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Beer yeast vesicles may improve hair follicle health.

Araliadiol may promote hair growth like minoxidil without being toxic.

A new method using a microfluidic device can prepare hair follicle germs efficiently for potential use in hair loss treatments.

GPC1 is important for blood vessel growth in hair follicles and could help treat hair loss.

GPC1 is important for hair growth by helping blood vessels form around hair follicles.

GPC1 is important for blood vessel growth in hair follicles and could help treat hair loss.

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

A new method quickly and efficiently isolates hair follicle stem cells from adult mice, promoting hair growth.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

Scientists made glow-in-the-dark dots from human hair that can detect iron, prevent counterfeiting, and reveal fingerprints.

Hataedock treatment improved skin health and reduced atopic dermatitis symptoms by enhancing the skin barrier and reducing inflammation.

Increased HSD11B1 enzyme expression is linked to higher body fat and insulin resistance.

Familial frontal fibrosing alopecia is rare, mostly affects women, and often occurs between sisters or mother-daughter pairs.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

The fuzzy gene is crucial for controlling hair growth cycles.

A new hair restoration technology was found to effectively increase hair thickness, density, and growth, while reducing hair loss and improving scalp health, with no side effects.

Arabidopsis Formin 2 stabilizes actin filaments to aid cell-to-cell trafficking.

The folate-cyclodextrin conjugate targets cancer cells more precisely, potentially reducing chemotherapy side effects.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

Neural crest-derived progenitor cells in the cornea could help treat corneal issues without transplants.

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

Human hair keratin might be good for filtering out harmful substances from water.

A patient with Ehlers-Danlos Syndrome improved after treatment for fat malabsorption and essential fatty acid deficiency.

Combining amino acid and stem cell therapy may help manage hepatocutaneous syndrome in dogs.

The protein FLCN is involved in cellular cleanup and is regulated by ULK1.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

Inhibitors of 11β-HSD1 show potential for treating type 2 diabetes but require more testing for safety and effectiveness.

A rare genetic skin condition usually affecting males was found in a 9-year-old girl.

Deferasirox combined with sorafenib reduces liver cancer risk and lessens treatment side effects.