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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.

CAG repeat numbers in the AR gene likely don't affect hair loss in Korean men.

Lipin-1 is important for skin cell differentiation and skin barrier function.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

HKN-2 antibody targets specific skin and hair cells, showing keratin complexity.

A specific gene mutation causes long hair in Angora rabbits.

The study found potential new DNA patterns in fertility genes, but further testing is needed.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Hair loss gene linked to prostate issues.

Ptprq has multiple forms that change during inner ear development.

Removing both Atr and Trp53 genes in adult mice causes severe tissue damage and death due to DNA damage.

TMPRSS2 is crucial for COVID-19 infection and is a potential target for treatment.

The Celsr1 gene is crucial for normal hair patterning in mice.

Controlling transposable elements is crucial for successful tissue regeneration.

K6hf is found in specific parts of hair follicles, nails, and tongue, and is linked to hair growth and structure.

Three genes linked to the development of trichilemmal cysts were found.

Foxn1 helps skin cells mature by controlling a specific protein's activity.

Keratin 17 is crucial for early hair strength and cell survival.

Mutations in the Sgk3 gene cause fuzzy hair in mice.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

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

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

Inhibiting SFRP1 may help treat hair loss.

A protein from fat-derived stem cells, DKK1, is linked to hair loss and blocking it may help treat alopecia areata.

Progerin affects cell shape but not hair or skin in mice.