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Olivier Elemento

Researcher at Cornell University

Publications -  596
Citations -  38936

Olivier Elemento is an academic researcher from Cornell University. The author has contributed to research in topics: Medicine & Biology. The author has an hindex of 82, co-authored 471 publications receiving 27739 citations. Previous affiliations of Olivier Elemento include Princeton University & Max Planck Society.

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Towards a better cancer precision medicine: systems biology meets immunotherapy.

TL;DR: It is argued that systems-level approaches are needed to help understand the concerted impact of tumor-specific and immune-specific molecular features on clinical outcomes, predict responders and unravel the complexity of tumor ecosystems.
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Correction: Unmasking Activation of the Zygotic Genome Using Chromosomal Deletions in the Drosophila Embryo

TL;DR: This work shows that the expression profile for at least one third of zygotically active genes is coupled to the concomitant degradation of the corresponding maternal mRNAs, and proposes that this regulatory mode links morphogen gradients with temporal regulation during the maternal-to-zygotic transition.
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Molecular and Pharmacological Bladder Cancer Therapy Screening: Discovery of Clofarabine as a Highly Active Compound.

TL;DR: In this paper , the authors used commercially available cell lines for the identification of novel drugs for the treatment of bladder cancer and confirmed the effects of one of these drugs, clofarabine, in patient derived cell lines and two different mouse models, thereby demonstrating the potential clinical relevance of this substance in bladder cancer treatment.
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Single-cell analysis of the muscle stem cell hierarchy identifies heterotypic communication signals involved in skeletal muscle regeneration

TL;DR: In this article, a hierarchical map of myogenic cell populations and identifying stage-specific regulatory programs that govern their contributions to muscle regeneration is provided. But, a unified organization of muscle stem and progenitor cells and their subpopulations remains unresolved.
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The cytidine deaminase APOBEC3G contributes to cancer mutagenesis and clonal evolution in bladder cancer.

TL;DR: In this article , the mutagenic signatures attributed to APOBEC3 cytidine deaminases are pervasive in human cancers and the authors showed that transgenic expression of human APEC3G promotes mutagenesis, genomic instability, and kataegis, leading to shorter survival in a murine bladder cancer model.