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A new genetic model may improve treatment and diagnosis for certain inherited skin diseases.

Repetin is a protein involved in skin and hair development, binding calcium and compensating for other proteins when needed.

CXCL7 is essential for muscle repair by aiding early neutrophil infiltration.

FOXN1 gene variants cause low T cells and immune issues from birth.

Two sisters with lipoedematous scalp suggest a genetic influence in the condition.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

Proteolytic enzymes damaged hair follicle stem cells in transgenic mice.

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.

Researchers found genes linked to hair growth cycles in Inner Mongolia cashmere goats, which could help understand and treat hair loss.

Sweat gland development involves two unique skin cell programs and a temporary skin environment.

IL-3 worsens lupus nephritis and blocking it improves kidney health.

A specific genetic trait in tumor cells is linked to longer survival without disease in certain lymphoma patients.

Plant roots respond to fungus smells by possibly using certain proteins and a plant hormone to change root growth, but more research is needed.

A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

Increased ODC expression makes normally tumor-resistant mice more prone to tumor development.

A new mouse mutation causes skin and hair defects due to a gene change.

FGF13 gene changes cause excessive hair growth in a rare condition.

Removing Mediator 1 causes teeth cells to turn into hair cells.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

Hoxc genes control hair growth through Wnt signaling.

Human hair has a protective lipid layer that can be damaged by moisture and treatments, affecting hair growth and health.

SCUBE3 is a potential target for cancer and alopecia treatment but is challenging to target due to its varied roles.

Cathepsin L deficiency causes large, abnormal cell structures and health issues in mice.

LEF1 interacts with Vitamin D Receptor, affecting hair follicle regeneration and this could be linked to hair loss conditions.

Loss of Pten in certain hair follicle stem cells increases skin cancer risk.

A patient with a new PLEC gene mutation showed symptoms of both muscular dystrophy and myasthenia gravis, which improved with steroid treatment.

A specific gene variation in goats is linked to better growth traits.

The three estrogen receptor genes are highly expressed in zebrafish neuromasts during development.

KAP9.2 and Hoxc13 genes are important for cashmere growth and vary in activity during different stages.