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Showing 1 to 12 of 434 entries
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Effectiveness of dietetic consultations in primary health care: a systematic review of randomized controlled trials

education interventions

Ball LE, Barnes KA, Ross LJ.
GSID: FLBXfXsBq78J
LJ Mitchell, LE Ball, LJ Ross, KA Barnes… - Journal of the Academy …, 2017 - Elsevier

Background A dietetic consultation is a structured process aimed at supporting individual patients to modify their dietary behaviors to improve health outcomes. The body of evidence …

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Mitchell, L. J., Ball, L. E., Ross, L. J., Barnes, K. A., & Williams, L. T. (2017). Effectiveness of dietetic consultations in primary health care: a systematic review of randomized controlled trials. Journal of the Academy of Nutrition and Dietetics, 117(12), 1941-1962.
Mitchell, Lana J., et al. "Effectiveness of dietetic consultations in primary health care: a systematic review of randomized controlled trials." Journal of the Academy of Nutrition and Dietetics 117.12 (2017): 1941-1962.
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Macrocyclization in the Design of Organic n-Type Electronic Materials.

Journal of the American Chemical Society

Ball M, Zhong Y, Fowler B, Zhang B, Li P, Etkin G, Paley DW, Decatur J, Dalsania AK, Li H, Xiao S, Ng F, Steigerwald ML, Nuckolls C.
PMID: 27666433
J Am Chem Soc. 2016 Oct 05;138(39):12861-12867. doi: 10.1021/jacs.6b05474. Epub 2016 Sep 26.

Here, we compare analogous cyclic and acyclic π-conjugated molecules as n-type electronic materials and find that the cyclic molecules have numerous benefits in organic photovoltaics. This is the first report of such a direct comparison. We designed two conjugated...

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Ball M, Zhong Y, Fowler B, et al. Macrocyclization in the Design of Organic n-Type Electronic Materials. J Am Chem Soc. 2016;138(39):12861-12867doi: 10.1021/jacs.6b05474.
Ball, M., Zhong, Y., Fowler, B., Zhang, B., Li, P., Etkin, G., Paley, D. W., Decatur, J., Dalsania, A. K., Li, H., Xiao, S., Ng, F., Steigerwald, M. L., & Nuckolls, C. (2016). Macrocyclization in the Design of Organic n-Type Electronic Materials. Journal of the American Chemical Society, 138(39), 12861-12867. https://doi.org/10.1021/jacs.6b05474
Ball, Melissa, et al. "Macrocyclization in the Design of Organic n-Type Electronic Materials." Journal of the American Chemical Society vol. 138,39 (2016): 12861-12867. doi: https://doi.org/10.1021/jacs.6b05474
Ball M, Zhong Y, Fowler B, Zhang B, Li P, Etkin G, Paley DW, Decatur J, Dalsania AK, Li H, Xiao S, Ng F, Steigerwald ML, Nuckolls C. Macrocyclization in the Design of Organic n-Type Electronic Materials. J Am Chem Soc. 2016 Oct 05;138(39):12861-12867. doi: 10.1021/jacs.6b05474. Epub 2016 Sep 26. PMID: 27666433.
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Cannabis use and treatment resistance in first episode psychosis: a natural language processing study.

Lancet (London, England)

Patel R, Wilson R, Jackson R, Ball M, Shetty H, Broadbent M, Stewart R, McGuire P, Bhattacharyya S.
PMID: 26312901
Lancet. 2015 Feb 26;385:S79. doi: 10.1016/S0140-6736(15)60394-4.

BACKGROUND: Cannabis is frequently used among individuals with first episode psychosis and is associated with poor clinical outcomes. However, little is known about the effect of cannabis use on the response to antipsychotic medications and how use could affect...

