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No difference in pain reduction after epidural steroid injections in diabetic versus nondiabetic patients: A retrospective cohort study.

Journal of anaesthesiology, clinical pharmacology

Wong F, Namdari B, Dupler S, Kovac MF, Makarova N, Dalton JE, Turan A.
PMID: 27006548
J Anaesthesiol Clin Pharmacol. 2016 Jan-Mar;32(1):84-8. doi: 10.4103/0970-9185.173334.

BACKGROUND AND AIMS: Diabetes affects peripheral and central neurons causing paresthesia, allodynia, hyperalgesia, and spontaneous pain. However, the effect of diabetes on response to epidural steroid injection (ESI) remains unknown. We hypothesized that diabetic patients receiving ESI will have...

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Wong F, Namdari B, Dupler S, et al. No difference in pain reduction after epidural steroid injections in diabetic versus nondiabetic patients: A retrospective cohort study. J Anaesthesiol Clin Pharmacol. 2016;32(1):84-8doi: 10.4103/0970-9185.173334.
Wong, F., Namdari, B., Dupler, S., Kovac, M. F., Makarova, N., Dalton, J. E., & Turan, A. (2016). No difference in pain reduction after epidural steroid injections in diabetic versus nondiabetic patients: A retrospective cohort study. Journal of anaesthesiology, clinical pharmacology, 32(1), 84-8. https://doi.org/10.4103/0970-9185.173334
Wong, Francis, et al. "No difference in pain reduction after epidural steroid injections in diabetic versus nondiabetic patients: A retrospective cohort study." Journal of anaesthesiology, clinical pharmacology vol. 32,1 (2016): 84-8. doi: https://doi.org/10.4103/0970-9185.173334
Wong F, Namdari B, Dupler S, Kovac MF, Makarova N, Dalton JE, Turan A. No difference in pain reduction after epidural steroid injections in diabetic versus nondiabetic patients: A retrospective cohort study. J Anaesthesiol Clin Pharmacol. 2016 Jan-Mar;32(1):84-8. doi: 10.4103/0970-9185.173334. PMID: 27006548; PMCID: PMC4784221.
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A Modified Reverse One-Hybrid Screen Identifies Transcriptional Activation Domains in PHYTOCHROME-INTERACTING FACTOR 3.

Frontiers in plant science

Dalton JC, Bätz U, Liu J, Curie GL, Quail PH.
PMID: 27379152
Front Plant Sci. 2016 Jun 17;7:881. doi: 10.3389/fpls.2016.00881. eCollection 2016.

Transcriptional activation domains (TADs) are difficult to predict and identify, since they are not conserved and have little consensus. Here, we describe a yeast-based screening method that is able to identify individual amino acid residues involved in transcriptional activation...

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Dalton JC, Bätz U, Liu J, et al. A Modified Reverse One-Hybrid Screen Identifies Transcriptional Activation Domains in PHYTOCHROME-INTERACTING FACTOR 3. Front Plant Sci. 2016;7:881doi: 10.3389/fpls.2016.00881.
Dalton, J. C., Bätz, U., Liu, J., Curie, G. L., & Quail, P. H. (2016). A Modified Reverse One-Hybrid Screen Identifies Transcriptional Activation Domains in PHYTOCHROME-INTERACTING FACTOR 3. Frontiers in plant science, 7881. https://doi.org/10.3389/fpls.2016.00881
Dalton, Jutta C, et al. "A Modified Reverse One-Hybrid Screen Identifies Transcriptional Activation Domains in PHYTOCHROME-INTERACTING FACTOR 3." Frontiers in plant science vol. 7 (2016): 881. doi: https://doi.org/10.3389/fpls.2016.00881
Dalton JC, Bätz U, Liu J, Curie GL, Quail PH. A Modified Reverse One-Hybrid Screen Identifies Transcriptional Activation Domains in PHYTOCHROME-INTERACTING FACTOR 3. Front Plant Sci. 2016 Jun 17;7:881. doi: 10.3389/fpls.2016.00881. eCollection 2016. PMID: 27379152; PMCID: PMC4911399.
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Finite-size scaling in silver nanowire films: design considerations for practical devices.

