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LGR5 mainly stays inside cells, moving to the trans-Golgi network, and this process is important for its role in cell signaling.

Lef1 helps stem cells become hair cells by interacting with specific signaling pathways.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

CCL5 is important for the hair growth potential of human dermal papilla cells.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

FGF20 is essential for hair follicle stem cell growth and development in fine-wool sheep.

LGR5 and LGR6 are expressed differently in various skin tumors, which may offer clues about their origins.

Targeting FGF5 could help treat prostate cancer.

KGF-1 135 is a stable and effective alternative for treating oral mucositis.

A gene mutation causes monilethrix in a Chinese family.

The Foxn1(-/-) nude mouse shows disrupted and expanded skin stem cell areas due to high Lhx2 levels.

LEF1 interacts with Vitamin D Receptor, affecting hair follicle regeneration and this could be linked to hair loss conditions.

Lhx2 helps retinal cells respond to signals for eye development.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

Gene regulatory regions evolve faster than protein coding regions, allowing new gene relationships without changing transcription factors.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

Two new gene clusters important for hair formation were found on human chromosome 11.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

Certain gene combinations improve cashmere quality and production in Liaoning goats.

Skin cell types develop when specific genes are turned on by removing certain chemical tags from DNA.

The human keratin 6a gene's specific sequences trigger expression in skin layers after injury.

Two new gene clusters important for hair formation were found on human chromosome 11.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

Nelfb is essential for dermal fat development and survival.