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CYP154C7 enzyme can effectively modify steroids and is promising for commercial use.

A woman's hair loss and scalp swelling, caused by a fungal infection, was wrongly treated but eventually cured with Terbinafine, emphasizing its effectiveness.

A new gene variant in a girl with Coffin-Lowry Syndrome may link the condition to early puberty.

An 8-year-old boy with a scabies infection was successfully treated with permethrin, antihistamines, and antibiotics.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Overexpressing SlCLE10 in tomatoes boosts root hair growth and drought tolerance.

Scalp condition healed with prednisone and tacrolimus.

PCOS is linked to changes in vaginal bacteria, with fewer good bacteria and more harmful ones.

A rare genetic disease caused severe, worsening hair loss from early childhood with poor treatment results.

Gloriosa superba poisoning can mimic severe tropical infections and cause rapid hair loss.

Erosive lichen sclerosus is a distinct subtype with specific skin features, and treatment led to complete resolution in half of the cases.

The saw palmetto extract effectively inhibits an enzyme linked to prostate issues, showing promise for prostate health.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

Lipids from Schizochytrium sp. help prevent hair loss by protecting hair cells from damage and promoting hair growth.

Sheep with chronic Sarcoptes scabiei dermatitis have altered keratin expression in their skin.

Poromas are related to sweat duct cells, and CK patterns help distinguish apocrine poromas from other neoplasms.

Human basal cell carcinomas and squamous cell carcinomas have unique gene expression patterns not fully mirrored in mouse models.

A boy's scalp rash and baldness were cured using oral medication and medicated shampoo.

Trichoscopy is useful for diagnosing and monitoring hair and scalp conditions.

Colorectal cancer cells can adapt without losing their traits or drug sensitivity.

Lack of cystatin M/E causes thin hair and dry skin.

Three different methods were compared for creating Titan cells, a type of fungus cell. The OZ method made the most cells initially, but the number dropped quickly. The EB method also made a lot of cells, but the number also dropped. The AA method made fewer cells, but the number stayed steady. The methods also affected which genes were active in the cells.

Cronkhite-Canada syndrome is a rare condition causing gut polyps, hair loss, skin changes, and nail issues, often with a poor outlook.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Chronic scalp lesions with crusts and pus indicate Erosive Pustular Dermatosis, which is confirmed by biopsy and effectively treated with strong topical steroids.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

The new model helps understand and develop treatments for genetic skin disorders like AEC.

A specific gene mutation causes Olmsted syndrome.

Regular endoscopic checks are crucial for Cronkhite-Canada syndrome patients to catch potential cancers early.

The hair and oil glands react by changing structure when stressed.