PUB - Publikationen an der Universität Bielefeld

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• [56]
  

  2022 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2969198

  Stoeger, T., Grant, R.A., McQuattie-Pimentel, A.C., Anekalla, K.R., Liu, S.S., Tejedor-Navarro, H., Singer, B.D., Abdala-Valencia, H., Schwake, M., Tetreault, M.-P., Perlman, H., Balch, W.E., Chandel, N.S., Ridge, K.M., Sznajder, J.I., Morimoto, R.I., Misharin, A.V., Budinger, G.R.S., Amaral, L.A.N.: Aging is associated with a systemic length-associated transcriptome imbalance. Nature Aging. 2, 1191-1206 (2022).

  PUB | DOI | WoS
   
• [55]
  

  2021 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2959493

  Donkervoort, S., Krause, N., Dergai, M., Yun, P., Koliwer, J., Gorokhova, S., Hauserman, J.G., Cummings, B.B., Hu, Y., Smith, R., Uapinyoying, P., Ganesh, V.S., Ghosh, P.S., Monaghan, K.G., Edassery, S.L., Ferle, P., Silverstein, S., Chao, K.R., Snyder, M., Ellingwood, S., Bharucha-Goebel, D., Iannaccone, S.T., Dal Peraro, M., Foley, A.R., Savas, J.N., Bolduc, V., Fasshauer, D., Bonnemann, C.G., Schwake, M.: BET1 variants establish impaired vesicular transport as a cause for muscular dystrophy with epilepsy. EMBO Molecular Medicine . : e13787 (2021).

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• [54]
  

  2020 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2948754

  Saminathan, A., Devany, J., Veetil, A.T., Suresh, B., Pillai, K.S., Schwake, M., Krishnan, Y.: A DNA-based voltmeter for organelles. Nature Nanotechnology. (2020).

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• [53]
  

  2019 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2936923

  Heybrock, S., Kanerva, K., Meng, Y., Ing, C., Liang, A., Xiong, Z.-J., Weng, X., Kim, Y.A., Collins, R., Trimble, W., Pomes, R., Prive, G.G., Annaert, W., Schwake, M., Heeren, J., Luellmann-Rauch, R., Grinstein, S., Ikonen, E., Saftig, P., Neculai, D.: Lysosomal integral membrane protein-2 (LIMP-2/SCARB2) is involved in lysosomal cholesterol export. Nature Communications. 10, : 3521 (2019).

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• [52]
  

  2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2931407

  Strigli, A., Raab, C., Hessler, S., Huth, T., Schuldt, A.J.T., Alzheimer, C., Friedrich, T., Burridge, P.W., Luedde, M., Schwake, M.: Doxorubicin induces caspase-mediated proteolysis of KV7.1. Communications Biology. 1, : 155 (2018).

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• [51]
  

  2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2932410

  Donkervoort, S., Hu, Y., Shieh, P., Koliwer, J., Tsai, L., Cummings, B., Snyder, M., Chao, K., Kaur, R., Bharucha-Goebel, D., Iannaccone, S., MacArthur, D., Foley, A.R., Schwake, M., Bonnemann, C.: Recessive mutations in BET1 and GOSR2 establish Q-SNARE Golgi-vesicle-transport genes as a cause for congenital muscular dystrophy with epilepsy. NEUROMUSCULAR DISORDERS. 28, : S30 (2018).

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• [50]
  

  2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953333

  Conrad, K.S., Cheng, T.-W., Ysselstein, D., Heybrock, S., Hoth, L.R., Chrunyk, B.A., am Ende, C.W., Krainc, D., Schwake, M., Saftig, P., Liu, S., Qiu, X., Ehlers, M.D.: Lysosomal integral membrane protein-2 as a phospholipid receptor revealed by biophysical and cellular studies. Nature Communications. 8, : 1908 (2017).

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• [49]
  

  2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953334

  Valdez, C., Wong, Y.C., Schwake, M., Bu, G., Wszolek, Z.K., Krainc, D.: Progranulin-mediated deficiency of cathepsin D results in FTD and NCL-like phenotypes in neurons derived from FTD patients. Human Molecular Genetics. 26, 4861-4872 (2017).

