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Removing a specific gene in certain skin cells causes hair loss in mice by disrupting hair follicle development.

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New mutations in hair keratin genes can change hair structure and cause monilethrix, with nail issues more common in certain gene mutations.

Gene expression regulates keratin production for normal hair growth.

Vogt–Koyanagi–Harada disease can cause rare hair growth on normally hairless thumb skin.

mHa2 and mHa3 keratins have different structures and roles in mouse hair and tongue tissues.

A girl had rickets due to a gene mutation affecting vitamin D response.

EZH1 and EZH2 are crucial for healthy hair growth and skin repair.

Human growth hormone treatment improved skin thickness and structure in osteoporosis patients.

A gene called HDAC9 might be a new factor in male-pattern baldness.

KRTAP2 genes are crucial for hair structure and may impact hair disorders and treatments.

The ovine Hoxc-13 gene is crucial for hair formation and may have other skin functions.

LHTric-1 is a specific antibody useful for studying hair and nail formation.

New mutations in the DSG4 gene cause a rare hair condition.

Epithelial proliferation and hyperkeratosis are linked to gastric ulcers in pigs.

FGF5 spliceosomes inhibit rabbit hair growth by affecting gene expression.

Fibroblast bioelectric signaling can promote hair growth and may help treat hair loss.

LHX2 is essential for hair follicle development, controlled by NF-κB and TGFβ2 signaling.

Keratins K1 and K10 are found in the inner root sheath and cuticle of human hair follicles.

HOXC13 is essential for hair and nail development by regulating Foxn1.

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

EGFR is crucial for preventing hair follicle inflammation and hair loss.

HAPLN1 can promote hair growth and may help treat hair loss.

Gamma-ray exposure can cause long-lasting damage to hair follicles, affecting hair structure and color.

The method successfully created stable transfection donor cells for goat hair follicle research.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

Kartogenin may help treat hair loss by promoting hair growth and extending the hair growth phase.

Too much IKZF1 and Ikaros protein may cause alopecia areata.