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A clinically suspected melanoma appeared benign under the microscope but was confirmed by specific tests and a rare mutation.

Overexpressing Merkel cell virus proteins in human hair follicles can create clusters of cells that resemble Merkel cell cancer.

Gsdma3 affects hair growth by controlling Wnt5a, which influences hair cell development.

Early diagnosis and treatment are crucial for managing Folliculotropic Mycosis Fungoides on the scalp.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

Activated LEF/TCF complexes are crucial for hair development and cycling.

BMS-470539 reduces skin fibrosis and inflammation.

Skin cells can naturally limit the growth of cancerous changes by balancing cell renewal and differentiation.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

LPAR6 has a unique way of binding and activating, which helps in designing treatments for hair loss and cancer.

Akt2 and SGK3 are both important for normal hair growth and development.

Foxi3 expression in developing teeth and hair is controlled by the ectodysplasin pathway.

Activating TLR3 boosts autophagy gene expression in skin cells.

A man with a type of skin lymphoma had unusual yellowish skin growths despite normal blood lipid levels, and treatment reduced some symptoms but not the growths.

IGF2BP3 and other m6A-related genes are linked to keloid formation and could be potential treatment targets.

LncRNA018392 helps goat skin cells grow by increasing CSF1R.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

TAK-279 effectively reduces psoriasis symptoms and is safe.

IL-3 worsens lupus nephritis and blocking it improves kidney health.

MOF controls skin development by regulating genes for mitochondria and cilia.

The research suggests that Tourette syndrome is linked to both brain signaling and immune system pathways.

Hair follicle sampling is a practical method for measuring biomarkers in children with and without Fragile X syndrome.

Some leukemia treatments can cause skin reactions similar to keratosis pilaris.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Human and mouse TGase3 enzymes are similar but differ near the activation site, crucial for their function in skin and hair development.

Blocking miR-27a increases sheep hair follicle stem cell growth and decreases cell death, which could help improve wool quality and treat hair loss.

The balance between cell renewal and differentiation controls the growth of cancerous cells in mouse skin.

DNAJB9 cfRNA could help diagnose and treat female hair loss.

MITF+ melanoma patients are more likely to have multiple melanomas and unique skin patterns.