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hsa_circ_0002980 can help stop liver cancer cells from growing and spreading.

Early diagnosis and treatment of haemochromatosis are crucial for reversing organ damage and improving fertility.

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

Skin organoids with NCSTN mutation show changes in hair follicle development and higher inflammation, key features of Hidradenitis Suppurativa.

Hedgehog signaling controls hair follicle development and can affect skin cancer growth.

Two siblings with a genetic mutation had a form of rickets that doesn't respond to vitamin D.

People with hidradenitis suppurativa have a higher risk of heart attacks and strokes.

The name Janus is fitting for JAK inhibitors as they revolutionize dermatology treatments.

The therapies improved ejaculation disorders and sexual function in middle-aged men.

JAM-A modification speeds up skin wound healing by boosting fibroblast growth.

Finasteride improves hidradenitis suppurativa in children with no adverse effects.

Patients with hidradenitis suppurativa have higher levels of cell-free DNA in their blood.

There is no gold standard treatment for hidradenitis suppurativa due to insufficient evidence.

Severe Hidradenitis Suppurativa increases missed and unproductive workdays.

Researchers made a detailed map of gene activity for different parts of human hair follicles to help create targeted hair disorder treatments.

Reduced AhR signaling in HS tunnels leads to persistent inflammation and microbial imbalance.

New hair spray caused a hair shaft disorder.

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

Hidradenitis suppurativa negatively affects patients' sexual lives and relationships, highlighting the need for better support and communication about sexual health.

Hair analysis can track haloperidol dosage history.

GnRH agonist effectively diagnoses and treats postmenopausal hyperandrogenism from ovarian sources.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

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A specific gene mutation causes vitamin D resistance, but certain vitamin D analogs might help.