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Book
Mobile Genetic Elements in Cellular Differentiation, Genome Stability, and Cancer
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Year: 2018 Publisher: Frontiers Media SA

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Abstract

The human genome, as with the genome of most organisms, is comprised of various types of mobile genetic element derived repeats. Mobile genetic elements that mobilize by an RNA intermediate, include both autonomous and non-autonomous retrotransposons, and mobilize by a “copy and paste” mechanism that relies of the presence of a functional reverse transcriptase activity. The extent to which these different types of elements are actively mobilizing varies among organisms, as revealed with the advent of Next Generation DNA sequencing (NGS).To understand the normal and aberrant mechanisms that impact the mobility of these elements requires a more extensive understanding of how these elements interact with molecular pathways of the cell, including DNA repair, recombination and chromatin. In addition, epigenetic based-mechanisms can also influence the mobility of these elements, likely by transcriptional activation or repression in certain cell types. Studies regarding how mobile genetic elements interface and evolve with these pathways will rely on genomic studies from various model organisms. In addition, the mechanistic details of how these elements are regulated will continue to be elucidated with the use of genetic, biochemical, molecular, cellular, and bioinformatic approaches. Remarkably, the current understanding regarding the biology of these elements in the human genome, suggests these elements may impact developmental biology, including cellular differentiation, neuronal development, and immune function. Thus, aberrant changes in these molecular pathways may also impact disease, including neuronal degeneration, autoimmunity, and cancer.


Book
Mobile Genetic Elements in Cellular Differentiation, Genome Stability, and Cancer
Authors: ---
Year: 2018 Publisher: Frontiers Media SA

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Abstract

The human genome, as with the genome of most organisms, is comprised of various types of mobile genetic element derived repeats. Mobile genetic elements that mobilize by an RNA intermediate, include both autonomous and non-autonomous retrotransposons, and mobilize by a “copy and paste” mechanism that relies of the presence of a functional reverse transcriptase activity. The extent to which these different types of elements are actively mobilizing varies among organisms, as revealed with the advent of Next Generation DNA sequencing (NGS).To understand the normal and aberrant mechanisms that impact the mobility of these elements requires a more extensive understanding of how these elements interact with molecular pathways of the cell, including DNA repair, recombination and chromatin. In addition, epigenetic based-mechanisms can also influence the mobility of these elements, likely by transcriptional activation or repression in certain cell types. Studies regarding how mobile genetic elements interface and evolve with these pathways will rely on genomic studies from various model organisms. In addition, the mechanistic details of how these elements are regulated will continue to be elucidated with the use of genetic, biochemical, molecular, cellular, and bioinformatic approaches. Remarkably, the current understanding regarding the biology of these elements in the human genome, suggests these elements may impact developmental biology, including cellular differentiation, neuronal development, and immune function. Thus, aberrant changes in these molecular pathways may also impact disease, including neuronal degeneration, autoimmunity, and cancer.


Book
Mobile Genetic Elements in Cellular Differentiation, Genome Stability, and Cancer
Authors: ---
Year: 2018 Publisher: Frontiers Media SA

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Bookmark

Abstract

The human genome, as with the genome of most organisms, is comprised of various types of mobile genetic element derived repeats. Mobile genetic elements that mobilize by an RNA intermediate, include both autonomous and non-autonomous retrotransposons, and mobilize by a “copy and paste” mechanism that relies of the presence of a functional reverse transcriptase activity. The extent to which these different types of elements are actively mobilizing varies among organisms, as revealed with the advent of Next Generation DNA sequencing (NGS).To understand the normal and aberrant mechanisms that impact the mobility of these elements requires a more extensive understanding of how these elements interact with molecular pathways of the cell, including DNA repair, recombination and chromatin. In addition, epigenetic based-mechanisms can also influence the mobility of these elements, likely by transcriptional activation or repression in certain cell types. Studies regarding how mobile genetic elements interface and evolve with these pathways will rely on genomic studies from various model organisms. In addition, the mechanistic details of how these elements are regulated will continue to be elucidated with the use of genetic, biochemical, molecular, cellular, and bioinformatic approaches. Remarkably, the current understanding regarding the biology of these elements in the human genome, suggests these elements may impact developmental biology, including cellular differentiation, neuronal development, and immune function. Thus, aberrant changes in these molecular pathways may also impact disease, including neuronal degeneration, autoimmunity, and cancer.

