The role of F508del variant of the gene CFTR contributing to the Cystic Fibrosis disease mechanism.
Reduced endocytosis of Abeta in the presence of apoE4 results in increased extracellular Abeta concentration and hence an increased rate of amyloid plaque formation.
Mechanism by which NOD2 1007fs variant causes increased Crohn's disease risk
Association of a truncating variant (rs63750245) in MSH2 gene with increased risk for Lynch syndrome.
Relationship between Crohn's risk genetic variants and Mongersen (drug) effectiveness
Effect of ATG16L1 genetic variant interaction with both commensal and pathogenic microbiomes.
Effect of ATG16L1 genetic variant towards Crohn's disease risk
What is the mechanism for TLR9 and NOD2 as epistatic pair for Crohn's disease?
How mutation in NOD2 is linked to increased Crohn's disease risk
The role of variants in TLR9 locus in Crohn's disease
The role of mutation in MUC2 gene for increasing Crohn’s disease risk.
The role of MUC1 genetic variant for Crohn’s disease.
How a GWAS marker on MST1MST1 gene is related to increased risk of Crohn's disease