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Beta-trace protein may help diagnose and predict treatment response in certain nerve disorders.

The enzyme steroid sulfatase is linked to breast cancer and other conditions, and inhibitors are being developed for treatment.

MCP@G improves diabetic wound healing by reducing stress and promoting tissue repair.

Ku80 is a key receptor for Thymosin β4, affecting cell migration and wound healing.

LPR1 regulates root growth under low phosphate stress independently of SIZ1 in Arabidopsis thaliana.

Longer treatment with vismodegib lowers relapse risk in basal cell carcinoma.

The specific skin disease variant p.(Arg2000Trp) in plectin can cause a wide range of symptoms, which should be considered when diagnosing patients.

CAP1/Prss8 does not activate PAR2 or inhibit PN-1.

New mutations in the DSG4 gene cause a rare hair condition.

TMPRSS2 affects COVID-19 severity and treatment options.

In Singapore, most skin reactions to drugs were in females and Chinese, often caused by painkillers, antibiotics, and some other drugs, with serious cases linked to genetics.

Profilin1 speeds up wound healing.

A specific enzyme that activates the hair growth medication minoxidil when applied to the skin was identified.

Dapagliflozin helps protect heart cells under stress by improving mitochondrial function and reducing cell damage.

Inhibitors of 11β-HSD1 show potential for treating type 2 diabetes but require more testing for safety and effectiveness.

Researchers created specific antibodies that detect a protein important in development and various conditions, and can be used for research and diagnosis.

Researchers developed a cost-effective 66 K SNP chip for cashmere goats that is accurate and useful for genetic studies.

Adalimumab significantly improved symptoms and quality of life in two patients with Hidradenitis Suppurativa.

BIVV009 is a safe treatment for bullous pemphigoid that reduces C3 deposition without harmful side effects.

Loss of OGG1 increases skin inflammation and auto-antibodies in lupus.

MIS-A is a severe complication after COVID-19, mostly in young black males, needing more research and awareness.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

The S9 fraction with GC-IDMS is effective for measuring 5α-reductase activity.

Box A of HMGB1 can improve stem cell function, aiding anti-aging therapy.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Hidradenitis suppurativa may be more severe in people with Mediterranean fever gene mutations.

Suplatast tosilate successfully treated a woman's systemic sclerosis symptoms.

Increased HSD11B1 enzyme expression is linked to higher body fat and insulin resistance.