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PBX1 helps hair stem cells grow and change by turning on certain cell signals and preventing cell death, which may be useful for hair regrowth treatments.

Finasteride helps female-pattern hair loss.

Two new mutations in the AR gene linked to severe androgen insensitivity were found.

ILC1-like cells can cause alopecia areata by themselves.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

mEphA1 receptor tyrosine kinase is important for skin and hair development and may play a role in certain diseases.

Scientists discovered two versions of a new human hair keratin gene.

PINK1 is important for controlling gut immune responses linked to early Parkinson's disease.

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

CD8A and FOXD2-AS1 may be key for diagnosing and treating alopecia areata.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

Mutations in the Whn gene affect hair keratin gene expression differently.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

FOXN1 mutations can cause varying immune and physical issues, with severity influenced by gene activity and possibly other factors.

BLMP-1 is important for regular molting and gene expression cycles in worms.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

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

Mutations in the p63 gene affect skin adhesion, barrier integrity, and hair growth.

Different PADI isoforms help cells develop diverse functions.

The study mapped keratin 15 and 19 genes, aiding future genetic disorder research.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Aire mutation reduces alopecia areata, while Notch4 mutation prevents it in mice.

AP-1 and TGFß work together to drive resistance in basal cell carcinoma, suggesting new treatment options.

Genetic marker rs12558842 strongly linked to male hair loss.

The oncoprotein causes abnormal hair growth without increasing skin cancer risk.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.