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UV radiation may cause DNA changes in skin, certain UVB therapy helps psoriasis, a new gene mutation is linked to mild piebaldism, different immune cells affect psoriasis, a drug promotes hair growth, and some cancer drugs could treat skin barrier issues.

The polyG fragment in Hoxc13 protein helps evolve mammalian skin and hair by enhancing gene interactions.

Lack of KSR1 stops certain skin tumors in mice.

Seven new genetic risk areas for prostate cancer were found.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

The ZIP13 variant is linked to abnormal hair quality.

Trichothiodystrophy is a rare genetic disorder causing hair issues and sometimes linked to DNA repair defects.

The hairy ear mutation in mice is linked to changes in gene expression affecting hair growth.

The naked mutation in mice causes hair loss and helps identify keratin genes.

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

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

SQSTM1 is linked to increased risk of alopecia areata.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

Prenatal genetic diagnosis may not predict MELAS syndrome severity in offspring.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Ribonucleotide excision repair is crucial to prevent skin cancer.

A patient with Werner syndrome showed a range of aging-like symptoms and metabolic issues, underscoring the need for early detection and treatment.

DPR can cause skin, hair, and nail issues, sometimes appearing later in life.

FOXN1 mutations can cause varying immune and physical issues, with severity influenced by gene activity and possibly other factors.

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

The mouse model showed defects in adult stem cell maintenance related to Hutchinson-Gilford progeria syndrome.

Some prostate cancers have gene changes that may affect treatment with certain drugs.

Progerin affects cell shape but not hair or skin in mice.

Pregnancies in a woman with the Donohue mutation were managed with genetic testing, resulting in three healthy infants.

A mutation in the human hairless gene causes alopecia universalis.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Deleting TNFα gene reduces skin cancer risk in certain mice.