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Anatomical Variations in Clefts of the Lip with or without Cleft Palate.

Plastic surgery international

Carroll K, Mossey PA.
PMID: 23251795
Plast Surg Int. 2012;2012:542078. doi: 10.1155/2012/542078. Epub 2012 Nov 29.

Objective. Few orofacial cleft (OFC) studies have examined the severity of clefts of the lip or palate. This study examined associations between the severity of cleft of the lip with cleft type, laterality, and sex in four regional British...

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Carroll K, Mossey PA. Anatomical Variations in Clefts of the Lip with or without Cleft Palate. Plast Surg Int. 2012;2012:542078doi: 10.1155/2012/542078.
Carroll, K., & Mossey, P. A. (2012). Anatomical Variations in Clefts of the Lip with or without Cleft Palate. Plastic surgery international, 2012542078. https://doi.org/10.1155/2012/542078
Carroll, K, and Mossey, P A. "Anatomical Variations in Clefts of the Lip with or without Cleft Palate." Plastic surgery international vol. 2012 (2012): 542078. doi: https://doi.org/10.1155/2012/542078
Carroll K, Mossey PA. Anatomical Variations in Clefts of the Lip with or without Cleft Palate. Plast Surg Int. 2012;2012:542078. doi: 10.1155/2012/542078. Epub 2012 Nov 29. PMID: 23251795; PMCID: PMC3517834.
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Direct Observation of the Coulomb Correlation Gap in a Nonmetallic Semiconductor, Si:B.

Physical review letters

Lee M, Massey JG.
PMID: 10059861
Phys Rev Lett. 1995 Dec 04;75(23):4266-4269. doi: 10.1103/PhysRevLett.75.4266.

No abstract available.

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Lee M, Massey JG. Direct Observation of the Coulomb Correlation Gap in a Nonmetallic Semiconductor, Si:B. Phys Rev Lett. 1995;75(23):4266-4269doi: 10.1103/PhysRevLett.75.4266.
Lee, M., & Massey, J. G. (1995). Direct Observation of the Coulomb Correlation Gap in a Nonmetallic Semiconductor, Si:B. Physical review letters, 75(23), 4266-4269. https://doi.org/10.1103/PhysRevLett.75.4266
Lee, and Massey. "Direct Observation of the Coulomb Correlation Gap in a Nonmetallic Semiconductor, Si:B." Physical review letters vol. 75,23 (1995): 4266-4269. doi: https://doi.org/10.1103/PhysRevLett.75.4266
Lee M, Massey JG. Direct Observation of the Coulomb Correlation Gap in a Nonmetallic Semiconductor, Si:B. Phys Rev Lett. 1995 Dec 04;75(23):4266-4269. doi: 10.1103/PhysRevLett.75.4266. PMID: 10059861.
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Cognitive Functional Abilities in Parkinson's Disease: Agreement Between Patients and Informants.

Movement disorders clinical practice

Deck BL, Xie SX, Choi G, Rick J, Siderowf A, Rudovsky S, Chen-Plotkin A, Duda JE, Morley JF, Dahodwala N, Trojanowski JQ, Weintraub D.
PMID: 31392244
Mov Disord Clin Pract. 2019 May 17;6(6):440-445. doi: 10.1002/mdc3.12781. eCollection 2019 Jul.

BACKGROUND: The Penn Parkinson's Daily Activities Questionnaire-15 (PDAQ-15) assesses cognition-related instrumental activities of daily living (IADL) in Parkinson's disease (PD).OBJECTIVES: To assess the degree and predictors of disagreement between patients (PT) and knowledgeable informants (KI) on the PDAQ-15.METHODS: We...

