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Zooplankton From a Reef System Under the Influence of the Amazon River Plume.

Frontiers in microbiology

Neumann-Leitão S, Melo PAMC, Schwamborn R, Diaz XFG, Figueiredo LGP, Silva AP, Campelo RPS, de Melo Júnior M, Melo NFAC, Costa AESF, Araújo M, Veleda DRA, Moura RL, Thompson F.
PMID: 29545783
Front Microbiol. 2018 Mar 01;9:355. doi: 10.3389/fmicb.2018.00355. eCollection 2018.

At the mouth of the Amazon River, a widespread carbonate ecosystem exists below the river plume, generating a hard-bottom reef (∼9500 km

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Neumann-Leitão S, Melo PAMC, Schwamborn R, et al. Zooplankton From a Reef System Under the Influence of the Amazon River Plume. Front Microbiol. 2018;9:355doi: 10.3389/fmicb.2018.00355.
Neumann-Leitão, S., Melo, P. A. M. C., Schwamborn, R., Diaz, X. F. G., Figueiredo, L. G. P., Silva, A. P., Campelo, R. P. S., de Melo Júnior, M., Melo, N. F. A. C., Costa, A. E. S. F., Araújo, M., Veleda, D. R. A., Moura, R. L., & Thompson, F. (2018). Zooplankton From a Reef System Under the Influence of the Amazon River Plume. Frontiers in microbiology, 9355. https://doi.org/10.3389/fmicb.2018.00355
Neumann-Leitão, Sigrid, et al. "Zooplankton From a Reef System Under the Influence of the Amazon River Plume." Frontiers in microbiology vol. 9 (2018): 355. doi: https://doi.org/10.3389/fmicb.2018.00355
Neumann-Leitão S, Melo PAMC, Schwamborn R, Diaz XFG, Figueiredo LGP, Silva AP, Campelo RPS, de Melo Júnior M, Melo NFAC, Costa AESF, Araújo M, Veleda DRA, Moura RL, Thompson F. Zooplankton From a Reef System Under the Influence of the Amazon River Plume. Front Microbiol. 2018 Mar 01;9:355. doi: 10.3389/fmicb.2018.00355. eCollection 2018. PMID: 29545783; PMCID: PMC5838004.
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The neural stem cell fate determinant TRIM32 regulates complex behavioral traits.

Frontiers in cellular neuroscience

Hillje AL, Beckmann E, Pavlou MA, Jaeger C, Pacheco MP, Sauter T, Schwamborn JC, Lewejohann L.
PMID: 25852471
Front Cell Neurosci. 2015 Mar 18;9:75. doi: 10.3389/fncel.2015.00075. eCollection 2015.

In mammals, new neurons are generated throughout the entire lifespan in two restricted areas of the brain, the dentate gyrus (DG) of the hippocampus and the subventricular zone (SVZ)-olfactory bulb (OB) system. In both regions newborn neurons display unique...

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Hillje AL, Beckmann E, Pavlou MA, et al. The neural stem cell fate determinant TRIM32 regulates complex behavioral traits. Front Cell Neurosci. 2015;9:75doi: 10.3389/fncel.2015.00075.
Hillje, A. L., Beckmann, E., Pavlou, M. A., Jaeger, C., Pacheco, M. P., Sauter, T., Schwamborn, J. C., & Lewejohann, L. (2015). The neural stem cell fate determinant TRIM32 regulates complex behavioral traits. Frontiers in cellular neuroscience, 975. https://doi.org/10.3389/fncel.2015.00075
Hillje, Anna-Lena, et al. "The neural stem cell fate determinant TRIM32 regulates complex behavioral traits." Frontiers in cellular neuroscience vol. 9 (2015): 75. doi: https://doi.org/10.3389/fncel.2015.00075
Hillje AL, Beckmann E, Pavlou MA, Jaeger C, Pacheco MP, Sauter T, Schwamborn JC, Lewejohann L. The neural stem cell fate determinant TRIM32 regulates complex behavioral traits. Front Cell Neurosci. 2015 Mar 18;9:75. doi: 10.3389/fncel.2015.00075. eCollection 2015. PMID: 25852471; PMCID: PMC4364253.
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Evolution of melanoma cross-resistance to CD8.

