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Showing 1 to 12 of 106 entries
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SU-E-T-583: Feasibility of Constraining Dose to the Nausea Center (area Postrema and Dorsal Vagal Complex) in IMRT Treatment Planning of the Head and Neck.

Medical physics

Fontenla S, Wang T, Lee N, McCann P, Young R, Mechalakos J.
PMID: 28517096
Med Phys. 2012 Jun;39(6):3840. doi: 10.1118/1.4735672.

PURPOSE: Nausea and vomiting have been known to occur in patients undergoing external beam radiation treatments for head&neck cancers. We sought to determine the feasibility of limiting the dose delivered to the nausea center, area postrema (AP) and dorsal...

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Fontenla S, Wang T, Lee N, et al. SU-E-T-583: Feasibility of Constraining Dose to the Nausea Center (area Postrema and Dorsal Vagal Complex) in IMRT Treatment Planning of the Head and Neck. Med Phys. 2012;39(6):3840doi: 10.1118/1.4735672.
Fontenla, S., Wang, T., Lee, N., McCann, P., Young, R., & Mechalakos, J. (2012). SU-E-T-583: Feasibility of Constraining Dose to the Nausea Center (area Postrema and Dorsal Vagal Complex) in IMRT Treatment Planning of the Head and Neck. Medical physics, 39(6), 3840. https://doi.org/10.1118/1.4735672
Fontenla, S, et al. "SU-E-T-583: Feasibility of Constraining Dose to the Nausea Center (area Postrema and Dorsal Vagal Complex) in IMRT Treatment Planning of the Head and Neck." Medical physics vol. 39,6 (2012): 3840. doi: https://doi.org/10.1118/1.4735672
Fontenla S, Wang T, Lee N, McCann P, Young R, Mechalakos J. SU-E-T-583: Feasibility of Constraining Dose to the Nausea Center (area Postrema and Dorsal Vagal Complex) in IMRT Treatment Planning of the Head and Neck. Med Phys. 2012 Jun;39(6):3840. doi: 10.1118/1.4735672. PMID: 28517096.
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The influence of rotator cuff pathology on functional outcome in total shoulder replacement.

International journal of shoulder surgery

Ahearn N, McCann PA, Tasker A, Sarangi PP.
PMID: 24403759
Int J Shoulder Surg. 2013 Oct;7(4):127-31. doi: 10.4103/0973-6042.123509.

INTRODUCTION: Total shoulder replacement (TSR) is a reliable treatment for glenohumeral osteoarthritis. In addition to proper component orientation, successful arthroplasty requires accurate restoration of soft tissues forces around the joint to maximize function. We hypothesized that pathological changes within...

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Ahearn N, McCann PA, Tasker A, et al. The influence of rotator cuff pathology on functional outcome in total shoulder replacement. Int J Shoulder Surg. 2013;7(4):127-31doi: 10.4103/0973-6042.123509.
Ahearn, N., McCann, P. A., Tasker, A., & Sarangi, P. P. (2013). The influence of rotator cuff pathology on functional outcome in total shoulder replacement. International journal of shoulder surgery, 7(4), 127-31. https://doi.org/10.4103/0973-6042.123509
Ahearn, Nathanael, et al. "The influence of rotator cuff pathology on functional outcome in total shoulder replacement." International journal of shoulder surgery vol. 7,4 (2013): 127-31. doi: https://doi.org/10.4103/0973-6042.123509
Ahearn N, McCann PA, Tasker A, Sarangi PP. The influence of rotator cuff pathology on functional outcome in total shoulder replacement. Int J Shoulder Surg. 2013 Oct;7(4):127-31. doi: 10.4103/0973-6042.123509. PMID: 24403759; PMCID: PMC3883186.
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Copper-Catalyzed Aerobic Oxidations of Organic Molecules: Pathways for Two-Electron Oxidation with a Four-Electron Oxidant and a One-Electron Redox-Active Catalyst.

Accounts of chemical research

McCann SD, Stahl SS.
PMID: 26020118
Acc Chem Res. 2015 Jun 16;48(6):1756-66. doi: 10.1021/acs.accounts.5b00060. Epub 2015 May 28.

