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TNFα and interleukin-1 blockers reduce skin inflammation from EGFR antibody therapy.

Keratin-gelatin films improve skin graft success in dogs.

DAB labeling effectively identifies collagen type III and PDGFR in horse skin, but may show false positives.

A patient with Alopecia Areata had complete hair regrowth after using the drug baricitinib.

JW0061 may be a new treatment for hair loss by promoting hair growth through WNT signaling.

Activin B helps start and grow hair follicles in mice.

Mouse and human keratin 16 can both form filaments, with differences likely due to the tail domain, not the helical domain.

AP-2α and AP-2β are crucial for healthy skin and hair.

Tofacitinib is a promising treatment for children with rheumatic diseases.

α- and γ-catenins help develop fetal skin by 23 weeks.

A new therapy for a skin blistering condition has not been developed yet.

The study created hair-bearing skin models that lack a key protein for skin layer attachment, limiting their use for certain skin disease research.

Targeting the PIEZO1 and MLCK axis may offer a new treatment for hair loss.

Glypican-1 is important for hair follicle blood vessel growth and could be a target for treating hair loss.

Tofacitinib is effective and safe for treating severe alopecia areata and related conditions.

Club-like receptors detect light touch but not whisking.

Trichohyalin, a hair follicle protein, has a part with repeating patterns of 23 amino acids.

Baricitinib combined with other immune therapies may safely and effectively treat severe scalp hair loss.

lncRNA VIM-AS1 helps heal diabetic wounds by boosting energy production and reducing cell aging.

Higher levels of MIG and IP-10 may help diagnose and monitor Alopecia Areata.

The treatment was not recommended due to limited effectiveness and significant side effects.

The enzyme 5α-reductase type 1 is important for blood vessel development and fertility in the uterus.

A specific type of immune cells, called CD301b-expressing macrophages, are crucial for skin repair processes.

Desmosomes are crucial for skin and heart development, and JNK may help regulate them.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

WIF1 helps keep skin stem cells inactive to prevent excessive cell growth.