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A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

Different wool coat types in goats are linked to specific gene expressions, which could improve cashmere quality.

K6/ODC transgenic mice are effective for quickly identifying cancer-causing chemicals.

CMG2 and TEM8 receptors have distinct roles in skin and growth disorders, affecting collagen breakdown and growth.

Pax9 is crucial for proper tongue surface development and preventing skin-like changes.

FGF20 is essential for hair follicle stem cell growth and development in fine-wool sheep.

Runx1 is crucial for proper hair structure and development.

Exosomal miR-199a-3p from dermal papilla cells helps control hair color by affecting melanocytes.

Csdc2 helps hair growth in cashmere goats by regulating specific genes.

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

The study mapped keratin 15 and 19 genes, aiding future genetic disorder research.

Hoxd gene regulation in mammals and birds is robust despite differences in DNA sequences, due to 3D chromatin structures.

BMI1 is essential for preventing hair greying and maintaining hair color.

Exosomes from small-tailed Han sheep can boost hair growth and thickness in mice.

Accurate diagnosis and early specialist referral are crucial for managing 46,XY Disorders of Sex Development.

Primary and secondary hair follicle cells in Cashmere goats have different gene expressions affecting hair growth and size.

Minoxidil improved hair growth in a child with a rare genetic disorder.

The enzyme system in hair follicles is similar to the liver's and is inhibited by certain substances.

Fibre optic confocal imaging can visualize skin layers, blood vessels, and nerves in live mice.

Steroid sulfatase inhibitors could help treat hormone-related disorders and cancers.

Gene variation affects prostate issues and hair loss.

DPC-Exos can help regenerate hair follicles and heal wounds by activating the Wnt/β-catenin pathway.

Goat skin adapts to seasonal changes through genes that respond to daylight length, affecting hormone levels and potentially making skin cells light-sensitive.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

Apoptosis and ribosomal proteins are key in hair follicle cycle changes in cashmere goats.

Fetuin A levels are higher in PCOS patients, while asprosin levels show no difference.

Blocking the NOTCH pathway can prevent fibrosis in systemic sclerosis.

Foxc1 helps keep hair follicle stem cells inactive, preventing hair loss.

Early over-expression of FoxN1 harms immune and skin development.