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The ALADIN score can predict how well patients with alopecia areata will respond to JAK inhibitor treatments.

Tofacitinib helped regrow hair in a woman with alopecia areata.

CTCF protein is essential for skin and hair follicle development in mice.

A woman with severe hair loss saw significant hair regrowth after adding platelet-rich plasma injections to her treatment with tofacitinib.

People with palmoplantar pustulosis, especially with bone issues, have different mouth bacteria compared to healthy people.

TRIV-509 quickly improves skin barrier and cell health in atopic dermatitis.

Tofacitinib is a potential alternative treatment for alopecia totalis, especially in patients with a shorter duration of the condition and more preserved hair follicles, but the overall response rate is low.

A 3-year-old boy was diagnosed with a rare, non-scarring hair loss condition called temporal triangular alopecia.

Trichoscopy effectively diagnoses temporal triangular alopecia in children.

TGF-β2 helps yak hair follicles enter the regression phase, while HSP70 tries to prevent it.

Tofacitinib is a safe and effective treatment for hair loss in children with Alopecia Areata.

Mutations in the HOXC13 gene cause hair and nail development issues.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

The KRTAP19-5 gene affects wool curvature in Chinese Tan sheep, with Variant B reducing curvature.

Thrombospondin-1 is crucial for hair follicle regression and reduced blood vessel growth during the catagen phase.

Using testosterone-stimulated weanling rats can effectively replace castrated rats for anti-androgen testing, reducing animal stress.

KRT72 gene helps form hair.

Skin tumor cells in patients with tuberous sclerosis have higher levels of a protein called cathepsin B.

A specific gene mutation causes woolly hair and hair loss.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

FOXN1 duplication can cause excessive hair growth.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

Trichohyalin is a versatile protein involved in hair and skin structure.