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Patel R, Wilson R, Jackson R, et al. Cannabis use and treatment resistance in first episode psychosis: a natural language processing study. Lancet. 2015;385:S79doi: 10.1016/S0140-6736(15)60394-4.
Patel, R., Wilson, R., Jackson, R., Ball, M., Shetty, H., Broadbent, M., Stewart, R., McGuire, P., & Bhattacharyya, S. (2015). Cannabis use and treatment resistance in first episode psychosis: a natural language processing study. Lancet (London, England), 385S79. https://doi.org/10.1016/S0140-6736(15)60394-4
Patel, Rashmi, et al. "Cannabis use and treatment resistance in first episode psychosis: a natural language processing study." Lancet (London, England) vol. 385 (2015): S79. doi: https://doi.org/10.1016/S0140-6736(15)60394-4
Patel R, Wilson R, Jackson R, Ball M, Shetty H, Broadbent M, Stewart R, McGuire P, Bhattacharyya S. Cannabis use and treatment resistance in first episode psychosis: a natural language processing study. Lancet. 2015 Feb 26;385:S79. doi: 10.1016/S0140-6736(15)60394-4. PMID: 26312901.
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Hydrophobically Modified siRNAs Silence Huntingtin mRNA in Primary Neurons and Mouse Brain.

Molecular therapy. Nucleic acids

Alterman JF, Hall LM, Coles AH, Hassler MR, Didiot MC, Chase K, Abraham J, Sottosanti E, Johnson E, Sapp E, Osborn MF, Difiglia M, Aronin N, Khvorova A.
PMID: 26623938
Mol Ther Nucleic Acids. 2015 Dec 01;4:e266. doi: 10.1038/mtna.2015.38.

Applications of RNA interference for neuroscience research have been limited by a lack of simple and efficient methods to deliver oligonucleotides to primary neurons in culture and to the brain. Here, we show that primary neurons rapidly internalize hydrophobically...

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Alterman JF, Hall LM, Coles AH, et al. Hydrophobically Modified siRNAs Silence Huntingtin mRNA in Primary Neurons and Mouse Brain. Mol Ther Nucleic Acids. 2015;4:e266doi: 10.1038/mtna.2015.38.
Alterman, J. F., Hall, L. M., Coles, A. H., Hassler, M. R., Didiot, M. C., Chase, K., Abraham, J., Sottosanti, E., Johnson, E., Sapp, E., Osborn, M. F., Difiglia, M., Aronin, N., & Khvorova, A. (2015). Hydrophobically Modified siRNAs Silence Huntingtin mRNA in Primary Neurons and Mouse Brain. Molecular therapy. Nucleic acids, 4e266. https://doi.org/10.1038/mtna.2015.38
Alterman, Julia F, et al. "Hydrophobically Modified siRNAs Silence Huntingtin mRNA in Primary Neurons and Mouse Brain." Molecular therapy. Nucleic acids vol. 4 (2015): e266. doi: https://doi.org/10.1038/mtna.2015.38
Alterman JF, Hall LM, Coles AH, Hassler MR, Didiot MC, Chase K, Abraham J, Sottosanti E, Johnson E, Sapp E, Osborn MF, Difiglia M, Aronin N, Khvorova A. Hydrophobically Modified siRNAs Silence Huntingtin mRNA in Primary Neurons and Mouse Brain. Mol Ther Nucleic Acids. 2015 Dec 01;4:e266. doi: 10.1038/mtna.2015.38. PMID: 26623938; PMCID: PMC5014532.
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Catalysis. Self-control tames the coupling of reactive radicals.

Science (New York, N.Y.)

Lloyd-Jones GC, Ball LT.
PMID: 25061190
Science. 2014 Jul 25;345(6195):381-2. doi: 10.1126/science.1256755. Epub 2014 Jul 24.

No abstract available.

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Lloyd-Jones GC, Ball LT. Catalysis. Self-control tames the coupling of reactive radicals. Science. 2014;345(6195):381-2doi: 10.1126/science.1256755.
Lloyd-Jones, G. C., & Ball, L. T. (2014). Catalysis. Self-control tames the coupling of reactive radicals. Science (New York, N.Y.), 345(6195), 381-2. https://doi.org/10.1126/science.1256755
Lloyd-Jones, Guy C, and Ball, Liam T. "Catalysis. Self-control tames the coupling of reactive radicals." Science (New York, N.Y.) vol. 345,6195 (2014): 381-2. doi: https://doi.org/10.1126/science.1256755
Lloyd-Jones GC, Ball LT. Catalysis. Self-control tames the coupling of reactive radicals. Science. 2014 Jul 25;345(6195):381-2. doi: 10.1126/science.1256755. Epub 2014 Jul 24. PMID: 25061190.
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Stepping into the Light: Conjugated Macrocycles with Donor-Acceptor Motifs.

