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[Not Available].

Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke

Frich JC.
PMID: 27637031
Tidsskr Nor Laegeforen. 2016 Sep 13;136(16):1323. doi: 10.4045/tidsskr.16.0659. eCollection 2016 Sep.

No abstract available.

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Frich JC. Re: Oslo 2014 fra studentenes perspektiv. [Not Available]. Tidsskr Nor Laegeforen. 2016;136(16):1323doi: 10.4045/tidsskr.16.0659.
Frich, J. C. (2016). Re: Oslo 2014 fra studentenes perspektiv. [Not Available]. Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke, 136(16), 1323. https://doi.org/10.4045/tidsskr.16.0659
Frich, Jan C. "Re: Oslo 2014 fra studentenes perspektiv." [Not Available]. Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke vol. 136,16 (2016): 1323. doi: https://doi.org/10.4045/tidsskr.16.0659
Frich JC. Re: Oslo 2014 fra studentenes perspektiv. [Not Available]. Tidsskr Nor Laegeforen. 2016 Sep 13;136(16):1323. doi: 10.4045/tidsskr.16.0659. eCollection 2016 Sep. Norwegian. PMID: 27637031.
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Charge-transfer states in triazole linked donor-acceptor materials: strong effects of chemical modification and solvation.

Physical chemistry chemical physics : PCCP

Kautny P, Glöcklhofer F, Kader T, Mewes JM, Stöger B, Fröhlich J, Lumpi D, Plasser F.
PMID: 28671704
Phys Chem Chem Phys. 2017 Jul 21;19(27):18055-18067. doi: 10.1039/c7cp01664f. Epub 2017 Jul 03.

A series of 1,2,3-triazole linked donor-acceptor chromophores are prepared by Click Chemistry from ene-yne starting materials. The effects of three distinct chemical variations are investigated: enhancing the acceptor strength through oxidation of the sulphur atom, alteration of the double...

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Kautny P, Glöcklhofer F, Kader T, et al. Charge-transfer states in triazole linked donor-acceptor materials: strong effects of chemical modification and solvation. Phys Chem Chem Phys. 2017;19(27):18055-18067doi: 10.1039/c7cp01664f.
Kautny, P., Glöcklhofer, F., Kader, T., Mewes, J. M., Stöger, B., Fröhlich, J., Lumpi, D., & Plasser, F. (2017). Charge-transfer states in triazole linked donor-acceptor materials: strong effects of chemical modification and solvation. Physical chemistry chemical physics : PCCP, 19(27), 18055-18067. https://doi.org/10.1039/c7cp01664f
Kautny, Paul, et al. "Charge-transfer states in triazole linked donor-acceptor materials: strong effects of chemical modification and solvation." Physical chemistry chemical physics : PCCP vol. 19,27 (2017): 18055-18067. doi: https://doi.org/10.1039/c7cp01664f
Kautny P, Glöcklhofer F, Kader T, Mewes JM, Stöger B, Fröhlich J, Lumpi D, Plasser F. Charge-transfer states in triazole linked donor-acceptor materials: strong effects of chemical modification and solvation. Phys Chem Chem Phys. 2017 Jul 21;19(27):18055-18067. doi: 10.1039/c7cp01664f. Epub 2017 Jul 03. PMID: 28671704.
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Synthesis of zearalenone-16-β,D-glucoside and zearalenone-16-sulfate: A tale of protecting resorcylic acid lactones for regiocontrolled conjugation.

Beilstein journal of organic chemistry

Mikula H, Weber J, Svatunek D, Skrinjar P, Adam G, Krska R, Hametner C, Fröhlich J.
PMID: 24991263
Beilstein J Org Chem. 2014 May 15;10:1129-34. doi: 10.3762/bjoc.10.112. eCollection 2014.

The development of a reliable procedure for the synthesis of the 16-glucoside and 16-sulfate of the resorcylic acid lactone (RAL) type compound zearalenone is presented. Different protective group strategies were considered and applied to enable the preparation of glucosides...

