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Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

The specific skin disease variant p.(Arg2000Trp) in plectin can cause a wide range of symptoms, which should be considered when diagnosing patients.

PSENEN gene mutations can cause both Dowling-Degos disease and acne inversa.

The hydrogel helps heal diabetic wounds faster by reducing inflammation.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

A specific enzyme is essential for proper hair follicle stem cell development and healthy skin.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

Ceramide Synthase 4 is essential for normal hair growth and preventing hair loss.

Deleting a specific protein in skin cells disrupts normal hair growth and development.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Meis2 is essential for touch sensation and proper nerve connection to touch receptors in certain skin areas of mice.

Type IV collagen chains vary in different parts of human skin, with specific patterns linked to melanocytes.

Delta1 is crucial for controlling skin cell growth and preventing tumors in mice.

A unique skin cell similar to hair bulb melanocytes was identified, with better preservation using permanganate fixation.

Par3–mInsc and Gαi3 work together to ensure proper cell division orientation in skin development.

Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

Lack of a key enzyme causes severe skin issues and death in mice.

N,N-Dimethylglycine Sodium Salt helps reduce skin inflammation and improves skin cell growth and healing.

TGM3 is important for skin and hair structure and may help diagnose cancer.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

Two new enzymes, PAD-R11 and PAD-R4, were cloned and showed activity, with PAD-R11 resembling epidermal enzymes.

Ceramide synthase 4 deficiency in mice leads to hair loss due to altered sebum lipids.

Vitamin D receptor is important for regulating hair growth and wound healing in mice.

Laminin-511 is essential for proper melanocyte movement and development in mice.