J
Julius Fredens
Researcher at Laboratory of Molecular Biology
Publications - 13
Citations - 619
Julius Fredens is an academic researcher from Laboratory of Molecular Biology. The author has contributed to research in topics: Genome & Gene. The author has an hindex of 7, co-authored 12 publications receiving 398 citations. Previous affiliations of Julius Fredens include University of Southern Denmark.
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Journal ArticleDOI
Total synthesis of Escherichia coli with a recoded genome
Julius Fredens,Kaihang Wang,Kaihang Wang,Daniel de la Torre,Louise F. H. Funke,Wesley E. Robertson,Yonka Christova,Tiongsun Chia,Wolfgang H. Schmied,Daniel L. Dunkelmann,Václav Beránek,Chayasith Uttamapinant,Andres Gonzalez Llamazares,Thomas S. Elliott,Jason W. Chin +14 more
TL;DR: The number of codons used to encode the canonical amino acids can be reduced, through the genome-wide substitution of target codons by defined synonyms, through a high-fidelity convergent total synthesis.
Journal ArticleDOI
Defining synonymous codon compression schemes by genome recoding
Kaihang Wang,Julius Fredens,Simon F. Brunner,Samuel H. Kim,Samuel H. Kim,Tiongsun Chia,Jason W. Chin,Jason W. Chin +7 more
TL;DR: This work endow E. coli with a system for efficient, programmable replacement of genomic DNA with long synthetic DNA, through the in vivo excision of double-stranded DNA from an episomal replicon by CRISPR/Cas9, coupled to lambda-red-mediated recombination and simultaneous positive and negative selection.
Journal ArticleDOI
Sense codon reassignment enables viral resistance and encoded polymer synthesis.
Wesley E. Robertson,Louise F. H. Funke,Daniel de la Torre,Julius Fredens,Thomas S. Elliott,Martin Spinck,Yonka Christova,Daniele Cervettini,Franz L. Böge,Kim C. Liu,Salvador Buse,Sarah L. Maslen,George P. C. Salmond,Jason W. Chin +13 more
TL;DR: In this article, the authors showed that removing cellular transfer RNAs (tRNAs) might create a genetic firewall to viral infection and enable sense codon reassignment, but it has been impossible to test these hypotheses.
Journal ArticleDOI
Quantitative proteomics by amino acid labeling in C. elegans
Julius Fredens,Kasper Engholm-Keller,Anders M.B. Giessing,Dennis Pultz,Martin R. Larsen,Peter Højrup,Jakob Møller-Jensen,Nils J. Færgeman +7 more
TL;DR: Using heavy isotope–labeled worms and quantitative proteomics methods, several proteins that are regulated in response to loss or RNAi-mediated knockdown of the nuclear hormone receptor 49 in C. elegans are identified.
Journal ArticleDOI
Axon-Dependent Patterning and Maintenance of Somatosensory Dendritic Arbors
Nelson J. Ramirez-Suarez,Helen M. Belalcazar,Christopher J. Salazar,Burcu Beyaz,Benjamin Raja,Ken C. Q. Nguyen,Kevin Celestrin,Julius Fredens,Nils J. Færgeman,David H. Hall,Hannes E. Bülow +10 more
TL;DR: In Caenorhabditis elegans, the SAX-7/L1CAM cell adhesion molecule engages in distinct molecular mechanisms to mediate extensions of PVD 1° dendrites and maintain the ALA-PVD axon-dendritic fascicle, respectively, showing that axons can serve as critical scaffolds to pattern and maintain dendrite formation through contact-dependent but activity-independent mechanisms.