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Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

Keratin2-6g is crucial for hair follicle development, with mutations causing cell degeneration and vacuolation.

New genes and pathways are important for testosterone production and male sexual development.

A rabbit gene important for hair development was identified and detailed.

Recombinant keratin K31 makes damaged hair thicker, stronger, and straighter.

Human anagen hair follicles have unique carbohydrate patterns during keratinization.

Human basal cell carcinomas and squamous cell carcinomas have unique gene expression patterns not fully mirrored in mouse models.

NBCCS and BFHS might be the same syndrome, helping better identify and manage cases.

SETDB1 is essential for controlling DNA methylation, silencing retrotransposons, and maintaining skin cell health, with its absence leading to skin inflammation and hair loss.

Different PADI isoforms help cells develop diverse functions.

Ptprq has multiple forms that change during inner ear development.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Two new enzymes, PAD-R11 and PAD-R4, were cloned and showed activity, with PAD-R11 resembling epidermal enzymes.

Hsc70 protein may influence hair growth by responding to androgens.

Two genetic variations in Moa buffalo help them adapt to heat.

A truncated protein linked to breast cancer may change cell adhesion.

Hair differentiation starts earlier than thought, involving multiple type-II keratins.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

Keratin gene regulation is similar across mammals, affecting hair follicle differentiation.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

The skin of both rat strains showed similar lectin binding patterns.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

A mycobacterial protein shares a similar region with a human skin protein, possibly affecting skin diseases.

PRO-C22 can help diagnose and monitor the severity of hidradenitis suppurativa.

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.