56 Publikationen

Alle markieren

  • [56]
    2022 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2969198
    T. Stoeger, R. A. Grant, A. C. McQuattie-Pimentel, K. R. Anekalla, S. S. Liu, H. Tejedor-Navarro, B. D. Singer, H. Abdala-Valencia, M. Schwake, M. - P. Tetreault, et al., “Aging is associated with a systemic length-associated transcriptome imbalance”, Nature Aging, 2022, 2, 1191-1206.
    PUB | DOI | WoS
     
  • [55]
    2021 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2959493 OA
    S. Donkervoort, N. Krause, M. Dergai, P. Yun, J. Koliwer, S. Gorokhova, J. G. Hauserman, B. B. Cummings, Y. Hu, R. Smith, et al., “BET1 variants establish impaired vesicular transport as a cause for muscular dystrophy with epilepsy”, EMBO Molecular Medicine , 2021, : e13787.
    PUB | PDF | DOI | WoS | PubMed | Europe PMC
     
  • [54]
    2020 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2948754
    A. Saminathan, J. Devany, A. T. Veetil, B. Suresh, K. S. Pillai, M. Schwake, and Y. Krishnan, “A DNA-based voltmeter for organelles”, Nature Nanotechnology, 2020.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [53]
    2019 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2936923
    S. Heybrock, K. Kanerva, Y. Meng, C. Ing, A. Liang, Z. - J. Xiong, X. Weng, Y. A. Kim, R. Collins, W. Trimble, et al., “Lysosomal integral membrane protein-2 (LIMP-2/SCARB2) is involved in lysosomal cholesterol export”, Nature Communications, 2019, 10, : 3521.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [52]
    2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2931407 OA
    A. Strigli, C. Raab, S. Hessler, T. Huth, A. J. T. Schuldt, C. Alzheimer, T. Friedrich, P. W. Burridge, M. Luedde, and M. Schwake, “Doxorubicin induces caspase-mediated proteolysis of KV7.1”, Communications Biology, 2018, 1, : 155.
    PUB | PDF | DOI | WoS | PubMed | Europe PMC
     
  • [51]
    2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2932410
    S. Donkervoort, Y. Hu, P. Shieh, J. Koliwer, L. Tsai, B. Cummings, M. Snyder, K. Chao, R. Kaur, D. Bharucha-Goebel, et al., “Recessive mutations in BET1 and GOSR2 establish Q-SNARE Golgi-vesicle-transport genes as a cause for congenital muscular dystrophy with epilepsy”, NEUROMUSCULAR DISORDERS, 2018, 28, : S30.
    PUB | DOI | WoS
     
  • [50]
    2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953333 OA
    K. S. Conrad, T. - W. Cheng, D. Ysselstein, S. Heybrock, L. R. Hoth, B. A. Chrunyk, C. W. am Ende, D. Krainc, M. Schwake, P. Saftig, et al., “Lysosomal integral membrane protein-2 as a phospholipid receptor revealed by biophysical and cellular studies”, Nature Communications, 2017, 8, : 1908.
    PUB | PDF | DOI | WoS | PubMed | Europe PMC
     
  • [49]
    2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953334
    C. Valdez, Y. C. Wong, M. Schwake, G. Bu, Z. K. Wszolek, and D. Krainc, “Progranulin-mediated deficiency of cathepsin D results in FTD and NCL-like phenotypes in neurons derived from FTD patients”, Human Molecular Genetics, 2017, 26, 4861-4872.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [48]
    2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2916109 OA
    M. A. Rujano, M. C. Serio, G. Panasyuk, R. A. P, J. Reunert, D. Rymen, V. Hauser, J. H. Park, P. Freisinger, E. Souche, et al., “Mutations in the X-linked ATP6AP2 cause a glycosylation disorder with autophagic defects”, JOURNAL OF EXPERIMENTAL MEDICINE, 2017, 214, 3707-3729.
    PUB | PDF | DOI | WoS | PubMed | Europe PMC
     
