Pathogenesis of bacterial infections and immunity

@article{Liégeois2020b,

title = {An atlas for hemocytes in an insect},

author = {Samuel Liégeois and Dominique Ferrandon},

editor = {Elife},

url = {https://elifesciences.org/articles/59113},

doi = {10.7554/eLife.59113},

year  = {2020},

date = {2020-06-30},

journal = {Elife},

abstract = {Single-cell RNA sequencing has revealed distinct subpopulations of hemocytes in fruit fly larvae},

keywords = {Drosophila, ferrandon, Hemocytes, M3i, single-cell},

pubstate = {published},

tppubtype = {article}

}

@article{Autour2017,

title = {Ultrahigh-Throughput Improvement and Discovery of Enzymes Using Droplet-Based Microfluidic Screening},

author = {A Autour and M Ryckelynck},

url = {https://doi.org/10.3390/mi8040128},

doi = {10.3390/mi8040128},

year  = {2017},

date = {2017-04-18},

journal = {Micromachines},

volume = {8},

number = {4},

pages = {128},

abstract = {Enzymes are extremely valuable tools for industrial, environmental, and biotechnological applications and there is a constant need for improving existing biological catalysts and for discovering new ones. Screening microbe or gene libraries is an efficient way of identifying new enzymes. In this view, droplet-based microfluidics appears to be one of the most powerful approaches as it allows inexpensive screenings in well-controlled conditions and an ultrahigh-throughput regime. This review aims to introduce the main microfluidic devices and concepts to be considered for such screening before presenting and discussing the latest successful applications of the technology for enzyme discovery. },

keywords = {directed evolution, droplet-based microfluidics, enzyme improvement, high-throughput screening, RYCKELYNCK, single-cell, Unité ARN},

pubstate = {published},

tppubtype = {article}

}