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A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Melanocyte-associated antigens may play a key role in alopecia areata and could be targets for new treatments.

Bcl-2 affects hair growth and pigmentation by controlling cell death.

Arg1+ macrophages may play a role in causing alopecia areata.

CS12192 effectively treats alopecia areata with better safety than current options.

hsa_circ_0001079 may help diagnose and treat hair loss.

Monilethrix is linked to a gene cluster on chromosome 12.

Mutations in the p63 gene affect skin adhesion, barrier integrity, and hair growth.

Two key genetic areas linked to male-pattern baldness were identified.

The conclusion is that a treatment called cp-asiAR can reduce hair loss and promote hair growth, making it a potential new therapy for androgenetic alopecia.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

A gene in Arabidopsis thaliana, AtPRPL1, affects root hair length but not cell wall composition.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

CARASIL, a rare genetic disorder, was confirmed in an Arabic woman, highlighting its rarity and need for stroke prevention.

Targeting the TNFRSF1B gene may help treat hair loss.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

Researchers found 15 new genetic links to skin traits in Japanese women.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

BMI should be considered in future research on dutasteride's effects on fertility.

Hair loss in androgenic alopecia patients is linked to changes in certain genes that control cell growth and death.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

CD28 is a promising target for treating alopecia areata with belatacept.

CD28 is a promising target for treating alopecia areata with belatacept.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

Genetic mutations linked to ectodermal dysplasias and hair loss were identified in Pakistani families.

Snail2 is crucial for hair growth and affects skin cancer development.

Metabolic processes and key genes like FGF5, FGFR1, and RRAS significantly affect hair follicle growth in Inner Mongolian Cashmere goats.