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Researchers found that certain RNA circles in the brain are linked to disease risk, but their exact role in disease is still unknown.

Dogs with dermatomyositis, especially Collies and Shetland Sheepdogs, need better treatments for their skin and muscle inflammation.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

New research has found 14 genes linked to the risk of developing alopecia areata, improving understanding and treatment options.

The Rotterdam Study updated its design and objectives in 2012, providing insights into various diseases in the elderly, including skin cancer, bone health, liver disease, neurological and psychiatric conditions, and respiratory issues.

Testosterone is linked to cardiovascular risk factors and stroke, but its exact role is unclear.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

Certain gene variations are linked to a higher risk of severe acne, suggesting a genetic influence on the condition.

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

Certain genetic variations are linked to increased androgen levels in PCOS, but more research is needed to understand these connections fully.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

New models predict male pattern baldness better than old ones but still need improvement.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

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

PCOS has a strong genetic basis, but more research is needed to fully understand it.

No strong genetic link to other skin conditions was found, but some genetic factors may make people more likely to get seborrheic dermatitis.

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

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.

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

The conclusion is that certain genetic factors and blood types may affect COVID-19 severity, but changes in ACE2 and TMPRSS2 genes are not clearly linked to it.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

A specific gene variant is linked to a higher risk of hair loss from chemotherapy in breast cancer patients.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

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

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

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

The document concludes that more research is needed to fully understand the causes of PCOS.

Atopic dermatitis increases the risk of some autoimmune diseases.

Genetics and hormones play a role in male and female hair loss, but more research is needed to fully understand it.