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Mikula H, Weber J, Svatunek D, et al. Synthesis of zearalenone-16-β,D-glucoside and zearalenone-16-sulfate: A tale of protecting resorcylic acid lactones for regiocontrolled conjugation. Beilstein J Org Chem. 2014;10:1129-34doi: 10.3762/bjoc.10.112.
Mikula, H., Weber, J., Svatunek, D., Skrinjar, P., Adam, G., Krska, R., Hametner, C., & Fröhlich, J. (2014). Synthesis of zearalenone-16-β,D-glucoside and zearalenone-16-sulfate: A tale of protecting resorcylic acid lactones for regiocontrolled conjugation. Beilstein journal of organic chemistry, 101129-34. https://doi.org/10.3762/bjoc.10.112
Mikula, Hannes, et al. "Synthesis of zearalenone-16-β,D-glucoside and zearalenone-16-sulfate: A tale of protecting resorcylic acid lactones for regiocontrolled conjugation." Beilstein journal of organic chemistry vol. 10 (2014): 1129-34. doi: https://doi.org/10.3762/bjoc.10.112
Mikula H, Weber J, Svatunek D, Skrinjar P, Adam G, Krska R, Hametner C, Fröhlich J. Synthesis of zearalenone-16-β,D-glucoside and zearalenone-16-sulfate: A tale of protecting resorcylic acid lactones for regiocontrolled conjugation. Beilstein J Org Chem. 2014 May 15;10:1129-34. doi: 10.3762/bjoc.10.112. eCollection 2014. PMID: 24991263; PMCID: PMC4077526.
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Detection of Botulinum Toxins A, B, E, and F in Foods by Endopep-MS.

Journal of agricultural and food chemistry

Kalb SR, Krilich JC, Dykes JK, Lúquez C, Maslanka SE, Barr JR.
PMID: 25578960
J Agric Food Chem. 2015 Feb 04;63(4):1133-1141. doi: 10.1021/jf505482b. Epub 2015 Jan 22.

Botulism is caused by exposure to botulinum neurotoxins (BoNTs). BoNTs are proteins secreted by some species of clostridia; these neurotoxins are known to interfere with nerve impulse transmission, thus causing paralysis. Botulism may be contracted through consumption of food...

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Kalb SR, Krilich JC, Dykes JK, et al. Detection of Botulinum Toxins A, B, E, and F in Foods by Endopep-MS. J Agric Food Chem. 2015;63(4):1133-1141doi: 10.1021/jf505482b.
Kalb, S. R., Krilich, J. C., Dykes, J. K., Lúquez, C., Maslanka, S. E., & Barr, J. R. (2015). Detection of Botulinum Toxins A, B, E, and F in Foods by Endopep-MS. Journal of agricultural and food chemistry, 63(4), 1133-1141. https://doi.org/10.1021/jf505482b
Kalb, Suzanne R, et al. "Detection of Botulinum Toxins A, B, E, and F in Foods by Endopep-MS." Journal of agricultural and food chemistry vol. 63,4 (2015): 1133-1141. doi: https://doi.org/10.1021/jf505482b
Kalb SR, Krilich JC, Dykes JK, Lúquez C, Maslanka SE, Barr JR. Detection of Botulinum Toxins A, B, E, and F in Foods by Endopep-MS. J Agric Food Chem. 2015 Feb 04;63(4):1133-1141. doi: 10.1021/jf505482b. Epub 2015 Jan 22. PMID: 25578960; PMCID: PMC4523457.
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Complications Related to Metal-on-Metal Articulation in Trapeziometacarpal Joint Total Joint Arthroplasty.

Journal of functional biomaterials

Frølich C, Hansen TB.
PMID: 26020592
J Funct Biomater. 2015 May 25;6(2):318-27. doi: 10.3390/jfb6020318.

Adverse reactions to metal-on-metal (MoM) prostheses are well known from total hip joint resurfacing arthroplasty with elevated serum chrome or cobalt, pain and pseudo tumor formation. It may, however, also be seen after total joint replacement of the trapeziometacarpal...

