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

Malondialdehyde-modified DNA may trigger an immune response in alopecia areata patients.

Measuring minimal residual disease on day 15 helps identify high-risk leukemia patients.

Vitamin D receptor mutations can cause alopecia by affecting hair growth genes.

A woman with chronic hepatitis C had a rare skin condition linked to her illness.

Certain CD8+ T cells attack hair follicles in alopecia areata, suggesting they could be targeted for treatment.

Patients with the same vitamin D receptor mutation showed different symptoms due to other factors.

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

The document describes previously unreported unique skin changes in a rare genetic disorder called Hereditary mucoepithelial dysplasia.

TH antibodies in vitiligo and AA patients recognize the same protein parts.

Genetics play a role in acne, but how exactly they contribute is not fully understood.

Lack of certain fatty acids causes skin, immune, and fertility issues in mice.

LHX2, with other markers, can identify hair placodes in rats.

Androgenetic alopecia negatively impacts quality of life, especially for women, due to social reactions.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

Discoid lupus erythematosus involves immune activation and fibrosis around hair follicles, with shared pathways across humans, dogs, and mice, suggesting potential treatments for both humans and animals.

The electronic version of the Dermatology Life Quality Index is as effective as the paper version, with most patients preferring it.

Oral lichen planus is not linked to sex hormone levels.

Genetic marker rs12558842 strongly linked to male hair loss.

DHA-NLC may improve drug delivery and reduce side effects for cancer treatment.

Lack of Vitamin D receptor changes skin structure and increases certain immune cells in the skin.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Swedish men with the E213 A-allele of the androgen receptor have a lower risk of prostate cancer.

A new mutation in the HR gene causes hair loss in a specific family.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

CD117 and platelet-derived growth factor receptor α may play a role in alopecia areata.

Cells that move well may improve hair loss treatments by entering hair follicles.

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