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Paving the Way to Understand Autoantibody-Mediated Epilepsy on the Molecular Level.

Frontiers in neurology

Seebohm G, Piccini I, Strutz-Seebohm N.
PMID: 26217297
Front Neurol. 2015 Jul 06;6:149. doi: 10.3389/fneur.2015.00149. eCollection 2015.

Correct function of neuronal networks is enabled by a delicate interplay among neurons communicating with each other. One of the keys is the communication at chemical synapses where neurotransmitters like glutamate, GABA, and glycine enable signal transfer over the...

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Seebohm G, Piccini I, Strutz-Seebohm N. Paving the Way to Understand Autoantibody-Mediated Epilepsy on the Molecular Level. Front Neurol. 2015;6:149doi: 10.3389/fneur.2015.00149.
Seebohm, G., Piccini, I., & Strutz-Seebohm, N. (2015). Paving the Way to Understand Autoantibody-Mediated Epilepsy on the Molecular Level. Frontiers in neurology, 6149. https://doi.org/10.3389/fneur.2015.00149
Seebohm, Guiscard, et al. "Paving the Way to Understand Autoantibody-Mediated Epilepsy on the Molecular Level." Frontiers in neurology vol. 6 (2015): 149. doi: https://doi.org/10.3389/fneur.2015.00149
Seebohm G, Piccini I, Strutz-Seebohm N. Paving the Way to Understand Autoantibody-Mediated Epilepsy on the Molecular Level. Front Neurol. 2015 Jul 06;6:149. doi: 10.3389/fneur.2015.00149. eCollection 2015. PMID: 26217297; PMCID: PMC4491625.
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Functional high-resolution time-course expression analysis of human embryonic stem cells undergoing cardiac induction.

Genomics data

Piccini I, Araúzo-Bravo M, Seebohm G, Greber B.
PMID: 27722090
Genom Data. 2016 Sep 28;10:71-74. doi: 10.1016/j.gdata.2016.09.007. eCollection 2016 Dec.

Cardiac induction of human embryonic stem cells (hESCs) is a process bearing increasing medical relevance, yet it is poorly understood from a developmental biology perspective. Anticipated technological progress in deriving stably expandable cardiac precursor cells or in advancing cardiac...

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Piccini I, Araúzo-Bravo M, Seebohm G, et al. Functional high-resolution time-course expression analysis of human embryonic stem cells undergoing cardiac induction. Genom Data. 2016;10:71-74doi: 10.1016/j.gdata.2016.09.007.
Piccini, I., Araúzo-Bravo, M., Seebohm, G., & Greber, B. (2016). Functional high-resolution time-course expression analysis of human embryonic stem cells undergoing cardiac induction. Genomics data, 1071-74. https://doi.org/10.1016/j.gdata.2016.09.007
Piccini, Ilaria, et al. "Functional high-resolution time-course expression analysis of human embryonic stem cells undergoing cardiac induction." Genomics data vol. 10 (2016): 71-74. doi: https://doi.org/10.1016/j.gdata.2016.09.007
Piccini I, Araúzo-Bravo M, Seebohm G, Greber B. Functional high-resolution time-course expression analysis of human embryonic stem cells undergoing cardiac induction. Genom Data. 2016 Sep 28;10:71-74. doi: 10.1016/j.gdata.2016.09.007. eCollection 2016 Dec. PMID: 27722090; PMCID: PMC5048627.
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Familial hypertrophic cardiomyopathy: functional variance among individual cardiomyocytes as a trigger of FHC-phenotype development.

Frontiers in physiology

Brenner B, Seebohm B, Tripathi S, Montag J, Kraft T.
PMID: 25346696
Front Physiol. 2014 Oct 10;5:392. doi: 10.3389/fphys.2014.00392. eCollection 2014.

Familial hypertrophic cardiomyopathy (FHC) is the most frequent inherited cardiac disease. It has been related to numerous mutations in many sarcomeric and even some non-sarcomeric proteins. So far, however, no common mechanism has been identified by which the many...