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• [48]
  

  2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2916109

  Rujano, M.A., Serio, M.C., Panasyuk, G., P, R.A., Reunert, J., Rymen, D., Hauser, V., Park, J.H., Freisinger, P., Souche, E., Guida, M.C., Maier, E.M., Wada, Y., Jager, S., Krogan, N.J., Kretz, O., Nobre, S., Garcia, P., Quelhas, D., Bird, T.D., Raskind, W.H., Schwake, M., Duvet, S., Foulquier, F., Matthijs, G., Marquardt, T., Simons, M.: Mutations in the X-linked ATP6AP2 cause a glycosylation disorder with autophagic defects. JOURNAL OF EXPERIMENTAL MEDICINE. 214, 3707-3729 (2017).

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• [47]
  

  2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2916411

  Völker, J.M., Dergai, M., Abriata, L.A., Mingard, Y., Ysselstein, D., Krainc, D., Dal Peraro, M., Fischer von Mollard, G., Fasshauer, D., Koliwer, J., Schwake, M.: Functional assays for the assessment of the pathogenicity of variants of GOSR2, an ER-to-Golgi SNARE involved in progressive myoclonus epilepsies. DISEASE MODELS & MECHANISMS. 10, 1391-1398 (2017).

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• [46]
  

  2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953335

  Zheng, J., Chen, L., Schwake, M., Silverman, R.B., Krainc, D.: Design and Synthesis of Potent Quinazolines as Selective β-Glucocerebrosidase Modulators. Journal of Medicinal Chemistry. 59, 8508-8520 (2016).

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [45]
  

  2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2913169

  Dibbens, L., Schwake, M., Saftig, P., Rubboli, G.: SCARB2/LIMP2 deficiency in action myoclonus-renal failure syndrome. EPILEPTIC DISORDERS. 18, S63-S72 (2016).

  PUB | DOI | WoS
   
• [44]
  

  2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2903027

  Zunke, F., Andresen, L., Wesseler, S., Groth, J., Arnold, P., Rothaug, M., Mazzulli, J.R., Krainc, D., Blanz, J., Saftig, P., Schwake, M.: Characterization of the complex formed by beta-glucocerebrosidase and the lysosomal integral membrane protein type-2. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA. 113, 3791-3796 (2016).

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• [43]
  

  2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2904109

  Kook, S., Wang, P., Young, L.R., Schwake, M., Saftig, P., Weng, X., Meng, Y., Neculai, D., Marks, M.S., Gonzales, L., Beers, M.F., Guttentag, S.: Impaired Lysosomal Integral Membrane Protein 2-dependent Peroxiredoxin 6 Delivery to Lamellar Bodies Accounts for Altered Alveolar Phospholipid Content in Adaptor Protein-3-deficient pearl Mice. JOURNAL OF BIOLOGICAL CHEMISTRY. 291, 8414-8427 (2016).

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• [42]
  

  2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2901299

  Agsten, M., Hessler, S., Lehnert, S., Volk, T., Rittger, A., Hartmann, S., Raab, C., Kim, D.Y., Groemer, T.W., Schwake, M., Alzheimer, C., Huth, T.: BACE1 modulates gating of KCNQ1 (Kv7.1) and cardiac delayed rectifier KCNQ1/KCNE1 (I-Ks). Journal of Molecular and Cellular Cardiology. 89, 335-348 (2015).

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• [41]
  

  2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2731234

  Hessler, S., Zheng, F., Hartmann, S., Rittger, A., Lehnert, S., Voelkel, M., Nissen, M., Edelmann, E., Saftig, P., Schwake, M., Huth, T., Alzheimer, C.: beta-Secretase BACE1 Regulates Hippocampal and Reconstituted M-Currents in a beta-Subunit-Like Fashion. Journal of Neuroscience. 35, 3298-3311 (2015).

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• [40]
  

  2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2731248

  Peters, J., Rittger, A., Weisner, R., Knabbe, J., Zunke, F., Rothaug, M., Damme, M., Berkovic, S.F., Blanz, J., Saftig, P., Schwake, M.: Lysosomal integral membrane protein type-2 (LIMP-2/SCARB2) is a substrate of cathepsin-F, a cysteine protease mutated in type-B-Kufs-disease. Biochemical and Biophysical Research Communications. 457, 334-340 (2015).

