Sequence Features of Mitochondrial Transporter Protein Families by Gergely Gyimesi, Matthias A. Hediger

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Transporter-Mediated Drug Delivery by Gergely Gyimesi, Matthias A. Hediger

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Systematic in silico discovery of novel solute carrier-like proteins from proteomes. by Gergely Gyimesi, Matthias A Hediger

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The Less Well-Known Little Brothers: The SLC9B/NHA Sodium Proton Exchanger Subfamily—Structure, Function, Regulation and Potential Drug-Target Approaches by Manuel A. Anderegg, Gergely Gyimesi, Gergely Gyimesi, Tin Manh Ho, Matthias A. Hediger, Matthias A. Hediger, Daniel G. Fuster

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A novel proton transfer mechanism in the SLC11 family of divalent metal ion transporters by Jonai Pujol-Giménez, Matthias A. Hediger, Gergely Gyimesi

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Applications of the Microscale Thermophoresis Binding Assay in COVID-19 Research by Damian T. Nydegger, Jonai Pujol-Giménez, Palanivel Kandasamy, Bruno Vogt, Matthias A. Hediger

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Investigation of the Inhibitory Effects of the Benzodiazepine Derivative, 5-BDBD on P2X4 Purinergic Receptors by two Complementary Methods by Bernadett Balázs, Tamás Dankó, Gergely Kovács, László Köles, Matthias A. Hediger, Ákos Zsembery

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New Insights into the Physiology of Iron Transport: An Interdisciplinary Approach by Jonas Zaugg, Jonai Pujol Giménez, Romina Silvia Cabra, Wilhelm Hofstetter, Matthias A. Hediger, Christiane Albrecht

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Mechanistic basis of the inhibition of SLC11/NRAMP-mediated metal ion transport by bis-isothiourea substituted compounds by Cristina Manatschal, Jonai Pujol-Giménez, Marion Poirier, Jean-Louis Reymond, Matthias A Hediger, Raimund Dutzler

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Ca2+/Calmodulin Binding to STIM1 Hydrophobic Residues Facilitates Slow Ca2+-Dependent Inactivation of the Orai1 Channel by Rajesh Bhardwaj, Bartłomiej S. Augustynek, Ebru Ercan-Herbst, Palanivel Kandasamy, Matthias Seedorf, Christine Peinelt, Matthias A. Hediger

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Oncogenic KRAS mutations enhance amino acid uptake by colorectal cancer cells via the hippo signaling effector YAP1 by Palanivel Kandasamy, Inti Zlobec, Damian T. Nydegger, Jonai Pujol‐Giménez, Rajesh Bhardwaj, Senji Shirasawa, Toshiyuki Tsunoda, Matthias A. Hediger

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Expression, purification, and structural insights for the human uric acid transporter, GLUT9, using the Xenopus laevis oocytes system. by Benjamin Clémençon, Benjamin P Lüscher, Michael Fine, Marc U Baumann, Daniel V Surbek, Olivier Bonny, Matthias A Hediger

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Different Pharmacological Properties of GLUT9a and GLUT9b: Potential Implications in Preeclampsia by Benjamin P. Lüscher, Daniel V. Surbek, Benjamin Clémençon, Xiao Huang, Christiane Albrecht, Camilla Marini, Matthias A. Hediger, Marc U. Baumann

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Synthesis and Pharmacological Characterization of 2-Aminoethyl Diphenylborinate (2-APB) Derivatives for Inhibition of Store-Operated Calcium Entry (SOCE) in MDA-MB-231 Breast Cance... by Achille Schild, Rajesh Bhardwaj, Nicolas Wenger, Dominic Tscherrig, Palanivel Kandasamy, Jan Dernič, Roland Baur, Christine Peinelt, Matthias A. Hediger, Martin Lochner

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The Allelic Variant A391T of Metal Ion Transporter ZIP8 (SLC39A8) Leads to Hypotension and Enhanced Insulin Resistance by Sophia N. Verouti, Sophia N. Verouti, Jonai Pujol-Giménez, Jonai Pujol-Giménez, Paola Bermudez-Lekerika, Paola Bermudez-Lekerika, Laeticia Scherler, Laeticia Scherler, Rajesh Bhardwaj, Rajesh Bhardwaj, Rajesh Bhardwaj, Aurélien Thomas, Aurélien Thomas, Sébastien Lenglet, Mark Siegrist, Willy Hofstetter, Daniel G. Fuster, Daniel G. Fuster, Matthias A. Hediger, Matthias A. Hediger, Geneviève Escher, Geneviève Escher, Bruno Vogt, Bruno Vogt

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Store-Operated Calcium Entry in Breast Cancer Cells Is Insensitive to Orai1 and STIM1 N-Linked Glycosylation by Jose Sanchez-Collado, Joel Nieto-Felipe, Isaac Jardin, Rajesh Bhardwaj, Alejandro Berna-Erro, Gines M. Salido, Tarik Smani, Matthias A Hediger, Jose J. Lopez, Juan A. Rosado

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Orai1 Boosts SK3 Channel Activation by Adéla Tiffner, Valentina Hopl, Romana Schober, Matthias Sallinger, Herwig Grabmayr, Carmen Höglinger, Marc Fahrner, Victoria Lunz, Lena Maltan, Irene Frischauf, Denis Krivic, Rajesh Bhardwaj, Rainer Schindl, Matthias A. Hediger, Isabella Derler

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Dominant‐negative variant in SLC1A4 causes an autosomal dominant epilepsy syndrome by Jonai Pujol‐Giménez, Ghayda Mirzaa, Elizabeth E. Blue, Giuseppe Albano, Danny E. Miller, Aimee Allworth, James T. Bennett, Peter H. Byers, Sirisak Chanprasert, Jingheng Chen, Daniel Doherty, Andrew B. Folta, Madelyn A. Gillentine, Ian Glass, Anne Hing, Martha Horike‐Pyne, Kathleen A. Leppig, Azma Parhin, Jane Ranchalis, Wendy H. Raskind, Elisabeth A. Rosenthal, Ulrike Schwarze, Sam Sheppeard, Samuel Strohbehn, Virginia P. Sybert, Andrew Timms, Mark Wener, University of Washington Center for Mendelian Genomics (UW‐CMG)a, Undiagnosed Diseases Network (UDN), Michael J. Bamshad, Fuki M. Hisama, Gail P. Jarvik, Katrina M. Dipple, Matthias A. Hediger, Andrew B. Stergachis

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