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Brenner B, Seebohm B, Tripathi S, et al. Familial hypertrophic cardiomyopathy: functional variance among individual cardiomyocytes as a trigger of FHC-phenotype development. Front Physiol. 2014;5:392doi: 10.3389/fphys.2014.00392.
Brenner, B., Seebohm, B., Tripathi, S., Montag, J., & Kraft, T. (2014). Familial hypertrophic cardiomyopathy: functional variance among individual cardiomyocytes as a trigger of FHC-phenotype development. Frontiers in physiology, 5392. https://doi.org/10.3389/fphys.2014.00392
Brenner, Bernhard, et al. "Familial hypertrophic cardiomyopathy: functional variance among individual cardiomyocytes as a trigger of FHC-phenotype development." Frontiers in physiology vol. 5 (2014): 392. doi: https://doi.org/10.3389/fphys.2014.00392
Brenner B, Seebohm B, Tripathi S, Montag J, Kraft T. Familial hypertrophic cardiomyopathy: functional variance among individual cardiomyocytes as a trigger of FHC-phenotype development. Front Physiol. 2014 Oct 10;5:392. doi: 10.3389/fphys.2014.00392. eCollection 2014. PMID: 25346696; PMCID: PMC4193225.
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Human pluripotent stem cell-derived cardiomyocytes: Genome-wide expression profiling of long-term in vitro maturation in comparison to human heart tissue.

Genomics data

Piccini I, Rao J, Seebohm G, Greber B.
PMID: 26484180
Genom Data. 2015 Apr 01;4:69-72. doi: 10.1016/j.gdata.2015.03.008. eCollection 2015 Jun.

Cardiomyocyte-like cells (CMs) derived from human pluripotent stem cells (hPSCs) present a valuable model for human disease modeling, studying early human development and, potentially, developing cell therapeutic approaches. However, the specification of early hPSC-derived CMs into defined cardiac subtypes...

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Piccini I, Rao J, Seebohm G, et al. Human pluripotent stem cell-derived cardiomyocytes: Genome-wide expression profiling of long-term in vitro maturation in comparison to human heart tissue. Genom Data. 2015;4:69-72doi: 10.1016/j.gdata.2015.03.008.
Piccini, I., Rao, J., Seebohm, G., & Greber, B. (2015). Human pluripotent stem cell-derived cardiomyocytes: Genome-wide expression profiling of long-term in vitro maturation in comparison to human heart tissue. Genomics data, 469-72. https://doi.org/10.1016/j.gdata.2015.03.008
Piccini, Ilaria, et al. "Human pluripotent stem cell-derived cardiomyocytes: Genome-wide expression profiling of long-term in vitro maturation in comparison to human heart tissue." Genomics data vol. 4 (2015): 69-72. doi: https://doi.org/10.1016/j.gdata.2015.03.008
Piccini I, Rao J, Seebohm G, Greber B. Human pluripotent stem cell-derived cardiomyocytes: Genome-wide expression profiling of long-term in vitro maturation in comparison to human heart tissue. Genom Data. 2015 Apr 01;4:69-72. doi: 10.1016/j.gdata.2015.03.008. eCollection 2015 Jun. PMID: 26484180; PMCID: PMC4535944.
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Adrenergic Stress Protection of Human iPS Cell-Derived Cardiomyocytes by Fast K.

Frontiers in physiology

Piccini I, Fehrmann E, Frank S, Müller FU, Greber B, Seebohm G.
PMID: 28959214
Front Physiol. 2017 Sep 14;8:705. doi: 10.3389/fphys.2017.00705. eCollection 2017.

The fight-or-flight response (FFR), a physiological acute stress reaction, involves positive chronotropic and inotropic effects on heart muscle cells mediated through β-adrenoceptor activation. Increased systolic calcium is required to enable stronger heart contractions whereas elevated potassium currents are to...

