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The C-terminal tail of AHF/trichohyalin is essential for organizing keratin filaments in keratinocytes.

No significant link between CAG repeat numbers and female pattern hair loss in Han Chinese population.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

Stem cells from whiskers can be transplanted to stimulate hair growth.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

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

Skin cancer often starts from Lgr5+ progenitor cells.

A rare case of a transplant patient developing a skin condition linked to HPV-49.

Hair follicle stem cells change states with age, affecting hair growth and aging.

Increased methylation of the Filip1l gene may contribute to aggressive skin cancer.

Hoxc13 is important for hair and tongue development by controlling hair keratin genes.

Targeting the TNFRSF1B gene may help treat hair loss.

A specific genetic mutation may increase male pattern baldness risk, especially in Europeans.

A Japanese patient with a rare genetic disorder had a less severe case than others, suggesting other factors may affect symptoms.

A mouse gene mutation increases the risk of skin cancer.

Certain gene variations may increase the risk and severity of alopecia areata.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

Budesonide and N-acetylcysteine reduced tumors and alopecia in mice, regardless of FHIT gene status.

High-content screening is useful for finding new treatments for rare diseases and has led to FDA-approved drugs.

Researchers found a new gene area linked to male-pattern baldness, which, along with another gene, significantly increases the risk of hair loss in men.

A specific enzyme is essential for proper hair follicle stem cell development and healthy skin.

Several genes, including Hox-7A, Stra6, and Lim-1, are involved in normal palate formation.

Variation in the TCHH gene affects wool curliness in sheep.

PBX1 reduces aging and cell death in stem cells by boosting SIRT1 and lowering PARP1.

miR-200c-3p could help diagnose and treat alopecia areata.

NSC167409 can effectively inhibit the virus causing hand, foot, and mouth disease.