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

A rare skin condition appeared on a 19-year-old woman's scalp.

Cross-linked proteins help maintain the structure of hair, feathers, and hagfish teeth.

Recognizing the "bamboo hair defect" is crucial for diagnosing Netherton's syndrome.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

Lower proximal cup cells, not bulge stem cells, regenerate hair follicles after chemotherapy.

Deleting MED1 in skin cells causes hair loss and skin changes.

The patient with EEC syndrome had scarring alopecia due to deep folliculitis, possibly linked to abnormal hair structure.

Arabidopsis collet hairs are good for studying nuclear movement and DNA content increase during growth.

A woman experienced severe side effects from a drug due to a specific genetic variation, suggesting genetic testing could prevent such risks.

The method shows how hair lipids form specific patterns and their roles in hair structure.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

Danthron from Rhubarb causes melanoma cells to stop growing and die.

The research created new azasteroids and pseudoazulenyl nitrones, which could be useful in medicine.

Activating Nrf2 in skin cells causes skin disease similar to chloracne in mice.

A rare skin reaction from cancer treatment was successfully managed with topical treatments and antihistamines.

Laser treatments are the most effective for porokeratotic adnexal ostial nevus.

Increasing type 17 collagen reduces aging signs in skin cells caused by UV light.

REV7 is crucial for genome stability and cancer treatment, making it a potential target for therapy.

Pyrene excimer nucleic acid probes are promising for detecting biomolecules accurately with potential for biological research and drug screening.

Hair thinning and loss in a girl with a rare metabolic disorder was linked to her condition.

Monitor for early signs of azathioprine toxicity and check blood counts regularly.

Dynlt3 is important for melanosome transport and skin coloration.

AKN is a chronic scalp condition in African-descended males, treated with topicals, antibiotics, steroids, and sometimes surgery or laser.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.