GABAergic regulation of cerebellar NG2 cell development is altered in perinatal white matter injury von Zonouzi, Marzieh, Scafidi, Joseph, Li, Peijun, McEllin, Brian, Edwards, Jorge, Dupree, Jeffrey L, Harvey, Lloyd, Sun, Dandan, Hübner, Christian A, Cull-Candy, Stuart G, Farrant, Mark, Gallo, Vittorio

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Role of FAM134 paralogues in endoplasmic reticulum remodeling, ER-phagy, and Collagen quality control von Reggio, Alessio, Buonomo, Viviana, Berkane, Rayene, Bhaskara, Ramachandra M, Tellechea, Mariana, Peluso, Ivana, Polishchuk, Elena, Di Lorenzo, Giorgia, Cirillo, Carmine, Esposito, Marianna, Hussain, Adeela, Huebner, Antje K, Hübner, Christian A, Settembre, Carmine, Hummer, Gerhard, Grumati, Paolo, Stolz, Alexandra

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Splicing factor YBX1 mediates persistence of JAK2-mutated neoplasms von Jayavelu, Ashok Kumar, Schnöder, Tina M., Perner, Florian, Herzog, Carolin, Meiler, Arno, Krishnamoorthy, Gurumoorthy, Huber, Nicolas, Mohr, Juliane, Edelmann-Stephan, Bärbel, Austin, Rebecca, Brandt, Sabine, Palandri, Francesca, Schröder, Nicolas, Isermann, Berend, Edlich, Frank, Sinha, Amit U., Ungelenk, Martin, Hübner, Christian A., Zeiser, Robert, Rahmig, Susann, Waskow, Claudia, Coldham, Iain, Ernst, Thomas, Hochhaus, Andreas, Jilg, Stefanie, Jost, Philipp J., Mullally, Ann, Bullinger, Lars, Mertens, Peter R., Lane, Steven W., Mann, Matthias, Heidel, Florian H.

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Intrinsic motions along an enzymatic reaction trajectory von HENZLER-WILDMAN, Katherine A, THAI, Vu, HÜBNER, Christian G, KERN, Dorothee, MING LEI, OTT, Maria, WOLF-WATZ, Magnus, FENN, Tim, POZHARSKI, Ed, WILSON, Mark A, PETSKO, Gregory A, KARPLUS, Martin

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Triac Treatment Prevents Neurodevelopmental and Locomotor Impairments in Thyroid Hormone Transporter Mct8/Oatp1c1 Deficient Mice von Chen, Jiesi, Salveridou, Eva, Liebmann, Lutz, Sundaram, Sivaraj M, Doycheva, Denica, Markova, Boyka, Hübner, Christian A, Boelen, Anita, Visser, W Edward, Heuer, Heike, Mayerl, Steffen

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Mutations in FAM134B , encoding a newly identified Golgi protein, cause severe sensory and autonomic neuropathy von Gal, Andreas, Huebner, Antje K, Baets, Jonathan, De Jonghe, Peter, Soehendra, Désirée, Nürnberg, Gudrun, Rotthier, Annelies, Senderek, Jan, Kaether, Christoph, Hübner, Christian A, Hennings, J Christopher, Timmerman, Vincent, Farrell, Sandra A, Pamminger, Torsten, Kurth, Ingo, Topaloglu, Haluk, Nürnberg, Peter

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A spastic paraplegia mouse model reveals REEP1-dependent ER shaping von Beetz, Christian, Koch, Nicole, Khundadze, Mukhran, Zimmer, Geraldine, Nietzsche, Sandor, Hertel, Nicole, Huebner, Antje-Kathrin, Mumtaz, Rizwan, Schweizer, Michaela, Dirren, Elisabeth, Karle, Kathrin N, Irintchev, Andrey, Alvarez, Victoria, Redies, Christoph, Westermann, Martin, Kurth, Ingo, Deufel, Thomas, Kessels, Michael M, Qualmann, Britta, Hübner, Christian A

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Overexpression of Pendrin in Intercalated Cells Produces Chloride-Sensitive Hypertension von JACQUES, Thibaut, PICARD, Nicolas, HASSAN, Hatim, ARONSON, Peter S, HENNINGS, Jean Christopher, HÜBNER, Christian A, NELSON, Raoul D, CHAMBREY, Régine, ELADARI, Dominique, MILLER, R. Lance, RIEMONDY, Kent A, HOUILLIER, Pascal, SOHET, Fabien, RAMAKRISHNAN, Suresh K, BÜSST, Cara J, JAYAT, Maximilien, CORNIERE, Nicolas

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Role of Cl−–HCO3− exchanger AE3 in intracellular pH homeostasis in cultured murine hippocampal neurons, and in crosstalk to adjacent astrocytes von Salameh, Ahlam I., Hübner, Christian A., Boron, Walter F.

