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Erratum to: Inhibition of pannexin1 channels alleviates acetaminophen-induced hepatotoxicity.

Archives of toxicology

Maes M, McGill MR, da Silva TC, Abels C, Lebofsky M, Weemhoff JL, Tiburcio T, Pereira IVA, Willebrords J, Yanguas SC, Farhood A, Beschin A, Van Ginderachter JA, Penuela S, Jaeschke H, Cogliati B, Vinken M.
PMID: 28243680
Arch Toxicol. 2017 May;91(5):2263-2264. doi: 10.1007/s00204-016-1929-y.

No abstract available.

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Maes M, McGill MR, da Silva TC, et al. Erratum to: Inhibition of pannexin1 channels alleviates acetaminophen-induced hepatotoxicity. Arch Toxicol. 2017;91(5):2263-2264doi: 10.1007/s00204-016-1929-y.
Maes, M., McGill, M. R., da Silva, T. C., Abels, C., Lebofsky, M., Weemhoff, J. L., Tiburcio, T., Pereira, I. V. A., Willebrords, J., Yanguas, S. C., Farhood, A., Beschin, A., Van Ginderachter, J. A., Penuela, S., Jaeschke, H., Cogliati, B., & Vinken, M. (2017). Erratum to: Inhibition of pannexin1 channels alleviates acetaminophen-induced hepatotoxicity. Archives of toxicology, 91(5), 2263-2264. https://doi.org/10.1007/s00204-016-1929-y
Maes, Michaël, et al. "Erratum to: Inhibition of pannexin1 channels alleviates acetaminophen-induced hepatotoxicity." Archives of toxicology vol. 91,5 (2017): 2263-2264. doi: https://doi.org/10.1007/s00204-016-1929-y
Maes M, McGill MR, da Silva TC, Abels C, Lebofsky M, Weemhoff JL, Tiburcio T, Pereira IVA, Willebrords J, Yanguas SC, Farhood A, Beschin A, Van Ginderachter JA, Penuela S, Jaeschke H, Cogliati B, Vinken M. Erratum to: Inhibition of pannexin1 channels alleviates acetaminophen-induced hepatotoxicity. Arch Toxicol. 2017 May;91(5):2263-2264. doi: 10.1007/s00204-016-1929-y. PMID: 28243680.
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Positive Tensor Network Approach for Simulating Open Quantum Many-Body Systems.

Physical review letters

Werner AH, Jaschke D, Silvi P, Kliesch M, Calarco T, Eisert J, Montangero S.
PMID: 27341253
Phys Rev Lett. 2016 Jun 10;116(23):237201. doi: 10.1103/PhysRevLett.116.237201. Epub 2016 Jun 07.

Open quantum many-body systems play an important role in quantum optics and condensed matter physics, and capture phenomena like transport, the interplay between Hamiltonian and incoherent dynamics, and topological order generated by dissipation. We introduce a versatile and practical...

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Werner AH, Jaschke D, Silvi P, et al. Positive Tensor Network Approach for Simulating Open Quantum Many-Body Systems. Phys Rev Lett. 2016;116(23):237201doi: 10.1103/PhysRevLett.116.237201.
Werner, A. H., Jaschke, D., Silvi, P., Kliesch, M., Calarco, T., Eisert, J., & Montangero, S. (2016). Positive Tensor Network Approach for Simulating Open Quantum Many-Body Systems. Physical review letters, 116(23), 237201. https://doi.org/10.1103/PhysRevLett.116.237201
Werner, A H, et al. "Positive Tensor Network Approach for Simulating Open Quantum Many-Body Systems." Physical review letters vol. 116,23 (2016): 237201. doi: https://doi.org/10.1103/PhysRevLett.116.237201
Werner AH, Jaschke D, Silvi P, Kliesch M, Calarco T, Eisert J, Montangero S. Positive Tensor Network Approach for Simulating Open Quantum Many-Body Systems. Phys Rev Lett. 2016 Jun 10;116(23):237201. doi: 10.1103/PhysRevLett.116.237201. Epub 2016 Jun 07. PMID: 27341253.
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FTIR and DFT studies of LiTFSI solvation in 3-methyl-2-oxazolidinone.

Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy

Jeschke S, Wiemhöfer HD.
PMID: 26774812
Spectrochim Acta A Mol Biomol Spectrosc. 2016 Mar 15;157:220-226. doi: 10.1016/j.saa.2015.12.021. Epub 2015 Dec 22.

Combined computational/FTIR spectroscopic analyses of 3-methyl-2-oxazolidinone (NMO) solutions with varying molar ratios of lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) are reported. Based on the second derivative spectral profile, overlapping peaks are distinguished as well as assigned to the vibrational modes of implicitly...

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Jeschke S, Wiemhöfer HD. FTIR and DFT studies of LiTFSI solvation in 3-methyl-2-oxazolidinone. Spectrochim Acta A Mol Biomol Spectrosc. 2015;157:220-226doi: 10.1016/j.saa.2015.12.021.
Jeschke, S., & Wiemhöfer, H. D. (2016). FTIR and DFT studies of LiTFSI solvation in 3-methyl-2-oxazolidinone. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 157220-226. https://doi.org/10.1016/j.saa.2015.12.021
Jeschke, Steffen, and Wiemhöfer, Hans-Dieter. "FTIR and DFT studies of LiTFSI solvation in 3-methyl-2-oxazolidinone." Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy vol. 157 (2016): 220-226. doi: https://doi.org/10.1016/j.saa.2015.12.021
Jeschke S, Wiemhöfer HD. FTIR and DFT studies of LiTFSI solvation in 3-methyl-2-oxazolidinone. Spectrochim Acta A Mol Biomol Spectrosc. 2016 Mar 15;157:220-226. doi: 10.1016/j.saa.2015.12.021. Epub 2015 Dec 22. PMID: 26774812.
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The Role of Glycosylation in Breast Cancer Metastasis and Cancer Control.

Frontiers in oncology

Kölbl AC, Andergassen U, Jeschke U.
PMID: 26528431
Front Oncol. 2015 Oct 13;5:219. doi: 10.3389/fonc.2015.00219. eCollection 2015.

Glycosylation and its correlation to the formation of remote metastasis in breast cancer had been an important scientific topic in the last 25 years. With the development of new analytical techniques, new insights were gained on the mechanisms underlying...

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Kölbl AC, Andergassen U, Jeschke U. The Role of Glycosylation in Breast Cancer Metastasis and Cancer Control. Front Oncol. 2015;5:219doi: 10.3389/fonc.2015.00219.
Kölbl, A. C., Andergassen, U., & Jeschke, U. (2015). The Role of Glycosylation in Breast Cancer Metastasis and Cancer Control. Frontiers in oncology, 5219. https://doi.org/10.3389/fonc.2015.00219
Kölbl, Alexandra C, et al. "The Role of Glycosylation in Breast Cancer Metastasis and Cancer Control." Frontiers in oncology vol. 5 (2015): 219. doi: https://doi.org/10.3389/fonc.2015.00219
Kölbl AC, Andergassen U, Jeschke U. The Role of Glycosylation in Breast Cancer Metastasis and Cancer Control. Front Oncol. 2015 Oct 13;5:219. doi: 10.3389/fonc.2015.00219. eCollection 2015. PMID: 26528431; PMCID: PMC4602128.
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EPR probes with well-defined, long distances between two or three unpaired electrons.

The Journal of organic chemistry

Godt A, Franzen C, Veit S, Enkelmann V, Pannier M, Jeschke G.
PMID: 11076617
J Org Chem. 2000 Nov 03;65(22):7575-82. doi: 10.1021/jo005556j.

The synthesis of rod- and star-shaped compounds carrying two or three spin labels as end groups is described. The unpaired electrons are 2.8-5.1 nm apart from each other. The shape-persistent scaffolds were obtained through Pd-Cu-catalyzed alkynyl-aryl coupling and Pd-Cu-catalyzed...

