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Flipping to engage students: Instructor perspectives on flipping large enrolment courses

flipped classroom

Cherrez NJ, Hassall L, Karabulut-Ilgu A.
GSID: YRuKVrHBnisJ
A Karabulut-Ilgu, NJ Cherrez, L Hassall - Australasian Journal of …, 2018 - ajet.org.au

The purpose of this study was to investigate instructor perspectives on the implementation of flipped classrooms in large enrolment classrooms. Five instructors teaching in different …

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Karabulut-Ilgu, A., Cherrez, N. J., & Hassall, L. (2018). Flipping to engage students: Instructor perspectives on flipping large enrolment courses. Australasian Journal of Educational Technology, 34(4).
Karabulut-Ilgu, Aliye, Nadia Jaramillo Cherrez, and Lesya Hassall. "Flipping to engage students: Instructor perspectives on flipping large enrolment courses." Australasian Journal of Educational Technology 34.4 (2018).
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Action research: Explaining the diversity

diversity

Cassell C.
GSID: IhNksP-3LAQJ
C Cassell, P Johnson - Human relations, 2006 - journals.sagepub.com

… diversity is not haphazard and that we must be cautious about developing all-embracing standards to differentiate the ‘good’ from the ‘bad’. Rather this diversity is … The aim of this article is to explain the apparent diversity of...

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Cassell, C., & Johnson, P. (2006). Action research: Explaining the diversity. Human relations, 59(6), 783-814.
Cassell, Catherine, and Phil Johnson. "Action research: Explaining the diversity." Human relations 59.6 (2006): 783-814.
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Increasing diversity in emerging non-religious communities

Broadening Participation in Computing AND Program Evaluation

Bushfield I, Hassall C.
GSID: PJ7j3C0_qf8J
C Hassall, I Bushfield - Secularism and Nonreligion, 2014 - secularismandnonreligion.org

Contemporary growth in non-religious populations has given rise to novel communities with unique perspectives on social issues. We describe a study of diversity within speakers at conferences organised by and attended by the atheist community. We analyse trends in...

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Hassall, C., & Bushfield, I. (2014). Increasing diversity in emerging non-religious communities. Secularism and Nonreligion, 3.
Hassall, Christopher, and Ian Bushfield. "Increasing diversity in emerging non-religious communities." Secularism and Nonreligion 3 (2014).
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The development of computer applications by non‐employed people in community settings

community settings

Cassell C.
GSID: Qfb-xXII8PYJ
C Cassell, M Fitter, D Fryer… - Journal of Occupational …, 1988 - Wiley Online Library

… SPRITE users stated a particular commitment to opening up the facilities to wider community use, for example: I think it would be nice to open up a community information service so if anyone wants to know where the...

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Cassell, C., Fitter, M., Fryer, D., & Smith, L. (1988). The development of computer applications by non‐employed people in community settings. Journal of Occupational psychology, 61(1), 89-102.
Cassell, Catherine, et al. "The development of computer applications by non‐employed people in community settings." Journal of Occupational psychology 61.1 (1988): 89-102.
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Choosing MUSE: Validation of a Low-Cost, Portable EEG System for ERP Research.

Frontiers in neuroscience

Krigolson OE, Williams CC, Norton A, Hassall CD, Colino FL.
PMID: 28344546
Front Neurosci. 2017 Mar 10;11:109. doi: 10.3389/fnins.2017.00109. eCollection 2017.

In recent years there has been an increase in the number of portable low-cost electroencephalographic (EEG) systems available to researchers. However, to date the validation of the use of low-cost EEG systems has focused on continuous recording of EEG...