  • [47]
    2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2916411
    J. M. Völker, M. Dergai, L. A. Abriata, Y. Mingard, D. Ysselstein, D. Krainc, M. Dal Peraro, G. Fischer von Mollard, D. Fasshauer, J. Koliwer, et al., “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, 2017, 10, 1391-1398.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [46]
    2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953335
    J. Zheng, L. Chen, M. Schwake, R. B. Silverman, and D. Krainc, “Design and Synthesis of Potent Quinazolines as Selective β-Glucocerebrosidase Modulators”, Journal of Medicinal Chemistry, 2016, 59, 8508-8520.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [45]
    2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2913169
    L. Dibbens, M. Schwake, P. Saftig, and G. Rubboli, “SCARB2/LIMP2 deficiency in action myoclonus-renal failure syndrome”, EPILEPTIC DISORDERS, 2016, 18, S63-S72.
    PUB | DOI | WoS
     
  • [44]
    2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2903027
    F. Zunke, L. Andresen, S. Wesseler, J. Groth, P. Arnold, M. Rothaug, J. R. Mazzulli, D. Krainc, J. Blanz, P. Saftig, et al., “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, 2016, 113, 3791-3796.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [43]
    2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2904109
    S. Kook, P. Wang, L. R. Young, M. Schwake, P. Saftig, X. Weng, Y. Meng, D. Neculai, M. S. Marks, L. Gonzales, et al., “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, 2016, 291, 8414-8427.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [42]
    2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2901299
    M. Agsten, S. Hessler, S. Lehnert, T. Volk, A. Rittger, S. Hartmann, C. Raab, D. Y. Kim, T. W. Groemer, M. Schwake, et al., “BACE1 modulates gating of KCNQ1 (Kv7.1) and cardiac delayed rectifier KCNQ1/KCNE1 (I-Ks)”, Journal of Molecular and Cellular Cardiology, 2015, 89, 335-348.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [41]
    2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2731234
    S. Hessler, F. Zheng, S. Hartmann, A. Rittger, S. Lehnert, M. Voelkel, M. Nissen, E. Edelmann, P. Saftig, M. Schwake, et al., “beta-Secretase BACE1 Regulates Hippocampal and Reconstituted M-Currents in a beta-Subunit-Like Fashion”, Journal of Neuroscience, 2015, 35, 3298-3311.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [40]
    2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2731248
    J. Peters, A. Rittger, R. Weisner, J. Knabbe, F. Zunke, M. Rothaug, M. Damme, S. F. Berkovic, J. Blanz, P. Saftig, et al., “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, 2015, 457, 334-340.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [39]
    2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2901039
    J. Blanz, F. Zunke, S. Markmann, M. Damme, T. Braulke, P. Saftig, and M. Schwake, “Mannose 6-phosphate-independent Lysosomal Sorting of Limp-2”, Traffic, 2015, 16, 1127-1136.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [38]
    2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2759802
    S. Kissing, C. Hermsen, U. Repnik, C. K. Nesset, K. von Bargen, G. Griffiths, A. Ichihara, B. S. Lee, M. Schwake, J. De Brabander, et al., “Vacuolar ATPase in Phagosome-Lysosome Fusion”, Journal of Biological Chemistry, 2015, 290, 14166-14180.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [37]
    2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2671368
    J. R. Lemke, R. Hendrickx, K. Geider, B. Laube, M. Schwake, R. J. Harvey, V. M. James, A. Pepler, I. Steiner, K. Hoertnagel, et al., “GRIN2B Mutations in West Syndrome and Intellectual Disability with Focal Epilepsy”, Annals of Neurology, 2014, 75, 147-154.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [36]
    2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2660866
    P. Gaspar, W. W. Kallemeijn, A. Strijland, S. Scheij, M. Van Eijk, J. Aten, H. S. Overkleeft, A. Balreira, F. Zunke, M. Schwake, et al., “Action myoclonus-renal failure syndrome: diagnostic applications of activity-based probes and lipid analysis”, The Journal of Lipid Research, 2014, 55, 138-145.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [35]
    2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2694992
    A. Rosendahl, G. Niemann, S. Lange, E. Ahadzadeh, C. Krebs, A. Contrepas, H. van Goor, T. Wiech, M. Bader, M. Schwake, et al., “Increased expression of (pro)renin receptor does not cause hypertension or cardiac and renal fibrosis in mice”, Laboratory Investigation, 2014, 94, 863-872.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [34]
    2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2707698
    M. Rothaug, F. Zunke, J. R. Mazzulli, M. Schweizer, H. Altmeppen, R. Luellmann-Rauch, W. W. Kallemeijn, P. Gaspar, J. M. Aerts, M. Glatzel, et al., “LIMP-2 expression is critical for beta-glucocerebrosidase activity and alpha-synuclein clearance”, Proceedings of the National Academy of Sciences, 2014, 111, 15573-15578.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [33]
    2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2681867
    J. Schwarz, S. Schmidt, O. Will, T. Koudelka, K. Koehler, M. Boss, B. Rabe, A. Tholey, J. Scheller, D. Schmidt-Arras, et al., “Polo-like Kinase 2, a Novel ADAM17 Signaling Component, Regulates Tumor Necrosis Factor similar to Ectodomain Shedding”, Journal of Biological Chemistry, 2014, 289, 3080-3093.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [32]
    2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953336
    K. R. Smith, H. - H. M. Dahl, L. Canafoglia, E. Andermann, J. Damiano, M. Morbin, A. C. Bruni, G. Giaccone, P. Cossette, P. Saftig, et al., “Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosis”, Human Molecular Genetics, 2013, 22, 1417-1423.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [31]
    2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953337
    M. Schwake, B. Schröder, and P. Saftig, “Lysosomal Membrane Proteins and Their Central Role in Physiology”, Traffic, 2013, 14, 739-748.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [30]
    2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953338
    J. Schmid, M. Oelbe, P. Saftig, M. Schwake, and F. Schweda, “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, 2013, 465, 895-905.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [29]
    2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953339
    A. Boehlen, M. Schwake, R. Dost, A. Kunert, P. Fidzinski, U. Heinemann, and C. Gebhardt, “The new KCNQ2 activator 4-Chlor-N-(6-chlor-pyridin-3-yl)-benzamid displays anticonvulsant potential”, British Journal of Pharmacology, 2013, 168, 1182-1200.
    PUB | DOI | Download (ext.) | WoS | PubMed | Europe PMC
     
