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Olfactory bulb encoding during learning under anesthesia.

Frontiers in behavioral neuroscience

Nicol AU, Sanchez-Andrade G, Collado P, Segonds-Pichon A, Kendrick KM.
PMID: 24926241
Front Behav Neurosci. 2014 Jun 05;8:193. doi: 10.3389/fnbeh.2014.00193. eCollection 2014.

Neural plasticity changes within the olfactory bulb are important for olfactory learning, although how neural encoding changes support new associations with specific odors and whether they can be investigated under anesthesia, remain unclear. Using the social transmission of food...

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Nicol AU, Sanchez-Andrade G, Collado P, et al. Olfactory bulb encoding during learning under anesthesia. Front Behav Neurosci. 2014;8:193doi: 10.3389/fnbeh.2014.00193.
Nicol, A. U., Sanchez-Andrade, G., Collado, P., Segonds-Pichon, A., & Kendrick, K. M. (2014). Olfactory bulb encoding during learning under anesthesia. Frontiers in behavioral neuroscience, 8193. https://doi.org/10.3389/fnbeh.2014.00193
Nicol, Alister U, et al. "Olfactory bulb encoding during learning under anesthesia." Frontiers in behavioral neuroscience vol. 8 (2014): 193. doi: https://doi.org/10.3389/fnbeh.2014.00193
Nicol AU, Sanchez-Andrade G, Collado P, Segonds-Pichon A, Kendrick KM. Olfactory bulb encoding during learning under anesthesia. Front Behav Neurosci. 2014 Jun 05;8:193. doi: 10.3389/fnbeh.2014.00193. eCollection 2014. PMID: 24926241; PMCID: PMC4046573.
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Electron spin relaxation of C60 monoanion in liquid solution: applicability of Kivelson-Orbach mechanism.

The journal of physical chemistry. A

Kundu K, Kattnig DR, Mladenova B, Grampp G, Das R.
PMID: 25789609
J Phys Chem A. 2015 Apr 02;119(13):3200-8. doi: 10.1021/jp5126409. Epub 2015 Mar 19.

We report the results of our investigation on the electron spin relaxation mechanism of the monoanion of C60 fullerene in liquid solution. The solvent chosen was carbon disulfide, which is rather uncommon in EPR spectroscopy but proved very useful...

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Kundu K, Kattnig DR, Mladenova B, et al. Electron spin relaxation of C60 monoanion in liquid solution: applicability of Kivelson-Orbach mechanism. J Phys Chem A. 2015;119(13):3200-8doi: 10.1021/jp5126409.
Kundu, K., Kattnig, D. R., Mladenova, B., Grampp, G., & Das, R. (2015). Electron spin relaxation of C60 monoanion in liquid solution: applicability of Kivelson-Orbach mechanism. The journal of physical chemistry. A, 119(13), 3200-8. https://doi.org/10.1021/jp5126409
Kundu, Krishnendu, et al. "Electron spin relaxation of C60 monoanion in liquid solution: applicability of Kivelson-Orbach mechanism." The journal of physical chemistry. A vol. 119,13 (2015): 3200-8. doi: https://doi.org/10.1021/jp5126409
Kundu K, Kattnig DR, Mladenova B, Grampp G, Das R. Electron spin relaxation of C60 monoanion in liquid solution: applicability of Kivelson-Orbach mechanism. J Phys Chem A. 2015 Apr 02;119(13):3200-8. doi: 10.1021/jp5126409. Epub 2015 Mar 19. PMID: 25789609.
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Selected topics related to occupational exposures. Part V. Occupational cardiovascular disease.

Disease-a-month : DM

Leikin JB, Davis A, Klodd DA, Thunder T, Kelafant GA, Paquette DL, Rothe MJ, Rubin R.
PMID: 10830614
Dis Mon. 2000 Apr;46(4):311-22. doi: 10.1016/s0011-5029(00)90037-3.

Cardiovascular disease is common in the United States. Several occupational exposures, such as carbon disulfide and organic nitrates, are believed to cause occupational cardiovascular disease. In addition some other agents, such as lead and cadmium, may indirectly cause cardiovascular...

