Venkatesh Ranjan

ORCID: 0000-0003-2406-1329
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About
Contact & Profiles
Research Areas
  • Chromosomal and Genetic Variations
  • CRISPR and Genetic Engineering
  • Animal Genetics and Reproduction
  • Synthesis and Characterization of Heterocyclic Compounds
  • Synthesis and Biological Evaluation
  • Advanced biosensing and bioanalysis techniques
  • RNA Interference and Gene Delivery
  • Ammonia Synthesis and Nitrogen Reduction
  • Bacteriophages and microbial interactions
  • Proteins in Food Systems
  • Protein Structure and Dynamics
  • Synthesis and biological activity
  • Prion Diseases and Protein Misfolding
  • NMR spectroscopy and applications
  • Graphene research and applications
  • Trace Elements in Health
  • Advanced Neuroimaging Techniques and Applications
  • 2D Materials and Applications

University of North Carolina at Charlotte
2019-2024

Optical Sciences (United States)
2024

Central University of Jharkhand
2015

A detailed discussion has been made for NH <sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">3</sub> affinity towards arsenene sheet. First principle calculations suggest that NH3 get adsorbed on pristine with weak binding. Doping Germanium and Selenium respectively decreased increased energy bnad gap. NBO analysis arsenic (As) valance-p orbital have active participations in binding Ge Se. doping results stronger of to sheet depend upon level...

10.1109/inis.2015.61 article EN 2015-12-01

Much attention has been given to studying the translational diffusion of globular proteins, whereas intrinsically disordered proteins (IDPs) is less studied. In this study, we investigate and how it affected by self-association an IDP, κ-casein, using pulsed-field gradient nuclear magnetic resonance time-resolved Förster energy transfer. Using analysis shape attenuation concentration dependence κ-casein coefficients intermolecular interactions, demonstrate that exhibits continuous...

10.1021/acs.jpcb.4c03625 article EN cc-by The Journal of Physical Chemistry B 2024-08-06

DNA transposons have emerged as promising tools in both gene therapy and functional genomics. In particular, the Sleeping Beauty (SB) transposon has advanced into clinical trials due to its ability stably integrate sequences of choice eukaryotic genomes. The efficiency system depends on interaction between transposase enzyme that facilitates transfer. this study, we assess DNA-binding capabilities variants SB demonstrate structural stability primary DNA-recognition subdomain, PAI, affects...

10.1093/nar/gkae1188 article EN cc-by Nucleic Acids Research 2024-12-09
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