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Natalie Artzi

Researcher at Massachusetts Institute of Technology

Publications -  89
Citations -  3381

Natalie Artzi is an academic researcher from Massachusetts Institute of Technology. The author has contributed to research in topics: Drug delivery & Medicine. The author has an hindex of 27, co-authored 82 publications receiving 2640 citations. Previous affiliations of Natalie Artzi include Broad Institute & Brigham and Women's Hospital.

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Local triple-combination therapy results in tumour regression and prevents recurrence in a colon cancer model

TL;DR: It is demonstrated that the combination of gene, drug and phototherapy delivered through a prophylactic hydrogel patch leads to complete tumour remission when applied to non-resected tumours and to the absence of tumour recurrence when applied following tumour resection.
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Self-assembled RNA-triple-helix hydrogel scaffold for microRNA modulation in the tumour microenvironment

TL;DR: It is shown that a self-assembled dual-colour RNA-triple-helix structure comprising two miRNAs-a miR mimic (tumour suppressor miRNA) and an antagomiR (oncomiR inhibitor)- provides outstanding capability to synergistically abrogate tumours.
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In vivo and in vitro tracking of erosion in biodegradable materials using non-invasive fluorescence imaging

TL;DR: In this article, the authors track the hydrolytic and enzymatic erosion of model materials by non-invasive fluorescence imaging, which allows the prediction of in vivo erosion from in vitro data.
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Designing Hydrogels for On-Demand Therapy

TL;DR: It is demonstrated that the hydrogel platform developed in the lab, based on dendrimer amine and dextran aldehyde, affords the delivery of a range of therapeutics to combat cancer, including nucleic acids, small molecules, and antibody drugs.
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Dual targeted immunotherapy via in vivo delivery of biohybrid RNAi-peptide nanoparticles to tumour-associated macrophages and cancer cells

TL;DR: The results here suggest that it is likely that the combination of silencing important genes in tumor cells and in their supporting immune cells in the tumor microenvironment, such as TAMs, will greatly improve cancer clinical outcomes.