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Merkel cells develop independently of nerves and are linked to specific hair follicles in mice.

The microneedles effectively kill MRSA and improve wound healing.

Electron microscopy helps understand skin structure and diseases.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

These methods help understand DNA changes in mouse skin.

MSC-CM cream speeds up burn wound healing better than the control treatment.

A rare skin condition causes red and dark patches on the face and limbs.

Matriptase is crucial for keeping epithelial tissues healthy and functioning properly.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

The marker 5-hmC changes in hair follicle stem cells when they start to grow.

Keratin 19 expression in certain skin cells is temporary and not a reliable stem cell marker.

Sheep have 17 keratin genes, similar to humans, but with different expression patterns affecting wool and hair.

Matrical tumors share a common growth mechanism involving the Wnt pathway and consistent PHLDA1 expression.

Biomimetic nanovesicles can speed up diabetic wound healing by regulating immune cell behavior and metabolism.

Eph receptors and ephrins may be promising targets for treating diseases, but more understanding is needed for effective and safe therapies.

Claudin expression changes help the skin respond to injury.

People with more than 11 skin tags, especially on the thigh, neck, or armpit, may have a higher chance of metabolic syndrome.

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

Extracellular vesicles could help tailor drug treatments, but more research is needed.

New laser particles can track thousands of cells in 3D models, improving single-cell analysis.

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

Erdr1 could be a new marker for diagnosing hair loss.

The guidelines ensure accurate genetic testing and reporting for 21-hydroxylase deficiency.

Low-oxygen conditions and ECM degradation products increase the healing abilities of perivascular stem cells.

Hair follicle samples effectively show how well the drug MK-0752 targets and engages with the Notch pathway.

The research identified unique metabolic activities in immune cells associated with hair loss in Alopecia Areata.

Different keratins have unique expression patterns in mouse skin cells.