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Deck BL, Xie SX, Choi G, et al. Cognitive Functional Abilities in Parkinson's Disease: Agreement Between Patients and Informants. Mov Disord Clin Pract. 2019;6(6):440-445doi: 10.1002/mdc3.12781.
Deck, B. L., Xie, S. X., Choi, G., Rick, J., Siderowf, A., Rudovsky, S., Chen-Plotkin, A., Duda, J. E., Morley, J. F., Dahodwala, N., Trojanowski, J. Q., & Weintraub, D. (2019). Cognitive Functional Abilities in Parkinson's Disease: Agreement Between Patients and Informants. Movement disorders clinical practice, 6(6), 440-445. https://doi.org/10.1002/mdc3.12781
Deck, Benjamin L, et al. "Cognitive Functional Abilities in Parkinson's Disease: Agreement Between Patients and Informants." Movement disorders clinical practice vol. 6,6 (2019): 440-445. doi: https://doi.org/10.1002/mdc3.12781
Deck BL, Xie SX, Choi G, Rick J, Siderowf A, Rudovsky S, Chen-Plotkin A, Duda JE, Morley JF, Dahodwala N, Trojanowski JQ, Weintraub D. Cognitive Functional Abilities in Parkinson's Disease: Agreement Between Patients and Informants. Mov Disord Clin Pract. 2019 May 17;6(6):440-445. doi: 10.1002/mdc3.12781. eCollection 2019 Jul. PMID: 31392244; PMCID: PMC6660222.
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Reaction-based Indicator displacement Assay (RIA) for the selective colorimetric and fluorometric detection of peroxynitrite.

Chemical science

Sun X, Lacina K, Ramsamy EC, Flower SE, Fossey JS, Qian X, Anslyn EV, Bull SD, James TD.
PMID: 28706677
Chem Sci. 2015 May 01;6(5):2963-2967. doi: 10.1039/c4sc03983a. Epub 2015 Mar 06.

Using the self-assembly of aromatic boronic acids with Alizarin Red S (ARS), we developed a new chemosensor for the selective detection of peroxynitrite. Phenylboronic acid (PBA), benzoboroxole (BBA) and 2-(

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Sun X, Lacina K, Ramsamy EC, et al. Reaction-based Indicator displacement Assay (RIA) for the selective colorimetric and fluorometric detection of peroxynitrite. Chem Sci. 2015;6(5):2963-2967doi: 10.1039/c4sc03983a.
Sun, X., Lacina, K., Ramsamy, E. C., Flower, S. E., Fossey, J. S., Qian, X., Anslyn, E. V., Bull, S. D., & James, T. D. (2015). Reaction-based Indicator displacement Assay (RIA) for the selective colorimetric and fluorometric detection of peroxynitrite. Chemical science, 6(5), 2963-2967. https://doi.org/10.1039/c4sc03983a
Sun, Xiaolong, et al. "Reaction-based Indicator displacement Assay (RIA) for the selective colorimetric and fluorometric detection of peroxynitrite." Chemical science vol. 6,5 (2015): 2963-2967. doi: https://doi.org/10.1039/c4sc03983a
Sun X, Lacina K, Ramsamy EC, Flower SE, Fossey JS, Qian X, Anslyn EV, Bull SD, James TD. Reaction-based Indicator displacement Assay (RIA) for the selective colorimetric and fluorometric detection of peroxynitrite. Chem Sci. 2015 May 01;6(5):2963-2967. doi: 10.1039/c4sc03983a. Epub 2015 Mar 06. PMID: 28706677; PMCID: PMC5490052.
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Additional data in the debate on stage I non-small cell lung cancer: surgery versus stereotactic ablative radiotherapy.

Annals of translational medicine

Simone CB, Dorsey JF.
PMID: 26366389
Ann Transl Med. 2015 Aug;3(13):172. doi: 10.3978/j.issn.2305-5839.2015.07.26.

Lobectomy has been the standard of care for patients with early stage non-small cell lung cancer (NSCLC), resulting in nearly universal local control and excellent overall survival. However, up to one-quarter of early stage patients are unable to undergo...

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Simone CB, Dorsey JF. Additional data in the debate on stage I non-small cell lung cancer: surgery versus stereotactic ablative radiotherapy. Ann Transl Med. 2015;3(13):172doi: 10.3978/j.issn.2305-5839.2015.07.26.
Simone, C. B., & Dorsey, J. F. (2015). Additional data in the debate on stage I non-small cell lung cancer: surgery versus stereotactic ablative radiotherapy. Annals of translational medicine, 3(13), 172. https://doi.org/10.3978/j.issn.2305-5839.2015.07.26
Simone, Charles B, and Dorsey, Jay F. "Additional data in the debate on stage I non-small cell lung cancer: surgery versus stereotactic ablative radiotherapy." Annals of translational medicine vol. 3,13 (2015): 172. doi: https://doi.org/10.3978/j.issn.2305-5839.2015.07.26
Simone CB, Dorsey JF. Additional data in the debate on stage I non-small cell lung cancer: surgery versus stereotactic ablative radiotherapy. Ann Transl Med. 2015 Aug;3(13):172. doi: 10.3978/j.issn.2305-5839.2015.07.26. PMID: 26366389; PMCID: PMC4543325.
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Asymmetric Synthesis of cis-3,4-Dihydrocoumarins via [4 + 2] Cycloadditions Catalyzed by Amidine Derivatives.

