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Quasi-experimental comparison group designs for social policy evaluation

quasi-experimental designs

Mueller CE, Gaus H.
GSID: -6ZMbgQxedoJ
CE Mueller, H Gaus - Handbook of social policy evaluation, 2017 - elgaronline.com

… have reported on quasi-experimental designs with nonequivalent comparison groups. Although we have made it clear that these designs do not … Finally, in discussing the potentials and pitfalls of the different types of quasi-experimental design we have only...

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Mueller, C. E., & Gaus, H. (2017). Quasi-experimental comparison group designs for social policy evaluation. In Handbook of social policy evaluation. Edward Elgar Publishing.
Mueller, Christoph E., and Hansjoerg Gaus. "Quasi-experimental comparison group designs for social policy evaluation." Handbook of social policy evaluation. Edward Elgar Publishing, 2017.
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Evaluating hydrogen bonding control in the diastereoselective Diels-Alder reactions of 9-(2-aminoethyl)-anthracene derivatives.

Organic & biomolecular chemistry

Bawa RA, Gautier FM, Adams H, Meijer AJ, Jones S.
PMID: 26340318
Org Biomol Chem. 2015 Nov 14;13(42):10569-77. doi: 10.1039/c5ob01343g. Epub 2015 Sep 04.

Several 9-(2-aminoethyl)anthracene derivatives were prepared with different nitrogen substitutents including alkyl, acetamide, trifluoroacaeamide and t-butyl carbamate. The selectivity in Diels-Alder cyclodaddition reaction with N-methyl maleimide was evaluated through single crystal X-ray analysis of the products. Models for the change...

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Bawa RA, Gautier FM, Adams H, et al. Evaluating hydrogen bonding control in the diastereoselective Diels-Alder reactions of 9-(2-aminoethyl)-anthracene derivatives. Org Biomol Chem. 2015;13(42):10569-77doi: 10.1039/c5ob01343g.
Bawa, R. A., Gautier, F. M., Adams, H., Meijer, A. J., & Jones, S. (2015). Evaluating hydrogen bonding control in the diastereoselective Diels-Alder reactions of 9-(2-aminoethyl)-anthracene derivatives. Organic & biomolecular chemistry, 13(42), 10569-77. https://doi.org/10.1039/c5ob01343g
Bawa, R A, et al. "Evaluating hydrogen bonding control in the diastereoselective Diels-Alder reactions of 9-(2-aminoethyl)-anthracene derivatives." Organic & biomolecular chemistry vol. 13,42 (2015): 10569-77. doi: https://doi.org/10.1039/c5ob01343g
Bawa RA, Gautier FM, Adams H, Meijer AJ, Jones S. Evaluating hydrogen bonding control in the diastereoselective Diels-Alder reactions of 9-(2-aminoethyl)-anthracene derivatives. Org Biomol Chem. 2015 Nov 14;13(42):10569-77. doi: 10.1039/c5ob01343g. Epub 2015 Sep 04. PMID: 26340318.
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No Difference in Myosin Kinetics and Spatial Distribution of the Lever Arm in the Left and Right Ventricles of Human Hearts.

Frontiers in physiology

Duggal D, Requena S, Nagwekar J, Raut S, Rich R, Das H, Patel V, Gryczynski I, Fudala R, Gryczynski Z, Blair C, Campbell KS, Borejdo J.
PMID: 29081749
Front Physiol. 2017 Oct 13;8:732. doi: 10.3389/fphys.2017.00732. eCollection 2017.

The systemic circulation offers larger resistance to the blood flow than the pulmonary system. Consequently, the left ventricle (LV) must pump blood with more force than the right ventricle (RV). The question arises whether the stronger pumping action of...

