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Rice bran extract and low-frequency electromagnetic fields together may help treat vitiligo and white hair.

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

TLR2 is crucial for hair growth and regeneration, and boosting it can help prevent hair loss.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

Tofacitinib effectively treated a woman's severe symptoms from a rare autoimmune condition.

Iron deficiency worsens inflammatory skin diseases by disrupting iron balance and increasing inflammation.

Specific mutations in a receptor cause facial abnormalities and hair loss.

Excessive sun protection might cause frontal fibrosing alopecia by disrupting skin immune balance.

TNC+ fibroblasts play a key role in skin inflammation by interacting with T cells.

Aryl hydrocarbon receptor overexpression found in miniaturized hair follicles in female hair loss.

Mutations in the TSPEAR gene cause a new form of ectodermal dysplasia affecting hair and tooth development.

Tcf3 helps cells move and heal wounds by controlling lipocalin 2.

Prdm1 is necessary for early whisker development in mice but not for other hair, and its absence changes nerve and brain patterns related to whiskers.

Scientists found a specific group of itch-sensing nerve cells in mice important for feeling itch but not for sensing heat or touch.

Vitamin D receptor binds similarly to natural and synthetic ligands, affecting gene regulation.

Excessive sun protection might contribute to frontal fibrosing alopecia.

Blue laser light reduces energy in mouse skin cells and creates harmful oxygen compounds, possibly harming the cells.

Early changes in skin gene expression can predict later bone mass loss after radiation exposure.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

Lack of FPR2 slows hair growth by affecting hair cell activity.

Using mesenchymal stem cells or their exosomes is safe for COVID-19 patients and helps improve lung healing and oxygen levels.

The protein STAT3 slows down cell growth by blocking the FST gene, which affects hair development in sheep.

Lymphoma should be considered in unusual scalp hair loss cases, as treatment can work but may lead to severe complications.

Mutating the gmds gene in zebrafish increases hair cell numbers and regeneration.

PINK1 is important for controlling gut immune responses linked to early Parkinson's disease.

Researchers made a detailed map of gene activity for different parts of human hair follicles to help create targeted hair disorder treatments.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Scientists made a mouse that shows how a specific protein in the skin changes and affects hair growth and shape.

Wnt signaling controls whether hair follicle stem cells stay inactive or regenerate hair.