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A review of research on procedures for teaching safety skills to persons with developmental disabilities

instructional interventions

Dixon DR, Tarbox J.
GSID: 1YJkSVFT78MJ
DR Dixon, R Bergstrom, MN Smith, J Tarbox - Research in developmental …, 2010 - Elsevier

Safety skills are an important but often neglected area of training for persons with developmental disabilities (DD). The present study reviewed the literature on teaching safety …

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Dixon, D. R., Bergstrom, R., Smith, M. N., & Tarbox, J. (2010). A review of research on procedures for teaching safety skills to persons with developmental disabilities. Research in developmental disabilities, 31(5), 985-994.
Dixon, Dennis R., et al. "A review of research on procedures for teaching safety skills to persons with developmental disabilities." Research in developmental disabilities 31.5 (2010): 985-994.
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'Back to nursing'--a sham.

Professional nurse (London, England)

Dixon MA.
PMID: 3353404
Prof Nurse. 1988 Jan;3(4):119.

No abstract available.

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Dixon MA. 'Back to nursing'--a sham. Prof Nurse. 1988;3(4):119
Dixon, M. A. (1988). 'Back to nursing'--a sham. Professional nurse (London, England), 3(4), 119.
Dixon, M A. "'Back to nursing'--a sham." Professional nurse (London, England) vol. 3,4 (1988): 119.
Dixon MA. 'Back to nursing'--a sham. Prof Nurse. 1988 Jan;3(4):119. PMID: 3353404.
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Natrum sulphuricum.

The Homoeopathic recorder

DIXON CA, MOORE TK.
PMID: 20266830
Homoeopath Rec. 1947 Oct;63(4):104-9.

No abstract available.

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DIXON CA, MOORE TK. Natrum sulphuricum. Homoeopath Rec. 1947;63(4):104-9
DIXON, C. A., & MOORE, T. K. (1947). Natrum sulphuricum. The Homoeopathic recorder, 63(4), 104-9.
DIXON, C A, and MOORE, T K. "Natrum sulphuricum." The Homoeopathic recorder vol. 63,4 (1947): 104-9.
DIXON CA, MOORE TK. Natrum sulphuricum. Homoeopath Rec. 1947 Oct;63(4):104-9. PMID: 20266830.
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Methane to methanol conversion induced by thorium oxide through the CH3Th(O)H intermediate in solid argon.

Inorganic chemistry

Gong Y, Andrews L, Jackson VE, Dixon DA.
PMID: 23002994
Inorg Chem. 2012 Oct 15;51(20):11055-60. doi: 10.1021/ic301595h. Epub 2012 Sep 24.

Reactions of ThO molecules and CH(4) have been investigated in solid argon near 4 K. The CH(3)Th(O)H molecule is produced when the sample is exposed to UV irradiation. Identification of this new intermediate is substantiated by observation of the...

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Gong Y, Andrews L, Jackson VE, et al. Methane to methanol conversion induced by thorium oxide through the CH3Th(O)H intermediate in solid argon. Inorg Chem. 2012;51(20):11055-60doi: 10.1021/ic301595h.
Gong, Y., Andrews, L., Jackson, V. E., & Dixon, D. A. (2012). Methane to methanol conversion induced by thorium oxide through the CH3Th(O)H intermediate in solid argon. Inorganic chemistry, 51(20), 11055-60. https://doi.org/10.1021/ic301595h
Gong, Yu, et al. "Methane to methanol conversion induced by thorium oxide through the CH3Th(O)H intermediate in solid argon." Inorganic chemistry vol. 51,20 (2012): 11055-60. doi: https://doi.org/10.1021/ic301595h
Gong Y, Andrews L, Jackson VE, Dixon DA. Methane to methanol conversion induced by thorium oxide through the CH3Th(O)H intermediate in solid argon. Inorg Chem. 2012 Oct 15;51(20):11055-60. doi: 10.1021/ic301595h. Epub 2012 Sep 24. PMID: 23002994.
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Catalytic enantio- and diastereoselective Mannich reaction of α-substituted isocyanoacetates and ketimines.

Chemical communications (Cambridge, England)

de la Campa R, Gammack Yamagata AD, Ortín I, Franchino A, Thompson AL, Odell B, Dixon DJ.
PMID: 27500289
Chem Commun (Camb). 2016 Aug 23;52(70):10632-5. doi: 10.1039/c6cc04132a.

The highly diastereo- and enantioselective Mannich addition/cyclisation reaction of α-substituted isocyanoacetate ester pronucleophiles and (hetero)aryl and alkyl methyl ketone-derived ketimines using a silver acetate and a cinchona-derived amino phosphine binary catalyst system is reported.

