Search Results - "Runtsch, Leander"

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  1. 1

    Structure and mechanism of the RNA dependent RNase Cas13a from Rhodobacter capsulatus by Kick, Leonhard M., von Wrisberg, Marie-Kristin, Runtsch, Leander S., Schneider, Sabine

    Published in Communications biology (20-01-2022)
    “…Cas13a are single-molecule effectors of the Class II, Type VI family of CRISPR-Cas systems that are part of the bacterial and archaeal defense systems. These…”
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    Journal Article
  2. 2

    Comprehensive comparison between azacytidine and decitabine treatment in an acute myeloid leukemia cell line by Aumer, Tina, Gremmelmaier, Constanze B, Runtsch, Leander S, Pforr, Johannes C, Yeşiltaç, G Nur, Kaiser, Stefanie, Traube, Franziska R

    Published in Clinical epigenetics (11-09-2022)
    “…Azacytidine (AzaC) and decitabine (AzadC) are cytosine analogs that covalently trap DNA methyltransferases, which place the important epigenetic mark…”
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    Journal Article
  3. 3

    A Click‐Chemistry‐Based Enrichable Crosslinker for Structural and Protein Interaction Analysis by Mass Spectrometry by Stadlmeier, Michael, Runtsch, Leander Simon, Streshnev, Filipp, Wühr, Martin, Carell, Thomas

    “…Mass spectrometry is the method of choice for the characterisation of proteomes. Most proteins operate in protein complexes, in which their close association…”
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  4. 4

    Comparative Nucleosomal Reactivity of 5‐Formyl‐Uridine and 5‐Formyl‐Cytidine by Runtsch, Leander Simon, Stadlmeier, Michael, Schön, Alexander, Müller, Markus, Carell, Thomas

    Published in Chemistry : a European journal (06-09-2021)
    “…5‐Formyl‐deoxyuridine (fdU) and 5‐formyl‐deoxycytidine (fdC) are formyl‐containing nucleosides that are created by oxidative stress in differentiated cells…”
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  5. 5

    Azobenzene-based inhibitors of human carbonic anhydrase II by Runtsch, Leander Simon, Barber, David Michael, Mayer, Peter, Groll, Michael, Trauner, Dirk, Broichhagen, Johannes

    Published in Beilstein journal of organic chemistry (07-07-2015)
    “…Aryl sulfonamides are a widely used drug class for the inhibition of carbonic anhydrases. In the context of our program of photochromic pharmacophores we were…”
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