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Cis-UCA can form new compounds without enzymes, and sulphide donors reduce its UVB-induced toxicity in skin cells.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

Id proteins, especially Id2 and Id3, are crucial for hair follicle development and stem cell regulation.

A new Wnt surrogate specifically targets the Frizzled7 receptor, promoting organoid formation and hair growth.

Foxi3 expression in developing teeth and hair is controlled by the ectodysplasin pathway.

Higher STAT3 levels are found in hair loss areas, but not linked to hair loss severity.

Stat3 is essential for hair growth and wound healing.

Sgk3 kinase is essential for normal hair growth in mice.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

Two genetic variations in Moa buffalo help them adapt to heat.

Exosomal miR-199a-3p from dermal papilla cells helps control hair color by affecting melanocytes.

Mouse zigzag hair bends form due to a 3-day cycle of changes in hair progenitors and their environment.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

ΔNp63α stops TAp73β from working in skin cancer by blocking its access to specific genes, not by directly interacting with it.

LncRNA MSTRG.14227.1 hinders hair follicle development in cashmere goats, affecting cashmere quality.

Researchers found a gene mutation responsible for a rare hair loss condition.

Deleting MPZL3 increases skin oil production and reduces body fat.

Tet2 and Tet3 enzymes are essential for controlling hair growth by affecting DNA demethylation and gene expression in mice.

Retinoic acid, glucocorticoids, and IGF1 increase IGFBP-3 production in human dermal papilla cells, affecting hair growth.

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

miR-3606-3p reduces skin fibrosis by blocking key signaling pathways.

Activating TLR3 boosts autophagy gene expression in skin cells.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

miR-214-3p helps nerve repair and recovery.

miR-214-3p helps nerve repair and recovery.