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An investigation of students' perspectives on anxiety and speaking

classroom interventions

Young DJ.
GSID: 04G2ckJsvfUJ
DJ Young - Foreign Language Annals, 1990 - Wiley Online Library

Language anxiety is becoming an important area of research in our profession. Debilitating language anxiety can have profound consequences on the language learning process. The …

Children's time with fathers in intact families

ADVANCE: Organizational Change for Gender Equity in STEM Academic Professions AND Program Evaluation

Yeung WJ.
GSID: OvcA6WXBMaIJ
WJ Yeung, JF Sandberg… - Journal of Marriage …, 2001 - Wiley Online Library

This paper uses the Panel Study of Income Dynamics to examine children's involvement with their fathers in intact families as measured through time spent together. Our findings suggest that although mothers still shoulder the lion's share of the parenting,...

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Yeung, W. J., Sandberg, J. F., Davis‐Kean, P. E., & Hofferth, S. L. (2001). Children's time with fathers in intact families. Journal of Marriage and Family, 63(1), 136-154.
Yeung, W. Jean, et al. "Children's time with fathers in intact families." Journal of Marriage and Family 63.1 (2001): 136-154.
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A Neutron Diffraction Study of the Electrochemical Double Layer Capacitor Electrolyte Tetrapropylammonium Bromide in Acetonitrile.

The journal of physical chemistry. B

Humphreys EK, Allan PK, Welbourn RJ, Youngs TG, Soper AK, Grey CP, Clarke SM.
PMID: 26513141
J Phys Chem B. 2015 Dec 10;119(49):15320-33. doi: 10.1021/acs.jpcb.5b08248. Epub 2015 Dec 02.

Neutron diffraction with isotopic substitution has been used to characterize the bulk liquid structure of the technologically relevant electrolyte solution, 1 M tetrapropylammonium bromide (TPA Br) in acetonitrile (acn), and of pure deuterated acetonitrile. Empirical potential structure refinement modeling...

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Humphreys EK, Allan PK, Welbourn RJ, et al. A Neutron Diffraction Study of the Electrochemical Double Layer Capacitor Electrolyte Tetrapropylammonium Bromide in Acetonitrile. J Phys Chem B. 2015;119(49):15320-33doi: 10.1021/acs.jpcb.5b08248.
Humphreys, E. K., Allan, P. K., Welbourn, R. J., Youngs, T. G., Soper, A. K., Grey, C. P., & Clarke, S. M. (2015). A Neutron Diffraction Study of the Electrochemical Double Layer Capacitor Electrolyte Tetrapropylammonium Bromide in Acetonitrile. The journal of physical chemistry. B, 119(49), 15320-33. https://doi.org/10.1021/acs.jpcb.5b08248
Humphreys, Elizabeth K, et al. "A Neutron Diffraction Study of the Electrochemical Double Layer Capacitor Electrolyte Tetrapropylammonium Bromide in Acetonitrile." The journal of physical chemistry. B vol. 119,49 (2015): 15320-33. doi: https://doi.org/10.1021/acs.jpcb.5b08248
Humphreys EK, Allan PK, Welbourn RJ, Youngs TG, Soper AK, Grey CP, Clarke SM. A Neutron Diffraction Study of the Electrochemical Double Layer Capacitor Electrolyte Tetrapropylammonium Bromide in Acetonitrile. J Phys Chem B. 2015 Dec 10;119(49):15320-33. doi: 10.1021/acs.jpcb.5b08248. Epub 2015 Dec 02. PMID: 26513141.
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Structural, electronic and kinetic properties of the phase-change material Ge2Sb2Te5 in the liquid state.

Scientific reports

Schumacher M, Weber H, Jóvári P, Tsuchiya Y, Youngs TG, Kaban I, Mazzarello R.
PMID: 27272222
Sci Rep. 2016 Jun 08;6:27434. doi: 10.1038/srep27434.

Phase-change materials exhibit fast and reversible transitions between an amorphous and a crystalline state at high temperature. The two states display resistivity contrast, which is exploited in phase-change memory devices. The technologically most important family of phase-change materials consists...

