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Topical ceramide treatment partially improves the skin condition in Jack Russell Terriers with a genetic skin disorder.

Electrical stimulation with minoxidil boosts hair cell growth.

Removing certain hair follicle stem cells worsens skin reactions to allergens.

A specific metabolite, not a receptor protein, triggers the production of certain kidney enzymes, but this process is disrupted in mice with a mutation causing testicular feminization.

Mice with extra sheep genes had hair that fell out and regrew in cycles.

Both SMS1 and SMS2 are crucial for normal hair growth and cycle in mice.

Enhanced stem cells from the placenta can help treat Graves' eye disease by stopping fat cell growth.

Corneodesmosin is crucial for skin and hair health, and its dysfunction can cause skin and hair disorders.

Modified β-catenin causes different effects in hair and skin cells, leading to cysts or tumors.

The HGCA tool helps identify genes that work together by analyzing their co-expression patterns.

Increased ornithine decarboxylase makes normally tumor-resistant mice more sensitive to tumors.

ZNF750 and MPZL3 are important in causing seborrheic dermatitis.

Loss of Ten1 in mice causes telomere shortening and symptoms similar to human dyskeratosis congenita.

Dihydrotestosterone (DHT) promotes the growth and spread of aggressive brain tumor cells.

The mTurq2-Col4a1 mouse model shows how the basement membrane develops in live mammals.

Mouse high-glycine/tyrosine proteins have distinct patterns in hair follicles, peaking at specific hair cycle days.

The ABCG2 gene variant increases the risk of high uric acid and cholesterol, especially in overweight or obese young Mexican males.

Deleting a specific protein in skin cells disrupts normal hair growth and development.

Melatonin helps improve Cashmere goat hair quality by promoting hair follicle growth through a specific cell signaling pathway.

Transglutaminase-3 is often reduced in esophageal cancer.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

A specific gene mutation causes monilethrix in this family, and minoxidil treatment improves hair condition.

MPZL3 is crucial for seborrheic dermatitis development.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

A new gene mutation causes insulin resistance in a girl and her mother.

ODC overexpression in hair cells increases tumor growth by reducing Notch signaling.

Researchers found four genes that could help diagnose severe alopecia areata early.

No consistent link between genotype and phenotype in 5-α-Reductase type 2 deficiency.