Oncoimmunology

Pieper N, Zaremba A, Leonardelli S, Harbers FN, Schwamborn M, Lübcke S, Schrörs B, Baingo J, Schramm A, Haferkamp S, Seifert U, Sucker A, Lennerz V, Wölfel T, Schadendorf D, Schilling B, Paschen A, Zhao F.
PMID: 30221038
Oncoimmunology. 2018 Apr 18;7(8):e1450127. doi: 10.1080/2162402X.2018.1450127. eCollection 2018.

The profound but frequently transient clinical responses to BRAF

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Pieper N, Zaremba A, Leonardelli S, et al. Evolution of melanoma cross-resistance to CD8. Oncoimmunology. 2018;7(8):e1450127doi: 10.1080/2162402X.2018.1450127.
Pieper, N., Zaremba, A., Leonardelli, S., Harbers, F. N., Schwamborn, M., Lübcke, S., Schrörs, B., Baingo, J., Schramm, A., Haferkamp, S., Seifert, U., Sucker, A., Lennerz, V., Wölfel, T., Schadendorf, D., Schilling, B., Paschen, A., & Zhao, F. (2018). Evolution of melanoma cross-resistance to CD8. Oncoimmunology, 7(8), e1450127. https://doi.org/10.1080/2162402X.2018.1450127
Pieper, Natalia, et al. "Evolution of melanoma cross-resistance to CD8." Oncoimmunology vol. 7,8 (2018): e1450127. doi: https://doi.org/10.1080/2162402X.2018.1450127
Pieper N, Zaremba A, Leonardelli S, Harbers FN, Schwamborn M, Lübcke S, Schrörs B, Baingo J, Schramm A, Haferkamp S, Seifert U, Sucker A, Lennerz V, Wölfel T, Schadendorf D, Schilling B, Paschen A, Zhao F. Evolution of melanoma cross-resistance to CD8. Oncoimmunology. 2018 Apr 18;7(8):e1450127. doi: 10.1080/2162402X.2018.1450127. eCollection 2018. PMID: 30221038; PMCID: PMC6136878.
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3D Cultures of Parkinson's Disease-Specific Dopaminergic Neurons for High Content Phenotyping and Drug Testing.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)

Bolognin S, Fossépré M, Qing X, Jarazo J, Ščančar J, Moreno EL, Nickels SL, Wasner K, Ouzren N, Walter J, Grünewald A, Glaab E, Salamanca L, Fleming RMT, Antony PMA, Schwamborn JC.
PMID: 30643711
Adv Sci (Weinh). 2018 Nov 20;6(1):1800927. doi: 10.1002/advs.201800927. eCollection 2019 Jan 09.

Parkinson's disease (PD)-specific neurons, grown in standard 2D cultures, typically only display weak endophenotypes. The cultivation of PD patient-specific neurons, derived from induced pluripotent stem cells carrying the LRRK2-G2019S mutation, is optimized in 3D microfluidics. The automated image analysis...

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Bolognin S, Fossépré M, Qing X, et al. 3D Cultures of Parkinson's Disease-Specific Dopaminergic Neurons for High Content Phenotyping and Drug Testing. Adv Sci (Weinh). 2018;6(1):1800927doi: 10.1002/advs.201800927.
Bolognin, S., Fossépré, M., Qing, X., Jarazo, J., Ščančar, J., Moreno, E. L., Nickels, S. L., Wasner, K., Ouzren, N., Walter, J., Grünewald, A., Glaab, E., Salamanca, L., Fleming, R. M. T., Antony, P. M. A., & Schwamborn, J. C. (2019). 3D Cultures of Parkinson's Disease-Specific Dopaminergic Neurons for High Content Phenotyping and Drug Testing. Advanced science (Weinheim, Baden-Wurttemberg, Germany), 6(1), 1800927. https://doi.org/10.1002/advs.201800927
Bolognin, Silvia, et al. "3D Cultures of Parkinson's Disease-Specific Dopaminergic Neurons for High Content Phenotyping and Drug Testing." Advanced science (Weinheim, Baden-Wurttemberg, Germany) vol. 6,1 (2019): 1800927. doi: https://doi.org/10.1002/advs.201800927
Bolognin S, Fossépré M, Qing X, Jarazo J, Ščančar J, Moreno EL, Nickels SL, Wasner K, Ouzren N, Walter J, Grünewald A, Glaab E, Salamanca L, Fleming RMT, Antony PMA, Schwamborn JC. 3D Cultures of Parkinson's Disease-Specific Dopaminergic Neurons for High Content Phenotyping and Drug Testing. Adv Sci (Weinh). 2018 Nov 20;6(1):1800927. doi: 10.1002/advs.201800927. eCollection 2019 Jan 09. PMID: 30643711; PMCID: PMC6325628.
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Synthesis, Characterization, and in vivo Distribution of Intracellular Delivered Macrolide Short-Chain Fatty Acid Derivatives.

