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CP-690,550 significantly reduced itching in patients with moderate-to-severe plaque psoriasis.

Atropine and neosynephrine effectively prevent floppy iris syndrome during cataract surgery.

Besnoitiosis, a parasitic disease, has been found in donkeys in Italy and may be more common in Europe than previously thought.

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

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

Mutants of CYP154C2 enzyme significantly improved steroid conversion efficiency.

TRα and CRABPII genes change their activity levels during goat fetal skin development.

The QuantAnts machines can find cancer markers and create CRISPR targets for them.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

RORs may influence cashmere growth cycles.

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Mutations in the KRT16 gene can cause skin and nail disorders.

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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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YWS1903 is safe for pregnant rats at moderate doses but causes fetal issues at high doses.

Sry may regulate fatty acid metabolism and shows different expression levels in rat tissues.

The Msx2 gene affects feather development in Hungarian white geese and a specific gene variation could indicate feather quality.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

The most common sign of aging at the gene level is more Ectodysplasin A2 Receptor (EDA2R) being made.

Tsc2-deficient stem cells can help understand and treat TSC-related tumors.

Finasteride effectively inhibits the enzyme steroid 5 alpha-reductase II.