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The KCl-cotransporter KCC2 linked to epilepsy von Hubner, Christian A

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Genetic deficiency of tartrate-resistant acid phosphatase associated with skeletal dysplasia, cerebral calcifications and autoimmunity von Superti-Furga, Andrea, Lausch, Ekkehart, Janecke, Andreas, Bros, Matthias, Trojandt, Stefanie, Alanay, Yasemin, De Laet, Corinne, Hübner, Christian A, Meinecke, Peter, Nishimura, Gen, Matsuo, Mari, Hirano, Yoshiko, Tenoutasse, Sylvie, Kiss, Andrea, Machado Rosa, Rafael Fabiano, Unger, Sharon L, Renella, Raffaele, Bonafé, Luisa, Spranger, Jürgen, Unger, Sheila, Zabel, Bernhard

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Intercalated Cell Depletion and Vacuolar H + -ATPase Mistargeting in an Ae1 R607H Knockin Model von Mumtaz, Rizwan, Trepiccione, Francesco, Hennings, J Christopher, Huebner, Antje K, Serbin, Bettina, Picard, Nicolas, Ullah, A K M Shahid, Păunescu, Teodor G, Capen, Diane E, Lashhab, Rawad M, Mouro-Chanteloup, Isabelle, Alper, Seth L, Wagner, Carsten A, Cordat, Emmanuelle, Brown, Dennis, Eladari, Dominique, Hübner, Christian A

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DNA Methylation-Mediated Modulation of Endocytosis as Potential Mechanism for Synaptic Function Regulation in Murine Inhibitory Cortical Interneurons von Pensold, Daniel, Reichard, Julia, Van Loo, Karen M J, Ciganok, Natalja, Hahn, Anne, Bayer, Cathrin, Liebmann, Lutz, Groß, Jonas, Tittelmeier, Jessica, Lingner, Thomas, Salinas-Riester, Gabriela, Symmank, Judit, Halfmann, Claas, González-Bermúdez, Lourdes, Urbach, Anja, Gehrmann, Julia, Costa, Ivan, Pieler, Tomas, Hübner, Christian A, Vatter, Hartmut, Kampa, Björn, Becker, Albert J, Zimmer-Bensch, Geraldine

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NKCC1-Dependent GABAergic Excitation Drives Synaptic Network Maturation during Early Hippocampal Development von Pfeffer, Carsten K, Stein, Valentin, Keating, Damien J, Maier, Hannes, Rinke, Ilka, Rudhard, York, Hentschke, Moritz, Rune, Gabriele M, Jentsch, Thomas J, Hubner, Christian A

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Photoblinking and photobleaching of rylene diimide dyes von Haase, Mathias, Hübner, Christian G, Nolde, Fabian, Müllen, Klaus, Basché, Thomas

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Structural and functional annotation of PR/SET Domain (PRDM) protein family: In-silico study elaborating role of PRDM12 mutation in congenital insensitivity to pain von Mehmood, Sarmad, Dad, Rubina, Ahmad, Arsalan, Ullah, Muhammad Ikram, John, Peter, Ali, Amjad, Hubner, Christian A., Mohyuddin, Aisha, Hassan, Muhammad Jawad

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Ion channels: Function unravelled by dysfunction von Jentsch, Thomas J, Hübner, Christian A, Fuhrmann, Jens C

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Mutations in RDH12 encoding a photoreceptor cell retinol dehydrogenase cause childhood-onset severe retinal dystrophy von McHenry, Christina L, Hübner, Christian A, Gal, Andreas, Thompson, Debra A, Wissinger, Bernd, Rüschendorf, Franz, Heckenlively, John, Schmid, Eduard, Utermann, Gerd, Janecke, Andreas R, Nair, Anita R, Nürnberg, Peter, Becker, Christian

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Combined genetic disruption of K-Cl cotransporters and Gardos channel KCNN4 rescues erythrocyte dehydration in the SAD mouse model of sickle cell disease von Shmukler, Boris E., Rivera, Alicia, Bhargava, Parul, Nishimura, Katherine, Hsu, Ann, Kim, Edward H., Trudel, Marie, Rust, Marco B., Hubner, Christian A., Brugnara, Carlo, Alper, Seth L.

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Genetic disruption of KCC cotransporters in a mouse model of thalassemia intermedia von Shmukler, Boris E., Rivera, Alicia, Bhargava, Parul, Nishimura, Katherine, Kim, Edward H., Hsu, Ann, Wohlgemuth, Jay G., Morton, James, Snyder, L. Michael, De Franceschi, Lucia, Rust, Marco B., Hubner, Christian A., Brugnara, Carlo, Alper, Seth L.

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