Congenital glucose-galactose malabsorption

Glucose–galactose malabsorption (GGM) is an autosomal recessive disease caused by mutations in the Na+/glucose cotransporter gene… (More)

With the advent of high-throughput targeted metabolic profiling techniques, the question of how to interpret and analyze the… (More)

Biological networks characterize the interactions of biomolecules at a systems-level. One important property of biological… (More)

We describe a gene network for the Arabidopsis thaliana transcriptome based on a modified graphical Gaussian model (GGM). Through… (More)

There are two broad classes of models used to address the econometric problems caused by skewness in data commonly encountered in… (More)

Glucose-galactose malabsorption (GGM) is a rare autosomal recessive disorder of intestinal transport of glucose and galactose… (More)

MOTIVATION Recent advances in DNA microarray technologies have made it possible to measure the expression levels of thousands of… (More)

In a gauge theory of weak and associated interactions (electromagnetic, strong .... ) in which parity and time reversal are… (More)

Introduction Congenital glucose galactose malabsorption (CGGM) is a rare autosomal recessive disorder, which presents as a… (More)

Glucose/galactose malabsorption (GGM) is an autosomal recessive disease manifesting within the first weeks of life and… (More)