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Ultrafast Dynamics of o-Nitrophenol: An Experimental and Theoretical Study.

The journal of physical chemistry. A

Ernst HA, Wolf TJ, Schalk O, González-García N, Boguslavskiy AE, Stolow A, Olzmann M, Unterreiner AN.
PMID: 26266823
J Phys Chem A. 2015 Sep 03;119(35):9225-35. doi: 10.1021/acs.jpca.5b04900. Epub 2015 Aug 22.

The photolysis of o-nitrophenol (o-NP), a typical push-pull molecule, is of current interest in atmospheric chemistry as a possible source of nitrous acid (HONO). To characterize the largely unknown photolysis mechanism, the dynamics of the lowest lying excited singlet...

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Ernst HA, Wolf TJ, Schalk O, et al. Ultrafast Dynamics of o-Nitrophenol: An Experimental and Theoretical Study. J Phys Chem A. 2015;119(35):9225-35doi: 10.1021/acs.jpca.5b04900.
Ernst, H. A., Wolf, T. J., Schalk, O., González-García, N., Boguslavskiy, A. E., Stolow, A., Olzmann, M., & Unterreiner, A. N. (2015). Ultrafast Dynamics of o-Nitrophenol: An Experimental and Theoretical Study. The journal of physical chemistry. A, 119(35), 9225-35. https://doi.org/10.1021/acs.jpca.5b04900
Ernst, Hanna A, et al. "Ultrafast Dynamics of o-Nitrophenol: An Experimental and Theoretical Study." The journal of physical chemistry. A vol. 119,35 (2015): 9225-35. doi: https://doi.org/10.1021/acs.jpca.5b04900
Ernst HA, Wolf TJ, Schalk O, González-García N, Boguslavskiy AE, Stolow A, Olzmann M, Unterreiner AN. Ultrafast Dynamics of o-Nitrophenol: An Experimental and Theoretical Study. J Phys Chem A. 2015 Sep 03;119(35):9225-35. doi: 10.1021/acs.jpca.5b04900. Epub 2015 Aug 22. PMID: 26266823.
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Editorial. The lack of interspecialty communication.

American journal of orthodontics

Salzmann JA.
PMID: 5280428
Am J Orthod. 1971 Jun;59(6):611-2. doi: 10.1016/0002-9416(71)90009-1.

No abstract available.

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Salzmann JA. Editorial. The lack of interspecialty communication. Am J Orthod. 1971;59(6):611-2doi: 10.1016/0002-9416(71)90009-1.
Salzmann, J. A. (1971). Editorial. The lack of interspecialty communication. American journal of orthodontics, 59(6), 611-2. https://doi.org/10.1016/0002-9416(71)90009-1
Salzmann, J A. "Editorial. The lack of interspecialty communication." American journal of orthodontics vol. 59,6 (1971): 611-2. doi: https://doi.org/10.1016/0002-9416(71)90009-1
Salzmann JA. Editorial. The lack of interspecialty communication. Am J Orthod. 1971 Jun;59(6):611-2. doi: 10.1016/0002-9416(71)90009-1. PMID: 5280428.
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SPECIALIZATION.

American journal of orthodontics

SALZMANN JA.
PMID: 14247299
Am J Orthod. 1965 Mar;51:208-10. doi: 10.1016/0002-9416(65)90006-0.

No abstract available.

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SALZMANN JA. SPECIALIZATION. Am J Orthod. 1965;51:208-10doi: 10.1016/0002-9416(65)90006-0.
SALZMANN, J. A. (1965). SPECIALIZATION. American journal of orthodontics, 51208-10. https://doi.org/10.1016/0002-9416(65)90006-0
SALZMANN, J A. "SPECIALIZATION." American journal of orthodontics vol. 51 (1965): 208-10. doi: https://doi.org/10.1016/0002-9416(65)90006-0
SALZMANN JA. SPECIALIZATION. Am J Orthod. 1965 Mar;51:208-10. doi: 10.1016/0002-9416(65)90006-0. PMID: 14247299.
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Salt effects on the structure of water probed by attenuated total reflection infrared spectroscopy and molecular dynamics simulations.

Chemphyschem : a European journal of chemical physics and physical chemistry

Riemenschneider J, Holzmann J, Ludwig R.
PMID: 19035393
Chemphyschem. 2008 Dec 22;9(18):2731-6. doi: 10.1002/cphc.200800571.

We study aqueous solutions of alkaline chlorides (NaCl, KCl, RbCl and CsCl) with a combination of attenuated total reflection infrared (ATR-IR) spectroscopy and molecular dynamics (MD) simulations using the TIP4P-Ew water model (Horn et al., J. Chem. Phys. 2004,...