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Leikin JB, Davis A, Klodd DA, et al. Selected topics related to occupational exposures. Part V. Occupational cardiovascular disease. Dis Mon. 2000;46(4):311-22doi: 10.1016/s0011-5029(00)90037-3.
Leikin, J. B., Davis, A., Klodd, D. A., Thunder, T., Kelafant, G. A., Paquette, D. L., Rothe, M. J., & Rubin, R. (2000). Selected topics related to occupational exposures. Part V. Occupational cardiovascular disease. Disease-a-month : DM, 46(4), 311-22. https://doi.org/10.1016/s0011-5029(00)90037-3
Leikin, et al. "Selected topics related to occupational exposures. Part V. Occupational cardiovascular disease." Disease-a-month : DM vol. 46,4 (2000): 311-22. doi: https://doi.org/10.1016/s0011-5029(00)90037-3
Leikin JB, Davis A, Klodd DA, Thunder T, Kelafant GA, Paquette DL, Rothe MJ, Rubin R. Selected topics related to occupational exposures. Part V. Occupational cardiovascular disease. Dis Mon. 2000 Apr;46(4):311-22. doi: 10.1016/s0011-5029(00)90037-3. PMID: 10830614.
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Viscosity dependence of optical limiting in carbon black suspensions.

Applied optics

Hernández FE, Shensky W, Cohanoschi I, Hagan DJ, Van S.
PMID: 11900132
Appl Opt. 2002 Feb 20;41(6):1103-7. doi: 10.1364/ao.41.001103.

We measure the optical limiting behavior of carbon black suspensions in various viscosity solvents by using a 10-Hz repetition rate, 532-nm, 5-ns pulsed laser. We found that, for common solvents used in the past such as water and ethanol,...

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Hernández FE, Shensky W, Cohanoschi I, et al. Viscosity dependence of optical limiting in carbon black suspensions. Appl Opt. 2002;41(6):1103-7doi: 10.1364/ao.41.001103.
Hernández, F. E., Shensky, W., Cohanoschi, I., Hagan, D. J., & Van, S. (2002). Viscosity dependence of optical limiting in carbon black suspensions. Applied optics, 41(6), 1103-7. https://doi.org/10.1364/ao.41.001103
Hernández, Florencio E, et al. "Viscosity dependence of optical limiting in carbon black suspensions." Applied optics vol. 41,6 (2002): 1103-7. doi: https://doi.org/10.1364/ao.41.001103
Hernández FE, Shensky W, Cohanoschi I, Hagan DJ, Van S. Viscosity dependence of optical limiting in carbon black suspensions. Appl Opt. 2002 Feb 20;41(6):1103-7. doi: 10.1364/ao.41.001103. PMID: 11900132.
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Formation of novel sulfur-containing C60F16 cycloadducts between tetrathiafulvalene and C60F18; a unique six-electron cycloaddition of a fullerene involving F2 loss.

Chemistry (Weinheim an der Bergstrasse, Germany)

Darwish AD, Avent AG, Boltalina OV, Gol'dt I, Kuvytchko I, Da Ros T, Street JM, Taylor R.
PMID: 12740847
Chemistry. 2003 May 09;9(9):2008-12. doi: 10.1002/chem.200204549.

Co-evaporation of solutions of C(60)F(18) and tetrathiafulvalene in toluene produces an unsymmetrical C(60)F(16):tetrathiafulvalene adduct through a unique six-electron cycloaddition involving displacement of two fluorine atoms by a terminal Cdbond;C double bond of the fulvalene. The adduct rearranges into two...

