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Activating mitophagy may help manage a key immune response involved in the hair loss condition alopecia areata.

New compounds were developed that promote hair growth in mice.

Celsr1 is crucial for skin cell alignment, while Celsr2 has little effect on this process.

Whiskers can form without sensory nerves or Foxd1, thanks to Meis2 in mesenchymal cells.

Mice with too much Claudin-6 have skin barrier problems and abnormal hair growth.

Blocking Wnt signaling in young mice causes thymus shrinkage and cell loss, but recovery is possible when the block is removed.

Killing specific cells in hair follicles can lead to hair growth problems in mice.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

The mTurq2-Col4a1 mouse model shows that cells can divide while attached to stable basement membranes during development.

Activating Kras in mouse skin causes excess skin and hair loss.

Bcl-2 affects hair growth and pigmentation by controlling cell death.

Progesterone and its metabolites affect myelin protein expression differently in male and female rat Schwann cells.

MJ04, a new compound, effectively promotes hair growth and is a potential topical treatment for hair loss.

Msx2 is essential for proper enamel formation by preventing abnormal cell transformation.

Laminin 332 is essential for normal skin cell behavior and structure.

Scientists found a gene in mice that causes early hearing loss.

The PON1 192R gene variant is linked to a higher risk of psoriasis and heart disease in Western Mexico.

ARHGEF3 is essential for proper hair follicle development.

Polycomb Repressive Complex 2 is not needed for hair regeneration.

PRC2 is essential for maintaining intestinal cell balance and aiding regeneration after damage.

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

SGK3 is essential for proper hair growth and health.

AL136131.3 slows hair growth by affecting energy processes in hair loss.

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.

A mutation in the human hairless gene causes alopecia universalis.

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

Rapamycin reduces skin cell growth and tumor development by affecting cell signaling in mice.