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Molecular modeling studies were accomplished using Glide docking tool.
Several studies were accomplished on the interaction of electromagnetic fields with graphene.
Aerodynamic laboratory studies were accomplished in a boundary layer wind tunnel.
Pore volume studies were accomplished by BET, and XRD was used to study crystalline structure of nanotubes.
Biodistribution studies were accomplished in athymic mice with C6 induced tumors that had blocked and unblocked receptors.
Kinetic studies were accomplished by changing the phenol and cyanide concentration and samples were collected at several time intervals till the equilibrium reached.
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Various and comprehensive parametric studies are accomplished and various boundary conditions are considered to extract more precise conclusions.
Further, validation of the interaction studies was accomplished by carrying out molecular docking studies with DNA, RNA and Topo-II targets.
The discovery of potential lead compounds by analogue based design studies was accomplished using 3D-QSAR and pharmacophore modelling of non-nucleoside reverse transcriptase inhibitors.
Ortholog identification and gene annotation of gene array data obtained from published studies was accomplished using ArrayTrack (Food and Drug Administration, NTCR) and/or NetAffix™ (Affymetrix Inc).
When these additional studies are accomplished, we believe that they will have at least three important clinical implications for the study of language change in Alzheimer's disease and other neurodegenerative dementias.
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