Nanoscale

Large MJ, Cann M, Ogilvie SP, King AA, Jurewicz I, Dalton AB.
PMID: 27377048
Nanoscale. 2016 Jul 14;8(28):13701-7. doi: 10.1039/c6nr03960j.

We report the first application of finite-size scaling theory to nanostructured percolating networks, using silver nanowire (AgNW) films as a model system for experiment and simulation. AgNWs have been shown to be a prime candidate for replacing Indium Tin...

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Large MJ, Cann M, Ogilvie SP, et al. Finite-size scaling in silver nanowire films: design considerations for practical devices. Nanoscale. 2016;8(28):13701-7doi: 10.1039/c6nr03960j.
Large, M. J., Cann, M., Ogilvie, S. P., King, A. A., Jurewicz, I., & Dalton, A. B. (2016). Finite-size scaling in silver nanowire films: design considerations for practical devices. Nanoscale, 8(28), 13701-7. https://doi.org/10.1039/c6nr03960j
Large, Matthew J, et al. "Finite-size scaling in silver nanowire films: design considerations for practical devices." Nanoscale vol. 8,28 (2016): 13701-7. doi: https://doi.org/10.1039/c6nr03960j
Large MJ, Cann M, Ogilvie SP, King AA, Jurewicz I, Dalton AB. Finite-size scaling in silver nanowire films: design considerations for practical devices. Nanoscale. 2016 Jul 14;8(28):13701-7. doi: 10.1039/c6nr03960j. PMID: 27377048.
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Preparative semiconductor photoredox catalysis: An emerging theme in organic synthesis.

Beilstein journal of organic chemistry

Manley DW, Walton JC.
PMID: 26664577
Beilstein J Org Chem. 2015 Sep 09;11:1570-82. doi: 10.3762/bjoc.11.173. eCollection 2015.

Heterogeneous semiconductor photoredox catalysis (SCPC), particularly with TiO2, is evolving to provide radically new synthetic applications. In this review we describe how photoactivated SCPCs can either (i) interact with a precursor that donates an electron to the semiconductor thus...

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Manley DW, Walton JC. Preparative semiconductor photoredox catalysis: An emerging theme in organic synthesis. Beilstein J Org Chem. 2015;11:1570-82doi: 10.3762/bjoc.11.173.
Manley, D. W., & Walton, J. C. (2015). Preparative semiconductor photoredox catalysis: An emerging theme in organic synthesis. Beilstein journal of organic chemistry, 111570-82. https://doi.org/10.3762/bjoc.11.173
Manley, David W, and Walton, John C. "Preparative semiconductor photoredox catalysis: An emerging theme in organic synthesis." Beilstein journal of organic chemistry vol. 11 (2015): 1570-82. doi: https://doi.org/10.3762/bjoc.11.173
Manley DW, Walton JC. Preparative semiconductor photoredox catalysis: An emerging theme in organic synthesis. Beilstein J Org Chem. 2015 Sep 09;11:1570-82. doi: 10.3762/bjoc.11.173. eCollection 2015. PMID: 26664577; PMCID: PMC4660884.
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Absolute Rate Constants for the Reactions of Primary Alkyl Radicals with Aromatic Amines(1).

The Journal of organic chemistry

Burton A, Ingold KU, Walton JC.
PMID: 11667229
J Org Chem. 1996 May 31;61(11):3778-3782. doi: 10.1021/jo952162x.

Hydrogen abstraction from diarylamines (4-X-C(6)H(4))(2)NH [X = H, CH(3), C(8)H(17), CH(3)O, and Br] by the 2-methyl-2-phenylpropyl radical in n-dodecane solution was investigated by thermolysis of 3-methyl-3-phenylbutanoyl peroxide in the presence of various concentrations of the amines. The reaction is...

