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PRAME helps distinguish between benign and malignant skin cells in most cases.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

Frontal fibrosing alopecia is linked to four genetic areas, especially the HLA-B*07:02 allele.

Two new enzymes, PAD-R11 and PAD-R4, were cloned and showed activity, with PAD-R11 resembling epidermal enzymes.

Ritlecitinib is an effective new treatment for Alopecia Areata.

Keratin-associated proteins help link filaments and affect keratin's strength.

R-Spondin-1 is important for skin health and could help diagnose and treat various skin conditions.

Keratin 75 might be important in oral cancer progression.

CXXC5 can both suppress and promote cancer, making it a complex target for treatment.

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

PAR-1 may play a role in hair growth regulation in human hair follicles.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

Patched1 helps prevent tumors by controlling cell growth.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

Differences in androgen receptor expression and tissue properties may lead to higher cryptorchidism risk in certain rats.

Upadacitinib successfully regrew hair in a child with alopecia universalis and specific genetic mutations.

Possible link between hair loss and metabolic syndrome, with RANTES as a potential clue.

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

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

A new gene, JMJD1C, may affect testosterone levels in men.

Mutations in the hairless gene cause a rare form of permanent hair loss.

hsa_circ_0001079 may help diagnose and treat hair loss.

Strontium ranelate helps cartilage growth by blocking a specific cell pathway.