The Journal of organic chemistry

Jin JH, Li XY, Luo X, Fossey JS, Deng WP.
PMID: 28441490
J Org Chem. 2017 May 19;82(10):5424-5432. doi: 10.1021/acs.joc.7b00367. Epub 2017 May 01.

A highly efficient chiral amidine derivative-catalyzed tandem Michael addition/lactonization of carboxylic acids and o-quinone methides (o-QMs) has been developed that enables the asymmetric synthesis of cis-3,4-dihydrocoumarins bearing contiguous tertiary stereogenic centers in high yields with excellent stereoselectivities.

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Jin JH, Li XY, Luo X, et al. Asymmetric Synthesis of cis-3,4-Dihydrocoumarins via [4 + 2] Cycloadditions Catalyzed by Amidine Derivatives. J Org Chem. 2017;82(10):5424-5432doi: 10.1021/acs.joc.7b00367.
Jin, J. H., Li, X. Y., Luo, X., Fossey, J. S., & Deng, W. P. (2017). Asymmetric Synthesis of cis-3,4-Dihydrocoumarins via [4 + 2] Cycloadditions Catalyzed by Amidine Derivatives. The Journal of organic chemistry, 82(10), 5424-5432. https://doi.org/10.1021/acs.joc.7b00367
Jin, Jing-Hai, et al. "Asymmetric Synthesis of cis-3,4-Dihydrocoumarins via [4 + 2] Cycloadditions Catalyzed by Amidine Derivatives." The Journal of organic chemistry vol. 82,10 (2017): 5424-5432. doi: https://doi.org/10.1021/acs.joc.7b00367
Jin JH, Li XY, Luo X, Fossey JS, Deng WP. Asymmetric Synthesis of cis-3,4-Dihydrocoumarins via [4 + 2] Cycloadditions Catalyzed by Amidine Derivatives. J Org Chem. 2017 May 19;82(10):5424-5432. doi: 10.1021/acs.joc.7b00367. Epub 2017 May 01. PMID: 28441490.
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Vaxchora: The First FDA-Approved Cholera Vaccination in the United States.

P & T : a peer-reviewed journal for formulary management

Mosley JF, Smith LL, Brantley P, Locke D, Como M.
PMID: 29018300
P T. 2017 Oct;42(10):638-640.

Vaxchora is the first vaccine approved by the Food and Drug Administration for the prophylaxis of cholera infection. Cholera, a potentially life-threatening bacterial infection that occurs in the intestines and causes severe diarrhea and dehydration, has a low incidence...

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Mosley JF, Smith LL, Brantley P, et al. Vaxchora: The First FDA-Approved Cholera Vaccination in the United States. P T. 2017;42(10):638-640
Mosley, J. F., Smith, L. L., Brantley, P., Locke, D., & Como, M. (2017). Vaxchora: The First FDA-Approved Cholera Vaccination in the United States. P & T : a peer-reviewed journal for formulary management, 42(10), 638-640.
Mosley, Juan F, et al. "Vaxchora: The First FDA-Approved Cholera Vaccination in the United States." P & T : a peer-reviewed journal for formulary management vol. 42,10 (2017): 638-640.
Mosley JF, Smith LL, Brantley P, Locke D, Como M. Vaxchora: The First FDA-Approved Cholera Vaccination in the United States. P T. 2017 Oct;42(10):638-640. PMID: 29018300; PMCID: PMC5614415.
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Homogenization of three-dimensional metamaterial objects and validation by a fast surface-integral equation solver.

Optics express

Liu XX, Massey JW, Wu MF, Kim KT, Shore RA, Yılmaz AE, Alù A.
PMID: 24104066
Opt Express. 2013 Sep 23;21(19):21714-27. doi: 10.1364/OE.21.021714.

A homogenization model is applied to describe the wave interaction with finite three-dimensional metamaterial objects composed of periodic arrays of magnetodielectric spheres and is validated with full-wave numerical simulations. The homogenization is based on a dipolar model of the...

