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A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

P-SLN nanoparticles effectively deliver podophyllotoxin to the skin.

The method effectively measures spermidine in hair lotions.

Cathepsin L deficiency causes hair and skin issues in mice.

A 15-year-old girl has a skin condition causing blisters on her feet, likely inherited from her family.

LLPS is crucial for RALF signaling, aiding plant growth and stress resilience.

Lactiplantibacillus plantarum lysate from green tea may help treat scalp seborrheic dermatitis.

Three siblings with a rare genetic condition had abnormal sexual development and chose different gender identities, needing surgery and therapy.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

Three genes linked to the development of trichilemmal cysts were found.

A method was found to accurately measure spironolactone and canrenone in blood samples using liquid chromatography-mass spectrometry.

A woman with lupus and severe nerve damage improved with specific treatments.

Costovertebral arthritis can cause chronic back pain in SLE patients and needs thorough evaluation.

Photodynamic therapy successfully treated skin cancer in a 53-year-old woman.

Two specific genes are more active during hair growth in mice.

ECCL should be considered in patients with specific skin and eye lesions.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

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

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

A 12-year-old boy with PAIS successfully developed male characteristics using high-dose testosterone and anastrozole.

A newborn with severe low blood sugar due to a genetic issue needed major surgery after standard treatments failed.

IL-3 worsens lupus nephritis and blocking it improves kidney health.

CD4+ lymphocytopenia can occur in patients with systemic lupus erythematosus.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

GLABRA2 represses root hair formation by inhibiting a specific gene.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

Tay syndrome is a unique genetic disorder causing skin, hair, and developmental issues.

sPLA2-IIE is crucial for normal hair follicle structure and skin health.

OsUEV1B protein is essential for controlling phosphate levels in rice.

Strontium ranelate is no longer available for treatment.