Search Results - Min Ae Lee‐Kirsch

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  1. 1
    Aicardi–Goutières syndrome: a model disease for systemic autoimmunity

    Aicardi–Goutières syndrome: a model disease for systemic autoimmunity by Min Ae Lee‐Kirsch, Christine Wolf, Claudia Günther

    Published 2013
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  2. 2
    Distinct Renin Isoforms Generated by Tissue-Specific Transcription Initiation and Alternative Splicing

    Distinct Renin Isoforms Generated by Tissue-Specific Transcription Initiation and Alternative Splicing by Min Ae Lee‐Kirsch, François Gaudet, M. Cristina Cardoso, Klaus Lindpaintner

    Published 1999
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  3. 3
    The cytosolic exonuclease TREX1 inhibits the innate immune response to human immunodeficiency virus type 1

    The cytosolic exonuclease TREX1 inhibits the innate immune response to human immunodeficiency virus type 1 by Nan Yan, Ashton D. Regalado-Magdos, Bart Stiggelbout, Min Ae Lee‐Kirsch, Judy Lieberman

    Published 2010
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  4. 4
    Assessment of Clinical Response to Janus Kinase Inhibition in Patients With Familial Chilblain Lupus and<i>TREX1</i>Mutation

    Assessment of Clinical Response to Janus Kinase Inhibition in Patients With Familial Chilblain Lupus and<i>TREX1</i>Mutation by Nick Zimmermann, Christine Wolf, R Schwenke, Anne Lüth, Franziska Schmidt, Kerstin Engel, Min Ae Lee‐Kirsch, Claudia Günther

    Published 2019
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  5. 5
    Autoimmune phenotype with type I interferon signature in two brothers with ADA2 deficiency carrying a novel CECR1 mutation

    Autoimmune phenotype with type I interferon signature in two brothers with ADA2 deficiency carrying a novel CECR1 mutation by Andrea Skrabl‐Baumgartner, Barbara Plecko, Wolfgang M. Schmidt, N. König, Michael S. Hershfield, U Gruber‐Sedlmayr, Min Ae Lee‐Kirsch

    Published 2017
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  6. 6
    Efficient Generation and Correction of Mutations in Human iPS Cells Utilizing mRNAs of CRISPR Base Editors and Prime Editors

    Efficient Generation and Correction of Mutations in Human iPS Cells Utilizing mRNAs of CRISPR Base Editors and Prime Editors by Duran Sürün, Aksana Schneider, Jovan Mircetic, Katrin Neumann, Felix Lansing, Maciej Paszkowski‐Rogacz, Vanessa Hänchen, Min Ae Lee‐Kirsch, Frank Buchholz

    Published 2020
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  7. 7
    Familial Chilblain Lupus, a Monogenic Form of Cutaneous Lupus Erythematosus, Maps to Chromosome 3p

    Familial Chilblain Lupus, a Monogenic Form of Cutaneous Lupus Erythematosus, Maps to Chromosome 3p by Min Ae Lee‐Kirsch, Maolian Gong, Herbert Schulz, Franz Rüschendorf, Annette Stein, Christiane Pfeiffer, Annalisa Ballarini, Manfred Gahr, Norbert Hübner, Maja Linné

    Published 2006
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  8. 8
    Single-stranded nucleic acids promote SAMHD1 complex formation

    Single-stranded nucleic acids promote SAMHD1 complex formation by Victoria Tüngler, Wolfgang Staroske, Barbara Kind, Manuela Dobrick, Stefanie Kretschmer, Franziska Schmidt, Claudia Krug, Mike Lorenz, Osvaldo Chara, Petra Schwille, Min Ae Lee-Kirsch

    Published 2013
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  9. 9
    Trex1 regulates lysosomal biogenesis and interferon-independent activation of antiviral genes

    Trex1 regulates lysosomal biogenesis and interferon-independent activation of antiviral genes by Maroof Hasan, James P. Koch, Dinesh Rakheja, Asit K. Pattnaik, James Brugarolas, Igor Dozmorov, Beth Levine, Edward K. Wakeland, Min Ae Lee‐Kirsch, Nan Yan

    Published 2012
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  10. 10
    Association Screening in the Epidermal Differentiation Complex (EDC) Identifies an SPRR3 Repeat Number Variant as a Risk Factor for Eczema

    Association Screening in the Epidermal Differentiation Complex (EDC) Identifies an SPRR3 Repeat Number Variant as a Risk Factor for Eczema by Ingo Marenholz, Vladimir A. Gimenez Rivera, Jorge Esparza-Gordillo, Anja Bauerfeind, Min-Ae Lee-Kirsch, Andrzej Ciechanowicz, Michael Kurek, T. Piskáčková, Milan Maçek, Young‐Ae Lee

    Published 2011
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  11. 11
    Deregulated Type I IFN Response in TREX1-Associated Familial Chilblain Lupus

    Deregulated Type I IFN Response in TREX1-Associated Familial Chilblain Lupus by Katrin Peschke, Franziska Friebe, Nick Zimmermann, Tom Wahlicht, Tina Schumann, Martin Achleitner, Nicole Berndt, Hella Luksch, Rayk Behrendt, Min Ae Lee‐Kirsch, Axel Roers, Claudia Günther

