Author

A. S. Chauhan

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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Cell Biology· 2

Signature Assays, Organisms & Methods

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Research Focus:cancer & tumor microenvironment· 2 Research Focus:chromatin & epigenetic regulation· 2 Approach:experimental assay· 2 Organism:human· 2 Research Focus:cell signaling & trafficking· 1 Assay:ChIP-seq· 1 Assay:DNA methylation· 1 Approach:wet-lab / biochemical assay· 1

Frequent Co-Authors

J. R. Morris· 2 shared K. Starowicz· 2 shared M. Jamshad· 2 shared R. M. Densham· 2 shared A. J. Garvin· 1 shared A. K. Walker· 1 shared G. S. Stewart· 1 shared H. L. MacKay· 1 shared

Activity by Year

2018-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersCell Biology

J. R. Morris

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2 papers

Recent·Most cited

The deSUMOylase SENP2 coordinates homologous recombination and non-homologous end joining by independent mechanisms.

A. J. Garvin, A. K. Walker, R. M. Densham, A. S. Chauhan, H. R. Stone, H. L. MacKay, M. Jamshad, K. Starowicz, M. Daza-Martin, J. R. Morris

This study identifies SENP2 as a deSUMOylase that differentially regulates homologous recombination and non-homologous end joining through distinct mechanisms, impacting DSB repair and radioresistance.

Genes & Development · Feb 22, 2019Peer-reviewedCell Biology

PIN1 isomerisation of BRCA1 promotes replication fork protection.

M. R. Daza-Martin, M. Jamshad, K. Starowicz, A. S. Chauhan, J. F. J. Beesley, J. Coles, G. S. Stewart, R. M. Densham, J. R. Morris

This study identifies PIN1-mediated BRCA1 isomerisation as a regulator of replication fork protection through enhanced BRCA1-BARD1-RAD51 interaction, distinct from BRCA1's role in homologous recombination.

bioRxiv · Nov 28, 2018 · PreprintCell Biology