ChemMedChem

Straß S, Schwamborn A, Keppler M, Cloos N, Guezguez J, Guse JH, Burnet M, Laufer S.
PMID: 33787081
ChemMedChem. 2021 Jul 20;16(14):2254-2269. doi: 10.1002/cmdc.202100139. Epub 2021 May 11.

Short-chain fatty acids (SCFAs) have a range of effects in metabolism and immune regulation. We have observed that delivery of SCFAs to lysosomes has potent immune regulatory effects, possibly as a surrogate signal for the presence of anaerobic organisms....

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Straß S, Schwamborn A, Keppler M, et al. Synthesis, Characterization, and in vivo Distribution of Intracellular Delivered Macrolide Short-Chain Fatty Acid Derivatives. ChemMedChem. 2021;16(14):2254-2269doi: 10.1002/cmdc.202100139.
Straß, S., Schwamborn, A., Keppler, M., Cloos, N., Guezguez, J., Guse, J. H., Burnet, M., & Laufer, S. (2021). Synthesis, Characterization, and in vivo Distribution of Intracellular Delivered Macrolide Short-Chain Fatty Acid Derivatives. ChemMedChem, 16(14), 2254-2269. https://doi.org/10.1002/cmdc.202100139
Straß, Simon, et al. "Synthesis, Characterization, and in vivo Distribution of Intracellular Delivered Macrolide Short-Chain Fatty Acid Derivatives." ChemMedChem vol. 16,14 (2021): 2254-2269. doi: https://doi.org/10.1002/cmdc.202100139
Straß S, Schwamborn A, Keppler M, Cloos N, Guezguez J, Guse JH, Burnet M, Laufer S. Synthesis, Characterization, and in vivo Distribution of Intracellular Delivered Macrolide Short-Chain Fatty Acid Derivatives. ChemMedChem. 2021 Jul 20;16(14):2254-2269. doi: 10.1002/cmdc.202100139. Epub 2021 May 11. PMID: 33787081.
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The Impact of Histological Annotations for Accurate Tissue Classification Using Mass Spectrometry Imaging.

Metabolites

Gonçalves JPL, Bollwein C, Schlitter AM, Martin B, Märkl B, Utpatel K, Weichert W, Schwamborn K.
PMID: 34822410
Metabolites. 2021 Oct 30;11(11). doi: 10.3390/metabo11110752.

Knowing the precise location of analytes in the tissue has the potential to provide information about the organs' function and predict its behavior. It is especially powerful when used in diagnosis and prognosis prediction of pathologies, such as cancer....

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Gonçalves JPL, Bollwein C, Schlitter AM, et al. The Impact of Histological Annotations for Accurate Tissue Classification Using Mass Spectrometry Imaging. Metabolites. 2021;11(11)doi: 10.3390/metabo11110752.
Gonçalves, J. P. L., Bollwein, C., Schlitter, A. M., Martin, B., Märkl, B., Utpatel, K., Weichert, W., & Schwamborn, K. (2021). The Impact of Histological Annotations for Accurate Tissue Classification Using Mass Spectrometry Imaging. Metabolites, 11(11), . https://doi.org/10.3390/metabo11110752
Gonçalves, Juliana Pereira Lopes, et al. "The Impact of Histological Annotations for Accurate Tissue Classification Using Mass Spectrometry Imaging." Metabolites vol. 11,11 (2021). doi: https://doi.org/10.3390/metabo11110752
Gonçalves JPL, Bollwein C, Schlitter AM, Martin B, Märkl B, Utpatel K, Weichert W, Schwamborn K. The Impact of Histological Annotations for Accurate Tissue Classification Using Mass Spectrometry Imaging. Metabolites. 2021 Oct 30;11(11). doi: 10.3390/metabo11110752. PMID: 34822410; PMCID: PMC8624953.
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[No title available]

RoFo : Fortschritte auf dem Gebiete der Rontgenstrahlen und der Nuklearmedizin

Sasse D, Schwamborn K, Gaa J.
PMID: 33535265
Rofo. 2021 Jul;193(7):835-836. doi: 10.1055/a-1339-1871. Epub 2021 Feb 03.

