Water molecules that mediate the binding are shown as small red spheres.
These results demonstrate that in the pathophysiology of SGVHD, there is a redundancy in the TH17 effector molecules that mediate the development of SGVHD.
The authors also identify organelle-specific molecules that mediate the tethering between these two organelles and demonstrate that lysosome mitochondrion contacts allow bidirectional regulation of the dynamics of these organelles.
We will discuss several of the key signaling molecules that mediate the interactions between humans and their microbiomes, such as human-produced antimicrobial peptides, microbial pheromones, bacterial peptide toxins and neuroactive microbial metabolites.
We describe the signaling molecules that mediate the interactions of these cell types in their "fibrosis of two", including transforming growth factor-β, connective tissue growth factor, sonic hedgehog, prostaglandin E2, angiotensin II and reactive oxygen species.
The details of these functions are covered in other articles; here we focus on the interactions between DNA and other molecules that mediate the function of the genome.
Physically, the linker is constituted by the motor and other molecules that mediate its attachment to the organelle.
Traditionally, β-arrestins are recognized as molecules that mediate the homologous desensitization and clathrin-dependent endocytosis of 7TMRs [5].
Previously, those two integrins were shown to be dominant adhesion molecules that mediate the attachment of chondrocytes [ 36, 37].
HSPGs (heparan sulphate proteoglycans) are another group of molecules that mediate the lateral diffusion of Wnt proteins.
Endothelial cells express an array of adhesion molecules that mediate the process of leukocyte attachment to the vascular wall during inflammation [ 2].
