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

HLD10 can include increased body hair and Mongolian spots.

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

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

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

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

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

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

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

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

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

A specific gene mutation causes congenital hair loss.

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.

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

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

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.

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

The hr gene is linked to hair loss in Valle del Belice sheep.

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

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

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

Two new gene mutations cause a rare hair disorder.

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

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

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

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.