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Phosphodiesterase inhibitors like tadalafil can reduce cell growth in BPH caused by CD8+ T cells in low androgen conditions.

Some people have genetic mutations that make them resistant to vitamin D, leading to rickets even with enough vitamin D intake.

Noncoding dsRNA helps produce exosomes that aid in skin regeneration.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

Plaquenil can cause a severe skin reaction called AGEP, requiring prompt diagnosis and treatment.

Para-aminobenzoic acid in hair supplements can cause autoimmune hepatitis.

The diphosphonate was the most effective at preventing calcification in rats.

DNA methylation is essential for skin and hair follicle development, and could be a target for treating skin diseases.

Certain genetic differences may affect how likely someone is to get COVID-19 and how severe it might be.

Double-stranded RNA causes inflammation in hair follicle cells, which may help understand and treat alopecia areata.

Topical immunotherapy with DPCP is most effective for certain alopecia areata types, with success linked to age and disease duration, and influenced by a gene polymorphism.

Polymer-based nanocarriers can improve acne treatment by delivering drugs through hair follicles more effectively.

Microneedles offer a promising, less invasive way to treat and monitor psoriasis.

Low PON1 levels may indicate and predict the severity of hair loss.

PandaOmics uses AI to find new disease treatment targets and biomarkers.

The vitamin D receptor can affect gene activity even without its usual hormone in hair and skin.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

34% of patients on hepatitis C treatment had reversible skin issues.

Dupilumab significantly improved a 5-year-old girl's prurigo nodularis without side effects.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

Panniculitis in dermatomyositis is rare, more common in women, and may persist despite treatment.

The growth of the Epstein-Barr virus in the patient's cells was linked to the worsening of her lymphoma.

Lysophosphatidic acid affects sensory neurons and may cause neuropathic pain and itch.

An intact skin barrier is crucial to prevent infection in cases of tether-induced tenosynovitis.

Polynucleotide gel injections help reduce hair loss and increase hair thickness in people with pattern hair loss, with few side effects.

The technology can help diagnose and subtype autoimmune diseases by identifying specific autoantibodies.

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A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.