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Tight junctions help control skin shedding and may be targets for treating certain skin conditions.

Disrupting a specific protein's function in hair follicle stem cells triggers their activation and a self-healing process.

Hemidesmosomes and Notch signaling help skin cells mature by moving them to the outer layer.

Certain mutations in the hairless protein disrupt its ability to regulate the hair cycle.

CRISPR/Cas9 editing in spinach affects root hair growth by altering specific genes.

Harlequin ichthyosis involves abnormal skin cell structures and giant mitochondria, affecting skin and hair.

3D cell spheroids can help reduce scars by delivering therapeutic vesicles.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

A gene mutation in mice causes skin defects and early death.

lncRNA VIM-AS1 helps heal diabetic wounds by boosting energy production and reducing cell aging.

Deleting part of a gene in mice causes wavy hair and high pup loss.

Astrotactin-2 is cleaved in a specific way that helps understand its maturation.

Mutations in NIPAL4 cause skin issues by disrupting lipid layers, but some improvement is seen with topical treatment.

Changing protein kinase levels in pituitary cells affects calcium flow and beta-endorphin release.

Hair follicles in nonsegmental vitiligo are better protected from immune attacks than in alopecia areata.

Reactive oxygen species and calcium create a feedback loop that shapes root hair cells.

The method using ionic liquid improves observation of cell structures with less damage.

Autophagy is essential for proper skin cell development and function.

Lack of Cisd2 disrupts calcium balance in cells, leading to poorly functioning neutrophils.

Bacterial extracellular vesicles could revolutionize regenerative medicine but need safety improvements.

Estrogen and androgen signals control synaptic changes in rat brains.

Involucrin is crucial for skin cell maturation and protection.

Keratinocyte adhesion problems can cause skin and hair disorders.

Mutants of CYP154C2 enzyme significantly improved steroid conversion efficiency.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

CaBP1 and CaBP2 are important for maintaining hearing by supporting continuous calcium currents and nerve signaling in the ear.