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Dermal Papilla Cells grown in 3D and with stem cells better mimic natural hair growth conditions than cells grown in 2D.

DNA methylation affects BMP7 gene expression, influencing cell growth in Hu sheep.

Human leukocytes and beard hair follicle cells have internal daily clocks, and PER1 and PER3 genes may indicate individual circadian rhythms.

Overexpressing ATF3 in mice's epithelial cells may lead to oral cancer.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

PDRN helps repair tissue and improve wound healing with a high safety profile.

Placenderm® can improve hair health and promote hair regrowth.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

CLK1 is needed for skin cells to become epidermal cells but not sebocytes.

SOX18 helps sheep hair cells grow by activating a specific cell growth pathway.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

Early diagnosis and multidisciplinary care are crucial for managing CNOT3 syndrome.

Researchers identified genes in scalp hair follicles that may affect hair traits and hair loss.

The enzymes Tet2 and Tet3 are important for skin cell development and hair growth.

Methylene blue staining effectively highlights detailed nerve structures in rat fur.

Spt4 and Spt6 are essential for fat cell development.

A Gsdma3 mutation causes hair loss due to stem cell damage from skin inflammation.

The G allele of IFITM3 rs12252 is linked to more severe COVID-19.

STIM1 is essential for sweat secretion.

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A new method using poly(ethylene imine) improves hair dyeing at lower temperatures with better color retention.

The new hydrogel with curcumin speeds up wound healing safely and effectively.

Nexin 1 may help control hair growth.

Sema3A can both slow and speed up wound healing, depending on its form and combination with EGF.

The research suggests that SFRP2 and PTGDS proteins might be indicators of female pattern hair loss and could contribute to hair loss.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

The HSD3B1 variant increases hair loss risk in overweight women with PCOS.

New mouse models of Pemphigus show severe symptoms and need better treatments.