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Overexpressing NSD3 in mice causes breast cancer-like tumors and gland abnormalities.

TRPA1 is crucial for mechanical sensitivity in skin sensory neurons.

RIPK1 inhibitors might help prevent alopecia areata.

LncRNA018392 helps goat skin cells grow by increasing CSF1R.

Selective non-steroidal inhibitors of 5α-reductase type 1 can help treat DHT-related disorders.

miRNAs are crucial for hair growth and skin health.

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

A missing mK6irs1 gene causes hair loss in mice.

Topical IKKα inhibitors may help prevent CCS tumours.

Variants in the CCDC47 gene are linked to trichohepatoneurodevelopmental syndrome.

Damage to skin releases dsRNA, which activates TLR3 and helps in skin and hair follicle regeneration.

miR-29a-5p prevents the formation of early hair structures by targeting a gene important for hair growth and is regulated by a complex network involving lncRNA627.1.

The Tru9I variant in the VDR gene may influence alopecia areata risk and vitamin D levels.

Dopaminergic neurons in the gut have distinct subtypes, some releasing both dopamine and acetylcholine.

Activating Nrf2 in skin cells causes skin disease similar to chloracne in mice.

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

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

NuMA-microtubule interactions are vital for proper skin structure formation and function.

LHX2 is essential for hair follicle development, controlled by NF-κB and TGFβ2 signaling.

Frizzled 3 and Frizzled 6 together control the orientation of mouse hair follicles.

A new method helps detect androgen receptor movement in cells, aiding research on hair loss treatments.

Nucleic acids trigger chemokine production in skin cells, affecting skin inflammation.

The Celsr1 gene is crucial for normal hair patterning in mice.

Clim proteins are essential for maintaining healthy corneas and hair follicles.

NFATc1 controls hair stem cell activity, affecting hair growth and could be a target for hair loss treatments.

HVDRR is caused by VDR gene mutations, leading to vitamin D resistance, treatable with high calcium doses, but alopecia remains permanent.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

Strontium ranelate helps cartilage growth by blocking a specific cell pathway.