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Showing 1 to 12 of 227 entries
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Towards ultimate low frequency air-core magnetometer sensitivity.

Scientific reports

Pellicer-Guridi R, Vogel MW, Reutens DC, Vegh V.
PMID: 28536460
Sci Rep. 2017 May 23;7(1):2269. doi: 10.1038/s41598-017-02099-z.

Air-core magnetometers are amongst the most commonly used magnetic field detectors in biomedical instruments. They offer excellent sensitivity, low fabrication complexity and a robust, cost-effective solution. However, air-core magnetometers must be tailored to the specific application to achieve high...

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Pellicer-Guridi R, Vogel MW, Reutens DC, et al. Towards ultimate low frequency air-core magnetometer sensitivity. Sci Rep. 2017;7(1):2269doi: 10.1038/s41598-017-02099-z.
Pellicer-Guridi, R., Vogel, M. W., Reutens, D. C., & Vegh, V. (2017). Towards ultimate low frequency air-core magnetometer sensitivity. Scientific reports, 7(1), 2269. https://doi.org/10.1038/s41598-017-02099-z
Pellicer-Guridi, Ruben, et al. "Towards ultimate low frequency air-core magnetometer sensitivity." Scientific reports vol. 7,1 (2017): 2269. doi: https://doi.org/10.1038/s41598-017-02099-z
Pellicer-Guridi R, Vogel MW, Reutens DC, Vegh V. Towards ultimate low frequency air-core magnetometer sensitivity. Sci Rep. 2017 May 23;7(1):2269. doi: 10.1038/s41598-017-02099-z. PMID: 28536460; PMCID: PMC5442107.
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Cobalt(III) diazabutadiene precursors for metal deposition: nanoparticle and thin film growth.

Inorganic chemistry

Pugh T, Cosham SD, Hamilton JA, Kingsley AJ, Johnson AL.
PMID: 24236689
Inorg Chem. 2013 Dec 02;52(23):13719-29. doi: 10.1021/ic402317g. Epub 2013 Nov 15.

We report the synthesis and characterization of a family of cobalt(III) metal precursors, based around cyclopentadienyl and diazabutadiene ligands. The molecular structure of the complexes cyclopentadienyl-Cobalt(III)(N,N'-dicyclohexyl-diazabutadiene) (2c) and cyclopentadienyl-Cobalt(III)(N,N'-dimesityl-diazabutadiene) (2d) are described, as determined by single crystal X-ray diffraction...

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Pugh T, Cosham SD, Hamilton JA, et al. Cobalt(III) diazabutadiene precursors for metal deposition: nanoparticle and thin film growth. Inorg Chem. 2013;52(23):13719-29doi: 10.1021/ic402317g.
Pugh, T., Cosham, S. D., Hamilton, J. A., Kingsley, A. J., & Johnson, A. L. (2013). Cobalt(III) diazabutadiene precursors for metal deposition: nanoparticle and thin film growth. Inorganic chemistry, 52(23), 13719-29. https://doi.org/10.1021/ic402317g
Pugh, Thomas, et al. "Cobalt(III) diazabutadiene precursors for metal deposition: nanoparticle and thin film growth." Inorganic chemistry vol. 52,23 (2013): 13719-29. doi: https://doi.org/10.1021/ic402317g
Pugh T, Cosham SD, Hamilton JA, Kingsley AJ, Johnson AL. Cobalt(III) diazabutadiene precursors for metal deposition: nanoparticle and thin film growth. Inorg Chem. 2013 Dec 02;52(23):13719-29. doi: 10.1021/ic402317g. Epub 2013 Nov 15. PMID: 24236689.
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FPGA Simulation Engine for Customized Construction of Neural Microcircuits.

ICCAD. IEEE/ACM International Conference on Computer-Aided Design

Blair HT, Cong J, Wu D.
PMID: 25584120
ICCAD IEEE ACM Int Conf Comput Aided Des. 2013 Apr;2013:229. doi: 10.1109/FCCM.2013.22.

In this paper we describe an FPGA-based platform for high-performance and low-power simulation of neural microcircuits composed from integrate-and-fire (IAF) neurons. Based on high-level synthesis, our platform uses design templates to map hierarchies of neuron model to logic fabrics....

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Blair HT, Cong J, Wu D. FPGA Simulation Engine for Customized Construction of Neural Microcircuits. ICCAD IEEE ACM Int Conf Comput Aided Des. 2013;2013:229doi: 10.1109/FCCM.2013.22.
Blair, H. T., Cong, J., & Wu, D. (2013). FPGA Simulation Engine for Customized Construction of Neural Microcircuits. ICCAD. IEEE/ACM International Conference on Computer-Aided Design, 2013229. https://doi.org/10.1109/FCCM.2013.22
Blair, Hugh T, et al. "FPGA Simulation Engine for Customized Construction of Neural Microcircuits." ICCAD. IEEE/ACM International Conference on Computer-Aided Design vol. 2013 (2013): 229. doi: https://doi.org/10.1109/FCCM.2013.22
Blair HT, Cong J, Wu D. FPGA Simulation Engine for Customized Construction of Neural Microcircuits. ICCAD IEEE ACM Int Conf Comput Aided Des. 2013 Apr;2013:229. doi: 10.1109/FCCM.2013.22. PMID: 25584120; PMCID: PMC4288851.
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Theoretical insights into the nature of PtSn bond: Reevaluating the bonding/back-bonding properties of trichlorostannate with comparison to the cyano ligand.

