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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.

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

PGD2 increases androgen receptor activity in hair cells, which could be targeted to treat hair loss.

α-parvin is necessary for skin and hair growth and for the correct orientation of skin cells.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

BMP-2 activates the Dlx3 gene in mouse skin cells, important for hair and skin development.

A Korean baby with nevus sebaceus syndrome was found to have a KRAS gene mutation.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

A gene mutation causes curly hair and hair loss in rats.

Runx1 helps control the KAP5 gene in human hair follicles.

Hair loss gene found on chromosome 3q26.

The new model helps understand and develop treatments for genetic skin disorders like AEC.

A new genetic variant in the EEF2K gene may contribute to polycystic ovary syndrome.

Longer TA repeats in the SRD5A2 gene may increase acne risk in Chinese people.

Human hair keratin genes have unique simple sequence repeats that may help track genetic variations.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

A specific gene variant (rs4833095) is linked to a higher risk of alopecia areata in Koreans.

BLTP1 and KIF27 gene mutations can help breed better wool sheep.

Certain changes in the KAP6-1 gene affect the thickness and length of cashmere goat fibers.

CD271 is crucial for maintaining healthy skin and preventing inflammation.

Double-stranded RNA activates a pathway that causes a skin protein to be expressed in the wrong place.

A specific gene change is linked to severe hair loss.

MPA increases cancer spread by boosting Eph A2 activity.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

XEDAR deficiency prevents muscle degeneration in EDA-A2 transgenic mice.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.