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Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

Thymic transplantation normalized some T-cells but not others, maintaining immune function.

Mice with the 'lanceolate hair' mutation have abnormal hair and skin similar to human Netherton's syndrome.

The gene causing hair loss and heart issues in rough coat mice is still unknown.

Nelfb is essential for dermal fat development and survival.

FFA patients have fewer melanocytes and thinner skin compared to others.

Removing both Atr and Trp53 genes in adult mice causes severe tissue damage and death due to DNA damage.

Foxn1 helps skin cells mature by controlling a specific protein's activity.

A gene mutation in mice causes permanent hair loss and skin issues.

Lack of a key enzyme causes severe skin issues and death in mice.

The FOXN1 gene is crucial for developing immune cells and preventing immune disorders.

The protein's size was reduced, but more work is needed to confirm its function.

The flaky skin mouse mutation is a natural model for studying human psoriasis.

Overexpressing the human H-ferritin gene in mice causes mild growth delay and temporary hair loss.

FTase and GGTase-I are essential for skin keratinocyte health.

The protein FLCN is involved in cellular cleanup and is regulated by ULK1.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

KLF4 is important for maintaining skin stem cells and helps heal wounds.

A specific gene mutation causes long hair in Angora rabbits.

FGF5 gene mutations cause long hair in domestic cats.

Loss of Ten1 in mice causes telomere shortening and symptoms similar to human dyskeratosis congenita.

LGR5 is a common marker of hair follicle stem cells in different animals and is important for hair growth and regeneration.

A gene mutation in mice causes severe skin disorder similar to a human condition.

CD61 is important for mouse tooth cell growth and works through Lgr5.

The Fas/FasL pathway may play a role in alopecia areata.

Truncated LTBP-1 disrupts TGF-β signaling, affecting hair growth.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

Blocking EGFR in mice causes hair loss and skin changes.