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Liu XX, Massey JW, Wu MF, et al. Homogenization of three-dimensional metamaterial objects and validation by a fast surface-integral equation solver. Opt Express. 2013;21(19):21714-27doi: 10.1364/OE.21.021714.
Liu, X. X., Massey, J. W., Wu, M. F., Kim, K. T., Shore, R. A., Yılmaz, A. E., & Alù, A. (2013). Homogenization of three-dimensional metamaterial objects and validation by a fast surface-integral equation solver. Optics express, 21(19), 21714-27. https://doi.org/10.1364/OE.21.021714
Liu, Xing-Xiang, et al. "Homogenization of three-dimensional metamaterial objects and validation by a fast surface-integral equation solver." Optics express vol. 21,19 (2013): 21714-27. doi: https://doi.org/10.1364/OE.21.021714
Liu XX, Massey JW, Wu MF, Kim KT, Shore RA, Yılmaz AE, Alù A. Homogenization of three-dimensional metamaterial objects and validation by a fast surface-integral equation solver. Opt Express. 2013 Sep 23;21(19):21714-27. doi: 10.1364/OE.21.021714. PMID: 24104066.
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Coetaneous catalytic kinetic resolution of alkynes and azides through asymmetric triazole formation.

Scientific reports

Brittain WDG, Dalling AG, Sun Z, Duff CSL, Male L, Buckley BR, Fossey JS.
PMID: 31636274
Sci Rep. 2019 Oct 21;9(1):15086. doi: 10.1038/s41598-019-50940-4.

A non-enzymatic simultaneous (coined coetaneous) kinetic resolution of a racemic alkyne and racemic azide, utilising an asymmetric CuAAC reaction is reported. The use of a CuCl (R,R)-Ph-Pybox catalyst system effects a simultaneous kinetic resolution of two racemic starting materials...

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Brittain WDG, Dalling AG, Sun Z, et al. Coetaneous catalytic kinetic resolution of alkynes and azides through asymmetric triazole formation. Sci Rep. 2019;9(1):15086doi: 10.1038/s41598-019-50940-4.
Brittain, W. D. G., Dalling, A. G., Sun, Z., Duff, C. S. L., Male, L., Buckley, B. R., & Fossey, J. S. (2019). Coetaneous catalytic kinetic resolution of alkynes and azides through asymmetric triazole formation. Scientific reports, 9(1), 15086. https://doi.org/10.1038/s41598-019-50940-4
Brittain, William D G, et al. "Coetaneous catalytic kinetic resolution of alkynes and azides through asymmetric triazole formation." Scientific reports vol. 9,1 (2019): 15086. doi: https://doi.org/10.1038/s41598-019-50940-4
Brittain WDG, Dalling AG, Sun Z, Duff CSL, Male L, Buckley BR, Fossey JS. Coetaneous catalytic kinetic resolution of alkynes and azides through asymmetric triazole formation. Sci Rep. 2019 Oct 21;9(1):15086. doi: 10.1038/s41598-019-50940-4. PMID: 31636274; PMCID: PMC6803658.
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Rigid and concave, 2,4-cis-substituted azetidine derivatives: A platform for asymmetric catalysis.

Scientific reports

Yoshizawa A, Feula A, Male L, Leach AG, Fossey JS.
PMID: 29695806
Sci Rep. 2018 Apr 25;8(1):6541. doi: 10.1038/s41598-018-24784-3.

A series of single enantiomer, 2,4-cis-disubstituted amino azetidines were synthesised and used as ligands for copper-catalysed Henry reactions of aldehydes with nitromethane. Optimisation of ligand substituents and the reaction conditions was conducted. The enantiomeric excess of the formed products...

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Yoshizawa A, Feula A, Male L, et al. Rigid and concave, 2,4-cis-substituted azetidine derivatives: A platform for asymmetric catalysis. Sci Rep. 2018;8(1):6541doi: 10.1038/s41598-018-24784-3.
Yoshizawa, A., Feula, A., Male, L., Leach, A. G., & Fossey, J. S. (2018). Rigid and concave, 2,4-cis-substituted azetidine derivatives: A platform for asymmetric catalysis. Scientific reports, 8(1), 6541. https://doi.org/10.1038/s41598-018-24784-3
Yoshizawa, Akina, et al. "Rigid and concave, 2,4-cis-substituted azetidine derivatives: A platform for asymmetric catalysis." Scientific reports vol. 8,1 (2018): 6541. doi: https://doi.org/10.1038/s41598-018-24784-3
Yoshizawa A, Feula A, Male L, Leach AG, Fossey JS. Rigid and concave, 2,4-cis-substituted azetidine derivatives: A platform for asymmetric catalysis. Sci Rep. 2018 Apr 25;8(1):6541. doi: 10.1038/s41598-018-24784-3. PMID: 29695806; PMCID: PMC5916886.
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Failure to collaborate?.