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Riemenschneider J, Holzmann J, Ludwig R. Salt effects on the structure of water probed by attenuated total reflection infrared spectroscopy and molecular dynamics simulations. Chemphyschem. 2008;9(18):2731-6doi: 10.1002/cphc.200800571.
Riemenschneider, J., Holzmann, J., & Ludwig, R. (2008). Salt effects on the structure of water probed by attenuated total reflection infrared spectroscopy and molecular dynamics simulations. Chemphyschem : a European journal of chemical physics and physical chemistry, 9(18), 2731-6. https://doi.org/10.1002/cphc.200800571
Riemenschneider, Julian, et al. "Salt effects on the structure of water probed by attenuated total reflection infrared spectroscopy and molecular dynamics simulations." Chemphyschem : a European journal of chemical physics and physical chemistry vol. 9,18 (2008): 2731-6. doi: https://doi.org/10.1002/cphc.200800571
Riemenschneider J, Holzmann J, Ludwig R. Salt effects on the structure of water probed by attenuated total reflection infrared spectroscopy and molecular dynamics simulations. Chemphyschem. 2008 Dec 22;9(18):2731-6. doi: 10.1002/cphc.200800571. PMID: 19035393.
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Accurate computational determination of the binding energy of the SO3 x H2O complex.

The Journal of chemical physics

Fliegl H, Glöss A, Welz O, Olzmann M, Klopper W.
PMID: 16942218
J Chem Phys. 2006 Aug 07;125(5):054312. doi: 10.1063/1.2234372.

Reliable thermochemical data for the reaction SO3 + H2OSO3 x H2O (1a) are of crucial importance for an adequate modeling of the homogeneous H2SO4 formation in the atmosphere. We report on high-level quantum chemical calculations to predict the binding...

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Fliegl H, Glöss A, Welz O, et al. Accurate computational determination of the binding energy of the SO3 x H2O complex. J Chem Phys. 2006;125(5):054312doi: 10.1063/1.2234372.
Fliegl, H., Glöss, A., Welz, O., Olzmann, M., & Klopper, W. (2006). Accurate computational determination of the binding energy of the SO3 x H2O complex. The Journal of chemical physics, 125(5), 054312. https://doi.org/10.1063/1.2234372
Fliegl, Heike, et al. "Accurate computational determination of the binding energy of the SO3 x H2O complex." The Journal of chemical physics vol. 125,5 (2006): 054312. doi: https://doi.org/10.1063/1.2234372
Fliegl H, Glöss A, Welz O, Olzmann M, Klopper W. Accurate computational determination of the binding energy of the SO3 x H2O complex. J Chem Phys. 2006 Aug 07;125(5):054312. doi: 10.1063/1.2234372. PMID: 16942218.
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Shock-tube study of the thermal decomposition of CH3CHO and CH3CHO + H reaction.

The journal of physical chemistry. A

Bentz T, Striebel F, Olzmann M.
PMID: 18547039
J Phys Chem A. 2008 Jul 10;112(27):6120-4. doi: 10.1021/jp802030z. Epub 2008 Jun 12.

The thermal decomposition of acetaldehyde, CH3CHO + M --> CH3 + HCO + M (eq 1), and the reaction CH3CHO + H --> products (eq 6) have been studied behind reflected shock waves with argon as the bath gas...

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Bentz T, Striebel F, Olzmann M. Shock-tube study of the thermal decomposition of CH3CHO and CH3CHO + H reaction. J Phys Chem A. 2008;112(27):6120-4doi: 10.1021/jp802030z.
Bentz, T., Striebel, F., & Olzmann, M. (2008). Shock-tube study of the thermal decomposition of CH3CHO and CH3CHO + H reaction. The journal of physical chemistry. A, 112(27), 6120-4. https://doi.org/10.1021/jp802030z
Bentz, Tobias, et al. "Shock-tube study of the thermal decomposition of CH3CHO and CH3CHO + H reaction." The journal of physical chemistry. A vol. 112,27 (2008): 6120-4. doi: https://doi.org/10.1021/jp802030z
Bentz T, Striebel F, Olzmann M. Shock-tube study of the thermal decomposition of CH3CHO and CH3CHO + H reaction. J Phys Chem A. 2008 Jul 10;112(27):6120-4. doi: 10.1021/jp802030z. Epub 2008 Jun 12. PMID: 18547039.
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Kinetics of the NCN + NO reaction over a broad temperature and pressure range.

The journal of physical chemistry. A

Welz O, Olzmann M.
PMID: 22694482
J Phys Chem A. 2012 Jul 12;116(27):7293-301. doi: 10.1021/jp303069g. Epub 2012 Jul 03.

Rate coefficients for the reaction (3)NCN + NO → products (R3) were measured in the temperature range 251-487 K at pressures from 10 mbar up to 50 bar with helium as the bath gas. The experiments were carried out...