No abstract available.

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Sasse D, Schwamborn K, Gaa J. Hepatische Manifestation bei Morbus Waldenström. . Rofo. 2021;193(7):835-836doi: 10.1055/a-1339-1871.
Sasse, D., Schwamborn, K., & Gaa, J. (2021). Hepatische Manifestation bei Morbus Waldenström. . RoFo : Fortschritte auf dem Gebiete der Rontgenstrahlen und der Nuklearmedizin, 193(7), 835-836. https://doi.org/10.1055/a-1339-1871
Sasse, Daniel, et al. "Hepatische Manifestation bei Morbus Waldenström." . RoFo : Fortschritte auf dem Gebiete der Rontgenstrahlen und der Nuklearmedizin vol. 193,7 (2021): 835-836. doi: https://doi.org/10.1055/a-1339-1871
Sasse D, Schwamborn K, Gaa J. Hepatische Manifestation bei Morbus Waldenström. . Rofo. 2021 Jul;193(7):835-836. doi: 10.1055/a-1339-1871. Epub 2021 Feb 03. German. PMID: 33535265.
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The Parkinson's-disease-associated mutation LRRK2-G2019S alters dopaminergic differentiation dynamics via NR2F1.

Cell reports

Walter J, Bolognin S, Poovathingal SK, Magni S, Gérard D, Antony PMA, Nickels SL, Salamanca L, Berger E, Smits LM, Grzyb K, Perfeito R, Hoel F, Qing X, Ohnmacht J, Bertacchi M, Jarazo J, Ignac T, Monzel AS, Gonzalez-Cano L, Krüger R, Sauter T, Studer M, de Almeida LP, Tronstad KJ, Sinkkonen L, Skupin A, Schwamborn JC.
PMID: 34686322
Cell Rep. 2021 Oct 19;37(3):109864. doi: 10.1016/j.celrep.2021.109864.

Increasing evidence suggests that neurodevelopmental alterations might contribute to increase the susceptibility to develop neurodegenerative diseases. We investigate the occurrence of developmental abnormalities in dopaminergic neurons in a model of Parkinson's disease (PD). We monitor the differentiation of human...

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Walter J, Bolognin S, Poovathingal SK, et al. The Parkinson's-disease-associated mutation LRRK2-G2019S alters dopaminergic differentiation dynamics via NR2F1. Cell Rep. 2021;37(3):109864doi: 10.1016/j.celrep.2021.109864.
Walter, J., Bolognin, S., Poovathingal, S. K., Magni, S., Gérard, D., Antony, P. M. A., Nickels, S. L., Salamanca, L., Berger, E., Smits, L. M., Grzyb, K., Perfeito, R., Hoel, F., Qing, X., Ohnmacht, J., Bertacchi, M., Jarazo, J., Ignac, T., Monzel, A. S., Gonzalez-Cano, L., Krüger, R., Sauter, T., Studer, M., de Almeida, L. P., Tronstad, K. J., Sinkkonen, L., Skupin, A., & Schwamborn, J. C. (2021). The Parkinson's-disease-associated mutation LRRK2-G2019S alters dopaminergic differentiation dynamics via NR2F1. Cell reports, 37(3), 109864. https://doi.org/10.1016/j.celrep.2021.109864
Walter, Jonas, et al. "The Parkinson's-disease-associated mutation LRRK2-G2019S alters dopaminergic differentiation dynamics via NR2F1." Cell reports vol. 37,3 (2021): 109864. doi: https://doi.org/10.1016/j.celrep.2021.109864
Walter J, Bolognin S, Poovathingal SK, Magni S, Gérard D, Antony PMA, Nickels SL, Salamanca L, Berger E, Smits LM, Grzyb K, Perfeito R, Hoel F, Qing X, Ohnmacht J, Bertacchi M, Jarazo J, Ignac T, Monzel AS, Gonzalez-Cano L, Krüger R, Sauter T, Studer M, de Almeida LP, Tronstad KJ, Sinkkonen L, Skupin A, Schwamborn JC. The Parkinson's-disease-associated mutation LRRK2-G2019S alters dopaminergic differentiation dynamics via NR2F1. Cell Rep. 2021 Oct 19;37(3):109864. doi: 10.1016/j.celrep.2021.109864. PMID: 34686322.
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Single-cell sequencing of human midbrain reveals glial activation and a Parkinson-specific neuronal state.

