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The use of imagery by soccer players

interventions

Hall C.
GSID: mtlyejrQGJ4J
J Salmon, C Hall, I Haslam - Journal of Applied Sport Psychology, 1994 - Taylor & Francis

The purpose of this study was to investigate the motivational and cognitive use of imagery by soccer players of various skill levels. The instrument developed and employed in this study …

Implementing iPads in the inclusive classroom setting

classroom instruction

Hall C, Maich K.
GSID: JRSouHX9uDcJ
K Maich, C Hall - Intervention in School and Clinic, 2016 - journals.sagepub.com

This column provides practical suggestions to help guide teachers in utilizing classroom sets of iPads. Following a brief introduction to tablet technology in inclusive classrooms and the …

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Maich, K., & Hall, C. (2016). Implementing iPads in the inclusive classroom setting. Intervention in School and Clinic, 51(3), 145-150.
Maich, Kimberly, and Carmen Hall. "Implementing iPads in the inclusive classroom setting." Intervention in School and Clinic 51.3 (2016): 145-150.
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Targeting obesity through health promotion programs for school staff

Non-school settings

Hall C, Lohrmann DK.
GSID: 1ayMFJm0UnIJ
PC Herbert, DK Lohrmann, C Hall - Strategies, 2017 - Taylor & Francis

Health promotion programs for school staff are an overlooked and under-utilized resource that can lead to reductions in overweight and obesity among teachers and other staff …

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Herbert, P. C., Lohrmann, D. K., & Hall, C. (2017). Targeting obesity through health promotion programs for school staff. Strategies, 30(1), 28-34.
Herbert, Patrick C., David K. Lohrmann, and Cougar Hall. "Targeting obesity through health promotion programs for school staff." Strategies 30.1 (2017): 28-34.
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Science-policy interface: beyond assessments

diversity

Beck S, Görg C, Hulme M, Mahony M.
GSID: YVnVI2RdB2YJ
M Hulme, M Mahony, S Beck, C Görg, B Hansjürgens… - Science, 2011 - science.org

SERIOUS CONFUSION SURROUNDS THE ACCIDENT AT FUKUSHIMA DAIICHI NUCLEAR POWER Plant with regard to the amount of permissible radiation exposure …

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Hulme, M., Mahony, M., Beck, S., Görg, C., Hansjürgens, B., Hauck, J., ... & Van der Sluijs, J. P. (2011). Science-policy interface: beyond assessments. Science, 333(6043), 697-698.
Hulme, Mike, et al. "Science-policy interface: beyond assessments." Science 333.6043 (2011): 697-698.
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Laboratory instruction in undergraduate astronautics

laboratory instruction

Hall C.
GSID: i6UhumFjlAMJ
C Hall - 1999 Annual Conference, 1999 - peer.asee.org

… In the remainder of the paper we describe some field and laboratory work that can be used to enhance this standard approach. … With the Satellite Tracking Laboratory, the satellite visibility prediction assignment becomes more meaningful and leads...

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Hall, C. (1999, June). Laboratory instruction in undergraduate astronautics. In 1999 Annual Conference (pp. 4-355).
Hall, Christopher. "Laboratory instruction in undergraduate astronautics." 1999 Annual Conference. 1999.
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Perylene bisimide hydrogels and lyotropic liquid crystals with temperature-responsive color change.

Chemical science

Görl D, Soberats B, Herbst S, Stepanenko V, Würthner F.
PMID: 28451124
Chem Sci. 2016 Nov 01;7(11):6786-6790. doi: 10.1039/c6sc02249a. Epub 2016 Jul 22.

The self-assembly of perylene bisimide (PBI) dyes bearing oligo ethylene glycol (OEG) units in water affords responsive functional nanostructures characterized by their lower critical solution temperature (LCST). Tuning of the LCST is realized by a supramolecular approach that relies...

