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The Rotterdam Study found risk factors for elderly diseases, links between lifestyle and genetics with health conditions, and aimed to explore new areas like DNA methylation and sensory input effects on brain function.

The research found that PCOS has common genetic factors regardless of how it is diagnosed and is linked to metabolic and reproductive issues.

The document concludes that the fast-growing direct-to-consumer genetic testing market lacks sufficient regulation, posing risks to consumers due to questionable test quality and accuracy.

Pregnancy can cause various skin changes and diseases, with PUPPP being the most common skin condition specific to pregnancy.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Humans lost body hair relatively recently in evolution.

Polycystic Ovary Syndrome likely starts in childhood and may be genetic and influenced by early hormone exposure.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

Researchers found a new gene area linked to male-pattern baldness, which, along with another gene, significantly increases the risk of hair loss in men.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Androgens can both stimulate and cause hair loss, and understanding their effects is key to treating hair disorders.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

Six new genetic regions linked to early hair loss also connect to Parkinson's disease and prostate cancer, possibly leading to new treatments.

Aromatase gene variation may increase female hair loss risk.

Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.

Researchers found 63 genes linked to male-pattern baldness, which could help in understanding its biology and developing new treatments.

AR polyglycine repeat doesn't cause baldness.

Researchers found 15 new genetic links to skin traits in Japanese women.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.

Reduced AR gene methylation may cause early pubic hair growth in girls.

A gene called HDAC9 might be a new factor in male-pattern baldness.

Genes and hormones cause hair loss, with four genes contributing equally.

DNA variants can predict male pattern baldness, with higher risk scores increasing baldness likelihood.

Hair diversity is influenced by complex genetics and environmental factors, requiring more research for practical solutions.

Genetic variations affecting skin structure play a key role in severe acne.

Female pattern hair loss has unclear causes, possibly involving genetics, hormones, and environment, and needs better treatments.

Men with Kennedy disease have less chance of hair loss.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.