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Fromm, Katja, Ortelli, Monica, Boegli, Alexandra, & bioRxiv. Cold Spring Harbor Laboratory. https://doi.org/10.1101/2024.03.23.586424
. (2024). Translocation of YopJ family effector proteins through the VirB/VirD4 T4SS of Bartonella [Posted-content]. In
Fromm, Katja, Ortelli, Monica, Boegli, Alexandra, & bioRxiv. Cold Spring Harbor Laboratory. https://doi.org/10.1101/2024.03.23.586424
. (2024). Translocation of YopJ family effector proteins through the VirB/VirD4 T4SS of Bartonella [Posted-content]. In
Ketterer, Maren, Chiquet, Petra, Sedzicki, Jaroslaw, Québatte, Maxime, & bioRxiv. Cold Spring Harbor Laboratory. https://doi.org/10.1101/2024.03.18.585630
. (2024). The putative Type 4 secretion system effector BspD is involved in maintaining envelope integrity of the pathogen Brucella [Posted-content]. In
Ketterer, Maren, Chiquet, Petra, Sedzicki, Jaroslaw, Québatte, Maxime, & bioRxiv. Cold Spring Harbor Laboratory. https://doi.org/10.1101/2024.03.18.585630
. (2024). The putative Type 4 secretion system effector BspD is involved in maintaining envelope integrity of the pathogen Brucella [Posted-content]. In
Sedzicki, Jaroslaw, Ni, Dongchun, Lehmann, Frank, Stahlberg, Henning, & Nature Communications, 15. https://doi.org/10.1038/s41467-024-45415-8
. (2024). Structure-function analysis of the cyclic β-1,2-glucan synthase from Agrobacterium tumefaciens.
Sedzicki, Jaroslaw, Ni, Dongchun, Lehmann, Frank, Stahlberg, Henning, & Nature Communications, 15. https://doi.org/10.1038/s41467-024-45415-8
. (2024). Structure-function analysis of the cyclic β-1,2-glucan synthase from Agrobacterium tumefaciens.
Sollier, Julie, Basler, Marek, Broz, Petr, Dittrich, Petra S., Drescher, Knut, Egli, Adrian, Harms, Alexander, Hierlemann, Andreas, Hiller, Sebastian, King, Carolyn G., McKinney, John D., Moran-Gilad, Jacob, Neher, Richard A., Page, Malcolm G. P., Panke, Sven, Persat, Alexandre, Picotti, Paola, Rentsch, Katharina M., Rivera-Fuentes, Pablo, et al. (2024). Revitalizing antibiotic discovery and development through in vitro modelling of in-patient conditions. Nature Microbiology, 9(1), 1–3. https://doi.org/10.1038/s41564-023-01566-w
Sollier, Julie, Basler, Marek, Broz, Petr, Dittrich, Petra S., Drescher, Knut, Egli, Adrian, Harms, Alexander, Hierlemann, Andreas, Hiller, Sebastian, King, Carolyn G., McKinney, John D., Moran-Gilad, Jacob, Neher, Richard A., Page, Malcolm G. P., Panke, Sven, Persat, Alexandre, Picotti, Paola, Rentsch, Katharina M., Rivera-Fuentes, Pablo, et al. (2024). Revitalizing antibiotic discovery and development through in vitro modelling of in-patient conditions. Nature Microbiology, 9(1), 1–3. https://doi.org/10.1038/s41564-023-01566-w
Ma, Fengjiao, Kaufmann, Rainer, Sedzicki, Jaroslaw, Cseresnyés, Zoltán, PLoS ONE, 18. https://doi.org/10.1371/journal.pone.0282803
, Hoeppener, Stephanie, Figge, Marc Thilo, & Heintzmann, Rainer. (2023). Guided-deconvolution for correlative light and electron microscopy.
Ma, Fengjiao, Kaufmann, Rainer, Sedzicki, Jaroslaw, Cseresnyés, Zoltán, PLoS ONE, 18. https://doi.org/10.1371/journal.pone.0282803
, Hoeppener, Stephanie, Figge, Marc Thilo, & Heintzmann, Rainer. (2023). Guided-deconvolution for correlative light and electron microscopy.
