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Researchers made a detailed map of gene activity for different parts of human hair follicles to help create targeted hair disorder treatments.

Gene regulation evolved differently in mouse and chicken skin, but remained stable in their trunks.

Lhx2 is a crucial regulator of the Sonic Hedgehog signaling in early mouse retinal development.

Lhx2 is essential for effective Sonic Hedgehog signaling in early retinal development.

The HR protein's role as a repressor is essential for controlling hair growth.

Deleting the Hoxc13 gene in frogs shows its crucial role in developing skin structures similar to hair.

ATP-dependent chromatin remodeling is crucial for skin development and stem cell function.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

Overexpression of Hoxc13 in hair cells causes hair loss and skin issues.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.

CTCF protein is essential for skin and hair follicle development in mice.

RXR agonists may promote hair growth in humans.

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

A unique gene mutation was found in a family with monilethrix.

The hairless protein is important for skin, hair, and may influence cancer development.

Scientists found new genetic areas that affect how rice root hairs grow and develop.

Dual TCR Treg cells are common in various mouse tissues and show diverse characteristics.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

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

Targeting NCoR1 can help treat heart enlargement and dysfunction.

Dual TCR Treg cells are common in mouse tissues and vary by location.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

Calreticulin has roles in healing, immune response, and disease beyond its known functions in the endoplasmic reticulum.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

Connexin 30 is usually absent in normal skin but can appear in certain skin conditions.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

The near-naked hairless mutation causes hair loss but is not due to a mutation in the hairless gene itself.