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Telocytes in the scalp may help with skin regeneration and maintenance.

Scientists made a mouse model of a serious skin cancer by changing skin cells with a virus and a specific gene, which is similar to the disease in humans.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

Steroid treatment greatly improved the symptoms of a boy with a rare disorder called Satoyoshi syndrome.

Understanding how Regulatory T Cells work could help create treatments for certain skin diseases and cancers.

MITF+ melanoma patients are more likely to have multiple melanomas and unique skin patterns.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

Soft-tissue calcification is rare in systemic lupus erythematosus.

SCUBE3 is a potential target for cancer and alopecia treatment but is challenging to target due to its varied roles.

Trichogerminoma is a rare, benign skin tumor from hair cells, with a small risk of becoming cancerous.

Clouston syndrome causes issues with teeth, hair, nails, and skin, and has no cure, but recognition has improved.

Msx2-deficient mice experience irregular hair growth and loss due to disrupted hair cycle phases.

Tinea faciale can be mistaken for lupus due to similar symptoms.

TB lymphadenitis can occur in people with weakened immune systems, like those with SLE.

Cronkhite-Canada syndrome may be more treatable and less severe than previously thought.

Tislelizumab can cause cutaneous lupus erythematosus.

A 14-year-old girl with a condition that makes her hair easy to pull out also has a hair-pulling disorder, and treatment helped but she relapsed after a year.

Early detection and biotin treatment improve outcomes for biotinidase deficiency.

A 13-year-old boy had a rare, stable type of hair loss with little chance of regrowth, but treatment is available for looks.

The system allows precise control of gene expression in mouse skin, useful for studying skin biology.

A 16-year-old boy with lupus had a rare brain artery issue but fully recovered with treatment.

PTCH gene mutations contribute to basal cell carcinoma development.

A 5-year-old girl with a rare genetic disorder, lipoid proteinosis, showed reduced new lesions but persistent scars after avoiding skin trauma.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

Generalized trichoepitheliomas with hair loss may indicate myasthenia gravis.

Lack of KSR1 stops certain skin tumors in mice.

Cancer cells often have more copies of TERT and TERC genes, which helps them grow and could affect patient outcomes.

Reduced TRPS1 leads to increased STAT3 and SOX9 in hair follicles, affecting hair growth.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.