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HTLV-1-associated lichenoid dermatitis (HALD) is linked to an immune response against HTLV-1-infected cells.

Lysophospholipids like LPA and S1P are important for hair growth, immune responses, and vascular development, and could be targeted for treating diseases.

PCOS is a complex condition that affects women's hormonal balance and metabolism, requiring lifestyle changes and medical management.

Sphingosine 1-phosphate affects inflammation and gene expression in different aorta cells.

HLD10 can include increased body hair and Mongolian spots.

Cutaneous lupus patients have higher levels of certain immune cells in their blood and skin.

The SNP rs6457452 is linked to a higher risk of alopecia areata in Koreans.

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

A specific gene mutation causes sparse, brittle hair in a family.

A mycobacterial protein shares a similar region with a human skin protein, possibly affecting skin diseases.

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

Dermal IgA deposition without symptoms is rare in Dermatitis herpetiformis risk groups.

HKN-2 antibody targets specific skin and hair cells, showing keratin complexity.

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

Donor lymphocyte infusions effectively treated leukemia relapse but caused vitiligo and alopecia areata.

The gene LRRC15 is more active in balding areas of the scalp compared to non-balding areas.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

Human placenta extract reduces inflammation and symptoms in atopic dermatitis.

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

Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

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

The 2012 criteria are better for diagnosing atypical lupus cases.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

Autoimmune reactions may cause both alopecia areata and HAM.

Plucked hair follicles can help diagnose scalp lupus.

A new DSG4 gene mutation causes hair defects in a young girl.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

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.