Verbeke, Jérémy, Fayt, Youri, Martin, Lisa, Yilmaz, Oya, Sedzicki, Jaroslaw, Reboul, Angéline, Jadot, Michel, Renard, Patricia, EMBO Journal, 42. https://doi.org/10.15252/embj.2022112817
, Renard, Henri-François, Letesson, Jean-Jacques, De Bolle, Xavier, & Arnould, Thierry. (2023). Host cell egress of Brucella abortus requires BNIP3L-mediated mitophagy.
Verbeke, Jérémy, Fayt, Youri, Martin, Lisa, Yilmaz, Oya, Sedzicki, Jaroslaw, Reboul, Angéline, Jadot, Michel, Renard, Patricia, EMBO Journal, 42. https://doi.org/10.15252/embj.2022112817
, Renard, Henri-François, Letesson, Jean-Jacques, De Bolle, Xavier, & Arnould, Thierry. (2023). Host cell egress of Brucella abortus requires BNIP3L-mediated mitophagy.
Alt, Silke, Haggstrom, Douglas, Kessmann, Helmut, Kloss, Florian, Schneider, Christian Elias, Jäger, Timo, Schwede, Torsten, Brakhage, Axel, & Nature Reviews. Drug Discovery, 21(9), 621–622. https://doi.org/10.1038/d41573-022-00138-7
. (2022). INCATE: a partnership to boost the antibiotic pipeline.
Alt, Silke, Haggstrom, Douglas, Kessmann, Helmut, Kloss, Florian, Schneider, Christian Elias, Jäger, Timo, Schwede, Torsten, Brakhage, Axel, & Nature Reviews. Drug Discovery, 21(9), 621–622. https://doi.org/10.1038/d41573-022-00138-7
. (2022). INCATE: a partnership to boost the antibiotic pipeline.
Fromm, Katja, Boegli, Alexandra, Ortelli, Monica, Wagner, Alexander, Bohn, Erwin, Malmsheimer, Silke, Wagner, Samuel, & Frontiers in Microbiology, 13, 913434. https://doi.org/10.3389/fmicb.2022.913434
. (2022). Bartonella taylorii; : A Model Organism for Studying; Bartonella; Infection; in vitro; and; in vivo;
Fromm, Katja, Boegli, Alexandra, Ortelli, Monica, Wagner, Alexander, Bohn, Erwin, Malmsheimer, Silke, Wagner, Samuel, & Frontiers in Microbiology, 13, 913434. https://doi.org/10.3389/fmicb.2022.913434
. (2022). Bartonella taylorii; : A Model Organism for Studying; Bartonella; Infection; in vitro; and; in vivo;
Mode, Selma, Ketterer, Maren, Québatte, Maxime, & PLoS Neglected Tropical Diseases, 16(7), e0010635. https://doi.org/10.1371/journal.pntd.0010635
. (2022). Antibiotic persistence of intracellular Brucella abortus.
Mode, Selma, Ketterer, Maren, Québatte, Maxime, & PLoS Neglected Tropical Diseases, 16(7), e0010635. https://doi.org/10.1371/journal.pntd.0010635
. (2022). Antibiotic persistence of intracellular Brucella abortus.
Sedzicki, Jaroslaw, Ni, Dongchun, Lehmann, Frank, Wu, Na, Zenobi, Renato, Jung, Seunho, Stahlberg, Henning, & Nature Structural and Molecular Biology, 29(12), 1170–1177. https://doi.org/10.1038/s41594-022-00868-7
. (2022). Mechanism of cyclic β-glucan export by ABC transporter Cgt of Brucella.
Sedzicki, Jaroslaw, Ni, Dongchun, Lehmann, Frank, Wu, Na, Zenobi, Renato, Jung, Seunho, Stahlberg, Henning, & Nature Structural and Molecular Biology, 29(12), 1170–1177. https://doi.org/10.1038/s41594-022-00868-7
. (2022). Mechanism of cyclic β-glucan export by ABC transporter Cgt of Brucella.
Siewert, Lena K., PLoS Pathogens, 18(5), e1010489. https://doi.org/10.1371/journal.ppat.1010489
, & Pinschewer, Daniel D. (2022). Adaptive immune defense prevents Bartonella persistence upon trans-placental transmission.
Siewert, Lena K., PLoS Pathogens, 18(5), e1010489. https://doi.org/10.1371/journal.ppat.1010489
, & Pinschewer, Daniel D. (2022). Adaptive immune defense prevents Bartonella persistence upon trans-placental transmission.
