Author

N. Mandayam

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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Cancer Biology· 2

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1

Frequent Co-Authors

D. Hsu· 2 shared A. Pinzaru· 1 shared H. Alwaseem· 1 shared H. Asgharian· 1 shared H. Goodarzi· 1 shared J. Gao· 1 shared L. B. Earnest-Noble· 1 shared M. C. Passarelli· 1 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersCancer Biology

D. Hsu

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Arginine limitation causes a directed DNA sequence evolution response in colorectal cancer cells

D. Hsu, J. Gao, N. Yamaguchi, A. Pinzaru, N. Mandayam, M. Liberti, S. Heissel, H. Alwaseem, S. Tavazoie, S. Tavazoie

This study shows that arginine limitation in colorectal cancer cells drives DNA sequence evolution away from arginine codons, leading to altered proteins.

bioRxiv · Jan 2, 2023 · PreprintCancer Biology

Two Isoleucyl tRNAs that Decode 'Synonymous' Codons Divergently Regulate Breast Cancer Progression

L. B. Earnest-Noble, D. Hsu, H. Asgharian, N. Mandayam, M. C. Passarelli, H. Goodarzi, S. F. Tavazoie

The paper shows that two isoleucyl tRNAs decode synonymous codons and have opposing effects on breast cancer progression by regulating translation of growth-promoting genes.

bioRxiv · Apr 22, 2021 · PreprintCancer Biology