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• [39]
  

  2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2901039

  Blanz, J., Zunke, F., Markmann, S., Damme, M., Braulke, T., Saftig, P., Schwake, M.: Mannose 6-phosphate-independent Lysosomal Sorting of Limp-2. Traffic. 16, 1127-1136 (2015).

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [38]
  

  2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2759802

  Kissing, S., Hermsen, C., Repnik, U., Nesset, C.K., von Bargen, K., Griffiths, G., Ichihara, A., Lee, B.S., Schwake, M., De Brabander, J., Haas, A., Saftig, P.: Vacuolar ATPase in Phagosome-Lysosome Fusion. Journal of Biological Chemistry. 290, 14166-14180 (2015).

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• [37]
  

  2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2671368

  Lemke, J.R., Hendrickx, R., Geider, K., Laube, B., Schwake, M., Harvey, R.J., James, V.M., Pepler, A., Steiner, I., Hoertnagel, K., Neidhardt, J., Ruf, S., Wolff, M., Bartholdi, D., Caraballo, R., Platzer, K., Suls, A., De Jonghe, P., Biskup, S., Weckhuysen, S.: GRIN2B Mutations in West Syndrome and Intellectual Disability with Focal Epilepsy. Annals of Neurology. 75, 147-154 (2014).

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• [36]
  

  2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2660866

  Gaspar, P., Kallemeijn, W.W., Strijland, A., Scheij, S., Van Eijk, M., Aten, J., Overkleeft, H.S., Balreira, A., Zunke, F., Schwake, M., Miranda, C.S., Aerts, J.M.F.G.: Action myoclonus-renal failure syndrome: diagnostic applications of activity-based probes and lipid analysis. The Journal of Lipid Research. 55, 138-145 (2014).

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• [35]
  

  2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2694992

  Rosendahl, A., Niemann, G., Lange, S., Ahadzadeh, E., Krebs, C., Contrepas, A., van Goor, H., Wiech, T., Bader, M., Schwake, M., Peters, J., Stahl, R., Nguyen, G., Wenzel, U.: Increased expression of (pro)renin receptor does not cause hypertension or cardiac and renal fibrosis in mice. Laboratory Investigation. 94, 863-872 (2014).

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• [34]
  

  2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2707698

  Rothaug, M., Zunke, F., Mazzulli, J.R., Schweizer, M., Altmeppen, H., Luellmann-Rauch, R., Kallemeijn, W.W., Gaspar, P., Aerts, J.M., Glatzel, M., Saftig, P., Krainc, D., Schwake, M., Blanz, J.: LIMP-2 expression is critical for beta-glucocerebrosidase activity and alpha-synuclein clearance. Proceedings of the National Academy of Sciences. 111, 15573-15578 (2014).

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• [33]
  

  2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2681867

  Schwarz, J., Schmidt, S., Will, O., Koudelka, T., Koehler, K., Boss, M., Rabe, B., Tholey, A., Scheller, J., Schmidt-Arras, D., Schwake, M., Rose-John, S., Chalaris, A.: Polo-like Kinase 2, a Novel ADAM17 Signaling Component, Regulates Tumor Necrosis Factor similar to Ectodomain Shedding. Journal of Biological Chemistry. 289, 3080-3093 (2014).

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• [32]
  

  2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953336

  Smith, K.R., Dahl, H.-H.M., Canafoglia, L., Andermann, E., Damiano, J., Morbin, M., Bruni, A.C., Giaccone, G., Cossette, P., Saftig, P., Grotzinger, J., Schwake, M., Andermann, F., Staropoli, J.F., Sims, K.B., Mole, S.E., Franceschetti, S., Alexander, N.A., Cooper, J.D., Chapman, H.A., Carpenter, S., Berkovic, S.F., Bahlo, M.: Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosis. Human Molecular Genetics. 22, 1417-1423 (2013).

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• [31]
  

  2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953337

  Schwake, M., Schröder, B., Saftig, P.: Lysosomal Membrane Proteins and Their Central Role in Physiology. Traffic. 14, 739-748 (2013).

