Showing 1 - 16 results of 16 for search 'Matthias A. Hediger', query time: 0.05s
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Sequence Features of Mitochondrial Transporter Protein Families by Gergely Gyimesi, Matthias A. Hediger
Published 2020-11-01
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Transporter-Mediated Drug Delivery by Gergely Gyimesi, Matthias A. Hediger
Published 2023-01-01
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Systematic in silico discovery of novel solute carrier-like proteins from proteomes. by Gergely Gyimesi, Matthias A Hediger
Published 2022-01-01
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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
Published 2022-05-01
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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
Published 2020-03-01
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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
Published 2021-10-01
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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
Published 2022-06-01
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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
Published 2023-06-01
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