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Two new enzymes, PAD-R11 and PAD-R4, were cloned and showed activity, with PAD-R11 resembling epidermal enzymes.

Equisetum arvense extract in gels may enhance drug release for treatments.

Alkaline Ceramidase 1 prevents early hair loss in mice by keeping hair follicle stem cells balanced.

Abnormal ECM and immune cell interactions can cause skin diseases.

High levels of ERK activity are key for tissue regeneration in spiny mice, and activating ERK can potentially redirect scar-forming healing towards regenerative healing in mammals.

The ZIP13 variant is linked to abnormal hair quality.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

Significant progress was made in understanding PXE, but effective treatments are still needed.

A severe form of Netherton syndrome caused by a specific gene mutation led to neonatal deaths in a family.

New genetic mutations linked to rare skin disorders were found in three newborns.

Rodent spiny hair traits are due to genetic factors other than the Edar gene.

Daily use of emollients from birth may reduce atopic dermatitis in infants, but results are mixed.

Pre-existing skin conditions and drug reactions are the main causes of exfoliative erythroderma.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Plakophilin 1 helps control skin cell immune responses to prevent excessive inflammation.

Skin grafts from related donors significantly healed chronic wounds in patients with a severe skin condition over a year.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

Dopaminergic neurons in the gut have distinct subtypes, some releasing both dopamine and acetylcholine.

Erectile dysfunction is linked to hormone imbalances and vascular health, requiring personalized treatment approaches.

Dermatopathia pigmentosa reticularis causes skin discoloration, hair loss, and nail problems.

The new 3D sponge-like material helps cells grow and heals wounds effectively.

PRC1 is essential for proper skin development and stem cell formation by controlling gene activity.

Adipocytes in atopic dermatitis skin change and worsen inflammation and fibrosis.

Epidermal growth factor disrupts hair and gland formation in bandicoots.

Epidermolysis bullosa in UK calves is not caused by mutations in keratin genes.

A man with a rare lung-focused form of hypereosinophilic syndrome improved with steroid treatment.

The LMNA mutation affects skin structure even in asymptomatic carriers.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

The ethosomal delivery system improves topical drug delivery and promotes hair growth.

The F9 formulation of Finasteride tablets, using Eudragit, successfully controlled drug release.