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The protein Gnαs is found more in black mice than white mice and may influence their coat color.

MPA increases cancer spread by boosting Eph A2 activity.

A new gene mutation is linked to monilethrix in the studied family.

Lack of cystatin M/E causes thin hair and dry skin.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

The PIP5K1A gene helps cashmere growth in goats by promoting cell proliferation, and melatonin boosts its expression.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

CMG2 and TEM8 receptors have distinct roles in skin and growth disorders, affecting collagen breakdown and growth.

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

Melanocyte-associated antigens may play a key role in alopecia areata and could be targets for new treatments.

The KRTAP15-1 gene affects cashmere fiber thickness in goats.

Changing protein kinase levels in pituitary cells affects calcium flow and beta-endorphin release.

The patient with both scarring and non-scarring hair loss showed complex immune reactions and improved with steroid treatment.

Targeting CXXC5 and GSK-3β may help treat male pattern baldness.

Similar treatments might work for different types of scarring hair loss.

VDAC2 promotes cell death in cashmere goat hair follicles through the P53 pathway.

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.

A new mutation in mice causes crooked whiskers and messy hair.

Nelfb is crucial for forming skin fat tissue by regulating genes needed for fat cell development.

Researchers found WNT10A to be a key gene in developing goat hair follicles.

AP-1 controls tumor cell type by affecting key signaling pathways.

Researchers found a genetic region that influences the number of coat layers in dogs.

A specific gene variation in goats is linked to better growth traits.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

Increased PPARGC1α relates to hair thinning in common baldness.

Activating β-catenin in different skin stem cells causes various types of hair growth and skin tumors.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

The CORT, FGF5, and CD36 genes are crucial for the cold weather adaptation of Yanbian cattle.