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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.

The lentiviral array can monitor and predict gene activity during stem cell differentiation.

Thicker hair grows faster; hair loss patients have slower growth.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

Loss of the Y chromosome and UTY gene activity increases cancer risk in men.

Activating TLR3 boosts autophagy gene expression in skin cells.

The ITGB6 gene is important for tissue repair and hair growth, and mutations can lead to enamel defects and other health issues.

The Hairless gene is crucial for healthy skin and hair growth.

Grasp protein helps maintain skin health after UVB exposure.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

Knocking out the FGF5 gene in sheep increased wool production and hair-follicle density.

The E2 protein affects gene activity in hair follicles of mice.

BTNL proteins help control inflammatory bowel disease by maintaining specific immune cells.

The hairless gene is crucial for hair health, and its mutations cause hair loss.

Lactoferrin helps mice grow hair by increasing cell growth and hair follicle development.

Mutating the gmds gene in zebrafish increases hair cell numbers and regeneration.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

ERULUS controls root hair growth by regulating cell wall composition and pectin activity.

Overexpressing GLI-1 in mice skin can cause tumors like human basal cell carcinomas.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

Deleting a specific protein in skin cells disrupts normal hair growth and development.

Certain proteins and their receptors are more active during the growth phase of human hair and could be targeted to treat hair disorders.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Certain long non-coding RNAs are important for controlling hair growth cycles in sheep.

Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.

The 4C32 gene may help in mouse skin development and differentiation.

ARHGEF3 is essential for proper hair follicle development in mice.

lncRNA XLOC_008679 and gene KRT35 affect cashmere fineness in goats.