Siewert, Lena K., Korotaev, Aleksandr, Sedzicki, Jaroslaw, Fromm, Katja, Pinschewer, Daniel D., & Proceedings of the National Academy of Sciences of the United States of America, 119(25), e2202059119. https://doi.org/10.1073/pnas.2202059119
. (2022). Identification of the; Bartonella; autotransporter CFA as a protective antigen and hypervariable target of neutralizing antibodies in mice.
Siewert, Lena K., Korotaev, Aleksandr, Sedzicki, Jaroslaw, Fromm, Katja, Pinschewer, Daniel D., & Proceedings of the National Academy of Sciences of the United States of America, 119(25), e2202059119. https://doi.org/10.1073/pnas.2202059119
. (2022). Identification of the; Bartonella; autotransporter CFA as a protective antigen and hypervariable target of neutralizing antibodies in mice.
Dietz, Nikolaus, Huber, Markus, Sorg, Isabel, Goepfert, Arnaud, Harms, Alexander, Schirmer, Tilman, & Proceedings of the National Academy of Sciences, 118(12), e2023245118. https://doi.org/10.1073/pnas.2023245118
. (2021). Structural basis for selective AMPylation of Rac-subfamily GTPases by Bartonella effector protein 1 (Bep1).
Dietz, Nikolaus, Huber, Markus, Sorg, Isabel, Goepfert, Arnaud, Harms, Alexander, Schirmer, Tilman, & Proceedings of the National Academy of Sciences, 118(12), e2023245118. https://doi.org/10.1073/pnas.2023245118
. (2021). Structural basis for selective AMPylation of Rac-subfamily GTPases by Bartonella effector protein 1 (Bep1).
Fromm, Katja, & Frontiers in Microbiology, 12, 762582. https://doi.org/10.3389/fmicb.2021.762582
. (2021). The Impact of; Bartonella; VirB/VirD4 Type IV Secretion System Effectors on Eukaryotic Host Cells.
Fromm, Katja, & Frontiers in Microbiology, 12, 762582. https://doi.org/10.3389/fmicb.2021.762582
. (2021). The Impact of; Bartonella; VirB/VirD4 Type IV Secretion System Effectors on Eukaryotic Host Cells.
Marlaire, Simon, & PLoS pathogens, 17(1), e1008548. https://doi.org/10.1371/journal.ppat.1008548
. (2021). Bartonella effector protein C mediates actin stress fiber formation via recruitment of GEF-H1.
Marlaire, Simon, & PLoS pathogens, 17(1), e1008548. https://doi.org/10.1371/journal.ppat.1008548
. (2021). Bartonella effector protein C mediates actin stress fiber formation via recruitment of GEF-H1.
Schirmer, Tilman, de Beer, Tjaart A. P., Tamegger, Stefanie, Harms, Alexander, Dietz, Nikolaus, Dranow, David M., Edwards, Thomas E., Myler, Peter J., Phan, Isabelle, & Microorganisms, 9(8), 23. https://doi.org/10.3390/microorganisms9081645
. (2021). Evolutionary Diversification of Host-Targeted; Bartonella; Effectors Proteins Derived from a Conserved FicTA Toxin-Antitoxin Module.
Schirmer, Tilman, de Beer, Tjaart A. P., Tamegger, Stefanie, Harms, Alexander, Dietz, Nikolaus, Dranow, David M., Edwards, Thomas E., Myler, Peter J., Phan, Isabelle, & Microorganisms, 9(8), 23. https://doi.org/10.3390/microorganisms9081645
. (2021). Evolutionary Diversification of Host-Targeted; Bartonella; Effectors Proteins Derived from a Conserved FicTA Toxin-Antitoxin Module.
Dietz, Nikolaus Balthasar, Huber, Markus, Sorg, Isabel, Goepfert, Arnaud, Harms, Alexander, Schirmer, Tilman, & Structural basis for selective targeting of Rac subfamily GTPases by a bacterial effector protein. bioRxiv. https://doi.org/10.1101/2020.06.29.167221
. (2020).
Dietz, Nikolaus Balthasar, Huber, Markus, Sorg, Isabel, Goepfert, Arnaud, Harms, Alexander, Schirmer, Tilman, & Structural basis for selective targeting of Rac subfamily GTPases by a bacterial effector protein. bioRxiv. https://doi.org/10.1101/2020.06.29.167221
. (2020).
