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Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Vitamin D receptor gene variations are not linked to alopecia areata.

NKG2D gene polymorphism doesn't affect SLE risk but may influence symptoms like rash and hair loss.

Hydroxychloroquine may cause false results in tuberculosis tests for patients with autoimmune skin diseases.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Blocking certain pathways with kinase inhibitors may help treat cutaneous lupus erythematosus.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

These specific gene polymorphisms are not linked to Alopecia Areata in Egyptians.

ULBP3 could be a marker for diagnosing alopecia areata incognita and may be linked to its cause and development.

Tph cells are linked to the severity of systemic lupus erythematosus.

ARQ-234, a protein designed to treat atopic dermatitis, shows increased effectiveness in early testing.

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

A gene deletion in DSG4 causes sparse hair in some Pakistani families.

Dlx3 is essential for hair growth and regeneration.

The 2012 criteria are better for diagnosing atypical lupus cases.

Higher activity in lichen planopilaris is linked to certain immune and tissue genes.

Certain KIR genes in Indian SLE patients are linked to disease severity and could be biomarkers.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

Sex and race affect immune responses and treatment outcomes in Hidradenitis suppurativa.

Low quality of life and high HSS-29 scores increase risk of losing patients during treatment.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

High levels of 3 alpha-diol glucuronide in the blood are a marker of increased androgen action in women with excessive hair growth of unknown cause.

Mutations in the DSG4 gene cause specific hair and scalp issues.

Hirsutism significantly lowers the quality of life for Turkish women.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.