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Welz O, Olzmann M. Kinetics of the NCN + NO reaction over a broad temperature and pressure range. J Phys Chem A. 2012;116(27):7293-301doi: 10.1021/jp303069g.
Welz, O., & Olzmann, M. (2012). Kinetics of the NCN + NO reaction over a broad temperature and pressure range. The journal of physical chemistry. A, 116(27), 7293-301. https://doi.org/10.1021/jp303069g
Welz, Oliver, and Olzmann, Matthias. "Kinetics of the NCN + NO reaction over a broad temperature and pressure range." The journal of physical chemistry. A vol. 116,27 (2012): 7293-301. doi: https://doi.org/10.1021/jp303069g
Welz O, Olzmann M. Kinetics of the NCN + NO reaction over a broad temperature and pressure range. J Phys Chem A. 2012 Jul 12;116(27):7293-301. doi: 10.1021/jp303069g. Epub 2012 Jul 03. PMID: 22694482.
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Reaction of dimethyl ether with hydroxyl radicals: kinetic isotope effect and prereactive complex formation.

The journal of physical chemistry. A

Bänsch C, Kiecherer J, Szöri M, Olzmann M.
PMID: 23914942
J Phys Chem A. 2013 Sep 05;117(35):8343-51. doi: 10.1021/jp405724a. Epub 2013 Aug 20.

The kinetic isotope effect of the reactions OH + CH3OCH3 (DME) and OH + CD3OCD3 (DME-d6) was experimentally and theoretically studied. Experiments were carried out in a slow-flow reactor at pressures between 5 and 21 bar (helium as bath...

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Bänsch C, Kiecherer J, Szöri M, et al. Reaction of dimethyl ether with hydroxyl radicals: kinetic isotope effect and prereactive complex formation. J Phys Chem A. 2013;117(35):8343-51doi: 10.1021/jp405724a.
Bänsch, C., Kiecherer, J., Szöri, M., & Olzmann, M. (2013). Reaction of dimethyl ether with hydroxyl radicals: kinetic isotope effect and prereactive complex formation. The journal of physical chemistry. A, 117(35), 8343-51. https://doi.org/10.1021/jp405724a
Bänsch, Cornelie, et al. "Reaction of dimethyl ether with hydroxyl radicals: kinetic isotope effect and prereactive complex formation." The journal of physical chemistry. A vol. 117,35 (2013): 8343-51. doi: https://doi.org/10.1021/jp405724a
Bänsch C, Kiecherer J, Szöri M, Olzmann M. Reaction of dimethyl ether with hydroxyl radicals: kinetic isotope effect and prereactive complex formation. J Phys Chem A. 2013 Sep 05;117(35):8343-51. doi: 10.1021/jp405724a. Epub 2013 Aug 20. PMID: 23914942.
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Native mass spectrometry combined with enzymatic dissection unravels glycoform heterogeneity of biopharmaceuticals.

Nature communications

Wohlschlager T, Scheffler K, Forstenlehner IC, Skala W, Senn S, Damoc E, Holzmann J, Huber CG.
PMID: 29712889
Nat Commun. 2018 Apr 30;9(1):1713. doi: 10.1038/s41467-018-04061-7.

Robust manufacturing processes resulting in consistent glycosylation are critical for the efficacy and safety of biopharmaceuticals. Information on glycosylation can be obtained by conventional bottom-up methods but is often limited to the glycan or glycopeptide level. Here, we apply...

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Wohlschlager T, Scheffler K, Forstenlehner IC, et al. Native mass spectrometry combined with enzymatic dissection unravels glycoform heterogeneity of biopharmaceuticals. Nat Commun. 2018;9(1):1713doi: 10.1038/s41467-018-04061-7.
Wohlschlager, T., Scheffler, K., Forstenlehner, I. C., Skala, W., Senn, S., Damoc, E., Holzmann, J., & Huber, C. G. (2018). Native mass spectrometry combined with enzymatic dissection unravels glycoform heterogeneity of biopharmaceuticals. Nature communications, 9(1), 1713. https://doi.org/10.1038/s41467-018-04061-7
Wohlschlager, Therese, et al. "Native mass spectrometry combined with enzymatic dissection unravels glycoform heterogeneity of biopharmaceuticals." Nature communications vol. 9,1 (2018): 1713. doi: https://doi.org/10.1038/s41467-018-04061-7
Wohlschlager T, Scheffler K, Forstenlehner IC, Skala W, Senn S, Damoc E, Holzmann J, Huber CG. Native mass spectrometry combined with enzymatic dissection unravels glycoform heterogeneity of biopharmaceuticals. Nat Commun. 2018 Apr 30;9(1):1713. doi: 10.1038/s41467-018-04061-7. PMID: 29712889; PMCID: PMC5928108.
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The cytosolic glyoxalases of .

