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Alpha-difluoromethylornithine prevents cancer in mice but causes hair loss.

Human hair keratin has a 40% α-helix structure that changes to a random coil in 8 M urea.

IL-18 levels are higher in hidradenitis suppurativa patients and may indicate disease severity.

A new amino acid derivative, ATS, improves hair texture and moisture, making it easier to straighten curly hair.

A certain genetic variant in the androgen receptor may predict the severity of COVID-19 in men.

Antiandrogens affect androgen-dependent body functions and are used for various medical conditions, with some risks like fetus feminization, but new forms like 17α-propylmesterolone show promise for acne without systemic effects.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

Foreskin keratinocytes and SVK14 cells express certain cytochrome P450 enzymes, unlike hair follicle keratinocytes.

HOXC13 is essential for hair and nail development by regulating Foxn1.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Using 5-butylpicolinate esters improves the sensitivity and reliability of detecting testosterone and dihydrotestosterone in saliva.

Uncombable hair is inherited dominantly with complete penetrance.

Mixed coconut oil/solvent is suitable for cyproterone acetate injections, but more safety checks are needed.

The NUDT15 gene variant causes severe side effects from azathioprine in some Indian patients.

Four new genes related to sheep wool were discovered, showing genetic diversity.

HAIRCARECUBE TM (HCC) helps hair products work better by getting active ingredients deeper into the hair.

Carthamus caeruleus L. extracts have strong antioxidant and anti-inflammatory effects.

BcFLA1 protein is crucial for root hair growth in response to low phosphate in Brassica carinata.

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A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

Osthole inhibits the TRPV3 channel by binding to specific sites, potentially aiding drug development for skin diseases and cancers.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

Higher expression of the keratin-associated protein 8.1 gene in Liaoning cashmere goats is linked to finer cashmere fibers.

Different cells affect hair follicle blood vessels, endothelial cells react differently to inflammation and oxidized fats, and prasugrel better protects heart vessels during a procedure than clopidogrel.

The synthetic retinoid EC23 thickens skin and promotes hair growth more effectively and with a lower dose than natural retinoids.

A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

A genetic variant in "Blonde d'Aquitaine" calves causes death at birth due to a missing protein.