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Piccini I, Fehrmann E, Frank S, et al. Adrenergic Stress Protection of Human iPS Cell-Derived Cardiomyocytes by Fast K. Front Physiol. 2017;8:705doi: 10.3389/fphys.2017.00705.
Piccini, I., Fehrmann, E., Frank, S., Müller, F. U., Greber, B., & Seebohm, G. (2017). Adrenergic Stress Protection of Human iPS Cell-Derived Cardiomyocytes by Fast K. Frontiers in physiology, 8705. https://doi.org/10.3389/fphys.2017.00705
Piccini, Ilaria, et al. "Adrenergic Stress Protection of Human iPS Cell-Derived Cardiomyocytes by Fast K." Frontiers in physiology vol. 8 (2017): 705. doi: https://doi.org/10.3389/fphys.2017.00705
Piccini I, Fehrmann E, Frank S, Müller FU, Greber B, Seebohm G. Adrenergic Stress Protection of Human iPS Cell-Derived Cardiomyocytes by Fast K. Front Physiol. 2017 Sep 14;8:705. doi: 10.3389/fphys.2017.00705. eCollection 2017. PMID: 28959214; PMCID: PMC5603700.
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NDRG2 phosphorylation provides negative feedback for SGK1-dependent regulation of a kainate receptor in astrocytes.

Frontiers in cellular neuroscience

Matschke V, Theiss C, Hollmann M, Schulze-Bahr E, Lang F, Seebohm G, Strutz-Seebohm N.
PMID: 26500492
Front Cell Neurosci. 2015 Oct 06;9:387. doi: 10.3389/fncel.2015.00387. eCollection 2015.

Glutamate receptors play an important role in the function of astrocytes. Among their tasks is the regulation of gliotransmission, gene expression and exocytosis of the tissue-type plasminogen activator (tPA), which has an enhancing effect on N-methyl-D-aspartate (NMDA) receptors and...

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Matschke V, Theiss C, Hollmann M, et al. NDRG2 phosphorylation provides negative feedback for SGK1-dependent regulation of a kainate receptor in astrocytes. Front Cell Neurosci. 2015;9:387doi: 10.3389/fncel.2015.00387.
Matschke, V., Theiss, C., Hollmann, M., Schulze-Bahr, E., Lang, F., Seebohm, G., & Strutz-Seebohm, N. (2015). NDRG2 phosphorylation provides negative feedback for SGK1-dependent regulation of a kainate receptor in astrocytes. Frontiers in cellular neuroscience, 9387. https://doi.org/10.3389/fncel.2015.00387
Matschke, Veronika, et al. "NDRG2 phosphorylation provides negative feedback for SGK1-dependent regulation of a kainate receptor in astrocytes." Frontiers in cellular neuroscience vol. 9 (2015): 387. doi: https://doi.org/10.3389/fncel.2015.00387
Matschke V, Theiss C, Hollmann M, Schulze-Bahr E, Lang F, Seebohm G, Strutz-Seebohm N. NDRG2 phosphorylation provides negative feedback for SGK1-dependent regulation of a kainate receptor in astrocytes. Front Cell Neurosci. 2015 Oct 06;9:387. doi: 10.3389/fncel.2015.00387. eCollection 2015. PMID: 26500492; PMCID: PMC4594022.
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Stepwise Clearance of Repressive Roadblocks Drives Cardiac Induction in Human ESCs.

Cell stem cell

Rao J, Pfeiffer MJ, Frank S, Adachi K, Piccini I, Quaranta R, Araúzo-Bravo M, Schwarz J, Schade D, Leidel S, Schöler HR, Seebohm G, Greber B.
PMID: 27058939
Cell Stem Cell. 2016 Apr 07;18(4):554-6. doi: 10.1016/j.stem.2016.03.008.

No abstract available.

