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The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

Alopecia areata involves specific immune cells, offering potential treatment targets.

NKG2D+CD4+ T cells are higher in alopecia areata patients and may be involved in the disease.

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

Skin cells and certain hair follicle areas produce hemoglobin, which may help protect against oxidative stress like UV damage.

IL16 gene variations may affect the risk of alopecia areata in Koreans.

LRIG1 is linked to better survival in Merkel cell carcinoma.

Human hair is made up of different keratins, some strong and some weak, with specific types appearing at various stages of hair growth.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Different γδ T cell types have unique roles in causing alopecia areata.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

TCHHL1 is a protein important for hair growth, found in hair follicles.

The study suggests that a specific type of immune cell, memory-like NK cells, may increase during active hair loss in Alopecia areata.

Overexpressing Merkel cell virus proteins in human hair follicles can create clusters of cells that resemble Merkel cell cancer.

Melanocytes may trigger the immune response in alopecia areata, affecting hair regrowth.

Scarring alopecia involves increased immune cells and specific gene changes near damaged hair follicles.

Restoring hair follicle immune privilege may help treat alopecia areata.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

Increased Toll-like receptors in blood cells may contribute to alopecia areata and could be a target for new treatments.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

A woman with chronic hepatitis C had a rare skin condition linked to her illness.

Hemoglobin α acts as an antioxidant in skin cells, especially protecting hair follicle stem cells from UV damage.

Cell adhesion molecules are important in the development of certain skin diseases.

Alopecia areata is linked to reduced T cell function and auto-immunity.

Relapsing hepatitis A can cause prolonged abnormal liver tests even without symptoms.

A unique gene mutation was found in a family with monilethrix.

Arg1+ macrophages may play a role in Alopecia Areata, offering new treatment targets.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.