Journal of computational chemistry

Papp T, Kollár L, Kégl T.
PMID: 28488281
J Comput Chem. 2017 Jul 15;38(19):1712-1726. doi: 10.1002/jcc.24815. Epub 2017 May 10.

The coordinating properties of the trichlorostannate ligand in hydrido platinum trichlorostannato and platinum bis-trichlorostannato complexes, containing various phosphine ligands, have been elucidated by means of charge decomposition analysis, the Ziegler-Rauk Energy Decomposition with the Natural Orbitals for Chemical Valence,...

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Papp T, Kollár L, Kégl T. Theoretical insights into the nature of PtSn bond: Reevaluating the bonding/back-bonding properties of trichlorostannate with comparison to the cyano ligand. J Comput Chem. 2017;38(19):1712-1726doi: 10.1002/jcc.24815.
Papp, T., Kollár, L., & Kégl, T. (2017). Theoretical insights into the nature of PtSn bond: Reevaluating the bonding/back-bonding properties of trichlorostannate with comparison to the cyano ligand. Journal of computational chemistry, 38(19), 1712-1726. https://doi.org/10.1002/jcc.24815
Papp, Tamara, et al. "Theoretical insights into the nature of PtSn bond: Reevaluating the bonding/back-bonding properties of trichlorostannate with comparison to the cyano ligand." Journal of computational chemistry vol. 38,19 (2017): 1712-1726. doi: https://doi.org/10.1002/jcc.24815
Papp T, Kollár L, Kégl T. Theoretical insights into the nature of PtSn bond: Reevaluating the bonding/back-bonding properties of trichlorostannate with comparison to the cyano ligand. J Comput Chem. 2017 Jul 15;38(19):1712-1726. doi: 10.1002/jcc.24815. Epub 2017 May 10. PMID: 28488281.
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Reply.

Journal of gastrointestinal and liver diseases : JGLD

Golovics PA, Vegh Z, Lakatos PL.
PMID: 27014767
J Gastrointestin Liver Dis. 2016 Mar;25(1):122-3. doi: 10.15403/jgld.2014.1121.251.rly.

No abstract available.

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Golovics PA, Vegh Z, Lakatos PL. Reply. J Gastrointestin Liver Dis. 2016;25(1):122-3doi: 10.15403/jgld.2014.1121.251.rly.
Golovics, P. A., Vegh, Z., & Lakatos, P. L. (2016). Reply. Journal of gastrointestinal and liver diseases : JGLD, 25(1), 122-3. https://doi.org/10.15403/jgld.2014.1121.251.rly
Golovics, Petra Anna, et al. "Reply." Journal of gastrointestinal and liver diseases : JGLD vol. 25,1 (2016): 122-3. doi: https://doi.org/10.15403/jgld.2014.1121.251.rly
Golovics PA, Vegh Z, Lakatos PL. Reply. J Gastrointestin Liver Dis. 2016 Mar;25(1):122-3. doi: 10.15403/jgld.2014.1121.251.rly. PMID: 27014767.
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Combined electron-spin-resonance, X-ray-diffraction studies on phospholipid vesicles obtained from cold-hardened wheats : II. The role of free sterols.

Planta

Horváth I, Vigh L, Woltjes J, Farkas T, van Hasselt P, Kuiper PJ.
PMID: 24232837
Planta. 1987 Jan;170(1):20-5. doi: 10.1007/BF00392376.

The contents of free sterols and phospholipids in leaves of wheat, Triticum aestivum L., cultivars of different frost resistances, as well as the physical state of isolated phospholipids in the presence and absence of sterols, were compared before and...

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Horváth I, Vigh L, Woltjes J, et al. Combined electron-spin-resonance, X-ray-diffraction studies on phospholipid vesicles obtained from cold-hardened wheats : II. The role of free sterols. Planta. 1987;170(1):20-5doi: 10.1007/BF00392376.
Horváth, I., Vigh, L., Woltjes, J., Farkas, T., van Hasselt, P., & Kuiper, P. J. (1987). Combined electron-spin-resonance, X-ray-diffraction studies on phospholipid vesicles obtained from cold-hardened wheats : II. The role of free sterols. Planta, 170(1), 20-5. https://doi.org/10.1007/BF00392376
Horváth, I, et al. "Combined electron-spin-resonance, X-ray-diffraction studies on phospholipid vesicles obtained from cold-hardened wheats : II. The role of free sterols." Planta vol. 170,1 (1987): 20-5. doi: https://doi.org/10.1007/BF00392376
Horváth I, Vigh L, Woltjes J, Farkas T, van Hasselt P, Kuiper PJ. Combined electron-spin-resonance, X-ray-diffraction studies on phospholipid vesicles obtained from cold-hardened wheats : II. The role of free sterols. Planta. 1987 Jan;170(1):20-5. doi: 10.1007/BF00392376. PMID: 24232837.
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Iron- and Cobalt-Catalyzed Synthesis of Carbene Phosphinidenes.