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Godt A, Franzen C, Veit S, et al. EPR probes with well-defined, long distances between two or three unpaired electrons. J Org Chem. 2000;65(22):7575-82doi: 10.1021/jo005556j.
Godt, A., Franzen, C., Veit, S., Enkelmann, V., Pannier, M., & Jeschke, G. (2000). EPR probes with well-defined, long distances between two or three unpaired electrons. The Journal of organic chemistry, 65(22), 7575-82. https://doi.org/10.1021/jo005556j
Godt, et al. "EPR probes with well-defined, long distances between two or three unpaired electrons." The Journal of organic chemistry vol. 65,22 (2000): 7575-82. doi: https://doi.org/10.1021/jo005556j
Godt A, Franzen C, Veit S, Enkelmann V, Pannier M, Jeschke G. EPR probes with well-defined, long distances between two or three unpaired electrons. J Org Chem. 2000 Nov 03;65(22):7575-82. doi: 10.1021/jo005556j. PMID: 11076617.
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Transmission of herbicide resistance from a monoecious to a dioecious weedy Amaranthus species.

TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik

Tranel J, Wassom J, Jeschke R, Rayburn L.
PMID: 12582480
Theor Appl Genet. 2002 Oct;105(5):674-679. doi: 10.1007/s00122-002-0931-3. Epub 2002 May 18.

The genus Amaranthus includes several important monoecious and dioecious weed species, and several populations of these species have developed resistance to herbicides. These species are closely related and two or more species often coexist in agricultural settings. Collectively, these...

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Tranel J, Wassom J, Jeschke R, et al. Transmission of herbicide resistance from a monoecious to a dioecious weedy Amaranthus species. Theor Appl Genet. 2002;105(5):674-679doi: 10.1007/s00122-002-0931-3.
Tranel, J., Wassom, J., Jeschke, R., & Rayburn, L. (2002). Transmission of herbicide resistance from a monoecious to a dioecious weedy Amaranthus species. TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik, 105(5), 674-679. https://doi.org/10.1007/s00122-002-0931-3
Tranel, J., et al. "Transmission of herbicide resistance from a monoecious to a dioecious weedy Amaranthus species." TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik vol. 105,5 (2002): 674-679. doi: https://doi.org/10.1007/s00122-002-0931-3
Tranel J, Wassom J, Jeschke R, Rayburn L. Transmission of herbicide resistance from a monoecious to a dioecious weedy Amaranthus species. Theor Appl Genet. 2002 Oct;105(5):674-679. doi: 10.1007/s00122-002-0931-3. Epub 2002 May 18. PMID: 12582480.
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Microstructure fabrication with a CO2 laser system: characterization and fabrication of cavities produced by raster scanning of the laser beam.

Lab on a chip

Jensen MF, Noerholm M, Christensen LH, Geschke O.
PMID: 15007463
Lab Chip. 2003 Nov;3(4):302-7. doi: 10.1039/b308153b. Epub 2003 Oct 07.

In this paper we describe the use of a CO(2) laser for production of cavities and microstructures in poly(methyl methacrylate) (PMMA) by moving the laser beam over the PMMA surface in a raster pattern. The topography of the cavities...

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Jensen MF, Noerholm M, Christensen LH, et al. Microstructure fabrication with a CO2 laser system: characterization and fabrication of cavities produced by raster scanning of the laser beam. Lab Chip. 2003;3(4):302-7doi: 10.1039/b308153b.
Jensen, M. F., Noerholm, M., Christensen, L. H., & Geschke, O. (2003). Microstructure fabrication with a CO2 laser system: characterization and fabrication of cavities produced by raster scanning of the laser beam. Lab on a chip, 3(4), 302-7. https://doi.org/10.1039/b308153b
Jensen, Martin F, et al. "Microstructure fabrication with a CO2 laser system: characterization and fabrication of cavities produced by raster scanning of the laser beam." Lab on a chip vol. 3,4 (2003): 302-7. doi: https://doi.org/10.1039/b308153b
Jensen MF, Noerholm M, Christensen LH, Geschke O. Microstructure fabrication with a CO2 laser system: characterization and fabrication of cavities produced by raster scanning of the laser beam. Lab Chip. 2003 Nov;3(4):302-7. doi: 10.1039/b308153b. Epub 2003 Oct 07. PMID: 15007463.
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Peroxynitrite formation and sinusoidal endothelial cell injury during acetaminophen-induced hepatotoxicity in mice.