Brain : a journal of neurology

Smajić S, Prada-Medina CA, Landoulsi Z, Ghelfi J, Delcambre S, Dietrich C, Jarazo J, Henck J, Balachandran S, Pachchek S, Morris CM, Antony P, Timmermann B, Sauer S, Pereira SL, Schwamborn JC, May P, Grünewald A, Spielmann M.
PMID: 34919646
Brain. 2021 Dec 17; doi: 10.1093/brain/awab446. Epub 2021 Dec 17.

Idiopathic Parkinson's disease is characterized by a progressive loss of dopaminergic neurons, but the exact disease etiology remains largely unknown. To date, Parkinson's disease research has mainly focused on nigral dopaminergic neurons, although recent studies suggest disease-related changes also...

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Smajić S, Prada-Medina CA, Landoulsi Z, et al. Single-cell sequencing of human midbrain reveals glial activation and a Parkinson-specific neuronal state. Brain. 2021;doi: 10.1093/brain/awab446.
Smajić, S., Prada-Medina, C. A., Landoulsi, Z., Ghelfi, J., Delcambre, S., Dietrich, C., Jarazo, J., Henck, J., Balachandran, S., Pachchek, S., Morris, C. M., Antony, P., Timmermann, B., Sauer, S., Pereira, S. L., Schwamborn, J. C., May, P., Grünewald, A., & Spielmann, M. (2021). Single-cell sequencing of human midbrain reveals glial activation and a Parkinson-specific neuronal state. Brain : a journal of neurology, . https://doi.org/10.1093/brain/awab446
Smajić, Semra, et al. "Single-cell sequencing of human midbrain reveals glial activation and a Parkinson-specific neuronal state." Brain : a journal of neurology vol. (2021). doi: https://doi.org/10.1093/brain/awab446
Smajić S, Prada-Medina CA, Landoulsi Z, Ghelfi J, Delcambre S, Dietrich C, Jarazo J, Henck J, Balachandran S, Pachchek S, Morris CM, Antony P, Timmermann B, Sauer S, Pereira SL, Schwamborn JC, May P, Grünewald A, Spielmann M. Single-cell sequencing of human midbrain reveals glial activation and a Parkinson-specific neuronal state. Brain. 2021 Dec 17; doi: 10.1093/brain/awab446. Epub 2021 Dec 17. PMID: 34919646.
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Retraction Notice to: The E3 SUMO Ligase PIASy Is a Regulator of Cellular Senescence and Apoptosis.

Molecular cell

Bischof O, Schwamborn K, Martin N, Werner A, Sustmann C, Grosschedl R, Dejean A.
PMID: 33338405
Mol Cell. 2020 Dec 17;80(6):1140. doi: 10.1016/j.molcel.2020.11.049.

No abstract available.

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Bischof O, Schwamborn K, Martin N, et al. Retraction Notice to: The E3 SUMO Ligase PIASy Is a Regulator of Cellular Senescence and Apoptosis. Mol Cell. 2020;80(6):1140doi: 10.1016/j.molcel.2020.11.049.
Bischof, O., Schwamborn, K., Martin, N., Werner, A., Sustmann, C., Grosschedl, R., & Dejean, A. (2020). Retraction Notice to: The E3 SUMO Ligase PIASy Is a Regulator of Cellular Senescence and Apoptosis. Molecular cell, 80(6), 1140. https://doi.org/10.1016/j.molcel.2020.11.049
Bischof, Oliver, et al. "Retraction Notice to: The E3 SUMO Ligase PIASy Is a Regulator of Cellular Senescence and Apoptosis." Molecular cell vol. 80,6 (2020): 1140. doi: https://doi.org/10.1016/j.molcel.2020.11.049
Bischof O, Schwamborn K, Martin N, Werner A, Sustmann C, Grosschedl R, Dejean A. Retraction Notice to: The E3 SUMO Ligase PIASy Is a Regulator of Cellular Senescence and Apoptosis. Mol Cell. 2020 Dec 17;80(6):1140. doi: 10.1016/j.molcel.2020.11.049. PMID: 33338405.
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The Importance of Clinical Tissue Imaging.