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Burton A, Ingold KU, Walton JC. Absolute Rate Constants for the Reactions of Primary Alkyl Radicals with Aromatic Amines(1). J Org Chem. 1996;61(11):3778-3782doi: 10.1021/jo952162x.
Burton, A., Ingold, K. U., & Walton, J. C. (1996). Absolute Rate Constants for the Reactions of Primary Alkyl Radicals with Aromatic Amines(1). The Journal of organic chemistry, 61(11), 3778-3782. https://doi.org/10.1021/jo952162x
Burton, Alan, et al. "Absolute Rate Constants for the Reactions of Primary Alkyl Radicals with Aromatic Amines(1)." The Journal of organic chemistry vol. 61,11 (1996): 3778-3782. doi: https://doi.org/10.1021/jo952162x
Burton A, Ingold KU, Walton JC. Absolute Rate Constants for the Reactions of Primary Alkyl Radicals with Aromatic Amines(1). J Org Chem. 1996 May 31;61(11):3778-3782. doi: 10.1021/jo952162x. PMID: 11667229.
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Silylated cyclohexadienes as new radical chain reducing reagents: preparative and mechanistic aspects.

Journal of the American Chemical Society

Studer A, Amrein S, Schleth F, Schulte T, Walton JC.
PMID: 12733911
J Am Chem Soc. 2003 May 14;125(19):5726-33. doi: 10.1021/ja0341743.

Various silylated 1,4-cyclohexadienes are presented as superior tin hydride substitutes for the conduction of various radical chain reductions. Debrominations, deiodinations, and deselenations can be performed using these environmentally benign reagents. Furthermore, Barton-McCombie-type deoxygenations using silylated cyclohexadienes are described. Radical...

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Studer A, Amrein S, Schleth F, et al. Silylated cyclohexadienes as new radical chain reducing reagents: preparative and mechanistic aspects. J Am Chem Soc. 2003;125(19):5726-33doi: 10.1021/ja0341743.
Studer, A., Amrein, S., Schleth, F., Schulte, T., & Walton, J. C. (2003). Silylated cyclohexadienes as new radical chain reducing reagents: preparative and mechanistic aspects. Journal of the American Chemical Society, 125(19), 5726-33. https://doi.org/10.1021/ja0341743
Studer, Armido, et al. "Silylated cyclohexadienes as new radical chain reducing reagents: preparative and mechanistic aspects." Journal of the American Chemical Society vol. 125,19 (2003): 5726-33. doi: https://doi.org/10.1021/ja0341743
Studer A, Amrein S, Schleth F, Schulte T, Walton JC. Silylated cyclohexadienes as new radical chain reducing reagents: preparative and mechanistic aspects. J Am Chem Soc. 2003 May 14;125(19):5726-33. doi: 10.1021/ja0341743. PMID: 12733911.
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Super-tough carbon-nanotube fibres.

Nature

Dalton AB, Collins S, Muñoz E, Razal JM, Ebron VH, Ferraris JP, Coleman JN, Kim BG, Baughman RH.
PMID: 12802323
Nature. 2003 Jun 12;423(6941):703. doi: 10.1038/423703a.

No abstract available.

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Dalton AB, Collins S, Muñoz E, et al. Super-tough carbon-nanotube fibres. Nature. 2003;423(6941):703doi: 10.1038/423703a.
Dalton, A. B., Collins, S., Muñoz, E., Razal, J. M., Ebron, V. H., Ferraris, J. P., Coleman, J. N., Kim, B. G., & Baughman, R. H. (2003). Super-tough carbon-nanotube fibres. Nature, 423(6941), 703. https://doi.org/10.1038/423703a
Dalton, Alan B, et al. "Super-tough carbon-nanotube fibres." Nature vol. 423,6941 (2003): 703. doi: https://doi.org/10.1038/423703a
Dalton AB, Collins S, Muñoz E, Razal JM, Ebron VH, Ferraris JP, Coleman JN, Kim BG, Baughman RH. Super-tough carbon-nanotube fibres. Nature. 2003 Jun 12;423(6941):703. doi: 10.1038/423703a. PMID: 12802323.
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Effect of sometribove administration on LH concentration in dairy cattle.

