Sentence examples for binding studies have provided from inspiring English sources

Data from genomic analysis of yeast transcriptional profiling, yeast two-hybrid screen, cellular localization, and transcription factor binding studies have provided a very thorough understanding of the biological function and regulation of the yeast genome and proteome, as well as allowed computational methods to generate global models of the cellular responses to environmental agents [ 1].

Although providing a structural insight into gal-1 saccharide binding, previous studies have provided a biased picture of how galectins interact with, and affect, the properties of complex, heterogeneous cell-surface glycans.

In vitro binding analyses and structural studies have provided a molecular description of how the ZF-CxxC domain recognizes its DNA substrates.

Despite the lack of crystallographic evidence of a large finger subdomain motion upon nucleotide binding, several stopped-flow fluorescence studies have provided information about various conformational change steps during nucleotide incorporation by the Y-family DNA polymerases, leading to the development of an expanded minimal kinetic pathway.

Molecular docking studies have provided possible binding modes of these inhibitors.

Since the early work of Attali et al [ 1], binding, behavioral, and in vitro physiologic studies have provided evidence supporting the existence of two subtypes of kappa-opioid receptors, kappa-1 and kappa-2.

Preclinical studies have provided evidence for the specific binding of 111In-bevacizumab to VEGF [16, 26].

In the past decade, live-cell single molecule imaging studies have provided unique insights on how DNA-binding molecules such as transcription factors explore the nuclear environment to search for and bind to their targets.

These studies have provided information concerning the structural requirements of substrate binding pockets of enzymes and evaluation of enzyme kinetics.

Previous in vitro and ChIP-chip studies have provided conflicting consensus sequences for the FOXP2-binding site.

Several biochemical and structure-function studies have provided an insight into the molecular details of this binding and delivery.