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Triphenylphosphine oxide can increase oil production and reduce inflammation in skin cells without affecting TRPM5.

A new system for classifying curly hair types using precise measurements can improve hair care products and cultural inclusion.

Women with PCOS, especially if they are obese, are more likely to have an underactive thyroid than women without PCOS.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

The patient's hair improved after treatment, but the genetic link is unclear.

Overexpression of IKZF1 and Ikaros causes hair loss in mice similar to alopecia areata.

Removing GRK2 in skin cells causes hair loss similar to immune-related alopecia.

MITF+ melanoma patients are more likely to have multiple melanomas and unique skin patterns.

New methods to classify curly hair types were developed based on shape and strength.

Both atopy and eosinophilia are linked to more severe hair loss in people with alopecia areata.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

Postmenopausal ovary stromal cells have a unique makeup and limited steroid production, suggesting androgens come from the adrenal gland.

Removing anthrax toxin receptor 1 in pigs prevents Senecavirus A infection and causes a rare disease similar to GAPO syndrome.

Colorectal cancer cells can adapt without losing their traits or drug sensitivity.

Fibromodulin treatment helps reduce scarring and improves wound healing by making it more like fetal healing.

Sulfated hyaluronan in collagen helps hair follicle cells grow and develop better for skin grafts.

A new syndrome, Teelwani Syndrome, combines features of two rare genetic disorders.

Removing the ATR gene in adult mice causes rapid aging and stem cell loss.

Certain microRNAs in the fluid around eggs are linked to Polycystic Ovary Syndrome and may help diagnose it.

People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

Normal-range ALT levels can indicate metabolic and hormonal imbalances in young women.

IL-4 and IL-13 might play a role in a type of hair loss similar to alopecia areata.

The type of PCOS a woman has doesn't strongly predict her skin or metabolic symptoms; obesity is a more important factor.

CD4 T cells can cause alopecia areata by activating CD8 T cells to attack hair follicles.

High CCL11 levels may indicate poor response to baricitinib in severe alopecia areata.