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

Athletic trainers should understand and support the medical needs of transgender and gender-diverse patients.

Activated protein C helps protect mice from radiation damage.

During late pregnancy in rats, hormonal changes increased certain GABAA receptors in specific brain cells.

A gene mutation causes a rare hereditary hair loss, offering potential for new treatments.

Shorter GGC triplet repeats in the androgen receptor gene are linked to less hair loss in Han men.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

γδTregs may help treat autoimmune diseases like alopecia areata by promoting hair regrowth and reducing immune attacks.

Activating β-catenin increases melanocytes and decreases Schwann cells.

A new enzyme in rats may help regulate hair growth.

Melanocyte-associated antigens may play a key role in alopecia areata and could be targets for new treatments.

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

Sinapic acid and glabridin together help hair growth in androgenetic alopecia.

The FA2H gene improves cashmere fineness by enhancing hair growth in goats.

A specific gene change in APCDD1 increases the risk of hair loss.

KATP channels are important for energy balance and are targeted by drugs for diabetes, hypoglycemia, hypertension, and hair loss.

Both mouse and rat models are effective for testing alopecia areata treatments.

Adding a second method to PROTACs could improve cancer treatment.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

A DNA aptamer helps promote hair growth by enhancing a key cell growth signal in hair follicle cells.

TCDD changes skin cell growth and keratin production in mice.

PCA hydrogel promotes hair growth by enhancing blood vessel formation and hair follicle stem cell activity.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

Non-coding RNAs may be key in diagnosing and treating rare skin disorders.

Dapagliflozin improved blood sugar control in a man with Werner syndrome without side effects.

The RNA AL136131.3 slows down hair growth and speeds up hair loss by affecting sugar breakdown in hair follicles.

A specific gene mutation causes a severe skin disorder in a family.

Silencing NtNCED3-2 gene in tobacco reduces drought tolerance and impairs growth.