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Androgenetic alopecia in men is genetic and linked to health issues like obesity and heart disease, with treatments including minoxidil, finasteride, and hair transplants.

Certain genetic mutations can lower bad cholesterol and reduce heart disease risk, leading to effective cholesterol-lowering drugs.

The study developed a 3D model that closely imitates remaining ovarian cancer after treatment and identified a potential drug targeting resistant cancer cells.

Alopecia Areata is an autoimmune disease affecting hair follicles, influenced by genetic and environmental factors, with rodent models being essential for research.

Research on Hutchinson-Gilford progeria syndrome could help understand normal aging and heart disease.

Premature aging increases the risk of immune problems and autoimmune diseases.

Large data can lead to new medical discoveries and personalized medicine.

Alopecia areata is likely caused by a combination of genetic factors and immune system dysfunction, and may represent different diseases with various causes.

Genetic differences may affect COVID-19 deaths; anti-androgens could be potential treatment.

Polycystic ovary syndrome (PCOS) was first described in 1721, officially diagnosed in the 1990s, and is now known to be partly genetic and linked to insulin resistance, with increased risk of cardiovascular disease and carbohydrate metabolism issues.

Understanding intermediate filaments helps explain hair health and related diseases.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

Zebrafish are useful for studying and developing treatments for human skin diseases.

Alopecia areata is an autoimmune condition causing hair loss due to the immune system attacking hair follicles, often influenced by genetics and stress.

Men's sensitivity to male hormones might affect how severe COVID-19 gets for them.

Men are more likely to get infectious skin diseases, while women are more prone to autoimmune and pigment-related skin conditions, influenced by biological and environmental factors.

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

People with anhidrotic ectodermal dysplasia may get severe bronchitis if exposed to dust.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

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

Increasing isoleucine intake improved skin and health issues in an infant with maple syrup urine disease.

Atopic dermatitis increases the risk of some autoimmune diseases.

Some skin diseases and their treatments can negatively affect male fertility.

The A allele of the C2 gene increases the risk of lupus, while the G allele may protect against it.

Certain genetic differences may affect how likely someone is to get COVID-19 and how severe it might be.

The document concludes that periocular hair disorders have various causes and treatments, and proper evaluation by specialists is important for management and prognosis.

Antifungal treatment can improve severe skin infections with cutaneous horns.

The cause of Frontal fibrosing alopecia, a type of hair loss, is complex, likely involving immune responses and genetics, but is not fully understood.

Men may be more vulnerable to severe COVID-19 due to genetic and hormonal factors, but more research is needed.

Susan Lee Lindquist was a pioneering biologist who made significant contributions to understanding protein folding and its role in disease.