Clinical mass spectrometry (Del Mar, Calif.)

Spraggins JM, Schwamborn K, Heeren RMA, Eberlin LS.
PMID: 32483555
Clin Mass Spectrom. 2019 Apr;12:47-49. doi: 10.1016/j.clinms.2019.04.001. Epub 2019 Apr 19.

No abstract available.

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Spraggins JM, Schwamborn K, Heeren RMA, et al. The Importance of Clinical Tissue Imaging. Clin Mass Spectrom. 2019;12:47-49doi: 10.1016/j.clinms.2019.04.001.
Spraggins, J. M., Schwamborn, K., Heeren, R. M. A., & Eberlin, L. S. (2019). The Importance of Clinical Tissue Imaging. Clinical mass spectrometry (Del Mar, Calif.), 1247-49. https://doi.org/10.1016/j.clinms.2019.04.001
Spraggins, Jeffrey M, et al. "The Importance of Clinical Tissue Imaging." Clinical mass spectrometry (Del Mar, Calif.) vol. 12 (2019): 47-49. doi: https://doi.org/10.1016/j.clinms.2019.04.001
Spraggins JM, Schwamborn K, Heeren RMA, Eberlin LS. The Importance of Clinical Tissue Imaging. Clin Mass Spectrom. 2019 Apr;12:47-49. doi: 10.1016/j.clinms.2019.04.001. Epub 2019 Apr 19. PMID: 32483555; PMCID: PMC7263479.
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Melanoma Differentiation Trajectories Determine Sensitivity toward Pre-Existing CD8.

The Journal of investigative dermatology

Harbers FN, Thier B, Stupia S, Zhu S, Schwamborn M, Peller V, Chauvistré H, Crivello P, Fleischhauer K, Roesch A, Sucker A, Schadendorf D, Chen Y, Paschen A, Zhao F.
PMID: 33798535
J Invest Dermatol. 2021 Oct;141(10):2480-2489. doi: 10.1016/j.jid.2021.03.013. Epub 2021 Mar 30.

The highly plastic nature of melanoma enables its transition among diverse cell states to survive hostile conditions. However, the interplay between specific tumor cell states and intratumoral T cells remains poorly defined. With MAPK inhibitor‒treated BRAF

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Harbers FN, Thier B, Stupia S, et al. Melanoma Differentiation Trajectories Determine Sensitivity toward Pre-Existing CD8. J Invest Dermatol. 2021;141(10):2480-2489doi: 10.1016/j.jid.2021.03.013.
Harbers, F. N., Thier, B., Stupia, S., Zhu, S., Schwamborn, M., Peller, V., Chauvistré, H., Crivello, P., Fleischhauer, K., Roesch, A., Sucker, A., Schadendorf, D., Chen, Y., Paschen, A., & Zhao, F. (2021). Melanoma Differentiation Trajectories Determine Sensitivity toward Pre-Existing CD8. The Journal of investigative dermatology, 141(10), 2480-2489. https://doi.org/10.1016/j.jid.2021.03.013
Harbers, Franziska Noelle, et al. "Melanoma Differentiation Trajectories Determine Sensitivity toward Pre-Existing CD8." The Journal of investigative dermatology vol. 141,10 (2021): 2480-2489. doi: https://doi.org/10.1016/j.jid.2021.03.013
Harbers FN, Thier B, Stupia S, Zhu S, Schwamborn M, Peller V, Chauvistré H, Crivello P, Fleischhauer K, Roesch A, Sucker A, Schadendorf D, Chen Y, Paschen A, Zhao F. Melanoma Differentiation Trajectories Determine Sensitivity toward Pre-Existing CD8. J Invest Dermatol. 2021 Oct;141(10):2480-2489. doi: 10.1016/j.jid.2021.03.013. Epub 2021 Mar 30. PMID: 33798535.
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