N
Natalie J. Holl
Researcher at Missouri University of Science and Technology
Publications - 5
Citations - 104
Natalie J. Holl is an academic researcher from Missouri University of Science and Technology. The author has contributed to research in topics: Cytotoxicity & Cell. The author has an hindex of 3, co-authored 4 publications receiving 23 citations.
Papers
More filters
Journal ArticleDOI
MXene-Graphene Field-Effect Transistor Sensing of Influenza Virus and SARS-CoV-2
Yanxiao Li,Zhekun Peng,Natalie J. Holl,Md. Rifat Hassan,John M. Pappas,Congjie Wei,Omid Hoseini Izadi,Yang Wang,Xiangyang Dong,Cheng Wang,Yue-Wern Huang,Dong-Hyun Kim,Chenglin Wu +12 more
TL;DR: In this paper, an MXene-graphene field effect transistor (FET) sensor for both influenza virus and 2019-nCoV sensing was developed and characterized, which combines the high chemical sensitivity of MXene and the continuity of large-area high-quality graphene to form an ultra-sensitive virus-sensing transduction material (VSTM).
Journal ArticleDOI
Cytotoxicity of NiO and Ni(OH)2 Nanoparticles Is Mediated by Oxidative Stress-Induced Cell Death and Suppression of Cell Proliferation.
Melissa H. Cambre,Natalie J. Holl,Bolin Wang,Lucas Harper,Han-Jung Lee,Charles C. Chusuei,Fang Y S Hou,Ethan T. Williams,Jerry D Argo,Raja R. Pandey,Yue-Wern Huang +10 more
TL;DR: Physical and chemical properties of NPs such as total surface area and metal dissolution are in agreement with the observed differential cytotoxicity in which nickel NPs were toxic to A549 cells but relatively nontoxic to HepG2 cells.
Journal ArticleDOI
Differential Cytotoxicity Induced by Transition Metal Oxide Nanoparticles is a Function of Cell Killing and Suppression of Cell Proliferation.
Larry M. Tolliver,Natalie J. Holl,Fang Yao Stephen Hou,Han-Jung Lee,Melissa H. Cambre,Yue-Wern Huang +5 more
TL;DR: The hypothesis that cell killing and cell proliferative inhibition are essential independent variables in NP-mediated cytotoxicity are supported.
Book ChapterDOI
Lactoferricin-Derived L5a Cell-Penetrating Peptide for Delivery of DNA into Cells.
TL;DR: Methods to study noncovalent interactions between L5a and plasmid DNA, and the delivery of L5A/DNA complexes into cells are described.