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• [30]
  

  2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953338

  Schmid, J., Oelbe, M., Saftig, P., Schwake, M., Schweda, F.: Parallel regulation of renin and lysosomal integral membrane protein 2 in renin-producing cells: further evidence for a lysosomal nature of renin secretory vesicles. Pflügers Archiv - European Journal of Physiology. 465, 895-905 (2013).

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• [29]
  

  2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953339

  Boehlen, A., Schwake, M., Dost, R., Kunert, A., Fidzinski, P., Heinemann, U., Gebhardt, C.: The new KCNQ2 activator 4-Chlor-N-(6-chlor-pyridin-3-yl)-benzamid displays anticonvulsant potential. British Journal of Pharmacology. 168, 1182-1200 (2013).

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• [28]
  

  2013 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2953341

  Schwake, M., Saftig, P.: Lysosomal Membrane Defects. In: Mehta, A. and Winchester, B. (eds.) Lysosomal Storage Disorders. A Practical Guide. p. 131-136. Wiley-Blackwell, Oxford (2013).

  PUB | DOI | Download (ext.)
   
• [27]
  

  2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2625613

  Lemke, J.R., Lal, D., Reinthaler, E.M., Steiner, I., Nothnagel, M., Alber, M., Geider, K., Laube, B., Schwake, M., Finsterwalder, K., Franke, A., Schilhabel, M., Jaehn, J.A., Muhle, H., Boor, R., Van Paesschen, W., Caraballo, R., Fejerman, N., Weckhuysen, S., De Jonghe, P., Larsen, J., Moller, R.S., Hjalgrim, H., Addis, L., Tang, S., Hughes, E., Pal, D.K., Veri, K., Vaher, U., Talvik, T., Dimova, P., Lopez, R.G., Serratosa, J.M., Linnankivi, T., Lehesjoki, A.-E., Ruf, S., Wolff, M., Buerki, S., Wohlrab, G., Kroell, J., Datta, A.N., Fiedler, B., Kurlemann, G., Kluger, G., Hahn, A., Haberlandt, D.E., Kutzer, C., Sperner, J., Becker, F., Weber, Y.G., Feucht, M., Steinboeck, H., Neophythou, B., Ronen, G.M., Gruber-Sedlmayr, U., Geldner, J., Harvey, R.J., Hoffmann, P., Herms, S., Altmueller, J., Toliat, M.R., Thiele, H., Nuernberg, P., Wilhelm, C., Stephani, U., Helbig, I., Lerche, H., Zimprich, F., Neubauer, B.A., Biskup, S., von Spiczak, S.: Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes. Nature Genetics. 45, 1067-1072 (2013).

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• [26]
  

  2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2645175

  Neculai, D., Schwake, M., Ravichandran, M., Zunke, F., Collins, R.F., Peters, J., Neculai, M., Plumb, J., Loppnau, P., Pizarro, J.C., Seitova, A., Trimble, W.S., Saftig, P., Grinstein, S., Dhe-Paganon, S.: Structure of LIMP-2 provides functional insights with implications for SR-BI and CD36. Nature. 504, 172-176 (2013).

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• [25]
  

  2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953340

  Zachos, C., Blanz, J., Saftig, P., Schwake, M.: A Critical Histidine Residue Within LIMP-2 Mediates pH Sensitive Binding to Its Ligand β-Glucocerebrosidase. Traffic. 13, 1113-1123 (2012).

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• [24]
  

  2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953342

  Chadha, P.S., Zunke, F., Davis, A.J., Jepps, T.A., Linders, J.T.M., Schwake, M., Towart, R., Greenwood, I.A.: Pharmacological dissection of Kv7.1 channels in systemic and pulmonary arteries. British Journal of Pharmacology. 166, 1377-1387 (2012).

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• [23]
  

  2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953343

  Prox, J., Willenbrock, M., Weber, S., Lehmann, T., Schmidt-Arras, D., Schwanbeck, R., Saftig, P., Schwake, M.: Tetraspanin15 regulates cellular trafficking and activity of the ectodomain sheddase ADAM10. Cellular and Molecular Life Sciences. 69, 2919-2932 (2012).