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Darwish AD, Avent AG, Boltalina OV, et al. Formation of novel sulfur-containing C60F16 cycloadducts between tetrathiafulvalene and C60F18; a unique six-electron cycloaddition of a fullerene involving F2 loss. Chemistry. 2003;9(9):2008-12doi: 10.1002/chem.200204549.
Darwish, A. D., Avent, A. G., Boltalina, O. V., Gol'dt, I., Kuvytchko, I., Da Ros, T., Street, J. M., & Taylor, R. (2003). Formation of novel sulfur-containing C60F16 cycloadducts between tetrathiafulvalene and C60F18; a unique six-electron cycloaddition of a fullerene involving F2 loss. Chemistry (Weinheim an der Bergstrasse, Germany), 9(9), 2008-12. https://doi.org/10.1002/chem.200204549
Darwish, Adam D, et al. "Formation of novel sulfur-containing C60F16 cycloadducts between tetrathiafulvalene and C60F18; a unique six-electron cycloaddition of a fullerene involving F2 loss." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 9,9 (2003): 2008-12. doi: https://doi.org/10.1002/chem.200204549
Darwish AD, Avent AG, Boltalina OV, Gol'dt I, Kuvytchko I, Da Ros T, Street JM, Taylor R. Formation of novel sulfur-containing C60F16 cycloadducts between tetrathiafulvalene and C60F18; a unique six-electron cycloaddition of a fullerene involving F2 loss. Chemistry. 2003 May 09;9(9):2008-12. doi: 10.1002/chem.200204549. PMID: 12740847.
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Detection limits for time-resolved coherent two-dimensional vibrational spectroscopy.

Analytical chemistry

Meyer KA, Wright JC.
PMID: 11721894
Anal Chem. 2001 Nov 01;73(21):5020-5. doi: 10.1021/ac0107195.

Coherent two-dimensional vibrational spectroscopy is performed using doubly vibrationally enhanced four-wave mixing in dilute solutions of carbon disulfide using an ultrafast (< or = 1 ps) laser pulse system. The nonresonant electronic background and singly resonant coherent anti-Stokes Raman...

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Meyer KA, Wright JC. Detection limits for time-resolved coherent two-dimensional vibrational spectroscopy. Anal Chem. 2001;73(21):5020-5doi: 10.1021/ac0107195.
Meyer, K. A., & Wright, J. C. (2001). Detection limits for time-resolved coherent two-dimensional vibrational spectroscopy. Analytical chemistry, 73(21), 5020-5. https://doi.org/10.1021/ac0107195
Meyer, K A, and Wright, J C. "Detection limits for time-resolved coherent two-dimensional vibrational spectroscopy." Analytical chemistry vol. 73,21 (2001): 5020-5. doi: https://doi.org/10.1021/ac0107195
Meyer KA, Wright JC. Detection limits for time-resolved coherent two-dimensional vibrational spectroscopy. Anal Chem. 2001 Nov 01;73(21):5020-5. doi: 10.1021/ac0107195. PMID: 11721894.
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Terminal titanium-ligand multiple bonds. Cleavages of C=O and C=S double bonds with Ti imido complexes.

Inorganic chemistry

Hsu SH, Chang JC, Lai CL, Hu CH, Lee HM, Lee GH, Peng SM, Huang JH.
PMID: 15476379
Inorg Chem. 2004 Oct 18;43(21):6786-92. doi: 10.1021/ic049474f.

Treatment of (t-)BuN=TiCl(2)Py(3) with 2 equiv lithium ketiminate compound, Li[OCMeCHCMeN(Ar)] (where Ar = 2,6-diisopropylphenyl), in toluene at room temperature gave (t-)BuN=Ti[OCMeCHCMeN(Ar)](2) (1) in high yield. The reaction of 1 with phenyl isocyanate at room-temperature resulted in imido ligand exchange...

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Hsu SH, Chang JC, Lai CL, et al. Terminal titanium-ligand multiple bonds. Cleavages of C=O and C=S double bonds with Ti imido complexes. Inorg Chem. 2004;43(21):6786-92doi: 10.1021/ic049474f.
Hsu, S. H., Chang, J. C., Lai, C. L., Hu, C. H., Lee, H. M., Lee, G. H., Peng, S. M., & Huang, J. H. (2004). Terminal titanium-ligand multiple bonds. Cleavages of C=O and C=S double bonds with Ti imido complexes. Inorganic chemistry, 43(21), 6786-92. https://doi.org/10.1021/ic049474f
Hsu, Shih-Hsien, et al. "Terminal titanium-ligand multiple bonds. Cleavages of C=O and C=S double bonds with Ti imido complexes." Inorganic chemistry vol. 43,21 (2004): 6786-92. doi: https://doi.org/10.1021/ic049474f
Hsu SH, Chang JC, Lai CL, Hu CH, Lee HM, Lee GH, Peng SM, Huang JH. Terminal titanium-ligand multiple bonds. Cleavages of C=O and C=S double bonds with Ti imido complexes. Inorg Chem. 2004 Oct 18;43(21):6786-92. doi: 10.1021/ic049474f. PMID: 15476379.
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Calculation of crystal and molecular structures of carbon disulfide CS2.