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Rao J, Pfeiffer MJ, Frank S, et al. Stepwise Clearance of Repressive Roadblocks Drives Cardiac Induction in Human ESCs. Cell Stem Cell. 2016;18(4):554-6doi: 10.1016/j.stem.2016.03.008.
Rao, J., Pfeiffer, M. J., Frank, S., Adachi, K., Piccini, I., Quaranta, R., Araúzo-Bravo, M., Schwarz, J., Schade, D., Leidel, S., Schöler, H. R., Seebohm, G., & Greber, B. (2016). Stepwise Clearance of Repressive Roadblocks Drives Cardiac Induction in Human ESCs. Cell stem cell, 18(4), 554-6. https://doi.org/10.1016/j.stem.2016.03.008
Rao, Jyoti, et al. "Stepwise Clearance of Repressive Roadblocks Drives Cardiac Induction in Human ESCs." Cell stem cell vol. 18,4 (2016): 554-6. doi: https://doi.org/10.1016/j.stem.2016.03.008
Rao J, Pfeiffer MJ, Frank S, Adachi K, Piccini I, Quaranta R, Araúzo-Bravo M, Schwarz J, Schade D, Leidel S, Schöler HR, Seebohm G, Greber B. Stepwise Clearance of Repressive Roadblocks Drives Cardiac Induction in Human ESCs. Cell Stem Cell. 2016 Apr 07;18(4):554-6. doi: 10.1016/j.stem.2016.03.008. PMID: 27058939.
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K.

Cell research

Ruck T, Bock S, Pfeuffer S, Schroeter CB, Cengiz D, Marciniak P, Lindner M, Herrmann A, Liebmann M, Kovac S, Gola L, Rolfes L, Pawlitzki M, Opel N, Hahn T, Dannlowski U, Pap T, Luessi F, Schreiber JA, Wünsch B, Kuhlmann T, Seebohm G, Tackenberg B, Seja P, Döring F, Wischmeyer E, Chasan AI, Roth J, Klotz L, Meyer Zu Hörste G, Wiendl H, Marschall T, Floess S, Huehn J, Budde T, Bopp T, Bittner S, Meuth SG.
PMID: 34702947
Cell Res. 2021 Oct 26; doi: 10.1038/s41422-021-00580-z. Epub 2021 Oct 26.

It remains largely unclear how thymocytes translate relative differences in T cell receptor (TCR) signal strength into distinct developmental programs that drive the cell fate decisions towards conventional (Tconv) or regulatory T cells (Treg). Following TCR activation, intracellular calcium...

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Ruck T, Bock S, Pfeuffer S, et al. K. Cell Res. 2021;doi: 10.1038/s41422-021-00580-z.
Ruck, T., Bock, S., Pfeuffer, S., Schroeter, C. B., Cengiz, D., Marciniak, P., Lindner, M., Herrmann, A., Liebmann, M., Kovac, S., Gola, L., Rolfes, L., Pawlitzki, M., Opel, N., Hahn, T., Dannlowski, U., Pap, T., Luessi, F., Schreiber, J. A., Wünsch, B., Kuhlmann, T., Seebohm, G., Tackenberg, B., Seja, P., Döring, F., Wischmeyer, E., Chasan, A. I., Roth, J., Klotz, L., Meyer Zu Hörste, G., Wiendl, H., Marschall, T., Floess, S., Huehn, J., Budde, T., Bopp, T., Bittner, S., & Meuth, S. G. (2021). K. Cell research, . https://doi.org/10.1038/s41422-021-00580-z
Ruck, Tobias, et al. "K." Cell research vol. (2021). doi: https://doi.org/10.1038/s41422-021-00580-z
Ruck T, Bock S, Pfeuffer S, Schroeter CB, Cengiz D, Marciniak P, Lindner M, Herrmann A, Liebmann M, Kovac S, Gola L, Rolfes L, Pawlitzki M, Opel N, Hahn T, Dannlowski U, Pap T, Luessi F, Schreiber JA, Wünsch B, Kuhlmann T, Seebohm G, Tackenberg B, Seja P, Döring F, Wischmeyer E, Chasan AI, Roth J, Klotz L, Meyer Zu Hörste G, Wiendl H, Marschall T, Floess S, Huehn J, Budde T, Bopp T, Bittner S, Meuth SG. K. Cell Res. 2021 Oct 26; doi: 10.1038/s41422-021-00580-z. Epub 2021 Oct 26. PMID: 34702947; PMCID: PMC8547300.
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In Vitro Model Systems of Coxsackievirus B3-Induced Myocarditis: Comparison of Commonly Used Cell Lines and Characterization of CVB3-Infected iCell.

