Risultati della ricerca - Birte Möhlendick

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  1. 1
    The single nucleotide polymorphism rs4986790 (c.896A>G) in the gene TLR4 as a protective factor in corona virus disease 2019 (COVID-19)

    The single nucleotide polymorphism rs4986790 (c.896A>G) in the gene TLR4 as a protective factor in corona virus disease 2019 (COVID-19) di Christoph Zacher, Kristina Schönfelder, Hana Rohn, Winfried Siffert, Birte Möhlendick

    Pubblicazione 2024
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  2. 2
    GNB3 c.825c>T polymorphism influences T-cell but not antibody response following vaccination with the mRNA-1273 vaccine

    GNB3 c.825c>T polymorphism influences T-cell but not antibody response following vaccination with the mRNA-1273 vaccine di Ieva Čiučiulkaitė, Birte Möhlendick, Laura Thümmler, Neslinur Fisenkci, Carina Elsner, Ulf Dittmer, Winfried Siffert, Monika Lindemann

    Pubblicazione 2022
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  3. 3
    Patients with Liver Cirrhosis Show High Immunogenicity upon COVID-19 Vaccination but Develop Premature Deterioration of Antibody Titers

    Patients with Liver Cirrhosis Show High Immunogenicity upon COVID-19 Vaccination but Develop Premature Deterioration of Antibody Titers di Katharina Willuweit, Alexandra Frey, Moritz Passenberg, Johannes Korth, Nissrin Saka, Olympia E. Anastasiou, Birte Möhlendick, Andreas Schütte, Hartmut Schmidt, Jassin Rashidi‐Alavijeh

    Pubblicazione 2022
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  4. 4
    Individuals With Weaker Antibody Responses After Booster Immunization Are Prone to Omicron Breakthrough Infections

    Individuals With Weaker Antibody Responses After Booster Immunization Are Prone to Omicron Breakthrough Infections di Birte Möhlendick, Ieva Čiučiulkaitė, Carina Elsner, Olympia E. Anastasiou, Mirko Trilling, Bernd Wagner, Denise Zwanziger, Karl‐Heinz Jöckel, Ulf Dittmer, Winfried Siffert

    Pubblicazione 2022
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  5. 5
    BRAF<sup>V600E</sup> mutation: A promising target in colorectal neuroendocrine carcinoma

    BRAF<sup>V600E</sup> mutation: A promising target in colorectal neuroendocrine carcinoma di Levent Dizdar, Thomas Werner, Jasmin Drusenheimer, Birte Möhlendick, Katharina Raba, Inga Boeck, Martin Anlauf, M. Schott, Wolfgang Göring, Iréne Esposito, Nikolas H. Stoecklein, Wolfram Trudo Knoefel, Andreas Krieg

    Pubblicazione 2018
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  6. 6
    The influence of IFITM3 polymorphisms on susceptibility to SARS-CoV-2 infection and severity of COVID-19

    The influence of IFITM3 polymorphisms on susceptibility to SARS-CoV-2 infection and severity of COVID-19 di Kristina Schönfelder, Katharina Breuckmann, Carina Elsner, Ulf Dittmer, David Fistera, Frank Herbstreit, Joachim Riße, Karsten Schmidt, Sivagurunathan Sutharsan, Christian Taube, Karl‐Heinz Jöckel, Winfried Siffert, Andreas Kribben, Birte Möhlendick

    Pubblicazione 2021
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  7. 7
    Transmembrane serine protease 2 Polymorphisms and Susceptibility to Severe Acute Respiratory Syndrome Coronavirus Type 2 Infection: A German Case-Control Study

    Transmembrane serine protease 2 Polymorphisms and Susceptibility to Severe Acute Respiratory Syndrome Coronavirus Type 2 Infection: A German Case-Control Study di Kristina Schönfelder, Katharina Breuckmann, Carina Elsner, Ulf Dittmer, David Fistera, Frank Herbstreit, Joachim Riße, Karsten Schmidt, Sivagurunathan Sutharsan, Christian Taube, Karl‐Heinz Jöckel, Winfried Siffert, Andreas Kribben, Birte Möhlendick

    Pubblicazione 2021
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  8. 8
    ACE2 polymorphism and susceptibility for SARS-CoV-2 infection and severity of COVID-19

    ACE2 polymorphism and susceptibility for SARS-CoV-2 infection and severity of COVID-19 di Birte Möhlendick, Kristina Schönfelder, Katharina Breuckmann, Carina Elsner, Nina Babel, Paul Balfanz, Edgar Dahl, Michael Dreher, David Fistera, Frank Herbstreit, Bodo Hölzer, Michael Koch, M. Kohnle, Nikolaus Marx, Joachim Riße, Karsten Schmidt, Sarah Skrzypczyk, Sivagurunathan Sutharsan, Christian Taube, Timm H. Westhoff, Karl‐Heinz Jöckel, Ulf Dittmer, Winfried Siffert, Andreas Kribben

    Pubblicazione 2021
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  9. 9
    Unscrambling the genomic chaos of osteosarcoma reveals extensive transcript fusion, recurrent rearrangements and frequent novel TP53 aberrations

    Unscrambling the genomic chaos of osteosarcoma reveals extensive transcript fusion, recurrent rearrangements and frequent novel TP53 aberrations di Susanne Lorenz, Tale Barøy, Jinchang Sun, Torfinn Nome, Daniel Vodák, Jan-Christian Bryne, Anne-Mari Håkelien, Lynnette Fernandez‐Cuesta, Birte Möhlendick, Harald Rieder, Károly Szuhai, Olga Zaikova, Terje Ahlquist, Gard O. S. Thomassen, Rolf I. Skotheim, Ragnhild A. Lothe, Patrick Tarpey, Peter J. Campbell, Adrienne M. Flanagan, Ola Myklebost, Leonardo A. Meza‐Zepeda

    Pubblicazione 2015
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