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Frølich C, Hansen TB. Complications Related to Metal-on-Metal Articulation in Trapeziometacarpal Joint Total Joint Arthroplasty. J Funct Biomater. 2015;6(2):318-27doi: 10.3390/jfb6020318.
Frølich, C., & Hansen, T. B. (2015). Complications Related to Metal-on-Metal Articulation in Trapeziometacarpal Joint Total Joint Arthroplasty. Journal of functional biomaterials, 6(2), 318-27. https://doi.org/10.3390/jfb6020318
Frølich, Christina, and Hansen, Torben Bæk. "Complications Related to Metal-on-Metal Articulation in Trapeziometacarpal Joint Total Joint Arthroplasty." Journal of functional biomaterials vol. 6,2 (2015): 318-27. doi: https://doi.org/10.3390/jfb6020318
Frølich C, Hansen TB. Complications Related to Metal-on-Metal Articulation in Trapeziometacarpal Joint Total Joint Arthroplasty. J Funct Biomater. 2015 May 25;6(2):318-27. doi: 10.3390/jfb6020318. PMID: 26020592; PMCID: PMC4493514.
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Neutrino-induced nucleosynthesis of A>64 nuclei: the nu p process.

Physical review letters

Fröhlich C, Martínez-Pinedo G, Liebendörfer M, Thielemann FK, Bravo E, Hix WR, Langanke K, Zinner NT.
PMID: 16712066
Phys Rev Lett. 2006 Apr 14;96(14):142502. doi: 10.1103/PhysRevLett.96.142502. Epub 2006 Apr 10.

We present a new nucleosynthesis process that we denote as the nu p process, which occurs in supernovae (and possibly gamma-ray bursts) when strong neutrino fluxes create proton-rich ejecta. In this process, antineutrino absorptions in the proton-rich environment produce...

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Fröhlich C, Martínez-Pinedo G, Liebendörfer M, et al. Neutrino-induced nucleosynthesis of A>64 nuclei: the nu p process. Phys Rev Lett. 2006;96(14):142502doi: 10.1103/PhysRevLett.96.142502.
Fröhlich, C., Martínez-Pinedo, G., Liebendörfer, M., Thielemann, F. K., Bravo, E., Hix, W. R., Langanke, K., & Zinner, N. T. (2006). Neutrino-induced nucleosynthesis of A>64 nuclei: the nu p process. Physical review letters, 96(14), 142502. https://doi.org/10.1103/PhysRevLett.96.142502
Fröhlich, C, et al. "Neutrino-induced nucleosynthesis of A>64 nuclei: the nu p process." Physical review letters vol. 96,14 (2006): 142502. doi: https://doi.org/10.1103/PhysRevLett.96.142502
Fröhlich C, Martínez-Pinedo G, Liebendörfer M, Thielemann FK, Bravo E, Hix WR, Langanke K, Zinner NT. Neutrino-induced nucleosynthesis of A>64 nuclei: the nu p process. Phys Rev Lett. 2006 Apr 14;96(14):142502. doi: 10.1103/PhysRevLett.96.142502. Epub 2006 Apr 10. PMID: 16712066.
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Double-resonance polarization spectroscopy using modulation sidebands.

Optics letters

Mlynek J, Drake KH, Kersten G, Frölich D, Lange W.
PMID: 19701336
Opt Lett. 1981 Feb 01;6(2):87-9. doi: 10.1364/ol.6.000087.

A novel technique for ultrahigh-resolution laser spectroscopy is described. Coherence between atomic substates created by an amplitude-modulated light beam is monitored in transmission of a weak probe beam by polarizationselective optical heterodyne detection. As a demonstration, the technique is...

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Mlynek J, Drake KH, Kersten G, et al. Double-resonance polarization spectroscopy using modulation sidebands. Opt Lett. 1981;6(2):87-9doi: 10.1364/ol.6.000087.
Mlynek, J., Drake, K. H., Kersten, G., Frölich, D., & Lange, W. (1981). Double-resonance polarization spectroscopy using modulation sidebands. Optics letters, 6(2), 87-9. https://doi.org/10.1364/ol.6.000087
Mlynek, J, et al. "Double-resonance polarization spectroscopy using modulation sidebands." Optics letters vol. 6,2 (1981): 87-9. doi: https://doi.org/10.1364/ol.6.000087
Mlynek J, Drake KH, Kersten G, Frölich D, Lange W. Double-resonance polarization spectroscopy using modulation sidebands. Opt Lett. 1981 Feb 01;6(2):87-9. doi: 10.1364/ol.6.000087. PMID: 19701336.
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Characterization of pyrgeometers and the accuracy of atmospheric long-wave radiation measurements.

Applied optics

Philipona R, Fröhlich C, Betz C.
PMID: 21037701
Appl Opt. 1995 Mar 20;34(9):1598-605. doi: 10.1364/AO.34.001598.

