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A new keratin, hK6irs1, is found in all layers of the hair follicle's inner root sheath.

The study identified key genes involved in goat hair growth.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

Tunisian children with hereditary vitamin D-resistant rickets showed improvement with calcium treatment, and new genetic mutations were identified.

Rushton's hyaline bodies form from hair keratin and blood substances.

Researchers found 19 genes important for root hair growth in a plant called Arabidopsis.

The Kras mutation changes normal cell signals, leading to disrupted tissue structure and potential cancer.

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

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

The rs1128977 gene variant may affect cholesterol and body measurements.

Excessive hair growth in women often has no known cause and is not linked to race or other hormonal symptoms.

BRG1 is essential for skin cells to move and heal wounds properly.

Hibiscus leaf extract may help hair grow better than flower extract.

Signaling pathways are crucial for hair growth in goats.

A genetic marker linked to a type of hair loss was found in most patients studied.

Defective nuclear transport may cause gene expression changes in Progeria.

Intranasal delivery of gene therapy shows promise for treating ischemic stroke.

Overexpression of Hoxc13 in hair cells causes hair loss and skin issues.

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

Increased PHGDH expression causes early melanin buildup in hair follicles.

Impaired LEF1 activation speeds up skin cell development in Hutchinson-Gilford Progeria Syndrome.

R-spondin2 may help treat hair loss, gene differences could explain baldness, a peptide's regulation is linked to psoriasis, B-defensin gene copies may affect a skin condition's risk and severity, and potential markers and targets for alopecia areata were identified.

Certain ESR1 gene variations may affect hormone levels and fat distribution in women with high male hormone levels.

Certain genes may promote longer root hairs in plants when phosphorus is low.

Specific keratin gene mutations can cause monilethrix.