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The study found that alopecia areata and hypothyroidism increase the risk of each other, but androgenetic alopecia and hypothyroidism do not.

Genetic research may lead to better ways to predict and treat male-pattern hair loss.

New gene discoveries have improved diagnosis and treatment for skin and hair disorders, but more research is needed to fully understand them.

More precise, personalized therapies are needed for autoimmune diseases.

Most COVID-19 patients in hospitals have androgenetic alopecia, more in men, suggesting a link between androgen sensitivity and severe COVID-19 symptoms.

Shift work disrupts the body's natural clock, leading to health problems.

Women may need different blood pressure guidelines than men for heart disease prevention.

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

Sex hormones like estrogen and testosterone may affect COVID-19 severity differently in men and women, potentially influencing prevention and treatment strategies.

Men who start puberty later may have lower sperm quality and different hormone levels in adulthood.

Atopic dermatitis increases the risk of some autoimmune diseases.

Some nutraceuticals may help in COVID-19 prevention and treatment, but more research is needed.

About 19.4% of Iranian women in the study have Polycystic Ovary Syndrome, with the most common type involving irregular periods and high male hormone levels, but their heart and metabolic health is similar to women without the condition.

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

Understanding hair growth involves complex factors, and more research is needed to improve treatments for hair loss conditions.

Hair loss affects attractiveness but can suggest intelligence, and face perception is complex, involving factors like age and smile.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

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.

Blocking a certain signal in the gp130 receptor can improve tissue healing and lessen osteoarthritis symptoms.

Drug repositioning is a promising way to quickly develop new treatments, especially for rare diseases.

Taller men are seen as more attractive, and hair loss negatively affects attractiveness.

Personalized treatments for hair loss are becoming more effective by using genetic information.

The new hydrogel treatment promotes faster hair growth and better skin health for hair loss.

Multi-omics techniques help understand the molecular causes of androgenetic alopecia.

Men with hair loss are seen as less attractive and shorter, and height is a key factor in attractiveness ratings.

Identified genes linked to male-pattern baldness may help develop new treatments.

Genetic risk for PCOS can affect children's growth, metabolism, and development from early life into adulthood.

Men and women respond differently to drugs for COVID-19, high cholesterol, and diabetes, which suggests a need for personalized treatments.

Male-pattern hair loss is largely influenced by genetics, with key genes identified.