Publications with the contribution of LGSA PhD candidates

The goal of a PhD thesis program is to publish at least one first-author paper in an international peer-reviewed journal. We are very happy that our young researchers highly contribute to the publication record of the participating institutions.

2022

  • Characterization of RNA content in individual phase-separated coacervate microdroplets.
    Wollny D, Vernot B, Wang J, Hondele M, Safrastyan A, Aron F, Micheel J, He Z, Hyman A, Weis K, Camp JG, Tang TYD, Treutlein B
    Nat Commun 2022, 13(1), 2626
  • ASPM promotes ATR-CHK1 activation and stabilizes stalled replication forks in response to replication stress.
    Wu* X, Xu* S, Wang P, Wang ZQ, Chen H, Xu X, Peng B
    Proc Natl Acad Sci U S A 2022, 119(40), e2203783119 * equal contribution
  • S-nitrosoglutathione reductase (GSNOR) deficiency impairs hematopoietic stem cell proteostasis
    Yi W
    Dissertation 2022, Jena, Germany
  • PARP1: Liaison of Chromatin Remodeling and Transcription.
    Zong W, Gong Y, Sun W, Li T, Wang ZQ
    Cancers (Basel) 2022, 14(17), 4162

2021

  • The Cdc14 Phosphatase Controls Resolution of Recombination Intermediates and Crossover Formation during Meiosis.
    Alonso-Ramos P, Álvarez-Melo D, Strouhalova K, Pascual-Silva C, Garside GB, Arter M, Bermejo T, Grigaitis R, Wettstein R, Fernández-Díaz M, Matos J, Geymonat M, San-Segundo PA, Carballo JA
    Int J Mol Sci 2021, 22(18), 9811
  • Analysis of intestinal stem cell competition in calorie restriction and aging
    Annunziata F
    Dissertation 2021, Jena
  • Antithetic hTERT Regulation by Androgens in Prostate Cancer Cells: hTERT Inhibition Is Mediated by the ING1 and ING2 Tumor Suppressors.
    Bartsch S, Mirzakhani K, Neubert L, Stenzel A, Ehsani M, Esmaeili M, Pungsrinont T, Kacal M, Rasa SMM, Kallenbach J, Damodaran D, Ribaudo F, Grimm MO, Neri F, Baniahmad A
    Cancers (Basel) 2021, 13(16), 4025
  • Targeting enzyme aging.
    Becker F, Rudolph KL
    Science 2021, 371(6528), 462-3
  • The role of Atlastin-3 in hereditary axonopathies / by B.Sc., M.Sc., Laura Behrendt
    Behrendt L
    Dissertation 2021, Jena, Germany
  • Disease-causing mutated ATLASTIN 3 is excluded from distal axons and reduces axonal autophagy.
    Behrendt L, Hoischen C, Kaether C
    Neurobiol Dis 2021, 155, 105400