Injecting 6-OHDA in newborn mice delays hair growth and thins skin.

CS12192 effectively treats alopecia areata with better safety than current options.

Prostasin has two roles in skin: one for normal skin development without needing activation, and another for proper hair growth that requires activation.

NKIRAS2 can suppress certain skin tumors but its effect on cancer varies with context and expression level.

Overexpressing PKCepsilon in mice reduces papillomas but increases carcinomas.

Type VII collagen absence helps skin development by allowing tissue remodeling.

Mice with human-like EGFR had growth issues, skin defects, heart problems, and unusual bone development.

Bimekizumab quickly improves psoriasis symptoms and skin at the molecular level.

Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

TB and BCC tumors show similar follicular differentiation patterns.

Defects in certain proteins cause major heart abnormalities during early development.

FP-1 is a key protein in rat hair growth, active only during the growth phase.

A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

Mutations in the Sgk3 gene cause fuzzy hair in mice.

The study found that p63 needs signals from morphogens to help skin cells differentiate properly.

The enzyme pyruvate kinase M2 helps hair regrowth and could be a potential treatment for hair loss.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Inward rectifier potassium channels are important in many body functions and diseases, and could be potential drug targets.

Keratin is crucial for skin barrier formation and affects mitochondrial function.

The new keratin film without KAPs stains better and could help study keratin functions.