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de la Campa R, Gammack Yamagata AD, Ortín I, et al. Catalytic enantio- and diastereoselective Mannich reaction of α-substituted isocyanoacetates and ketimines. Chem Commun (Camb). 2016;52(70):10632-5doi: 10.1039/c6cc04132a.
de la Campa, R., Gammack Yamagata, A. D., Ortín, I., Franchino, A., Thompson, A. L., Odell, B., & Dixon, D. J. (2016). Catalytic enantio- and diastereoselective Mannich reaction of α-substituted isocyanoacetates and ketimines. Chemical communications (Cambridge, England), 52(70), 10632-5. https://doi.org/10.1039/c6cc04132a
de la Campa, Raquel, et al. "Catalytic enantio- and diastereoselective Mannich reaction of α-substituted isocyanoacetates and ketimines." Chemical communications (Cambridge, England) vol. 52,70 (2016): 10632-5. doi: https://doi.org/10.1039/c6cc04132a
de la Campa R, Gammack Yamagata AD, Ortín I, Franchino A, Thompson AL, Odell B, Dixon DJ. Catalytic enantio- and diastereoselective Mannich reaction of α-substituted isocyanoacetates and ketimines. Chem Commun (Camb). 2016 Aug 23;52(70):10632-5. doi: 10.1039/c6cc04132a. PMID: 27500289.
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Enantioselective Construction of the ABCDE Pentacyclic Core of the Strychnos Alkaloids.

Organic letters

Gammack Yamagata AD, Dixon DJ.
PMID: 28357866
Org Lett. 2017 Apr 07;19(7):1894-1897. doi: 10.1021/acs.orglett.7b00669. Epub 2017 Mar 30.

An efficient enantioselective 12-step synthesis of the ABCDE pentacyclic core of the Strychnos alkaloids is described. A key feature of this approach is an organocatalyzed enantioselective desymmetrization to generate the morphan core in high ee and dr. After palladium-catalyzed...

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Gammack Yamagata AD, Dixon DJ. Enantioselective Construction of the ABCDE Pentacyclic Core of the Strychnos Alkaloids. Org Lett. 2017;19(7):1894-1897doi: 10.1021/acs.orglett.7b00669.
Gammack Yamagata, A. D., & Dixon, D. J. (2017). Enantioselective Construction of the ABCDE Pentacyclic Core of the Strychnos Alkaloids. Organic letters, 19(7), 1894-1897. https://doi.org/10.1021/acs.orglett.7b00669
Gammack Yamagata, Adam D, and Dixon, Darren J. "Enantioselective Construction of the ABCDE Pentacyclic Core of the Strychnos Alkaloids." Organic letters vol. 19,7 (2017): 1894-1897. doi: https://doi.org/10.1021/acs.orglett.7b00669
Gammack Yamagata AD, Dixon DJ. Enantioselective Construction of the ABCDE Pentacyclic Core of the Strychnos Alkaloids. Org Lett. 2017 Apr 07;19(7):1894-1897. doi: 10.1021/acs.orglett.7b00669. Epub 2017 Mar 30. PMID: 28357866.
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Single-Site Zeolite-Anchored Organoiridium Carbonyl Complexes: Characterization of Structure and Reactivity by Spectroscopy and Computational Chemistry.

Chemistry (Weinheim an der Bergstrasse, Germany)

Martinez-Macias C, Chen M, Dixon DA, Gates BC.
PMID: 26140330
Chemistry. 2015 Aug 10;21(33):11825-35. doi: 10.1002/chem.201501277. Epub 2015 Jul 03.

A family of HY zeolite-supported cationic organoiridium carbonyl complexes was formed by reaction of Ir(CO)2 (acac) (acac=acetylacetonate) to form supported Ir(CO)2 complexes, which were treated at 298 K and 1 atm with flowing gas-phase reactants, including C2 H4 ,...

