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Urotensin II increases growth and VEGF production in rat skin cells by turning on the Wnt-β-catenin pathway.

The ID2 gene can help distinguish between sensitizers and irritants in skin cells.

TCDD disrupts skin stem cells, causing skin issues like chloracne.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

A KRT32 gene variant causes loose anagen hair syndrome.

Trichothiodystrophy hair is structurally abnormal with protein and organization issues.

Targeting cholesterol, fatty acids, fibrosis, and mast cells may help treat CCCA.

TGF-β1 and 2 in hair follicles may be linked to hair loss in AGA.

Dickkopf-related Protein 2 can help hair grow by activating a specific cell pathway.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

TSC2-/meth cells can cause skin lesions, hair growth, and lung issues, and may be treated with chromatin remodeling agents.

TCF/Lef1 is essential for skin barrier function by regulating lipid metabolism.

A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

The C-CAT tool helps assess and improve treatment for central centrifugal cicatricial alopecia.

Pvalb8 is essential for zebrafish hearing and hair cell development, and its mutation causes hearing loss.

CircAGK affects cell death in hair cells by controlling the miR-3180-5p/BAX pathway, which can lead to hair loss.

Blocking adenosine A2B receptor may prevent or treat hearing loss.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.

Cathepsin L is essential for normal hair growth and development.

Baricitinib and its combination with lonafarnib improve fat cell formation in certain genetic disorders.

A new mouse mutation causes skin and hair issues, influenced by another gene.

Cyclooxygenase-2 overexpression in mice skin causes hair loss like human androgenetic alopecia.

The FDA approved the first gene therapy for a blood disorder after overcoming early challenges and demonstrating patient benefits.

Low oxygen levels affect the behavior of certain proteins in human skin cells.

Meis2 is essential for touch sensation and nerve function in mice.

Inhibiting TYK2 can restore hair growth in alopecia areata.