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Görl D, Soberats B, Herbst S, et al. Perylene bisimide hydrogels and lyotropic liquid crystals with temperature-responsive color change. Chem Sci. 2016;7(11):6786-6790doi: 10.1039/c6sc02249a.
Görl, D., Soberats, B., Herbst, S., Stepanenko, V., & Würthner, F. (2016). Perylene bisimide hydrogels and lyotropic liquid crystals with temperature-responsive color change. Chemical science, 7(11), 6786-6790. https://doi.org/10.1039/c6sc02249a
Görl, Daniel, et al. "Perylene bisimide hydrogels and lyotropic liquid crystals with temperature-responsive color change." Chemical science vol. 7,11 (2016): 6786-6790. doi: https://doi.org/10.1039/c6sc02249a
Görl D, Soberats B, Herbst S, Stepanenko V, Würthner F. Perylene bisimide hydrogels and lyotropic liquid crystals with temperature-responsive color change. Chem Sci. 2016 Nov 01;7(11):6786-6790. doi: 10.1039/c6sc02249a. Epub 2016 Jul 22. PMID: 28451124; PMCID: PMC5356028.
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Synthesis of Functionalized 1,4-Azaborinines by the Cyclization of Di-tert-butyliminoborane and Alkynes.

Journal of the American Chemical Society

Schäfer M, Beattie NA, Geetharani K, Schäfer J, Ewing WC, Krahfuß M, Hörl C, Dewhurst RD, Macgregor SA, Lambert C, Braunschweig H.
PMID: 27286231
J Am Chem Soc. 2016 Jul 06;138(26):8212-20. doi: 10.1021/jacs.6b04128. Epub 2016 Jun 27.

Di-tert-butyliminoborane is found to be a very useful synthon for the synthesis of a variety of functionalized 1,4-azaborinines by the Rh-mediated cyclization of iminoboranes with alkynes. The reactions proceed via [2 + 2] cycloaddition of iminoboranes and alkynes in...

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Schäfer M, Beattie NA, Geetharani K, et al. Synthesis of Functionalized 1,4-Azaborinines by the Cyclization of Di-tert-butyliminoborane and Alkynes. J Am Chem Soc. 2016;138(26):8212-20doi: 10.1021/jacs.6b04128.
Schäfer, M., Beattie, N. A., Geetharani, K., Schäfer, J., Ewing, W. C., Krahfuß, M., Hörl, C., Dewhurst, R. D., Macgregor, S. A., Lambert, C., & Braunschweig, H. (2016). Synthesis of Functionalized 1,4-Azaborinines by the Cyclization of Di-tert-butyliminoborane and Alkynes. Journal of the American Chemical Society, 138(26), 8212-20. https://doi.org/10.1021/jacs.6b04128
Schäfer, Marius, et al. "Synthesis of Functionalized 1,4-Azaborinines by the Cyclization of Di-tert-butyliminoborane and Alkynes." Journal of the American Chemical Society vol. 138,26 (2016): 8212-20. doi: https://doi.org/10.1021/jacs.6b04128
Schäfer M, Beattie NA, Geetharani K, Schäfer J, Ewing WC, Krahfuß M, Hörl C, Dewhurst RD, Macgregor SA, Lambert C, Braunschweig H. Synthesis of Functionalized 1,4-Azaborinines by the Cyclization of Di-tert-butyliminoborane and Alkynes. J Am Chem Soc. 2016 Jul 06;138(26):8212-20. doi: 10.1021/jacs.6b04128. Epub 2016 Jun 27. PMID: 27286231.
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Emergency General Surgery: evolution of a subspecialty by stealth.

World journal of emergency surgery : WJES

Pearce L, Smith SR, Parkin E, Hall C, Kennedy J, Macdonald A.
PMID: 26733342
World J Emerg Surg. 2016 Jan 04;11:2. doi: 10.1186/s13017-015-0058-x. eCollection 2016.

BACKGROUND: Emergency surgical patients account for around half of all NHS surgical workload and 80 % of surgical deaths. Few trainees opt to CCT in General Surgery, and there is no recognised subspecialty training program in Emergency General Surgery...

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Pearce L, Smith SR, Parkin E, et al. Emergency General Surgery: evolution of a subspecialty by stealth. World J Emerg Surg. 2016;11:2doi: 10.1186/s13017-015-0058-x.
Pearce, L., Smith, S. R., Parkin, E., Hall, C., Kennedy, J., & Macdonald, A. (2016). Emergency General Surgery: evolution of a subspecialty by stealth. World journal of emergency surgery : WJES, 112. https://doi.org/10.1186/s13017-015-0058-x
Pearce, L, et al. "Emergency General Surgery: evolution of a subspecialty by stealth." World journal of emergency surgery : WJES vol. 11 (2016): 2. doi: https://doi.org/10.1186/s13017-015-0058-x
Pearce L, Smith SR, Parkin E, Hall C, Kennedy J, Macdonald A. Emergency General Surgery: evolution of a subspecialty by stealth. World J Emerg Surg. 2016 Jan 04;11:2. doi: 10.1186/s13017-015-0058-x. eCollection 2016. PMID: 26733342; PMCID: PMC4700620.
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Impact of the individualization of the first-line chemotherapy for advanced colorectal cancer based on collagen gel droplet-embedded drug sensitivity test.

