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

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

Trichostatin A helps restore hair-growing ability in skin cells used for hair regeneration.

Two new gene clusters important for hair formation were found on human chromosome 11.

SPRY1 deficiency in skin cells causes stem cells to move to the skin surface, leading to increased pigmentation.

A new compound from Royoporus badius activates immune cells and induces inflammatory responses.

External factors can cause skin cancer cells that usually don't spread to grow and form tumors in mice.

Reduced matriptase activity causes skin and hair issues in both humans and mice.

TRPV4 channel affects skin health and could be a target for treating skin disorders.

Mice without the Sept4/ARTS gene heal wounds better due to more stem cells that don't die easily.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

TAF4 is important for skin cell growth and helps prevent skin cancer in mice.

A new DSG4 gene mutation causes hair defects in a young girl.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

A man with a weakened immune system was diagnosed with a rare skin condition called trichodysplasia spinulosa using skin examination techniques.

A protein called sFRP4 can partly inhibit hair growth.

Sulfur-35 can be used to track hair growth and past exposure.

Trichodysplasia spinulosa can occur after a heart transplant due to immunosuppressive drugs.

LEKTI is crucial for skin barrier and immune function, affecting conditions like Netherton syndrome and atopic dermatitis.

Deep Brain Stimulation helps manage Parkinson's symptoms when medication isn't enough.

A man's relapsed leprosy was successfully treated with the antibiotic sparfloxacin.

Identical p53 gene mutations in different cancers suggest the need for careful treatment.

The research identified specific genes that are active in the cells crucial for hair growth.

The care model improved timely diagnosis and treatment for psoriasis and psoriatic arthritis.

Tiger tail banding and hair abnormalities are reliable indicators for diagnosing trichothiodystrophy.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

N1-methylspermidine helps hair growth and reduces inflammation in hair follicles.

Overexpressing SSAT in mice makes them highly sensitive to polyamine analogues, causing liver damage and high mortality.

Spiny keratoderma may be ectopic hair formation on palms and soles.