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The research created a detailed map of skin cells, showing that certain cells in basal cell carcinoma may come from hair follicles and could help the cancer grow.

Lymphangiosarcoma was confirmed in cats with specific skin symptoms using a lymphatic marker.

A JAK1 variant causes hair loss, skin issues, and thyroid disease, but treatment with a specific inhibitor can help.

The study developed a mouse model for Alopecia Areata that responds to treatment, useful for future research.

Sacituzumab tirumotecan shows promise in treating breast cancer with manageable side effects.

Proinflammatory fibroblasts and vascular endothelial cells are key in keloid development.

Innate immunity genes in hair follicle stem cells might have new roles beyond traditional immune functions.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Genetic testing is crucial for diagnosing and treating acrodermatitis enteropathica effectively.

Activating Notch signaling can kill basal cell carcinoma cells.

Melanocyte stem cells are crucial for skin pigmentation and have potential in disease modeling and regenerative medicine.

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

Higher CRHR1 levels in AA patients lead to increased inflammation.

HT-scCAT-seq helps understand gene regulation in embryonic skin development.

Keratinocytes can reverse the effects of the GNAQ oncogene, inhibiting melanoma cell growth.

A combination of ixekizumab and tofacitinib successfully treated severe scalp cellulitis, leading to hair regrowth.

A 65-year-old man developed a serious skin cancer linked to a drug he was taking for a fungal infection after a bone marrow transplant.

Hair protects the scalp from skin cancer by aiding immune defense.

Keratin 14 may be an autoantigen in autoimmune skin diseases.

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

A woman with unexplained hair loss was found to have harmless skin tumors and a scarring hair loss condition, but the tumors didn't cause the hair loss.

Clonally expanded CD8+ T cells cause alopecia areata.

BKN-1 antibody targets specific keratin in basal cell epithelioma and normal skin basal cells.

FOXN1 mutations can cause varying immune and physical issues, with severity influenced by gene activity and possibly other factors.

Researchers improved a method to study individual cells in newborn mouse skin and found a way to assess the severity of a skin condition in humans.

LL-37 helps stem cells grow and move, aiding tissue regeneration and hair growth.

Certain mutations in the PADI3 gene may increase the risk of developing a type of scarring hair loss common in women of African descent.

Certain CD8+ T cells attack hair follicles in alopecia areata, suggesting they could be targeted for treatment.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.