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A scale was made to measure hair loss severity in African American women.

Targeting the Smoothened receptor shows promise for treating certain cancers.

Ustekinumab treatment may reveal a genetic tendency for steatocystoma multiplex in psoriasis patients.

CYLD deficiency in skin tumors disrupts hair follicle cell processes and protein secretion.

The International Society of Hair Restoration Surgery created a standard curriculum in 2008 to guide doctors in diagnosing and treating hair loss effectively.

Sulfur-based treatments combined with simparica effectively treat scabies in puppies.

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.

Ceramide Synthase 4 is crucial for maintaining hair follicle stem cells and preventing hair loss.

Using a collagen sponge scaffold helps stem cells become more like skin cells.

Cutaneous angiosarcomas require a combined treatment approach, but prognosis is generally poor.

SHISA6 helps maintain certain stem cells in mouse testes by blocking signals that would otherwise cause them to differentiate.

The scraggly mutation causes hair loss and skin defects in mice.

Disrupting the Tsc2 gene in certain cells leads to thicker skin, larger hair, and changes in hair growth signaling, which can be partly reversed with specific treatment.

Early shedding of the inner root sheath in noninflamed hair follicles is a relatively specific sign of Central Centrifugal Cicatricial Alopecia.

T cell subsets are crucial in kidney cancer, and a new model predicts patient outcomes using key genes.

Stereotactic body radiation therapy and radiosurgery are advanced, precise treatments that target tumors while protecting healthy tissue.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

A neck lesion misdiagnosed as benign was later treated successfully with Mohs Micrographic Surgery.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

A woman was diagnosed with a rare adrenal gland cancer that did not show usual hormone-related symptoms.

Melanocyte stem cells hold promise for skin regeneration and treating pigmentation issues.

A novel CLDN1 mutation in a 2-month-old with NISCH showed improvement with symptom management.

External factors can cause skin cancer cells that usually don't spread to grow and form tumors in mice.

A rare lupus case on the chin was successfully treated with steroids and immunomodulators after accurate diagnosis using advanced imaging techniques.

Raman spectroscopy could effectively guide skin cancer surgery by identifying tumor margins.

Skin stem cells can help treat many skin diseases without invasive procedures.

A rare type of skin cancer on the scalp can be mistaken for hair loss, causing delayed diagnosis and severe damage.

Combining Western chemotherapy with Traditional Chinese Medicine can reduce side effects and improve immune response in treating bone and soft tissue tumors.