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cGEL hydrogel improves melanin production in skin cells, making it a promising option for skin treatments.

Circular RNA ERCC6 helps activate stem cells important for cashmere goat hair growth by interacting with specific molecules in an m6A modification-dependent way.

Activating TRPV4 in skin cells helps regrow hair in mice, possibly offering a treatment for hair loss.

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Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

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Polycaprolactone and barium titanate composites show promise for use in biomedical applications.

Lipid content and structure affect water absorption in different hair types.

Mangkokan leaf contains various beneficial compounds like alkaloids, flavonoids, and steroids.

Mouse Scube3 affects teeth, tongue, vibrissae, and eye development, but not facial structure or limb growth.

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Defects in certain proteins cause major heart abnormalities during early development.

Removing the Crif1 gene in mouse skin disrupts skin balance and hair growth.

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Finasteride complexes with HPβCD and polymers improve solubility, potentially enhancing hair loss treatment.

The lotion CG428 did not show effectiveness in treating permanent hair loss in breast cancer survivors.

A method was developed to grow millions of hair cells from a single hair for research and storage.

TRF1 is crucial for creating and maintaining stem cells and marks both pluripotent and adult stem cells.

A new staining method helps tell growing from resting hairs to diagnose hair loss.

CDK4/6 inhibitors may cause hair loss in breast cancer patients.

Chick embryo extract helps rat hair follicle stem cells become more like neurons.

Fusion proteins can protect hair from heat damage.

ROP GTPase helps control the growth of pollen tubes and root hairs by managing cell structure and movement.

MYB30 and EIN3 work against each other to control root hair growth and phosphorus uptake in plants when phosphate is low.

Keratins K4 and K13 form stable dimers in mature esophageal cells, aiding cell stability.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.