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Melanoma risk tools need improvement, a gene mutation causes a hair disorder that might be treated by managing cell stress, a potential therapy for a skin-ear disorder involves blocking cell channels, skin wrinkling may indicate lung aging regardless of smoking, and oxidative stress might contribute to common baldness.

Removing HIF-P4H-2 from certain skin cells in mice causes hair loss on the body but not the head.

Trichoscopy is useful for diagnosing Netherton syndrome in children with skin issues.

Whn is essential for hair growth, and its malfunction causes hair loss.

High androgen levels and genetic factors likely cause Becker's nevus and related symptoms.

A 12-year-old girl was diagnosed with monilethrix, a genetic condition causing fragile, beaded hair that breaks easily, with no effective treatment available.

PC-associated alopecia has unique microscopic features.

Research on skin disorders in humans and mice has improved understanding of hair and skin development.

Increased PHGDH expression causes early melanin buildup in hair follicles.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

The model can effectively test gene functions and drug responses in human skin.

Scientists created a long-lasting stem cell line from human hair that can turn into different skin and hair cell types.

Excessive minoxidil use can damage hair structure.

CAL-PDT is safer and more effective for treating actinic keratosis on the scalp.

Mutations in the Whn gene affect hair keratin gene expression differently.

Lichenoid keratosis can cause localized hair loss.

Acitretin significantly reduced inflammatory attacks in a woman with Naevus Comedonicus Syndrome but caused side effects.

Cornification is how skin cells die to form the protective outer layer of skin, hair, and nails.

The new keratin film without KAPs stains better and could help study keratin functions.

Some scalp sores are linked to different inherited skin conditions.

New mutations in the DSG4 gene cause a rare hair condition.

Hemidesmosomes and Notch signaling help skin cells mature by moving them to the outer layer.

Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

Trichilemmal cysts may form from hair follicle outer root sheath growth.

RPGRIP1L helps skin cells stick together by blocking PKCβII, which can prevent skin blistering like in pemphigus.

Hair cells grown in a lab showed specific hair proteins.

TB and BCC tumors show similar follicular differentiation patterns.