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  1. Article ; Online: Cardiac involvement in patients with rheumatic disorders: Data of the RHEU-M(A)R study.

    Greulich, Simon / Kitterer, Daniel / Kurmann, Reto / Henes, Joerg / Latus, Joerg / Gloekler, Steffen / Wahl, Andreas / Buss, Sebastian J / Katus, Hugo A / Bobbo, Marco / Lombardi, Massimo / Backes, Maik / Steubing, Hannah / Schepat, Pascal / Braun, Niko / Alscher, M Dominik / Sechtem, Udo / Mahrholdt, Heiko

    International journal of cardiology

    2016  Volume 224, Page(s) 37–49

    Abstract: Background: The diagnosis of cardiac involvement in rheumatic disorders is challenging due to its varying clinical presentation. Since clinical consequences range from immediate treatment changes to adverse long-term outcome, individual risk ... ...

    Abstract Background: The diagnosis of cardiac involvement in rheumatic disorders is challenging due to its varying clinical presentation. Since clinical consequences range from immediate treatment changes to adverse long-term outcome, individual risk stratification is of great clinical interest. Primary aim was to evaluate the prevalence of cardiac involvement in patients with different rheumatic disorders using late gadolinium enhancement-cardiac magnetic resonance imaging (LGE-CMR). In addition, we sought to investigate if different rheumatic disorders would demonstrate different LGE patterns.
    Methods: Two-hundred-ninety-seven patients with rheumatic disorders were included and underwent LGE-CMR for work-up of cardiac involvement, which was defined by the presence of LGE in the myocardium. Patients were divided into five subgroups: 1) ANCA-associated vasculitis, 2) non-ANCA-associated vasculitis, 3) connective tissue disorders, 4) arthritis, and 5) sarcoidosis.
    Results: Mean ejection fraction in the overall population was 65%, with a mean age of 55yrs. Prevalence of cardiac involvement in the five subgroups were as follows: 54% in the ANCA-associated vasculitis group, 22% in the non-ANCA-associated vasculitis group, 14% in the group with connective tissue disorders, 21% in the arthritis group, and 24% in sarcoid patients. Each of the five subgroups demonstrated a distinct pattern of LGE.
    Conclusion: There is a wide range in the prevalence of cardiac involvement in different rheumatic disorders (54%-14%). Different groups of rheumatic disorders demonstrate different patterns of LGE.
    Condensed abstract: Primary aim of the study was to evaluate the presence of cardiac involvement in patients with different rheumatic disorders using LGE-CMR. In addition, we sought to investigate if different rheumatic disorders would reveal different LGE patterns. In our 297 patients, the highest prevalence of cardiac involvement was found in patients with ANCA-associated vasculitis (54%), whereas the lowest prevalence was demonstrated in patients with connective tissue disorders (14%). Furthermore, different groups of rheumatic disorders demonstrate distinct patterns of LGE.
    MeSH term(s) Adult ; Aged ; Cardiovascular Diseases/diagnostic imaging ; Cardiovascular Diseases/epidemiology ; Cardiovascular Diseases/physiopathology ; Electrocardiography/trends ; Female ; Humans ; Magnetic Resonance Imaging, Cine/trends ; Male ; Middle Aged ; Rheumatic Diseases/diagnostic imaging ; Rheumatic Diseases/epidemiology ; Rheumatic Diseases/physiopathology ; Statistics as Topic/trends
    Language English
    Publishing date 2016-12-01
    Publishing country Netherlands
    Document type Journal Article ; Multicenter Study
    ZDB-ID 779519-1
    ISSN 1874-1754 ; 0167-5273
    ISSN (online) 1874-1754
    ISSN 0167-5273
    DOI 10.1016/j.ijcard.2016.08.298
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Book: Volkseigene Gesundheit

    Wahl, Markus

    Reflexionen zur Sozialgeschichte des Gesundheitswesens der DDR

    (Medizin, Gesellschaft und Geschichte. Beiheft ; 75)