Sorg, Isabel, Schmutz, Christoph, Lu, Yun-Yueh, Fromm, Katja, Siewert, Lena K., Bögli, Alexandra, Strack, Kathrin, Harms, Alexander, & Cell host & microbe, 27(3), 476–485. https://doi.org/10.1016/j.chom.2020.01.015
. (2020). A Bartonella effector acts as signaling hub for intrinsic STAT3 activation to trigger anti-inflammatory responses.
Sorg, Isabel, Schmutz, Christoph, Lu, Yun-Yueh, Fromm, Katja, Siewert, Lena K., Bögli, Alexandra, Strack, Kathrin, Harms, Alexander, & Cell host & microbe, 27(3), 476–485. https://doi.org/10.1016/j.chom.2020.01.015
. (2020). A Bartonella effector acts as signaling hub for intrinsic STAT3 activation to trigger anti-inflammatory responses.
Balaban, Nathalie Q., Helaine, Sophie, Lewis, Kim, Ackermann, Martin, Aldridge, Bree, Andersson, Dan I., Brynildsen, Mark P., Bumann, Dirk, Camilli, Andrew, Collins, James J., Nature Reviews Microbiology, 17(7), 441–448. https://doi.org/10.1038/s41579-019-0196-3
, Fortune, Sarah M., Ghigo, Jean-Marc, Hardt, Wolf-Dietrich, Harms, Alexander, Heinemann, Matthias, Hung, Deborah T., Jenal, Urs, Levin, Bruce R., et al. (2019). Definitions and guidelines for research on antibiotic persistence.
Balaban, Nathalie Q., Helaine, Sophie, Lewis, Kim, Ackermann, Martin, Aldridge, Bree, Andersson, Dan I., Brynildsen, Mark P., Bumann, Dirk, Camilli, Andrew, Collins, James J., Nature Reviews Microbiology, 17(7), 441–448. https://doi.org/10.1038/s41579-019-0196-3
, Fortune, Sarah M., Ghigo, Jean-Marc, Hardt, Wolf-Dietrich, Harms, Alexander, Heinemann, Matthias, Hung, Deborah T., Jenal, Urs, Levin, Bruce R., et al. (2019). Definitions and guidelines for research on antibiotic persistence.
Casanova, Alain, Low, Shyan Huey, Québatte, Maxime, Sedzicki, Jaroslaw, Tschon, Therese, Ketterer, Maren, Smith, Kevin, Emmenlauer, Mario, Ben-Tekaya, Houchaima, & mSphere, 4(3), e00380–19. https://doi.org/10.1128/msphere.00380-19
. (2019). A Role for the VPS Retromer in Brucella Intracellular Replication Revealed by Genomewide siRNA Screening.
Casanova, Alain, Low, Shyan Huey, Québatte, Maxime, Sedzicki, Jaroslaw, Tschon, Therese, Ketterer, Maren, Smith, Kevin, Emmenlauer, Mario, Ben-Tekaya, Houchaima, & mSphere, 4(3), e00380–19. https://doi.org/10.1128/msphere.00380-19
. (2019). A Role for the VPS Retromer in Brucella Intracellular Replication Revealed by Genomewide siRNA Screening.
Cunrath, Olivier, Meinel, Dominik M., Maturana, Pauline, Fanous, Joseph, Buyck, Julien M., Saint Auguste, Pamela, Seth-Smith, Helena M. B., Körner, Jonas, EBioMedicine, 41, 479–487. https://doi.org/10.1016/j.ebiom.2019.02.061
, Trebosc, Vincent, Kemmer, Christian, Neher, Richard, Egli, Adrian, & Bumann, Dirk. (2019). Quantitative contribution of efflux to multi-drug resistance of clinical Escherichia coli and Pseudomonas aeruginosa strains.
Cunrath, Olivier, Meinel, Dominik M., Maturana, Pauline, Fanous, Joseph, Buyck, Julien M., Saint Auguste, Pamela, Seth-Smith, Helena M. B., Körner, Jonas, EBioMedicine, 41, 479–487. https://doi.org/10.1016/j.ebiom.2019.02.061
, Trebosc, Vincent, Kemmer, Christian, Neher, Richard, Egli, Adrian, & Bumann, Dirk. (2019). Quantitative contribution of efflux to multi-drug resistance of clinical Escherichia coli and Pseudomonas aeruginosa strains.
