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Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

The trial aims to understand how obesity and lifestyle affect circadian rhythms in people with schizophrenia and bipolar disorder.

The document concludes that patient outcomes for Congenital Adrenal Hyperplasia are often not ideal because of poor management and a need for better diagnosis and treatment methods.

The meeting highlighted the genetic basis of female pattern hair loss and various skin health insights.

Researchers created human hair follicles using a new method that could help treat hair loss.

Male hormones like testosterone may make COVID-19 worse, and testing for sensitivity to these hormones could help predict how severe a patient's symptoms might be. Treatments that reduce these hormones are being explored.

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

Acne is caused by genetics, diet, hormones, and bacteria, with treatments not yet curative.

The document concludes that more research is needed to understand excessive hair growth in women with normal hormone levels and regular ovulation.

Male hormones cause different growth in identical human hair follicles due to their unique epigenetic characteristics.

Hormones and genetics play key roles in male and female baldness, which can affect mental health and may be linked to other health issues.

New technologies help us better understand how skin microbes affect skin diseases.

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

Fluconazole can cause hair loss, but the exact cause is unknown.

Genetic differences within ethnic groups may affect prostate cancer treatment effectiveness.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

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.

A special gene region controls the re-emergence of a primitive wool type in Merino sheep, improving their wool yield and adaptability.

The conclusion is that adult males with muscle weakness and hormonal imbalances should be tested for Kennedy's disease.

UK medical students lack dermatology education, liver biopsy patients with risk factors show more fibrosis, and certain fungi resist drugs due to melanin; genetics may influence female hair loss.

The workshop highlighted the genetic links and psychological impacts of hair loss and skin disorders.

Thymic mesenchymal cells have unique gene expression that supports their specific functions in the thymus.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

Mutations in the glucocorticoid receptor gene cause reduced sensitivity to glucocorticoids and may lead to poor response to treatment.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

Melatonin increased the activity of a hair growth gene in Cashmere goats.

AR polyglycine repeat doesn't cause baldness.

Sleep, testosterone levels, and a specific enzyme activity affect skin oil production in women.

Scientists made a mouse that shows how a specific protein in the skin changes and affects hair growth and shape.