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Arjun Raj

Researcher at University of Pennsylvania

Publications -  142
Citations -  21547

Arjun Raj is an academic researcher from University of Pennsylvania. The author has contributed to research in topics: RNA & Gene. The author has an hindex of 50, co-authored 131 publications receiving 18166 citations. Previous affiliations of Arjun Raj include Rutgers University & University of California, San Diego.

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Systems biology: Molecular memoirs of a cellular family

TL;DR: A system that introduces random modifications to barcode sequences embedded in cells' DNA allows lineage relationships between cells to be discerned, while preserving the cells' spatial relationships.
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Systematically quantifying morphological features reveals constraints on organoid phenotypes

TL;DR: In this article, the authors establish a framework to identify constraints on an organoid's morphological features by quantifying them from microscopy images of organoids exposed to a range of perturbations.
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Replication defective viral genomes exploit a cellular pro-survival mechanism to establish paramyxovirus persistence

TL;DR: TNF is identified as a pivotal factor in determining cell fate during a viral infection and a MAVS/TNFR2-mediated mechanism that drives the persistence of otherwise acute viruses is delineated.
Posted ContentDOI

Responsiveness to perturbations is a hallmark of transcription factors that maintain cell identity

TL;DR: Perturbation Panel Profiling (P3) was developed as a framework for perturbing cells in dozens of conditions and measuring gene expression responsiveness transcriptome-wide and it was proposed that responsiveness to perturbations is a property of factors that help maintain cellular identity.
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Metastatic potential in clonal melanoma cells is driven by a rare, early-invading subpopulation

TL;DR: It is shown that rare, highly invasive melanoma cells can appear even within clonal cell lines due to non-genetic fluctuations, and these differences were intrinsic to the cells independent of their external context, and were marked by transiently high levels of SEMA3C expression.