Theriogenology

Dalton JC, Marcinkowski DP.
PMID: 16727401
Theriogenology. 1994 Feb;41(2):437-45. doi: 10.1016/0093-691x(94)90079-x.

Sixteen lactating, normally cycling Holstein cows were used to study 1) the effects of sometribove (recombinant methionyl bST) administration on basal LH concentrations and 2) the pituitary response to a GnRH challenge during the breeding period. The cows received...

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Dalton JC, Marcinkowski DP. Effect of sometribove administration on LH concentration in dairy cattle. Theriogenology. 1994;41(2):437-45doi: 10.1016/0093-691x(94)90079-x.
Dalton, J. C., & Marcinkowski, D. P. (1994). Effect of sometribove administration on LH concentration in dairy cattle. Theriogenology, 41(2), 437-45. https://doi.org/10.1016/0093-691x(94)90079-x
Dalton, J C, and Marcinkowski, D P. "Effect of sometribove administration on LH concentration in dairy cattle." Theriogenology vol. 41,2 (1994): 437-45. doi: https://doi.org/10.1016/0093-691x(94)90079-x
Dalton JC, Marcinkowski DP. Effect of sometribove administration on LH concentration in dairy cattle. Theriogenology. 1994 Feb;41(2):437-45. doi: 10.1016/0093-691x(94)90079-x. PMID: 16727401.
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Kinetic and theoretical study of 4-exo ring closures of carbamoyl radicals onto C=C and C=N bonds.

Organic letters

Dilabio GA, Scanlan EM, Walton JC.
PMID: 15625001
Org Lett. 2005 Jan 06;7(1):155-8. doi: 10.1021/ol047716+.

Carbamoyl radicals were generated from oxime oxalate amides, and the kinetics of their 4-exo cyclizations onto C=C and C=NO bonds, leading to beta-lactam-containing species, were studied by EPR spectroscopy. DFT computations with model carbamoyl radicals predicted 4-exo ring closures...

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Dilabio GA, Scanlan EM, Walton JC. Kinetic and theoretical study of 4-exo ring closures of carbamoyl radicals onto C=C and C=N bonds. Org Lett. 2005;7(1):155-8doi: 10.1021/ol047716+.
Dilabio, G. A., Scanlan, E. M., & Walton, J. C. (2005). Kinetic and theoretical study of 4-exo ring closures of carbamoyl radicals onto C=C and C=N bonds. Organic letters, 7(1), 155-8. https://doi.org/10.1021/ol047716+
Dilabio, Gino A, et al. "Kinetic and theoretical study of 4-exo ring closures of carbamoyl radicals onto C=C and C=N bonds." Organic letters vol. 7,1 (2005): 155-8. doi: https://doi.org/10.1021/ol047716+
Dilabio GA, Scanlan EM, Walton JC. Kinetic and theoretical study of 4-exo ring closures of carbamoyl radicals onto C=C and C=N bonds. Org Lett. 2005 Jan 06;7(1):155-8. doi: 10.1021/ol047716+. PMID: 15625001.
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Radical-carbanion cyclo-coupling in armed aromatics: overriding steric hindrance to ring closure.

Chemical communications (Cambridge, England)

Roydhouse MD, Walton JC.
PMID: 16136248
Chem Commun (Camb). 2005 Sep 21;(35):4453-5. doi: 10.1039/b506391d. Epub 2005 Aug 04.

Omega-(2-Halophenyl)alkyl-2-oxazolines were prepared and reacted via base promoted intramolecular coupling of radical with carbanionic centres to yield 1-phenyl-1-oxazolino-indan and -tetralin derivatives containing quaternary C-atoms.

