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Hidradenitis suppurativa tunnels have different microenvironments, suggesting targeted treatments could be more effective.

3D microenvironments in microwells improve hair follicle stem cell behavior and hair regeneration.

Cosmetic products or emotional factors might contribute to Frontal Fibrosing Alopecia, and trichoscopy is useful for diagnosis.

Hair shaft malformation contributes to Central Centrifugal Cicatricial Alopecia.

Local testosterone treatment improved sexual desire in a female with fragile X syndrome.

Curly and straight hair differ in how their internal fibers are arranged.

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Brownish halos around axillary hair can help diagnose frontal fibrosing alopecia.

The SHJH hr mice with a mutated Hr gene show signs of faster skin aging due to poor antioxidative protection.

A comprehensive human skin cell atlas was created to better understand skin biology and disease.

A 46-year-old man was diagnosed with frontal fibrosing alopecia, a condition usually seen in postmenopausal women.

Friedreich's ataxia causes thin, weak hair with surface damage and cavities.

The girl has an inflammatory type of scarring hair loss.

Hair follicle stem cells from aged eyelid skin can become corneal endothelial-like cells for potential eye treatments.

Human cells in plasma-derived gels can potentially mimic hair follicle environments, improving hair regeneration therapies.

Hair restoration surgeons undergo comprehensive training and exams to ensure competence.

Mouse skin cells can become sperm-like cells in the lab.

Patients with Systemic Sclerosis have much higher levels of GDF-15, which could help predict organ involvement and guide treatment.

Frontal fibrosing alopecia has occurred in two related male families.

Culturing Dermal Papilla Cells and Hair Follicle Stem Cells in 3D conditions can significantly improve hair regeneration potential.

FR-1 reduces skin scarring and promotes healing without harmful effects.

The document concludes that facial feminization surgery improves psychological well-being and social acceptance for transgender individuals.

The document reports three sisters with Woodhouse-Sakati syndrome showing typical symptoms and unusual gynecological anomalies.

Certain eye surgery complications can be managed effectively, especially in patients who have used specific prostate medications.

hsa_circ_0002980 can help stop liver cancer cells from growing and spreading.

Early detection and intensive treatment of diseases caused by Staphylococcus aureus toxins are crucial for reducing severe health effects.

Keratosis Follicularis Spinulosa Decalvans is a rare genetic disorder causing skin and hair issues, often inherited through the X chromosome.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

Seven genes are highly expressed in both germ-line and hematopoietic stem cells.