LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 10 of total 24644

Search options

  1. Article: First report of the emergence of CTX-M-type extended-spectrum beta-lactamases (ESBLs) as the predominant ESBL isolated in a U.S. health care system.

    Lewis, James S / Herrera, Monica / Wickes, Brian / Patterson, Jan E / Jorgensen, James H

    Antimicrobial agents and chemotherapy

    2007  Volume 51, Issue 11, Page(s) 4015–4021

    Abstract: CTX-M-type extended-spectrum beta-lactamases (ESBLs) have become increasingly common worldwide ... than ceftazidime, suggesting the possibility of CTX-M-type enzymes. Microbiology laboratory records were reviewed ... of CTX-M, TEM, and SHV ESBLs. Only small numbers of retained ESBL-producing isolates were available ...

    Abstract CTX-M-type extended-spectrum beta-lactamases (ESBLs) have become increasingly common worldwide, with the notable exception of the United States, where TEM- and SHV-type ESBLs have appeared to predominate. We have noted the emergence of ESBLs in our health care system (the University Health System in San Antonio, TX), especially in Escherichia coli isolates, that preferentially hydrolyze cefotaxime rather than ceftazidime, suggesting the possibility of CTX-M-type enzymes. Microbiology laboratory records were reviewed to identify ESBL-producing isolates and to compare the diameters of ceftazidime disk diffusion zones of inhibition to cefotaxime zone diameters. All isolates had been initially detected and confirmed using the procedures recommended by the Clinical and Laboratory Standards Institute. A total of 94 stored ESBL-producing isolates recovered between January 2000 and June 2006 (predominately from blood and normally sterile fluids) were retrieved for further study and screened using PCR primers specific for the presence of CTX-M, TEM, and SHV ESBLs. Only small numbers of retained ESBL-producing isolates were available for study in 2000 and 2002. The percentages of available ESBL-producing organisms in the following years were found to produce CTX-M enzymes: 2000, 25%; 2001, 10%; 2002, 0%; 2003, 60%; 2004, 69%; 2005, 89%; and 2006, 70%. The most common CTX-M-type ESBL was CTX-M-15, followed by CTX-M-16, CTX-M-8, and CTX-M-14. Comparing the disk diffusion zone diameters of cefotaxime and ceftazidime was helpful with the initial recognition of CTX-M-producing E. coli, which had an average cefotaxime zone diameter 7 mm smaller than the ceftazidime zone. However, comparing ceftazidime and cefotaxime zones for CTX-M-producing Klebsiella spp. was not helpful with initial recognition. CTX-M enzymes were also identified in Proteus mirabilis, Enterobacter spp., and Morganella morganii. Based on pulsed-field gel electrophoresis typing of the E. coli isolates, the CTX-M-producing isolates did not represent the spread of a single clone in the institution or in the community. In conclusion, CTX-M-type ESBLs are now the most common ESBL type isolated from patients in our health care system and may also be present but unrecognized in other U.S. locales.
    MeSH term(s) Bacterial Infections/drug therapy ; Bacterial Infections/microbiology ; Cefotaxime/metabolism ; Cefotaxime/pharmacology ; Ceftazidime/metabolism ; Ceftazidime/pharmacology ; Cluster Analysis ; Enterobacteriaceae/drug effects ; Enterobacteriaceae/genetics ; Escherichia coli/classification ; Escherichia coli/drug effects ; Escherichia coli/genetics ; Humans ; Isoenzymes/genetics ; Isoenzymes/metabolism ; Klebsiella/drug effects ; Klebsiella/genetics ; Klebsiella pneumoniae/drug effects ; Klebsiella pneumoniae/genetics ; Microbial Sensitivity Tests ; Phylogeny ; Polymerase Chain Reaction ; Texas ; beta-Lactam Resistance/genetics ; beta-Lactamases/genetics ; beta-Lactamases/metabolism
    Chemical Substances Isoenzymes ; Ceftazidime (9M416Z9QNR) ; beta-Lactamases (EC 3.5.2.6) ; Cefotaxime (N2GI8B1GK7)
    Language English
    Publishing date 2007-11
    Publishing country United States
    Document type Journal Article ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 217602-6
    ISSN 1098-6596 ; 0066-4804
    ISSN (online) 1098-6596
    ISSN 0066-4804
    DOI 10.1128/AAC.00576-07
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  2. Article ; Online: Professor J. L. Harley: C.B.E., M.A., D.Phil. (Oxon), Hon. Fil. Dr (Uppsala), Hon. D.Sc. (Sheffield) F.L.S., C.Biol., F.I.Biol., F.R.S. (Editor of The New Phytologist, 1961-1983, Advisor to The New Phytologist Trust 1983-1990).