Transposition : forty-third symposium of the Society for general microbiology held at Warwick, April 1988
Authors: --- --- ---
ISBN: 0521354641 Year: 1988 Volume: vol 43 Publisher: Cambridge London New York Cambridge University Press


Book
Plasmids of eukaryotes : fundamentals and applications
Author:
ISBN: 3540157980 0387157980 3642825850 9783540157984 Year: 1986 Publisher: Berlin Springer


Book
Carbapenemase-Producing Enterobacterales
Author:
Year: 2022 Publisher: Basel MDPI - Multidisciplinary Digital Publishing Institute

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Abstract

Carbapenem-resistant Enterobacterales (CRE) are a common cause of infections in both community and healthcare settings and have become an increasing threat to public health worldwide. The focus of this Special Issue includes aspects concerning plasmid-mediated antimicrobial resistance along with other carbapenem resistance mechanisms. Understanding the prevalence and routes of transmission of CRE is important in developing specific interventions for healthcare facilities, as well as the general impact of CRE circulation on the environment. Attention has also been focused on carbapenemase testing in order to provide advanced phenotypic and molecular assays for the identification of CRE, as a valid tool for active global surveillance, and from this perspective, the study of resistance mechanisms can provide significant support for the development of new and appropriate antimicrobial molecules. For all of these reasons, the phenomenon of carbapenem resistance deserves more attention, for the sake of public health.

Keywords

Research & information: general --- Biology, life sciences --- Microbiology (non-medical) --- carbapenem resistance --- carbapenemase --- whole genome sequencing --- long reads, plasmid --- Klebsiella pneumoniae --- extensively drug-resistant --- molecular typing --- carbapenemases --- Enterobacteriales --- human --- animal --- food --- environment --- carbapenemase-producing Enterobacterales --- KPC --- carbapenem --- multidrug resistance --- nosocomial --- Enterobacteriaceae --- ESBL --- resistance genes --- cattle --- blaOXA-48 --- ERIC-PCR --- plasmid profile analysis --- biofilm formation --- PCR-based replicon typing --- antibiotic-resistance --- sequence types --- multilocus sequence typing --- plasmids --- antimicrobial resistance --- carbapenem inactivation method --- carbapenem-resistant Enterobacterales --- real-time multiplex PCR --- whole-genome sequencing --- carbapenem-resistance --- Qatar --- CRE --- OXA-48 --- carbapenems resistance --- Gram-negative bacteria --- infection --- colonization --- COVID-19 --- K. pneumoniae --- porins --- ceftazidime/avibactam --- ESKAPE --- healthcare-associated infections --- antimicrobial peptides --- Temporin L --- Klebsiella michiganensis --- Citrobacter farmeri --- KPC-2 --- plasmid --- transposon --- carbapenem-resistant Enterobacteriaceae (CRE) --- outbreak --- infection control --- pulsed-field gel electrophoresis (PFGE) --- multilocus sequence typing (MLST) --- IMP-6 --- porin --- efflux pump --- nosocomial infections --- NDM-1 --- Fourier transform infrared spectroscopy --- Eazyplex® SuperBug CRE assay --- extended-spectrum beta-lactamases --- gram-negative rods --- LAMP method --- NDM --- VIM --- molecular epidemiology --- PFGE --- Carbapenemase producing Enterobacterales --- IncX-3 --- one health --- water --- colistin susceptibility testing --- broth microdilution --- colistin broth disc elution --- Vitek 2 compact --- rapid polymyxin NP test --- Etest --- ChromID colistin R agar --- micronaut MIC-strip colistin --- population analysis profiling --- Enterobacterales --- neonates --- plasmid-typing --- sequence type --- wastewater --- virulence --- carbapenem resistance --- carbapenemase --- whole genome sequencing --- long reads, plasmid --- Klebsiella pneumoniae --- extensively drug-resistant --- molecular typing --- carbapenemases --- Enterobacteriales --- human --- animal --- food --- environment --- carbapenemase-producing Enterobacterales --- KPC --- carbapenem --- multidrug resistance --- nosocomial --- Enterobacteriaceae --- ESBL --- resistance genes --- cattle --- blaOXA-48 --- ERIC-PCR --- plasmid profile analysis --- biofilm formation --- PCR-based replicon typing --- antibiotic-resistance --- sequence types --- multilocus sequence typing --- plasmids --- antimicrobial resistance --- carbapenem inactivation method --- carbapenem-resistant Enterobacterales --- real-time multiplex PCR --- whole-genome sequencing --- carbapenem-resistance --- Qatar --- CRE --- OXA-48 --- carbapenems resistance --- Gram-negative bacteria --- infection --- colonization --- COVID-19 --- K. pneumoniae --- porins --- ceftazidime/avibactam --- ESKAPE --- healthcare-associated infections --- antimicrobial peptides --- Temporin L --- Klebsiella michiganensis --- Citrobacter farmeri --- KPC-2 --- plasmid --- transposon --- carbapenem-resistant Enterobacteriaceae (CRE) --- outbreak --- infection control --- pulsed-field gel electrophoresis (PFGE) --- multilocus sequence typing (MLST) --- IMP-6 --- porin --- efflux pump --- nosocomial infections --- NDM-1 --- Fourier transform infrared spectroscopy --- Eazyplex® SuperBug CRE assay --- extended-spectrum beta-lactamases --- gram-negative rods --- LAMP method --- NDM --- VIM --- molecular epidemiology --- PFGE --- Carbapenemase producing Enterobacterales --- IncX-3 --- one health --- water --- colistin susceptibility testing --- broth microdilution --- colistin broth disc elution --- Vitek 2 compact --- rapid polymyxin NP test --- Etest --- ChromID colistin R agar --- micronaut MIC-strip colistin --- population analysis profiling --- Enterobacterales --- neonates --- plasmid-typing --- sequence type --- wastewater --- virulence


