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The ID2 gene can help distinguish between sensitizers and irritants in skin cells.

Mutations in the KLHL24 gene cause skin blistering in epidermolysis bullosa simplex.

Akt2 protein is essential for normal cell division in early mouse embryos.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

RAR-gamma 1 is important for normal skin maintenance and differentiation.

AKR1D1 controls glucocorticoid levels and receptor activity in liver cells.

K6hf is a unique protein found only in a specific layer of hair follicles.

Fibroblasts from healthy donors can prevent changes seen in recessive epidermolysis bullosa simplex.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

Pmg-1 and Pmg-2 are new genes important for skin and mammary gland development.

KLHL24-mutant stem cells help understand skin and heart disease.

KGF-1 135 is a stable and effective alternative for treating oral mucositis.

A KLK5 inhibitor effectively improved skin symptoms in a mouse model of Netherton Syndrome.

LRIG1 is linked to better survival in Merkel cell carcinoma.

Trichoblastic fibroma and basal cell carcinoma are similar but different from trichoepithelioma.

SP1 promotes and KROX20 inhibits hair cell growth by affecting the CUX1 gene.

Signals from skin cells controlled by Rac proteins help turn certain precursor cells into white fat cells.

Mrp3 may aid in wound healing and hair growth.

Monilethrix is linked to a gene cluster on chromosome 12.

Ptprq has multiple forms that change during inner ear development.

ERULUS controls root hair growth by regulating cell wall composition and pectin activity.

A high-fat diet may weaken tongue structure by reducing certain protein genes.

Activating cannabinoid receptor 1 reduces certain keratin levels, potentially aiding psoriasis treatment.

The Kras mutation changes normal cell signals, leading to disrupted tissue structure and potential cancer.

Mouse and human keratin 16 can both form filaments, with differences likely due to the tail domain, not the helical domain.

A rare EGFR mutation in newborns leads to severe health issues and early death.

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