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MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

The nude gene causes skin cell overgrowth and improper development, leading to hair and urinary issues.

Tretinoin cream successfully treated a woman's skin condition called Fox-Fordyce disease.

Runx1 affects hair growth, cancer development, and autoimmune diseases in epithelial tissues.

CD18-deficient mice developed psoriasis-like skin disease, useful for studying inflammatory skin disorders.

Tranexamic acid turns white hair brown in certain mice by affecting specific proteins.

Sox9 is crucial for hair follicle stem cells to become melanocytes instead of glial cells.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

A KLK5 inhibitor effectively improved skin symptoms in a mouse model of Netherton Syndrome.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

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

TGFβ1 expression in skin causes hair loss and skin thickening, but these effects are reversible.

Runx1 is crucial for proper hair structure and development.

A new gene mutation causes a rare type of hair loss.

Miz1 is essential for proper hair structure and growth.

Laser hair reduction can sometimes cause a rare skin condition called Fox-Fordyce disease.

Erythropoietin overexpression disrupts hair growth and fat formation in mice.

Deleting the Sox21 gene changes hair lipid composition and increases cholesterol sulfate levels.

Prdm1 is necessary for early whisker development in mice but not for other hair, and its absence changes nerve and brain patterns related to whiskers.

MFN2 mutations cause mitochondrial problems, leading to more upper body fat and lower leptin levels.

Lhx2 helps retinal cells respond to signals for eye development.

Linoleate deficiency in rats reduces growth and n-6 polyunsaturate accumulation, causing mild symptoms.

Removing the p75 gene in mouse skin cells didn't affect their skin or hair growth.

Disrupting the Tsc2 gene in certain cells leads to thicker skin, larger hair, and changes in hair growth signaling, which can be partly reversed with specific treatment.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

Iron deficiency in mothers causes hair loss in their baby mice.

Iron contributes to skin fibrosis in nephrogenic systemic fibrosis.

Nicastrin deficiency may cause skin cell damage and pigmentation disorders in humans, similar to effects seen in fish.

Lack of certain fatty acids causes skin, immune, and fertility issues in mice.