ACS central science

Ball M, Nuckolls C.
PMID: 27163002
ACS Cent Sci. 2015 Nov 25;1(8):416-7. doi: 10.1021/acscentsci.5b00339. Epub 2015 Oct 27.

No abstract available.

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Ball M, Nuckolls C. Stepping into the Light: Conjugated Macrocycles with Donor-Acceptor Motifs. ACS Cent Sci. 2015;1(8):416-7doi: 10.1021/acscentsci.5b00339.
Ball, M., & Nuckolls, C. (2015). Stepping into the Light: Conjugated Macrocycles with Donor-Acceptor Motifs. ACS central science, 1(8), 416-7. https://doi.org/10.1021/acscentsci.5b00339
Ball, Melissa, and Nuckolls, Colin. "Stepping into the Light: Conjugated Macrocycles with Donor-Acceptor Motifs." ACS central science vol. 1,8 (2015): 416-7. doi: https://doi.org/10.1021/acscentsci.5b00339
Ball M, Nuckolls C. Stepping into the Light: Conjugated Macrocycles with Donor-Acceptor Motifs. ACS Cent Sci. 2015 Nov 25;1(8):416-7. doi: 10.1021/acscentsci.5b00339. Epub 2015 Oct 27. PMID: 27163002; PMCID: PMC4827538.
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Au-Catalyzed Biaryl Coupling To Generate 5- to 9-Membered Rings: Turnover-Limiting Reductive Elimination versus π-Complexation.

Journal of the American Chemical Society

Corrie TJ, Ball LT, Russell CA, Lloyd-Jones GC.
PMID: 27936749
J Am Chem Soc. 2017 Jan 11;139(1):245-254. doi: 10.1021/jacs.6b10018. Epub 2016 Dec 29.

The intramolecular gold-catalyzed arylation of arenes by aryl-trimethylsilanes has been investigated from both mechanistic and preparative aspects. The reaction generates 5- to 9-membered rings, and of the 44 examples studied, 10 include a heteroatom (N, O). Tethering of the...

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Corrie TJ, Ball LT, Russell CA, et al. Au-Catalyzed Biaryl Coupling To Generate 5- to 9-Membered Rings: Turnover-Limiting Reductive Elimination versus π-Complexation. J Am Chem Soc. 2016;139(1):245-254doi: 10.1021/jacs.6b10018.
Corrie, T. J., Ball, L. T., Russell, C. A., & Lloyd-Jones, G. C. (2017). Au-Catalyzed Biaryl Coupling To Generate 5- to 9-Membered Rings: Turnover-Limiting Reductive Elimination versus π-Complexation. Journal of the American Chemical Society, 139(1), 245-254. https://doi.org/10.1021/jacs.6b10018
Corrie, Tom J A, et al. "Au-Catalyzed Biaryl Coupling To Generate 5- to 9-Membered Rings: Turnover-Limiting Reductive Elimination versus π-Complexation." Journal of the American Chemical Society vol. 139,1 (2017): 245-254. doi: https://doi.org/10.1021/jacs.6b10018
Corrie TJ, Ball LT, Russell CA, Lloyd-Jones GC. Au-Catalyzed Biaryl Coupling To Generate 5- to 9-Membered Rings: Turnover-Limiting Reductive Elimination versus π-Complexation. J Am Chem Soc. 2017 Jan 11;139(1):245-254. doi: 10.1021/jacs.6b10018. Epub 2016 Dec 29. PMID: 27936749.
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Effects of halogens on European air-quality.

Faraday discussions

Sherwen T, Evans MJ, Sommariva R, Hollis LDJ, Ball SM, Monks PS, Reed C, Carpenter LJ, Lee JD, Forster G, Bandy B, Reeves CE, Bloss WJ.
PMID: 28581558
Faraday Discuss. 2017 Aug 24;200:75-100. doi: 10.1039/c7fd00026j.