  • [28]
    2013 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2953341
    M. Schwake, and P. Saftig, in Lysosomal Storage Disorders. A Practical Guide (Eds.: A. Mehta, B. Winchester), Wiley-Blackwell, Oxford, 2013, p. 131-136.
    PUB | DOI | Download (ext.)
     
  • [27]
    2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2625613
    J. R. Lemke, D. Lal, E. M. Reinthaler, I. Steiner, M. Nothnagel, M. Alber, K. Geider, B. Laube, M. Schwake, K. Finsterwalder, et al., “Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes”, Nature Genetics, 2013, 45, 1067-1072.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [26]
    2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2645175
    D. Neculai, M. Schwake, M. Ravichandran, F. Zunke, R. F. Collins, J. Peters, M. Neculai, J. Plumb, P. Loppnau, J. C. Pizarro, et al., “Structure of LIMP-2 provides functional insights with implications for SR-BI and CD36”, Nature, 2013, 504, 172-176.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [25]
    2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953340
    C. Zachos, J. Blanz, P. Saftig, and M. Schwake, “A Critical Histidine Residue Within LIMP-2 Mediates pH Sensitive Binding to Its Ligand β-Glucocerebrosidase”, Traffic, 2012, 13, 1113-1123.
    PUB | DOI | Download (ext.) | WoS | PubMed | Europe PMC
     
  • [24]
    2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953342
    P. S. Chadha, F. Zunke, A. J. Davis, T. A. Jepps, J. T. M. Linders, M. Schwake, R. Towart, and I. A. Greenwood, “Pharmacological dissection of Kv7.1 channels in systemic and pulmonary arteries”, British Journal of Pharmacology, 2012, 166, 1377-1387.
    PUB | DOI | Download (ext.) | WoS | PubMed | Europe PMC
     