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Roydhouse MD, Walton JC. Radical-carbanion cyclo-coupling in armed aromatics: overriding steric hindrance to ring closure. Chem Commun (Camb). 2005;(35):4453-5doi: 10.1039/b506391d.
Roydhouse, M. D., & Walton, J. C. (2005). Radical-carbanion cyclo-coupling in armed aromatics: overriding steric hindrance to ring closure. Chemical communications (Cambridge, England), (35), 4453-5. https://doi.org/10.1039/b506391d
Roydhouse, Mark D, and Walton, John C. "Radical-carbanion cyclo-coupling in armed aromatics: overriding steric hindrance to ring closure." Chemical communications (Cambridge, England) vol. ,35 (2005): 4453-5. doi: https://doi.org/10.1039/b506391d
Roydhouse MD, Walton JC. Radical-carbanion cyclo-coupling in armed aromatics: overriding steric hindrance to ring closure. Chem Commun (Camb). 2005 Sep 21;(35):4453-5. doi: 10.1039/b506391d. Epub 2005 Aug 04. PMID: 16136248.
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Axial and equatorial cyclohexylacyl and tetrahydropyranyl-2-acyl radicals. An experimental and theoretical study.

Organic letters

DiLabio GA, Ingold KU, Roydhouse MD, Walton JC.
PMID: 15524473
Org Lett. 2004 Nov 11;6(23):4319-22. doi: 10.1021/ol0481683.

Axial and equatorial cyclohexylacyl and tetrahydropyranyl-2-acyl radicals gave distinct EPR spectra thanks to surprisingly large beta-hydrogen atom hyperfine splittings that enabled them to be characterized and monitored. DFT computations indicated that the axial species (X = CH(2)) had a...

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DiLabio GA, Ingold KU, Roydhouse MD, et al. Axial and equatorial cyclohexylacyl and tetrahydropyranyl-2-acyl radicals. An experimental and theoretical study. Org Lett. 2004;6(23):4319-22doi: 10.1021/ol0481683.
DiLabio, G. A., Ingold, K. U., Roydhouse, M. D., & Walton, J. C. (2004). Axial and equatorial cyclohexylacyl and tetrahydropyranyl-2-acyl radicals. An experimental and theoretical study. Organic letters, 6(23), 4319-22. https://doi.org/10.1021/ol0481683
DiLabio, Gino A, et al. "Axial and equatorial cyclohexylacyl and tetrahydropyranyl-2-acyl radicals. An experimental and theoretical study." Organic letters vol. 6,23 (2004): 4319-22. doi: https://doi.org/10.1021/ol0481683
DiLabio GA, Ingold KU, Roydhouse MD, Walton JC. Axial and equatorial cyclohexylacyl and tetrahydropyranyl-2-acyl radicals. An experimental and theoretical study. Org Lett. 2004 Nov 11;6(23):4319-22. doi: 10.1021/ol0481683. PMID: 15524473.
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Digestion of haemoglobin by schistosomes: 35 years on.

Parasitology today (Personal ed.)

Dalton JP, Smith AM, Clough KA, Brindley PJ.
PMID: 15275329
Parasitol Today. 1995 Aug;11(8):299-303. doi: 10.1016/0169-4758(95)80045-x.

Adult schistosomes obtain nutrients by digesting haemoglobin, which they obtain from ingested host red blood cells. Here John Dalton, Angela Smith, Karen Clough and Paul Brindley argue that a cathepsin L proteinase recently identified in their laboratory as the...

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Dalton JP, Smith AM, Clough KA, et al. Digestion of haemoglobin by schistosomes: 35 years on. Parasitol Today. 1995;11(8):299-303doi: 10.1016/0169-4758(95)80045-x.
Dalton, J. P., Smith, A. M., Clough, K. A., & Brindley, P. J. (1995). Digestion of haemoglobin by schistosomes: 35 years on. Parasitology today (Personal ed.), 11(8), 299-303. https://doi.org/10.1016/0169-4758(95)80045-x
Dalton, J P, et al. "Digestion of haemoglobin by schistosomes: 35 years on." Parasitology today (Personal ed.) vol. 11,8 (1995): 299-303. doi: https://doi.org/10.1016/0169-4758(95)80045-x
Dalton JP, Smith AM, Clough KA, Brindley PJ. Digestion of haemoglobin by schistosomes: 35 years on. Parasitol Today. 1995 Aug;11(8):299-303. doi: 10.1016/0169-4758(95)80045-x. PMID: 15275329.
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Showing 1 to 12 of 282 entries