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Schumacher M, Weber H, Jóvári P, et al. Structural, electronic and kinetic properties of the phase-change material Ge2Sb2Te5 in the liquid state. Sci Rep. 2016;6:27434doi: 10.1038/srep27434.
Schumacher, M., Weber, H., Jóvári, P., Tsuchiya, Y., Youngs, T. G., Kaban, I., & Mazzarello, R. (2016). Structural, electronic and kinetic properties of the phase-change material Ge2Sb2Te5 in the liquid state. Scientific reports, 627434. https://doi.org/10.1038/srep27434
Schumacher, Mathias, et al. "Structural, electronic and kinetic properties of the phase-change material Ge2Sb2Te5 in the liquid state." Scientific reports vol. 6 (2016): 27434. doi: https://doi.org/10.1038/srep27434
Schumacher M, Weber H, Jóvári P, Tsuchiya Y, Youngs TG, Kaban I, Mazzarello R. Structural, electronic and kinetic properties of the phase-change material Ge2Sb2Te5 in the liquid state. Sci Rep. 2016 Jun 08;6:27434. doi: 10.1038/srep27434. PMID: 27272222; PMCID: PMC4897623.
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S-(1-Oxido-2-pyridinyl)-1,1,3,3-tetramethylthiouronium Hexafluorophosphate. A New Reagent for Preparing Hindered Barton Esters.

The Journal of organic chemistry

Garner P, Anderson JT, Dey S, Youngs WJ, Galat K.
PMID: 11672163
J Org Chem. 1998 Aug 21;63(17):5732-5733. doi: 10.1021/jo980870n.

No abstract available.

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Garner P, Anderson JT, Dey S, et al. S-(1-Oxido-2-pyridinyl)-1,1,3,3-tetramethylthiouronium Hexafluorophosphate. A New Reagent for Preparing Hindered Barton Esters. J Org Chem. 1998;63(17):5732-5733doi: 10.1021/jo980870n.
Garner, P., Anderson, J. T., Dey, S., Youngs, W. J., & Galat, K. (1998). S-(1-Oxido-2-pyridinyl)-1,1,3,3-tetramethylthiouronium Hexafluorophosphate. A New Reagent for Preparing Hindered Barton Esters. The Journal of organic chemistry, 63(17), 5732-5733. https://doi.org/10.1021/jo980870n
Garner, Philip, et al. "S-(1-Oxido-2-pyridinyl)-1,1,3,3-tetramethylthiouronium Hexafluorophosphate. A New Reagent for Preparing Hindered Barton Esters." The Journal of organic chemistry vol. 63,17 (1998): 5732-5733. doi: https://doi.org/10.1021/jo980870n
Garner P, Anderson JT, Dey S, Youngs WJ, Galat K. S-(1-Oxido-2-pyridinyl)-1,1,3,3-tetramethylthiouronium Hexafluorophosphate. A New Reagent for Preparing Hindered Barton Esters. J Org Chem. 1998 Aug 21;63(17):5732-5733. doi: 10.1021/jo980870n. PMID: 11672163.
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A Novel High-Yield Synthesis of Substituted Isoindolequinones.

The Journal of organic chemistry

Chakraborty M, McConville DB, Koser GF, Tessier CA, Saito T, Rinaldi PL, Youngs WJ.
PMID: 11671931
J Org Chem. 1997 Nov 14;62(23):8193-8197. doi: 10.1021/jo971671r.

The high-yield, general, one-pot synthesis of substituted isoindolequinones, a group of important radiosensitizers which sensitize hypoxic cells to the lethal effect of radiation in cancer radiotherapy, is described. Primary amines react with 2,3-bis[2-(trimethylsilyl)ethynyl]-5,6-dimethylhydroquinone (2) in methanol at room temperature...

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Chakraborty M, McConville DB, Koser GF, et al. A Novel High-Yield Synthesis of Substituted Isoindolequinones. J Org Chem. 1997;62(23):8193-8197doi: 10.1021/jo971671r.
Chakraborty, M., McConville, D. B., Koser, G. F., Tessier, C. A., Saito, T., Rinaldi, P. L., & Youngs, W. J. (1997). A Novel High-Yield Synthesis of Substituted Isoindolequinones. The Journal of organic chemistry, 62(23), 8193-8197. https://doi.org/10.1021/jo971671r
Chakraborty, Manisha, et al. "A Novel High-Yield Synthesis of Substituted Isoindolequinones." The Journal of organic chemistry vol. 62,23 (1997): 8193-8197. doi: https://doi.org/10.1021/jo971671r
Chakraborty M, McConville DB, Koser GF, Tessier CA, Saito T, Rinaldi PL, Youngs WJ. A Novel High-Yield Synthesis of Substituted Isoindolequinones. J Org Chem. 1997 Nov 14;62(23):8193-8197. doi: 10.1021/jo971671r. PMID: 11671931.
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Reactions of Primary and Secondary Amines with Substituted Hydroquinones: Nuclear Amination, Side-Chain Amination, and Indolequinone Formation.

