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Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

HAP stem cells can repair nerves, grow hair follicle nerves, and become heart muscle cells, making them useful for regenerative medicine.

HAPLN1 can promote hair growth and may help treat hair loss.

Targeting LPA could help treat skin disorders.

The N gene affects the protein makeup of mouse hair.

EZH2 is essential for hair growth and skin cell development.

EGFR helps control how hair grows and forms without needing p53 protein.

Delta1 is crucial for controlling skin cell growth and preventing tumors in mice.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Polycomb Repressive Complex 1 is crucial for keeping stem cells stable and maintaining healthy adult tissues.

PEA boosts allopregnanolone production and reduces oxidative stress in brain cells.

Removing both KLK5 and KLK7 proteins can prevent death and skin issues in Netherton syndrome.

Egfl6 is not needed for zebrafish face development.

p63 is essential for controlling epithelial stem cells and tissue health.

Non-coding RNAs may be key in diagnosing and treating rare skin disorders.

Defective nuclear transport may cause gene expression changes in Progeria.

β1 integrin is essential for the survival, growth, and movement of human epithelial progenitor cells.

The Paxbp1 gene is crucial for healthy hair follicles.

Targeting NCoR1 can help treat heart enlargement and dysfunction.

P311 helps skin stem cells become myofibroblast-like cells, aiding wound healing.

Deleting the PTEN gene in mice causes nerve cells to grow larger and heal better after injury, but may cause overgrowth and hair loss in older mice.

Neurotrophins regulate nerve growth by balancing promotion and suppression.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

Mutations in the FOXN1 gene cause severe immune issues but don't affect hair and nails.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.