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Showing 349 to 353 of 353 entries
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Is semantic processing impaired near the hands?.

Acta psychologica

Grossi G, Olmstead AJ, Stoudt S.
PMID: 34739901
Acta Psychol (Amst). 2021 Oct 30;221:103443. doi: 10.1016/j.actpsy.2021.103443. Epub 2021 Oct 30.

In a sentence decision task, Davoli et al. (2010) found that the semantic analysis of sentences differed depending on whether the participants' hands were close to or far from the computer screen. According to the authors, the findings reflected...

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Grossi G, Olmstead AJ, Stoudt S. Is semantic processing impaired near the hands?. Acta Psychol (Amst). 2021;221:103443doi: 10.1016/j.actpsy.2021.103443.
Grossi, G., Olmstead, A. J., & Stoudt, S. (2021). Is semantic processing impaired near the hands?. Acta psychologica, 221103443. https://doi.org/10.1016/j.actpsy.2021.103443
Grossi, Giordana, et al. "Is semantic processing impaired near the hands?." Acta psychologica vol. 221 (2021): 103443. doi: https://doi.org/10.1016/j.actpsy.2021.103443
Grossi G, Olmstead AJ, Stoudt S. Is semantic processing impaired near the hands?. Acta Psychol (Amst). 2021 Oct 30;221:103443. doi: 10.1016/j.actpsy.2021.103443. Epub 2021 Oct 30. PMID: 34739901.
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Benefits of auditory-verbal intervention for adult cochlear implant users: perspectives of users and their coaches.

International journal of audiology

Fitzpatrick EM, Carrier V, Turgeon G, Olmstead T, McAfee A, Whittingham J, Schramm D.
PMID: 35015968
Int J Audiol. 2022 Jan 11;1-10. doi: 10.1080/14992027.2021.1993361. Epub 2022 Jan 11.

OBJECTIVE: Post-implant rehabilitation is limited for adult cochlear implant (CI) recipients. The objective of this research was to capture the perspectives of CI users and their coaches regarding their experiences with auditory-verbal intervention as an example of post-implant rehabilitation...

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Fitzpatrick EM, Carrier V, Turgeon G, et al. Benefits of auditory-verbal intervention for adult cochlear implant users: perspectives of users and their coaches. Int J Audiol. 2022;1-10doi: 10.1080/14992027.2021.1993361.
Fitzpatrick, E. M., Carrier, V., Turgeon, G., Olmstead, T., McAfee, A., Whittingham, J., & Schramm, D. (2022). Benefits of auditory-verbal intervention for adult cochlear implant users: perspectives of users and their coaches. International journal of audiology, 1-10. https://doi.org/10.1080/14992027.2021.1993361
Fitzpatrick, Elizabeth M, et al. "Benefits of auditory-verbal intervention for adult cochlear implant users: perspectives of users and their coaches." International journal of audiology vol. (2022): 1-10. doi: https://doi.org/10.1080/14992027.2021.1993361
Fitzpatrick EM, Carrier V, Turgeon G, Olmstead T, McAfee A, Whittingham J, Schramm D. Benefits of auditory-verbal intervention for adult cochlear implant users: perspectives of users and their coaches. Int J Audiol. 2022 Jan 11;1-10. doi: 10.1080/14992027.2021.1993361. Epub 2022 Jan 11. PMID: 35015968.
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Dipeptide Surrogates Containing Asparagine-Derived Tetrahydropyrimidinones:  Structure and Amide Rotomer Stereochemistry of a Proline Mimic.

The Journal of organic chemistry

Konopelski JP, Wei Y, Olmstead MM.
PMID: 34237879
J Org Chem. 1999 Jul 09;64(14):5148-5151. doi: 10.1021/jo9901790.

Novel dipeptide surrogates Fmoc-Xaa-(cyclo)Asn-OBu

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Konopelski JP, Wei Y, Olmstead MM. Dipeptide Surrogates Containing Asparagine-Derived Tetrahydropyrimidinones:  Structure and Amide Rotomer Stereochemistry of a Proline Mimic. J Org Chem. 1999;64(14):5148-5151doi: 10.1021/jo9901790.
Konopelski, J. P., Wei, Y., & Olmstead, M. M. (1999). Dipeptide Surrogates Containing Asparagine-Derived Tetrahydropyrimidinones:  Structure and Amide Rotomer Stereochemistry of a Proline Mimic. The Journal of organic chemistry, 64(14), 5148-5151. https://doi.org/10.1021/jo9901790
Konopelski, Joseph P, et al. "Dipeptide Surrogates Containing Asparagine-Derived Tetrahydropyrimidinones:  Structure and Amide Rotomer Stereochemistry of a Proline Mimic." The Journal of organic chemistry vol. 64,14 (1999): 5148-5151. doi: https://doi.org/10.1021/jo9901790
Konopelski JP, Wei Y, Olmstead MM. Dipeptide Surrogates Containing Asparagine-Derived Tetrahydropyrimidinones:  Structure and Amide Rotomer Stereochemistry of a Proline Mimic. J Org Chem. 1999 Jul 09;64(14):5148-5151. doi: 10.1021/jo9901790. PMID: 34237879.
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The PhyloCode, types, ranks and monophyly: a response to Pickett.

