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AIRE protein, defective in APECED patients, is found in skin and hair cells and interacts with cytokeratin 17.

Removing MCPIP1 from myeloid cells in mice leads to hair loss and prevents skin tumors but causes pigmented spots.

Alopecia areata's causes are unclear, treatments exist but relapses are common.

Activating TERT in mice skin boosts hair growth by waking up hair follicle stem cells.

Tofacitinib is an effective and safe treatment for alopecia areata.

A new gene mutation causes insulin resistance in a girl and her mother.

A woman with undifferentiated connective tissue disease was diagnosed with renal amyloidosis and carpal tunnel syndrome.

Alopecia areata is the most common type of baldness treated with corticosteroids and minoxidil.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

DHT increases scalp heat, causing hair loss.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

Contact immunotherapy can change immune responses in alopecia areata, suggesting new treatment targets.

A rare EGFR mutation in newborns leads to severe health issues and early death.

Terminalia bellirica extracts effectively promote hair regrowth and treat androgenetic alopecia.

A certain signaling pathway in mice, when increased, causes hair to gray by depleting the cells that give hair its color.

Mutations in the PADI3 gene may cause central centrifugal cicatricial alopecia in women of African ancestry.

Non-motor symptoms in myasthenia gravis are common and need early diagnosis for better management.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

JAK inhibitors may help treat alopecia areata and promote hair regrowth.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

JAK inhibitors helped treat hair loss in two people with Down syndrome.

EGFR helps mouse hair follicles stop growing by reducing certain growth regulators.

Eating vitamin A affects hair growth and health by changing cell signals in mice.

Cantú syndrome may be linked to pituitary adenomas.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Lymphocytes, especially CD8+ T cells, play a key role in causing alopecia areata, and targeting them may lead to new treatments.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

Erlotinib can cause hair loss and texture changes.