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GI198745 is more potent and longer-lasting than finasteride, potentially better for treating hair loss.

UHP-sCESr is as effective as HESr for treating BPH symptoms.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Certain miRNAs are linked to Cashmere goat hair quality.

DS-2325a is safe and well-tolerated, supporting further development for Netherton Syndrome treatment.

The document's conclusion cannot be provided because the document is not accessible.

Ritlecitinib is being tested for safety and effectiveness in young children with severe alopecia areata.

IL-15 promotes hair growth and protects hair follicles.

Risankizumab effectively treats and maintains skin clearance in moderate-to-severe psoriasis.

P chinensis may help treat stress-related hair loss.

An 11-year-old girl with a rare skin disorder also had cornea issues and dry eye, needing careful management.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Clinical trials for hair loss in the USA show differences in participation among different races and ethnic groups.

Ritlecitinib may cause serious side effects like blood clots in alopecia areata patients.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

Certain genetic variants in PRLR and PCCA genes may lead to shorter hair in cattle, which could help with heat tolerance.

M50054 may help treat hepatitis and hair loss from chemotherapy.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

A rare skin disorder affecting the face was found in a 28-year-old Saudi man.

DKK4 can be used to improve wool quality in Zhexi Angora rabbits.

5-alpha reductase inhibitors don't increase breast cancer or benign breast disorder risk in women.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.