Viruses

Kraft L, Sauter M, Seebohm G, Klingel K.
PMID: 34578416
Viruses. 2021 Sep 14;13(9). doi: 10.3390/v13091835.

Coxsackievirus B3 (CVB3) belongs to the enteroviruses, which are a well-known cause of acute and chronic myocarditis, primarily infecting cardiac myocytes. As primary human cardiomyocytes are difficult to obtain, viral myocarditis is quite frequently studied in vitro in different...

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Kraft L, Sauter M, Seebohm G, et al. In Vitro Model Systems of Coxsackievirus B3-Induced Myocarditis: Comparison of Commonly Used Cell Lines and Characterization of CVB3-Infected iCell. Viruses. 2021;13(9)doi: 10.3390/v13091835.
Kraft, L., Sauter, M., Seebohm, G., & Klingel, K. (2021). In Vitro Model Systems of Coxsackievirus B3-Induced Myocarditis: Comparison of Commonly Used Cell Lines and Characterization of CVB3-Infected iCell. Viruses, 13(9), . https://doi.org/10.3390/v13091835
Kraft, Lisa, et al. "In Vitro Model Systems of Coxsackievirus B3-Induced Myocarditis: Comparison of Commonly Used Cell Lines and Characterization of CVB3-Infected iCell." Viruses vol. 13,9 (2021). doi: https://doi.org/10.3390/v13091835
Kraft L, Sauter M, Seebohm G, Klingel K. In Vitro Model Systems of Coxsackievirus B3-Induced Myocarditis: Comparison of Commonly Used Cell Lines and Characterization of CVB3-Infected iCell. Viruses. 2021 Sep 14;13(9). doi: 10.3390/v13091835. PMID: 34578416; PMCID: PMC8472939.
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Selective Inhibition of .

The Journal of pharmacology and experimental therapeutics

Gresch A, Hurtado HN, Wörmeyer L, De Luca V, Wiggers R, Seebohm G, Wünsch B, Düfer M.
PMID: 34593560
J Pharmacol Exp Ther. 2021 Nov;379(3):235-244. doi: 10.1124/jpet.121.000807. Epub 2021 Sep 30.

Participation of

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Gresch A, Hurtado HN, Wörmeyer L, et al. Selective Inhibition of . J Pharmacol Exp Ther. 2021;379(3):235-244doi: 10.1124/jpet.121.000807.
Gresch, A., Hurtado, H. N., Wörmeyer, L., De Luca, V., Wiggers, R., Seebohm, G., Wünsch, B., & Düfer, M. (2021). Selective Inhibition of . The Journal of pharmacology and experimental therapeutics, 379(3), 235-244. https://doi.org/10.1124/jpet.121.000807
Gresch, Anne, et al. "Selective Inhibition of ." The Journal of pharmacology and experimental therapeutics vol. 379,3 (2021): 235-244. doi: https://doi.org/10.1124/jpet.121.000807
Gresch A, Hurtado HN, Wörmeyer L, De Luca V, Wiggers R, Seebohm G, Wünsch B, Düfer M. Selective Inhibition of . J Pharmacol Exp Ther. 2021 Nov;379(3):235-244. doi: 10.1124/jpet.121.000807. Epub 2021 Sep 30. PMID: 34593560.
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K.

Cell research

Ruck T, Bock S, Pfeuffer S, Schroeter CB, Cengiz D, Marciniak P, Lindner M, Herrmann A, Liebmann M, Kovac S, Gola L, Rolfes L, Pawlitzki M, Opel N, Hahn T, Dannlowski U, Pap T, Luessi F, Schreiber JA, Wünsch B, Kuhlmann T, Seebohm G, Tackenberg B, Seja P, Döring F, Wischmeyer E, Chasan AI, Roth J, Klotz L, Meyer Zu Hörste G, Wiendl H, Marschall T, Floess S, Huehn J, Budde T, Bopp T, Bittner S, Meuth SG.
PMID: 34702947
Cell Res. 2022 Jan;32(1):72-88. doi: 10.1038/s41422-021-00580-z. Epub 2021 Oct 26.

