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A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

The ZIP7 gene helps control zinc levels in cells by moving zinc from the Golgi apparatus to the cytoplasm.

Mutations in the hairless gene cause a rare form of permanent hair loss.

H1 increases risk for neurodegenerative diseases, while H2 offers protection but is linked to other disorders.

The gene SDR5A1 is found in scalp hair of both hirsute and normal individuals, but it does not explain differences in hair growth.

A gene in Arabidopsis thaliana, AtPRPL1, affects root hair length but not cell wall composition.

Toll-like receptor 3 helps repair the skin barrier after UV damage.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

A mutation in the KRT74 gene causes woolly hair by affecting hair texture.

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

Certain genetic changes in the KRT82 gene may cause patchy skin in New Zealand rabbits.

ROR2 is essential for hair follicle stem cell renewal and maintenance.

Lhx2 is essential for effective Sonic Hedgehog signaling in early retinal development.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

The FA2H gene improves cashmere fineness by enhancing hair growth in goats.

KRT85 gene variations can help improve wool traits in sheep through selective breeding.

Overexpressing the human H-ferritin gene in mice causes mild growth delay and temporary hair loss.

Hair differentiation starts earlier than thought, involving multiple type-II keratins.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

OsPHR2 gene in rice enhances root growth and phosphorus accumulation.

The ND1 gene of the Asian black bear Sichuan subspecies is similar to other bear species.

Suppressing the HGPS mutation may improve symptoms and suggest reversibility.

An individual's morning or evening preference can predict changes in their body clock gene expression.

Hair follicle analysis can track body changes from high-intensity interval training.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.