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NB-002 is a promising new topical treatment for fungal nail infections, showing better results than a non-medicated option.

Nevus psiloliparus lacks mature hair follicles but keeps other skin structures intact.

Researchers found three types of melanocytes in developing mouse skin, each with different genes and locations.

Mice with the 'lanceolate hair' mutation have abnormal hair and skin similar to human Netherton's syndrome.

Higher levels of nidogen1 and type IV collagen are found in basal cell carcinoma compared to normal skin.

Snail2 is crucial for hair growth and affects skin cancer development.

UC.145 may be a new biomarker for predicting gastric cancer.

Hoxc13 gene is essential for hair, nail, and papilla development.

Nuclear Factor I-C is important for controlling hair growth by affecting the TGF-β1 pathway.

Nude mice are hairless due to a shared defect affecting both skin and thymus, not just thymic issues.

The Korean study found that twenty-nail dystrophy mainly affects adults, more often women, and has five distinct types with different clinical progressions.

A rare genetic mutation causes severe immune issues, hair loss, and nail problems.

Certain RNAs may help diagnose alopecia areata by affecting keratin genes.

A new method accurately measures cell changes in breast cancer.

RNase L hinders hair follicle regeneration by altering immune signals.

Cystatin M/E helps in the final stages of hair and nail formation by controlling certain enzymes.

Loose anagen hair syndrome is caused by structural abnormalities in the hair follicle's inner root sheath.

Mutations in the SNRPE gene cause hereditary hair loss.

RNase L suppresses regeneration in mammals.

The first pediatric case of naevus trichilemmocysticus was documented.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

ILC1-like cells may contribute to hair loss in alopecia areata and could be new treatment targets.

UV-enhanced trichoscopy helps diagnose hair shaft disorders like pili annulati.

Netherton syndrome causes specific skin and hair changes that help in early diagnosis.

New molecules can prevent cell death in hair follicles.

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

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Benign tumors from hair follicles can look like other skin cancers but have distinct features under dermoscopy.

Apoptotic cells help cause hair follicle cell death during regression.