Search Results - Chloë Scheldeman

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  1. 1
    Gain-of-function <i>FHF1</i> mutation causes early-onset epileptic encephalopathy with cerebellar atrophy

    Gain-of-function <i>FHF1</i> mutation causes early-onset epileptic encephalopathy with cerebellar atrophy by Aleksandra Siekierska, Mala Isrie, Yue Liu, Chloë Scheldeman, Niels Vanthillo, Lieven Lagae, Peter de Witte, Hilde Van Esch, Mitchell Goldfarb, Gunnar Buyse

    Published 2016
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  2. 2
    G3BPs tether the TSC complex to lysosomes and suppress mTORC1 signaling

    G3BPs tether the TSC complex to lysosomes and suppress mTORC1 signaling by Mirja Tamara Prentzell, Ulrike Rehbein, Marti Cadena Sandoval, Ann‐Sofie De Meulemeester, Ralf Baumeister, Laura Brohée, Bianca Berdel, Mathias Bockwoldt, Bernadette Carroll, Suvagata Roy Chowdhury, Andreas von Deimling, Constantinos Demetriades, Gianluca Figlia, Mariana E. G. de Araújo, Alexander Martin Heberle, Ines Heiland, Birgit Holzwarth, Lukas A. Huber, Jacek Jaworski, Magdalena Kedra, Katharina Kern, Andrii Kopach, Viktor I. Korolchuk, Ineke Kuper, Matylda Macias, Mark Nellist, Wilhelm Palm, Stefan Pusch, José M. Ramos Pittol, Michèle Reil, Anja Reintjes, Friederike Reuter, Julian R. Sampson, Chloë Scheldeman, Aleksandra Siekierska, Eduard Stefan, Aurelio A. Teleman, Laura E. Thomas, Omar Torres‐Quesada, Saskia Trump, Hannah D. West, Peter de Witte, Sandra Woltering, Teodor E. Yordanov, Justyna Zmorzyńska, Christiane A. Opitz, Kathrin Thedieck

    Published 2021
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