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

Some new progesterone derivatives are better at blocking testosterone conversion than a common drug.

A new, quick method was developed to analyze skin lipids, discovering a new ceramide subclass.

New technologies help us better understand how skin microbes affect skin diseases.

Quercetin can boost hair follicle stem cell growth in cashmere goats, potentially improving cashmere quality.

Lichen planus pigmentosus mainly affects middle-aged women with darker skin, is underreported, and is hard to treat.

A specific gene mutation causes severe skin and nail issues and hair loss.

Gene knockout mice developed scars similar to human hypertrophic scars, useful for studying scar progression.

EGFR and mTOR inhibitors may help manage Olmsted syndrome symptoms.

Hyper-keratinisation in Meibomian glands contributes to gland dysfunction.

Key genes, including KRT39 and KRT74, influence hair length in Inner Mongolia cashmere goats.

Monilethrix causes short, fragile hair with no specific treatment available.

Proteoglycans are vital for tissue growth and healing, with potential as treatment targets.

Early sunburn treatment with certain inhibitors may reduce skin cancer risk.

Nitrogen starvation in microalgae increases lipid production, making it a potential biofuel source.

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.

Reduced TRPS1 leads to increased STAT3 and SOX9 in hair follicles, affecting hair growth.

Skin organoids can regenerate hair by forming specific cell units with certain signals.

Not having enough cystatin M/E protein causes less hair growth and dry skin.

RORs may influence cashmere growth cycles.

Accurate diagnosis and management of rare genian fistulas require combined clinical, radiologic, and histopathologic evaluations.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

Classical PCOS types A and B are most common and linked to higher health risks.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

Using cosmetics made elderly people feel more comfortable and attractive.

Genetic testing is crucial for diagnosing rare hair loss disorders.

Msx2 is essential for proper enamel formation by preventing abnormal cell transformation.

A 36-year-old person with a female appearance but male chromosomes was diagnosed with a rare enzyme deficiency affecting sexual development.

A 5-year-old girl has lipoid proteinosis, causing voice issues, hair thinning, skin lesions, and tongue movement problems.

CRISPR/Cas9 gene editing in cashmere goats increases hair follicles and fiber length, boosting cashmere yield.