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Stem cell behavior varies with stimuli, and lineage changes can happen without affecting stem cell division.

LEF1 is essential for the development of airway glands and is regulated by the Wnt/ß-catenin pathway.

Mutations in β1 integrins cause embryonic death but have milder effects on skin.

The Cashmere goat hair keratin gene is crucial for hair structure.

Wnt and Shh signaling are key in noggin-induced tumors, and blocking them can slow tumor growth.

The LncRNA AC010789.1 slows down hair loss by promoting hair follicle growth and interacting with miR-21 and the Wnt/β-catenin pathway.

A new genetic model may improve treatment and diagnosis for certain inherited skin diseases.

HLD10 can include increased body hair and Mongolian spots.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

Key genes and pathways influence wool traits in Merino sheep.

Skin cells can naturally limit the growth of cancerous changes by balancing cell renewal and differentiation.

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

Intermediate filaments are crucial for cell structure and function, regulated by specific genes and proteins.

Increasing Wnt10b levels can help grow new hair follicles in mice.

The RNA AL136131.3 slows down hair growth and speeds up hair loss by affecting sugar breakdown in hair follicles.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

Different sheep breeds share similar genetic factors affecting wool fineness.

RD26 controls root hair growth during drought by repressing key genes, helping plants save energy.

The study found specific skin cells and genes that may affect the quality of cashmere in Liaoning Cashmere Goats.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

Vitamin D receptor is essential for hair growth signaling.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

FGF13 gene changes cause excessive hair growth in a rare condition.

Cells with active Wnt signaling are less likely to turn into cancer when exposed to a cancer-causing gene.

Gene expression affects fur development in rex rabbits.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

Pangolins have lost some skin-related genes, but kept others, showing complex skin evolution.