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GRHL3 is important for controlling gene activity in skin cells during different stages of their development.

CD18-deficient mice developed psoriasis-like skin disease, useful for studying inflammatory skin disorders.

The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

Estrogen and MLL enzymes work together to regulate genes important for hair growth and leukemia.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

A gene mutation in Lama3 is linked to a common type of hair loss.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

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

pCLCA2 protein may help maintain skin structure and function.

Removing Gsdma1/2/3 genes reduces skin cell overgrowth by blocking a specific cell pathway.

The SLICK1 allele in Holstein heifers affects hair and immune traits without altering prolactin signaling.

Prolactin affects hair growth cycles and can cause early hair follicle regression.

Basement membrane changes in lichen planopilaris cause scarring and permanent hair loss.

Mice with a mutated Dsg3 gene showed severe symptoms but not the typical blistering of pemphigus vulgaris.

Scarring alopecia involves increased immune cells and specific gene changes near damaged hair follicles.

Phospholipase A2 enzymes play key roles in skin health and disease.

A woman with a rare autoimmune disorder had a blister on her eye and unique immune reaction, which was effectively treated with medication.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

PDO, PLLA, and PCL threads increase collagen in ageing skin but don't change MMP1 gene expression.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

PLAU and SerpinB2 affect cell death differently in various forms of leprosy and could be targets for new treatments.

Ixekizumab may be an effective first treatment for a rare skin condition causing hair loss.

Different sPLA2 enzymes affect immunity, skin and hair health, reproduction, and may be potential targets for therapy.

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

Bovine milk fats applied to mouse skin can promote hair growth similar to known hair growth treatments.

Mechanical stress causes ligament thickening through WISP-1 and Hedgehog signaling.

The LMNA mutation affects skin structure even in asymptomatic carriers.