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Methionine supplementation in low-protein diets improves growth, fur quality, and gut health in blue foxes.

TCF/Lef1 is essential for skin barrier function by regulating lipid metabolism.

Mice lacking fibromodulin have disrupted healing patterns, leading to abnormal skin repair and scarring.

Kidney cancer cells without folliculin are more sensitive to radiation due to increased self-eating cell death.

Signals from skin cells controlled by Rac proteins help turn certain precursor cells into white fat cells.

Researchers created a new mouse model for studying scleroderma.

Deleting part of a gene in mice causes wavy hair and high pup loss.

Removing certain hair follicle stem cells worsens skin reactions to allergens.

Over-expression of Sp2 can lead to cancer by preventing proper stem cell differentiation.

Verteporfin reduces growth and stem cell traits in rat hair follicle cells by blocking the Hippo pathway.

MED1 affects skin wound healing differently in young and old mice.

Lack of 5α-Reductase type 1 can lead to insulin resistance and liver problems.

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

Overexpression of Hoxc13 in hair cells causes hair loss and skin issues.

NFATc1 controls hair stem cell activity, affecting hair growth and could be a target for hair loss treatments.

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.

Rat hair follicle stem cells have functional oxytocin receptors, useful for studying neuropsychiatric disorders.

The LMNA mutation affects skin structure even in asymptomatic carriers.

A rare EGFR mutation in newborns leads to severe health issues and early death.

Trps1 is essential for proper hair follicle development.

Adam10 enzyme is crucial for healthy skin and proper Notch signaling.

Zebrafish help understand genetic causes of skin pigment disorders like albinism.

Removing MCPIP1 from myeloid cells in mice leads to hair loss and prevents skin tumors but causes pigmented spots.

ANXA1 influences hair growth in mice through the EGF signaling pathway.

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

The compound additive improved growth and fur quality in blue foxes.

SOX9 is crucial for cell development and repair but can cause fibrosis and cancer if misregulated.

Lack of TrkC receptor delays hair follicle development.

Krox20 is important for maintaining stem cells in the skin and affects hair growth and color.