Nanofabricated structures, recapitulating the length scale of naturally occurring nanotopographic structures, are now being used to elucidate how physical cues can direct cell behaviour and orchestrate complex cellular processes such as stem cell differentiation and tissue organization.
In order to elucidate how zeolite structure and alkylating agent play roles in the shape-selective catalysis, the alkylation, i.e., isopropylation, sec-butylation, and tert-butylation, of naphthalene (NP) was examined over three-dimensional twelve-membered (12-MR) zeolites, Y (FAU), Beta (BEA), and CIT-1 (CON), and compared to that of H-mordenite (MOR).
To elucidate how βB1 structure and stability are affected by the S228P mutation, we compared the behaviors of the wild type (WT) βB1 and the S228P mutant at the protein and cellular levels.
The average oxygen diffusion and reduction in each CL is directly calculated using pore-scale simulations, and the results are then used in an electrode model to elucidate how the CL structure affects cell performance.
In this paper, our aim is to elucidate how the network structure drives the functional dynamics, and consequently, analyze the ability to reconstruct the physical connectivity of an underlying network.
Although recent studies have begun to elucidate how airway microbial community structure relates to lung disease in cystic fibrosis (CF), microbial community activity and the host's response to changes in this activity are poorly understood.
To elucidate how maturation impacts the structure and mechanics of meniscus extracellular matrix (ECM) at the length scale of collagen fibrils and fibers, we tested the micromechanical properties of fetal and adult bovine menisci via atomic force microscopy (AFM -nanoindentation.
The direct and indirect effects of Dot1 on chromatin organization and gene regulation [ 20, 24, 41] and the redundancy of Dot1 with other pathways of silencing has made it difficult to elucidate how Dot1 affects chromatin structure and function.
To elucidate how unique mRNA secondary structures interact with the translation initiation complex and the scanning ribosome, it will require the development of techniques to determine simultaneously the position of ribosomes on mRNAs and the precise secondary structures at that particular location.
The present study conducted detailed histopathological analyses to elucidate how gastric carcinoma cells may affect the structure and hemodynamics of pulmonary arteries.
To elucidate how its binding to microtubules is regulated, we performed a structure-function analysis of Jvl (Fig. 7L).
