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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.

Genes play a significant role in male-pattern baldness, and understanding them could lead to new treatments and insights into related health issues.

Human leukocytes and beard hair follicle cells have internal daily clocks, and PER1 and PER3 genes may indicate individual circadian rhythms.

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.

The document concludes that validated methods are needed to ensure the quality of fluconazole drugs and that new antifungal medications are necessary due to safety and resistance concerns.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

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.

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

Removing a testicular tumor in a dog reduced its aggressive behavior and skin problems.

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

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

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

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.

Scientists successfully edited a goat's genes to grow more and longer cashmere hair.

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

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

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.

Men with early balding showed higher levels of certain genes linked to hair loss and possibly prostate cancer.

Four genetic risk areas related to male-pattern baldness were identified, with WNT signaling playing a role in its development.

Dr. Rodney Sinclair uses a detailed grading system to diagnose female pattern hair loss, recommends daily spironolactone and minoxidil for treatment, and believes genetics play a role in the condition.