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

Spt4 and Spt6 are essential for fat cell development.

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A Korean baby with nevus sebaceus syndrome was found to have a KRAS gene mutation.

AcSDKP may help prevent skin and hair aging and promote their growth.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

Short-term treatment with ROCKi increases skin cell growth without changing stem cell features.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

TRPV3 in skin cells causes inflammation and cell death.

YAP and TAZ proteins control skin cell growth and repair.

Taking 5-ARI before prostate laser surgery may lead to more blood changes, longer surgery, and more urinary issues.

CTCF protein is essential for skin and hair follicle development in mice.

RK81 can help promote hair growth.

Mrp3 helps in wound healing and hair growth.

SK2 channels help control sensory signals in rat muscle spindles and hair follicles.

Recombinant thymosin β4 promotes blood vessel growth and reduces muscle damage.

AKR1D1 controls glucocorticoid levels and receptor activity in liver cells.

The KAP8-1 gene affects skin, hair follicle development, and wool quality in different sheep varieties.

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

Activating certain potassium channels in honey bees can lower antioxidant levels and reduce death rates during heavy mite infestations, potentially aiding their immune response.

mHa2 and mHa3 keratins have different structures and roles in mouse hair and tongue tissues.

Keratin 17 is modified by RSK1 in response to growth and stress, affecting skin growth and stress response.

Esrp1 is important for skin health by helping form and maintain the skin barrier.

Ginsenoside Rg4 from ginseng may help hair growth by activating certain cell signals.

The newborn with Klippel-Trénaunay syndrome was healthy but needed regular check-ups for possible complications.