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Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

Mutations in the KLHL24 gene cause skin blistering in epidermolysis bullosa simplex.

Basement membrane changes are crucial for hair follicle development.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

Quiescent cells have increased mitochondrial activity and ECM gene expression, but reduced glycolysis.

The 4C32 gene may help in mouse skin development and differentiation.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

Loss of Ten1 in mice causes telomere shortening and symptoms similar to human dyskeratosis congenita.

A mutation in the KRT25 gene causes woolly hair and hair loss.

XEDAR triggers a specific signaling pathway in cells.

Circular RNA ERCC6 helps activate stem cells important for cashmere goat hair growth by interacting with specific molecules in an m6A modification-dependent way.

Protease Nexin-1 is found in human hair growth cells and is affected by male hormones.

The research found that the molecule lncRNA-H19 helps hair follicle cells grow by affecting certain cell pathways in cashmere goats.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

New mutations in the DSG4 gene cause a rare hair condition.

SLVs help maintain muscle stretch sensitivity and could aid in treating hypertension and muscle spasticity.

Trichohyalin helps in hair and skin cell structure and function by binding calcium and linking proteins.

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

The DiLiCre mouse model is an effective tool for precise genome editing using light.

Gene expression affects fur development in rex rabbits.

Targeting NMMHC IIA may help treat blood-brain barrier damage.

Repetin is a protein involved in skin and hair development, binding calcium and compensating for other proteins when needed.

A specific gene mutation causes woolly hair and hair loss.

The gene Msx2 is crucial for hair follicle regeneration during wound healing.

Researchers found that certain RNA circles in the brain are linked to disease risk, but their exact role in disease is still unknown.

TACE/ADAM17 is essential for maintaining healthy hair and hair follicle stem cells.

ERG increases SOX9, promoting prostate cancer growth and invasion.