Search

everythingexperts & clinicslearnresearchcommunity

for

Search:↓

Using polymeric micelles to deliver spironolactone topically could improve wound healing in skin affected by glucocorticoids.

ARL15 is important for fat cell development and the release of the hormone adiponectin.

The biofilm enhances skin healing by promoting cell growth and blood vessel formation.

Phospholipase Cδ1 is crucial for normal skin and hair development.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Microfluidic technology improves cell spheroid creation for better drug testing and tissue engineering.

Biotin mega-dose therapy led to dramatic improvement in a newborn with a rare metabolic disorder.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

ABCD1 gene mutations cause adrenomyeloneuropathy, leading to symptoms like limb weakness and spasticity, with management focusing on rehabilitation and spasticity treatment.

A compound from Calophyllum inophyllum L. leaf may help treat non-small cell lung cancer.

Different sPLA2 enzymes have unique roles in phospholipid metabolism and biological processes.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

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

The study created a mouse model to mimic degenerative diseases for testing tissue repair and new therapies.

Solid lipid nanoparticles can improve how well drugs that don't dissolve in water work and are safe.

Chitosan-coated spironolactone nano carriers effectively treat acne without side effects.

Targeting lipid metabolism can help treat advanced, resistant cancers.

Monoclonal antibodies LT-1, LT-2, and LT-7 help diagnose certain blood cancers.

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

New treatments targeting genetic mutations in lung cancer are needed for better outcomes.

A new therapy for a skin blistering condition has not been developed yet.

A baby with maple syrup urine disease improved from skin problems by adjusting his diet to correct amino acid levels.

Lrig1 could be a marker for advanced sebaceous carcinoma.

Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

A girl had rickets due to a gene mutation affecting vitamin D response.

CLK1 is needed for skin cells to become epidermal cells but not sebocytes.

Altering SSAT affects fat metabolism and body fat in mice.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

CT60 polymorphism might increase the risk of Alopecia Areata.