Gotowa bibliografia na temat „Aminoglycosides uptake”
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Artykuły w czasopismach na temat "Aminoglycosides uptake"
Ford, D. M., R. H. Dahl, C. A. Lamp i B. A. Molitoris. "Apically and basolaterally internalized aminoglycosides colocalize in LLC-PK1 lysosomes and alter cell function". American Journal of Physiology-Cell Physiology 266, nr 1 (1.01.1994): C52—C57. http://dx.doi.org/10.1152/ajpcell.1994.266.1.c52.
Pełny tekst źródłaRodriguez, Mônica B., i Sérgio O. P. Costa. "Spontaneous kanamycin-resistant Escherichia coli mutant with altered periplasmic oligopeptide permease protein (OppA) and impermeability to aminoglycosides". Revista de Microbiologia 30, nr 2 (kwiecień 1999): 153–56. http://dx.doi.org/10.1590/s0001-37141999000200013.
Pełny tekst źródłaMcCollister, Bruce D., Matthew Hoffman, Maroof Husain i Andrés Vázquez-Torres. "Nitric Oxide Protects Bacteria from Aminoglycosides by Blocking the Energy-Dependent Phases of Drug Uptake". Antimicrobial Agents and Chemotherapy 55, nr 5 (22.02.2011): 2189–96. http://dx.doi.org/10.1128/aac.01203-10.
Pełny tekst źródłaEzraty, Benjamin, Alexandra Vergnes, Manuel Banzhaf, Yohann Duverger, Allison Huguenot, Ana Rita Brochado, Shu-Yi Su i in. "Fe-S Cluster Biosynthesis Controls Uptake of Aminoglycosides in a ROS-Less Death Pathway". Science 340, nr 6140 (27.06.2013): 1583–87. http://dx.doi.org/10.1126/science.1238328.
Pełny tekst źródłaMao, Weimin, Mark S. Warren, Angela Lee, Anita Mistry i Olga Lomovskaya. "MexXY-OprM Efflux Pump Is Required for Antagonism of Aminoglycosides by Divalent Cations inPseudomonas aeruginosa". Antimicrobial Agents and Chemotherapy 45, nr 7 (1.07.2001): 2001–7. http://dx.doi.org/10.1128/aac.45.7.2001-2007.2001.
Pełny tekst źródłaKang, Hyung Sub, Dirk Kerstan, Long-jun Dai, Gordon Ritchie i Gary A. Quamme. "Aminoglycosides inhibit hormone-stimulated Mg2+ uptake in mouse distal convoluted tubule cells". Canadian Journal of Physiology and Pharmacology 78, nr 8 (1.08.2000): 595–602. http://dx.doi.org/10.1139/y00-038.
Pełny tekst źródłaJassem, Agatha N., James E. A. Zlosnik, Deborah A. Henry, Robert E. W. Hancock, Robert K. Ernst i David P. Speert. "In VitroSusceptibility of Burkholderia vietnamiensis to Aminoglycosides". Antimicrobial Agents and Chemotherapy 55, nr 5 (14.02.2011): 2256–64. http://dx.doi.org/10.1128/aac.01434-10.
Pełny tekst źródłaHadidi, Kaivin, Ezequiel Wexselblatt, Jeffrey D. Esko i Yitzhak Tor. "Cellular uptake of modified aminoglycosides". Journal of Antibiotics 71, nr 1 (1.11.2017): 142–45. http://dx.doi.org/10.1038/ja.2017.131.
Pełny tekst źródłaJiang, Meiyan, Hongzhe Li, Anastasiya Johnson, Takatoshi Karasawa, Yuan Zhang, William B. Meier, Farshid Taghizadeh, Allan Kachelmeier i Peter S. Steyger. "Inflammation up-regulates cochlear expression of TRPV1 to potentiate drug-induced hearing loss". Science Advances 5, nr 7 (lipiec 2019): eaaw1836. http://dx.doi.org/10.1126/sciadv.aaw1836.
Pełny tekst źródłaSchlessinger, D. "Failure of aminoglycoside antibiotics to kill anaerobic, low-pH, and resistant cultures." Clinical Microbiology Reviews 1, nr 1 (styczeń 1988): 54–59. http://dx.doi.org/10.1128/cmr.1.1.54.
Pełny tekst źródłaRozprawy doktorskie na temat "Aminoglycosides uptake"
Subedi, Yagya P. "Cost-Effective Synthesis, Bioactivity and Cellular Uptake Study of Aminoglycosides with Antimicrobial and Connexin Hemichannel Inhibitory Activity". DigitalCommons@USU, 2019. https://digitalcommons.usu.edu/etd/7699.
Pełny tekst źródłaLang, Manon. "Un nouveau mécanisme d’entrée des aminosides dans les bactéries Gram-négative". Electronic Thesis or Diss., Sorbonne université, 2023. http://www.theses.fr/2023SORUS143.
Pełny tekst źródłaThe number of deaths due to multidrug-resistant bacteria was over one million in 2019, demonstrating that the fight against pathogenic bacteria is a major public health issue. Aminoglycosides (AGs) are broad-spectrum antibiotics, effective against Gram-negative bacteria due to their ability to cross the double membrane barrier using the proton motive force, but the precise mechanism remains to be elucidated. Our laboratory has discovered a novel mechanism of entry of AGs into V. cholerae via sugar transporters. In this study, we showed that overexpression in Escherichia coli of multiple carbohydrate transporters increased sensitivity to AGs while deletion of a single transporter had little impact on sensitivity, suggesting a redundancy of these transporters capable of compensating for each other and limiting the development of resistance. Using a "proof-of-concept" transporter called CmtA, we confirmed that differential entry of AGs was linked to the deletion or overexpression of this transporter. This mechanism is shared with other pathogens, since the same sensitivity to AGs was observed upon overexpression of sugar transporters in Pseudomonas aeruginosa. Increasing the production of these transporters in response to the presence of a substrate in vivo could allow for greater efficacy and lower side effects of AG therapies by allowing better uptake by bacteria. We therefore sought a substrate capable of increasing the expression of transporters involved in AG uptake, and identified the ribonucleoside uridine as an activator. The addition of uridine to the culture medium allows for greater AG uptake in E. coli and did not show a mutant appearance. By mimicking a urinary tract infection with a synthetic medium, the addition of uridine potentiates AG treatment by decreasing the minimum inhibitory concentration of AGs and accelerating death kinetics. We propose uridine as a potentiator of GA treatment by co-administering an AG with uridine to stimulate its entry. This study paves the way for improving these treatments by using carbohydrates to stimulate AGs molecules uptake
Części książek na temat "Aminoglycosides uptake"
Sidders, Ashelyn E., Lauren C. Radlinski, Sarah E. Rowe i Brian P. Conlon. "Stimulating Aminoglycoside Uptake to Kill Staphylococcus aureus Persisters". W Methods in Molecular Biology, 223–36. New York, NY: Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1621-5_15.
Pełny tekst źródłaTulkens, Paul M., i Zoltan Kallay. "Uptake and Subcellular Distribution of Poly-L-Aspartic Acid, a Protectant Against Aminoglycoside-Induced Nephrotoxicity, in Rat Kidney Cortex". W Nephrotoxicity, 189–92. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4757-2040-2_27.
Pełny tekst źródłaBuchanan, Ruaridh, i David Wareham. "Mechanisms of Antibiotic Resistance". W Tutorial Topics in Infection for the Combined Infection Training Programme. Oxford University Press, 2019. http://dx.doi.org/10.1093/oso/9780198801740.003.0055.
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