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DermaCult™ Keratinocyte Expansion Medium allows human skin cells to grow longer while keeping their ability to develop properly.

Artemis phosphorylation at Ser516 may help regulate skin and hair structures.

Increasing type 17 collagen reduces aging signs in skin cells caused by UV light.

DS-2325a is safe and well-tolerated, supporting further development for Netherton Syndrome treatment.

Keratin 15 helps maintain skin cell growth and repair.

BKN-1 antibody targets specific keratin in basal cell epithelioma and normal skin basal cells.

Isotretinoin can raise CPK levels, so patients need monitoring, especially before surgery.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

The ABHRS held a test in Capri, Italy.

Researchers created a cell line to study hair growth and found specific genes affected by dihydrotestosterone.

ZPK helps skin cells mature and may affect skin health.

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

Kerion is a rare but serious scalp infection that needs proper treatment.

A rare skin condition in a 17-year-old was diagnosed late, stressing the need for careful evaluation and genetic testing.

Syntaxin 9 helps in transporting and signaling of the EGF receptor in skin and stomach cells.

KAP-depleted hair causes less immune response and is more biocompatible for implants.

K14 expression in young rats differs from adults.

L-threonate may help prevent balding by blocking a key protein.

The new model helps understand and develop treatments for genetic skin disorders like AEC.

H3K4me3 helps control RSPO3 to influence hair growth and development.

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Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

Signals from skin cells controlled by Rac proteins help turn certain precursor cells into white fat cells.

A new mutation in mice causes crooked whiskers and messy hair.

Caspase-14 is important for skin and hair development in all mammals.

A 5-year-old girl with a rare skin disorder was effectively treated with skin creams instead of oral medication.