The Journal of chemical physics

Thiéry MM, Rérat C.
PMID: 15740263
J Chem Phys. 2005 Jan 22;122(4):44503. doi: 10.1063/1.1834896.

Crystal and molecular structures of carbon disulfide CS(2) were investigated by molecular packing analysis with a computed dynamical model. This model includes thermal motions, molecular deformations, and anisotropic atomic repulsive interactions. Several crystalline structures with orthorhombic symmetry Cmca have...

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Thiéry MM, Rérat C. Calculation of crystal and molecular structures of carbon disulfide CS2. J Chem Phys. 2005;122(4):44503doi: 10.1063/1.1834896.
Thiéry, M. M., & Rérat, C. (2005). Calculation of crystal and molecular structures of carbon disulfide CS2. The Journal of chemical physics, 122(4), 44503. https://doi.org/10.1063/1.1834896
Thiéry, M-M, and Rérat, C. "Calculation of crystal and molecular structures of carbon disulfide CS2." The Journal of chemical physics vol. 122,4 (2005): 44503. doi: https://doi.org/10.1063/1.1834896
Thiéry MM, Rérat C. Calculation of crystal and molecular structures of carbon disulfide CS2. J Chem Phys. 2005 Jan 22;122(4):44503. doi: 10.1063/1.1834896. PMID: 15740263.
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Time-resolved optical Kerr-effect investigation on CS2/polystyrene mixtures.

The Journal of chemical physics

Heisler IA, Correia RR, Buckup T, Cunha SL, da Silveira NP.
PMID: 16108671
J Chem Phys. 2005 Aug 01;123(5):054509. doi: 10.1063/1.1994850.

The relaxation dynamics of carbon disulfide are investigated in mixtures with polystyrene (PS) using the time-resolved optical heterodyne-detected optical Kerr effect (OHD-OKE). The data are analyzed using both the model-dependent approach, which assumes four distinct temporal responses, and the...

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Heisler IA, Correia RR, Buckup T, et al. Time-resolved optical Kerr-effect investigation on CS2/polystyrene mixtures. J Chem Phys. 2005;123(5):054509doi: 10.1063/1.1994850.
Heisler, I. A., Correia, R. R., Buckup, T., Cunha, S. L., & da Silveira, N. P. (2005). Time-resolved optical Kerr-effect investigation on CS2/polystyrene mixtures. The Journal of chemical physics, 123(5), 054509. https://doi.org/10.1063/1.1994850
Heisler, Ismael A, et al. "Time-resolved optical Kerr-effect investigation on CS2/polystyrene mixtures." The Journal of chemical physics vol. 123,5 (2005): 054509. doi: https://doi.org/10.1063/1.1994850
Heisler IA, Correia RR, Buckup T, Cunha SL, da Silveira NP. Time-resolved optical Kerr-effect investigation on CS2/polystyrene mixtures. J Chem Phys. 2005 Aug 01;123(5):054509. doi: 10.1063/1.1994850. PMID: 16108671.
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Shape-controlled synthesis and self-assembly of hexagonal covellite (CuS) nanoplatelets.

Chemistry (Weinheim an der Bergstrasse, Germany)

Du W, Qian X, Ma X, Gong Q, Cao H, Yin J.
PMID: 17200918
Chemistry. 2007;13(11):3241-7. doi: 10.1002/chem.200601368.

Single-crystalline, hexagonal covellite (CuS) nanoplatelets were successfully synthesized through a facile, inexpensive, reproducible, and improved solvothermal process in toluene at 120 degrees C for 24 h with hexadecylamine as a capping agent and copper acetate and carbon disulfide as...

