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New gene mutations linked to skin conditions were found, bacteria and chemicals may worsen acne, a dog mutation could exist in humans, virus-like elements might be involved in psoriasis, and a vitamin D3 treatment doesn't prevent chemotherapy-related hair loss.

Genetic mutations that disrupt homocysteine breakdown lead to increased damage in mouse hair keratin.

A specific gene mutation causes a severe skin disorder in a family.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

A specific gene mutation in Japanese people can cause varying degrees of hair thinning in adulthood.

A specific gene mutation causes different hair defects in Indian monilethrix families.

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

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

A specific gene mutation causes long hair in Angora rabbits.

Melanocyte pathology requires keratinocyte hyperplasia and regulation dysfunction.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

The PML protein helps prevent skin cancer in mice.

A mutation in the MAP2 gene causes reduced hair follicle density, leading to hairlessness.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

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

A gene mutation in mice causes permanent hair loss and skin issues.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

A Gsdma3 mutation causes hair loss due to stem cell damage from skin inflammation.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

A new genetic mutation in mice causes permanent hair loss and skin wrinkling.

Sun exposure and genetics increase skin cancer risk from precancerous lesions.

Mutations in the p63 gene affect skin adhesion, barrier integrity, and hair growth.

Inactivating both p53 and Rb genes in mice speeds up aggressive skin cancer development.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

5% topical minoxidil improves hair density and quality in monilethrix patients.

CARASIL can cause different symptoms even with the same genetic mutation.

Defective mitochondrial DNA replication causes aging symptoms and increased oxidative damage in mice.