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Localized dystrophic epidermolysis bullosa (DEB) can lead to scarring alopecia, highlighting the need to recognize and address this complication.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

3-Deoxysappanchalcone helps human hair cells grow and stimulates hair growth in mice by affecting certain cell signaling pathways.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Diphenylcyclopropenone treatment helps hair growth in alopecia areata by promoting blood vessel growth and cell survival.

EBF1 controls hair type and length.

MCHR2 gene duplications may be linked to alopecia areata.

Hair shaft changes may be linked to CCCA, but their role is unclear.

Hair follicle cells change their DNA packaging during growth cycles and when grown in the lab.

Dissecting cellulitis may have genetic links and can cause permanent hair loss.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

Dermoscopy shows that diffuse alopecia areata progresses through specific hair growth stages.

Deucravacitinib helped a man regrow hair significantly.

The medicine Cyclosporin A might cause excessive hair growth by reducing a protein that controls hair growth.

The conclusion is that Darier-White disease was accurately described by White but he missed the key feature of dyskeratotic cells which Darier identified.

MAD2B slows down the growth of skin cells that are important for hair development by interacting with TCF4.

The gene LRRC15 is more active in balding areas of the scalp compared to non-balding areas.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

Norgalanthamine helps hair cells grow by activating certain pathways related to hair growth.

Dermal cell activity increases during hair growth in rats.

Actin filaments help stabilize and reshape cell membranes.

Researchers created immortal human skin cells with constant testosterone receptor activity to study hair loss and test treatments.

Actin filaments help stabilize and integrate cell membranes during transfer.

Early shedding of the inner root sheath in noninflamed hair follicles is a relatively specific sign of Central Centrifugal Cicatricial Alopecia.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

A specific gene mutation causes a severe skin disorder in a family.

Familial dyskeratotic comedones are a rare, inherited skin condition that is hard to treat but may improve slightly with topical retinoids and urea cream.

β-catenin in the dermal papilla is crucial for normal hair growth and repair.

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