scholarly journals New Peptide-Based Antimicrobials for Tackling Drug Resistance in Bacteria: Single-Cell Fluorescence Imaging

2013 ◽  
Vol 4 (6) ◽  
pp. 556-559 ◽  
Author(s):  
Jean-Marie Pagès ◽  
Slavka Kascàkovà ◽  
Laure Maigre ◽  
Anas Allam ◽  
Mickael Alimi ◽  
...  
The Analyst ◽  
2018 ◽  
Vol 143 (1) ◽  
pp. 164-174 ◽  
Author(s):  
Yong Zhang ◽  
Ludi Jin ◽  
Jingjing Xu ◽  
Yuezhou Yu ◽  
Lin Shen ◽  
...  

Drug resistance and heterogeneous characteristics of human gastric carcinoma cells (BGC823) under the treatment of paclitaxel (PTX) were investigated using single-cell Raman spectroscopy (RS).


2019 ◽  
Vol 411 (19) ◽  
pp. 4339-4347
Author(s):  
Siwen Wang ◽  
Fei Ji ◽  
Zhonghan Li ◽  
Min Xue

2018 ◽  
Vol 13 (5) ◽  
pp. 1034-1061 ◽  
Author(s):  
David Lando ◽  
Srinjan Basu ◽  
Tim J Stevens ◽  
Andy Riddell ◽  
Kai J Wohlfahrt ◽  
...  

2019 ◽  
Vol 13 (7) ◽  
pp. 1883-1889 ◽  
Author(s):  
Jan-Hendrik Hehemann ◽  
Greta Reintjes ◽  
Leeann Klassen ◽  
Adam D. Smith ◽  
Didier Ndeh ◽  
...  

2017 ◽  
Vol 33 (3) ◽  
pp. 207-210 ◽  
Author(s):  
William Wang ◽  
Xiangdong Wang
Keyword(s):  

2017 ◽  
Vol 35 (1) ◽  
pp. 81-89 ◽  
Author(s):  
Jennifer B. Glass ◽  
Si Chen ◽  
Katherine S. Dawson ◽  
Damian R. Horton ◽  
Stefan Vogt ◽  
...  

2018 ◽  
Author(s):  
Clare Rebbeck ◽  
Florian Raths ◽  
Bassem Ben Cheik ◽  
Kenneth Gouin ◽  
Gregory J. Hannon ◽  
...  

AbstractMolecular barcoding has provided means to link genotype to phenotype, to individuate cells in single-cell analyses, to enable the tracking of evolving lineages, and to facilitate the analysis of complex mixtures containing phenotypically distinct lineages. To date, all existing approaches enable retrospective associations to be made between characteristics and the lineage harbouring them, but provide no path toward isolating or manipulating those lineages within the complex mixture. Here, we describe a strategy for creating functionalized barcodes that enable straightforward manipulation of lineages within complex populations of cells, either marking and retrieval of selected lineages, or modification of their phenotype within the population, including their elimination. These “SmartCodes” rely on a simple CRISPR-based, molecular barcode reader that can switch measurable, or selectable markers, on or off in a binary fashion. While this approach could have broad impact, we envision initial approaches to the study of tumour heterogeneity, focused on issues of tumour progression, metastasis, and drug resistance.


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