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Two new enzymes, PAD-R11 and PAD-R4, were cloned and showed activity, with PAD-R11 resembling epidermal enzymes.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

Testosterone treatment may change estrogen receptor methylation in AFAB individuals.

β1 integrin is essential for the survival, growth, and movement of human epithelial progenitor cells.

Defective protein folding due to a mutation is key in ANE syndrome.

A specific gene mutation (Y449H in K10) was found in a patient with severe skin disorder.

Valproic acid can cause a rare allergic reaction leading to fluid around the lungs and heart, which is treatable by changing medication.

A mycobacterial protein shares a similar region with a human skin protein, possibly affecting skin diseases.

Targeting amphiregulin may improve treatment for fibrotic diseases and cancer.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

PGF_2α receptors in human eyelids are found in specific parts of hair follicles, explaining eyelash changes with glaucoma treatment.

Early diagnosis and comprehensive management improve life quality for Netherton syndrome patients.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

BerEP4 and CD34 staining can help tell apart tricholemmoma from basal cell carcinoma.

Resident memory T cells and necroptosis may drive fibrosis in eosinophilic fasciitis and morphea.

Prostaglandin E2 affects human platelet activity in complex ways that could lead to personalized heart disease treatments.

Mouse epidermal growth factor temporarily stops wool growth and causes cell changes in Merino sheep.

Focal palmoplantar callosities may help diagnose non-Herlitz junctional epidermolysis bullosa.

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

A brain-made hormone can protect against memory-related brain damage caused by harmful proteins.

Two mutations in KRT74 and EDAR genes cause sheep to have finer wool.

Corneous beta-proteins evolved uniquely in reptiles and birds, forming scales, claws, beaks, and feathers.

PAD3 plays a key role in hair and skin protein structure and may be linked to skin diseases.

Promising cancer treatments were found, but the manufacturer closed.

A genetic variant in "Blonde d'Aquitaine" calves causes death at birth due to a missing protein.

Genetic testing is crucial for diagnosing and treating acrodermatitis enteropathica effectively.

Diphenyl ethers can potentially reduce excess oil production when applied on the skin, helping treat conditions like acne.

Mutations in the hHb6 gene cause the hair disorder monilethrix.