    Smith, David / Lewis, David

    The New phytologist

    2013  Volume 119, Issue 1, Page(s) 5–7

    Language English
    Publishing date 2013-08-23
    Publishing country England
    Document type Journal Article
    ZDB-ID 208885-x
    ISSN 1469-8137 ; 0028-646X
    ISSN (online) 1469-8137
    ISSN 0028-646X
    DOI 10.1111/j.1469-8137.1991.tb01003.x
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  3. Article ; Online: Measurement of signs of chemical shift differences between ground and excited protein states: a comparison between H(S/M)QC and R1rho methods.

    Auer, Renate / Hansen, D Flemming / Neudecker, Philipp / Korzhnev, Dmitry M / Muhandiram, D Ranjith / Konrat, Robert / Kay, Lewis E

    Journal of biomolecular NMR

    2009  Volume 46, Issue 3, Page(s) 205–216

    Abstract: ... H(S/M)QC approach for measuring the signs of chemical shift differences. For the Abp1p and Fyn SH3 ... domains considered here it is found that while H(S/M)QC measurements provide signs for more residues ... frequently produces signs for more residues than when the H(S/M)QC method is used alone. ...

    Abstract Carr-Purcell-Meiboom-Gill (CPMG) relaxation dispersion NMR spectroscopy has emerged as a powerful tool for quantifying the kinetics and thermodynamics of millisecond exchange processes between a major, populated ground state and one or more minor, low populated and often invisible 'excited' conformers. Analysis of CPMG data-sets also provides the magnitudes of the chemical shift difference(s) between exchanging states (|Deltavarpi|), that inform on the structural properties of the excited state(s). The sign of Deltavarpi is, however, not available from CPMG data. Here we present one-dimensional NMR experiments for measuring the signs of (1)H(N) and (13)C(alpha) Deltavarpi values using weak off-resonance R (1rho ) relaxation measurements, extending the spin-lock approach beyond previous applications focusing on the signs of (15)N and (1)H(alpha) shift differences. The accuracy of the method is established by using an exchanging system where the invisible, excited state can be converted to the visible, ground state by altering conditions so that the signs of Deltavarpi values obtained from the spin-lock approach can be validated with those measured directly. Further, the spin-lock experiments are compared with the established H(S/M)QC approach for measuring the signs of chemical shift differences. For the Abp1p and Fyn SH3 domains considered here it is found that while H(S/M)QC measurements provide signs for more residues than the spin-lock data, the two different methodologies are complementary, so that combining both approaches frequently produces signs for more residues than when the H(S/M)QC method is used alone.
    MeSH term(s) Models, Statistical ; Nitrogen Isotopes ; Nuclear Magnetic Resonance, Biomolecular/methods ; Protein Conformation ; Proteins/chemistry ; Thermodynamics
    Chemical Substances Nitrogen Isotopes ; Proteins
    Language English
    Publishing date 2009-12-22
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1081696-3
    ISSN 1573-5001 ; 0925-2738
    ISSN (online) 1573-5001
    ISSN 0925-2738
    DOI 10.1007/s10858-009-9394-z
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  4. Book: Radiopharmaceutical Therapy

    Bodei, Lisa / Zeglis, Brian M. / Lewis, Jason S.

    2023  

    Author's details Lisa Bodei, MD, PhD is a nuclear medicine physician with extensive experience and expertise in therapeutic and diagnostic applications of nuclear medicine in oncology, particularly with theranostics and the application of genomic technology to further defining the efficacy of theranostics. She is the Director of the Targeted Radionuclide Therapy Section of the Molecular Imaging and Therapy Service in the Department of Radiology, MSKCC. She has authored more than 200 peer-reviewed publications and serves on the editorial boards of several scientific journals. Jason S. Lewis, PhD, is the Emily Tow Chair, Chief of the Radiochemistry and Imaging Sciences Service, and Director of the Radiochemistry and Molecular Imaging Probe Core Facility in the Department of Radiology, MSKCC. He heads a laboratory in the Sloan Kettering Institute's molecular pharmacology program and is a professor at the Gerstner Sloan Kettering Graduate School of BiomedicalSciences. He has published more than 300 pape
    Keywords Radiotherapy ; Cancer therapy ; endoradiotherapy ; Radiotherapeutics ; Cancer Imaging ; Radiobiology ; biochemistry ; Medical Physics ; radiopharmaceutical chemistry ; Radioimmunotherapy ; radiotherapy ; cancer therapy ; cancer imaging ; Medical physics
    Language English
    Size 576 p.
    Edition 1
    Publisher Springer International Publishing
    Document type Book
    Note PDA Manuell_23
    Format 183 x 260 x 35
    ISBN 9783031390043 ; 3031390040
    Database PDA