Microbial cell (Graz, Austria)

Wezena CA, Alisch R, Golzmann A, Liedgens L, Staudacher V, Pradel G, Deponte M.
PMID: 29354648
Microb Cell. 2017 Nov 20;5(1):32-41. doi: 10.15698/mic2018.01.608.

The enzymes glyoxalase 1 and 2 (Glo1 and Glo2) are found in most eukaryotes and catalyze the glutathione-dependent conversion of 2-oxoaldehydes to 2-hydroxycarboxylic acids. Four glyoxalases are encoded in the genome of the malaria parasite

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Wezena CA, Alisch R, Golzmann A, et al. The cytosolic glyoxalases of . Microb Cell. 2017;5(1):32-41doi: 10.15698/mic2018.01.608.
Wezena, C. A., Alisch, R., Golzmann, A., Liedgens, L., Staudacher, V., Pradel, G., & Deponte, M. (2017). The cytosolic glyoxalases of . Microbial cell (Graz, Austria), 5(1), 32-41. https://doi.org/10.15698/mic2018.01.608
Wezena, Cletus A, et al. "The cytosolic glyoxalases of ." Microbial cell (Graz, Austria) vol. 5,1 (2017): 32-41. doi: https://doi.org/10.15698/mic2018.01.608
Wezena CA, Alisch R, Golzmann A, Liedgens L, Staudacher V, Pradel G, Deponte M. The cytosolic glyoxalases of . Microb Cell. 2017 Nov 20;5(1):32-41. doi: 10.15698/mic2018.01.608. PMID: 29354648; PMCID: PMC5772037.
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Ending on a sour note: Lipids orchestrate ferroptosis in cancer.

Cell metabolism

Lange M, Olzmann JA.
PMID: 34348094
Cell Metab. 2021 Aug 03;33(8):1507-1509. doi: 10.1016/j.cmet.2021.07.011.

Lipid metabolism is altered in the acidic tumor microenvironment. Here, the authors show that polyunsaturated fatty acid supplementation, together with concomitant inhibition of lipid droplet biogenesis, induces ferroptosis in acidic cancer cells. These findings highlight the potential to exploit...

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Lange M, Olzmann JA. Ending on a sour note: Lipids orchestrate ferroptosis in cancer. Cell Metab. 2021;33(8):1507-1509doi: 10.1016/j.cmet.2021.07.011.
Lange, M., & Olzmann, J. A. (2021). Ending on a sour note: Lipids orchestrate ferroptosis in cancer. Cell metabolism, 33(8), 1507-1509. https://doi.org/10.1016/j.cmet.2021.07.011
Lange, Mike, and Olzmann, James A. "Ending on a sour note: Lipids orchestrate ferroptosis in cancer." Cell metabolism vol. 33,8 (2021): 1507-1509. doi: https://doi.org/10.1016/j.cmet.2021.07.011
Lange M, Olzmann JA. Ending on a sour note: Lipids orchestrate ferroptosis in cancer. Cell Metab. 2021 Aug 03;33(8):1507-1509. doi: 10.1016/j.cmet.2021.07.011. PMID: 34348094.
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Temperature- and pressure-dependent kinetics of the competing C-O bond fission reactions of dimethoxymethane.

Physical chemistry chemical physics : PCCP

Golka L, Gratzfeld D, Weber I, Olzmann M.
PMID: 32104877
Phys Chem Chem Phys. 2020 Mar 11;22(10):5523-5530. doi: 10.1039/d0cp00136h.

Oxymethylene ethers are often considered as promising fuel additives to reduce the emissions of soot and NOx from diesel engines. Dimethoxymethane (DMM) is the smallest member of this class of compounds and therefore particularly suitable to study the reactivity...

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Golka L, Gratzfeld D, Weber I, et al. Temperature- and pressure-dependent kinetics of the competing C-O bond fission reactions of dimethoxymethane. Phys Chem Chem Phys. 2020;22(10):5523-5530doi: 10.1039/d0cp00136h.
Golka, L., Gratzfeld, D., Weber, I., & Olzmann, M. (2020). Temperature- and pressure-dependent kinetics of the competing C-O bond fission reactions of dimethoxymethane. Physical chemistry chemical physics : PCCP, 22(10), 5523-5530. https://doi.org/10.1039/d0cp00136h
Golka, Leonie, et al. "Temperature- and pressure-dependent kinetics of the competing C-O bond fission reactions of dimethoxymethane." Physical chemistry chemical physics : PCCP vol. 22,10 (2020): 5523-5530. doi: https://doi.org/10.1039/d0cp00136h
Golka L, Gratzfeld D, Weber I, Olzmann M. Temperature- and pressure-dependent kinetics of the competing C-O bond fission reactions of dimethoxymethane. Phys Chem Chem Phys. 2020 Mar 11;22(10):5523-5530. doi: 10.1039/d0cp00136h. PMID: 32104877.
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Showing 1 to 12 of 55 entries