The Journal of organic chemistry

Chakraborty M, McConville DB, Niu Y, Tessier CA, Youngs WJ.
PMID: 11672419
J Org Chem. 1998 Oct 16;63(21):7563-7567. doi: 10.1021/jo980541v.

No abstract available.

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Chakraborty M, McConville DB, Niu Y, et al. Reactions of Primary and Secondary Amines with Substituted Hydroquinones: Nuclear Amination, Side-Chain Amination, and Indolequinone Formation. J Org Chem. 1998;63(21):7563-7567doi: 10.1021/jo980541v.
Chakraborty, M., McConville, D. B., Niu, Y., Tessier, C. A., & Youngs, W. J. (1998). Reactions of Primary and Secondary Amines with Substituted Hydroquinones: Nuclear Amination, Side-Chain Amination, and Indolequinone Formation. The Journal of organic chemistry, 63(21), 7563-7567. https://doi.org/10.1021/jo980541v
Chakraborty, Manisha, et al. "Reactions of Primary and Secondary Amines with Substituted Hydroquinones: Nuclear Amination, Side-Chain Amination, and Indolequinone Formation." The Journal of organic chemistry vol. 63,21 (1998): 7563-7567. doi: https://doi.org/10.1021/jo980541v
Chakraborty M, McConville DB, Niu Y, Tessier CA, Youngs WJ. Reactions of Primary and Secondary Amines with Substituted Hydroquinones: Nuclear Amination, Side-Chain Amination, and Indolequinone Formation. J Org Chem. 1998 Oct 16;63(21):7563-7567. doi: 10.1021/jo980541v. PMID: 11672419.
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Solution of the heawood map-coloring problem.

Proceedings of the National Academy of Sciences of the United States of America

Ringel G, Youngs JW.
PMID: 16591648
Proc Natl Acad Sci U S A. 1968 Jun;60(2):438-45. doi: 10.1073/pnas.60.2.438.

No abstract available.

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Ringel G, Youngs JW. Solution of the heawood map-coloring problem. Proc Natl Acad Sci U S A. 1968;60(2):438-45doi: 10.1073/pnas.60.2.438.
Ringel, G., & Youngs, J. W. (1968). Solution of the heawood map-coloring problem. Proceedings of the National Academy of Sciences of the United States of America, 60(2), 438-45. https://doi.org/10.1073/pnas.60.2.438
Ringel, G, and Youngs, J W. "Solution of the heawood map-coloring problem." Proceedings of the National Academy of Sciences of the United States of America vol. 60,2 (1968): 438-45. doi: https://doi.org/10.1073/pnas.60.2.438
Ringel G, Youngs JW. Solution of the heawood map-coloring problem. Proc Natl Acad Sci U S A. 1968 Jun;60(2):438-45. doi: 10.1073/pnas.60.2.438. PMID: 16591648; PMCID: PMC225066.
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A molecular dynamics study of glucose solvation in the ionic liquid 1,3-dimethylimidazolium chloride.

Chemphyschem : a European journal of chemical physics and physical chemistry

Youngs TG, Holbrey JD, Deetlefs M, Nieuwenhuyzen M, Costa Gomes MF, Hardacre C.
PMID: 17086590
Chemphyschem. 2006 Nov 13;7(11):2279-81. doi: 10.1002/cphc.200600569.

No abstract available.

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Youngs TG, Holbrey JD, Deetlefs M, et al. A molecular dynamics study of glucose solvation in the ionic liquid 1,3-dimethylimidazolium chloride. Chemphyschem. 2006;7(11):2279-81doi: 10.1002/cphc.200600569.
Youngs, T. G., Holbrey, J. D., Deetlefs, M., Nieuwenhuyzen, M., Costa Gomes, M. F., & Hardacre, C. (2006). A molecular dynamics study of glucose solvation in the ionic liquid 1,3-dimethylimidazolium chloride. Chemphyschem : a European journal of chemical physics and physical chemistry, 7(11), 2279-81. https://doi.org/10.1002/cphc.200600569
Youngs, Tristan G A, et al. "A molecular dynamics study of glucose solvation in the ionic liquid 1,3-dimethylimidazolium chloride." Chemphyschem : a European journal of chemical physics and physical chemistry vol. 7,11 (2006): 2279-81. doi: https://doi.org/10.1002/cphc.200600569
Youngs TG, Holbrey JD, Deetlefs M, Nieuwenhuyzen M, Costa Gomes MF, Hardacre C. A molecular dynamics study of glucose solvation in the ionic liquid 1,3-dimethylimidazolium chloride. Chemphyschem. 2006 Nov 13;7(11):2279-81. doi: 10.1002/cphc.200600569. PMID: 17086590.
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A Reduction Theorem Concerning the Representation Problem for Fréchet Varieties.

