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Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

TNC+ fibroblasts play a key role in skin inflammation by interacting with T cells.

HoxC genes are crucial for normal hair and nail development.

Cantú syndrome is caused by mutations in the ABCC9 gene.

Nephronectin is linked to worse breast cancer outcomes and helps cancer spread.

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

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

Lack of Cisd2 disrupts calcium balance in cells, leading to poorly functioning neutrophils.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

NGAL may help maintain skin balance and is linked to skin disorders and cancers.

PKC ε increases hair follicle stem cell turnover and may raise skin cancer risk.

Key genes, including KRT39 and KRT74, influence hair length in Inner Mongolia cashmere goats.

The nude gene is important for skin and hair development.

lncRNAs may help control cashmere goat hair growth by responding to light changes.

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

The study identified key genes and pathways that influence goat wool quality and growth.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

The human K5 promoter controls specific gene expression in skin cells, with key regulatory elements near the TATA box.

CAP1 decreases the expression of a hair-related protein in young Tan sheep's skin.

The Foxn1(-/-) phenotype disrupts hair growth and affects skin stem cells.

The gene GJA1 is important for regulating coarse hair density in goats.

The system allows precise control of gene expression in mouse skin, useful for studying skin biology.

Human basal cell carcinomas and squamous cell carcinomas have unique gene expression patterns not fully mirrored in mouse models.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

Different body areas have unique skin cell communication patterns, explaining why certain skin diseases occur in specific regions.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.