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The study found that androgen receptors in skin cells mainly affect the focal adhesion pathway and control the caveolin-1 gene, with implications for new treatments for related diseases.

Male and female bodies respond differently to stress, influenced by hormones and development stages, with implications for stress-related diseases.

The ACE1 gene variant doesn't affect long-COVID symptoms.

The ABCG2 gene variant increases the risk of high uric acid and cholesterol, especially in overweight or obese young Mexican males.

Increased EGFR gene variations may predict chemotherapy outcomes in small cell lung cancer patients.

A specific gene variation increases the risk of high uric acid and cholesterol in young Mexican males.

Low-penetration genes might help personalize colorectal cancer prevention.

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

A specific gene mutation causes severe skin and nail issues and hair loss.

Cell membrane-coated nanoparticles could improve gene therapy by enhancing delivery and targeting of nucleic acids.

Genetic differences affect COVID-19 severity and treatment effectiveness.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

Gene expression in hair follicles can help diagnose methamphetamine use disorder.

Vitiligo is influenced by genetics and environment, and combining these factors can improve early detection and prevention.

Certain genetic mutations can lower bad cholesterol and reduce heart disease risk, leading to effective cholesterol-lowering drugs.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

Certain genetic differences may affect how likely someone is to get COVID-19 and how severe it might be.

Certain gene changes and hormone levels are linked to female hair loss.

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

LEF1 is essential for the development of airway glands and is regulated by the Wnt/ß-catenin pathway.

AB+ blood group is more common in alopecia areata patients.

Finasteride may lower cholesterol and slow heart disease progression.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

High TSPEAR levels in colorectal cancer predict worse outcomes.

The study suggests smoking is common in HS patients but its role is unclear, and more research is needed to understand HS causes.

Genes linked to fibrosis are more active in people with central centrifugal cicatricial alopecia.

Hormones affect prostate health and disease, with certain hormone imbalances linked to prostate cancer and benign prostatic hyperplasia.

DNA methylation changes in women with PCOS could be used as disease markers and suggest new treatment targets.

Frontal fibrosing alopecia might be linked to autoimmune diseases.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.