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Involvement of the L-Type Amino Acid Transporter Lat2 in the Transport of 3,3′-Diiodothyronine across the Plasma Membrane

2015 . Kinne, Anita | Wittner, Melanie | Wirth, Eva K. | Hinz, Katrin M. | Schülein, Ralf | Köhrle, Josef | Krause, Gerd

Lipids, GTPases, and their regulators in membrane dynamics: an intracellular ménage à trois

2015 . Echard, Arnaud | Haucke, Volker

Structural heterogeneity in microcrystalline ubiquitin studied by solid-state NMR

2015 . Fasshuber, Hannes Klaus | Lakomek, Nils-Alexander | Habenstein, Birgit | Loquet, Antoine | Shi, Chaowei | Giller, Karin | Wolff, Sebastian | Becker, Stefan | Lange, Adam

Syntaxin 1B is important for mouse postnatal survival and proper synaptic function at the mouse neuromuscular junctions

2015 . Wu, Yuan-Ju | Tejero, Rocio | Arancillo, Marife | Vardar, Gülcin | Korotkova, Tatiana | Kintscher, Michael | Schmitz, Dietmar | Tabares, Lucia | Rosenmund, Christian | Ponomarenko, Alexey

Discovery of CLC transport proteins: cloning, structure, function and pathophysiology

2015 . https://frl.publisso.de/authors/ | Jentsch, Thomas

Structural Insights Into Thyroid Hormone Transport Mechanisms of the L-Type Amino Acid Transporter 2

2015 . Hinz, Katrin M. | Meyer, Katja | Kinne, Anita | Schülein, Ralf | Köhrle, Josef | Krause, Gerd

Loss of Gadkin Affects Dendritic Cell Migration 'In Vitro'

2015 . Schachtner, Hannah | Weimershaus, Mirjana | Stache, Vanessa | Plewa, Natalia | Legler, Daniel F. | Höpken, Uta E. | Maritzen, Tanja

Finding new drugs to enhance anion secretion in cystic fibrosis: Toward suitable systems for better drug screening. Report on the pre-conference meeting to the 12th ECFS Basic Science Conference, Albufeira, 25–28 March 2015

2015 . Verkman, Alan S. | Edelman, Aleksander | Amaral, Margarida | Mall, Marcus A. | Beekman, Jeffrey M. | Meiners, Torsten | Galietta, Luis J.V. | Bear, Christine E.

Plasma proteomic analysis of active and torpid greater mouse-eared bats (Myotis myotis)

2015 . Hecht, Alexander M. | Braun, Beate C. | Krause, Eberhard | Voigt, Christian | Greenwood, Alex | Czirják, Gábor Árpád

X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes

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