Selective oxidation reactions have extraordinary value in organic chemistry, ranging from the conversion of petrochemical feedstocks into industrial chemicals and polymer precursors to the introduction of heteroatom functional groups into pharmaceutical and agrochemical intermediates. Molecular oxygen (O2) would be...

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McCann SD, Stahl SS. Copper-Catalyzed Aerobic Oxidations of Organic Molecules: Pathways for Two-Electron Oxidation with a Four-Electron Oxidant and a One-Electron Redox-Active Catalyst. Acc Chem Res. 2015;48(6):1756-66doi: 10.1021/acs.accounts.5b00060.
McCann, S. D., & Stahl, S. S. (2015). Copper-Catalyzed Aerobic Oxidations of Organic Molecules: Pathways for Two-Electron Oxidation with a Four-Electron Oxidant and a One-Electron Redox-Active Catalyst. Accounts of chemical research, 48(6), 1756-66. https://doi.org/10.1021/acs.accounts.5b00060
McCann, Scott D, and Stahl, Shannon S. "Copper-Catalyzed Aerobic Oxidations of Organic Molecules: Pathways for Two-Electron Oxidation with a Four-Electron Oxidant and a One-Electron Redox-Active Catalyst." Accounts of chemical research vol. 48,6 (2015): 1756-66. doi: https://doi.org/10.1021/acs.accounts.5b00060
McCann SD, Stahl SS. Copper-Catalyzed Aerobic Oxidations of Organic Molecules: Pathways for Two-Electron Oxidation with a Four-Electron Oxidant and a One-Electron Redox-Active Catalyst. Acc Chem Res. 2015 Jun 16;48(6):1756-66. doi: 10.1021/acs.accounts.5b00060. Epub 2015 May 28. PMID: 26020118.
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Second-Order Biomimicry: In Situ Oxidative Self-Processing Converts Copper(I)/Diamine Precursor into a Highly Active Aerobic Oxidation Catalyst.

ACS central science

McCann SD, Lumb JP, Arndtsen BA, Stahl SS.
PMID: 28470049
ACS Cent Sci. 2017 Apr 26;3(4):314-321. doi: 10.1021/acscentsci.7b00022. Epub 2017 Feb 24.

A homogeneous Cu-based catalyst system consisting of [Cu(MeCN)

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McCann SD, Lumb JP, Arndtsen BA, et al. Second-Order Biomimicry: In Situ Oxidative Self-Processing Converts Copper(I)/Diamine Precursor into a Highly Active Aerobic Oxidation Catalyst. ACS Cent Sci. 2017;3(4):314-321doi: 10.1021/acscentsci.7b00022.
McCann, S. D., Lumb, J. P., Arndtsen, B. A., & Stahl, S. S. (2017). Second-Order Biomimicry: In Situ Oxidative Self-Processing Converts Copper(I)/Diamine Precursor into a Highly Active Aerobic Oxidation Catalyst. ACS central science, 3(4), 314-321. https://doi.org/10.1021/acscentsci.7b00022
McCann, Scott D, et al. "Second-Order Biomimicry: In Situ Oxidative Self-Processing Converts Copper(I)/Diamine Precursor into a Highly Active Aerobic Oxidation Catalyst." ACS central science vol. 3,4 (2017): 314-321. doi: https://doi.org/10.1021/acscentsci.7b00022
McCann SD, Lumb JP, Arndtsen BA, Stahl SS. Second-Order Biomimicry: In Situ Oxidative Self-Processing Converts Copper(I)/Diamine Precursor into a Highly Active Aerobic Oxidation Catalyst. ACS Cent Sci. 2017 Apr 26;3(4):314-321. doi: 10.1021/acscentsci.7b00022. Epub 2017 Feb 24. PMID: 28470049; PMCID: PMC5408333.
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Real-time diode laser measurements of vapor-phase benzene.

Analytical chemistry

Jeffers JD, Roller CB, Namjou K, Evans MA, McSpadden L, Grego J, McCann PJ.
PMID: 14719893
Anal Chem. 2004 Jan 15;76(2):424-32. doi: 10.1021/ac0345392.

An absorption spectrometer equipped with a IV-VI semiconductor tunable mid-IR diode laser was used to make sensitive measurements of benzene (C(6)H(6)) gas in the 5.1-microm spectral range. Wavelength modulation coupled with second-harmonic detection achieved accurate real-time quantification of benzene...

