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The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

The research suggests that the global distribution of PCOS is likely due to historical human migration and that genes affecting PCOS may have different impacts on males and females.

HLA-DRB5 and other genes may be linked to alopecia universalis.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

Genetic data can predict male-pattern baldness with moderate accuracy, especially for early-onset cases in some European men.

Swedish men with the E213 A-allele of the androgen receptor have a lower risk of prostate cancer.

DNA profiling in forensics has improved, but predicting physical traits and ancestry from DNA has limitations and requires ethical consideration.

Nellore cattle have genetic variations linked to their adaptation to tropical environments.

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

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

A gene variation is linked to hair thickness in Asians.

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.

The EDAR gene greatly affects hair thickness in Asian populations.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

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.

The study found that in Latin America, ancestry varies by location, influences physical traits, and affects how people perceive their own heritage.

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 Rotterdam Study aims to understand disease causes in the elderly and has found new risk factors and genetic influences on various conditions.

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

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.

AR polyglycine repeat doesn't cause baldness.

Researchers identified specific genes that are important for mouse skin cell development and healing.

Researchers found that most genes affecting drug responses are not fully covered by commercial SNP chips, suggesting the need for more comprehensive tools to optimize drug selection based on genetics.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

Genetic differences within ethnic groups may affect prostate cancer treatment effectiveness.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.