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Artykuły w czasopismach na temat "Warnericin RK"
Verdon, Julien, Nicolas Girardin, Adrienne Marchand, Yann Héchard i Jean-Marc Berjeaud. "Purification and antibacterial activity of recombinant warnericin RK expressed in Escherichia coli". Applied Microbiology and Biotechnology 97, nr 12 (4.10.2012): 5401–12. http://dx.doi.org/10.1007/s00253-012-4417-1.
Pełny tekst źródłaVerdon, Julien, Mirjam Falge, Elke Maier, Heike Bruhn, Michael Steinert, Cornelius Faber, Roland Benz i Yann Héchard. "Detergent-Like Activity and α-Helical Structure of Warnericin RK, an Anti-Legionella Peptide". Biophysical Journal 97, nr 7 (październik 2009): 1933–40. http://dx.doi.org/10.1016/j.bpj.2009.06.053.
Pełny tekst źródłaVerdon, Julien, Jérome Labanowski, Tobias Sahr, Thierry Ferreira, Christian Lacombe, Carmen Buchrieser, Jean-Marc Berjeaud i Yann Héchard. "Fatty acid composition modulates sensitivity of Legionella pneumophila to warnericin RK, an antimicrobial peptide". Biochimica et Biophysica Acta (BBA) - Biomembranes 1808, nr 4 (kwiecień 2011): 1146–53. http://dx.doi.org/10.1016/j.bbamem.2010.12.011.
Pełny tekst źródłaVerdon, Julien, Jean-Marc Berjeaud, Christian Lacombe i Yann Héchard. "Characterization of anti-Legionella activity of warnericin RK and delta-lysin I from Staphylococcus warneri". Peptides 29, nr 6 (czerwiec 2008): 978–84. http://dx.doi.org/10.1016/j.peptides.2008.01.017.
Pełny tekst źródłaIslam, M. Amirul, Walid M. Hassen, Azam F. Tayabali i Jan J. Dubowski. "Antimicrobial warnericin RK peptide functionalized GaAs/AlGaAs biosensor for highly sensitive and selective detection of Legionella pneumophila". Biochemical Engineering Journal 154 (luty 2020): 107435. http://dx.doi.org/10.1016/j.bej.2019.107435.
Pełny tekst źródłaMarchand, Adrienne, Jacques Augenstreich, Clémence Loiseau, Julien Verdon, Sophie Lecomte i Jean-Marc Berjeaud. "Effect of amino acid substitution in the staphylococcal peptides warnericin RK and PSMα on their anti-Legionella and hemolytic activities". Molecular and Cellular Biochemistry 405, nr 1-2 (14.04.2015): 159–67. http://dx.doi.org/10.1007/s11010-015-2407-1.
Pełny tekst źródłaLoiseau, Clémence, Jacques Augenstreich, Adrienne Marchand, Etienne Harté, Martine Garcia, Julien Verdon, Marc Mesnil, Sophie Lecomte i Jean-Marc Berjeaud. "Specific Anti-Leukemic Activity of the Peptide Warnericin RK and Analogues and Visualization of Their Effect on Cancer Cells by Chemical Raman Imaging". PLOS ONE 11, nr 9 (6.09.2016): e0162007. http://dx.doi.org/10.1371/journal.pone.0162007.
Pełny tekst źródłaIslam, M. Amirul, Walid M. Hassen, Azam F. Tayabali i Jan J. Dubowski. "Short Ligand, Cysteine-Modified Warnericin RK Antimicrobial Peptides Favor Highly Sensitive Detection of Legionella pneumophila". ACS Omega, 6.01.2021. http://dx.doi.org/10.1021/acsomega.0c04753.
Pełny tekst źródłaRozprawy doktorskie na temat "Warnericin RK"
Loison, Lea. "Rôle des interactiοns hôte-micrοbiοte dans la physiοlοgie intestinale et dans les Τrοubles du Cοmpοrtement Alimentaire". Electronic Thesis or Diss., Normandie, 2024. http://www.theses.fr/2024NORMR049.
Pełny tekst źródłaThe gut microbiota constantly interacts with the host. It communicates directly with neighboring intestinal cells as well as with distant organs, including the brain. As a result, the microbiota regulates numerous biological processes and is involved in the pathophysiology of many diseases.We first investigated whether commensal bacteria from the gut microbiota modulate an essential post-translational modification in intestinal physiology, i.e. SUMOylation. It has been demonstrated that gut commensal bacteria can promote SUMOylation through the production of short- and branched-chain fatty acids (SCFA/BCFA). In the present study, we demonstrated that the commensal bacterium Staphylococcus warneri secretes a protein, named Warnericin RK, which targets key components of the SUMOylation machinery, leading to a decrease in intestinal cell’s SUMOylation. This decrease in SUMOylation promotes gut inflammation, and more particularly TNF-dependent inflammatory responses. Collectively, these findings highlight the versatility of mechanisms used by non-pathogenic bacteria in the gut microbiota to regulate host SUMOylation. Additionally, they show that changes in the composition of the gut microbiota may have an impact on gut inflammation by modulating the equilibrium between bacterial effectors enhancing or suppressing SUMOylation.Secondly, we investigated the role of the gut microbiota in the pathophysiology of Binge-Eating Disorder. Indeed, the microbiota is involved in the regulation of eating behaviors through communication along the gut-brain axis. Consequently, it has been hypothesized that the microbiota may be a contributing factor to binge-eating disorder. To investigate the potential causal role of the gut microbiota in this disease, we have transplanted fecal microbiota from patients to recipient mice. Our experimental model did not allow us to demonstrate a role for the microbiota in changes in eating behavior, or in the gastrointestinal and anxiety-depressive disorders associated with binge-eating disorder