Proceedings of the National Academy of Sciences of the United States of America

Youngs JW.
PMID: 16578229
Proc Natl Acad Sci U S A. 1946 Dec;32(12):328-30. doi: 10.1073/pnas.32.12.328.

No abstract available.

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Youngs JW. A Reduction Theorem Concerning the Representation Problem for Fréchet Varieties. Proc Natl Acad Sci U S A. 1946;32(12):328-30doi: 10.1073/pnas.32.12.328.
Youngs, J. W. (1946). A Reduction Theorem Concerning the Representation Problem for Fréchet Varieties. Proceedings of the National Academy of Sciences of the United States of America, 32(12), 328-30. https://doi.org/10.1073/pnas.32.12.328
Youngs, J W. "A Reduction Theorem Concerning the Representation Problem for Fréchet Varieties." Proceedings of the National Academy of Sciences of the United States of America vol. 32,12 (1946): 328-30. doi: https://doi.org/10.1073/pnas.32.12.328
Youngs JW. A Reduction Theorem Concerning the Representation Problem for Fréchet Varieties. Proc Natl Acad Sci U S A. 1946 Dec;32(12):328-30. doi: 10.1073/pnas.32.12.328. PMID: 16578229; PMCID: PMC1078963.
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Solvent extraction and lanthanide complexation studies with new terdentate ligands containing two 1,3,5-triazine moieties.

Dalton transactions (Cambridge, England : 2003)

Drew MG, Hill C, Hudson MJ, Iveson PB, Madic C, Youngs TG.
PMID: 15356719
Dalton Trans. 2004 Jan 21;(2):244-51. doi: 10.1039/b312582c. Epub 2003 Dec 05.

The extracting agent 2,6-bis(4,6-di-pivaloylamino-1,3,5-triazin-2-yl)-pyridine (L(5)) in n-octanol was found, in synergy with 2-bromodecanoic acid, to give D(Am)/D(Eu) separation factors (SFs) between 2.4 and 3.7 when used to extract the metal ions from 0.02-0.12 M HNO(3). Slightly higher SFs (4-6)...

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Drew MG, Hill C, Hudson MJ, et al. Solvent extraction and lanthanide complexation studies with new terdentate ligands containing two 1,3,5-triazine moieties. Dalton Trans. 2003;(2):244-51doi: 10.1039/b312582c.
Drew, M. G., Hill, C., Hudson, M. J., Iveson, P. B., Madic, C., & Youngs, T. G. (2004). Solvent extraction and lanthanide complexation studies with new terdentate ligands containing two 1,3,5-triazine moieties. Dalton transactions (Cambridge, England : 2003), (2), 244-51. https://doi.org/10.1039/b312582c
Drew, Michael G B, et al. "Solvent extraction and lanthanide complexation studies with new terdentate ligands containing two 1,3,5-triazine moieties." Dalton transactions (Cambridge, England : 2003) vol. ,2 (2004): 244-51. doi: https://doi.org/10.1039/b312582c
Drew MG, Hill C, Hudson MJ, Iveson PB, Madic C, Youngs TG. Solvent extraction and lanthanide complexation studies with new terdentate ligands containing two 1,3,5-triazine moieties. Dalton Trans. 2004 Jan 21;(2):244-51. doi: 10.1039/b312582c. Epub 2003 Dec 05. PMID: 15356719.
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Apparatus for Collecting and Measuring the Gases evolved during Fermentation.

The Biochemical journal

Harden A, Thompson J, Young WJ.
PMID: 16742158
Biochem J. 1911;5(5):230-5. doi: 10.1042/bj0050230.

No abstract available.

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Harden A, Thompson J, Young WJ. Apparatus for Collecting and Measuring the Gases evolved during Fermentation. Biochem J. 1911;5(5):230-5doi: 10.1042/bj0050230.
Harden, A., Thompson, J., & Young, W. J. (1911). Apparatus for Collecting and Measuring the Gases evolved during Fermentation. The Biochemical journal, 5(5), 230-5. https://doi.org/10.1042/bj0050230
Harden, A, et al. "Apparatus for Collecting and Measuring the Gases evolved during Fermentation." The Biochemical journal vol. 5,5 (1911): 230-5. doi: https://doi.org/10.1042/bj0050230
Harden A, Thompson J, Young WJ. Apparatus for Collecting and Measuring the Gases evolved during Fermentation. Biochem J. 1911;5(5):230-5. doi: 10.1042/bj0050230. PMID: 16742158; PMCID: PMC1276362.
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Showing 1 to 12 of 447 entries