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Removing a methyl group from the ITGAV gene speeds up bone formation in a specific type of bone disease model.

Seven genes are highly expressed in both germ-line and hematopoietic stem cells.

LIPH mutations cause woolly hair in some Chinese people.

FOXN1 mutations can cause varying immune and physical issues, with severity influenced by gene activity and possibly other factors.

Vitamin D receptor and hairless protein are essential for hair growth.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

This enzyme helps metabolize fatty acids and isoleucine, and could be key in treating neurological diseases and certain cancers.

Hox genes control hair follicle stem cell regeneration in different body regions.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

The rhg mutation in mice affects the Oat gene, causing hair growth issues and other symptoms.

Targeting the HEDGEHOG-GLI1 pathway could help treat keloids.

The POMP gene is active in various goat tissues and affects hair growth, with certain treatments influencing its expression.

Glypicans help hair follicle stem cells differentiate by interacting with specific receptors, influencing hair growth.

Phospholipase C-δ1 is crucial for normal hair development.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

Lrig1 marks a unique group of stem cells in mouse skin that can become different skin cell types.

BTNL2 helps protect hair follicles from immune attacks, which could aid in treating alopecia areata.

Changes in certain RNA and protein levels may contribute to alopecia areata and could be treatment targets.

A gene mutation in mice causes hair loss, weak bones, and protein buildup, showing how protein processing issues can lead to diseases.

A new gene mutation causes a rare type of hair loss.

A new genetic mutation linked to Hutchinson-Gilford progeria syndrome was found in China.

An Australian with rare hair loss and eye conditions had a gene linked to both, not seen together before.

Mice with a changed Hr gene lose and regrow hair due to changes in the gene's activity.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

Increased HSD11B1 enzyme expression is linked to higher body fat and insulin resistance.