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Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

Two mouse mutants have defective hair cuticle cross-linking.

KAP genes show significant genetic variability, but its impact on hair traits is unclear.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

Corneodesmosin is essential for skin and hair health, and its dysfunction can lead to skin and hair disorders.

Keratinocyte gene expression is controlled by multiple modules with specific binding sites.

Keratins are important for skin cell health and their problems can cause diseases.

Hedgehog signaling is crucial for hair development, cadherins affect cell adhesion, neutrophils play a role in skin lesions, and BP230 autoantibodies impact skin stability.

TAF4 is important for skin cell growth and helps prevent skin cancer in mice.

Coordinated gene activities are crucial for normal hair growth.

Basonuclin may help control ribosomal RNA gene activity in skin cells.

Hydrophilic carbon dots cause one protein to clump more and prevent another from clumping.

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

Cysteines in wool fibers are accessible and form important disulfide bonds.

The arrector pili muscle attaches to the extracellular matrix using α5β1 integrin and connects muscle cells using α1β1 integrin.

A gene mutation in mice causes severe skin disorder similar to a human condition.

Terrestrial vertebrates have balanced keratin gene clusters, unlike teleost fish.

Overexpressing 14-3-3σ in mice skin reduces cell growth and hair density.

Specific proteins and molecules play key roles in the development of human hair follicles.

Corneodesmosin is crucial for skin and hair health, and its dysfunction can cause skin and hair disorders.

Human hair keratin genes hHa2 and hHb1 are located on chromosomes 17 and 12.

The tumor suppressor BRCA2 helps in cell division by bringing key proteins to the area where cells split.

Mutations in the KLHL24 gene cause a skin disorder in some Russian families.

Scientists used stem cells to create a model of the skin disease Epidermolysis Bullosa simplex, which helped them understand its molecular mechanisms and could aid in finding treatments.

Two new proteins, hKAP1.6 and hKAP1.7, are found in the hair follicle cortex.

Antibodies help identify glycoproteins in normal skin and tumor cells.

Modified β-catenin causes different effects in hair and skin cells, leading to cysts or tumors.

LEKTI is crucial for skin barrier and immune function, affecting conditions like Netherton syndrome and atopic dermatitis.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

Keratin 15 helps keep skin cells in a young, undifferentiated state.