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A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

LGR5 and LGR6 are expressed differently in various skin tumors, which may offer clues about their origins.

A gene mutation in Lama3 is linked to a common type of hair loss.

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

Lhx2 helps retinal cells respond to signals for eye development.

The protein RSL4 is crucial for making root hairs longer by controlling genes related to cell growth.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

A specific RNA molecule blocks hair growth by affecting a protein related to hair loss conditions.

Circular RNA ERCC6 helps activate stem cells important for cashmere goat hair growth by interacting with specific molecules in an m6A modification-dependent way.

The LAMTOR3 gene is involved in cashmere goat hair growth and is affected by certain treatments and other genes.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

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

Certain changes in the KAP6-1 gene affect the thickness and length of cashmere goat fibers.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

Researchers cloned a gene from Xinjiang fine-wool sheep, finding it very similar to other sheep and somewhat similar to goats, humans, and rabbits.

A gene mutation in mice causes severe skin disorder similar to a human condition.

A rabbit gene important for hair development was identified and detailed.

Hex gene plays a crucial role in starting feather development in chick embryos.

mrp/plf-mRNA can indicate tumor-promoting effects in skin.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

Keratin K6irs is a marker for the inner root sheath of hair follicles in mice and humans.

LGR6+ stem cells may improve bone healing.

Mutant MK6a transgenes in mice cause blistering, hair loss, and potential human alopecia.

UV exposure reduces Lgr6+ stem cells in mouse skin and they don't significantly contribute to skin cancer development.

Higher activity in lichen planopilaris is linked to certain immune and tissue genes.

Egfl6 is not needed for zebrafish face development.

Not having the gene PLAAT3 leads to fat loss, high insulin resistance, and abnormal fat levels in the blood due to a disruption in fat cell development and function.