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Duggal D, Requena S, Nagwekar J, et al. No Difference in Myosin Kinetics and Spatial Distribution of the Lever Arm in the Left and Right Ventricles of Human Hearts. Front Physiol. 2017;8:732doi: 10.3389/fphys.2017.00732.
Duggal, D., Requena, S., Nagwekar, J., Raut, S., Rich, R., Das, H., Patel, V., Gryczynski, I., Fudala, R., Gryczynski, Z., Blair, C., Campbell, K. S., & Borejdo, J. (2017). No Difference in Myosin Kinetics and Spatial Distribution of the Lever Arm in the Left and Right Ventricles of Human Hearts. Frontiers in physiology, 8732. https://doi.org/10.3389/fphys.2017.00732
Duggal, Divya, et al. "No Difference in Myosin Kinetics and Spatial Distribution of the Lever Arm in the Left and Right Ventricles of Human Hearts." Frontiers in physiology vol. 8 (2017): 732. doi: https://doi.org/10.3389/fphys.2017.00732
Duggal D, Requena S, Nagwekar J, Raut S, Rich R, Das H, Patel V, Gryczynski I, Fudala R, Gryczynski Z, Blair C, Campbell KS, Borejdo J. No Difference in Myosin Kinetics and Spatial Distribution of the Lever Arm in the Left and Right Ventricles of Human Hearts. Front Physiol. 2017 Oct 13;8:732. doi: 10.3389/fphys.2017.00732. eCollection 2017. PMID: 29081749; PMCID: PMC5645524.
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Fragments of layered manganese oxide are the real water oxidation catalyst after transformation of molecular precursor on clay.

Journal of the American Chemical Society

Najafpour MM, Moghaddam AN, Dau H, Zaharieva I.
PMID: 24798550
J Am Chem Soc. 2014 May 21;136(20):7245-8. doi: 10.1021/ja5028716. Epub 2014 May 07.

A binuclear manganese molecular complex [(OH2)(terpy)Mn(μ-O)2Mn(terpy)(OH2)](3+) (1) is the most prominent structural and functional model of the water-oxidizing Mn complex operating in plants and cyanobacteria. Supported on montmorillonite clay and using Ce(IV) as a chemical oxidant, 1 has been...

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Najafpour MM, Moghaddam AN, Dau H, et al. Fragments of layered manganese oxide are the real water oxidation catalyst after transformation of molecular precursor on clay. J Am Chem Soc. 2014;136(20):7245-8doi: 10.1021/ja5028716.
Najafpour, M. M., Moghaddam, A. N., Dau, H., & Zaharieva, I. (2014). Fragments of layered manganese oxide are the real water oxidation catalyst after transformation of molecular precursor on clay. Journal of the American Chemical Society, 136(20), 7245-8. https://doi.org/10.1021/ja5028716
Najafpour, M M, et al. "Fragments of layered manganese oxide are the real water oxidation catalyst after transformation of molecular precursor on clay." Journal of the American Chemical Society vol. 136,20 (2014): 7245-8. doi: https://doi.org/10.1021/ja5028716
Najafpour MM, Moghaddam AN, Dau H, Zaharieva I. Fragments of layered manganese oxide are the real water oxidation catalyst after transformation of molecular precursor on clay. J Am Chem Soc. 2014 May 21;136(20):7245-8. doi: 10.1021/ja5028716. Epub 2014 May 07. PMID: 24798550.
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Chemoselective silicification of synthetic peptides and polyamines.

Beilstein journal of nanotechnology

Abacilar M, Daus F, Geyer A.
PMID: 25671155
Beilstein J Nanotechnol. 2015 Jan 08;6:103-10. doi: 10.3762/bjnano.6.10. eCollection 2015.

Biosilicification sets the standard for the localized in vitro precipitation of silica at low orthosilicate concentrations in aqueous environment under ambient conditions. Numerous parameters must be controlled for the development of new technologies in designing inventive nanosilica structures, which...

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Abacilar M, Daus F, Geyer A. Chemoselective silicification of synthetic peptides and polyamines. Beilstein J Nanotechnol. 2015;6:103-10doi: 10.3762/bjnano.6.10.
Abacilar, M., Daus, F., & Geyer, A. (2015). Chemoselective silicification of synthetic peptides and polyamines. Beilstein journal of nanotechnology, 6103-10. https://doi.org/10.3762/bjnano.6.10
Abacilar, Maryna, et al. "Chemoselective silicification of synthetic peptides and polyamines." Beilstein journal of nanotechnology vol. 6 (2015): 103-10. doi: https://doi.org/10.3762/bjnano.6.10
Abacilar M, Daus F, Geyer A. Chemoselective silicification of synthetic peptides and polyamines. Beilstein J Nanotechnol. 2015 Jan 08;6:103-10. doi: 10.3762/bjnano.6.10. eCollection 2015. PMID: 25671155; PMCID: PMC4311759.
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Listening to disembodied voices: anthropological and psychiatric challenges.