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Martinez-Macias C, Chen M, Dixon DA, et al. Single-Site Zeolite-Anchored Organoiridium Carbonyl Complexes: Characterization of Structure and Reactivity by Spectroscopy and Computational Chemistry. Chemistry. 2015;21(33):11825-35doi: 10.1002/chem.201501277.
Martinez-Macias, C., Chen, M., Dixon, D. A., & Gates, B. C. (2015). Single-Site Zeolite-Anchored Organoiridium Carbonyl Complexes: Characterization of Structure and Reactivity by Spectroscopy and Computational Chemistry. Chemistry (Weinheim an der Bergstrasse, Germany), 21(33), 11825-35. https://doi.org/10.1002/chem.201501277
Martinez-Macias, Claudia, et al. "Single-Site Zeolite-Anchored Organoiridium Carbonyl Complexes: Characterization of Structure and Reactivity by Spectroscopy and Computational Chemistry." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 21,33 (2015): 11825-35. doi: https://doi.org/10.1002/chem.201501277
Martinez-Macias C, Chen M, Dixon DA, Gates BC. Single-Site Zeolite-Anchored Organoiridium Carbonyl Complexes: Characterization of Structure and Reactivity by Spectroscopy and Computational Chemistry. Chemistry. 2015 Aug 10;21(33):11825-35. doi: 10.1002/chem.201501277. Epub 2015 Jul 03. PMID: 26140330.
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HOCCO versus OCCO: Comparative spectroscopy of the radical and diradical reactive intermediates.

The Journal of chemical physics

Dixon AR, Xue T, Sanov A.
PMID: 27334160
J Chem Phys. 2016 Jun 21;144(23):234305. doi: 10.1063/1.4953774.

We present a photoelectron imaging study of three glyoxal derivatives: the ethylenedione anion (OCCO(-)), ethynediolide (HOCCO(-)), and glyoxalide (OHCCO(-)). These anions provide access to the corresponding neutral reactive intermediates: the OCCO diradical and the HOCCO and OHCCO radicals. Contrasting...

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Dixon AR, Xue T, Sanov A. HOCCO versus OCCO: Comparative spectroscopy of the radical and diradical reactive intermediates. J Chem Phys. 2016;144(23):234305doi: 10.1063/1.4953774.
Dixon, A. R., Xue, T., & Sanov, A. (2016). HOCCO versus OCCO: Comparative spectroscopy of the radical and diradical reactive intermediates. The Journal of chemical physics, 144(23), 234305. https://doi.org/10.1063/1.4953774
Dixon, Andrew R, et al. "HOCCO versus OCCO: Comparative spectroscopy of the radical and diradical reactive intermediates." The Journal of chemical physics vol. 144,23 (2016): 234305. doi: https://doi.org/10.1063/1.4953774
Dixon AR, Xue T, Sanov A. HOCCO versus OCCO: Comparative spectroscopy of the radical and diradical reactive intermediates. J Chem Phys. 2016 Jun 21;144(23):234305. doi: 10.1063/1.4953774. PMID: 27334160.
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High Conductivity, High Strength Solid Electrolytes Formed by in Situ Encapsulation of Ionic Liquids in Nanofibrillar Methyl Cellulose Networks.

ACS applied materials & interfaces

Mantravadi R, Chinnam PR, Dikin DA, Wunder SL.
PMID: 27153318
ACS Appl Mater Interfaces. 2016 Jun 01;8(21):13426-36. doi: 10.1021/acsami.6b02903. Epub 2016 May 19.

Strong, solid polymer electrolyte ion gels, with moduli in the MPa range, a capacitance of 2 μF/cm(2), and high ambient ionic conductivities (>1 × 10(-3) S/cm), all at room temperature, have been prepared from butyl-N-methyl pyrrolidinium bis(trifluoromethylsulfonyl) imide (PYR14TFSI)...

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Mantravadi R, Chinnam PR, Dikin DA, et al. High Conductivity, High Strength Solid Electrolytes Formed by in Situ Encapsulation of Ionic Liquids in Nanofibrillar Methyl Cellulose Networks. ACS Appl Mater Interfaces. 2016;8(21):13426-36doi: 10.1021/acsami.6b02903.
Mantravadi, R., Chinnam, P. R., Dikin, D. A., & Wunder, S. L. (2016). High Conductivity, High Strength Solid Electrolytes Formed by in Situ Encapsulation of Ionic Liquids in Nanofibrillar Methyl Cellulose Networks. ACS applied materials & interfaces, 8(21), 13426-36. https://doi.org/10.1021/acsami.6b02903
Mantravadi, Ramya, et al. "High Conductivity, High Strength Solid Electrolytes Formed by in Situ Encapsulation of Ionic Liquids in Nanofibrillar Methyl Cellulose Networks." ACS applied materials & interfaces vol. 8,21 (2016): 13426-36. doi: https://doi.org/10.1021/acsami.6b02903
Mantravadi R, Chinnam PR, Dikin DA, Wunder SL. High Conductivity, High Strength Solid Electrolytes Formed by in Situ Encapsulation of Ionic Liquids in Nanofibrillar Methyl Cellulose Networks. ACS Appl Mater Interfaces. 2016 Jun 01;8(21):13426-36. doi: 10.1021/acsami.6b02903. Epub 2016 May 19. PMID: 27153318.
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Reaction of CO.

