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Activating CB1 can reduce keratin levels, potentially helping manage psoriasis and aid wound healing.

Stress can cause a type of hair loss in mice lacking the CCHCR1 gene.

A rare gene variant causes hair and nail issues in a family.

Bioengineered skin models aging well, useful for studying aging and testing treatments.

The study found that mouse sweat glands develop before birth, mature after birth, and have specific keratin patterns.

Beta-catenin boosts hair follicle cell growth by increasing c-myc expression.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

Protein kinase C epsilon may increase skin cancer risk by affecting nearby cells.

ROR2 is essential for hair follicle stem cell renewal and maintenance.

BRG1 is essential for skin cells to move and heal wounds properly.

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

The KRTAP21-1 gene affects wool yield and can help improve wool production.

A protein called IL-36γ causes skin side effects from certain cancer treatments when combined with a common skin bacteria.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

OR2AT4 helps reduce aging and cell damage in human skin cells.

Twist1 helps maintain important features of cells crucial for hair growth by working with Tcf4 and β-catenin.

FOXN1 mutations can cause varying immune and physical issues, with severity influenced by gene activity and possibly other factors.

A new genetic region, 17q21.31, is linked to higher ovarian cancer risk.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

Two new gene mutations cause a rare hair disorder.

The OVOL1 gene, controlled by β-catenin, is crucial for creating hair follicles.

Removing GRK2 in skin cells causes hair loss similar to immune-related alopecia.

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

The Foxn1 gene is essential for normal nail and hair development.

A specific group of slow-growing stem cells marked by Thy1 is crucial for skin maintenance and healing in mice.

Jumonji genes are important for development and their mutations can cause abnormalities, especially in the heart and brain.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.