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New mutations in hair keratin genes cause the rare hair disorder monilethrix.

Bexxar treatment led to a high response rate in patients with advanced-stage, treatment-resistant follicular lymphoma.

Atopic dermatitis shows a link between skin layers in inflammation, detectable with detailed gene analysis.

Higher levels of certain proteins may increase or decrease rosacea risk.

Ruxolitinib helps regrow hair in alopecia areata by blocking inflammation, reducing stress, and controlling cell death.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

Losing both ERBB2 and ERBB3 receptors in mice causes significant skin problems and inflammation.

Certain gene variations in the Vitamin D Receptor are linked to higher risk of female hair loss.

Aromoline and DRD4 are potential targets for osteoarthritis treatment.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Mice lacking the PPARγ gene in their fat cells had almost no fat tissue, severe metabolic problems, and abnormal development of other fat-related tissues.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

Ptprq has multiple forms that change during inner ear development.

Dermal fibroblasts have adjustable roles in wound healing, with specific cells promoting regeneration or scar formation.

Polycomb Repressive Complex 1 is crucial for keeping stem cells stable and maintaining healthy adult tissues.

Recent advances show zebrafish can model anemia, Alx4 affects craniofacial and hair development, and mTORC1 is crucial for retinal development.

ERβ has potential in treating prostate cancer and neurodegenerative diseases, but human studies are needed before clinical use.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

A certain genetic variant in the androgen receptor may predict the severity of COVID-19 in men.

RADA16-I can effectively deliver and release mangiferin, improving its solubility and bioavailability.

A genetic variant in "Blonde d'Aquitaine" calves causes death at birth due to a missing protein.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

RNA is crucial for controlling cell flexibility and regeneration.

17β-estradiol can reduce inflammation in the skin.

Keratinocytes can reduce the survival of certain melanoma cells, suggesting new therapy paths.