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Genetic manipulations that extend lifespan in mice may not work as effectively in humans.

The SNP rs6457452 is linked to a higher risk of alopecia areata in Koreans.

Mutation in hairless gene may increase hair loss risk.

Certain gene variations increase male hair loss risk, influenced by hormone levels.

Mutation in hairless gene may increase hair loss risk.

Hair loss may indicate a higher risk of heart disease and other health issues related to metabolism.

Human enzymes can detoxify harmful substances but might also increase their cancer risk.

The research found that male pattern hair loss is mostly genetic and involves hair thinning due to hormonal effects and changes in gene expression.

Pediatric endocrinologists should provide early fertility counseling and preservation options to young patients at risk of infertility.

Keratins are crucial for cell structure, growth, and disease risk.

Male hormones affect COVID-19 severity and certain drugs targeting these hormones could help reduce the risk.

The document concludes that early recognition and treatment of PCOS in adolescents is crucial for managing symptoms and long-term health risks.

Longer CAG and GGN repeats increase alopecia risk, but no significant link to post-finasteride syndrome found.

Testosterone therapy in transgender men can lead to hair loss, with the risk increasing over time and influenced by family history.

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.

People with Major Depressive Disorder have a higher chance of getting Alopecia Areata, and vice versa; antidepressants may lower this risk.

Family history, especially on the mother's side, increases the risk of female pattern hair loss.

Early-onset baldness is linked to genetics, lifestyle, and can indicate higher risk for heart and metabolic diseases, and affects mental health.

Alopecia areata causes sudden hair loss, has genetic links, and can be managed but not cured.

Genetic marker rs12558842 strongly linked to male hair loss.

Genetic factors alone might not cause pemphigus vulgaris; other factors like birth complications and puberty may trigger it.

iPSCs can help treat genetic skin disorders by creating healthy skin cells from a small biopsy.

Birt–Hogg–Dubé Syndrome requires genetic testing for accurate diagnosis due to its similarities with tuberous sclerosis.

Certain genes are linked to the risk of developing Alopecia Areata.

Afro-textured hair needs personalized care due to its unique genetic traits.

Alopecia Areata affects people of all ages worldwide, is likely caused by genetic and environmental factors, and can lead to stress and depression, highlighting the need for treatments that address both physical and mental health.

Melanoma risk tools need improvement, a gene mutation causes a hair disorder that might be treated by managing cell stress, a potential therapy for a skin-ear disorder involves blocking cell channels, skin wrinkling may indicate lung aging regardless of smoking, and oxidative stress might contribute to common baldness.

Premature aging increases the risk of immune problems and autoimmune diseases.

Rare genetic variants in 125 genes are linked to male-pattern hair loss.

Men with genetic hair loss are more likely to have abnormal blood lipid levels, especially if the hair loss is severe.