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Both HLA-B and MICA are independently linked to alopecia areata.

ME1 and PPAR signaling may influence hair loss in androgenetic alopecia.

A mutation in the KRTHB5 gene causes hair and nail issues.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

PRC1 is essential for proper skin development and stem cell formation by controlling gene activity.

Increased PHGDH expression causes early melanin buildup in hair follicles.

MC1R gene variations affect skin, hair color, UV sensitivity, and melanoma risk.

A certain gene variation can affect protein production and is linked to male pattern baldness.

SLC24A5 shows a clear selective sweep, but no link to UV radiation intensity.

The PLP2 gene affects cashmere fiber quality in goats and is linked to hair growth and loss.

Laminin-511 is involved in psoriasis development and can be regulated by cannabinoid receptor type 1.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

Removing Mediator 1 causes teeth cells to turn into hair cells.

Epigenetic changes in blood cells may contribute to alopecia areata.

GLI2 activates GLI1, promoting skin tumor growth and hair development.

Removing Mediator 1 from certain mouse cells causes teeth to grow hair instead of enamel.

A truncated protein linked to breast cancer may change cell adhesion.

Disrupting Acvr1b in mice causes severe hair loss and thicker skin.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

Some cells may slow melanoma growth, a protein could affect skin pigmentation, a gene-silencing method might treat hair defects, skin bacteria changes likely result from eczema, and a defensin protein could help treat multiple sclerosis.

Kdm6b is crucial for skin cell differentiation.

New findings suggest the protein linked to Birt–Hogg–Dubé syndrome is important in cell signaling and could affect treatment understanding.

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

SLC45A2 and GPNMB genes help control chicken feather color by promoting melanin.

Researchers found specific genes in the part of hair follicles that could help treat hair disorders.

Overexpressing CtBP1 in skin cells causes skin and hair problems.

Tmem30b is essential for hearing by maintaining hair cell structure in the ear.

Gene linked to common hair loss found, may lead to new treatments.