Works by Bultynck, Geert


Results: 86
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    Correction to: Disruption of MAM integrity in mutant FUS oligodendroglial progenitors from hiPSCs.

    Published in:
    Acta Neuropathologica, 2024, v. 147, n. 1, p. 1, doi. 10.1007/s00401-024-02748-4
    By:
    • Zhu, Yingli;
    • Burg, Thibaut;
    • Neyrinck, Katrien;
    • Vervliet, Tim;
    • Nami, Fatemeharefeh;
    • Vervoort, Ellen;
    • Ahuja, Karan;
    • Sassano, Maria Livia;
    • Chai, Yoke Chin;
    • Tharkeshwar, Arun Kumar;
    • De Smedt, Jonathan;
    • Hu, Haibo;
    • Bultynck, Geert;
    • Agostinis, Patrizia;
    • Swinnen, Johannes V.;
    • Van Den Bosch, Ludo;
    • da Costa, Rodrigo Furtado Madeiro;
    • Verfaillie, Catherine
    Publication type:
    Article
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    Disruption of MAM integrity in mutant FUS oligodendroglial progenitors from hiPSCs.

    Published in:
    Acta Neuropathologica, 2024, v. 147, n. 1, p. 1, doi. 10.1007/s00401-023-02666-x
    By:
    • Zhu, Yingli;
    • Burg, Thibaut;
    • Neyrinck, Katrien;
    • Vervliet, Tim;
    • Nami, Fatemeharefeh;
    • Vervoort, Ellen;
    • Ahuja, Karan;
    • Sassano, Maria Livia;
    • Chai, Yoke Chin;
    • Tharkeshwar, Arun Kumar;
    • De Smedt, Jonathan;
    • Hu, Haibo;
    • Bultynck, Geert;
    • Agostinis, Patrizia;
    • Swinnen, Johannes V.;
    • Van Den Bosch, Ludo;
    • da Costa, Rodrigo Furtado Madeiro;
    • Verfaillie, Catherine
    Publication type:
    Article
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    MICAL2 is essential for myogenic lineage commitment.

    Published in:
    Cell Death & Disease, 2020, v. 11, n. 8, p. 1, doi. 10.1038/s41419-020-02886-z
    By:
    • Giarratana, Nefele;
    • Conti, Filippo;
    • La Rovere, Rita;
    • Gijsbers, Rik;
    • Carai, Paolo;
    • Duelen, Robin;
    • Vervliet, Tim;
    • Bultynck, Geert;
    • Ronzoni, Flavio;
    • Piciotti, Roberto;
    • Costamagna, Domiziana;
    • Fulle, Stefania;
    • Barravecchia, Ivana;
    • Angeloni, Debora;
    • Torrente, Yvan;
    • Sampaolesi, Maurilio
    Publication type:
    Article
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    ER calcium depletion as a key driver for impaired ER-to-mitochondria calcium transfer and mitochondrial dysfunction in Wolfram syndrome.

    Published in:
    Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-50502-x
    By:
    • Liiv, Mailis;
    • Vaarmann, Annika;
    • Safiulina, Dzhamilja;
    • Choubey, Vinay;
    • Gupta, Ruby;
    • Kuum, Malle;
    • Janickova, Lucia;
    • Hodurova, Zuzana;
    • Cagalinec, Michal;
    • Zeb, Akbar;
    • Hickey, Miriam A.;
    • Huang, Yi-Long;
    • Gogichaishvili, Nana;
    • Mandel, Merle;
    • Plaas, Mario;
    • Vasar, Eero;
    • Loncke, Jens;
    • Vervliet, Tim;
    • Tsai, Ting-Fen;
    • Bultynck, Geert
    Publication type:
    Article
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    Polycystin-1 but not polycystin-2 deficiency causes upregulation of the mTOR pathway and can be synergistically targeted with rapamycin and metformin.

