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Patients with chronic graft-versus-host disease often have skin problems like vitiligo and alopecia areata.

Vitamin C deficiency changes gene expression, affecting skin and hair health.

Geranium sibiricum extract helps hair grow and is more effective than minoxidil but can be toxic in high concentrations.

Modified red ginseng extract promotes hair growth and has antioxidant and anti-inflammatory effects.

The NUDT15 gene variant causes severe side effects from azathioprine in some Indian patients.

Suppressing ODC activity reduces tumor growth in hair follicles.

Liver damage in PCOS is linked to iron overload and cell death due to the miR-761-hepcidin/GPX4 pathway.

AGD1 is important for root hair development in Arabidopsis, working with phosphoinositide signaling and the actin cytoskeleton.

Applying DMG-Na to the skin increases blood flow and may help with skin conditions.

IGF2BP3 gene is up-regulated in keloid patients, suggesting potential targets for treatment.

Genetic defects in androgen production are linked to male developmental disorders and are improving treatment understanding.

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

Gamma-ray exposure improves genome editing efficiency in mice using the i-GONAD method.

Giant axonal neuropathy changes the structure of keratin in human hair.

The enzyme CD73 helps control human hair growth and could be targeted to treat hair growth disorders.

Targeting CXXC5 and GSK-3β may help treat male pattern baldness.

Most patients experienced mild to moderate skin problems during a trial for a desmoid tumor treatment.

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

Hair glycation levels can indicate long-term blood sugar control.

Chronic ethanol increases certain brain receptor levels, influenced by steroids and protein changes.

Improved genetic diagnosis of PCOS can lead to better patient outcomes.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

New mutations in the DSG4 gene cause a rare hair condition.

5α reductase type 2 enzyme mutation and oxidative stress may increase androgenetic alopecia risk in Egyptians.

The P133R mutation in AKR1D1 enzyme causes harmful bile acid buildup, explaining related health issues.

Enhanced stem cells from the placenta can reduce fat buildup in eye tissue for Graves' disease.

Injecting newborn mice with a niacin blocker caused skin, gut, and brain damage similar to human pellagra.

Newborn screening for biotinidase deficiency is effective in preventing severe complications.