Halogens (Cl, Br) have a profound influence on stratospheric ozone (O

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Sherwen T, Evans MJ, Sommariva R, et al. Effects of halogens on European air-quality. Faraday Discuss. 2017;200:75-100doi: 10.1039/c7fd00026j.
Sherwen, T., Evans, M. J., Sommariva, R., Hollis, L. D. J., Ball, S. M., Monks, P. S., Reed, C., Carpenter, L. J., Lee, J. D., Forster, G., Bandy, B., Reeves, C. E., & Bloss, W. J. (2017). Effects of halogens on European air-quality. Faraday discussions, 20075-100. https://doi.org/10.1039/c7fd00026j
Sherwen, T, et al. "Effects of halogens on European air-quality." Faraday discussions vol. 200 (2017): 75-100. doi: https://doi.org/10.1039/c7fd00026j
Sherwen T, Evans MJ, Sommariva R, Hollis LDJ, Ball SM, Monks PS, Reed C, Carpenter LJ, Lee JD, Forster G, Bandy B, Reeves CE, Bloss WJ. Effects of halogens on European air-quality. Faraday Discuss. 2017 Aug 24;200:75-100. doi: 10.1039/c7fd00026j. PMID: 28581558.
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Vertical or horizontal orientation of foot radiographs does not affect image interpretation.

Muscles, ligaments and tendons journal

Ferran NA, Ball L, Maffulli N.
PMID: 23738310
Muscles Ligaments Tendons J. 2013 Jan 21;2(4):278-81. Print 2012 Oct.

This study determined whether the orientation of dorsoplantar and oblique foot radiographs has an effect on radiograph interpretation. A test set of 50 consecutive foot radiographs were selected (25 with fractures, and 25 normal), and duplicated in the horizontal...

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Ferran NA, Ball L, Maffulli N. Vertical or horizontal orientation of foot radiographs does not affect image interpretation. Muscles Ligaments Tendons J. 2013;2(4):278-81
Ferran, N. A., Ball, L., & Maffulli, N. (2012). Vertical or horizontal orientation of foot radiographs does not affect image interpretation. Muscles, ligaments and tendons journal, 2(4), 278-81.
Ferran, Nicholas Antonio, et al. "Vertical or horizontal orientation of foot radiographs does not affect image interpretation." Muscles, ligaments and tendons journal vol. 2,4 (2012): 278-81.
Ferran NA, Ball L, Maffulli N. Vertical or horizontal orientation of foot radiographs does not affect image interpretation. Muscles Ligaments Tendons J. 2013 Jan 21;2(4):278-81. Print 2012 Oct. PMID: 23738310; PMCID: PMC3666538.
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GENE GENEALOGIES WITHIN THE ORGANISMAL PEDIGREES OF RANDOM-MATING POPULATIONS.

Evolution; international journal of organic evolution

Ball RM, Neigel JE, Avise JC.
PMID: 28564387
Evolution. 1990 Mar;44(2):360-370. doi: 10.1111/j.1558-5646.1990.tb05205.x.

Using computer simulations, we generated and analyzed genetic distances among selectively neutral haplotypes transmitted through gene genealogies with random-mating organismal pedigrees. Constraints and possible biases on haplotype distances due to correlated ancestry were evaluated by comparing observed distributions of...

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Ball RM, Neigel JE, Avise JC. GENE GENEALOGIES WITHIN THE ORGANISMAL PEDIGREES OF RANDOM-MATING POPULATIONS. Evolution. 1990;44(2):360-370doi: 10.1111/j.1558-5646.1990.tb05205.x.
Ball, R. M., Neigel, J. E., & Avise, J. C. (1990). GENE GENEALOGIES WITHIN THE ORGANISMAL PEDIGREES OF RANDOM-MATING POPULATIONS. Evolution; international journal of organic evolution, 44(2), 360-370. https://doi.org/10.1111/j.1558-5646.1990.tb05205.x
Ball, R Martin, et al. "GENE GENEALOGIES WITHIN THE ORGANISMAL PEDIGREES OF RANDOM-MATING POPULATIONS." Evolution; international journal of organic evolution vol. 44,2 (1990): 360-370. doi: https://doi.org/10.1111/j.1558-5646.1990.tb05205.x
Ball RM, Neigel JE, Avise JC. GENE GENEALOGIES WITHIN THE ORGANISMAL PEDIGREES OF RANDOM-MATING POPULATIONS. Evolution. 1990 Mar;44(2):360-370. doi: 10.1111/j.1558-5646.1990.tb05205.x. PMID: 28564387.
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The evolution of a stereoselective synthesis of the C1-C16 fragment of bryostatins.