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• [22]
  

  2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953344

  Corbett, M.A., Schwake, M., Bahlo, M., Dibbens, L.M., Lin, M., Gandolfo, L.C., Vears, D.F., O'Sullivan, J.D., Robertson, T., Bayly, M.A., Gardner, A.E., Vlaar, A.M., Korenke, G.C., Bloem, B.R., de Coo, I. F., Verhagen, J.M.A., Lehesjoki, A.-E., Gecz, J., Berkovic, S.F.: A Mutation in the Golgi Qb-SNARE Gene GOSR2 Causes Progressive Myoclonus Epilepsy with Early Ataxia. The American Journal of Human Genetics. 88, 657-663 (2011).

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• [21]
  

  2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953345

  Valkova, C., Albrizio, M., Roder, I.V., Schwake, M., Betto, R., Rudolf, R., Kaether, C.: Sorting receptor Rer1 controls surface expression of muscle acetylcholine receptors by ER retention of unassembled α-subunits. Proceedings of the National Academy of Sciences. 108, 621-625 (2011).

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• [20]
  

  2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953346

  Desmond, M.J., Lee, D., Fraser, S.A., Katerelos, M., Gleich, K., Martinello, P., Li, Y.Q., Thomas, M.C., Michelucci, R., Cole, A.J., Saftig, P., Schwake, M., Stapleton, D., Berkovic, S.F., Power, D.A.: Tubular proteinuria in mice and humans lacking the intrinsic lysosomal protein SCARB2/Limp-2. American Journal of Physiology-Renal Physiology. 300, F1437-F1447 (2011).

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• [19]
  

  2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953347

  Blanz, J., Groth, J., Zachos, C., Wehling, C., Saftig, P., Schwake, M.: Disease-causing mutations within the lysosomal integral membrane protein type 2 (LIMP-2) reveal the nature of binding to its ligand β-glucocerebrosidase. Human Molecular Genetics. 19, 563-572 (2010).

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• [18]
  

  2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953348

  Lange, W., Geißendörfer, J., Schenzer, A., Grötzinger, J., Seebohm, G., Friedrich, T., Schwake, M.: Refinement of the Binding Site and Mode of Action of the Anticonvulsant Retigabine on KCNQ K Channels. Molecular Pharmacology. 75, 272-280 (2009).

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• [17]
  

  2008 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953349

  Yeung, S.Y.M., Schwake, M., Pucovský, V., Greenwood, I.A.: Bimodal effects of the K 7 channel activator retigabine on vascular K+ currents. British Journal of Pharmacology. 155, 62-72 (2008).

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• [16]
  

  2008 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953350

  Yeung, S.Y.M., Lange, W., Schwake, M., Greenwood, I.A.: Expression profile and characterisation of a truncated KCNQ5 splice variant. Biochemical and Biophysical Research Communications. 371, 741-746 (2008).

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• [15]
  

  2007 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953351

  Yamasaki, R., Zhang, J., Koshiishi, I., Sastradipura Suniarti, D.F., Wu, Z., Peters, C., Schwake, M., Uchiyama, Y., Kira, J.-ichi, Saftig, P., Utsumi, H., Nakanishi, H.: Involvement of lysosomal storage-induced p38 MAP kinase activation in the overproduction of nitric oxide by microglia in cathepsin D-deficient mice. Molecular and Cellular Neuroscience. 35, 573-584 (2007).

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• [14]
  

  2007 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953352

  Reczek, D., Schwake, M., Schröder, J., Hughes, H., Blanz, J., Jin, X., Brondyk, W., Van Patten, S., Edmunds, T., Saftig, P.: LIMP-2 Is a Receptor for Lysosomal Mannose-6-Phosphate-Independent Targeting of β-Glucocerebrosidase. Cell. 131, 770-783 (2007).

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• [13]
  

  2007 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953353

  Schroen, B., Leenders, J.J., van Erk, A., Bertrand, A.T., van Loon, M., van Leeuwen, R.E., Kubben, N., Duisters, R.F., Schellings, M.W., Janssen, B.J., Debets, J.J., Schwake, M., Høydal, M.A., Heymans, S., Saftig, P., Pinto, Y.M.: Lysosomal integral membrane protein 2 is a novel component of the cardiac intercalated disc and vital for load-induced cardiac myocyte hypertrophy. Journal of Experimental Medicine. 204, 1227-1235 (2007).

