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A man got six skin cancers within a year after a cell transplant for leukemia but was cancer-free 32 months later; skin checks are important post-transplant.

Alopecia areata patients have higher levels of certain immune receptors, suggesting new treatment possibilities.

BioPlex-11 improves DNA profiling from telogen hair roots in forensic work.

A rare genetic mutation causes Woodhouse-Sakati syndrome symptoms.

The risk of skin tumors becoming malignant depends on the specific skin cell type affected.

Thymic LCH may be underdiagnosed, so thymic ultrasound should be considered in infants with cutaneous LCH.

Patients with RASopathies are at risk for autoimmune disorders and should be routinely screened.

Targeting the TNFRSF1B gene may help treat hair loss.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

The research developed methods to test drugs that could protect and restore hair follicle protection in a hair loss condition.

People with late-stage HIV-1 often experience a specific type of hair loss linked to multiple factors, including nutritional issues and immune responses.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

Certain VDR gene changes can affect melanoma risk.

LHX2, with other markers, can identify hair placodes in rats.

New hair regrowth model introduced, imiquimod kills skin cancer cells, T-cadherin loss makes skin cancer more invasive, no strong link between PTCH1 gene and skin cancer after transplant, and male teens more likely to have hereditary hair loss.

A gene mutation causes a rare hereditary hair loss, offering potential for new treatments.

ILC1-like cells can cause alopecia areata by disrupting hair follicle immunity, suggesting a new treatment approach.

Targeting TCR-Vβ2 in cutaneous T cell lymphoma shows promise for safer, more specific treatment.

Shorter GGC triplet repeats in the androgen receptor gene are linked to less hair loss in Han men.

VDC-1101 shows potential as a treatment for canine cutaneous T-cell lymphoma.

Ruxolitinib helped a woman with a genetic mutation regrow her hair and improved her health.

The study suggests that analyzing DNA can help treat hair loss, but more research is needed.

Alopecia can be caused by multicentric reticulohistiocytosis.

CD271 is crucial for maintaining healthy skin and preventing inflammation.

HSP90 and lamin A/C are crucial for hair growth and could be targets for treating hair loss.

Lack of KSR1 stops certain skin tumors in mice.

VDDR I and II are genetic disorders affecting vitamin D use, causing rickets, with VDDR I treatable by vitamin D supplements and VDDR II needing high doses and calcium.