It remains largely unclear how thymocytes translate relative differences in T cell receptor (TCR) signal strength into distinct developmental programs that drive the cell fate decisions towards conventional (Tconv) or regulatory T cells (Treg). Following TCR activation, intracellular calcium...

Cite
Ruck T, Bock S, Pfeuffer S, et al. K. Cell Res. 2021;32(1):72-88doi: 10.1038/s41422-021-00580-z.
Ruck, T., Bock, S., Pfeuffer, S., Schroeter, C. B., Cengiz, D., Marciniak, P., Lindner, M., Herrmann, A., Liebmann, M., Kovac, S., Gola, L., Rolfes, L., Pawlitzki, M., Opel, N., Hahn, T., Dannlowski, U., Pap, T., Luessi, F., Schreiber, J. A., Wünsch, B., Kuhlmann, T., Seebohm, G., Tackenberg, B., Seja, P., Döring, F., Wischmeyer, E., Chasan, A. I., Roth, J., Klotz, L., Meyer Zu Hörste, G., Wiendl, H., Marschall, T., Floess, S., Huehn, J., Budde, T., Bopp, T., Bittner, S., & Meuth, S. G. (2022). K. Cell research, 32(1), 72-88. https://doi.org/10.1038/s41422-021-00580-z
Ruck, Tobias, et al. "K." Cell research vol. 32,1 (2022): 72-88. doi: https://doi.org/10.1038/s41422-021-00580-z
Ruck T, Bock S, Pfeuffer S, Schroeter CB, Cengiz D, Marciniak P, Lindner M, Herrmann A, Liebmann M, Kovac S, Gola L, Rolfes L, Pawlitzki M, Opel N, Hahn T, Dannlowski U, Pap T, Luessi F, Schreiber JA, Wünsch B, Kuhlmann T, Seebohm G, Tackenberg B, Seja P, Döring F, Wischmeyer E, Chasan AI, Roth J, Klotz L, Meyer Zu Hörste G, Wiendl H, Marschall T, Floess S, Huehn J, Budde T, Bopp T, Bittner S, Meuth SG. K. Cell Res. 2022 Jan;32(1):72-88. doi: 10.1038/s41422-021-00580-z. Epub 2021 Oct 26. PMID: 34702947; PMCID: PMC8547300.
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The role of internal pressure and muscle activation during locust oviposition.

Journal of insect physiology

Rose U, Seebohm G, Hustert R.
PMID: 12770260
J Insect Physiol. 2000 Jan;46(1):69-80. doi: 10.1016/s0022-1910(99)00103-1.

The oviposition of female locusts is a complex behaviour that includes a dramatic extension of the abdomen. The role of internal pressure during oviposition was investigated by monitoring the intra-tracheal pressure and the activity of selected longitudinal muscles, while...

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Rose U, Seebohm G, Hustert R. The role of internal pressure and muscle activation during locust oviposition. J Insect Physiol. 2000;46(1):69-80doi: 10.1016/s0022-1910(99)00103-1.
Rose, U., Seebohm, G., & Hustert, R. (2000). The role of internal pressure and muscle activation during locust oviposition. Journal of insect physiology, 46(1), 69-80. https://doi.org/10.1016/s0022-1910(99)00103-1
Rose, U, et al. "The role of internal pressure and muscle activation during locust oviposition." Journal of insect physiology vol. 46,1 (2000): 69-80. doi: https://doi.org/10.1016/s0022-1910(99)00103-1
Rose U, Seebohm G, Hustert R. The role of internal pressure and muscle activation during locust oviposition. J Insect Physiol. 2000 Jan;46(1):69-80. doi: 10.1016/s0022-1910(99)00103-1. PMID: 12770260.
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