Z
Zev J. Gartner
Researcher at University of California, San Francisco
Publications - 127
Citations - 6907
Zev J. Gartner is an academic researcher from University of California, San Francisco. The author has contributed to research in topics: Medicine & Biology. The author has an hindex of 34, co-authored 105 publications receiving 4824 citations. Previous affiliations of Zev J. Gartner include University of California & Daegu Gyeongbuk Institute of Science and Technology.
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Journal ArticleDOI
DoubletFinder: Doublet Detection in Single-Cell RNA Sequencing Data Using Artificial Nearest Neighbors.
TL;DR: A computational doublet detection tool-DoubletFinder-that identifies doublets using only gene expression data is presented, allowing its application across scRNA-seq datasets with diverse distributions of cell types.
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Boron Nitride Nanotubes Are Noncytotoxic and Can Be Functionalized for Interaction with Proteins and Cells
Xing Chen,Peng Wu,Michael Rousseas,David Okawa,Zev J. Gartner,Alex Zettl,Carolyn R. Bertozzi +6 more
TL;DR: The discovery that boron nitride nanotubes (BNNTs), isosteres of CNTs with unique physical properties, are inherently noncytotoxic is reported and it is shown that BNNTs can deliver DNA oligomers to the interior of cells with no apparent toxicity.
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DNA-Templated Organic Synthesis and Selection of a Library of Macrocycles
TL;DR: This work used multistep DNA-templated organic synthesis to translate libraries of DNA sequences, each containing three “codons,” into libraries of sequence-programmed synthetic small-molecule macrocycles, subjected to in vitro selections for protein affinity.
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MULTI-seq: sample multiplexing for single-cell RNA sequencing using lipid-tagged indices.
Christopher S. McGinnis,David M. Patterson,Juliane Winkler,Daniel N. Conrad,Marco Y. Hein,Marco Y. Hein,Vasudha Srivastava,Jennifer L. Hu,Lyndsay M. Murrow,Jonathan S. Weissman,Jonathan S. Weissman,Zena Werb,Eric D. Chow,Zev J. Gartner +13 more
TL;DR: Tagging live single cells and nuclei with lipid- or cholesterol-modified oligonucleotides enables massive scRNA-seq sample multiplexing, identifies doublets and recovers cells with low RNA content.
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Programmed assembly of 3-dimensional microtissues with defined cellular connectivity
TL;DR: It is demonstrated that the kinetic parameters of the assembly process depend on DNA sequence complexity, density, and total cell concentration, and cell assembly can be highly controlled, enabling the design of microtissues with defined cell composition and stoichiometry.