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Jeffers JD, Roller CB, Namjou K, et al. Real-time diode laser measurements of vapor-phase benzene. Anal Chem. 2004;76(2):424-32doi: 10.1021/ac0345392.
Jeffers, J. D., Roller, C. B., Namjou, K., Evans, M. A., McSpadden, L., Grego, J., & McCann, P. J. (2004). Real-time diode laser measurements of vapor-phase benzene. Analytical chemistry, 76(2), 424-32. https://doi.org/10.1021/ac0345392
Jeffers, J D, et al. "Real-time diode laser measurements of vapor-phase benzene." Analytical chemistry vol. 76,2 (2004): 424-32. doi: https://doi.org/10.1021/ac0345392
Jeffers JD, Roller CB, Namjou K, Evans MA, McSpadden L, Grego J, McCann PJ. Real-time diode laser measurements of vapor-phase benzene. Anal Chem. 2004 Jan 15;76(2):424-32. doi: 10.1021/ac0345392. PMID: 14719893.
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Dissociation of the ground state vinoxy radical and its photolytic precursor chloroacetaldehyde: electronic nonadiabaticity and the suppression of the H+ketene channel.

The Journal of chemical physics

Miller JL, McCunn LR, Krisch MJ, Butler LJ, Shu J.
PMID: 15260734
J Chem Phys. 2004 Jul 22;121(4):1830-8. doi: 10.1063/1.1765653.

This work is a study of the competition between the two unimolecular reaction channels available to the vinoxy radical (CH(2)CHO), C-H fission to form H+ketene, and isomerization to the acetyl radical (CH(3)CO) followed by C-C fission to form CH(3)...

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Miller JL, McCunn LR, Krisch MJ, et al. Dissociation of the ground state vinoxy radical and its photolytic precursor chloroacetaldehyde: electronic nonadiabaticity and the suppression of the H+ketene channel. J Chem Phys. 2004;121(4):1830-8doi: 10.1063/1.1765653.
Miller, J. L., McCunn, L. R., Krisch, M. J., Butler, L. J., & Shu, J. (2004). Dissociation of the ground state vinoxy radical and its photolytic precursor chloroacetaldehyde: electronic nonadiabaticity and the suppression of the H+ketene channel. The Journal of chemical physics, 121(4), 1830-8. https://doi.org/10.1063/1.1765653
Miller, Johanna L, et al. "Dissociation of the ground state vinoxy radical and its photolytic precursor chloroacetaldehyde: electronic nonadiabaticity and the suppression of the H+ketene channel." The Journal of chemical physics vol. 121,4 (2004): 1830-8. doi: https://doi.org/10.1063/1.1765653
Miller JL, McCunn LR, Krisch MJ, Butler LJ, Shu J. Dissociation of the ground state vinoxy radical and its photolytic precursor chloroacetaldehyde: electronic nonadiabaticity and the suppression of the H+ketene channel. J Chem Phys. 2004 Jul 22;121(4):1830-8. doi: 10.1063/1.1765653. PMID: 15260734.
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Ornithine decarboxylase, polyamines, and pyrrolizidine alkaloids in senecio and crotalaria.

Plant physiology

Birecka H, Birecki M, Cohen EJ, Bitonti AJ, McCann PP.
PMID: 16665870
Plant Physiol. 1988 Jan;86(1):224-30. doi: 10.1104/pp.86.1.224.

When tested for ornithine and arginine decarboxylases, pyrrolizidine alkaloid-bearing Senecio riddellii, S. longilobus (Compositae), and Crotalaria retusa (Leguminosae) plants exhibited only ornithine decarboxylase activity. This contrasts with previous studies of four species of pyrrolizidine alkaloid-bearing Heliotropium (Boraginaceae) in which...

