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Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

Low oxygen levels help hair follicle stem cells turn into heart muscle cells faster.

HSPGs help control stem cell behavior, affecting hair growth and offering a target for hair loss treatments.

Keratinocyte gene expression is controlled by multiple modules with specific binding sites.

Lower IGFBP4 promoter methylation is linked to finer wool in sheep.

Heparanase is essential for hair follicle health and inner root sheath differentiation.

A specific mutation in PA-PLA1α causes abnormal hair growth.

KAP genes are crucial for hair development and show both shared and unique traits in humans, chimpanzees, and baboons.

Disrupting the Sox21 gene in mice causes hair loss and regrowth cycles.

Sweat glands and hair follicles are determined by opposing signals, with BMPs promoting sweat glands and blocking BMPs leading to hair follicles.

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

Hair and nail cells share similar proteins, indicating a common differentiation pathway.

Too much IKZF1 and Ikaros protein may cause alopecia areata.

Overactivating Hedgehog signaling makes hair follicle cells in mice grow hair faster and create more follicles.

CD8A and FOXD2-AS1 may be key for diagnosing and treating alopecia areata.

A mutation in the human hairless gene causes alopecia universalis.

New genetic mutations causing hair loss were found in a Chinese family.

Mice hair follicles take in the amino acid cystine.

ODC expression in mouse skin and tumors is varied and can be inhibited by retinoic acid or cycloheximide.

NADPH oxidase 4 is key for stem cell activity and growth under low oxygen.

The hr gene is linked to hair loss in Valle del Belice sheep.

Hair samples can't reliably detect hypercortisolism in anorexia nervosa patients.

Targeting LGR4 may help treat cancer by reducing cancer stem cell traits and drug resistance.

The hexosamine pathway helps maintain healthy skin by affecting the skin's structure and possibly increasing hair follicle stem cells.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

Alkylated keratin from human hair can help deliver growth factors for bone healing.