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Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

Matriptase-2 helps control iron levels by suppressing hepcidin, and its deficiency can cause iron-deficiency anemia.

Arabidopsis Formin 2 stabilizes actin filaments, affecting cell-to-cell movement and virus susceptibility.

IGF2BP3 gene is up-regulated in keloid patients, suggesting potential targets for treatment.

A KRT32 gene variant causes loose anagen hair syndrome.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

The same gene mutation can cause different symptoms in family members.

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

circRNA-1926 helps goat stem cells turn into hair follicles by affecting miR-148a/b-3p and CDK19.

Mutations in the androgen receptor gene cause Androgen Insensitivity Syndrome, affecting sexual development.

The type of tumor suppressor gene lost affects the behavior of skin cancer.

N1-acetylspermidine promotes hair follicle stem cell self-renewal.

Key genes linked to hair growth and cancer were identified in hairless mice.

CaBP1 and 2 are necessary for maintaining calcium currents and hearing in inner ear cells.

Shikimic acid promotes hair growth.

A specific DNA region controls skin cell gene expression by working with certain proteins.

A five-year-old girl has a harmless, unchanging bald patch on her scalp.

Squaric acid dibutylester promotes hair growth by activating immune cells, especially macrophages.

R-Spondin-1 is important for skin health and could help diagnose and treat various skin conditions.

A new technology showed that the SOX9 gene might control heart scar formation after injury, suggesting new treatment possibilities.

OsPHR3 can help breed rice that efficiently uses phosphate without growth issues.

Sox13 is a marker for early hair follicle development but not essential for skin and hair growth.

Mutations in Far2 mice cause hair loss due to sebaceous gland issues.

Unique fat cells near fibrotic areas contribute to systemic sclerosis progression.