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A protein complex called mTORC1 likely affects when hair growth starts in mice.

The BUZZ gene is important for root hair growth and overall root structure in the plant Brachypodium distachyon.

Two siblings have a rare hair condition caused by a new genetic variant.

A unique gene mutation was found in a family with monilethrix.

Tiny particles from brain cells help hair grow by targeting a specific hair growth pathway.

Different keratins have unique expression patterns in mouse skin cells.

RXR and RAR proteins in skin may help with cell growth, hair growth, and gland function.

A specific genetic deletion in goats affects cashmere yield and thickness.

ESR2 gene linked to female-pattern hair loss.

Tmem50b and 2610305D13Rik genes play key roles in early mouse embryo development.

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

The IRE gene is important for normal root hair growth in Arabidopsis plants.

A girl had rickets due to a gene mutation affecting vitamin D response.

Ginsenoside Rg1 protects mouse skin from UVB damage and helps control inflammation.

Increased PPARGC1α relates to hair thinning in common baldness.

A gene variation is linked to hair thickness in Asians.

New LPA receptors (LPA4, LPA5, LPA6) have diverse roles in the body.

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

Skin cells can naturally limit the growth of cancerous changes by balancing cell renewal and differentiation.

PRC2 is not essential for hair follicle stem cell maintenance or hair growth.

The genetic variation in the KAP13-3 gene may affect cashmere fiber traits in Liaoning goats.

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.

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

The KRTAP15-1 gene affects cashmere fiber thickness in goats.

A new mutation in the KRT86 gene causes monilethrix in a Han family.