For these two systems, we characterize the protein interactions of the leaving group, the degree of ordering in the active site solvent, and the extent of opening of the TcTS acceptor site and quantify the various contributions to the computed binding free energy for interaction of lactose or Mu with sialyl-TcTS.
Using this system, we characterized the replication and fitness of 2 isolates of the Makona variant.
As a validation of the system, we characterized the home-cage behaviours of two standard inbred and two non-standard mouse strains.
To clarify how the information carried by different OSNs is integrated by the olfactory system, we characterized the response properties of local inhibitory interneurons and projection neurons in the antennal lobe.
Taking advantage of the efficient reporter design of yeast two-hybrid system, we characterized the TEF3-1 domains in activating gene expression.
Using this system, we characterized the cytoplasmic transcripts from HeLa cells.
Using this system, we characterized control of hydrogen peroxide in various cell systems, such as cells deficient in thioredoxin reductase, sulfhydryl oxidases or subjected to selenium deficiency.
In particular, using the ER-positive MCF7 and ER-negative SkBr3 breast cancer cells as a model system, we characterized the biological properties of MIBE.
Prior to characterizing this variable by organ system, we characterized this variable according to the presence/absence of congenital anomalies, developmental delay, and neuropsychiatric disorders (eg, autism spectrum disorder), as others have reported.
In order to see whether the mtDNA abnormalities observed in tissues could also be reproduced in a cell culture system, we characterized Mpv17−/− and Mpv17+/+ mouse embryonic fibroblasts (MEFs) at different passages.