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Du W, Qian X, Ma X, et al. Shape-controlled synthesis and self-assembly of hexagonal covellite (CuS) nanoplatelets. Chemistry. 2007;13(11):3241-7doi: 10.1002/chem.200601368.
Du, W., Qian, X., Ma, X., Gong, Q., Cao, H., & Yin, J. (2007). Shape-controlled synthesis and self-assembly of hexagonal covellite (CuS) nanoplatelets. Chemistry (Weinheim an der Bergstrasse, Germany), 13(11), 3241-7. https://doi.org/10.1002/chem.200601368
Du, Weimin, et al. "Shape-controlled synthesis and self-assembly of hexagonal covellite (CuS) nanoplatelets." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 13,11 (2007): 3241-7. doi: https://doi.org/10.1002/chem.200601368
Du W, Qian X, Ma X, Gong Q, Cao H, Yin J. Shape-controlled synthesis and self-assembly of hexagonal covellite (CuS) nanoplatelets. Chemistry. 2007;13(11):3241-7. doi: 10.1002/chem.200601368. PMID: 17200918.
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Gaseous constituents in the plume from eruptions of mount st. Helens.

Science (New York, N.Y.)

Inn EC, Vedder JF, Condon EP, O'hara D.
PMID: 17740390
Science. 1981 Feb 20;211(4484):821-3. doi: 10.1126/science.211.4484.821.

Measurements in the stratosphere of gaseous constituents in the plume of Mount St. Helens were obtained during five flights of the NASA U-2 aircraft between 19 May and 17 June 1980. Mixing ratios from gas chromatographic measurements on samples...

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Inn EC, Vedder JF, Condon EP, et al. Gaseous constituents in the plume from eruptions of mount st. Helens. Science. 1981;211(4484):821-3doi: 10.1126/science.211.4484.821.
Inn, E. C., Vedder, J. F., Condon, E. P., & O'hara, D. (1981). Gaseous constituents in the plume from eruptions of mount st. Helens. Science (New York, N.Y.), 211(4484), 821-3. https://doi.org/10.1126/science.211.4484.821
Inn, E C, et al. "Gaseous constituents in the plume from eruptions of mount st. Helens." Science (New York, N.Y.) vol. 211,4484 (1981): 821-3. doi: https://doi.org/10.1126/science.211.4484.821
Inn EC, Vedder JF, Condon EP, O'hara D. Gaseous constituents in the plume from eruptions of mount st. Helens. Science. 1981 Feb 20;211(4484):821-3. doi: 10.1126/science.211.4484.821. PMID: 17740390.
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An efficient one-pot, three-component synthesis of 5-hydrazinoalkylidene rhodanines from 1,2-diaza-1,3-dienes.

Organic letters

Attanasi OA, Crescentini LD, Favi G, Filippone P, Giorgi G, Mantellini F, Moscatelli G, Behalo MS.
PMID: 19397335
Org Lett. 2009 Jun 04;11(11):2265-8. doi: 10.1021/ol900545v.

A novel three-component synthesis of 5-hydrazinoalkylidene rhodanine derivatives starting from aliphatic primary amines, carbon disulfide, and 1,2-diaza-1,3-dienes is described. The reaction proceeds successfully under both solution and solid-phase conditions.

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Attanasi OA, Crescentini LD, Favi G, et al. An efficient one-pot, three-component synthesis of 5-hydrazinoalkylidene rhodanines from 1,2-diaza-1,3-dienes. Org Lett. 2009;11(11):2265-8doi: 10.1021/ol900545v.
Attanasi, O. A., Crescentini, L. D., Favi, G., Filippone, P., Giorgi, G., Mantellini, F., Moscatelli, G., & Behalo, M. S. (2009). An efficient one-pot, three-component synthesis of 5-hydrazinoalkylidene rhodanines from 1,2-diaza-1,3-dienes. Organic letters, 11(11), 2265-8. https://doi.org/10.1021/ol900545v
Attanasi, Orazio A, et al. "An efficient one-pot, three-component synthesis of 5-hydrazinoalkylidene rhodanines from 1,2-diaza-1,3-dienes." Organic letters vol. 11,11 (2009): 2265-8. doi: https://doi.org/10.1021/ol900545v
Attanasi OA, Crescentini LD, Favi G, Filippone P, Giorgi G, Mantellini F, Moscatelli G, Behalo MS. An efficient one-pot, three-component synthesis of 5-hydrazinoalkylidene rhodanines from 1,2-diaza-1,3-dienes. Org Lett. 2009 Jun 04;11(11):2265-8. doi: 10.1021/ol900545v. PMID: 19397335.
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Showing 13 to 24 of 343 entries