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Overexpression of sPLA2-IIA in mouse skin reduces hair stem cells and increases cell differentiation through JNK/c-Jun pathway activation.

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

Lhx2 helps retinal cells respond to signals for eye development.

Cathepsin L is essential for normal hair growth and development.

Different sPLA2 enzymes have unique roles in phospholipid metabolism and biological processes.

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

New mutations in hair keratin genes cause the rare hair disorder monilethrix.

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

sPLA2-IIA increases growth in hair follicle stem cells and cancer cells, suggesting it could be targeted for hair growth and cancer treatment.

SLC3A2 is crucial for hair follicle stem cell function and hair growth.

Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

sPLA2-IIE is crucial for normal hair follicle structure and skin health.

Dermal EZH2 controls skin cell growth and differentiation in mice.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

The enzyme is crucial for skin cell development and can be activated without proteolytic activation.

A new gene mutation is linked to monilethrix in the studied family.

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

Pyruvate Kinase M2 helps hair grow by linking energy production and a key hair growth pathway.

Turning off the Lhx2 gene in mouse embryos leads to slower wound healing and scars.

Skin acetyl-CoA synthesis is crucial for overall lipid balance.

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

TET enzymes are important for skin and hair development by controlling gene activity in specific areas.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

TYK2 inhibition may help treat alopecia areata by promoting hair growth and reducing immune response.

The B2 genes are crucial for hair growth in rats.

Recessive X-linked ichthyosis involves a less efficient enzyme in hair follicles, suggesting two distinct enzymes.

Human sebaceous glands contain enzymes that affect androgen production and may influence sebum production and acne.

A new protein linked to hair strength was identified, aiding in understanding brittle hair conditions.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.