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Krigolson OE, Williams CC, Norton A, et al. Choosing MUSE: Validation of a Low-Cost, Portable EEG System for ERP Research. Front Neurosci. 2017;11:109doi: 10.3389/fnins.2017.00109.
Krigolson, O. E., Williams, C. C., Norton, A., Hassall, C. D., & Colino, F. L. (2017). Choosing MUSE: Validation of a Low-Cost, Portable EEG System for ERP Research. Frontiers in neuroscience, 11109. https://doi.org/10.3389/fnins.2017.00109
Krigolson, Olave E, et al. "Choosing MUSE: Validation of a Low-Cost, Portable EEG System for ERP Research." Frontiers in neuroscience vol. 11 (2017): 109. doi: https://doi.org/10.3389/fnins.2017.00109
Krigolson OE, Williams CC, Norton A, Hassall CD, Colino FL. Choosing MUSE: Validation of a Low-Cost, Portable EEG System for ERP Research. Front Neurosci. 2017 Mar 10;11:109. doi: 10.3389/fnins.2017.00109. eCollection 2017. PMID: 28344546; PMCID: PMC5344886.
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Effects of microclimate on behavioural and life history traits of terrestrial isopods: implications for responses to climate change.

ZooKeys

Dixie B, White H, Hassall M.
PMID: 26261446
Zookeys. 2015 Jul 30;(515):145-57. doi: 10.3897/zookeys.515.9399. eCollection 2015.

The sensitivity of terrestrial isopods to changes in both temperature and moisture make them suitable models for examining possible responses of arthropod macro-decomposers to predicted climate change. Effects of changes in both temperature and relative humidity on aggregation, growth...

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Dixie B, White H, Hassall M. Effects of microclimate on behavioural and life history traits of terrestrial isopods: implications for responses to climate change. Zookeys. 2015;(515):145-57doi: 10.3897/zookeys.515.9399.
Dixie, B., White, H., & Hassall, M. (2015). Effects of microclimate on behavioural and life history traits of terrestrial isopods: implications for responses to climate change. ZooKeys, (515), 145-57. https://doi.org/10.3897/zookeys.515.9399
Dixie, Bernice, et al. "Effects of microclimate on behavioural and life history traits of terrestrial isopods: implications for responses to climate change." ZooKeys vol. ,515 (2015): 145-57. doi: https://doi.org/10.3897/zookeys.515.9399
Dixie B, White H, Hassall M. Effects of microclimate on behavioural and life history traits of terrestrial isopods: implications for responses to climate change. Zookeys. 2015 Jul 30;(515):145-57. doi: 10.3897/zookeys.515.9399. eCollection 2015. PMID: 26261446; PMCID: PMC4525041.
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Institutional and technological barriers to the use of open educational resources (OERs) in physiology and medical education.

Advances in physiology education

Hassall C, Lewis DI.
PMID: 28143826
Adv Physiol Educ. 2017 Mar 01;41(1):77-81. doi: 10.1152/advan.00171.2016.

Open educational resources (OERs) are becoming increasingly common as a tool in education, particularly in medical and biomedical education. However, three key barriers have been identified to their use: 1) lack of awareness of OERs, 2) lack of motivation...

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Hassall C, Lewis DI. Institutional and technological barriers to the use of open educational resources (OERs) in physiology and medical education. Adv Physiol Educ. 2017;41(1):77-81doi: 10.1152/advan.00171.2016.
Hassall, C., & Lewis, D. I. (2017). Institutional and technological barriers to the use of open educational resources (OERs) in physiology and medical education. Advances in physiology education, 41(1), 77-81. https://doi.org/10.1152/advan.00171.2016
Hassall, Christopher, and Lewis, David I. "Institutional and technological barriers to the use of open educational resources (OERs) in physiology and medical education." Advances in physiology education vol. 41,1 (2017): 77-81. doi: https://doi.org/10.1152/advan.00171.2016
Hassall C, Lewis DI. Institutional and technological barriers to the use of open educational resources (OERs) in physiology and medical education. Adv Physiol Educ. 2017 Mar 01;41(1):77-81. doi: 10.1152/advan.00171.2016. PMID: 28143826.
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Assuring high-quality evidence reviews for chemical risk assessment: Five lessons from guest editing the first environmental health journal special issue dedicated to systematic review.

Environment international

Whaley P, Halsall C.
PMID: 27133460
Environ Int. 2016 Jul-Aug;92:553-5. doi: 10.1016/j.envint.2016.04.016. Epub 2016 Apr 29.

No abstract available.

