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A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Researchers found a new mutation causing total hair loss from birth.

The keratin 19 promoter effectively targets genes in specific epithelial cells in mice.

Krox20 is crucial for hair growth and maintaining skin stem cells.

TCF/Lef1 is essential for skin barrier function by regulating lipid metabolism.

MPZL3 is important for controlling the hair growth cycle in mice and humans.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

CD8+ T cells attack hair follicle stem cells, causing scarring and hair loss.

Two patients with the same genetic mutation had both blistering skin and easily pulled out hair.

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.

Targeting Hedgehog signaling may help treat ligamentum flavum fibrosis.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

Minoxidil affects collagen-related genes, potentially helping treat fibrosis.

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

The HR protein helps hair grow by blocking a hair growth inhibitor, aiding in hair follicle regeneration.

A specific DNA region is crucial for Foxn1 gene expression in thymus cells but not in hair follicles.

HDAC4 and HDAC7 are crucial for Th17 cell development and could be targeted to treat inflammatory diseases.

Deleting part of a gene in mice causes wavy hair and high pup loss.

Sonic hedgehog signaling is needed for the development of touch-receptor cells in the skin, and the loss of Polycomb repressive complex 2 can lead to more of these cells.

Lykoi cats' unique sparse hair is linked to specific genetic variants in the Hairless gene.

LncRNA018392 helps goat skin cells grow by increasing CSF1R.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

Researchers found that the Leptin receptor is a consistent marker for hair follicle dermal cells, which may help future hair research.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

Ixekizumab may be an effective first treatment for a rare skin condition causing hair loss.

A protein called lfTSLP is important in causing allergic and other skin diseases and could be a target for treatment.

LGR5 is a marker found in hair follicle stem cells in various species and is important for hair growth and skin repair.