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K39 and K40 are the last keratins expressed in hair development, completing the hair keratin catalog.

The study created a mouse model to better understand hair follicle stem cells' role in hair growth and repair.

CLK1 is needed for skin cells to become epidermal cells but not sebocytes.

Cnicus Benedictus leaf extract can kill cervical cancer cells without harming normal cells.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

Transcutaneous vaccination using nanoparticles can enhance immune responses and reduce basal cell carcinomas.

Genetic mutations that disrupt homocysteine breakdown lead to increased damage in mouse hair keratin.

The man was diagnosed with Cronkhite-Canada syndrome, a rare disorder with GI polyps, skin issues, hair loss, and nail problems.

Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.

Neurokinin B levels are higher in the placentas of women with PCOS who have female babies.

Hexi cashmere goats' hair growth varies by stage, with Hoxc13 linked to hair activity.

The investigation found no work-related causes for employee hair loss at Equifax Payment Services, and the environment was not hazardous.

A genetic variant linked to hair thinning in Japanese women was found.

CAG repeat numbers in the AR gene likely don't affect male pattern baldness in Korean men.

Hair cortisol measurement can help diagnose and monitor Cushing’s disease.

L-Cystine and L-Cystine with Kera-Diet® safely improved hair and nail quality in healthy women.

Certain SPINK5 gene mutations are common in Israeli families with Comèl-Netherton syndrome.

The CAP1 gene helps control ammonium levels and is necessary for the proper growth of root hairs in Arabidopsis.

HOXC13 is crucial for regulating hair keratin genes in hair follicles.

HBCs in the olfactory epithelium can self-renew or differentiate into other cell types, with specific patterns during regeneration.

A missing mK6irs1 gene causes hair loss in mice.

Mutant MK6a transgenes in mice cause blistering, hair loss, and potential human alopecia.

Netherton syndrome causes skin and hair issues, confirmed by "bamboo hair" under dermoscopy, with no cure but managed with topical treatments.