This gives you an approximation on how ZINC affects the functionality of the insulin receptor. Insulin resistance or dysfunction and eventual failure occurs when the zinc becomes deficient intracellularly.
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Same as zinc, CHROMIUM is critical to insulin receptor functionality at many different sites on the receptor. Without CR (i.e. chromium) (see the areas I starred in red) the receptors not only become dysfuncyional but die eventually. No rev
Chromium is even more critical than zinc to the glucose transport by the insulin receptor on the cell surface.
Intracellular Chromium deficiencies are fairly common in my practice.
Again early lack of chromium causes reversible insulin re
Zinc is critical for Glucose Transport through the cell wall via the Insulin Receptor.
If you have low intracellular zinc level (much more telling and accurate versus serum levels) then this transport does not occur.
Early and milder is j
…reviews for a solo practitioner MD than any other MD in the country. So I think 1,200 plus I think we figured out um and um doctors aren't very popular. Usually MDs aren't I mean I've known Nature Pass that probably have 10,000 five star re…
…erferon-gamma, and related immune pathways.
Understand the connection
IL-18 belongs to the IL-1 family. It is made as an inactive precursor and can be activated by caspase-1 through inflammasome pathways.
Follow the pathway
Dr. Purser con…
ESR1 encodes estrogen receptor alpha, which helps cells respond to estrogen. Receptor signaling is different from the amount of estrogen measured in blood.
FOLR1 encodes folate receptor alpha, which helps cells take up folate and has an important role in folate transport at the brain’s barriers. Blood folate and folate availability in the nervous system are not identical measurements.
FOLR2 encodes folate receptor beta, a folate-binding protein expressed in particular cell types, including subsets of immune cells. It is distinct from the FOLR1 receptor and the SLC19A1 reduced folate carrier.
G6PC2 encodes a glucose-6-phosphatase-related protein expressed in pancreatic islet cells. Common variation is associated with differences in fasting glucose regulation; it is not the insulin receptor.
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