KRT4 gene
The KRT4 gene, also known as Keratin 4, is a gene that plays a crucial role in the health of the human body. It is a scientific gene that has been extensively studied and researched by professionals in the field.…
Expert
What are some of the challenges facing precision medicine and the Precision Medicine Initiative
Precision medicine is a medical approach that takes into account individual variability in genes, environment, and lifestyle when developing tailored treatment plans. It aims to provide more accurate diagnoses, deliver personalized treatment options, and improve patient outcomes. Precision medicine utilizes…
CDC6 gene
The CDC6 gene is a genetic variant that encodes a protein involved in the regulation of cell division. This gene is also known as the Meier-Gorlin syndrome gene, as mutations in CDC6 have been linked to this condition. The Meier-Gorlin…
RYR2 gene
The RYR2 gene, also known as the Ryanodine receptor 2 gene, is a gene that encodes for the ryanodine receptor 2 protein. Mutations in this gene can lead to various diseases and conditions, including arrhythmogenic right ventricular cardiomyopathy, catecholaminergic polymorphic…
TRPV4 gene
The TRPV4 gene is associated with various diseases and disorders characterized by a wide range of symptoms. This gene is listed in databases such as Auer-Grumbach and PubMed, along with other genes and disorders. References and resources on TRPV4-associated diseases…
DHEA Sulfate Test
The DHEA Sulfate Test is a blood test that measures the level of DHEA-S (dehydroepiandrosterone sulfate) in the body. DHEA-S is a hormone produced by the adrenal glands and testicles (in men) that can be converted into other hormones, such…
Genetic Conditions B
Genetic conditions are disorders caused by abnormalities in an individual’s genetic material. These conditions can be inherited from one or both parents or arise spontaneously due to mutations in genes. One such genetic condition is Genetic Conditions B. Genetic Conditions…
TAP1 gene
The TAP1 gene, also known as the Transporter Associated with Antigen Processing 1 gene, is a genetic variant that is related to a number of diseases and conditions. The gene is part of a complex that is involved in processing…
F12 gene
The F12 gene is responsible for coding the coagulation factor XII, which plays a crucial role in the blood clotting cascade. This gene is located on chromosome 5 and is involved in the production of a protein that is essential…
Colorectal Cancer Screening Tests
Colorectal cancer is a serious disease that affects the colon or rectum. It usually starts as benign growths called polyps, which can become cancerous over time. Detecting and treating colorectal cancer early is crucial for a successful outcome. One of…