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Birecka H, Birecki M, Cohen EJ, et al. Ornithine decarboxylase, polyamines, and pyrrolizidine alkaloids in senecio and crotalaria. Plant Physiol. 1988;86(1):224-30doi: 10.1104/pp.86.1.224.
Birecka, H., Birecki, M., Cohen, E. J., Bitonti, A. J., & McCann, P. P. (1988). Ornithine decarboxylase, polyamines, and pyrrolizidine alkaloids in senecio and crotalaria. Plant physiology, 86(1), 224-30. https://doi.org/10.1104/pp.86.1.224
Birecka, H, et al. "Ornithine decarboxylase, polyamines, and pyrrolizidine alkaloids in senecio and crotalaria." Plant physiology vol. 86,1 (1988): 224-30. doi: https://doi.org/10.1104/pp.86.1.224
Birecka H, Birecki M, Cohen EJ, Bitonti AJ, McCann PP. Ornithine decarboxylase, polyamines, and pyrrolizidine alkaloids in senecio and crotalaria. Plant Physiol. 1988 Jan;86(1):224-30. doi: 10.1104/pp.86.1.224. PMID: 16665870; PMCID: PMC1054458.
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Assaying ornithine and arginine decarboxylases in some plant species.

Plant physiology

Birecka H, Bitonti AJ, McCann PP.
PMID: 16664441
Plant Physiol. 1985 Oct;79(2):509-14. doi: 10.1104/pp.79.2.509.

A release of (14)CO(2) not related to ornithine decarboxylase activity was found in crude leaf extracts from Lycopersicon esculentum, Avena sativa, and especially from the pyrrolizidine alkaloid-bearing Heliotropium angiospermum when incubated with [1-(14)C]- or [U-(14)C]ornithine. The total (14)CO(2) produced...

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Birecka H, Bitonti AJ, McCann PP. Assaying ornithine and arginine decarboxylases in some plant species. Plant Physiol. 1985;79(2):509-14doi: 10.1104/pp.79.2.509.
Birecka, H., Bitonti, A. J., & McCann, P. P. (1985). Assaying ornithine and arginine decarboxylases in some plant species. Plant physiology, 79(2), 509-14. https://doi.org/10.1104/pp.79.2.509
Birecka, H, et al. "Assaying ornithine and arginine decarboxylases in some plant species." Plant physiology vol. 79,2 (1985): 509-14. doi: https://doi.org/10.1104/pp.79.2.509
Birecka H, Bitonti AJ, McCann PP. Assaying ornithine and arginine decarboxylases in some plant species. Plant Physiol. 1985 Oct;79(2):509-14. doi: 10.1104/pp.79.2.509. PMID: 16664441; PMCID: PMC1074916.
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Response of photosynthesis and cellular antioxidants to ozone in populus leaves.

Plant physiology

Gupta AS, Alscher RG, McCune D.
PMID: 16668235
Plant Physiol. 1991 Jun;96(2):650-5. doi: 10.1104/pp.96.2.650.

Atmospheric ozone causes formation of various highly reactive intermediates (e.g. peroxyl and superoxide radicals, H(2)O(2), etc.) in plant tissues. A plant's productivity in environments with ozone may be related to its ability to scavenge the free radicals formed. The...

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Gupta AS, Alscher RG, McCune D. Response of photosynthesis and cellular antioxidants to ozone in populus leaves. Plant Physiol. 1991;96(2):650-5doi: 10.1104/pp.96.2.650.
Gupta, A. S., Alscher, R. G., & McCune, D. (1991). Response of photosynthesis and cellular antioxidants to ozone in populus leaves. Plant physiology, 96(2), 650-5. https://doi.org/10.1104/pp.96.2.650
Gupta, A S, et al. "Response of photosynthesis and cellular antioxidants to ozone in populus leaves." Plant physiology vol. 96,2 (1991): 650-5. doi: https://doi.org/10.1104/pp.96.2.650
Gupta AS, Alscher RG, McCune D. Response of photosynthesis and cellular antioxidants to ozone in populus leaves. Plant Physiol. 1991 Jun;96(2):650-5. doi: 10.1104/pp.96.2.650. PMID: 16668235; PMCID: PMC1080820.
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Customer satisfaction: are hospitals "hospitable"?.

American journal of orthopedics (Belle Mead, N.J.)

McCann PD.
PMID: 16584076
Am J Orthop (Belle Mead NJ). 2006 Feb;35(2):59.

No abstract available.

