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

Biosimilars lower costs but don't significantly improve access.

The UHS promoter is specific to mouse hair follicles.

CD8+ T cells attack hair follicle stem cells, causing scarring and hair loss.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

A new gene, mrp4, is found in mice and may play a unique role in hair follicle development in tails and ears.

A new topical treatment for hair loss shows strong hair growth effects with low toxicity.

A man had two rare autoimmune diseases that might be connected.

Clq deficiency is linked to systemic lupus erythematosus symptoms.

The new microneedle system promotes hair growth by improving the hair follicle environment.

CEP135 may predict cancer outcomes, and targeting PLK1 could help treat certain sarcomas.

A certain medication improved severe itching in a boy with liver and bowel disease by reducing histamine levels, suggesting a new treatment target.

SACUMAN, a rare condition causing hair loss without clear signs, is often misdiagnosed and needs scalp biopsies for accurate detection.

50-mg ritlecitinib capsules are bioequivalent to 100-mg capsules.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

Samcyprone ointment is effective for treating common warts if a sensitization reaction occurs first.

The study found a specific peptide that helps detect TGase 3 activity in skin and hair follicles.

Keratin 75 might be important in oral cancer progression.

Sex and race affect immune responses and treatment outcomes in Hidradenitis suppurativa.

The enzyme from human skin can cross-link proteins and needs calcium to work.

5% topical minoxidil improves hair density and quality in monilethrix patients.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

The combination of tadalafil and finasteride improves urinary symptoms and erectile function in men with enlarged prostates.

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

A patient with a nerve disorder died from infection complications after developing insulin resistance from a treatment.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

A new method using human lung cells helps find drugs to block and reduce inflammation from SARS-CoV-2.

Antibodies help identify glycoproteins in normal skin and tumor cells.