Dirmeier, Simon, Emmenlauer, Mario, BMC Bioinformatics, 20(1), 564. https://doi.org/10.1186/s12859-019-3087-8
, & Beerenwinkel, Niko. (2019). PyBDA: a command line tool for automated analysis of big biological data sets.
Dirmeier, Simon, Emmenlauer, Mario, BMC Bioinformatics, 20(1), 564. https://doi.org/10.1186/s12859-019-3087-8
, & Beerenwinkel, Niko. (2019). PyBDA: a command line tool for automated analysis of big biological data sets.
Liu, Yansheng, Mi, Yang, Müller, Torsten, Kreibich, Saskia, Williams, Evan G., Van Drogen, Audry, Borel, Christelle, Frank, Max, Germain, Pierre-Luc, Bludau, Isabell, Mehnert, Martin, Seifert, Michael, Emmenlauer, Mario, Sorg, Isabel, Bezrukov, Fedor, Sloan Bena, Frederique, Zhou, Hu, Nature Biotechnology, 37(3), 314–322. https://doi.org/10.1038/s41587-019-0037-y
, Testa, Giuseppe, et al. (2019). Multi-omic measurements of heterogeneity in HeLa cells across laboratories.
Liu, Yansheng, Mi, Yang, Müller, Torsten, Kreibich, Saskia, Williams, Evan G., Van Drogen, Audry, Borel, Christelle, Frank, Max, Germain, Pierre-Luc, Bludau, Isabell, Mehnert, Martin, Seifert, Michael, Emmenlauer, Mario, Sorg, Isabel, Bezrukov, Fedor, Sloan Bena, Frederique, Zhou, Hu, Nature Biotechnology, 37(3), 314–322. https://doi.org/10.1038/s41587-019-0037-y
, Testa, Giuseppe, et al. (2019). Multi-omic measurements of heterogeneity in HeLa cells across laboratories.
Québatte, Maxime, & Cellular Microbiology, 21(11), e13068. https://doi.org/10.1111/cmi.13068
. (2019). Bartonella gene transfer agent: Evolution, function, and proposed role in host adaptation.
Québatte, Maxime, & Cellular Microbiology, 21(11), e13068. https://doi.org/10.1111/cmi.13068
. (2019). Bartonella gene transfer agent: Evolution, function, and proposed role in host adaptation.
Wagner, Alexander, & Cellular microbiology, 21(3), e13004. https://doi.org/10.1111/cmi.13004
. (2019). Role of distinct type-IV-secretion systems and secreted effector sets in host adaptation by pathogenic Bartonella species.
Wagner, Alexander, & Cellular microbiology, 21(3), e13004. https://doi.org/10.1111/cmi.13004
. (2019). Role of distinct type-IV-secretion systems and secreted effector sets in host adaptation by pathogenic Bartonella species.
Wagner, Alexander, Tittes, Colin, & Frontiers in Microbiology, 10, 921. https://doi.org/10.3389/fmicb.2019.00921
. (2019). Versatility of the BID Domain: Conserved Function as Type-IV-Secretion-Signal and Secondarily Evolved Effector Functions Within; Bartonella; -Infected Host Cells.
Wagner, Alexander, Tittes, Colin, & Frontiers in Microbiology, 10, 921. https://doi.org/10.3389/fmicb.2019.00921
. (2019). Versatility of the BID Domain: Conserved Function as Type-IV-Secretion-Signal and Secondarily Evolved Effector Functions Within; Bartonella; -Infected Host Cells.
Daga, Neha, Eicher, Simone, Kannan, Abhilash, Casanova, Alain, Low, Shyan H., Kreibich, Saskia, Andritschke, Daniel, Emmenlauer, Mario, Jenkins, Jeremy L., Hardt, Wolf-Dietrich, Greber, Urs F., Nucleic Acids Research, 46(18), 9309–9320. https://doi.org/10.1093/nar/gky798
, & von Mering, Christian. (2018). Growth-restricting effects of siRNA transfections: a largely deterministic combination of off-target binding and hybridization-independent competition.
Daga, Neha, Eicher, Simone, Kannan, Abhilash, Casanova, Alain, Low, Shyan H., Kreibich, Saskia, Andritschke, Daniel, Emmenlauer, Mario, Jenkins, Jeremy L., Hardt, Wolf-Dietrich, Greber, Urs F., Nucleic Acids Research, 46(18), 9309–9320. https://doi.org/10.1093/nar/gky798
, & von Mering, Christian. (2018). Growth-restricting effects of siRNA transfections: a largely deterministic combination of off-target binding and hybridization-independent competition.