    Published in:
    Pflügers Archiv: European Journal of Physiology, 2014, v. 466, n. 8, p. 1591, doi. 10.1007/s00424-013-1394-x
    By:
    • Mekahli, Djalila;
    • Decuypere, Jean-Paul;
    • Sammels, Eva;
    • Welkenhuyzen, Kirsten;
    • Schoeber, Joost;
    • Audrezet, Marie-Pierre;
    • Corvelyn, Anniek;
    • Dechênes, Georges;
    • Ong, Albert;
    • Wilmer, Martijn;
    • Heuvel, Lambertus;
    • Bultynck, Geert;
    • Parys, Jan;
    • Missiaen, Ludwig;
    • Levtchenko, Elena;
    • Smedt, Humbert
    Publication type:
    Article
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    Intracellular Ca<sup>2+</sup> signaling.

    Published in:
    Communicative & Integrative Biology, 2013, v. 6, n. 5, p. 1, doi. 10.4161/cib.25429
    By:
    • Decuypere, Jean-Paul;
    • Chandra Paudel, Ram;
    • Parys, Jan B.;
    • Bultynck, Geert
    Publication type:
    Article
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    Bcl-2 and IP<sub>3</sub> compete for the ligand-binding domain of IP<sub>3</sub>Rs modulating Ca<sup>2+</sup> signaling output.

    Published in:
    Cellular & Molecular Life Sciences, 2019, v. 76, n. 19, p. 3843, doi. 10.1007/s00018-019-03091-8
    By:
    • Ivanova, Hristina;
    • Wagner II, Larry E.;
    • Tanimura, Akihiko;
    • Vandermarliere, Elien;
    • Luyten, Tomas;
    • Welkenhuyzen, Kirsten;
    • Alzayady, Kamil J.;
    • Wang, Liwei;
    • Hamada, Kozo;
    • Mikoshiba, Katsuhiko;
    • De Smedt, Humbert;
    • Martens, Lennart;
    • Yule, David I.;
    • Parys, Jan B.;
    • Bultynck, Geert
    Publication type:
    Article
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    TMBIM5 loss of function alters mitochondrial matrix ion homeostasis and causes a skeletal myopathy.

    Published in:
    Life Science Alliance, 2022, v. 5, n. 10, p. 1, doi. 10.26508/lsa.202201478
    By:
    • Li Zhang;
    • Dietsche, Felicia;
    • Seitaj, Bruno;
    • Rojas-Charry, Liliana;
    • Latchman, Nadina;
    • Tomar, Dhanendra;
    • Wüst, Rob C. I.;
    • Nickel, Alexander;
    • Frauenknecht, Katrin B. M.;
    • Schoser, Benedikt;
    • Schumann, Sven;
    • Schmeisser, Michael J.;
    • vom Berg, Johannes;
    • Buch, Thorsten;
    • Finger, Stefanie;
    • Wenzel, Philip;
    • Maack, Christoph;
    • Elrod, John W.;
    • Parys, Jan B.;
    • Bultynck, Geert
    Publication type:
    Article
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    Dominant mutations in ITPR3 cause Charcot‐Marie‐Tooth disease.

    Published in:
    Annals of Clinical & Translational Neurology, 2020, v. 7, n. 10, p. 1962, doi. 10.1002/acn3.51190
    By:
    • Rönkkö, Julius;
    • Molchanova, Svetlana;
    • Revah‐Politi, Anya;
    • Pereira, Elaine M.;
    • Auranen, Mari;
    • Toppila, Jussi;
    • Kvist, Jouni;
    • Ludwig, Anastasia;
    • Neumann, Julika;
    • Bultynck, Geert;
    • Humblet‐Baron, Stéphanie;
    • Liston, Adrian;
    • Paetau, Anders;
    • Rivera, Claudio;
    • Harms, Matthew B.;
    • Tyynismaa, Henna;
    • Ylikallio, Emil
    Publication type:
    Article
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