    Published 2013
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  12. 12
    Diabetes and Neurodegeneration in Wolfram Syndrome

    Diabetes and Neurodegeneration in Wolfram Syndrome by Julia Rohayem, Christian Ehlers, B. Wiedemann, Reinhard W. Holl, Konrad Oexle, Olga Kordonouri, Giuseppina Salzano, Thomas Meißner, Walter Burger, Edith Schober, Angela Huebner, Min Ae Lee‐Kirsch

    Published 2011
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  13. 13
    Familial chilblain lupus due to a gain-of-function mutation in STING

    Familial chilblain lupus due to a gain-of-function mutation in STING by N. König, Christoph Fiehn, Christine Wolf, Max Schuster, Emanuel Cura Costa, Victoria Tüngler, H. Ariel Alvarez, Osvaldo Chara, Kerstin Engel, Raphaela Goldbach‐Mansky, Claudia Günther, Min Ae Lee‐Kirsch

    Published 2016
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  14. 14
    Disrupted degradative sorting of TLR7 is associated with human lupus

    Disrupted degradative sorting of TLR7 is associated with human lupus by Harshita Mishra, Claire Schlack-Leigers, Ee Lyn Lim, Oliver Thieck, Thomas Magg, Johannes Raedler, Christine Wolf, Christoph Klein, Helge Ewers, Min Ae Lee‐Kirsch, David Meierhofer, Fabian Hauck, Olivia Majer

    Published 2024
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  15. 15
    RPA and Rad51 constitute a cell intrinsic mechanism to protect the cytosol from self DNA

    RPA and Rad51 constitute a cell intrinsic mechanism to protect the cytosol from self DNA by Christine Wolf, Alexander Rapp, Nicole Berndt, Wolfgang Staroske, Max Schuster, Manuela Dobrick-Mattheuer, Stefanie Kretschmer, N. König, Thomas Kurth, Dagmar Wieczorek, Karin Kast, M. Cristina Cardoso, Claudia Günther, Min Ae Lee‐Kirsch

    Published 2016
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  16. 16
    SAMHD1 prevents autoimmunity by maintaining genome stability

    SAMHD1 prevents autoimmunity by maintaining genome stability by Stefanie Kretschmer, Christine Wolf, N. König, Wolfgang Staroske, Jochen Guck, Martin Häusler, Hella Luksch, L.A. Nguyen, Baek Kim, Dimitra Alexopoulou, Andreas Dahl, Alexander Rapp, M. Cristina Cardoso, Anna Shevchenko, Min Ae Lee‐Kirsch

    Published 2014
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  17. 17
    Rat<i>hd</i>Mutation Reveals an Essential Role of Centrobin in Spermatid Head Shaping and Assembly of the Head-Tail Coupling Apparatus1

    Rat<i>hd</i>Mutation Reveals an Essential Role of Centrobin in Spermatid Head Shaping and Assembly of the Head-Tail Coupling Apparatus1 by František Liška, Claudia Gösele, Eugene Rivkin, Laura L. Tres, M. Cristina Cardoso, Petra Domaing, Eliška Krejčí, Pavel Šnajdr, Min Ae Lee‐Kirsch, Dirk G. de Rooij, Vladimı́r Kr̆en, D Křenová, Abraham L. Kierszenbaum, Norbert Hübner

    Published 2009
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  18. 18
    Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia

    Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia by Claus‐Eric Ott, Gundula Leschik, Fabienne Trotier, Louise Brueton, Han G. Brunner, Wim Brussel, Encarna Guillén‐Navarro, Claudia M. Haase, Juergen Kohlhase, Dieter Kotzot, Andrew Lane, Min Ae Lee‐Kirsch, Susanne Morlot, Marleen Simon, Elisabeth Steichen‐Gersdorf, David Tegay, Hartmut Peters, Stefan Mundlos, Eva Klopocki

    Published 2010
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  19. 19
    SAMHD1 controls innate immunity by regulating condensation of immunogenic self RNA

    SAMHD1 controls innate immunity by regulating condensation of immunogenic self RNA by Shovamayee Maharana, Stefanie Kretschmer, Susan Hunger, Xiao Yan, David Kuster, Sofia Traikov, Thomas Zillinger, Marc Gentzel, Shobha Elangovan, Padmanava Dasgupta, Nagaraja Chappidi, Nadja Lucas, Katharina Isabell Maser, Henrike Maatz, Alexander Rapp, Virginie Marchand, Young‐Tae Chang, Yuri Motorin, Norbert Hübner, Gunther Hartmann, Anthony A. Hyman, Simon Alberti, Min Ae Lee‐Kirsch

    Published 2022
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  20. 20
    Structural basis for OAS2 regulation and its antiviral function

    Structural basis for OAS2 regulation and its antiviral function by Veronika Merold, Indra Bekere, Stefanie Kretschmer, Adrian F. Schnell, Dorota Kmieć, Rinu Sivarajan, Katja Lammens, R. Liu, Julia Mergner, Julia Teppert, Maximilian Hirschenberger, Alexander Henrici, Sarah Hammes, Kathrin Buder, Marcus Weitz, Karl Hackmann, Lars M. König, Andreas Pichlmair, Nadine Schwierz, Konstantin M. J. Sparrer, Min Ae Lee‐Kirsch, Carina C. de Oliveira Mann

    Published 2025
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