    Kategorien

  5. Article: Differential maturation and subcellular localization of severe acute respiratory syndrome coronavirus surface proteins S, M and E.

    Nal, Béatrice / Chan, Cheman / Kien, Francois / Siu, Lewis / Tse, Jane / Chu, Kid / Kam, Jason / Staropoli, Isabelle / Crescenzo-Chaigne, Bernadette / Escriou, Nicolas / van der Werf, Sylvie / Yuen, Kwok-Yung / Altmeyer, Ralf

    The Journal of general virology

    2004  Volume 86, Issue Pt 5, Page(s) 1423–1434

    Abstract: ... In this study, the subcellular distribution and maturation of SARS-CoV surface proteins S, M and E were analysed ... mannosylated S assembles into trimers prior to acquisition of complex N-glycans in the Golgi. Like S, M ... S, M and E show differential subcellular localizations when expressed alone suggesting ...

    Abstract Post-translational modifications and correct subcellular localization of viral structural proteins are prerequisites for assembly and budding of enveloped viruses. Coronaviruses, like the severe acute respiratory syndrome-associated virus (SARS-CoV), bud from the endoplasmic reticulum-Golgi intermediate compartment. In this study, the subcellular distribution and maturation of SARS-CoV surface proteins S, M and E were analysed by using C-terminally tagged proteins. As early as 30 min post-entry into the endoplasmic reticulum, high-mannosylated S assembles into trimers prior to acquisition of complex N-glycans in the Golgi. Like S, M acquires high-mannose N-glycans that are subsequently modified into complex N-glycans in the Golgi. The N-glycosylation profile and the absence of O-glycosylation on M protein relate SARS-CoV to the previously described group 1 and 3 coronaviruses. Immunofluorescence analysis shows that S is detected in several compartments along the secretory pathway from the endoplasmic reticulum to the plasma membrane while M predominantly localizes in the Golgi, where it accumulates, and in trafficking vesicles. The E protein is not glycosylated. Pulse-chase labelling and confocal microscopy in the presence of protein translation inhibitor cycloheximide revealed that the E protein has a short half-life of 30 min. E protein is found in bright perinuclear patches colocalizing with endoplasmic reticulum markers. In conclusion, SARS-CoV surface proteins S, M and E show differential subcellular localizations when expressed alone suggesting that additional cellular or viral factors might be required for coordinated trafficking to the virus assembly site in the endoplasmic reticulum-Golgi intermediate compartment.
    MeSH term(s) Animals ; Cytoplasmic Vesicles/chemistry ; Endoplasmic Reticulum/chemistry ; Glycosylation ; Golgi Apparatus/chemistry ; Humans ; Mannose/analysis ; Membrane Glycoproteins/analysis ; Membrane Glycoproteins/chemistry ; Membrane Glycoproteins/metabolism ; Microscopy, Confocal ; Polysaccharides/chemistry ; Protein Processing, Post-Translational ; Protein Transport ; SARS Virus/growth & development ; Spike Glycoprotein, Coronavirus ; Viral Envelope Proteins/analysis ; Viral Envelope Proteins/chemistry ; Viral Envelope Proteins/metabolism ; Viral Matrix Proteins/analysis ; Viral Matrix Proteins/chemistry ; Viral Matrix Proteins/metabolism
    Chemical Substances M protein, Coronavirus ; Membrane Glycoproteins ; Polysaccharides ; Spike Glycoprotein, Coronavirus ; Viral Envelope Proteins ; Viral Matrix Proteins ; Mannose (PHA4727WTP)
    Keywords covid19
    Language English
    Publishing date 2004-01-29
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 219316-4
    ISSN 1465-2099 ; 0022-1317
    ISSN (online) 1465-2099
    ISSN 0022-1317
    DOI 10.1099/vir.0.80671-0
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  6. Book ; Online: Quality assurance in haematology / by S. M. Lewis

    Lewis, Shirley Mitchell / World Health Organization. Health Laboratory Technology and Blood Safety Unit

    1998  

    Abstract: This document revises and replaces docs. WHO/LAB/86.5 Rev.1 and WHO/LBS/92.4 ... WHO/LAB/98.4 ... English only ...

