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Hair stem cells produce a protein called COL17A1 that plays a key role in their development and is linked to hair thinning and baldness.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

Gene expression in wool follicles changes with growth cycles, offering insights into wool and human hair growth.

Human hair keratins were cataloged, showing their roles in hair differentiation stages.

CRABP1 boosts hair cell growth in Hu sheep by affecting key genes.

A specific gene change in APCDD1 increases the risk of hair loss.

The Bsk mutation doesn't involve keratin gene recombination and its cause is unknown.

Keratin 16 delays skin maturation and affects skin and hair development in mice.

Hoxc13 gene is essential for hair, nail, and papilla development.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

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

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

The study found 65 intermediate filament genes, including new keratins, and suggested updating keratin naming.

Keratin 17 is important for skin development and may help define skin cell types.

Certain genetic changes in the KAP22-1 gene are linked to better wool quality in Egyptian sheep.

GKLF/KLF4 and Sp1 control Keratin 19 gene activity, influencing cancer-related changes.

Understanding intermediate filaments helps explain hair health and related diseases.

Keratin is crucial for skin barrier formation and affects mitochondrial function.

Keratin 79 marks a new group of cells that are key for creating and repairing the hair follicle's structure.

The method effectively analyzes human hair proteins, especially nonfilamentous ones.

BBS7 is essential for healthy gums by supporting cell function and blood flow.

The gene for Marie Unna hereditary hypotrichosis is located on chromosome 8p21.

Most mouse hair keratin genes are on chromosomes 11 and 15.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

Hedgehog signaling is essential for normal sebaceous gland development and affects keratin 6a expression.

Keratins help GLUT2 stay on the cell membrane in pancreatic β-cells.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

PBX1 helps hair stem cells grow and change by turning on certain cell signals and preventing cell death, which may be useful for hair regrowth treatments.