Comparative hepatology

Knight TR, Jaeschke H.
PMID: 14960198
Comp Hepatol. 2004 Jan 14;3:S46. doi: 10.1186/1476-5926-2-S1-S46.

INTRODUCTION: Vascular injury and accumulation of red blood cells in the space of Disse (hemorrhage) is a characteristic feature of acetaminophen hepatotoxicity. However, the mechanism of nonparenchymal cell injury is unclear. Therefore, the objective was to investigate if either...

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Knight TR, Jaeschke H. Peroxynitrite formation and sinusoidal endothelial cell injury during acetaminophen-induced hepatotoxicity in mice. Comp Hepatol. 2004;3:S46doi: 10.1186/1476-5926-2-S1-S46.
Knight, T. R., & Jaeschke, H. (2004). Peroxynitrite formation and sinusoidal endothelial cell injury during acetaminophen-induced hepatotoxicity in mice. Comparative hepatology, 3S46. https://doi.org/10.1186/1476-5926-2-S1-S46
Knight, Tamara R, and Jaeschke, Hartmut. "Peroxynitrite formation and sinusoidal endothelial cell injury during acetaminophen-induced hepatotoxicity in mice." Comparative hepatology vol. 3 (2004): S46. doi: https://doi.org/10.1186/1476-5926-2-S1-S46
Knight TR, Jaeschke H. Peroxynitrite formation and sinusoidal endothelial cell injury during acetaminophen-induced hepatotoxicity in mice. Comp Hepatol. 2004 Jan 14;3:S46. doi: 10.1186/1476-5926-2-S1-S46. PMID: 14960198; PMCID: PMC2410261.
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How flexible are poly(para-phenyleneethynylene)s?.

Angewandte Chemie (International ed. in English)

Godt A, Schulte M, Zimmermann H, Jeschke G.
PMID: 17051574
Angew Chem Int Ed Engl. 2006 Nov 20;45(45):7560-4. doi: 10.1002/anie.200602807.

No abstract available.

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Godt A, Schulte M, Zimmermann H, et al. How flexible are poly(para-phenyleneethynylene)s?. Angew Chem Int Ed Engl. 2006;45(45):7560-4doi: 10.1002/anie.200602807.
Godt, A., Schulte, M., Zimmermann, H., & Jeschke, G. (2006). How flexible are poly(para-phenyleneethynylene)s?. Angewandte Chemie (International ed. in English), 45(45), 7560-4. https://doi.org/10.1002/anie.200602807
Godt, Adelheid, et al. "How flexible are poly(para-phenyleneethynylene)s?." Angewandte Chemie (International ed. in English) vol. 45,45 (2006): 7560-4. doi: https://doi.org/10.1002/anie.200602807
Godt A, Schulte M, Zimmermann H, Jeschke G. How flexible are poly(para-phenyleneethynylene)s?. Angew Chem Int Ed Engl. 2006 Nov 20;45(45):7560-4. doi: 10.1002/anie.200602807. PMID: 17051574.
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Naphthalene amidine imide dyes by transamination of naphthalene bisimides.

Chemistry (Weinheim an der Bergstrasse, Germany)

Langhals H, Jaschke H.
PMID: 16425168
Chemistry. 2006 Mar 20;12(10):2815-24. doi: 10.1002/chem.200500899.

Derivatives of naphthalene-1,4,5,8-tetracarboxylic acid with amidine structures have been prepared. The light absorption of the bisimide derivatives in the UV region is shifted to the visible for the amidine imides, which also fluoresce with a large Stokes shift. It...

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Langhals H, Jaschke H. Naphthalene amidine imide dyes by transamination of naphthalene bisimides. Chemistry. 2006;12(10):2815-24doi: 10.1002/chem.200500899.
Langhals, H., & Jaschke, H. (2006). Naphthalene amidine imide dyes by transamination of naphthalene bisimides. Chemistry (Weinheim an der Bergstrasse, Germany), 12(10), 2815-24. https://doi.org/10.1002/chem.200500899
Langhals, Heinz, and Jaschke, Harald. "Naphthalene amidine imide dyes by transamination of naphthalene bisimides." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 12,10 (2006): 2815-24. doi: https://doi.org/10.1002/chem.200500899
Langhals H, Jaschke H. Naphthalene amidine imide dyes by transamination of naphthalene bisimides. Chemistry. 2006 Mar 20;12(10):2815-24. doi: 10.1002/chem.200500899. PMID: 16425168.
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Fully-automated assay by liquid chromatography for routine drug monitoring in body fluids--method development with biological samples.

