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A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

A man with myotonic dystrophy type 1 had 28 skin cancers, suggesting a link between the disease and skin cancer, emphasizing the need for sun protection and regular skin checks.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

Patients with myotonic dystrophy often have skin problems that suggest early aging and vitamin D issues, and the severity of these problems is linked to their genetic condition and vitamin D levels.

Myotonic dystrophy should be considered in patients with hair thinning, and genetic counseling is important.

Eating too much selenium can cause bad breath, hair loss, and nail changes, with harmful effects starting at low daily doses.

Intermediate filaments are crucial for cell differentiation and stem cell function.

The document is a detailed guide on skin conditions and treatments for dermatologists.

Small molecule drugs show promise for advancing regenerative medicine but still face development challenges.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

Gene therapy in mice increased lifespan and improved health without causing cancer.

Understanding skin structure and development helps diagnose and treat skin disorders.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

The document concludes that more research is needed to understand how to treat muscle pain with drugs.

The document concludes that Syndromes of Severe Insulin Resistance are rare disorders with limited treatment options.

The document concludes that more research is needed to reduce frequent hospital visits, addiction medicine education improves with specific training, early breast cancer surgery findings are emerging, nipple smears are not very accurate, surgery for older melanoma patients doesn't extend life, a genetic condition in infants can often be treated with one drug, doctors are inconsistent with blood clot medication, a certain gene may protect against cell damage, muscle gene overexpression affects many other genes, and some mitochondrial genes are less active in mice with tumors.

New therapies are being developed that target integrin pathways to treat various diseases.

Environmental factors can cause mutations in skin proteins, leading to skin disorders.

Epigenetic factors play a crucial role in skin health and disease.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Improving maternal diets can prevent severe health issues, including death, from goiter in goat kids.

IL-33 is linked to hair follicle damage in psoriasis and could be a treatment target for hair loss in this condition.

Knocking out certain genes in mice helps understand skin and hair growth problems.

Hair loss in male pattern baldness involves muscle degeneration and increased scalp fat.

Adrenal disorders can cause lasting brain and behavior issues in children.

The arrector pili muscle might play a role in hair loss and needs more research to understand its impact.

Severe insulin resistance can be managed with medication, lifestyle changes, and treatment for related conditions.

Finasteride increased hair count and regrowth in men with hair loss but also caused more sexual side effects than placebo.

Treg cells help repair and regenerate tissues by interacting with local cells.

Targeting and modifying the stem cell niche can improve regenerative therapies.