Organic & biomolecular chemistry

Ball M, Baron A, Bradshaw B, Dumeunier R, O'Brien M, Thomas EJ.
PMID: 27714213
Org Biomol Chem. 2016 Oct 12;14(40):9650-9681. doi: 10.1039/c6ob01804a.

The development of a synthesis of the C1-C16 fragment of bryostatins in which the key step is a stereoselective oxy-Michael reaction used to assemble the cis-2,6-disubstituted tetrahydropyran with the exocyclic alkene already installed, is described. Following early work using...

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Ball M, Baron A, Bradshaw B, et al. The evolution of a stereoselective synthesis of the C1-C16 fragment of bryostatins. Org Biomol Chem. 2016;14(40):9650-9681doi: 10.1039/c6ob01804a.
Ball, M., Baron, A., Bradshaw, B., Dumeunier, R., O'Brien, M., & Thomas, E. J. (2016). The evolution of a stereoselective synthesis of the C1-C16 fragment of bryostatins. Organic & biomolecular chemistry, 14(40), 9650-9681. https://doi.org/10.1039/c6ob01804a
Ball, Matthew, et al. "The evolution of a stereoselective synthesis of the C1-C16 fragment of bryostatins." Organic & biomolecular chemistry vol. 14,40 (2016): 9650-9681. doi: https://doi.org/10.1039/c6ob01804a
Ball M, Baron A, Bradshaw B, Dumeunier R, O'Brien M, Thomas EJ. The evolution of a stereoselective synthesis of the C1-C16 fragment of bryostatins. Org Biomol Chem. 2016 Oct 12;14(40):9650-9681. doi: 10.1039/c6ob01804a. PMID: 27714213.
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Tackling vitamin A deficiency with biofortified sweetpotato in sub-Saharan Africa.

Global food security

Low JW, Mwanga ROM, Andrade M, Carey E, Ball AM.
PMID: 28989861
Glob Food Sec. 2017 Sep;14:23-30. doi: 10.1016/j.gfs.2017.01.004.

Orange-fleshed sweetpotato (OFSP) is a rich plant-based source of beta-carotene, which the body converts into vitamin A. In sub-Saharan Africa, sweetpotato is known as a food security crop but most varieties grown are high dry matter white-fleshed types, lacking...

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Low JW, Mwanga ROM, Andrade M, et al. Tackling vitamin A deficiency with biofortified sweetpotato in sub-Saharan Africa. Glob Food Sec. 2017;14:23-30doi: 10.1016/j.gfs.2017.01.004.
Low, J. W., Mwanga, R. O. M., Andrade, M., Carey, E., & Ball, A. M. (2017). Tackling vitamin A deficiency with biofortified sweetpotato in sub-Saharan Africa. Global food security, 1423-30. https://doi.org/10.1016/j.gfs.2017.01.004
Low, Jan W, et al. "Tackling vitamin A deficiency with biofortified sweetpotato in sub-Saharan Africa." Global food security vol. 14 (2017): 23-30. doi: https://doi.org/10.1016/j.gfs.2017.01.004
Low JW, Mwanga ROM, Andrade M, Carey E, Ball AM. Tackling vitamin A deficiency with biofortified sweetpotato in sub-Saharan Africa. Glob Food Sec. 2017 Sep;14:23-30. doi: 10.1016/j.gfs.2017.01.004. PMID: 28989861; PMCID: PMC5614018.
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Showing 1 to 12 of 434 entries