Anthropology & medicine

Basu H.
PMID: 24962129
Anthropol Med. 2014 Dec;21(3):325-342. doi: 10.1080/13648470.2014.928095. Epub 2014 Jun 25.

What is the role of the voice in Indian explanatory models of madness and psychiatric nosology? Anthropological and psychiatric challenges, it is argued, are crystallised in the voice, a medium that signifies the intersection of models of occult madness...

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Basu H. Listening to disembodied voices: anthropological and psychiatric challenges. Anthropol Med. 2014;21(3):325-342doi: 10.1080/13648470.2014.928095.
Basu, H. (2014). Listening to disembodied voices: anthropological and psychiatric challenges. Anthropology & medicine, 21(3), 325-342. https://doi.org/10.1080/13648470.2014.928095
Basu, Helene. "Listening to disembodied voices: anthropological and psychiatric challenges." Anthropology & medicine vol. 21,3 (2014): 325-342. doi: https://doi.org/10.1080/13648470.2014.928095
Basu H. Listening to disembodied voices: anthropological and psychiatric challenges. Anthropol Med. 2014 Dec;21(3):325-342. doi: 10.1080/13648470.2014.928095. Epub 2014 Jun 25. PMID: 24962129.
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Biological variation of canine serum thyrotropin (TSH) concentration.

Veterinary clinical pathology

Iversen L, Jensen AL, Høier R, Aaes H.
PMID: 12075532
Vet Clin Pathol. 1999;28(1):16-19. doi: 10.1111/j.1939-165x.1999.tb01036.x.

The aim of the present study was to estimate the between-dog, within-dog and analytical components of variance for serum thyrotropin (TSH) in healthy dogs, and to use these components of variance to 1) estimate the critical difference for significance...

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Iversen L, Jensen AL, Høier R, et al. Biological variation of canine serum thyrotropin (TSH) concentration. Vet Clin Pathol. 1999;28(1):16-19doi: 10.1111/j.1939-165x.1999.tb01036.x.
Iversen, L., Jensen, A. L., Høier, R., & Aaes, H. (1999). Biological variation of canine serum thyrotropin (TSH) concentration. Veterinary clinical pathology, 28(1), 16-19. https://doi.org/10.1111/j.1939-165x.1999.tb01036.x
Iversen, Lars, et al. "Biological variation of canine serum thyrotropin (TSH) concentration." Veterinary clinical pathology vol. 28,1 (1999): 16-19. doi: https://doi.org/10.1111/j.1939-165x.1999.tb01036.x
Iversen L, Jensen AL, Høier R, Aaes H. Biological variation of canine serum thyrotropin (TSH) concentration. Vet Clin Pathol. 1999;28(1):16-19. doi: 10.1111/j.1939-165x.1999.tb01036.x. PMID: 12075532.
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Barium Templating Schiff-Base Lateral Macrobicycles.

Inorganic chemistry

Esteban D, Bañobre D, Bastida R, de Blas A, Macías A, Rodríguez A, Rodríguez-Blas T, Fenton DE, Adams H, Mahía J.
PMID: 11670968
Inorg Chem. 1999 Apr 19;38(8):1937-1944. doi: 10.1021/ic9811190.

Schiff-base lateral macrobicycles containing two different binding units, a rigid and unsaturated N(2)X set (X: N, O) and a flexible and cyclic N(2)O(n)() set, linked by two aromatic bridges, have been prepared by reaction of the appropriate bibracchial diamines...

