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Doxycycline or flucloxacillin can cause a rare, severe skin reaction that can be fatal, especially in the elderly.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

Solid lipid nanoparticles are promising for safe and effective drug delivery but need more research for clinical use.

A 532 nm laser at 15 J/cm2 speeds up tendon healing by increasing tendon stem cell growth and tendon-related gene activity.

Cystatin M/E strongly inhibits cathepsin V and cathepsin L, important for skin formation.

Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.

New technologies replicate human skin for testing without animals.

The method creates skin organoids with hair follicles for research on skin conditions and treatments.

Levetiracetam often causes behavioral issues, while oxcarbazepine is more likely to cause sleepiness in epilepsy patients.

LEF1 is essential for the development of airway glands and is regulated by the Wnt/ß-catenin pathway.

A PIK3CA mutation in Schwann cells causes severe nerve damage and increased glycolysis, but early treatment can help.

SH-SY5Y cell lysate is effective for diagnosing Satoyoshi syndrome.

A new engineered treatment shows promise in curing heart fibrosis.

Timely diagnosis and aggressive treatment with high-dose steroids and B-cell depletion therapies are effective for severe acute cutaneous lupus.

The PCL/PHB blend allows for slower, more controlled curcumin release than individual polymers.

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

S1PR1 helps control inflammation in blood vessel cells by affecting gene activity differently in various cell types and locations.

High-throughput LC-MS screening is effective for finding new autotaxin inhibitors for asthma treatment.

Trans-esophageal echocardiography is crucial for accurately diagnosing heart issues in lupus patients.

The system aims to extend human lifespan to 130-150 years by improving cellular health and reducing stress.

The system aims to extend human lifespan to 130-150 years by improving cellular health and reducing stress.

Increased liposome fluidity boosts skin penetration of sodium fluorescein.

A woman with X-linked chronic granulomatous disease developed lupus-like skin lesions, improved with treatment, suggesting a unique skin condition in carriers.

BLTP1 and KIF27 gene mutations can help breed better wool sheep.

Susan Lee Lindquist was a pioneering biologist who made significant contributions to understanding protein folding and its role in disease.