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

A specific gene variant may increase the risk of developing Alopecia Areata.

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

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

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.

Monoclonal antibodies LT-1, LT-2, and LT-7 help diagnose certain blood cancers.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

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

A girl had rickets due to a gene mutation affecting vitamin D response.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

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

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

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

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

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

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

RANKL improves the immune response against herpes simplex virus by enhancing T cell activation and could help develop better treatments or vaccines.

Crash dieting can cause hair loss due to severe calorie restriction.

The mtDNA N haplogroup is linked to a higher risk of late-onset lupus and specific symptoms in Han Chinese women.

High LGR5 levels in glioblastoma indicate poor prognosis and are essential for cancer stem cell survival.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

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

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

A vitamin D receptor mutation causes rickets and affects immune responses.

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

A truncated protein linked to breast cancer may change cell adhesion.