Lobet, Elodie, Willemart, Kevin, Ninane, Noëlle, Demazy, Catherine, Sedzicki, Jaroslaw, Lelubre, Christophe, De Bolle, Xavier, Renard, Patricia, Raes, Martine, Scientific Reports, 8(1), 5173. https://doi.org/10.1038/s41598-018-23483-3
, Letesson, Jean-Jacques, & Arnould, Thierry. (2018). Mitochondrial fragmentation affects neither the sensitivity to TNFα-induced apoptosis of Brucella-infected cells nor the intracellular replication of the bacteria.
Lobet, Elodie, Willemart, Kevin, Ninane, Noëlle, Demazy, Catherine, Sedzicki, Jaroslaw, Lelubre, Christophe, De Bolle, Xavier, Renard, Patricia, Raes, Martine, Scientific Reports, 8(1), 5173. https://doi.org/10.1038/s41598-018-23483-3
, Letesson, Jean-Jacques, & Arnould, Thierry. (2018). Mitochondrial fragmentation affects neither the sensitivity to TNFα-induced apoptosis of Brucella-infected cells nor the intracellular replication of the bacteria.
Sedzicki, Jaroslaw, Tschon, Therese, Low, Shyan Huey, Willemart, Kevin, Goldie, Kenneth N., Letesson, Jean-Jacques, Stahlberg, Henning, & Journal of Cell Science, 131(4), jcs. https://doi.org/10.1242/jcs.210799
. (2018). 3D correlative electron microscopy reveals continuity of Brucella -containing vacuoles with the endoplasmic reticulum.
Sedzicki, Jaroslaw, Tschon, Therese, Low, Shyan Huey, Willemart, Kevin, Goldie, Kenneth N., Letesson, Jean-Jacques, Stahlberg, Henning, & Journal of Cell Science, 131(4), jcs. https://doi.org/10.1242/jcs.210799
. (2018). 3D correlative electron microscopy reveals continuity of Brucella -containing vacuoles with the endoplasmic reticulum.
Srivatsa, Sumana, Kuipers, Jack, Schmich, Fabian, Eicher, Simone, Emmenlauer, Mario, Bioinformatics, 34(13), i519–i527. https://doi.org/10.1093/bioinformatics/bty240
, & Beerenwinkel, Niko. (2018). Improved pathway reconstruction from RNA interference screens by exploiting off-target effects.
Srivatsa, Sumana, Kuipers, Jack, Schmich, Fabian, Eicher, Simone, Emmenlauer, Mario, Bioinformatics, 34(13), i519–i527. https://doi.org/10.1093/bioinformatics/bty240
, & Beerenwinkel, Niko. (2018). Improved pathway reconstruction from RNA interference screens by exploiting off-target effects.
Current Opinion in Microbiology, 39, viii–vixi. https://doi.org/10.1016/j.mib.2017.11.024
, & Bumann, Dirk. (2017). Editorial overview: Bacterial systems biology.
Current Opinion in Microbiology, 39, viii–vixi. https://doi.org/10.1016/j.mib.2017.11.024
, & Bumann, Dirk. (2017). Editorial overview: Bacterial systems biology.
Dehio, C., & Tsolis, R. M. (2017). Type IV effector secretion and subversion of host functions by bartonella and brucella species (Vol. 413, pp. 269–295). Springer Verlagservice@springer.de. https://doi.org/10.1007/978-3-319-75241-9_11
Dehio, C., & Tsolis, R. M. (2017). Type IV effector secretion and subversion of host functions by bartonella and brucella species (Vol. 413, pp. 269–295). Springer Verlagservice@springer.de. https://doi.org/10.1007/978-3-319-75241-9_11
González-Prieto, Coral, Gabriel, Richard, Applied and Environmental Microbiology, 83(12), e00207–17. https://doi.org/10.1128/aem.00207-17
, Schmidt, Manfred, & Llosa, Matxalen. (2017). The Conjugative Relaxase TrwC Promotes Integration of Foreign DNA in the Human Genome.
González-Prieto, Coral, Gabriel, Richard, Applied and Environmental Microbiology, 83(12), e00207–17. https://doi.org/10.1128/aem.00207-17
, Schmidt, Manfred, & Llosa, Matxalen. (2017). The Conjugative Relaxase TrwC Promotes Integration of Foreign DNA in the Human Genome.