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Whaley P, Halsall C. Assuring high-quality evidence reviews for chemical risk assessment: Five lessons from guest editing the first environmental health journal special issue dedicated to systematic review. Environ Int. 2016;92:553-5doi: 10.1016/j.envint.2016.04.016.
Whaley, P., & Halsall, C. (2016). Assuring high-quality evidence reviews for chemical risk assessment: Five lessons from guest editing the first environmental health journal special issue dedicated to systematic review. Environment international, 92553-5. https://doi.org/10.1016/j.envint.2016.04.016
Whaley, Paul, and Halsall, Crispin. "Assuring high-quality evidence reviews for chemical risk assessment: Five lessons from guest editing the first environmental health journal special issue dedicated to systematic review." Environment international vol. 92 (2016): 553-5. doi: https://doi.org/10.1016/j.envint.2016.04.016
Whaley P, Halsall C. Assuring high-quality evidence reviews for chemical risk assessment: Five lessons from guest editing the first environmental health journal special issue dedicated to systematic review. Environ Int. 2016 Jul-Aug;92:553-5. doi: 10.1016/j.envint.2016.04.016. Epub 2016 Apr 29. PMID: 27133460.
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The chemists behind the crystals.

Nature chemistry

King B, Schlüter D, Hansell C.
PMID: 25143199
Nat Chem. 2014 Sep;6(9):751-3. doi: 10.1038/nchem.2033.

No abstract available.

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King B, Schlüter D, Hansell C. The chemists behind the crystals. Nat Chem. 2014;6(9):751-3doi: 10.1038/nchem.2033.
King, B., Schlüter, D., & Hansell, C. (2014). The chemists behind the crystals. Nature chemistry, 6(9), 751-3. https://doi.org/10.1038/nchem.2033
King, Benjamin, et al. "The chemists behind the crystals." Nature chemistry vol. 6,9 (2014): 751-3. doi: https://doi.org/10.1038/nchem.2033
King B, Schlüter D, Hansell C. The chemists behind the crystals. Nat Chem. 2014 Sep;6(9):751-3. doi: 10.1038/nchem.2033. PMID: 25143199.
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Isothiocyanate analogs targeting CD44 receptor as an effective strategy against colon cancer.

Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents

Misra S, Ghatak S, Vyas A, O'Brien P, Markwald RR, Khetmalas M, Hascall VC, McCarthy JB, Karamanos NK, Tammi MI, Tammi RH, Prestwitch GD, Padhye S.
PMID: 25013352
Med Chem Res. 2014 Aug 01;23(8):3836-3851. doi: 10.1007/s00044-014-0958-4.

Inflammatory pathway plays an important role in tumor cell progression of colorectal cancers. Although colon cancer is considered as one of the leading causes of death worldwide, very few drugs are available for its effective treatment. Many studies have...

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Misra S, Ghatak S, Vyas A, et al. Isothiocyanate analogs targeting CD44 receptor as an effective strategy against colon cancer. Med Chem Res. 2014;23(8):3836-3851doi: 10.1007/s00044-014-0958-4.
Misra, S., Ghatak, S., Vyas, A., O'Brien, P., Markwald, R. R., Khetmalas, M., Hascall, V. C., McCarthy, J. B., Karamanos, N. K., Tammi, M. I., Tammi, R. H., Prestwitch, G. D., & Padhye, S. (2014). Isothiocyanate analogs targeting CD44 receptor as an effective strategy against colon cancer. Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents, 23(8), 3836-3851. https://doi.org/10.1007/s00044-014-0958-4
Misra, Suniti, et al. "Isothiocyanate analogs targeting CD44 receptor as an effective strategy against colon cancer." Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents vol. 23,8 (2014): 3836-3851. doi: https://doi.org/10.1007/s00044-014-0958-4
Misra S, Ghatak S, Vyas A, O'Brien P, Markwald RR, Khetmalas M, Hascall VC, McCarthy JB, Karamanos NK, Tammi MI, Tammi RH, Prestwitch GD, Padhye S. Isothiocyanate analogs targeting CD44 receptor as an effective strategy against colon cancer. Med Chem Res. 2014 Aug 01;23(8):3836-3851. doi: 10.1007/s00044-014-0958-4. PMID: 25013352; PMCID: PMC4084864.
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Bis- and Tris(pyrazolyl)hydroborato Ligands with Bulky Triptycyl Substituents: The Synthesis and Structural Characterization of Tl[Bp(Trip)] and Tl[Tp(Trip)].