Oncology letters

Ochiai T, Nishimura K, Watanabe T, Kitajima M, Nakatani A, Nagayasu K, Naito S, Sato T, Kishine K, Abe Y, Hara C, Yamada S, Mashiko S, Nagaoka I.
PMID: 29113244
Oncol Lett. 2017 Nov;14(5):6045-6052. doi: 10.3892/ol.2017.6960. Epub 2017 Sep 15.

Leucovorin (FOL) and fluorouracil (5-FU) plus oxaliplatin (l-OHP; FOLFOX) or FOL and 5-FU plus irinotecan (SN-38; FOLFIRI) are widely used as first-line chemotherapy regimens in the treatment of advanced colorectal cancer (CRC). However, second-line chemotherapy must be abandoned in...

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Ochiai T, Nishimura K, Watanabe T, et al. Impact of the individualization of the first-line chemotherapy for advanced colorectal cancer based on collagen gel droplet-embedded drug sensitivity test. Oncol Lett. 2017;14(5):6045-6052doi: 10.3892/ol.2017.6960.
Ochiai, T., Nishimura, K., Watanabe, T., Kitajima, M., Nakatani, A., Nagayasu, K., Naito, S., Sato, T., Kishine, K., Abe, Y., Hara, C., Yamada, S., Mashiko, S., & Nagaoka, I. (2017). Impact of the individualization of the first-line chemotherapy for advanced colorectal cancer based on collagen gel droplet-embedded drug sensitivity test. Oncology letters, 14(5), 6045-6052. https://doi.org/10.3892/ol.2017.6960
Ochiai, Takumi, et al. "Impact of the individualization of the first-line chemotherapy for advanced colorectal cancer based on collagen gel droplet-embedded drug sensitivity test." Oncology letters vol. 14,5 (2017): 6045-6052. doi: https://doi.org/10.3892/ol.2017.6960
Ochiai T, Nishimura K, Watanabe T, Kitajima M, Nakatani A, Nagayasu K, Naito S, Sato T, Kishine K, Abe Y, Hara C, Yamada S, Mashiko S, Nagaoka I. Impact of the individualization of the first-line chemotherapy for advanced colorectal cancer based on collagen gel droplet-embedded drug sensitivity test. Oncol Lett. 2017 Nov;14(5):6045-6052. doi: 10.3892/ol.2017.6960. Epub 2017 Sep 15. PMID: 29113244; PMCID: PMC5661441.
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Correlated 3D Nanoscale Mapping and Simulation of Coupled Plasmonic Nanoparticles.

Nano letters

Haberfehlner G, Trügler A, Schmidt FP, Hörl A, Hofer F, Hohenester U, Kothleitner G.
PMID: 26495933
Nano Lett. 2015 Nov 11;15(11):7726-30. doi: 10.1021/acs.nanolett.5b03780. Epub 2015 Oct 28.

Electron tomography in combination with electron energy-loss spectroscopy (EELS) experiments and simulations was used to unravel the interplay between structure and plasmonic properties of a silver nanocuboid dimer. The precise 3D geometry of the particles fabricated by means of...

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Haberfehlner G, Trügler A, Schmidt FP, et al. Correlated 3D Nanoscale Mapping and Simulation of Coupled Plasmonic Nanoparticles. Nano Lett. 2015;15(11):7726-30doi: 10.1021/acs.nanolett.5b03780.
Haberfehlner, G., Trügler, A., Schmidt, F. P., Hörl, A., Hofer, F., Hohenester, U., & Kothleitner, G. (2015). Correlated 3D Nanoscale Mapping and Simulation of Coupled Plasmonic Nanoparticles. Nano letters, 15(11), 7726-30. https://doi.org/10.1021/acs.nanolett.5b03780
Haberfehlner, Georg, et al. "Correlated 3D Nanoscale Mapping and Simulation of Coupled Plasmonic Nanoparticles." Nano letters vol. 15,11 (2015): 7726-30. doi: https://doi.org/10.1021/acs.nanolett.5b03780
Haberfehlner G, Trügler A, Schmidt FP, Hörl A, Hofer F, Hohenester U, Kothleitner G. Correlated 3D Nanoscale Mapping and Simulation of Coupled Plasmonic Nanoparticles. Nano Lett. 2015 Nov 11;15(11):7726-30. doi: 10.1021/acs.nanolett.5b03780. Epub 2015 Oct 28. PMID: 26495933; PMCID: PMC4643356.
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A theoretical study of the aromaticity in neutral and anionic borole compounds.

