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Stress increases certain chemicals in the skin and nerves, which might worsen skin conditions.

AVT is highly conserved and may have antimicrobial properties.

A new gene mutation linked to a skin condition was found in a Spanish family.

Lower growth factors linked to balding in androgenetic alopecia.

Overexpressing noggin in mice causes severe osteoporosis.

The research identified new skin traits in mice, some linked to human skin conditions.

The technology can help diagnose and subtype autoimmune diseases by identifying specific autoantibodies.

Black hairs have more pigment-related genes, while gray hairs have more keratin-related genes.

FilaggrinHigh melanomas have active FGFR signaling and weak GNA14 and Th1 signatures.

Truncated LTBP-1 disrupts TGF-β signaling, affecting hair growth.

A specific gene segment can make mouse skin cells glow, helping study hair growth and gene effects.

The mutation causing Hutchinson-Gilford progeria syndrome leads to severe skin problems and early death in mice.

The PP2A-B55α protein is essential for brain and skin development in embryos.

LRIG1 protein affects hair growth by regulating skin receptors, leading to hair loss when overexpressed.

Epimorphin helps shape and develop epithelial cells, like those in hair follicles.

Basonuclin 1 (BNC1) helps skin cells multiply and move, which is crucial for wound healing.

Human skin has less GDNF and its receptor with age.

Mouse Notch is important for determining cell roles in hair follicles.

QR 678 and QR 678 Neo are safe and promote hair growth, potentially helping chemotherapy-induced hair loss.

Mrp3 helps in wound healing and hair growth.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

Neurotrophins are important for hair growth and response to stress.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

lncRNA MTC affects protein levels in goat skin cells, impacting hair growth.

PSENEN gene mutations can cause both Dowling-Degos disease and acne inversa.

Melanocyte-associated antigens may play a key role in alopecia areata and could be targets for new treatments.

A person with a new mutation in the SCN1A gene developed brain inflammation after COVID-19.

A specific gene change in APCDD1 increases the risk of hair loss.

The patient had paraneoplastic pemphigus without mucosal involvement.