Journal of professional nursing : official journal of the American Association of Colleges of Nursing

Massey JA, Reimels EM.
PMID: 3503070
J Prof Nurs. 1986 Sep-Oct;2(5):276. doi: 10.1016/s8755-7223(86)80026-6.

No abstract available.

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Massey JA, Reimels EM. Failure to collaborate?. J Prof Nurs. 1986;2(5):276doi: 10.1016/s8755-7223(86)80026-6.
Massey, J. A., & Reimels, E. M. (1986). Failure to collaborate?. Journal of professional nursing : official journal of the American Association of Colleges of Nursing, 2(5), 276. https://doi.org/10.1016/s8755-7223(86)80026-6
Massey, J A, and Reimels, E M. "Failure to collaborate?." Journal of professional nursing : official journal of the American Association of Colleges of Nursing vol. 2,5 (1986): 276. doi: https://doi.org/10.1016/s8755-7223(86)80026-6
Massey JA, Reimels EM. Failure to collaborate?. J Prof Nurs. 1986 Sep-Oct;2(5):276. doi: 10.1016/s8755-7223(86)80026-6. PMID: 3503070.
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Proteomic profiling reveals biomarkers and pathways in type 2 diabetes risk.

JCI insight

Ngo D, Benson MD, Long JZ, Chen ZZ, Wang R, Nath AK, Keyes MJ, Shen D, Sinha S, Kuhn E, Morningstar JE, Shi X, Peterson BD, Chan C, Katz DH, Tahir UA, Farrell LA, Melander O, Mosley JD, Carr SA, Vasan RS, Larson MG, Smith JG, Wang TJ, Yang Q, Gerszten RE.
PMID: 33591955
JCI Insight. 2021 Mar 08;6(5). doi: 10.1172/jci.insight.144392.

Recent advances in proteomic technologies have made high-throughput profiling of low-abundance proteins in large epidemiological cohorts increasingly feasible. We investigated whether aptamer-based proteomic profiling could identify biomarkers associated with future development of type 2 diabetes (T2DM) beyond known risk...

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Ngo D, Benson MD, Long JZ, et al. Proteomic profiling reveals biomarkers and pathways in type 2 diabetes risk. JCI Insight. 2021;6(5)doi: 10.1172/jci.insight.144392.
Ngo, D., Benson, M. D., Long, J. Z., Chen, Z. Z., Wang, R., Nath, A. K., Keyes, M. J., Shen, D., Sinha, S., Kuhn, E., Morningstar, J. E., Shi, X., Peterson, B. D., Chan, C., Katz, D. H., Tahir, U. A., Farrell, L. A., Melander, O., Mosley, J. D., Carr, S. A., Vasan, R. S., Larson, M. G., Smith, J. G., Wang, T. J., Yang, Q., & Gerszten, R. E. (2021). Proteomic profiling reveals biomarkers and pathways in type 2 diabetes risk. JCI insight, 6(5), . https://doi.org/10.1172/jci.insight.144392
Ngo, Debby, et al. "Proteomic profiling reveals biomarkers and pathways in type 2 diabetes risk." JCI insight vol. 6,5 (2021). doi: https://doi.org/10.1172/jci.insight.144392
Ngo D, Benson MD, Long JZ, Chen ZZ, Wang R, Nath AK, Keyes MJ, Shen D, Sinha S, Kuhn E, Morningstar JE, Shi X, Peterson BD, Chan C, Katz DH, Tahir UA, Farrell LA, Melander O, Mosley JD, Carr SA, Vasan RS, Larson MG, Smith JG, Wang TJ, Yang Q, Gerszten RE. Proteomic profiling reveals biomarkers and pathways in type 2 diabetes risk. JCI Insight. 2021 Mar 08;6(5). doi: 10.1172/jci.insight.144392. PMID: 33591955; PMCID: PMC8021115.
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Showing 13 to 24 of 176 entries