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R-spondin2 may help treat hair loss, gene differences could explain baldness, a peptide's regulation is linked to psoriasis, B-defensin gene copies may affect a skin condition's risk and severity, and potential markers and targets for alopecia areata were identified.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

SH-SY5Y cell lysate is effective for diagnosing Satoyoshi syndrome.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

CEP135 may predict cancer outcomes, and targeting PLK1 could help treat certain sarcomas.

PRSS35 enzyme may help start skin tumors and could be a target for cancer treatment.

GATA6 is important for maintaining and differentiating cells in a key area of human skin.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

A protein called COMP is part of the connective tissue in normal human hair follicles and may be important for hair health.

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Keratin 6a is important for quick wound healing from hair follicles.

Mouse and human keratin 16 can both form filaments, with differences likely due to the tail domain, not the helical domain.

Topical IKKα inhibitors may help prevent CCS tumours.

Different versions of the KRTAP6-2 gene in goats can lead to thinner cashmere fibers.

Beta-trace protein may help diagnose and predict treatment response in certain nerve disorders.

The protein's size was reduced, but more work is needed to confirm its function.

The gene NM_026333 slows down aging by affecting the NCX1 pathway and could be targeted for anti-aging treatments.

Targeting NMMHC IIA may help treat blood-brain barrier damage.

Human hair proteins have similar cysteine and glycine levels to skin proteins.

Prostasin has two roles in skin: one for normal skin development without needing activation, and another for proper hair growth that requires activation.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

Overexpression of sPLA2-IIA in mouse skin reduces hair stem cells and increases cell differentiation through JNK/c-Jun pathway activation.

A mutation in the Sgkl gene causes defective hair growth in mice.

HPV8 E6 gene causes growth of certain skin stem cells.

Scientists found new, better-working inhibitors for a hormone-related enzyme.

Scientists successfully created and analyzed the structure of a part of the human androgen receptor with specific modulators and a peptide to understand how it binds differently in various tissues.