Book
Carbapenemase-Producing Enterobacterales
Author:
Year: 2022 Publisher: Basel MDPI - Multidisciplinary Digital Publishing Institute

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Bookmark

Abstract

Carbapenem-resistant Enterobacterales (CRE) are a common cause of infections in both community and healthcare settings and have become an increasing threat to public health worldwide. The focus of this Special Issue includes aspects concerning plasmid-mediated antimicrobial resistance along with other carbapenem resistance mechanisms. Understanding the prevalence and routes of transmission of CRE is important in developing specific interventions for healthcare facilities, as well as the general impact of CRE circulation on the environment. Attention has also been focused on carbapenemase testing in order to provide advanced phenotypic and molecular assays for the identification of CRE, as a valid tool for active global surveillance, and from this perspective, the study of resistance mechanisms can provide significant support for the development of new and appropriate antimicrobial molecules. For all of these reasons, the phenomenon of carbapenem resistance deserves more attention, for the sake of public health.

Keywords

Research & information: general --- Biology, life sciences --- Microbiology (non-medical) --- carbapenem resistance --- carbapenemase --- whole genome sequencing --- long reads, plasmid --- Klebsiella pneumoniae --- extensively drug-resistant --- molecular typing --- carbapenemases --- Enterobacteriales --- human --- animal --- food --- environment --- carbapenemase-producing Enterobacterales --- KPC --- carbapenem --- multidrug resistance --- nosocomial --- Enterobacteriaceae --- ESBL --- resistance genes --- cattle --- blaOXA-48 --- ERIC-PCR --- plasmid profile analysis --- biofilm formation --- PCR-based replicon typing --- antibiotic-resistance --- sequence types --- multilocus sequence typing --- plasmids --- antimicrobial resistance --- carbapenem inactivation method --- carbapenem-resistant Enterobacterales --- real-time multiplex PCR --- whole-genome sequencing --- carbapenem-resistance --- Qatar --- CRE --- OXA-48 --- carbapenems resistance --- Gram-negative bacteria --- infection --- colonization --- COVID-19 --- K. pneumoniae --- porins --- ceftazidime/avibactam --- ESKAPE --- healthcare-associated infections --- antimicrobial peptides --- Temporin L --- Klebsiella michiganensis --- Citrobacter farmeri --- KPC-2 --- plasmid --- transposon --- carbapenem-resistant Enterobacteriaceae (CRE) --- outbreak --- infection control --- pulsed-field gel electrophoresis (PFGE) --- multilocus sequence typing (MLST) --- IMP-6 --- porin --- efflux pump --- nosocomial infections --- NDM-1 --- Fourier transform infrared spectroscopy --- Eazyplex® SuperBug CRE assay --- extended-spectrum beta-lactamases --- gram-negative rods --- LAMP method --- NDM --- VIM --- molecular epidemiology --- PFGE --- Carbapenemase producing Enterobacterales --- IncX-3 --- one health --- water --- colistin susceptibility testing --- broth microdilution --- colistin broth disc elution --- Vitek 2 compact --- rapid polymyxin NP test --- Etest --- ChromID colistin R agar --- micronaut MIC-strip colistin --- population analysis profiling --- Enterobacterales --- neonates --- plasmid-typing --- sequence type --- wastewater --- virulence


