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Certain defective glucocorticoid receptor mutants move faster inside cell nuclei and work less effectively.

The postnatal thymus has cells like mesenchymal stem cells that can become different cell types and help maintain thymus structure.

Two genetic variations in Moa buffalo help them adapt to heat.

C-scores can help predict gain-of-function and loss-of-function mutations.

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3D models from confocal microscopy improve melanoma detection on sun-damaged skin.

Keratin 15 affects cell behavior and characteristics in skin cells.

A new compound effectively inhibits human 5α-reductase 1.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.

The ventral matrix is the main source of the nail plate.

B2m-free HLA variants may be a new class of HLA important in immune responses and diseases.

Researchers found a specific immune receptor in patients that causes severe skin reactions to a drug.

Twist1 is crucial for UVB-induced skin cancer development.

Genetic mutations that disrupt homocysteine breakdown lead to increased damage in mouse hair keratin.

Protein Kinase Cε increases skin sensitivity to UV damage and skin cancer risk.

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

CT-707 is effective and safe for treating certain Chinese lung cancer patients.

Cetaceans lost hair due to changes in the Hr and FGF5 genes.

Catalytic antibodies are early indicators and active participants in the development of systemic lupus erythematosus.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

FOL-005, a hair growth promoter, acts locally on mouse skin where injected and could be a promising hair loss treatment.

A new test more accurately detects citrulline in hair follicles and pilomatrixomas.

CMG2 and TEM8 receptors have distinct roles in skin and growth disorders, affecting collagen breakdown and growth.

Suppressing ODC activity reduces tumor growth in hair follicles.

Hair shaft malformation contributes to Central Centrifugal Cicatricial Alopecia.

Different types of skin gland tumors have unique genetic traits, which can guide personalized treatments.