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Blocking a key energy pathway in human hair follicles can trigger stress responses that stop cell growth.

Adding a second method to PROTACs could improve cancer treatment.

The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

People with atopic dermatitis have more CD4+ T cells that respond to a certain bacterial lipid, which may play a role in the skin condition's inflammation.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

Phosphatide distribution in mouse skin remains consistent in both normal and cancerous growths.

The enzyme PA-PLA1α is important for proper hair follicle development.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

Two genetic disorders affect biotin metabolism, causing severe skin, hair, and metabolic issues.

LPAR6 has a unique way of binding and activating, which helps in designing treatments for hair loss and cancer.

This enzyme helps metabolize fatty acids and isoleucine, and could be key in treating neurological diseases and certain cancers.

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

Pilomatricomas don't follow the usual hair follicle cell differentiation process.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Lysophosphatidic acid boosts stem cell growth and movement by creating reactive oxygen species.

Scientists found new, better-working inhibitors for a hormone-related enzyme.

A new gene mutation linked to a skin condition was found in a Spanish family.

Retinoids increase steroid sulfatase activity in leukemia cells through RARα/RXR and involves certain pathways like phosphoinositide 3-kinase and ERK-MAP kinase.

Mice studies show that Protein Phosphatase 2A is crucial for cell growth, development, and disease prevention.

Reduced matriptase activity causes skin and hair issues in both humans and mice.

A specific chemical change in the S100A3 protein leads to the formation of a four-part structure important for hair formation.

Topical 6% salicylic acid effectively reduced skin plaques in a patient with wooly hair and palmoplantar keratoderma.

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

Trichohyalin is modified by enzymes to form strong structures in hair cells.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

The enzyme steroid sulfatase is linked to breast cancer and other conditions, and inhibitors are being developed for treatment.

Blocking cholesterol production may help control hair loss in Primary Cicatricial Alopecia by affecting key regulators.

Two enzyme defects in biotin metabolism cause severe skin, hair, and metabolic issues.