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

A two-step method was created in 2015 to make more cells that help with hair growth, but they need to be combined with other cells for 4 days to actually form new hair.

RANKL causes lymph nodes to grow by making certain cells multiply.

Loss of a specific protein in skin cells causes symptoms similar to psoriasis.

STAT3 signaling is important for healthy skin and hair follicles, and its disruption can lead to skin conditions like atopic dermatitis.

Th22 cells are essential for Tβ15-induced hair growth in mice.

mEphA1 receptor tyrosine kinase is important for skin and hair development and may play a role in certain diseases.

The local environment is crucial for cell development in the tongue.

Fibroblast growth factors are crucial for hair follicle development and regeneration.

B2m-free HLA variants may be a new class of HLA important in immune responses and diseases.

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

AIRE-deficient rats developed severe autoimmune disease similar to APECED, useful for testing treatments.

Targeting immune tolerance issues in Alopecia Areata could restore hair growth and maintain remission.

Human scalp hair follicles can be used to study how prolactin affects hair growth and cell death.

Researchers created specific antibodies that detect a protein important in development and various conditions, and can be used for research and diagnosis.

A rare case showed hair regrowth after chemotherapy for thymoma, suggesting a link between alopecia areata and thymoma.

A cat had a rare skin disorder with hair loss and scaling, linked to a suspected tumor.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

New protein changes may be involved in the immune attack on hair follicles in alopecia areata.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

Ruxolitinib significantly improves multiple autoimmune conditions in APS-1 patients.

Thymoma in cats can cause hair loss without inflammation.

FOXN1 is crucial for thymus development and immune response in Xenopus laevis.

Fox genes are important for hair growth and development in cashmere goats.

Mutations in the FOXN1 gene cause severe immune issues but don't affect hair and nails.

AIRE deficiency causes hair loss similar to alopecia areata in mice.

Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.