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A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

Hairless protein can both repress and activate vitamin D receptor functions, affecting gene regulation.

Lack of small, fine hair on the front hairline is a key sign of frontal fibrosing alopecia.

A patient with advanced kidney cancer and no hepatitis C developed skin inflammation due to a drug called interferon alpha-2a.

A new genetic variant of Woodhouse-Sakati syndrome was found in two adult sisters in Russia.

Two brothers from Bangladesh were diagnosed with X-linked adrenoleukodystrophy, showing neurological and adrenal symptoms.

PN hydrates skin; PDRN heals and regenerates skin and hair.

Autoimmune Polyendocrine Syndromes involve specific combinations of autoimmune diseases.

Different skin conditions show distinct types of vessel inflammation, a new quality of life index for vulval disease is reliable, a certain intrauterine system might be linked to chronic vaginal yeast infections, and oral minoxidil reduces hair loss in women.

Genetic analysis is crucial for diagnosing and managing cerebral arteriopathy.

AIRE-deficient rats developed severe autoimmune disease similar to APECED, useful for testing treatments.

CD117 and platelet-derived growth factor receptor α may play a role in alopecia areata.

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

Type-2 immunity may influence skin diseases and could be targeted for treatment.

These specific gene polymorphisms are not linked to Alopecia Areata in Egyptians.

Hair dye ingredient PPD can cause severe allergic reactions, including facial swelling.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Ezh2 controls skin development by balancing signals for dermal and epidermal growth.

TRPV3 channels are involved in skin processes and are affected by shear stress, influencing itch and mechanotransduction.

The B2 genes are crucial for hair growth in rats.

Hair follicles in nonsegmental vitiligo are better protected from immune attacks than in alopecia areata.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

Different types of PPARγ are found in varying amounts in human skin and its parts, which could affect how skin treatments work.

TRPA1 and TRPV1 channels don't affect mechanotransduction in rat sinus hair follicles.

Segmental vitiligo affects hair follicle melanocytes, causing small, uniform depigmented spots.

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

A small group of slow-growing cells causes basal cell carcinoma to return after treatment.

Oral difelikefalin significantly reduces itch in notalgia paresthetica.

Microarray analysis helps find hidden chromosomal changes in patients with intellectual disabilities and birth defects.