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Researchers found new hair and nail genes, how hair reacts to UV, differences in white and pigmented hair growth, nerve changes in alopecia, treatments for baldness and alopecia, a toenail condition linked to a genetic disorder, and that nail fungus is more common in people with psoriasis.

A bull with a gene mutation was asymptomatic, synthetic retinoids cause hair loss, and new therapeutic targets were identified for skin diseases.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

Deleting the Hoxc13 gene in frogs shows its crucial role in developing skin structures similar to hair.

A specific RNA, circNlgn, contributes to heart damage and scarring caused by the cancer drug doxorubicin.

Adding TERT and BMI1 to certain skin cells can improve their ability to create hair follicles in mice.

Defective protein folding due to a mutation is key in ANE syndrome.

BTNL2 helps protect hair follicles from immune attacks.

Mutating the gmds gene in zebrafish increases hair cell numbers and regeneration.

Three genes, BMP4, POSTN, and WNT5A, may help treat keloids.

A new genetic region, 17q21.31, is linked to higher ovarian cancer risk.

Removing certain hair follicle stem cells worsens skin reactions to allergens.

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

New markers and pathways have been found in skin tumors, helping better understand and diagnose them.

A specific DNA region is crucial for Foxn1 gene expression in thymus cells but not in hair follicles.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

BTNL2 helps protect hair follicles from immune attacks, which could aid in treating alopecia areata.

Keratin 15 cells from hair follicles help develop and maintain skin tumors in mice.

ErbB2 signaling is crucial for skin cell growth and cancer development in mice.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

A rare genetic mutation causes Woodhouse-Sakati syndrome symptoms.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

The ITGB6 gene is important for tissue repair and hair growth, and mutations can lead to enamel defects and other health issues.

WNT10A helps esophageal cancer cells spread and keep renewing themselves.

mrp/plf-mRNA can indicate tumor-promoting effects in skin.

The EDAR gene mutation leads to thinner and more deformed hair shafts.

Netherton syndrome causes skin and hair issues, confirmed by "bamboo hair" under dermoscopy, with no cure but managed with topical treatments.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

A new goat gene affects cashmere fiber thickness; certain variations can make the fibers coarser.

Mutations in the SHH pathway in certain skin cells can cause skin tumors and abnormal hair growth.