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Keratin 75 is important for fast wound healing and works with SOX2 and the LINC complex to help skin cells move and repair damage.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

Mutations in the KLHL24 gene cause skin blistering in epidermolysis bullosa simplex.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

LPA3 signaling in the uterus is crucial for placental formation and fetal development.

Lactate production is important for activating hair growth stem cells.

Deleting the Hoxc13 gene in frogs shows its crucial role in developing skin structures similar to hair.

Lizard claws have hair-like keratins similar to those in mammals.

New mutations in hair keratin genes cause the rare hair disorder monilethrix.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

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

Monilethrix involves multiple genes affecting hair structure, including DSG4 mutations.

Hoxc genes control hair growth through Wnt signaling.

Msx2 is essential for proper enamel formation by preventing abnormal cell transformation.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Lysophosphatidic acid affects sensory neurons and may cause neuropathic pain and itch.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

Cathepsin L is essential for normal hair growth and development.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

Deleting a specific protein in skin cells disrupts normal hair growth and development.

A specific DNA region controls skin cell gene expression by working with certain proteins.

Hairless protein can both repress and activate vitamin D receptor functions, affecting gene regulation.

miR‑339‑5p can slow down hair follicle stem cell differentiation by targeting DLX5.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

A boy developed a rare skin condition after recovering from a severe skin reaction, and it improved with lotion treatment.

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