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The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.

KRTAP28-1 gene can help breed sheep with finer wool.

A specific microRNA, chi-miR-30b-5p, slows down the growth of hair-related cells by affecting the CaMKIIδ gene in cashmere goats.

CXCR2 in skin cells promotes tumor growth.

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.

Krt15+ cells in mice can resist radiation, regenerate tissue, and start tumors, suggesting new cancer treatment targets.

Genetic testing for hairless gene mutations is crucial to correctly diagnose and treat atrichia with papular lesions.

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

Removing UBE2N from skin cells causes inflammation and immune response, which can be lessened with specific inhibitors.

A new model uses specific blood markers to predict if children's hair loss will return.

Double-stranded RNA activates a pathway that causes a skin protein to be expressed in the wrong place.

Deleting NIPP1 in mouse skin cells causes early aging and chronic skin issues.

Alopecia from CDK 4/6 inhibitors worsens quality of life in breast cancer patients.

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

MPA increases cancer spread by boosting Eph A2 activity.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

Brepocitinib improves cicatricial alopecia and reduces key immune markers.

Harlequin mutant mice have hair loss due to low AIF protein levels and retroviral element activity.

Genetic marker rs12558842 strongly linked to male hair loss.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

A genetic variant in the KRT25 gene causes tightly curled hair.

Certain mutations in the PADI3 gene may increase the risk of developing a type of scarring hair loss common in women of African descent.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Sheep have a unique gene, KAP8-2, that humans don't have, which may affect wool properties.