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PPAR activation can improve diabetic wound healing by enhancing blood vessel function.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

The girl in "The Girl with a Pearl Earring" might have had alopecia areata, causing her lack of eyebrows and sparse eyelashes.

Sca-1+ cells in newborn mouse skin may become fat cells.

Combining amino acid and stem cell therapy may help manage hepatocutaneous syndrome in dogs.

AL136131.3 slows hair growth by affecting energy processes in hair loss.

The symposium concluded that a specific lipid might cause hair loss, inflammation is a key factor, and stem cells in bald scalps aren't working right, suggesting new treatment targets.

Soy oil and genistein reduce hair loss risk in mice.

Treatment improved symptoms in a woman with HAIR-AN syndrome.

A 13-year-old boy with a rare genetic condition survived a heart attack and improved with treatment.

NAFLD is common in women with PCOS and may signal metabolic syndrome.

Deleting the Sox21 gene changes hair lipid composition and increases cholesterol sulfate levels.

An infant with complete hair loss was diagnosed with a genetic disorder affecting hair growth.

A defective protein in progeria causes cell death and atherosclerosis, but a treatment targeting cell stress may reduce these effects.

The woman has a skin condition involving nodules, scars, and hair loss.

Targeting gut microbiome and metabolome may help treat autoimmune skin diseases like alopecia areata.

hsa_circ_0002980 can help stop liver cancer cells from growing and spreading.

Wnt/β-catenin signaling is important for keeping skin cell attachment structures stable.

The conditions alopecia areata, primary sclerosing cholangitis, and ulcerative colitis may be linked by shared autoimmune and cell death mechanisms.

A low-starch/low-dairy diet may help overweight women with PCOS lose weight and improve metabolism, but more research is needed.

Harlequin ichthyosis involves abnormal skin cell structures and giant mitochondria, affecting skin and hair.

The clinical signs of Adams-Oliver syndrome can vary greatly, even among family members.

Zinc supplements effectively treat acrodermatitis enteropathica.

Pseudopelade is a rare inherited hair loss condition with a genetic cause.

Epilation and DHT cause skin calcification by increasing ATP and calcium deposits.

Certain gene variations and low adiponectin levels may increase the risk of hair loss in Egyptians.