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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.

Activating β-catenin in mammary cells leads to changes that cause early-stage abnormal growths similar to skin structures.

Male pattern hair loss caused by follicular miniaturization; early diagnosis and treatment can reduce psychological burden.

The document concludes that hair transplantation and gene therapy may be important for future hair loss treatment.

NSG mice had the most mites, and genetic factors affect immune response and susceptibility.

A specific thyroid hormone resistance mutation may be linked to different types of hair loss.

Managing metabolic syndrome needs both lifestyle changes and medical treatments.

CDP is crucial for lung and hair follicle cell development.

Acne is a chronic disease linked to various systemic conditions and has significant psychological and social effects.

Overexpressing the mineralocorticoid receptor in mouse skin causes skin thinning, early skin barrier development, eye issues, and hair loss.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Asian hair is generally straight and thick, with unique disorders and properties, and more research is needed to understand it fully.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Selective breeding caused the unique curly hair in Mangalitza pigs.

Hidradenitis Suppurativa is a chronic skin condition best treated early with surgery for better outcomes and less recurrence.

Lipase H is important for hair follicle function and shaping hair fibers.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

A specific DNA sequence caused hair loss in male mice by activating immune cells and increasing a certain immune signal.

Discoid Lupus Erythematosus often causes scarring hair loss, is influenced by genetics and environment, and requires early treatment to prevent worsening.

Epidermal stem cells are diverse and vary in activity, playing key roles in skin maintenance and repair.

Noggin overexpression delays eyelid opening by affecting cell death and skin cell development.

Mice lacking Insig proteins had hair growth problems due to cholesterol buildup, but this was fixed by the drug simvastatin.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

No consistent link between genotype and phenotype in 5-α-Reductase type 2 deficiency.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

South American camelids should be sheared early, fleece type affects fiber quality, and the S/P follicle ratio doesn't distinguish between Bolivian llama genotypes.

Thyroid diseases may contribute to autoimmune skin diseases, and more research is needed on their relationship.

Whale genes show changes that help them live in water, like less hair and better flippers.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

MC4R gene variants not linked to female hair loss.