    Abstract This document revises and replaces docs. WHO/LAB/86.5 Rev.1 and WHO/LBS/92.4

    WHO/LAB/98.4

    English only

    113 p.
    Keywords Hematology ; Quality assurance ; Health care ; Quality control ; Laboratories ; Manuals ; Medical Technology and Radiation Medicine ; standards laboratory manuals ; standards
    Language English
    Publisher Geneva : World Health Organization
    Document type Book ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  7. Book ; Online: Quality assurance in haematology / by S. M. Lewis

    Lewis, Shirley Mitchell / World Health Organization. Health Laboratory Technology and Blood Safety Unit

    1998  

    Abstract: This document revises and replaces docs. WHO/LAB/86.5 Rev.1 and WHO/LBS/92.4 ... WHO/LAB/98.4 ... 113 p. ...

    Abstract This document revises and replaces docs. WHO/LAB/86.5 Rev.1 and WHO/LBS/92.4

    WHO/LAB/98.4

    113 p.
    Keywords Hematology ; Quality Assurance ; Health Care ; Quality Control ; Laboratories ; Handbook ; Medical Technology and Radiation Medicine ; standards laboratory manuals ; standards
    Language English
    Publisher World Health Organization
    Document type Book ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  8. Article ; Online: Answer to the Letter to the Editor of Gui-Tao Li et al. concerning: "A systematic review and meta-analysis of biological treatments targeting tumour necrosis factor α for sciatica" by Williams NH, Lewis R, Din NU, Matar HE, Fitzsimmons D, Phillips CJ, Sutton A, Burton K, Hendry M, Nafees S, Wilkinson C (2013) Eur Spine J; 22:1921-1935.

    Williams, Nefyn H / Lewis, Ruth

    European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society

    2014  Volume 23, Issue 4, Page(s) 939

    MeSH term(s) Antibodies, Monoclonal/therapeutic use ; Antibodies, Monoclonal, Humanized/therapeutic use ; Humans ; Immunoglobulin G/therapeutic use ; Receptors, Tumor Necrosis Factor/therapeutic use ; Sciatica/drug therapy ; Tumor Necrosis Factor-alpha/antagonists & inhibitors
    Chemical Substances Antibodies, Monoclonal ; Antibodies, Monoclonal, Humanized ; Immunoglobulin G ; Receptors, Tumor Necrosis Factor ; Tumor Necrosis Factor-alpha
    Language English
    Publishing date 2014-01-17
    Publishing country Germany
    Document type Letter ; Comment
    ZDB-ID 1115375-1
    ISSN 1432-0932 ; 0940-6719
    ISSN (online) 1432-0932
    ISSN 0940-6719
    DOI 10.1007/s00586-014-3171-8
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  9. Article: Distribution of S- and M-cones in normal and experimentally detached cat retina.

    Linberg, K A / Lewis, G P / Shaaw, C / Rex, T S / Fisher, S K

    The Journal of comparative neurology

    2000  Volume 430, Issue 3, Page(s) 343–356

    Abstract: The lectin peanut agglutinin (PNA) and antibodies to short (S)- and medium to long wavelength (M/L ... distribution in the normal cat's retina is established by the preponderance of M-cones that constitute between 80% and 90 ... of all cones. Their peak density of over 26,000 cells/mm(2) resides at the area centralis. Though M-cone ...