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McCann PD. Customer satisfaction: are hospitals "hospitable"?. Am J Orthop (Belle Mead NJ). 2006;35(2):59
McCann, P. D. (2006). Customer satisfaction: are hospitals "hospitable"?. American journal of orthopedics (Belle Mead, N.J.), 35(2), 59.
McCann, Peter D. "Customer satisfaction: are hospitals "hospitable"?." American journal of orthopedics (Belle Mead, N.J.) vol. 35,2 (2006): 59.
McCann PD. Customer satisfaction: are hospitals "hospitable"?. Am J Orthop (Belle Mead NJ). 2006 Feb;35(2):59. PMID: 16584076.
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A study of the unimolecular dissociation of the 2-buten-2-yl radical via the 193 nm photodissociation of 2-chloro-2-butene.

The journal of physical chemistry. A

McCunn LR, Krisch MJ, Liu Y, Butler LJ, Shu J.
PMID: 16833987
J Phys Chem A. 2005 Jul 28;109(29):6430-9. doi: 10.1021/jp050970e.

This work investigates the unimolecular dissociation of the 2-buten-2-yl radical. This radical has three potentially competing reaction pathways: C-C fission to form CH3 + propyne, C-H fission to form H + 1,2-butadiene, and C-H fission to produce H +...

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McCunn LR, Krisch MJ, Liu Y, et al. A study of the unimolecular dissociation of the 2-buten-2-yl radical via the 193 nm photodissociation of 2-chloro-2-butene. J Phys Chem A. 2005;109(29):6430-9doi: 10.1021/jp050970e.
McCunn, L. R., Krisch, M. J., Liu, Y., Butler, L. J., & Shu, J. (2005). A study of the unimolecular dissociation of the 2-buten-2-yl radical via the 193 nm photodissociation of 2-chloro-2-butene. The journal of physical chemistry. A, 109(29), 6430-9. https://doi.org/10.1021/jp050970e
McCunn, Laura R, et al. "A study of the unimolecular dissociation of the 2-buten-2-yl radical via the 193 nm photodissociation of 2-chloro-2-butene." The journal of physical chemistry. A vol. 109,29 (2005): 6430-9. doi: https://doi.org/10.1021/jp050970e
McCunn LR, Krisch MJ, Liu Y, Butler LJ, Shu J. A study of the unimolecular dissociation of the 2-buten-2-yl radical via the 193 nm photodissociation of 2-chloro-2-butene. J Phys Chem A. 2005 Jul 28;109(29):6430-9. doi: 10.1021/jp050970e. PMID: 16833987.
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Rapid gel-like latex film formation through controlled ionic coacervation of latex polymer particles containing strong cationic and protonated weak acid functionalities.

Langmuir : the ACS journal of surfaces and colloids

Rose GD, Harris JK, McCann GD, Weishuhn JM, Schmidt DL.
PMID: 15697260
Langmuir. 2005 Feb 15;21(4):1192-200. doi: 10.1021/la048309+.

We introduce a controlled ionic coacervation (CIC) process that rapidly forms uniform, gel-like latex films with significant mechanical integrity without loss of water from the film. This process uses latex particles that contain both strong cationic charges and weak...

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Rose GD, Harris JK, McCann GD, et al. Rapid gel-like latex film formation through controlled ionic coacervation of latex polymer particles containing strong cationic and protonated weak acid functionalities. Langmuir. 2005;21(4):1192-200doi: 10.1021/la048309+.
Rose, G. D., Harris, J. K., McCann, G. D., Weishuhn, J. M., & Schmidt, D. L. (2005). Rapid gel-like latex film formation through controlled ionic coacervation of latex polymer particles containing strong cationic and protonated weak acid functionalities. Langmuir : the ACS journal of surfaces and colloids, 21(4), 1192-200. https://doi.org/10.1021/la048309+
Rose, Gene D, et al. "Rapid gel-like latex film formation through controlled ionic coacervation of latex polymer particles containing strong cationic and protonated weak acid functionalities." Langmuir : the ACS journal of surfaces and colloids vol. 21,4 (2005): 1192-200. doi: https://doi.org/10.1021/la048309+
Rose GD, Harris JK, McCann GD, Weishuhn JM, Schmidt DL. Rapid gel-like latex film formation through controlled ionic coacervation of latex polymer particles containing strong cationic and protonated weak acid functionalities. Langmuir. 2005 Feb 15;21(4):1192-200. doi: 10.1021/la048309+. PMID: 15697260.
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Showing 1 to 12 of 106 entries