    2020  

    Author's details herausgegeben von Markus Wahl
    Series title Medizin, Gesellschaft und Geschichte. Beiheft ; 75
    Medizin, Gesellschaft und Geschichte
    Collection Medizin, Gesellschaft und Geschichte
    Keywords Geschichte der Medizin ; Deutschland ; Gesundheitswesen ; Sozialgeschichte
    Subject Gesundheitsdienst ; Gesundheitssystem ; Gesundheitswirtschaft ; Medizinalwesen ; Medizinalsystem
    Subject code 900
    Language German
    Size 211 Seiten, Illustrationen, 24 cm x 17 cm
    Publisher Franz Steiner Verlag
    Publishing place Stuttgart
    Publishing country Germany
    Document type Book
    HBZ-ID HT020490373
    ISBN 978-3-515-12671-7 ; 3-515-12671-6 ; 9783515126731 ; 3515126732
    Database Catalogue ZB MED Medicine, Health

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  3. Book ; Thesis: Chronisch oxidativer Stress reguliert durch Induktion der mikroRNA-1 die Connexin-43-Expression in einem neuen Zellmodell ventrikulärer Arrhythmien

    Wahl, Carl-Mattheis / Hecker, Markus

    2022  

    Institution Universität Heidelberg
    Author's details vorgelegt von Carl-Mattheis Martin Wahl ; Doktorvater: Prof. Dr. Markus Hecker
    Language German
    Size V, 95 Blätter, Illustrationen, Diagramme
    Publishing place Heidelberg
    Publishing country Germany
    Document type Book ; Thesis
    Thesis / German Habilitation thesis Dissertation, Ruprecht-Karls-Universität Heidelberg, 2022
    HBZ-ID HT030727523
    Database Catalogue ZB MED Medicine, Health

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  4. Article: Oncostatin M in the anti-inflammatory response.

    Wahl, A F / Wallace, P M

    Annals of the rheumatic diseases

    2001  Volume 60 Suppl 3, Page(s) iii75–80

    Abstract: Oncostatin M (OM) is a pleiotropic cytokine of the interleukin 6 family, whose in vivo properties ...

    Abstract Oncostatin M (OM) is a pleiotropic cytokine of the interleukin 6 family, whose in vivo properties and physiological function remain in dispute and poorly defined. These in vivo studies strongly suggest that OM is anabolic, promoting wound healing and bone formation, and anti-inflammatory. In models of inflammation OM is produced late in the cytokine response and protects from lipopolysaccharide (LPS)-induced toxicities, promoting the re-establishment of homoeostasis by cooperating with proinflammatory cytokines and acute phase molecules to alter and attenuate the inflammatory response. Administration of OM inhibited bacterial LPS-induced production of tumour necrosis factor alpha and septic lethality in a dose dependent manner. Consistent with these findings, in animal models of chronic inflammatory disease OM potently suppressed inflammation and tissue destruction in murine models of rheumatoid arthritis and multiple sclerosis. T cell function and antibody production were not impaired by OM treatment. Taken together, these data indicate that the activities of this cytokine in vivo are anti-inflammatory without concordant immunosuppression.
    MeSH term(s) Animals ; Arthritis, Experimental/drug therapy ; Bacterial Infections/metabolism ; Humans ; Inflammation Mediators/physiology ; Lipopolysaccharides ; Mice ; Models, Animal ; Multiple Sclerosis/drug therapy ; Oncostatin M ; Peptides/physiology ; Peptides/therapeutic use ; Tumor Necrosis Factor-alpha/metabolism ; Wound Healing/physiology
    Chemical Substances Inflammation Mediators ; Lipopolysaccharides ; OSM protein, human ; Osm protein, mouse ; Peptides ; Tumor Necrosis Factor-alpha ; Oncostatin M (106956-32-5)
    Language English
    Publishing date 2001-11
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 7090-7
    ISSN 1468-2060 ; 0003-4967
    ISSN (online) 1468-2060
    ISSN 0003-4967
    DOI 10.1136/ard.60.90003.iii75
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Book ; Thesis: Erzeugung und immunhistochemisches Reaktionsmuster des monoklonalen Antikörpers Ki-M7 [Ki-M]

