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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Functional Characterization of the Lysosomal Peptide/Histidine Transporter PHT1 (<i>SLC15A4</i>) by Solid Supported Membrane Electrophysiology (SSME) by Jonai Pujol-Giménez, Sven P. Baumann, Tin Manh Ho, Bartlomiej Augustynek, Matthias A. Hediger

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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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Electrophysiological characterization of a diverse group of sugar transporters from Trichoderma reesei by Sami Havukainen, Jonai Pujol-Giménez, Mari Valkonen, Ann Westerholm-Parvinen, Matthias A. Hediger, Christopher P. Landowski

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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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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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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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