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The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

A specific mutation in PA-PLA1α causes abnormal hair growth.

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

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

BAF200 is essential for proper heart and coronary artery formation.

Higher expression of the keratin-associated protein 8.1 gene in Liaoning cashmere goats is linked to finer cashmere fibers.

Stress can cause a type of hair loss in mice lacking the CCHCR1 gene.

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

The IRE gene is important for normal root hair growth in Arabidopsis plants.

JAK1 gene variation may increase alopecia areata risk.

The Engrailed-1 gene plays a key role in the development of sweat glands in mice.

AIRE protein, defective in APECED patients, is found in skin and hair cells and interacts with cytokeratin 17.

A gene called BMAL1 plays a role in controlling hair growth.

TRα and CRABPII genes change their activity levels during goat fetal skin development.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

Deleting MED1 in skin cells causes hair loss and skin changes.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

The FAT1 gene and its variations can help improve wool quality in Chinese Merino sheep through selective breeding.

BMI1 is essential for preventing hair greying and maintaining hair color.

The LncRNA AC010789.1 slows down hair loss by promoting hair follicle growth and interacting with miR-21 and the Wnt/β-catenin pathway.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

A gene mutation causes monilethrix in a Chinese family.

OXI1 kinase is essential for plant defense and root hair growth in Arabidopsis.

The P133R mutation in AKR1D1 enzyme causes harmful bile acid buildup, explaining related health issues.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.