  • [23]
    2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953343
    J. Prox, M. Willenbrock, S. Weber, T. Lehmann, D. Schmidt-Arras, R. Schwanbeck, P. Saftig, and M. Schwake, “Tetraspanin15 regulates cellular trafficking and activity of the ectodomain sheddase ADAM10”, Cellular and Molecular Life Sciences, 2012, 69, 2919-2932.
    PUB | DOI | Download (ext.) | WoS | PubMed | Europe PMC
     
  • [22]
    2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953344
    M. A. Corbett, M. Schwake, M. Bahlo, L. M. Dibbens, M. Lin, L. C. Gandolfo, D. F. Vears, J. D. O'Sullivan, T. Robertson, M. A. Bayly, et al., “A Mutation in the Golgi Qb-SNARE Gene GOSR2 Causes Progressive Myoclonus Epilepsy with Early Ataxia”, The American Journal of Human Genetics, 2011, 88, 657-663.
    PUB | DOI | Download (ext.) | WoS | PubMed | Europe PMC
     
  • [21]
    2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953345
    C. Valkova, M. Albrizio, I. V. Roder, M. Schwake, R. Betto, R. Rudolf, and C. Kaether, “Sorting receptor Rer1 controls surface expression of muscle acetylcholine receptors by ER retention of unassembled α-subunits”, Proceedings of the National Academy of Sciences, 2011, 108, 621-625.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [20]
    2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953346
    M. J. Desmond, D. Lee, S. A. Fraser, M. Katerelos, K. Gleich, P. Martinello, Y. Q. Li, M. C. Thomas, R. Michelucci, A. J. Cole, et al., “Tubular proteinuria in mice and humans lacking the intrinsic lysosomal protein SCARB2/Limp-2”, American Journal of Physiology-Renal Physiology, 2011, 300, F1437-F1447.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [19]
    2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953347
    J. Blanz, J. Groth, C. Zachos, C. Wehling, P. Saftig, and M. Schwake, “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, 2010, 19, 563-572.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [18]
    2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953348
    W. Lange, J. Geißendörfer, A. Schenzer, J. Grötzinger, G. Seebohm, T. Friedrich, and M. Schwake, “Refinement of the Binding Site and Mode of Action of the Anticonvulsant Retigabine on KCNQ K Channels”, Molecular Pharmacology, 2009, 75, 272-280.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [17]
    2008 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953349
    S. Y. M. Yeung, M. Schwake, V. Pucovský, and I. A. Greenwood, “Bimodal effects of the K 7 channel activator retigabine on vascular K+ currents”, British Journal of Pharmacology, 2008, 155, 62-72.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [16]
    2008 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953350
    S. Y. M. Yeung, W. Lange, M. Schwake, and I. A. Greenwood, “Expression profile and characterisation of a truncated KCNQ5 splice variant”, Biochemical and Biophysical Research Communications, 2008, 371, 741-746.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [15]
    2007 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953351
    R. Yamasaki, J. Zhang, I. Koshiishi, D. F. Sastradipura Suniarti, Z. Wu, C. Peters, M. Schwake, Y. Uchiyama, J. -ichi Kira, P. Saftig, et al., “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, 2007, 35, 573-584.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [14]
    2007 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953352
    D. Reczek, M. Schwake, J. Schröder, H. Hughes, J. Blanz, X. Jin, W. Brondyk, S. Van Patten, T. Edmunds, and P. Saftig, “LIMP-2 Is a Receptor for Lysosomal Mannose-6-Phosphate-Independent Targeting of β-Glucocerebrosidase”, Cell, 2007, 131, 770-783.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [13]
    2007 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953353
    B. Schroen, J. J. Leenders, A. van Erk, A. T. Bertrand, M. van Loon, R. E. van Leeuwen, N. Kubben, R. F. Duisters, M. W. Schellings, B. J. Janssen, et al., “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, 2007, 204, 1227-1235.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [12]
    2007 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953354
