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A protein from fat-derived stem cells, DKK1, is linked to hair loss and blocking it may help treat alopecia areata.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

Foxn1 helps skin cells mature by controlling a specific protein's activity.

AMPK activation may reduce melanoma risk in red-haired individuals.

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

A mutation in the VDR gene affects hair cycling without needing ligand binding.

SNP rs2479106 in the DENND1A gene may increase PCOS risk in Saudi Arabian females.

Keratinocyte gene expression is controlled by multiple modules with specific binding sites.

AGC2-1 protein is essential for root hair growth in Arabidopsis.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

A mutation in the Sgkl gene causes defective hair growth in mice.

Increasing PDCD4 protein may help prevent or treat some skin cancers.

Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

The protein FLCN is involved in cellular cleanup and is regulated by ULK1.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

The DMI3 gene is essential for nodule development and symbiosis in certain plants.

Keratinocytes can reduce the survival of certain melanoma cells, suggesting new therapy paths.

K6/ODC transgenic mice are effective for quickly identifying cancer-causing chemicals.

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

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

Dermal EZH2 controls skin cell development and hair growth in mice.

A new keratin 6 type in mice explains why some mice without certain keratin genes still have normal hair and nails.

PCR genotyping in cre-loxP mice can be inaccurate due to unintended gene deletions in non-target tissues.

Removing GRK2 in skin cells causes hair loss similar to immune-related alopecia.

A faulty KLHL24 gene leads to hair loss by damaging hair follicle stem cells.

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.

Deleting TNFα gene reduces skin cancer risk in certain mice.

A new gene mutation is linked to monilethrix in the studied family.

ETS2 drives cancer progression in squamous cell carcinoma and is linked to poor patient outcomes.