Dalton transactions (Cambridge, England : 2003)

Jimenez-Halla JO, Matito E, Solà M, Braunschweig H, Hörl C, Krummenacher I, Wahler J.
PMID: 25494445
Dalton Trans. 2015 Apr 21;44(15):6740-7. doi: 10.1039/c4dt03445g.

In this contribution, we have evaluated the (anti)aromatic character of thirty-four different borole compounds in their neutral and reduced states based on two aromaticity indices, namely nucleus-independent chemical shift (NICS) and multicenter indices (MCI), calculated at the PBE0/6-31+G(d,p) level...

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Jimenez-Halla JO, Matito E, Solà M, et al. A theoretical study of the aromaticity in neutral and anionic borole compounds. Dalton Trans. 2015;44(15):6740-7doi: 10.1039/c4dt03445g.
Jimenez-Halla, J. O., Matito, E., Solà, M., Braunschweig, H., Hörl, C., Krummenacher, I., & Wahler, J. (2015). A theoretical study of the aromaticity in neutral and anionic borole compounds. Dalton transactions (Cambridge, England : 2003), 44(15), 6740-7. https://doi.org/10.1039/c4dt03445g
Jimenez-Halla, J Oscar C, et al. "A theoretical study of the aromaticity in neutral and anionic borole compounds." Dalton transactions (Cambridge, England : 2003) vol. 44,15 (2015): 6740-7. doi: https://doi.org/10.1039/c4dt03445g
Jimenez-Halla JO, Matito E, Solà M, Braunschweig H, Hörl C, Krummenacher I, Wahler J. A theoretical study of the aromaticity in neutral and anionic borole compounds. Dalton Trans. 2015 Apr 21;44(15):6740-7. doi: 10.1039/c4dt03445g. PMID: 25494445.
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Optoelectronic crystal of artificial atoms in strain-textured molybdenum disulphide.

Nature communications

Li H, Contryman AW, Qian X, Ardakani SM, Gong Y, Wang X, Weisse JM, Lee CH, Zhao J, Ajayan PM, Li J, Manoharan HC, Zheng X.
PMID: 26088550
Nat Commun. 2015 Jun 19;6:7381. doi: 10.1038/ncomms8381.

The isolation of the two-dimensional semiconductor molybdenum disulphide introduced a new optically active material possessing a band gap that can be facilely tuned via elastic strain. As an atomically thin membrane with exceptional strength, monolayer molybdenum disulphide subjected to...

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Li H, Contryman AW, Qian X, et al. Optoelectronic crystal of artificial atoms in strain-textured molybdenum disulphide. Nat Commun. 2015;6:7381doi: 10.1038/ncomms8381.
Li, H., Contryman, A. W., Qian, X., Ardakani, S. M., Gong, Y., Wang, X., Weisse, J. M., Lee, C. H., Zhao, J., Ajayan, P. M., Li, J., Manoharan, H. C., & Zheng, X. (2015). Optoelectronic crystal of artificial atoms in strain-textured molybdenum disulphide. Nature communications, 67381. https://doi.org/10.1038/ncomms8381
Li, Hong, et al. "Optoelectronic crystal of artificial atoms in strain-textured molybdenum disulphide." Nature communications vol. 6 (2015): 7381. doi: https://doi.org/10.1038/ncomms8381
Li H, Contryman AW, Qian X, Ardakani SM, Gong Y, Wang X, Weisse JM, Lee CH, Zhao J, Ajayan PM, Li J, Manoharan HC, Zheng X. Optoelectronic crystal of artificial atoms in strain-textured molybdenum disulphide. Nat Commun. 2015 Jun 19;6:7381. doi: 10.1038/ncomms8381. PMID: 26088550; PMCID: PMC4557352.
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Showing 1 to 12 of 712 entries