Book
Carbapenemase-Producing Enterobacterales
Author:
Year: 2022 Publisher: Basel MDPI - Multidisciplinary Digital Publishing Institute

Loading...
Export citation

Choose an application

Bookmark

Abstract

Carbapenem-resistant Enterobacterales (CRE) are a common cause of infections in both community and healthcare settings and have become an increasing threat to public health worldwide. The focus of this Special Issue includes aspects concerning plasmid-mediated antimicrobial resistance along with other carbapenem resistance mechanisms. Understanding the prevalence and routes of transmission of CRE is important in developing specific interventions for healthcare facilities, as well as the general impact of CRE circulation on the environment. Attention has also been focused on carbapenemase testing in order to provide advanced phenotypic and molecular assays for the identification of CRE, as a valid tool for active global surveillance, and from this perspective, the study of resistance mechanisms can provide significant support for the development of new and appropriate antimicrobial molecules. For all of these reasons, the phenomenon of carbapenem resistance deserves more attention, for the sake of public health.

Keywords

carbapenem resistance --- carbapenemase --- whole genome sequencing --- long reads, plasmid --- Klebsiella pneumoniae --- extensively drug-resistant --- molecular typing --- carbapenemases --- Enterobacteriales --- human --- animal --- food --- environment --- carbapenemase-producing Enterobacterales --- KPC --- carbapenem --- multidrug resistance --- nosocomial --- Enterobacteriaceae --- ESBL --- resistance genes --- cattle --- blaOXA-48 --- ERIC-PCR --- plasmid profile analysis --- biofilm formation --- PCR-based replicon typing --- antibiotic-resistance --- sequence types --- multilocus sequence typing --- plasmids --- antimicrobial resistance --- carbapenem inactivation method --- carbapenem-resistant Enterobacterales --- real-time multiplex PCR --- whole-genome sequencing --- carbapenem-resistance --- Qatar --- CRE --- OXA-48 --- carbapenems resistance --- Gram-negative bacteria --- infection --- colonization --- COVID-19 --- K. pneumoniae --- porins --- ceftazidime/avibactam --- ESKAPE --- healthcare-associated infections --- antimicrobial peptides --- Temporin L --- Klebsiella michiganensis --- Citrobacter farmeri --- KPC-2 --- plasmid --- transposon --- carbapenem-resistant Enterobacteriaceae (CRE) --- outbreak --- infection control --- pulsed-field gel electrophoresis (PFGE) --- multilocus sequence typing (MLST) --- IMP-6 --- porin --- efflux pump --- nosocomial infections --- NDM-1 --- Fourier transform infrared spectroscopy --- Eazyplex® SuperBug CRE assay --- extended-spectrum beta-lactamases --- gram-negative rods --- LAMP method --- NDM --- VIM --- molecular epidemiology --- PFGE --- Carbapenemase producing Enterobacterales --- IncX-3 --- one health --- water --- colistin susceptibility testing --- broth microdilution --- colistin broth disc elution --- Vitek 2 compact --- rapid polymyxin NP test --- Etest --- ChromID colistin R agar --- micronaut MIC-strip colistin --- population analysis profiling --- Enterobacterales --- neonates --- plasmid-typing --- sequence type --- wastewater --- virulence

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