Author

V. Mahajan

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Immunology· 3 Biophysics· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 4 Approach:experimental assay· 3 Assay:bulk RNA-seq· 2 Research Focus:cell signaling & trafficking· 2 Research Focus:differential expression· 2 Organism:human· 2 Organism:mouse· 2 Approach:statistical model· 2

Frequent Co-Authors

S. Pillai· 3 shared F. Alsufyani· 2 shared G. J. Yuen· 2 shared H. Mattoo· 2 shared A. Ruland· 1 shared A. V. Taubenberger· 1 shared C. Werner· 1 shared D. J. Irvine· 1 shared

Activity by Year

2018-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

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3 shared papersImmunology

S. Pillai

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Mapping tumor spheroid mechanics in dependence of 3D microenvironment stiffness and degradability by Brillouin microscopy

V. Mahajan, T. Beck, P. Gregorczyk, A. Ruland, S. Alberti, J. Guck, C. Werner, R. Schluessler, A. V. Taubenberger

This study uses Brillouin microscopy to map tumor spheroid mechanics in 3D hydrogels, showing that stiffness and degradability affect mechanical properties and cell invasion.

bioRxiv · Oct 12, 2021Biophysics

DOCK2 sets the threshold for entry into the virtual memory CD8+ T cell compartment by negatively regulating tonic TCR triggering

E. Demissie, V. Mahajan, F. Alsufyani, S. Kumari, G. J. Yuen, V. Viswanadham, J. Q. Tran, J. J. Moon, D. J. Irvine, S. Pillai

This study shows that DOCK2 deficiency leads to increased virtual memory CD8+ T cells by enhancing TCR sensitivity to weak agonists and reducing tonic TCR triggering.

bioRxiv · Mar 20, 2019Immunology

Alterations in sialic-acid O-acetylation glycoforms during murine erythrocyte development

V. Mahajan, F. Alsufyani, H. Mattoo, I. Rosenberg, S. Pillai

This study shows that CASD1 is essential for 9-O-acetylation of sialic acids on erythroid cells in vivo, and that this modification is recognized by specific virolectins and contributes to the TER-119 epitope.

bioRxiv · Nov 14, 2018Immunology

The expansion in lymphoid organs of IL-4+ BATF+ T follicular helper cells is linked to IgG4 class switching in vivo

S. Pillai, J. Stone, S. Nakamura, T. Kiyoshima, J. Daccache, M. Yamauchi, H. Yamamoto, T. Saeki, M. Moriyama, M. Ohta, N. Ishiguro, G. J. Yuen, S. L. Murphy, V. Mahajan, H. Mattoo, T. Maehara

The paper identifies IL-4+ BATF+ T follicular helper cells in IgG4-related disease that correlate with IgG4 class switching in lymphoid organs.

bioRxiv · Mar 19, 2018Immunology