Harms, Alexander, Liesch, Marius, Körner, Jonas, Québatte, Maxime, Engel, Philipp, & PLoS Genetics, 13(10), e1007077. https://doi.org/10.1371/journal.pgen.1007077
. (2017). A bacterial toxin-antitoxin module is the origin of inter-bacterial and inter-kingdom effectors of Bartonella.
Harms, Alexander, Liesch, Marius, Körner, Jonas, Québatte, Maxime, Engel, Philipp, & PLoS Genetics, 13(10), e1007077. https://doi.org/10.1371/journal.pgen.1007077
. (2017). A bacterial toxin-antitoxin module is the origin of inter-bacterial and inter-kingdom effectors of Bartonella.
Harms, Alexander, Segers, Francisca H. I. D., Quebatte, Maxime, Mistl, Claudia, Manfredi, Pablo, Körner, Jonas, Chomel, Bruno B., Kosoy, Michael, Maruyama, Soichi, Engel, Philipp, & Genome biology and evolution, 9(3), 761–776. https://doi.org/10.1093/gbe/evx042
. (2017). Evolutionary Dynamics of Pathoadaptation Revealed by Three Independent Acquisitions of the VirB/D4 Type IV Secretion System in Bartonella.
Harms, Alexander, Segers, Francisca H. I. D., Quebatte, Maxime, Mistl, Claudia, Manfredi, Pablo, Körner, Jonas, Chomel, Bruno B., Kosoy, Michael, Maruyama, Soichi, Engel, Philipp, & Genome biology and evolution, 9(3), 761–776. https://doi.org/10.1093/gbe/evx042
. (2017). Evolutionary Dynamics of Pathoadaptation Revealed by Three Independent Acquisitions of the VirB/D4 Type IV Secretion System in Bartonella.
Omasits, Ulrich, Varadarajan, Adithi R., Schmid, Michael, Goetze, Sandra, Melidis, Damianos, Bourqui, Marc, Nikolayeva, Olga, Québatte, Maxime, Patrignani, Andrea, Genome Research, 27(12), 2083–2095. https://doi.org/10.1101/gr.218255.116
, Frey, Juerg E., Robinson, Mark D., Wollscheid, Bernd, & Ahrens, Christian H. (2017). An integrative strategy to identify the entire protein coding potential of prokaryotic genomes by proteogenomics.
Omasits, Ulrich, Varadarajan, Adithi R., Schmid, Michael, Goetze, Sandra, Melidis, Damianos, Bourqui, Marc, Nikolayeva, Olga, Québatte, Maxime, Patrignani, Andrea, Genome Research, 27(12), 2083–2095. https://doi.org/10.1101/gr.218255.116
, Frey, Juerg E., Robinson, Mark D., Wollscheid, Bernd, & Ahrens, Christian H. (2017). An integrative strategy to identify the entire protein coding potential of prokaryotic genomes by proteogenomics.
Québatte, Maxime, Christen, Matthias, Harms, Alexander, Körner, Jonas, Christen, Beat, & Cell Systems, 4(6), 611–621. https://doi.org/10.1016/j.cels.2017.05.011
. (2017). Gene Transfer Agent Promotes Evolvability within the Fittest Subpopulation of a Bacterial Pathogen.
Québatte, Maxime, Christen, Matthias, Harms, Alexander, Körner, Jonas, Christen, Beat, & Cell Systems, 4(6), 611–621. https://doi.org/10.1016/j.cels.2017.05.011
. (2017). Gene Transfer Agent Promotes Evolvability within the Fittest Subpopulation of a Bacterial Pathogen.
Québatte, Maxime, & Current Opinion in Microbiology, 39, 34–41. https://doi.org/10.1016/j.mib.2017.08.002
. (2017). Systems-level interference strategies to decipher host factors involved in bacterial pathogen interaction: from RNAi to CRISPRi.
Québatte, Maxime, & Current Opinion in Microbiology, 39, 34–41. https://doi.org/10.1016/j.mib.2017.08.002
. (2017). Systems-level interference strategies to decipher host factors involved in bacterial pathogen interaction: from RNAi to CRISPRi.
Riba, Andrea, Emmenlauer, Mario, Chen, Amy, Sigoillot, Frederic, Cong, Feng, Cell Systems, 4(2), 182–193. https://doi.org/10.1016/j.cels.2017.01.011
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