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The research found a way to identify and study skin cells with stem cell traits, revealing they behave differently in culture and questioning current stemness assessment methods.

A new genetic variant of Woodhouse-Sakati syndrome was found in two adult sisters in Russia.

Cyclosporine may cause hair loss, so patients need monitoring.

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Intralesional steroid injections can effectively treat calcinosis and ulcers in scleroderma.

SCD1 is crucial for skin health and overall energy balance.

Cathepsin L is essential for heart health and its absence causes heart problems and hair loss.

A U.S. Naval fighter pilot suffered permanent vision loss in one eye due to recurrent central serous retinopathy.

The tool iCOUNT helps understand how stem cells divide and affect tissue development and repair.

Reducing SOX2 in colorectal cancer cells decreases tumor growth and self-renewal.

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

PKC ε increases hair follicle stem cell turnover and may raise skin cancer risk.

A 31-year-old woman was diagnosed with Complete Androgen Insensitivity Syndrome much later than usual, leading to a call for earlier detection and treatment guidelines.

Activating Sonic Hedgehog signaling in cancer stroma may help treat basal cell carcinoma.

Researchers found a specific T cell receptor linked to severe drug reactions like Stevens-Johnson syndrome when patients take carbamazepine.

Syndecan-1 is essential for maintaining skin fat and preventing cold stress.

The folate-cyclodextrin conjugate targets cancer cells more precisely, potentially reducing chemotherapy side effects.

The CLASI is useful but needs revision to accurately assess all cutaneous lupus erythematosus subtypes.

Cellulose nanocrystals are promising for making effective, sustainable sensors for various uses.

The journal emphasizes the importance of combining basic and clinical science to improve health.

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

848 genes related to fat and metabolism are less active in people with Central Centrifugal Cicatricial Alopecia.

NISCH syndrome is a rare genetic disorder affecting skin and liver, with variable symptoms and limited treatment options.

Blocking CXXC5 speeds up diabetic wound healing by improving blood vessel growth and skin repair.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Mice with extra PKCδ resist chemical-induced skin cancer but not UV-induced.