Inorganic chemistry

Fillebeen T, Hascall T, Parkin G.
PMID: 11670076
Inorg Chem. 1997 Aug 13;36(17):3787-3790. doi: 10.1021/ic970259r.

No abstract available.

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Fillebeen T, Hascall T, Parkin G. Bis- and Tris(pyrazolyl)hydroborato Ligands with Bulky Triptycyl Substituents: The Synthesis and Structural Characterization of Tl[Bp(Trip)] and Tl[Tp(Trip)]. Inorg Chem. 1997;36(17):3787-3790doi: 10.1021/ic970259r.
Fillebeen, T., Hascall, T., & Parkin, G. (1997). Bis- and Tris(pyrazolyl)hydroborato Ligands with Bulky Triptycyl Substituents: The Synthesis and Structural Characterization of Tl[Bp(Trip)] and Tl[Tp(Trip)]. Inorganic chemistry, 36(17), 3787-3790. https://doi.org/10.1021/ic970259r
Fillebeen, Tauqir, et al. "Bis- and Tris(pyrazolyl)hydroborato Ligands with Bulky Triptycyl Substituents: The Synthesis and Structural Characterization of Tl[Bp(Trip)] and Tl[Tp(Trip)]." Inorganic chemistry vol. 36,17 (1997): 3787-3790. doi: https://doi.org/10.1021/ic970259r
Fillebeen T, Hascall T, Parkin G. Bis- and Tris(pyrazolyl)hydroborato Ligands with Bulky Triptycyl Substituents: The Synthesis and Structural Characterization of Tl[Bp(Trip)] and Tl[Tp(Trip)]. Inorg Chem. 1997 Aug 13;36(17):3787-3790. doi: 10.1021/ic970259r. PMID: 11670076.
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Pentalene complexes of group 7 metal carbonyls: an organometallic mixed-valence system with very large metal-metal electronic coupling.

Journal of the American Chemical Society

Jones SC, Hascall T, Barlow S, O'Hare D.
PMID: 12296722
J Am Chem Soc. 2002 Oct 02;124(39):11610-1. doi: 10.1021/ja027705g.

The bimetallic complexes [M(CO)(3)](2)(mu:eta(5):eta(5)-Pn) (Pn = pentalene, C(8)H(6); M = Mn, Re) have been synthesized and characterized crystallographically; the Mn compound was isolated as solely the anti-isomer, while the Re analogue was formed as a mixture of anti- and...

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Jones SC, Hascall T, Barlow S, et al. Pentalene complexes of group 7 metal carbonyls: an organometallic mixed-valence system with very large metal-metal electronic coupling. J Am Chem Soc. 2002;124(39):11610-1doi: 10.1021/ja027705g.
Jones, S. C., Hascall, T., Barlow, S., & O'Hare, D. (2002). Pentalene complexes of group 7 metal carbonyls: an organometallic mixed-valence system with very large metal-metal electronic coupling. Journal of the American Chemical Society, 124(39), 11610-1. https://doi.org/10.1021/ja027705g
Jones, Simon C, et al. "Pentalene complexes of group 7 metal carbonyls: an organometallic mixed-valence system with very large metal-metal electronic coupling." Journal of the American Chemical Society vol. 124,39 (2002): 11610-1. doi: https://doi.org/10.1021/ja027705g
Jones SC, Hascall T, Barlow S, O'Hare D. Pentalene complexes of group 7 metal carbonyls: an organometallic mixed-valence system with very large metal-metal electronic coupling. J Am Chem Soc. 2002 Oct 02;124(39):11610-1. doi: 10.1021/ja027705g. PMID: 12296722.
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Showing 1 to 12 of 167 entries