Kaether Research Group

Publications

2024

  • IER3IP1-mutations cause microcephaly by selective inhibition of ER-Golgi transport.
    Anitei M, Bruno F, Valkova C, Dau T, Cirri E, Mestres I, Calegari F, Kaether C
    Cell Mol Life Sci 2024, 81(1), 334

2023

  • Triac Treatment Prevents Neurodevelopmental and Locomotor Impairments in Thyroid Hormone Transporter Mct8/Oatp1c1 Deficient Mice.
    Chen J, Salveridou E, Liebmann L, Sundaram SM, Doycheva D, Markova B, Hübner CA, Boelen A, Visser WE, Heuer H, Mayerl S
    Int J Mol Sci 2023, 24(4), 3452
  • A YIPF5-GOT1A/B complex directs a transcription-independent function of ATF6 in ER export
    Cramer P, Yonemura Y, Behrendt L, Marszalek A, Sannai M, Durso W, Günes C, Szafranski K, Nakamura N, Nasrashvili T, Mayer J, von Eyss** B, Kaether** C
    bioRxiv 2023, 10.1101/2023.12.12.569033 ** co-corresponding authors
  • Impact of Hypermannosylation on the Structure and Functionality of the ER and the Golgi Complex.
    Franzka P, Schüler SC, Kentache T, Storm R, Bock A, Katona I, Weis J, Buder K, Kaether C, Hübner CA
    Biomedicines 2023, 11(1), 146.doi: 10.3390/biomedicines110

2022

  • Conserved exchange of paralog proteins during neuronal differentiation.
    Di Fraia D, Anitei M, Mackmull MT, Parca L, Behrendt L, Andres-Pons A, Gilmour D, Helmer Citterich M, Kaether C, Beck M, Ori A
    Life Sci Alliance 2022, 5(6)
  • Hanging the coat on a collar: Same function but different localization and mechanism for COPII.
    Malis Y, Hirschberg K, Kaether C
    Bioessays 2022, 44(10), e2200064
  • Meprin β knockout reduces brain Aβ levels and rescues learning and memory impairments in the APP/lon mouse model for Alzheimer's disease.
    Marengo L, Armbrust F, Schoenherr C, Storck SE, Schmitt U, Zampar S, Wirths O, Altmeppen H, Glatzel M, Kaether C, Weggen S, Becker-Pauly C, Pietrzik CU
    Cell Mol Life Sci 2022, 79(3), 168

2021

  • 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
  • GMPPA defects cause a neuromuscular disorder with α-dystroglycan hyperglycosylation.
    Franzka P, Henze* H, Jung* MJ, Schüler SC, Mittag S, Biskup K, Liebmann L, Kentache T, Morales J, Martínez B, Katona I, Herrmann T, Huebner AK, Hennings JC, Groth S, Gresing LJ, Horstkorte R, Marquardt T, Weis J, Kaether C, Mutchinick OM, Ori A, Huber O, Blanchard V, von Maltzahn J, Hübner CA
    J Clin Invest 2021, 131(9), e139076 * equal contribution