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Low-dose DMSO may help treat castration-resistant prostate cancer by reducing key cancer cell receptors.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

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

AKR1B10 enzyme may cause keloid scars and could be a treatment target.

Male hormones and reduced plakoglobin can impair heart electrical function and increase arrhythmia risk in males.

Androgens may influence bladder cancer progression by affecting cellular behavior.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

CS-891 may effectively treat hair loss by blocking enzymes in hair follicles.

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

The enzyme 5α-reductase is key in causing psychotic-like effects from sleep deprivation.

p2y5, now called LPA6, is a receptor important for human hair growth.

Prostate cells have proteins that bind to specific hormones, which can increase protein production when activated by these hormones.

Mutations in the NR3C1 gene cause a rare condition that affects hormone signaling and can lead to various symptoms, with dexamethasone as a treatment option.

Androgens increase muscle mass by promoting myoblast growth through ornithine decarboxylase.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

Sfrp2 increases during hair follicle catagen phase and slows keratinocyte growth.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

Editing the FGF5 gene in sheep increases wool length, confirming its role in hair growth.

Starting 5-alpha reductase inhibitors does not significantly increase the risk of rhabdomyolysis in older men, but is linked to a higher risk of muscle conditions.

Rats had lasting erectile problems after stopping a certain medication.

Androgen treatment with dihydrotestosterone may help maintain height in patients with 5-α-reductase type 2 deficiency, especially before puberty.

A new syndrome, Teelwani Syndrome, combines features of two rare genetic disorders.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Three siblings with a rare genetic condition had abnormal sexual development and chose different gender identities, needing surgery and therapy.

Mutations in the KRT85 gene cause hair and nail problems.

The index to ring finger ratio may indicate disease severity in female ankylosing spondylitis patients, but not in males.

5-alpha-reductase inhibitors help treat urinary symptoms from an enlarged prostate.

5-Alpha reductase inhibitors help treat enlarged prostate but may cause sexual side effects.