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Current treatments for male pattern baldness include minoxidil and finasteride, with new options being developed.

Hairless protein reduces Msx2 gene activity, affecting hair follicle development.

Different ACE2 gene versions may affect COVID-19 impact based on age and suggest some hair loss drugs could be potential treatments.

Changes in KRT17 gene activity linked to wool production in Angora rabbits.

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

The document concludes that Cutaneous Lupus Erythematosus has different forms, is influenced by genetic and environmental factors, and can be treated with various medications, but more targeted therapies are needed.

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

Higher miR-34a levels and the A variant of the MIR-34A gene are linked to increased risk and severity of alopecia areata.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

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.

The rhg mutation in mice affects the Oat gene, causing hair growth issues and other symptoms.

Case-only trees and random forests improve predictions of treatment effects in clinical trials.

DNA profiling in forensics has improved, but predicting physical traits and ancestry from DNA has limitations and requires ethical consideration.

High levels of TNF-α may contribute to obesity and insulin resistance in PCOS, but not due to the C850T genetic variation.

Mutations in certain receptors can cause diseases and offer new treatment options.

Researchers identified genes in scalp hair follicles that may affect hair traits and hair loss.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

Certain genes and nutrients like vitamin D, zinc, and omega fatty acids affect COVID-19 severity and infection risk.

The conclusion is that many small genetic variations influence claw disorders in cows, and using genomic selection could help reduce these disorders.

The document concludes that insulin resistance is key in PCOS development and early treatment is crucial to prevent complications.

Exposure to too much androgen before birth might cause polycystic ovary syndrome later in life.

Androgen receptors are key for development and health, affecting conditions like prostate cancer and male pattern baldness.

Insulin resistance contributes to hormone imbalances in many women with polycystic ovary syndrome.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

Low and ultralow doses of flutamide can cause liver damage in young women with high androgen levels, regardless of dose or birth control use, with higher risk for those with higher BMI and liver enzyme levels before treatment.

Genes related to pigmentation, body rhythms, and behavior change during hares' seasonal coat color transition, with a common genetic mechanism in two hare species.

Night shift work disrupts the body's natural clock genes.

Low birthweight and rapid weight gain after birth may increase the risk of developing polycystic ovary syndrome.