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A patient with "strawberry gingivitis" improved after correct treatment for Granulomatosis with polyangiitis, highlighting the need for early diagnosis.

The research found that a protein called PPARg is important for the formation and healing of sebaceous glands, which can regenerate independently from hair follicles.

A special gel with medicine helps prevent melanoma from coming back after surgery.

Late dumping syndrome after fundoplication can be diagnosed with an oral glucose tolerance test and managed with diet changes.

The TGM3 gene's promoter region is key for skin and hair cell function and may aid gene therapy.

The hydrogel dressings speed up healing and reduce scarring.

The new chemotherapy combination for advanced lung cancer showed a 35.7% response rate but caused significant side effects.

Growth hormone therapy can improve growth in Netherton syndrome patients with growth hormone deficiency.

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

A 2-year-old girl with a rare vitamin D disorder had rickets and hair loss, but treatment was ineffective due to poor compliance.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

Removing Dicer from pigment cells in newborn mice causes early hair graying and changes in cell migration molecules.

PDGFA helps activate hair growth in cashmere goats.

A 17-year-old girl with Kartagener's syndrome also has unusual skin, hair, and nail issues.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

Inhibiting ODC can prevent UV-induced skin cancer.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

Hair root analysis can effectively detect somatic mosaicism in double cortex syndrome.

Skin issues from chronic graft-versus-host disease greatly affect daily life, needing teamwork between blood and skin doctors.

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

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

Hair dye may trigger anti-GBM disease relapse, and rituximab can help manage it.

Different human hair follicle stem cells grow at different rates and respond differently to a baldness-related compound.

Microsponges delivery system is a safe, versatile method for controlled drug release in various treatments.

BST2 protein and certain T cells increase in early alopecia areata.

New inhibitors may reduce gut toxicity from cancer drugs.

People with Down's syndrome are more likely to have syringomas.

Four new FGF5 gene variants cause long hair in dogs.