The journal of physical chemistry. A

Flores LA, Murphy JG, Copeland WB, Dixon DA.
PMID: 29028336
J Phys Chem A. 2017 Nov 09;121(44):8518-8524. doi: 10.1021/acs.jpca.7b09107. Epub 2017 Oct 25.

Adsorption of CO

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Flores LA, Murphy JG, Copeland WB, et al. Reaction of CO. J Phys Chem A. 2017;121(44):8518-8524doi: 10.1021/acs.jpca.7b09107.
Flores, L. A., Murphy, J. G., Copeland, W. B., & Dixon, D. A. (2017). Reaction of CO. The journal of physical chemistry. A, 121(44), 8518-8524. https://doi.org/10.1021/acs.jpca.7b09107
Flores, Luis A, et al. "Reaction of CO." The journal of physical chemistry. A vol. 121,44 (2017): 8518-8524. doi: https://doi.org/10.1021/acs.jpca.7b09107
Flores LA, Murphy JG, Copeland WB, Dixon DA. Reaction of CO. J Phys Chem A. 2017 Nov 09;121(44):8518-8524. doi: 10.1021/acs.jpca.7b09107. Epub 2017 Oct 25. PMID: 29028336.
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Elicitor-mediated induction of chalcone isomerase in Phaseolus vulgaris cell suspension cultures.

Planta

Dixon RA, Gerrish C, Lamb CJ, Robbins MP.
PMID: 24258333
Planta. 1983 Dec;159(6):561-9. doi: 10.1007/BF00409146.

Approximately fourfold increases in the extractable activity of the enzyme chalcone isomerase (CHI, EC 5.5.1.6) were observed within 24 h of treatment of cell suspension cultures of Phaseolus vulgaris with a crude elicitor preparation heatreleased from the cell walls...

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Dixon RA, Gerrish C, Lamb CJ, et al. Elicitor-mediated induction of chalcone isomerase in Phaseolus vulgaris cell suspension cultures. Planta. 1983;159(6):561-9doi: 10.1007/BF00409146.
Dixon, R. A., Gerrish, C., Lamb, C. J., & Robbins, M. P. (1983). Elicitor-mediated induction of chalcone isomerase in Phaseolus vulgaris cell suspension cultures. Planta, 159(6), 561-9. https://doi.org/10.1007/BF00409146
Dixon, R A, et al. "Elicitor-mediated induction of chalcone isomerase in Phaseolus vulgaris cell suspension cultures." Planta vol. 159,6 (1983): 561-9. doi: https://doi.org/10.1007/BF00409146
Dixon RA, Gerrish C, Lamb CJ, Robbins MP. Elicitor-mediated induction of chalcone isomerase in Phaseolus vulgaris cell suspension cultures. Planta. 1983 Dec;159(6):561-9. doi: 10.1007/BF00409146. PMID: 24258333.
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Dose responses for Colletotrichum lindemuthianum elicitor-mediated enzyme induction in French bean cell suspension cultures.

Planta

Dixon RA, Dey PM, Murphy DL, Whitehead IM.
PMID: 24301854
Planta. 1981 Mar;151(3):272-80. doi: 10.1007/BF00395180.

The induction of L-phenylalanine ammonialyase (PAL, EC 4.3.1.5) and flavanone synthase in French bean cell suspension cultures in response to heat-released elicitor from cell walls of the phytopathogenic fungus Colletotrichum lindemuthianum is highly dependent upon elicitor concentration. The elicitor...

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Dixon RA, Dey PM, Murphy DL, et al. Dose responses for Colletotrichum lindemuthianum elicitor-mediated enzyme induction in French bean cell suspension cultures. Planta. 1981;151(3):272-80doi: 10.1007/BF00395180.
Dixon, R. A., Dey, P. M., Murphy, D. L., & Whitehead, I. M. (1981). Dose responses for Colletotrichum lindemuthianum elicitor-mediated enzyme induction in French bean cell suspension cultures. Planta, 151(3), 272-80. https://doi.org/10.1007/BF00395180
Dixon, R A, et al. "Dose responses for Colletotrichum lindemuthianum elicitor-mediated enzyme induction in French bean cell suspension cultures." Planta vol. 151,3 (1981): 272-80. doi: https://doi.org/10.1007/BF00395180
Dixon RA, Dey PM, Murphy DL, Whitehead IM. Dose responses for Colletotrichum lindemuthianum elicitor-mediated enzyme induction in French bean cell suspension cultures. Planta. 1981 Mar;151(3):272-80. doi: 10.1007/BF00395180. PMID: 24301854.
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Showing 1 to 12 of 858 entries