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Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

Li2CO3 improved skin disease in a mouse model of Focal Dermal Hypoplasia without toxicity.

VPS13C variants are linked to more severe REM sleep disorder and faster progression to Parkinson's disease.

The EDAR gene mutation leads to thinner and more deformed hair shafts.

LPA3 signaling in the uterus is crucial for placental formation and fetal development.

A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

Matriptase imbalance contributes to cancer development and spread.

A new compound slows cancer cell growth and causes cell death by blocking cell cycle progression and increasing cell-damaging molecules.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

The HSD3B1 variant increases hair loss risk in overweight women with PCOS.

New gene variants were found for rare skin and hair disorders, improving understanding and treatment.

A girl with citrullinemia developed pili torti, suggesting a link between the hair condition and the metabolic disorder.

Researchers found two new genetic variants linked to Alzheimer's disease.

Methylation in specific gene region causes finasteride resistance in some BPH patients.

PDRN is effective and safe for healing wounds and skin issues.

PP2Acα is essential for proper hair and skin development.

CRISPR gene editing reduces harmful molecules in cells from Emery–Dreifuss Muscular Dystrophy patients.

The patient's hair was thinner and had fewer lipids due to a genetic mutation.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

A specific gene mutation causes different hair defects in Indian monilethrix families.

Four new cases of Bachmann-Bupp syndrome suggest potential for targeted treatment.

Gene differences affect finasteride side effects in men with hair loss.

A woman with a specific mutation causing adrenal gland issues faced fertility problems, but careful hormone therapy helped her manage it successfully.

GasderminA3 is important for normal hair cycle transitions by controlling Wnt signaling.

A new mutation in the HR gene causes hair loss in a specific family.

Removing MCPIP1 from myeloid cells in mice leads to hair loss and prevents skin tumors but causes pigmented spots.

Zebrafish help understand genetic causes of skin pigment disorders like albinism.

High levels of ODC and a mutant Ha-ras gene cause tumors in mice.