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Double-stranded RNA causes inflammation in hair follicle cells, which may help understand and treat alopecia areata.

Tofacitinib helped most teenagers in the study regrow hair with mild side effects.

Enhanced stem cells from the placenta can reduce fat buildup in eye tissue for Graves' disease.

A new peptide, FOL-005, may help treat excessive hair growth by reducing a hair growth promoter, FGF7.

The study suggests a possible increase in androgen receptors in patients with frontal fibrosing alopecia, but more research is needed.

BAF200 is essential for proper heart and coronary artery formation.

Inhibiting PDE8A may help treat hair loss by boosting fat cell growth and hair regeneration.

Fibroblasts can be mistaken for neural cells, so functional validation is needed.

FOL-005 peptide can reduce human hair growth by lowering FGF7 levels.

Pmg-1 and Pmg-2 are new genes important for skin and mammary gland development.

Grasp protein helps maintain skin health after UVB exposure.

Lef1 is essential for normal skin, hair growth, and healing wounds in mice.

The enzyme PA-PLA1α is important for proper hair follicle development.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

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

Researchers found a gene in hamsters that responds to male hormones and may be indirectly controlled by them.

ANXA1 influences hair growth in mice through the EGF signaling pathway.

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

Oral isotretinoin effectively treats yellow facial papules in frontal fibrosing alopecia patients.

ILC1-like cells can cause alopecia areata by affecting hair follicles.

Excessive sun protection might contribute to frontal fibrosing alopecia.

Tofacitinib helped over half of the patients with severe hair loss regrow at least 50% of their hair.

FGF-1 causes spiral ganglion neurites to branch more.

A JAK1 variant causes hair loss, skin issues, and thyroid disease, but treatment with a specific inhibitor can help.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

ME1 and PPAR signaling may influence hair loss in androgenetic alopecia.

Phosphorylation controls TFEB's location in the cell, affecting cell metabolism and stress response.

An 18-year-old man was diagnosed with a rare genetic disorder causing hair loss, severe light sensitivity, and skin issues.