    C. Wehling, C. Beimgraben, C. Gelhaus, T. Friedrich, P. Saftig, J. Grötzinger, and M. Schwake, “Self-assembly of the isolated KCNQ2 subunit interaction domain”, FEBS Letters, 2007, 581, 1594-1598.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [11]
    2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953358
    M. Schwake, “Structural Determinants of M-Type KCNQ (Kv7) K+ Channel Assembly”, Journal of Neuroscience, 2006, 26, 3757-3766.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [10]
    2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953355
    M. Knipper, C. Claussen, L. Rüttiger, U. Zimmermann, R. Lüllmann-Rauch, E. - L. Eskelinen, J. Schröder, M. Schwake, and P. Saftig, “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, 2006, 576, 73-86.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [9]
    2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953356
    K. Caeyenberghs, D. Balschun, D. P. Roces, M. Schwake, P. Saftig, and R. D'Hooge, “Multivariate neurocognitive and emotional profile of a mannosidosis murine model for therapy assessment”, Neurobiology of Disease, 2006, 23, 422-432.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [8]
    2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953357
    A. Pachnio, S. Dietrich, W. Klapper, A. Humpe, M. Schwake, R. Sedlacek, M. Gramatzki, and C. Beck, “Proliferation-based T-cell selection for immunotherapy and graft-versus-host-disease prophylaxis in the context of bone marrow transplantation”, Bone Marrow Transplantation, 2006, 38, 157-167.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [7]
    2005 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953361
    D. Dominguez, J. Tournoy, D. Hartmann, T. Huth, K. Cryns, S. Deforce, L. Serneels, I. E. Camacho, E. Marjaux, K. Craessaerts, et al., “Phenotypic and Biochemical Analyses of BACE1- and BACE2-deficient Mice”, Journal of Biological Chemistry, 2005, 280, 30797-30806.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [6]
    2005 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953360
    R. D'Hooge, R. Lüllmann-Rauch, T. Beckers, D. Balschun, M. Schwake, K. Reiss, K. von Figura, and P. Saftig, “Neurocognitive and Psychotiform Behavioral Alterations and Enhanced Hippocampal Long-Term Potentiation in Transgenic Mice Displaying Neuropathological Features of Human  α-Mannosidosis”, Journal of Neuroscience, 2005, 25, 6539-6549.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [5]
    2005 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953359
    A. Schenzer, T. Friedrich, M. Pusch, P. Saftig, T. J. Jentsch, J. Grötzinger, and M. Schwake, “Molecular Determinants of KCNQ (Kv7) K+ Channel Sensitivity to the Anticonvulsant Retigabine”, Journal of Neuroscience, 2005, 25, 5051-5060.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [4]
    2003 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953362
    M. Schwake, T. J. Jentsch, and T. Friedrich, “A carboxy‐terminal domain determines the subunit specificity of KCNQ K+ channel assembly”, EMBO reports, 2003, 4, 76-81.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [3]
    2001 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953363 OA
    M. Schwake, T. Friedrich, and T. J. Jentsch, “An Internalization Signal in ClC-5, an Endosomal Cl−Channel Mutated in Dent's Disease”, Journal of Biological Chemistry, 2001, 276, 12049-12054.
    PUB | PDF | DOI | WoS | PubMed | Europe PMC
     
  • [2]
    2000 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953364
    N. Piwon, W. Günther, M. Schwake, M. R. Bösl, and T. J. Jentsch, “ClC-5 Cl--channel disruption impairs endocytosis in a mouse model for Dent's disease”, Nature, 2000, 408, 369-373.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [1]
    2000 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2953365 OA
    M. Schwake, M. Pusch, T. Kharkovets, and T. J. Jentsch, “Surface Expression and Single Channel Properties of KCNQ2/KCNQ3, M-type K+ Channels Involved in Epilepsy”, Journal of Biological Chemistry, 2000, 275, 13343-13348.
    PUB | PDF | DOI | WoS | PubMed | Europe PMC
     

Suche

Publikationen filtern

Darstellung / Sortierung

Export / Einbettung