    Wahl, Robert

    1987  

    Title variant Erzeugung und immunhistochemisches Reaktionsmuster des monoklonalen Antikörpers Ki-M7
    Size 33 S. : Ill.
    Document type Book ; Thesis
    Thesis / German Habilitation thesis Kiel, Univ., Diss., 1987
    HBZ-ID HT003080442
    Database Catalogue ZB MED Medicine, Health

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  6. Book ; Online ; E-Book: Medical memories and experiences in Postwar East Germany

    Wahl, Markus

    treatments of the past

    (Routledge studies in the history of science, technology and medicine)

    2019  

    Abstract: List of Figures List of Tables Acknowledgements Abbreviations Introduction: Medical Memories and Experiences Chapter 1 Treating the Past: Narratives of the Medical Profession after 1945 Chapter 2 Treatments from the Past: Continuities in Treating ... ...

    Author's details Markus Wahl
    Series title Routledge studies in the history of science, technology and medicine
    Abstract List of Figures List of Tables Acknowledgements Abbreviations Introduction: Medical Memories and Experiences Chapter 1 Treating the Past: Narratives of the Medical Profession after 1945 Chapter 2 Treatments from the Past: Continuities in Treating Venereal Diseases Chapter 3 Treatments for the Past? 'War Children' and the New State Chapter 4 Institutionalised Treatments of the Past: The Fürsorgeheim Leuben in Postwar Dresden Epilogue Appendix Index
    Keywords Medicine ; Germany ; History ; 20th century
    Language English
    Size 1 Online-Ressource (xiv, 224 Seiten), Illustrationen
    Publisher Routledge
    Publishing place London
    Publishing country Great Britain
    Document type Book ; Online ; E-Book
    Remark Zugriff für angemeldete ZB MED-Nutzerinnen und -Nutzer
    HBZ-ID HT020170450
    ISBN 978-1-00-000492-2 ; 978-0-367-13871-4 ; 9780367138707 ; 1-00-000492-9 ; 0-367-13871-9 ; 0367138700
    Database ZB MED Catalogue: Medicine, Health, Nutrition, Environment, Agriculture

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  7. Article ; Online: Construction and nonclinical testing of a Puumala virus synthetic M gene-based DNA vaccine.

    Brocato, R L / Josleyn, M J / Wahl-Jensen, V / Schmaljohn, C S / Hooper, J W

    Clinical and vaccine immunology : CVI

    2012  Volume 20, Issue 2, Page(s) 218–226

    Abstract: ... the synthesis of a codon-optimized, full-length M segment open reading frame and its cloning into a DNA vaccine ... vector to produce the plasmid pWRG/PUU-M(s2). pWRG/PUU-M(s2) delivered by gene gun produced high-titer ... neutralizing antibodies in hamsters and nonhuman primates. Vaccination with pWRG/PUU-M(s2) protected hamsters against ...

    Abstract Puumala virus (PUUV) is a causative agent of hemorrhagic fever with renal syndrome (HFRS). Although PUUV-associated HFRS does not result in high case-fatality rates, the social and economic impact is considerable. There is no licensed vaccine or specific therapeutic to prevent or treat HFRS. Here we report the synthesis of a codon-optimized, full-length M segment open reading frame and its cloning into a DNA vaccine vector to produce the plasmid pWRG/PUU-M(s2). pWRG/PUU-M(s2) delivered by gene gun produced high-titer neutralizing antibodies in hamsters and nonhuman primates. Vaccination with pWRG/PUU-M(s2) protected hamsters against infection with PUUV but not against infection by related HFRS-associated hantaviruses. Unexpectedly, vaccination protected hamsters in a lethal disease model of Andes virus (ANDV) in the absence of ANDV cross-neutralizing antibodies. This is the first evidence that an experimental DNA vaccine for HFRS can provide protection in a hantavirus lethal disease model.
    MeSH term(s) Animals ; Antibodies, Neutralizing/immunology ; Antibodies, Viral/immunology ; COS Cells ; Cell Line ; Chlorocebus aethiops ; Cricetinae ; Cross Reactions ; DNA, Viral/immunology ; Hantavirus/immunology ; Hantavirus Infections/immunology ; Hemorrhagic Fever with Renal Syndrome/immunology ; Hemorrhagic Fever with Renal Syndrome/prevention & control ; Hemorrhagic Fever with Renal Syndrome/virology ; Macaca mulatta/immunology ; Neutralization Tests ; Puumala virus/immunology ; Vaccination ; Vaccines, DNA/administration & dosage ; Vaccines, DNA/immunology ; Vero Cells ; Viral Matrix Proteins/genetics ; Viral Matrix Proteins/immunology ; Viral Plaque Assay ; Viral Vaccines/administration & dosage ; Viral Vaccines/immunology
    Chemical Substances Antibodies, Neutralizing ; Antibodies, Viral ; DNA, Viral ; Vaccines, DNA ; Viral Matrix Proteins ; Viral Vaccines
    Language English
    Publishing date 2012-12-12
    Publishing country United States
    Document type Journal Article ; Research Support, U.S. Gov't, Non-P.H.S. ; Research Support, U.S. Gov't, P.H.S.
    ZDB-ID 2221082-9
    ISSN 1556-679X ; 1556-6811
    ISSN (online) 1556-679X
    ISSN 1556-6811
    DOI 10.1128/CVI.00546-12
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: A Microarray-Matrix-assisted Laser Desorption/Ionization-Mass Spectrometry Approach for Site-specific Protein N-glycosylation Analysis, as Demonstrated for Human Serum Immunoglobulin M (IgM).