A detailed characterization is performed to calibrate pyrgeometers, using a newly developed apparatus that contains a blackbody radiation source and the means to vary the temperatures of the pyrgeometer under testing. Calibration measurements cover the parameter space of radiation...

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Philipona R, Fröhlich C, Betz C. Characterization of pyrgeometers and the accuracy of atmospheric long-wave radiation measurements. Appl Opt. 1995;34(9):1598-605doi: 10.1364/AO.34.001598.
Philipona, R., Fröhlich, C., & Betz, C. (1995). Characterization of pyrgeometers and the accuracy of atmospheric long-wave radiation measurements. Applied optics, 34(9), 1598-605. https://doi.org/10.1364/AO.34.001598
Philipona, R, et al. "Characterization of pyrgeometers and the accuracy of atmospheric long-wave radiation measurements." Applied optics vol. 34,9 (1995): 1598-605. doi: https://doi.org/10.1364/AO.34.001598
Philipona R, Fröhlich C, Betz C. Characterization of pyrgeometers and the accuracy of atmospheric long-wave radiation measurements. Appl Opt. 1995 Mar 20;34(9):1598-605. doi: 10.1364/AO.34.001598. PMID: 21037701.
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New determination of Rayleigh scattering in the terrestrial atmosphere.

Applied optics

Fröhlich C, Shaw GE.
PMID: 20221123
Appl Opt. 1980 Jun 01;19(11):1773-5. doi: 10.1364/AO.19.001773.

New Rayleigh-scattering optical thickness values for the terrestrial atmosphere in the 260 < lambda < 1500-nm wavelength range have been calculated using updated data on atmospheric optical parameters. The calculations include molecular scattering from water vapor and take into...

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Fröhlich C, Shaw GE. New determination of Rayleigh scattering in the terrestrial atmosphere. Appl Opt. 1980;19(11):1773-5doi: 10.1364/AO.19.001773.
Fröhlich, C., & Shaw, G. E. (1980). New determination of Rayleigh scattering in the terrestrial atmosphere. Applied optics, 19(11), 1773-5. https://doi.org/10.1364/AO.19.001773
Fröhlich, C, and Shaw, G E. "New determination of Rayleigh scattering in the terrestrial atmosphere." Applied optics vol. 19,11 (1980): 1773-5. doi: https://doi.org/10.1364/AO.19.001773
Fröhlich C, Shaw GE. New determination of Rayleigh scattering in the terrestrial atmosphere. Appl Opt. 1980 Jun 01;19(11):1773-5. doi: 10.1364/AO.19.001773. PMID: 20221123.
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Cerebral blood flow during propofol induced sedation.

Molecular imaging and biology

Byas-Smith M, Frölich MA, Votaw JR, Faber TL, Hoffman JM.
PMID: 14537136
Mol Imaging Biol. 2002 Mar;4(2):139-46. doi: 10.1016/s1536-1632(01)00006-3.

PURPOSE: This work determined if 2, 6-diisopropylphenol (propofol) selectively affects cerebral blood flow in regions associated with wakefulness.PROCEDURES: Cerebral blood flow (CBF) was measured with positron emission tomography (PET) using the 15O-water bolus technique in 10 subjects while awake...

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Byas-Smith M, Frölich MA, Votaw JR, et al. Cerebral blood flow during propofol induced sedation. Mol Imaging Biol. 2002;4(2):139-46doi: 10.1016/s1536-1632(01)00006-3.
Byas-Smith, M., Frölich, M. A., Votaw, J. R., Faber, T. L., & Hoffman, J. M. (2002). Cerebral blood flow during propofol induced sedation. Molecular imaging and biology, 4(2), 139-46. https://doi.org/10.1016/s1536-1632(01)00006-3
Byas-Smith, Michael, et al. "Cerebral blood flow during propofol induced sedation." Molecular imaging and biology vol. 4,2 (2002): 139-46. doi: https://doi.org/10.1016/s1536-1632(01)00006-3
Byas-Smith M, Frölich MA, Votaw JR, Faber TL, Hoffman JM. Cerebral blood flow during propofol induced sedation. Mol Imaging Biol. 2002 Mar;4(2):139-46. doi: 10.1016/s1536-1632(01)00006-3. PMID: 14537136.
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4-[(Z)-2-(methylsulfanyl)ethenyl]-1-phenyl-1H-1,2,3-triazole: an order-disorder (OD) interpretation of twinning.

