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IL-17 plays a key role in severe hair loss in chronic alopecia areata.

Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

The KRTAP15-1 gene affects cashmere fiber thickness in goats.

Coinheritance of BRCA2 and CYLD genes may lead to new treatment options for certain cancers.

DKK2 and SOSTDC1 together are necessary for the normal timing of the first regression phase in the hair growth cycle.

New therapies and trials are needed for Merkel cell carcinoma, a tough skin cancer.

Collagen XVIII and Bmx tyrosine kinase are important for hair growth and skin cancer development.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

High-dose radiation speeds up aging in skin stem cells.

Keratinocytes can reverse the effects of the GNAQ oncogene, inhibiting melanoma cell growth.

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

Mutations in the SNRPE gene cause hereditary hair loss.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

KAP6 genes are conserved across species and active in hair follicles.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

MCHR2 gene duplications may be linked to alopecia areata.

Hirsute women have lower type 2 17β-HSD enzyme levels, which improve with treatment.

The gene for Marie Unna hereditary hypotrichosis is located on chromosome 8p21, near the hairless gene.

The PCR technique can identify genetic differences in a wool-related gene among different sheep breeds, which may help improve wool and pelt quality.

Keratin K14 expression varies between hair follicles and epidermis, affecting cell differentiation.

CARASIL can cause different symptoms even with the same genetic mutation.

STK11 gene variations do not predict how well metformin will work for PCOS, but may affect hair loss and excess hair growth.

PSENEN gene mutations can cause both Dowling-Degos disease and acne inversa.

A new method, iSiMPRe, effectively identifies key protein regions in cancer genes, highlighting potential drug targets.

Mice with extra PKCδ resist chemical-induced skin cancer but not UV-induced.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

Hairless protein helps control hair growth by regulating vitamin D receptor activity.