Let’s explore “Inhibin B — lab reference”

The older Purser genetics reference uses the heading “DAOA (AOC1)” in its gut section.

CYP1B1 is the gene name for Cytochrome P450 Family 1 Subfamily B Member 1. Learn what a specific result could mean and what to ask about it.

CYP27B1 is the gene name for Cytochrome P450 Family 27 Subfamily B Member 1. Learn what a specific result could mean and what to ask about it.

We’re going LIVE tomorrow! Join Dan Purser MD on September 5th at 9:00 AM Mountain Time across our social media platforms for a live conversation about health, wellness, and the questions you want answered. Come listen. Come learn. B

Explore B-cell attracting chemokine-1, CXCR5, B cells, follicular helper T cells, and lymphoid structures.

Explore CXCL13, B-cell and follicular helper T-cell movement, germinal centers, and immune-cell organization.

Explore the IFNG variant rs2430561, the +874 T/A position, NF-kappa B, and interferon-gamma regulation.

Explore interleukin-18 receptor 1, IL-18, IFN-gamma, NF-kappa B, NLRP3, and related inflammation and treatment research.

What if the key to feeling better isn't another health trend—but understanding the nutrients your body depends on every day? Vitamin C. B vitamins. Iron. These essential nutrients influence everything from energy production and immune fun

What if the answers you've been searching for aren't found in another prescription—but inside your own cells? Most lab tests tell you what's circulating in your blood. But what if your cells are telling a different story? A Cellular Micro

What if everything you’ve been told about PCOS is missing the real culprit? Homocysteine isn’t just a random lab marker—it may be the hidden thread tying together hormone imbalance, inflammation, and the symptoms so many are struggling to m

PURSER WELLNESSHow To Know If You Have High Homocysteine?A conversation with Dr. Purser

High homocysteine often shows up first as widespread inflammation—pain all over, poor circulation, or even early warning signs of cardiovascular problems like stroke and heart attack. The best way to know for sure is through testing: a blood test can measure homocysteine directly, while a CMA with Redox uncovers the vitamin deficiencies driving it. For genetic causes, the DRP Genetics panel screens 15–16 of the 17 known SNPs that can cause permanently high homocysteine. If your levels are fixed by genetics, reduced glutathione and targeted B vitamins (like MTHFR Daily) are key to balancing the