Acta crystallographica. Section C, Crystal structure communications

Stöger B, Lumpi D, Fröhlich J.
PMID: 22051964
Acta Crystallogr C. 2011 Nov;67:o464-8. doi: 10.1107/S0108270111043083. Epub 2011 Oct 31.

The title compound, C(11)H(11)SN(3), crystallizes as twins with a twin volume fraction of 0.4232 (13). An order-disorder (OD) interpretation gives a plausible explanation of the crystallization behaviour. The structure is a polytype with a maximum degree of order (MDO)....

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Stöger B, Lumpi D, Fröhlich J. 4-[(Z)-2-(methylsulfanyl)ethenyl]-1-phenyl-1H-1,2,3-triazole: an order-disorder (OD) interpretation of twinning. Acta Crystallogr C. 2011;67:o464-8doi: 10.1107/S0108270111043083.
Stöger, B., Lumpi, D., & Fröhlich, J. (2011). 4-[(Z)-2-(methylsulfanyl)ethenyl]-1-phenyl-1H-1,2,3-triazole: an order-disorder (OD) interpretation of twinning. Acta crystallographica. Section C, Crystal structure communications, 67o464-8. https://doi.org/10.1107/S0108270111043083
Stöger, Berthold, et al. "4-[(Z)-2-(methylsulfanyl)ethenyl]-1-phenyl-1H-1,2,3-triazole: an order-disorder (OD) interpretation of twinning." Acta crystallographica. Section C, Crystal structure communications vol. 67 (2011): o464-8. doi: https://doi.org/10.1107/S0108270111043083
Stöger B, Lumpi D, Fröhlich J. 4-[(Z)-2-(methylsulfanyl)ethenyl]-1-phenyl-1H-1,2,3-triazole: an order-disorder (OD) interpretation of twinning. Acta Crystallogr C. 2011 Nov;67:o464-8. doi: 10.1107/S0108270111043083. Epub 2011 Oct 31. PMID: 22051964.
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Fibre optic ATR-IR spectroscopy at cryogenic temperatures: in-line reaction monitoring on organolithium compounds.

Chemical communications (Cambridge, England)

Lumpi D, Wagner C, Schöpf M, Horkel E, Ramer G, Lendl B, Fröhlich J.
PMID: 22274536
Chem Commun (Camb). 2012 Feb 28;48(18):2451-3. doi: 10.1039/c2cc16016a. Epub 2012 Jan 25.

A reliable methodology, utilising an ATR-IR fibre probe, for in-line monitoring of low temperature reactions is presented. The application of this convenient set-up enables a fast and safe exploration of highly reactive substrates. Hence, in situ monitoring of lithiation...

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Lumpi D, Wagner C, Schöpf M, et al. Fibre optic ATR-IR spectroscopy at cryogenic temperatures: in-line reaction monitoring on organolithium compounds. Chem Commun (Camb). 2012;48(18):2451-3doi: 10.1039/c2cc16016a.
Lumpi, D., Wagner, C., Schöpf, M., Horkel, E., Ramer, G., Lendl, B., & Fröhlich, J. (2012). Fibre optic ATR-IR spectroscopy at cryogenic temperatures: in-line reaction monitoring on organolithium compounds. Chemical communications (Cambridge, England), 48(18), 2451-3. https://doi.org/10.1039/c2cc16016a
Lumpi, Daniel, et al. "Fibre optic ATR-IR spectroscopy at cryogenic temperatures: in-line reaction monitoring on organolithium compounds." Chemical communications (Cambridge, England) vol. 48,18 (2012): 2451-3. doi: https://doi.org/10.1039/c2cc16016a
Lumpi D, Wagner C, Schöpf M, Horkel E, Ramer G, Lendl B, Fröhlich J. Fibre optic ATR-IR spectroscopy at cryogenic temperatures: in-line reaction monitoring on organolithium compounds. Chem Commun (Camb). 2012 Feb 28;48(18):2451-3. doi: 10.1039/c2cc16016a. Epub 2012 Jan 25. PMID: 22274536.
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Showing 1 to 12 of 140 entries