Join Here   |   Log In
New research on FTO gene variants, FTO and heart disease, viral susceptibility

FTO and m6A Methylation

Recently, researchers discovered that FTO is an m6A eraser that removes methyl groups from mRNA. This discovery has opened up huge avenues of research on topics from cancer to immune response to heart disease.

Hemochromatosis Symptoms, genetics

Building Up Iron: Hemochromatosis mutations

A couple of common mutations can cause you to build up iron, leading to iron overload or hemochromatosis. It is one genetic disease where knowledge is really powerful – you can completely prevent hemochromatosis through blood donations.

PCSK9 gene: Cancer Recurrence & Prevention

PCSK9: Cancer Recurrence & Prevention

Lower PCSK9 levels have been shown in research studies to correlate to a significantly reduced risk of metastatic recurrence in certain types of cancer.

Parkinson's Disease genetic factors and environmental factors, Parkinson's symptoms

Parkinson’s Disease: Genetics plus Environmental Factors

Parkinson’s disease (PD) is not yet fully understood. Researchers think that it is caused by a combo of genetics and environmental factors. Learn more about this disease and the factors that lead to susceptibility.

Back Pain: Genetics, Root Causes, and Solutions

Back Pain: Genetics, Root Causes, and Solutions

For some people, back pain is a daily occurrence that drastically affects their quality of life. For others, it may be an intermittent nagging problem, often without rhyme or reason. Your genes play a role in whether disc degeneration gives you back pain.

Fragile X Syndrome, FMR1 gene variants

Fragile X Syndrome

Fragile X Syndrome is a genetic disorder that can cause changes in a person’s ability to learn and causes alterations in behavior. It is caused by mutations in the FMR1 gene.

COMT and Chronic Pain, Fibromyalgia, chronic back pain, natural supplements to avoid for slow COMT

COMT in Pain Disorders

Genetic polymorphisms in COMT affect how we feel certain types of pain. These variants are linked to increased susceptibility to chronic pain disorders.

Ehlers-Danlos Syncrome, symptoms, genetics of hEDS

Ehlers Danlos Syndrome: Genes, Types, and Treatments

Ehlers-Danlos Syndromes causes changes in the way that collagen forms in the joints, ligaments, and skin. Explore the research on EDS and the genetic mutations that cause some of the subtypes of the disorder.

Lymphedema: Causes and Genetic Pathways

Lymphedema: Causes and Genetic Pathways

Lymphedema can be caused by various factors such as a traumatic injury, genetics, or even cancer. Discover how your genetics influence the risk of developing the condition.

Butyrylcholinesterase (BChE) gene variants

BChE gene: Nightshade sensitivity, Anesthesia risk

Genetic variants of the BChE gene decrease its enzyme’s activity. This can lead to various and seemingly unconnected consequences…such as an increased risk for Parkinson’s or food sensitivity to potatoes.