Search

everythinglearnresearchcommunity

for

Search:↓

Viral reactivation is rare at the time of DRESS diagnosis in the U.S.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

Timely and aggressive treatment is crucial for improving outcomes in severe complications of adult-onset Still's disease.

RCS-01 cell therapy is safe and improves skin gene expression.

A missing mK6irs1 gene causes hair loss in mice.

Surgery may help infants with sagittal craniosynostosis develop more typical language processing.

Children under 18 had milder SARS with no deaths, but teenagers faced higher severe illness risk, and effective treatments were uncertain.

Self-amplifying RNA could be a better option for protein replacement therapy with lower doses and lasting effects, but delivering it into cells is still challenging.

A deep learning model was developed to help diagnose trichothiodystrophy by analyzing hair patterns.

Aging in one type of stem cell can cause aging-like changes in various organs.

The project created a standardized system for classifying skin lesions in lab rats and mice.

Lack of sleep in mice leads to prostatitis by reducing certain hormones and activating an inflammatory pathway, which can be temporarily fixed with normal sleep.

These methods help understand cell structures and reactions.

5α-reductase affects dopamine receptors linked to sensorimotor gating, which may help understand disorders like schizophrenia.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

A 6-year-old girl had a rare allergic reaction to a hair regrowth treatment.

RORs may influence cashmere growth cycles.

Clq deficiency is linked to systemic lupus erythematosus symptoms.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

PDRN is effective and safe for healing wounds and skin issues.

SQSTM1 is linked to increased risk of alopecia areata.

Scientists made a sensor that can detect a specific type of RNA related to androgen receptors quickly and accurately.

Most skin conditions in Down syndrome are benign and involve dry or thickened skin.

Combining red LED therapy with beta-carotene is more effective for treating photoaging than red LED therapy alone.

Rituximab leads to longer remission and fewer side effects than cyclophosphamide.

Early diagnosis and multidisciplinary care are crucial for improving the quality of life in patients with ectodermal dysplasia.

A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.