Cladistics : the international journal of the Willi Hennig Society

Laurin M, de Queiroz K, Cantino P, Cellinese N, Olmstead R.
PMID: 34892947
Cladistics. 2005 Dec;21(6):605-607. doi: 10.1111/j.1096-0031.2005.00090.x.

A report from the First International Phylogenetic Nomenclature Meeting recently published in Cladistics conveys several misconceptions about the PhyloCode and presents an erroneous interpretation of discussions that took place at that meeting. Contrary to Pickett's assertions, the PhyloCode is...

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Laurin M, de Queiroz K, Cantino P, et al. The PhyloCode, types, ranks and monophyly: a response to Pickett. Cladistics. 2005;21(6):605-607doi: 10.1111/j.1096-0031.2005.00090.x.
Laurin, M., de Queiroz, K., Cantino, P., Cellinese, N., & Olmstead, R. (2005). The PhyloCode, types, ranks and monophyly: a response to Pickett. Cladistics : the international journal of the Willi Hennig Society, 21(6), 605-607. https://doi.org/10.1111/j.1096-0031.2005.00090.x
Laurin, Michel, et al. "The PhyloCode, types, ranks and monophyly: a response to Pickett." Cladistics : the international journal of the Willi Hennig Society vol. 21,6 (2005): 605-607. doi: https://doi.org/10.1111/j.1096-0031.2005.00090.x
Laurin M, de Queiroz K, Cantino P, Cellinese N, Olmstead R. The PhyloCode, types, ranks and monophyly: a response to Pickett. Cladistics. 2005 Dec;21(6):605-607. doi: 10.1111/j.1096-0031.2005.00090.x. PMID: 34892947.
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Single samarium atoms in large fullerene cages. Characterization of two isomers of Sm@C92 and four isomers of Sm@C94 with the X-ray crystallographic identification of Sm@C1(42)-C92, Sm@C(s)(24)-C92, and Sm@C3v(134)-C94.

Journal of the American Chemical Society

Jin H, Yang H, Yu M, Liu Z, Beavers CM, Olmstead MM, Balch AL.
PMID: 22536841
J Am Chem Soc. 2012 Jul 04;134(26):10933-41. doi: 10.1021/ja302859r. Epub 2012 Jun 25.

Two isomers of Sm@C(92) and four isomers of Sm@C(94) were isolated from carbon soot obtained by electric arc vaporization of carbon rods doped with Sm(2)O(3). Analysis of the structures by single-crystal X-ray diffraction on cocrystals formed with Ni(II)(octaethylporphyrin) reveals...

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Jin H, Yang H, Yu M, et al. Single samarium atoms in large fullerene cages. Characterization of two isomers of Sm@C92 and four isomers of Sm@C94 with the X-ray crystallographic identification of Sm@C1(42)-C92, Sm@C(s)(24)-C92, and Sm@C3v(134)-C94. J Am Chem Soc. 2012;134(26):10933-41doi: 10.1021/ja302859r.
Jin, H., Yang, H., Yu, M., Liu, Z., Beavers, C. M., Olmstead, M. M., & Balch, A. L. (2012). Single samarium atoms in large fullerene cages. Characterization of two isomers of Sm@C92 and four isomers of Sm@C94 with the X-ray crystallographic identification of Sm@C1(42)-C92, Sm@C(s)(24)-C92, and Sm@C3v(134)-C94. Journal of the American Chemical Society, 134(26), 10933-41. https://doi.org/10.1021/ja302859r
Jin, Hongxiao, et al. "Single samarium atoms in large fullerene cages. Characterization of two isomers of Sm@C92 and four isomers of Sm@C94 with the X-ray crystallographic identification of Sm@C1(42)-C92, Sm@C(s)(24)-C92, and Sm@C3v(134)-C94." Journal of the American Chemical Society vol. 134,26 (2012): 10933-41. doi: https://doi.org/10.1021/ja302859r
Jin H, Yang H, Yu M, Liu Z, Beavers CM, Olmstead MM, Balch AL. Single samarium atoms in large fullerene cages. Characterization of two isomers of Sm@C92 and four isomers of Sm@C94 with the X-ray crystallographic identification of Sm@C1(42)-C92, Sm@C(s)(24)-C92, and Sm@C3v(134)-C94. J Am Chem Soc. 2012 Jul 04;134(26):10933-41. doi: 10.1021/ja302859r. Epub 2012 Jun 25. PMID: 22536841.
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Showing 349 to 353 of 353 entries