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ISCK03 stops melanin production in human melanoma cells and lightens skin color in mice and guinea pigs.

Hair growth-related cells need the enzyme SCD1 to help maintain the area that supports hair growth.

A new DSG4 gene mutation causes hair defects in a young girl.

The DMI3 gene is essential for nodule development and symbiosis in certain plants.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

Sostdc1 controls the size and number of hair and mammary gland structures.

AtCSLD3 and GhCSLD3 genes enhance root growth and cell elongation in plants.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

The ZIP13 variant is linked to abnormal hair quality.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

The ASIP gene is crucial for determining cattle coat color.

Researchers created a new mouse model for studying scleroderma.

OCIAD2 and DCN genes affect hair growth in goats by having opposite effects on a growth signaling pathway and inhibiting each other.

A new gene mutation causes insulin resistance in a girl and her mother.

Tofacitinib helps improve skin conditions in people with Down syndrome, especially alopecia areata.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

cDermo-1 causes dense skin, feathers, and scales in chickens.

Unique genes in hair follicle cells help tissue regeneration.

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

Secreted inhibitors of Wnt and IGF signaling control hair and tooth development, creating species-specific patterns.

CD98hc's role in skin health decreases with age.