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Some cells may slow melanoma growth, a protein could affect skin pigmentation, a gene-silencing method might treat hair defects, skin bacteria changes likely result from eczema, and a defensin protein could help treat multiple sclerosis.

A mutation in the KRTHB5 gene causes hair and nail issues.

Accurate diagnosis and zinc supplements can improve life quality in acrodermatitis enteropathica, even with normal zinc levels.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

Isoproterenol helps hair follicle stem cells turn into beating heart muscle cells.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

High amphiregulin in the skin is a bad sign for acute graft-versus-host disease.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

EGF and KGF signalling prevent hair follicle formation and promote skin cell development in mice.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

Fish oil improves skin health in people with diabetes and high cholesterol.

The oncoprotein causes abnormal hair growth without increasing skin cancer risk.

Horse skin stem cells combined with platelet-rich plasma improve skin healing.

Human placental extract may help hair growth by affecting certain cell signals and could be more effective with minoxidil.

Extracellular vesicles may help prevent and repair spine disc degeneration.

Mice without certain skin proteins had abnormal skin and hair development.

Aptamers can improve wound healing and promote hair growth.

Dexamethasone may influence hair growth by altering estrogen receptor activity in hair cells.

TTD patients don't have a higher skin cancer risk because their main issue is with transcription, not DNA repair.

Platelet-derived extracellular vesicles can boost hair growth by activating a specific signaling pathway.

Certain gene variations may increase the risk and severity of alopecia areata.

CMG2 and TEM8 receptors have distinct roles in skin and growth disorders, affecting collagen breakdown and growth.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

Ruxolitinib reduced inflammation and improved symptoms in APECED patients but may cause anemia and weight gain.

A rare scalp condition was successfully treated with specific medications after 9 months.

Scientists found a new protein, AMY117, common in Alzheimer's patients, which could be important for treatment and diagnosis.

STIM1 is essential for sweat secretion.

Platelet-derived products can help regenerate the temporomandibular joint by enhancing natural healing processes.