    Pabst, Martin / Küster, Simon Karl / Wahl, Fabian / Krismer, Jasmin / Dittrich, Petra S / Zenobi, Renato

    Molecular & cellular proteomics : MCP

    2015  Volume 14, Issue 6, Page(s) 1645–1656

    Abstract: We demonstrate a new approach for the site-specific identification and characterization of protein N-glycosylation. It is based on a nano-liquid chromatography microarray-matrix assisted laser desorption/ionization-MS platform, which employs droplet ... ...

    Abstract We demonstrate a new approach for the site-specific identification and characterization of protein N-glycosylation. It is based on a nano-liquid chromatography microarray-matrix assisted laser desorption/ionization-MS platform, which employs droplet microfluidics for on-plate nanoliter reactions. A chromatographic separation of a proteolytic digest is deposited at a high frequency on the microarray. In this way, a short separation run is archived into thousands of nanoliter reaction cavities, and chromatographic peaks are spread over multiple array spots. After fractionation, each other spot is treated with PNGaseF to generate two correlated traces within one run, one with treated spots where glycans are enzymatically released from the peptides, and one containing the intact glycopeptides. Mining for distinct glycosites is performed by searching for the predicted deglycosylated peptides in the treated trace. An identified peptide then leads directly to the position of the "intact" glycopeptide clusters, which are located in the adjacent spots. Furthermore, the deglycosylated peptide can be sequenced efficiently in a simple collision-induced dissociation-MS experiment. We applied the microarray approach to a detailed site-specific glycosylation analysis of human serum IgM. By scanning the treated spots with low-resolution matrix assisted laser desorption/ionization-time-of-flight-MS, we observed all five deglycosylated peptides, including the one originating from the secretory chain. A detailed glycopeptide characterization was then accomplished on the adjacent, untreated spots with high mass resolution and high mass accuracy using a matrix assisted laser desorption ionization-Fourier transform-MS. We present the first detailed and comprehensive mass spectrometric analysis on the glycopeptide level for human polyclonal IgM with high mass accuracy. Besides complex type glycans on Asn 395, 332, 171, and on the J chain, we observed oligomannosidic glycans on Asn 563, Asn 402 and minor amounts of oligomannosidic glycans on the glycosite Asn 171. Furthermore, hybrid type glycans were found on Asn 402, Asn 171 and in traces Asn 332.
    MeSH term(s) Chromatography, Liquid ; Glycosylation ; Humans ; Immunoglobulin M/blood ; Immunoglobulin M/chemistry ; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
    Chemical Substances Immunoglobulin M
    Language English
    Publishing date 2015-03-23
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2075924-1
    ISSN 1535-9484 ; 1535-9476
    ISSN (online) 1535-9484
    ISSN 1535-9476
    DOI 10.1074/mcp.O114.046748
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article: Regulation of inflammatory responses by oncostatin M.

