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Trichohyalin helps in hair and skin cell structure and function by binding calcium and linking proteins.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

A protein called COMP is part of the connective tissue in normal human hair follicles and may be important for hair health.

Different signals work together to change gene activity and guide hair follicle stem cells to become specific cell types.

Deleting the MAD2L1 gene is tolerated in certain mouse cancer models.

Coordinated gene activities are crucial for normal hair growth.

The protein DDX6 helps keep skin cells renewing properly by controlling the production of certain other proteins and breaking down those that cause cells to mature too quickly.

Keratin proteins in hair are complex and come from multiple gene families.

BRG1 is essential for skin cells to move and heal wounds properly.

A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

The study found that p63 needs signals from morphogens to help skin cells differentiate properly.

The LEF-1 binding site enhances gene expression in hair follicles, with other proteins aiding specific regulation.

Polyamines help fix DNA damage accurately in cells.

Higher PHGDH levels cause unusual melanin buildup in hair follicles.

A new genetic mutation in mice causes permanent hair loss and skin wrinkling.

m6A-circHECA may affect cashmere goat hair growth and is possibly controlled by gene promoter methylation.

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

The gene Foxq1, controlled by Hoxc13, is crucial for hair follicle differentiation.

Hex gene plays a crucial role in starting feather development in chick embryos.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

PRC2 is not essential for hair follicle stem cell maintenance or hair growth.

Keratin2-6g is crucial for hair follicle development, with mutations causing cell degeneration and vacuolation.

A new mutation in the HR gene causes hair loss in a specific family.

Human hair keratin has a 40% α-helix structure that changes to a random coil in 8 M urea.