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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.

Early and late matrix progenitors in hair follicles create different cell layers, with early ones forming the companion layer and later ones forming the inner root sheath and hair shaft.

The role of certain genes in skin cell development may be linked to psoriasis, but the connection is unclear.

Reactive lipids from aging cells change the extracellular matrix, affecting cell function and inflammation.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

A rare skin condition in a boy is likely due to a specific genetic mutation pattern.

The Ysc84/SH3yl1 protein family is important for cell movement and the process of taking in materials by interacting with actin and cell membranes.

SOX11 and SOX4 help skin cells act like embryonic cells to heal wounds in mice.

Hair keratin-associated proteins are essential for strong hair, with over 80 genes showing specific patterns and variations among people.

Disrupted cell interactions in hair follicles contribute to hair loss in androgenetic alopecia.

Collagen XVII is important for cell functions and its absence can worsen cancer outcomes.

Mouse tail skin has different keratinization near hair follicles and scales.

The extracellular matrix is crucial for maintaining and regulating epidermal stem cells in hair follicles.

Human and bovine hair follicles have distinct cytokeratins specific to hair-forming cells.

The Foxn1 gene is essential for normal nail and hair development.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Cell junctions are crucial for healthy skin by supporting sebaceous gland function and sebum production.

Sweat glands and hair follicles are structurally connected within a specific layer of skin fat.

Steatocystoma multiplex is a skin condition starting around age 26, linked to hair follicles, and related to eruptive vellus hair cysts.

A cluster of 21 keratin-associated protein genes important for hair growth was found on human chromosome 21.

Different body areas have unique skin cell communication patterns, explaining why certain skin diseases occur in specific regions.

Fibre optic confocal imaging can visualize skin layers, blood vessels, and nerves in live mice.

Giant axonal neuropathy changes the structure of keratin in human hair.

Mutations in certain receptors can cause diseases and offer new treatment options.

Small proline-rich proteins and trichohyalin help make epithelial tissues tougher and more flexible.

Hoxc8 gene helps start mammary gland development by controlling specific signals.