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Trichodysplasia spinulosa is a rare skin disease in immunocompromised patients caused by a specific virus targeting hair follicle cells.

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Woodhouse-Sakati Syndrome can include unique symptoms like liver issues and low growth hormone.

A specific enzyme is essential for proper hair follicle stem cell development and healthy skin.

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TRIV-509 quickly improves skin barrier and cell health in atopic dermatitis.

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

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

New mouse models of Pemphigus show severe symptoms and need better treatments.

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

SFRP2 and PTGDS may be key factors in female hair loss.

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The ZIP7 gene helps control zinc levels in cells by moving zinc from the Golgi apparatus to the cytoplasm.

Marine sponges from Tabuhan Island can inhibit enzymes linked to Alzheimer's and hair loss.

Researchers created human cells that can turn into sebocytes, which may help study and treat skin conditions like acne.

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

The study found that tight junctions reach the top layer of the skin's stratum granulosum, not just the second top layer as previously thought.

Trimethoprim-sulfamethoxazole can cause aseptic meningitis.

Mutations in the ST14 gene cause skin and hair issues by disrupting important protein processing.

Scientists created a 3D skin model to study a chronic skin disease and test treatments.

The research suggests that SFRP2 and PTGDS proteins might be indicators of female pattern hair loss and could contribute to hair loss.

K6hf is a unique protein found only in a specific layer of hair follicles.

A rabbit gene important for hair development was identified and detailed.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

Beta-trace protein may help diagnose and predict treatment response in certain nerve disorders.

Tph cells are linked to the severity of systemic lupus erythematosus.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive stomach cancer.