Glucose-galactose malabsorption (GGM) is a rare inherited metabolic disorder that prevents the body from absorbing two simple sugars: glucose and galactose. Glucose-galactose malabsorption (GGM) is a ...

Glucose-galactose malabsorption (GGM) is a rare metabolic condition. It occurs when a genetic variation makes the body unable to properly absorb the simple sugars glucose and galactose. Sugars are the ...

Next, we sought to explain the observation regarding absence of positive correlation between display level and activity using strain A6. Sodium dodecyl sulfate (SDS) is a strong anionic surfactant ...

Dietary nutrients are tightly linked to antitumour immune responses 1,2,3,4. Dietary trans-vaccenic acid directly promotes the tumour-infiltrating and cytotoxic functions of CD8 + T cells to suppress ...

We describe a 55-year-old man with the cardiac variant of Fabry's disease who had residual α-galactosidase A activity as the result of a missense mutation encoding a substitution of arginine for ...

Breast milk is full of good things that babies need -- key nutrients, hormones, and antibodies that protect them from disease and keep them healthy. It’s easy to test for galactosemia. It’s also ...

Galactosemia is a genetic disorder in which the body cannot process galactose, which is a simple sugar that is found in many foods. It is actually part of the sugar called lactose, (lactose contains ...

Galactosemia is a rare genetic disorder that affects how your body metabolizes galactose. Galactose is a simple sugar found in milk, cheese, yogurt, and other dairy products. When it’s combined with ...

The following represents disclosure information provided by authors of this manuscript. All relationships are considered compensated unless otherwise noted. Relationships are self-held unless noted. I ...

Cetuximab, a chimeric mouse–human IgG1 monoclonal antibody against the epidermal growth factor receptor, is approved for use in colorectal cancer and squamous-cell carcinoma of the head and neck. A ...