    Wallace, P M / MacMaster, J F / Rouleau, K A / Brown, T J / Loy, J K / Donaldson, K L / Wahl, A F

    Journal of immunology (Baltimore, Md. : 1950)

    1999  Volume 162, Issue 9, Page(s) 5547–5555

    Abstract: Oncostatin M (OM) is a pleiotropic cytokine produced late in the activation cycle of T cells and ...

    Abstract Oncostatin M (OM) is a pleiotropic cytokine produced late in the activation cycle of T cells and macrophages. In vitro it shares properties with related proteins of the IL-6 family of cytokines; however, its in vivo properties and physiological function are as yet ill defined. We show that administration of OM inhibited bacterial LPS-induced production of TNF-alpha and lethality in a dose-dependent manner. Consistent with these findings, OM potently suppressed inflammation and tissue destruction in murine models of rheumatoid arthritis and multiple sclerosis. T cell function and Ab production were not impaired by OM treatment. Taken together these data indicate the activities of this cytokine in vivo are antiinflammatory without concordant immunosuppression.
    MeSH term(s) Animals ; Arthritis, Rheumatoid/immunology ; Arthritis, Rheumatoid/pathology ; Arthritis, Rheumatoid/prevention & control ; Cytokines/administration & dosage ; Cytokines/biosynthesis ; Cytokines/physiology ; Disease Models, Animal ; Encephalomyelitis, Autoimmune, Experimental/immunology ; Encephalomyelitis, Autoimmune, Experimental/pathology ; Encephalomyelitis, Autoimmune, Experimental/prevention & control ; Female ; Hindlimb ; Humans ; Immunosuppressive Agents/administration & dosage ; Immunosuppressive Agents/pharmacology ; Inflammation Mediators/administration & dosage ; Inflammation Mediators/metabolism ; Inflammation Mediators/physiology ; Injections, Intravenous ; Lipopolysaccharides/administration & dosage ; Lymphocyte Activation/immunology ; Macrophage Activation/immunology ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Oncostatin M ; Peptides/administration & dosage ; Peptides/metabolism ; Peptides/physiology
    Chemical Substances Cytokines ; Immunosuppressive Agents ; Inflammation Mediators ; Lipopolysaccharides ; OSM protein, human ; Osm protein, mouse ; Peptides ; Oncostatin M (106956-32-5)
    Language English
    Publishing date 1999-05-01
    Publishing country United States
    Document type Journal Article
    ZDB-ID 3056-9
    ISSN 1550-6606 ; 0022-1767 ; 1048-3233 ; 1047-7381
    ISSN (online) 1550-6606
    ISSN 0022-1767 ; 1048-3233 ; 1047-7381
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Disentangling the Biological and Environmental Control of M. edulis Shell Chemistry

    Heinemann, Agnes / Hiebenthal, Claas / Fietzke, Jan / Eisenhauer, Anton / Wahl, Martin

    2011  

    Abstract: ... and “physiological variability”) on elemental ratios (79% on Mg/Ca and 41% on Sr/Ca) in M. edulis ...

    Abstract Blue mussel individuals (Mytilus edulis) were cultured at four different salinities (17, 20, 29, and 34). During the course of the experiment, temperature was gradually increased from 6°C to 14°C. Mg/Ca and Sr/Ca ratios of the shell calcite portions produced during the 9 weeks of experimental treatment as well parts that were precipitated before the treatment phase were measured by laser ablation–multicollector–inductively coupled plasma–mass spectrometry. Mg/Ca ratios show a positive correlation with temperature for individuals cultured at salinity 29 and 34 (Mg/Ca (mmol/mol) ∼ (0.2–0.3)*T (°C)), while for individuals cultured at low salinities (17, 20) no trend was observed. Sr/Ca ratios were not affected by temperature but strongly by salinity. The data show very strong biological influence (“individual differences” and “physiological variability”) on elemental ratios (79% on Mg/Ca and 41% on Sr/Ca) in M. edulis calcite. The results challenge the use of blue mussel shell data as environmental proxies.
    Language English
    Publisher AGU (American Geophysical Union)
    Publishing country de
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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