The scientist’s investigation covers issues in Biochemistry, Stereochemistry, Protein structure, Peptide sequence and Biophysics. In his study, Drug resistance, Microbiology and Xanthone is inextricably linked to Bacteria, which falls within the broad field of Biochemistry. His Protein structure study incorporates themes from Binding site and Cell biology.
His study focuses on the intersection of Peptide sequence and fields such as Peptide with connections in the field of Combinatorial chemistry and Phosphorylation. His work carried out in the field of Biophysics brings together such families of science as Plasma protein binding, Nanotechnology, Adhesive and Molecular dynamics. Chandra S. Verma studied Molecular dynamics and Transcription factor that intersect with Mutant, Mdm2, Cancer, Drug development and Drug discovery.
His scientific interests lie mostly in Biochemistry, Biophysics, Peptide, Stereochemistry and Cell biology. Binding site, Plasma protein binding, Protein–protein interaction and Small molecule are among the areas of Biochemistry where the researcher is concentrating his efforts. Chandra S. Verma has researched Biophysics in several fields, including Molecular dynamics, Mutant, Membrane, Lipid bilayer and Protein structure.
Chandra S. Verma interconnects Mutation, DNA-binding domain and Cancer research in the investigation of issues within Mutant. His research in Peptide intersects with topics in Amino acid, Peptide sequence, Computational biology and Mdm2. His Cell biology research includes elements of Molecular biology and Transcription factor.
Chandra S. Verma spends much of his time researching Cell biology, Biophysics, Cancer research, Peptide and Computational biology. His research integrates issues of Cleavage, Mutant and Binding site in his study of Cell biology. Chandra S. Verma combines subjects such as Molecular dynamics, Mutation, Membrane, Lipid bilayer and Molecule with his study of Biophysics.
His Cancer research research is multidisciplinary, relying on both Bladder cancer, Cancer, Receptor, Kinase and Ubiquitin ligase. His Peptide research is multidisciplinary, incorporating perspectives in Amino acid, Cancer cell, Stereochemistry, Small molecule and Intracellular. His Computational biology research incorporates elements of Eukaryotic translation, Binding affinities, Protein–protein interaction, EIF4E and Drug discovery.
The scientist’s investigation covers issues in Peptide, Cell biology, Small molecule, Computational biology and Biophysics. The various areas that he examines in his Peptide study include Ligand, Cancer cell, Mdm2 and Stereochemistry, Circular dichroism. His Mdm2 study combines topics in areas such as Phosphorylation and Stapled peptide.
His work on Mitochondrion as part of general Cell biology research is frequently linked to Protein glutathionylation, bridging the gap between disciplines. His Small molecule research incorporates themes from Platelet, Unfolded protein response, Allosteric regulation, Binding site and Drug discovery. His studies deal with areas such as Mutation, Lipid bilayer and Druggability as well as Biophysics.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Awakening guardian angels: drugging the p53 pathway
Christopher J. Brown;Sonia Lain;Chandra S. Verma;Alan R. Fersht.
Nature Reviews Cancer (2009)
Drugging the p53 pathway: understanding the route to clinical efficacy
Kian Hoe Khoo;Chandra S. Verma;Chandra S. Verma;Chandra S. Verma;David P. Lane.
Nature Reviews Drug Discovery (2014)
Lapatinib, a HER2 tyrosine kinase inhibitor, induces stabilization and accumulation of HER2 and potentiates trastuzumab-dependent cell cytotoxicity
M Scaltriti;C Verma;M Guzman;J Jimenez.
Oncogene (2009)
Translating p53 into the clinic
Chit Fang Cheok;Chandra S Verma;José Baselga;David P Lane.
Nature Reviews Clinical Oncology (2011)
The crystal structure of the L1 metallo-beta-lactamase from Stenotrophomonas maltophilia at 1.7 A resolution.
J.H. Ullah;T.R. Walsh;T.R. Walsh;I.A. Taylor;D.C. Emery.
Journal of Molecular Biology (1998)
Structural origins of the interfacial activation in Thermomyces (Humicola) lanuginosa lipase.
A M Brzozowski;H Savage;C S Verma;J P Turkenburg.
Biochemistry (2000)
Membrane Active Antimicrobial Peptides: Translating Mechanistic Insights to Design.
Jianguo Li;Jianguo Li;Jun-Jie Koh;Shouping Liu;Rajamani Lakshminarayanan.
Frontiers in Neuroscience (2017)
Stapled Peptides with Improved Potency and Specificity That Activate p53
Christopher J. Brown;Soo T. Quah;Janice Jong;Amanda M. Goh.
ACS Chemical Biology (2013)
The Crystal Structure of the Globular Domain of Sheep Prion Protein
L.F. Haire;S.M. Whyte;N. Vasisht;Andrew C. Gill.
Journal of Molecular Biology (2004)
Erratum: Drugging the p53 pathway: understanding the route to clinical efficacy
Kian Hoe Khoo;Chandra S. Verma;David P. Lane.
Nature Reviews Drug Discovery (2014)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:
Karolinska Institute
Agency for Science, Technology and Research
University of York
National University of Singapore
University of Cambridge
Memorial Sloan Kettering Cancer Center
University of York
MRC Laboratory of Molecular Biology
Nanyang Technological University
Huaqiao University
University of California, Berkeley
University of Cambridge
University of Notre Dame
Zhejiang University
Oregon State University
The Jackson Laboratory
University of Kentucky
The University of Texas Southwestern Medical Center
Oregon State University
Washington State University
University of Arizona
University of Sydney
Northwestern University
University Medical Center Groningen
University of Rouen
Centers for Disease Control and Prevention