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Certain long non-coding RNAs in cashmere goats affect hair growth when treated with a specific growth factor.

Monilethrix is linked to a gene cluster on chromosome 12.

A gene mutation causes monilethrix in a Chinese family.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

Genes affect cytokine production, which can influence chronic diseases, and certain interventions may help prevent related molecular damage.

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

FOL-026 peptide can help repair blood vessels and promote growth, offering potential treatment for vascular diseases.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

The FGF5 gene determines hair length in dogs.

Removing HIF-P4H-2 from certain skin cells in mice causes hair loss on the body but not the head.

Formononetin may help protect the brain and treat neurological diseases.

Understanding the APCDD1 gene can lead to new hair loss treatments.

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

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

NF-κB is crucial for zebrafish heart repair, affecting heart cell growth and repair processes.

Nitrate helps plants manage phosphate uptake and starvation responses through NIGT1 proteins.

A new gene mutation causes vitamin D resistance and hair loss in two unrelated girls.

Targeting FGFR-1 with antisense oligonucleotides may help treat baldness by increasing hair follicle activity.

A unique gene mutation was found in a family with monilethrix.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

Higher levels of nidogen1 and type IV collagen are found in basal cell carcinoma compared to normal skin.

The near-naked hairless mutation causes hair loss but is not due to a mutation in the hairless gene itself.