Journal of pharmaceutical and biomedical analysis

Roth W, Beschke K.
PMID: 16867756
J Pharm Biomed Anal. 1984;2(2):289-96. doi: 10.1016/0731-7085(84)80079-5.

A fully-automated liquid chromatograph based on alternated pre-column enrichment technique has been developed for routine drug monitoring of body fluids using a column switching technique. Advantages of the method include the facility of direct injection of the body fluid...

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Roth W, Beschke K. Fully-automated assay by liquid chromatography for routine drug monitoring in body fluids--method development with biological samples. J Pharm Biomed Anal. 1984;2(2):289-96doi: 10.1016/0731-7085(84)80079-5.
Roth, W., & Beschke, K. (1984). Fully-automated assay by liquid chromatography for routine drug monitoring in body fluids--method development with biological samples. Journal of pharmaceutical and biomedical analysis, 2(2), 289-96. https://doi.org/10.1016/0731-7085(84)80079-5
Roth, W, and Beschke, K. "Fully-automated assay by liquid chromatography for routine drug monitoring in body fluids--method development with biological samples." Journal of pharmaceutical and biomedical analysis vol. 2,2 (1984): 289-96. doi: https://doi.org/10.1016/0731-7085(84)80079-5
Roth W, Beschke K. Fully-automated assay by liquid chromatography for routine drug monitoring in body fluids--method development with biological samples. J Pharm Biomed Anal. 1984;2(2):289-96. doi: 10.1016/0731-7085(84)80079-5. PMID: 16867756.
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Spatial distribution of stabilizer-derived nitroxide radicals during thermal degradation of poly(acrylonitrile-butadiene-styrene) copolymers: a unified picture from pulsed ELDOR and ESR imaging.

Physical chemistry chemical physics : PCCP

Jeschke G, Schlick S.
PMID: 17028698
Phys Chem Chem Phys. 2006 Sep 21;8(35):4095-103. doi: 10.1039/b607826e. Epub 2006 Jul 31.

Double Electron-Electron Resonance (DEER) provides information on the spatial distribution of radicals on the length scale of a few nanometres, while Electron Spin Resonance Imaging (ESRI) provides information on a length scale of millimetres with a resolution of about...

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Jeschke G, Schlick S. Spatial distribution of stabilizer-derived nitroxide radicals during thermal degradation of poly(acrylonitrile-butadiene-styrene) copolymers: a unified picture from pulsed ELDOR and ESR imaging. Phys Chem Chem Phys. 2006;8(35):4095-103doi: 10.1039/b607826e.
Jeschke, G., & Schlick, S. (2006). Spatial distribution of stabilizer-derived nitroxide radicals during thermal degradation of poly(acrylonitrile-butadiene-styrene) copolymers: a unified picture from pulsed ELDOR and ESR imaging. Physical chemistry chemical physics : PCCP, 8(35), 4095-103. https://doi.org/10.1039/b607826e
Jeschke, Gunnar, and Schlick, Shulamith. "Spatial distribution of stabilizer-derived nitroxide radicals during thermal degradation of poly(acrylonitrile-butadiene-styrene) copolymers: a unified picture from pulsed ELDOR and ESR imaging." Physical chemistry chemical physics : PCCP vol. 8,35 (2006): 4095-103. doi: https://doi.org/10.1039/b607826e
Jeschke G, Schlick S. Spatial distribution of stabilizer-derived nitroxide radicals during thermal degradation of poly(acrylonitrile-butadiene-styrene) copolymers: a unified picture from pulsed ELDOR and ESR imaging. Phys Chem Chem Phys. 2006 Sep 21;8(35):4095-103. doi: 10.1039/b607826e. Epub 2006 Jul 31. PMID: 17028698.
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Showing 13 to 24 of 450 entries