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Esteban D, Bañobre D, Bastida R, et al. Barium Templating Schiff-Base Lateral Macrobicycles. Inorg Chem. 1999;38(8):1937-1944doi: 10.1021/ic9811190.
Esteban, D., Bañobre, D., Bastida, R., de Blas, A., Macías, A., Rodríguez, A., Rodríguez-Blas, T., Fenton, D. E., Adams, H., & Mahía, J. (1999). Barium Templating Schiff-Base Lateral Macrobicycles. Inorganic chemistry, 38(8), 1937-1944. https://doi.org/10.1021/ic9811190
Esteban, David, et al. "Barium Templating Schiff-Base Lateral Macrobicycles." Inorganic chemistry vol. 38,8 (1999): 1937-1944. doi: https://doi.org/10.1021/ic9811190
Esteban D, Bañobre D, Bastida R, de Blas A, Macías A, Rodríguez A, Rodríguez-Blas T, Fenton DE, Adams H, Mahía J. Barium Templating Schiff-Base Lateral Macrobicycles. Inorg Chem. 1999 Apr 19;38(8):1937-1944. doi: 10.1021/ic9811190. PMID: 11670968.
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Controlling substitution chemistry in ruthenium(II) systems. Synthesis of heteroleptic complexes incorporating the [Ru([9]aneS3)]2+ metal center.

Inorganic chemistry

Roche S, Adams H, Spey SE, Thomas JA.
PMID: 12526500
Inorg Chem. 2000 May 29;39(11):2385-90. doi: 10.1021/ic991336g.

The complex [Ru(py)3([9]aneS3)][PF6]2, 1 (py = pyridine), has proved to be a suitable starting material for the synthesis of heteroleptic Ru(II) complexes. By exploiting unfavorable steric interactions between 2-H and 6-H hydrogens of coordinated pyridyl ligands, we have synthesized...

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Roche S, Adams H, Spey SE, et al. Controlling substitution chemistry in ruthenium(II) systems. Synthesis of heteroleptic complexes incorporating the [Ru([9]aneS3)]2+ metal center. Inorg Chem. 2000;39(11):2385-90doi: 10.1021/ic991336g.
Roche, S., Adams, H., Spey, S. E., & Thomas, J. A. (2000). Controlling substitution chemistry in ruthenium(II) systems. Synthesis of heteroleptic complexes incorporating the [Ru([9]aneS3)]2+ metal center. Inorganic chemistry, 39(11), 2385-90. https://doi.org/10.1021/ic991336g
Roche, S, et al. "Controlling substitution chemistry in ruthenium(II) systems. Synthesis of heteroleptic complexes incorporating the [Ru([9]aneS3)]2+ metal center." Inorganic chemistry vol. 39,11 (2000): 2385-90. doi: https://doi.org/10.1021/ic991336g
Roche S, Adams H, Spey SE, Thomas JA. Controlling substitution chemistry in ruthenium(II) systems. Synthesis of heteroleptic complexes incorporating the [Ru([9]aneS3)]2+ metal center. Inorg Chem. 2000 May 29;39(11):2385-90. doi: 10.1021/ic991336g. PMID: 12526500.
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Accumulation of 15-Kilodalton Zein in Novel Protein Bodies in Transgenic Tobacco.

Plant physiology

Bagga S, Adams H, Kemp JD, Sengupta-Gopalan C.
PMID: 12228338
Plant Physiol. 1995 Jan;107(1):13-23. doi: 10.1104/pp.107.1.13.

Zeins, the seed storage proteins of maize, are a group of alcohol-soluble polypeptides of different molecular masses that share a similar amino acid composition but vary in their sulfur amino acid composition. They are synthesized on the rough endoplasmic...

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Bagga S, Adams H, Kemp JD, et al. Accumulation of 15-Kilodalton Zein in Novel Protein Bodies in Transgenic Tobacco. Plant Physiol. 1995;107(1):13-23doi: 10.1104/pp.107.1.13.
Bagga, S., Adams, H., Kemp, J. D., & Sengupta-Gopalan, C. (1995). Accumulation of 15-Kilodalton Zein in Novel Protein Bodies in Transgenic Tobacco. Plant physiology, 107(1), 13-23. https://doi.org/10.1104/pp.107.1.13
Bagga, S., et al. "Accumulation of 15-Kilodalton Zein in Novel Protein Bodies in Transgenic Tobacco." Plant physiology vol. 107,1 (1995): 13-23. doi: https://doi.org/10.1104/pp.107.1.13
Bagga S, Adams H, Kemp JD, Sengupta-Gopalan C. Accumulation of 15-Kilodalton Zein in Novel Protein Bodies in Transgenic Tobacco. Plant Physiol. 1995 Jan;107(1):13-23. doi: 10.1104/pp.107.1.13. PMID: 12228338; PMCID: PMC161159.
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One-dimensional manganese coordination polymers composed of polynuclear cluster blocks and polypyridyl linkers: structures and properties.

