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Lower levels of certain genes in hair cells improve hair loss treatment outcomes.

New methods efficiently isolate dermal papilla cells from hair follicles, preserving their characteristics better than traditional methods.

COVID-19 infection rates were low in patients with immune diseases, regardless of their treatment type.

A rare benign skin growth called melanocytic matricoma was identified in a 69-year-old man.

Tyrosinase and gp100 proteins can help diagnose and treat melanoma.

A 78-year-old man with Cronkhite-Canada syndrome improved significantly after treatment and remains symptom-free.

Polyamines are crucial for skin tumor development, and inhibiting them can prevent tumors.

A woman with dermatomyositis showed rare skin symptoms, was treated successfully, and her case suggests checking for cancer in similar patients.

Trichoblastic fibroma and basal cell carcinoma are similar but different from trichoepithelioma.

53BP1 focus analysis in hair cells can help estimate radiation doses.

Cutaneous Lymphadenoma is a unique skin tumor with specific protein markers and common gene mutations that may cause continuous cell growth.

The patient with both scarring and non-scarring hair loss showed complex immune reactions and improved with steroid treatment.

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

CD34+ cells from fat tissue help form hair follicles and blood vessels in skin.

Basal cell carcinoma shows keratin patterns similar to hair follicle structures.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

A 60-year-old man with Cronkhite-Canada syndrome improved with treatment, but the condition has a high mortality rate and a risk of colorectal cancer.

Cold Atmospheric Plasma shows promise in treating aggressive breast cancer by targeting cancer cells while sparing normal tissue.

Melanocyte-associated antigens may play a key role in alopecia areata and could be targets for new treatments.

Early diagnosis and treatment with corticosteroids can improve outcomes in Cronkhite–Canada syndrome.

Dysplastic nevi have unique gene expressions, making them distinct from common melanocytic nevi.

Plasmacytoid dendritic cells, which overproduce IFN-α, may play a crucial role in starting alopecia areata, an autoimmune disease causing hair loss.

The oils showed potential to kill certain cancer cells, especially from Dysphania ambrosioides.

A man with kidney tumors and lung cysts was diagnosed with Birt–Hogg–Dubé syndrome and treated successfully, with genetic testing confirming the diagnosis.

The CD4 protein may play a role in the behavior of certain skin cells, affecting their growth, movement, and differentiation.

RCS-01 cell therapy is safe and improves skin gene expression.

Cupric chloride treatment corrected abnormal Purkinje cell development in brindled mice.

CK 19 expression is higher in more severe skin cancers.

Small bowel lesions in Cronkhite-Canada syndrome persist despite steroid treatment.