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ASLAN004 was safe and well-tolerated, supporting further development for treating certain diseases.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Squaric acid dibutylester for alopecia areata can cause benign skin lymphoid growths.

Different types of skin gland tumors have unique genetic traits, which can guide personalized treatments.

The report shows a young man with Hutchinson-Gilford Progeria Syndrome had typical and additional eye problems related to the disease.

DMBT1 and galectin-3 may help suppress epithelial skin cancer.

These migraine prevention drugs can cause side effects like constipation, hair loss, injection site reactions, fatigue, and sometimes unexpected issues like Raynaud's phenomenon and weight gain.

Malondialdehyde-modified DNA may trigger an immune response in alopecia areata patients.

A 12-year-old girl was misdiagnosed with alopecia areata but actually had a nevus sebaceus with a genetic mutation.

Researchers created a new mouse model, G4, that mimics human PCOS symptoms and links the condition to a specific gene.

The study showed that a specific DNA sequence can control gene expression in hair growth areas of mice.

Cell membrane-coated nanoparticles could improve gene therapy by enhancing delivery and targeting of nucleic acids.

GRF is not safe for tubal occlusion.

Azelaic acid in a special gel is more effective against skin fungi than regular azelaic acid.

Personalized sonidegib dosing can effectively treat Gorlin-Goltz syndrome with fewer side effects.

Sugars from Sargassum and brown algae may have health benefits like fighting viruses and helping with wound healing, but there are challenges in using them.

Sheep hair follicle transglutaminases are calcium-dependent.

Topical patidegib gel effectively treats basal cell carcinoma in Gorlin syndrome patients without causing the side effects seen with oral treatments.

The infant with a urea cycle disorder improved with treatment and a liver transplant.

L-PGDS has specific binding sites for its functions and could help in drug delivery system design.

Early diagnosis and treatment with corticosteroids can improve outcomes in Cronkhite–Canada syndrome.

A baby girl had two brain-related growths removed and is developing normally.

Three dogs with a rare skin condition improved with treatment.

Elderly patients with eruptive skin bumps may have clear cell syringoma linked to glucose issues.

The N-K GM Series offers highly selective, eco-friendly medicines targeting harmful microbes, free for personal use.

A 44-year-old woman with Down's syndrome was diagnosed with both rheumatoid and gouty arthritis and treated with multiple medications.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

Treatment with moisturizers improved the skin condition of a girl with a rare genetic skin disorder.

GLABRA2 represses root hair formation by inhibiting a specific gene.

Lysocellin helps stop cell damage from etoposide and may prevent hair loss.