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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.

Blocking prolactin increases the activity of secondary hair follicles in cashmere goats.

Androgens may worsen COVID-19 and hair loss could indicate the disease's severity.

Alopecia areata is an autoimmune condition causing hair loss, linked to genetic factors and immune system issues, with no cure yet.

Certain genes influence immunoglobulin levels in Chinese Holstein cows, which can improve calf health.

The Rotterdam Study updated findings on elderly health, focusing on heart disease, genetics, lifestyle effects, and disease understanding.

Genetic variants linked to ten skin diseases were found, showing both immune and non-immune factors play a role.

Minoxidil can reduce functions related to androgen receptors.

Hair follicles are normally protected from the immune system, but when this protection fails, it can cause hair loss in alopecia areata.

Different hair types in mammals are linked to variations in specific protein genes, with changes influenced by their living environments.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

The research confirms that Hidradenitis Suppurativa is characterized by increased inflammation, disrupted skin cell organization, and abnormal metabolic processes.

Shorter telomeres in white blood cells may increase the risk of a common type of hair loss.

Some canine hair follicle tumors contain amyloid deposits, with a protein called CK5 involved in their formation.

Male pattern baldness does not cause an increased risk of prostate cancer.

DNA changes in tetraploid wheat improve root growth and nitrogen use.