Inorganic chemistry

Baca SG, Malaestean IL, Keene TD, Adams H, Ward MD, Hauser J, Neels A, Decurtins S.
PMID: 18959375
Inorg Chem. 2008 Dec 01;47(23):11108-19. doi: 10.1021/ic8014145.

The synthesis, crystal structures and magnetic properties of five new manganese compounds are reported. These include a linear trinuclear cluster [Mn(II)(3)(O(2)CCHMe(2))(6)(dpa)(2)].2MeCN (1) (dpa = 2,2'-dipyridylamine), a tetranuclear cluster [Mn(II)(2)Mn(III)(2)O(2)(O(2)CCMe(3))(6)(bpy)(2)] (3) (bpy = 2,2'-bipyridine), and chain coordination polymers composed of...

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Baca SG, Malaestean IL, Keene TD, et al. One-dimensional manganese coordination polymers composed of polynuclear cluster blocks and polypyridyl linkers: structures and properties. Inorg Chem. 2008;47(23):11108-19doi: 10.1021/ic8014145.
Baca, S. G., Malaestean, I. L., Keene, T. D., Adams, H., Ward, M. D., Hauser, J., Neels, A., & Decurtins, S. (2008). One-dimensional manganese coordination polymers composed of polynuclear cluster blocks and polypyridyl linkers: structures and properties. Inorganic chemistry, 47(23), 11108-19. https://doi.org/10.1021/ic8014145
Baca, Svetlana G, et al. "One-dimensional manganese coordination polymers composed of polynuclear cluster blocks and polypyridyl linkers: structures and properties." Inorganic chemistry vol. 47,23 (2008): 11108-19. doi: https://doi.org/10.1021/ic8014145
Baca SG, Malaestean IL, Keene TD, Adams H, Ward MD, Hauser J, Neels A, Decurtins S. One-dimensional manganese coordination polymers composed of polynuclear cluster blocks and polypyridyl linkers: structures and properties. Inorg Chem. 2008 Dec 01;47(23):11108-19. doi: 10.1021/ic8014145. PMID: 18959375.
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Kinetically locked, trinuclear Ru(II) metallo-macrocycles--synthesis, electrochemical, and optical properties.

Dalton transactions (Cambridge, England : 2003)

Shan N, Ingram JD, Easun TL, Vickers SJ, Adams H, Ward MD, Thomas JA.
PMID: 16751899
Dalton Trans. 2006 Jun 21;(23):2900-6. doi: 10.1039/b516080b. Epub 2006 May 04.

Using a [Ru(II)([9]aneS3)] templating moiety, kinetically-locked, metallomacrocycles incorporating adenine based ligands have been synthesised through self-assembly. The kinetically robust nature of these structures is confirmed by electrochemical studies: each can be reversibly oxidised in a four-member redox series, containing...

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Shan N, Ingram JD, Easun TL, et al. Kinetically locked, trinuclear Ru(II) metallo-macrocycles--synthesis, electrochemical, and optical properties. Dalton Trans. 2006;(23):2900-6doi: 10.1039/b516080b.
Shan, N., Ingram, J. D., Easun, T. L., Vickers, S. J., Adams, H., Ward, M. D., & Thomas, J. A. (2006). Kinetically locked, trinuclear Ru(II) metallo-macrocycles--synthesis, electrochemical, and optical properties. Dalton transactions (Cambridge, England : 2003), (23), 2900-6. https://doi.org/10.1039/b516080b
Shan, Naz, et al. "Kinetically locked, trinuclear Ru(II) metallo-macrocycles--synthesis, electrochemical, and optical properties." Dalton transactions (Cambridge, England : 2003) vol. ,23 (2006): 2900-6. doi: https://doi.org/10.1039/b516080b
Shan N, Ingram JD, Easun TL, Vickers SJ, Adams H, Ward MD, Thomas JA. Kinetically locked, trinuclear Ru(II) metallo-macrocycles--synthesis, electrochemical, and optical properties. Dalton Trans. 2006 Jun 21;(23):2900-6. doi: 10.1039/b516080b. Epub 2006 May 04. PMID: 16751899.
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