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• [12]
  

  2007 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953354

  Wehling, C., Beimgraben, C., Gelhaus, C., Friedrich, T., Saftig, P., Grötzinger, J., Schwake, M.: Self-assembly of the isolated KCNQ2 subunit interaction domain. FEBS Letters. 581, 1594-1598 (2007).

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• [11]
  

  2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953358

  Schwake, M.: Structural Determinants of M-Type KCNQ (Kv7) K+ Channel Assembly. Journal of Neuroscience. 26, 3757-3766 (2006).

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• [10]
  

  2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953355

  Knipper, M., Claussen, C., Rüttiger, L., Zimmermann, U., Lüllmann-Rauch, R., Eskelinen, E.-L., Schröder, J., Schwake, M., Saftig, P.: Deafness in LIMP2-deficient mice due to early loss of the potassium channel KCNQ1/KCNE1 in marginal cells of the stria vascularis. The Journal of Physiology. 576, 73-86 (2006).

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  2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953356

  Caeyenberghs, K., Balschun, D., Roces, D.P., Schwake, M., Saftig, P., D'Hooge, R.: Multivariate neurocognitive and emotional profile of a mannosidosis murine model for therapy assessment. Neurobiology of Disease. 23, 422-432 (2006).

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  2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953357

  Pachnio, A., Dietrich, S., Klapper, W., Humpe, A., Schwake, M., Sedlacek, R., Gramatzki, M., Beck, C.: Proliferation-based T-cell selection for immunotherapy and graft-versus-host-disease prophylaxis in the context of bone marrow transplantation. Bone Marrow Transplantation. 38, 157-167 (2006).

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  2005 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953361

  Dominguez, D., Tournoy, J., Hartmann, D., Huth, T., Cryns, K., Deforce, S., Serneels, L., Camacho, I.E., Marjaux, E., Craessaerts, K., Roebroek, A.J.M., Schwake, M., D'Hooge, R., Bach, P., Kalinke, U., Moechars, D., Alzheimer, C., Reiss, K., Saftig, P., De Strooper, B.: Phenotypic and Biochemical Analyses of BACE1- and BACE2-deficient Mice. Journal of Biological Chemistry. 280, 30797-30806 (2005).

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  2005 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953360

  D'Hooge, R., Lüllmann-Rauch, R., Beckers, T., Balschun, D., Schwake, M., Reiss, K., von Figura, K., Saftig, P.: Neurocognitive and Psychotiform Behavioral Alterations and Enhanced Hippocampal Long-Term Potentiation in Transgenic Mice Displaying Neuropathological Features of Human  α-Mannosidosis. Journal of Neuroscience. 25, 6539-6549 (2005).

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  2005 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953359

  Schenzer, A., Friedrich, T., Pusch, M., Saftig, P., Jentsch, T.J., Grötzinger, J., Schwake, M.: Molecular Determinants of KCNQ (Kv7) K+ Channel Sensitivity to the Anticonvulsant Retigabine. Journal of Neuroscience. 25, 5051-5060 (2005).

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  2003 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953362

  Schwake, M., Jentsch, T.J., Friedrich, T.: A carboxy‐terminal domain determines the subunit specificity of KCNQ K+ channel assembly. EMBO reports. 4, 76-81 (2003).

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  2001 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953363

  Schwake, M., Friedrich, T., Jentsch, T.J.: An Internalization Signal in ClC-5, an Endosomal Cl−Channel Mutated in Dent's Disease. Journal of Biological Chemistry. 276, 12049-12054 (2001).

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  2000 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953364

  Piwon, N., Günther, W., Schwake, M., Bösl, M.R., Jentsch, T.J.: ClC-5 Cl--channel disruption impairs endocytosis in a mouse model for Dent's disease. Nature. 408, 369-373 (2000).

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  2000 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953365

  Schwake, M., Pusch, M., Kharkovets, T., Jentsch, T.J.: Surface Expression and Single Channel Properties of KCNQ2/KCNQ3, M-type K+ Channels Involved in Epilepsy. Journal of Biological Chemistry. 275, 13343-13348 (2000).

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