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Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

The N gene affects the protein makeup of mouse hair.

The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

Genetically modified rats help reveal how vitamin D affects bone and skin health.

Basonuclin 1 (BNC1) helps skin cells multiply and move, which is crucial for wound healing.

Different body areas have unique skin cell communication patterns, explaining why certain skin diseases occur in specific regions.

Yorkshire Terriers with Colour Dilution Alopecia have reduced melanin and hair structure issues.

Enteral supplements can improve symptoms of Cronkhite-Canada syndrome.

The CTLA-4 gene polymorphism does not affect polycystic ovarian syndrome.

Regular endoscopic checks are crucial for Cronkhite-Canada syndrome patients to catch potential cancers early.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Activated β-catenin affects hair growth and skin thickness, and changes are reversible.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Familial dyskeratotic comedones are a rare, benign skin disorder that is hard to treat.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Lack of cystatin M/E causes thin hair and dry skin.

Certain gene variations increase the risk of alopecia areata in Koreans.

Androgens increase muscle mass by promoting myoblast growth through ornithine decarboxylase.

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

DNMT1 may help treat hypospadias by improving cell function and preventing unwanted cell changes.

Researchers created a cell line to study hair growth and found specific genes affected by dihydrotestosterone.

The most common sign of aging at the gene level is more Ectodysplasin A2 Receptor (EDA2R) being made.

Steroid treatment improved both gut and nerve symptoms in a man with Cronkhite–Canada syndrome.

Cancer-associated fibroblasts promote tumor growth in skin cancer.

CRABP1 boosts hair cell growth in Hu sheep by affecting key genes.