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Three genes in Arabidopsis are important for plant growth and development by affecting sugar attachment to proteins.

Mutations in the hairless gene cause hair loss and skin cysts in rhesus macaques.

A unique gene mutation causes vitamin D-resistant rickets without causing hair loss.

Human hair follicles can produce stem cells that turn into heart muscle cells.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

Injecting a peptide-hyaluronic acid mix improved hair growth in men with hair loss and was safe.

Psoriasis patients' immune response to a hair protein depends on their specific gene type.

The 5050 MHA42MCS45 hydrogel blend is suitable for repairing load-bearing soft tissues.

The hair erector muscle is involved in various skin conditions and disorders.

The HCR gene contributes to psoriasis risk.

HAIR-AN syndrome is common in young women and can be effectively managed with a comprehensive treatment plan.

A patient with HAIR-AN syndrome, PCOS, and Hashimoto's thyroiditis improved with early diagnosis and treatment to prevent serious health problems.

ZO-1 helps hair follicle stem cells renew better by changing their structure.

High levels of ODC and a mutant Ha-ras gene cause tumors in mice.

HR protein causes abnormal hair cycles by increasing Tgf-β2 and reducing miR-31.

Hairless protein can block vitamin D activation in skin cells.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

Alcohol dependence affects stress hormone levels more than childhood maltreatment.

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

HIF-1α in fibroblasts boosts hair growth and health.

The RHD4 gene is crucial for consistent root hair growth in Arabidopsis thaliana.

Hidradenitis Suppurativa has genetic links, with certain gene mutations more common in patients and a third of cases having a family history.

Understanding the properties of hyaluronic acid helps improve its use in facial aging treatments.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

The correction fixes an image mistake in the original publication, but the findings on the hair treatment's effectiveness are unchanged.

Low oxygen levels help hair follicle stem cells turn into heart muscle cells faster.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.