    Abstract The lectin peanut agglutinin (PNA) and antibodies to short (S)- and medium to long wavelength (M/L)-sensitive cones were utilized in order to define the relative distributions of the two spectral types of cone across the domestic cat's retina. These values, in turn, were compared to those from retinas that had been experimentally detached from the retinal pigment epithelium. The pattern of cone distribution in the normal cat's retina is established by the preponderance of M-cones that constitute between 80% and 90% of all cones. Their peak density of over 26,000 cells/mm(2) resides at the area centralis. Though M-cone density decreases smoothly to the ora serrata where they have densities as low as 2,200 cells/mm(2), the density decrease along the nasotemporal axis is slower,creating a horizontal region of higher cone density. S-cones constitute between 10% and 20% of all cones, the number being quite variable even between individual animals of similar age. The highest S-cone densities are found in three distinct locations: at the superior far periphery near the ora serrata, immediately at the area centralis itself, and in a broad zone comprising the central and lower half of the inferior hemiretina. S-cones in the cat retina do not form a regular geometrical array at any eccentricity. As for the detached cat retina, the density of labeled S-cone outer segments (OS) decreases rapidly as early as 1 day postdetachment and continues decreasing to day 28 when the density of cones labeling with anti-S opsin has dropped to less than 10% of normal. This response points to a profound difference between rods and cones; essentially all rods, including those without OS, continue to express their opsin even in long-term detachments. The implications of these results for visual recovery after retinal reattachment are discussed.
    MeSH term(s) Animals ; Calbindins ; Cats ; Cell Count ; Cell Death/physiology ; Female ; Immunohistochemistry ; Nerve Regeneration/physiology ; Peanut Agglutinin/pharmacology ; Recovery of Function/physiology ; Retinal Cone Photoreceptor Cells/cytology ; Retinal Cone Photoreceptor Cells/metabolism ; Retinal Detachment/pathology ; Retinal Detachment/physiopathology ; Rhodopsin/metabolism ; Rod Opsins/metabolism ; S100 Calcium Binding Protein G/metabolism ; Vision, Ocular/physiology
    Chemical Substances Calbindins ; Peanut Agglutinin ; Rod Opsins ; S100 Calcium Binding Protein G ; Rhodopsin (9009-81-8)
    Language English
    Publishing date 2000-02-23
    Publishing country United States
    Document type Journal Article ; Research Support, U.S. Gov't, P.H.S.
    ZDB-ID 3086-7
    ISSN 1096-9861 ; 0021-9967 ; 0092-7317
    ISSN (online) 1096-9861
    ISSN 0021-9967 ; 0092-7317
    DOI 10.1002/1096-9861(20010212)430:3<343::aid-cne1035>3.0.co;2-u
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  10. Article: Measurement of signs of chemical shift differences between ground and excited protein states: a comparison between H(S/M)QC and R ₁ρ methods

    Auer, Renate / Hansen, D. Flemming / Neudecker, Philipp / Korzhnev, Dmitry M. / Muhandiram, D. Ranjith / Konrat, Robert / Kay, Lewis E.

    Journal of biomolecular NMR. 2010 Mar., v. 46, no. 3

    2010  

    Abstract: ... with the established H(S/M)QC approach for measuring the signs of chemical shift differences. For the Abp1p and Fyn SH3 ... domains considered here it is found that while H(S/M)QC measurements provide signs for more residues ... frequently produces signs for more residues than when the H(S/M)QC method is used alone. ...

    Abstract Carr-Purcell-Meiboom-Gill (CPMG) relaxation dispersion NMR spectroscopy has emerged as a powerful tool for quantifying the kinetics and thermodynamics of millisecond exchange processes between a major, populated ground state and one or more minor, low populated and often invisible ‘excited' conformers. Analysis of CPMG data-sets also provides the magnitudes of the chemical shift difference(s) between exchanging states (|Δϖ|), that inform on the structural properties of the excited state(s). The sign of Δϖ is, however, not available from CPMG data. Here we present one-dimensional NMR experiments for measuring the signs of ¹HN and ¹³Cα Δϖ values using weak off-resonance R ₁ρ relaxation measurements, extending the spin-lock approach beyond previous applications focusing on the signs of ¹⁵N and ¹Hα shift differences. The accuracy of the method is established by using an exchanging system where the invisible, excited state can be converted to the visible, ground state by altering conditions so that the signs of Δϖ values obtained from the spin-lock approach can be validated with those measured directly. Further, the spin-lock experiments are compared with the established H(S/M)QC approach for measuring the signs of chemical shift differences. For the Abp1p and Fyn SH3 domains considered here it is found that while H(S/M)QC measurements provide signs for more residues than the spin-lock data, the two different methodologies are complementary, so that combining both approaches frequently produces signs for more residues than when the H(S/M)QC method is used alone.
    Keywords data collection ; nuclear magnetic resonance spectroscopy ; thermodynamics
    Language English
    Dates of publication 2010-03
    Size p. 205-216.
    Publisher Springer Netherlands
    Publishing place Dordrecht
    Document type Article
    ZDB-ID 1081696-3
    ISSN 0925-2738
    ISSN 0925-2738
    DOI 10.1007/s10858-009-9394-z
    Database NAL-Catalogue (AGRICOLA)

    More links

    Kategorien

To top