Angewandte Chemie (International ed. in English)

Pal K, Hemming OB, Day BM, Pugh T, Evans DJ, Layfield RA.
PMID: 26643712
Angew Chem Int Ed Engl. 2016 Jan 26;55(5):1690-3. doi: 10.1002/anie.201508303. Epub 2015 Dec 08.

In the presence of stoichiometric or catalytic amounts of [M{N(SiMe3 )2 }2 ] (M=Fe, Co), N-heterocyclic carbenes (NHCs) react with primary phosphines to give a series of carbene phosphinidenes of the type (NHC)⋅PAr. The formation of (IMe4 )⋅PMes (Mes=mesityl)...

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Pal K, Hemming OB, Day BM, et al. Iron- and Cobalt-Catalyzed Synthesis of Carbene Phosphinidenes. Angew Chem Int Ed Engl. 2015;55(5):1690-3doi: 10.1002/anie.201508303.
Pal, K., Hemming, O. B., Day, B. M., Pugh, T., Evans, D. J., & Layfield, R. A. (2016). Iron- and Cobalt-Catalyzed Synthesis of Carbene Phosphinidenes. Angewandte Chemie (International ed. in English), 55(5), 1690-3. https://doi.org/10.1002/anie.201508303
Pal, Kuntal, et al. "Iron- and Cobalt-Catalyzed Synthesis of Carbene Phosphinidenes." Angewandte Chemie (International ed. in English) vol. 55,5 (2016): 1690-3. doi: https://doi.org/10.1002/anie.201508303
Pal K, Hemming OB, Day BM, Pugh T, Evans DJ, Layfield RA. Iron- and Cobalt-Catalyzed Synthesis of Carbene Phosphinidenes. Angew Chem Int Ed Engl. 2016 Jan 26;55(5):1690-3. doi: 10.1002/anie.201508303. Epub 2015 Dec 08. PMID: 26643712; PMCID: PMC5064616.
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The cation radicals of free base and zinc bacteriochlorin, bacteriochlorophyll, and bacteriopheophytin.

Proceedings of the National Academy of Sciences of the United States of America

Fajer J, Borg DC, Forman A, Felton RH, Dolphin D, Vegh L.
PMID: 16592150
Proc Natl Acad Sci U S A. 1974 Mar;71(3):994-8. doi: 10.1073/pnas.71.3.994.

One-electron oxidation of zinc tetraphenylbacteriochlorin and its metal-free base yielded stable cation radicals. Electron spin resonance hyperfine splittings were assigned by selective deuterations. These results indicate that the protons of the saturated rings of the bacteriochlorins carry large spin...

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Fajer J, Borg DC, Forman A, et al. The cation radicals of free base and zinc bacteriochlorin, bacteriochlorophyll, and bacteriopheophytin. Proc Natl Acad Sci U S A. 1974;71(3):994-8doi: 10.1073/pnas.71.3.994.
Fajer, J., Borg, D. C., Forman, A., Felton, R. H., Dolphin, D., & Vegh, L. (1974). The cation radicals of free base and zinc bacteriochlorin, bacteriochlorophyll, and bacteriopheophytin. Proceedings of the National Academy of Sciences of the United States of America, 71(3), 994-8. https://doi.org/10.1073/pnas.71.3.994
Fajer, J, et al. "The cation radicals of free base and zinc bacteriochlorin, bacteriochlorophyll, and bacteriopheophytin." Proceedings of the National Academy of Sciences of the United States of America vol. 71,3 (1974): 994-8. doi: https://doi.org/10.1073/pnas.71.3.994
Fajer J, Borg DC, Forman A, Felton RH, Dolphin D, Vegh L. The cation radicals of free base and zinc bacteriochlorin, bacteriochlorophyll, and bacteriopheophytin. Proc Natl Acad Sci U S A. 1974 Mar;71(3):994-8. doi: 10.1073/pnas.71.3.994. PMID: 16592150; PMCID: PMC388144.
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Effect of frost hardening on lipid and Fatty Acid composition of chloroplast thylakoid membranes in two wheat varieties of contrasting hardiness.

Plant physiology

Vigh L, Horvàth I, van Hasselt PR, Kuiper PJ.
PMID: 16664487
Plant Physiol. 1985 Nov;79(3):756-9. doi: 10.1104/pp.79.3.756.

Lipid and fatty acid composition of chloroplast thylakoid membranes was determined in two varieties of wheat (Triticum aestivum L.), the hardy Miranovskaja and the sensitive Penjamo. Plants were grown at room temperature or under frost hardening conditions (1.5 degrees...

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Vigh L, Horvàth I, van Hasselt PR, et al. Effect of frost hardening on lipid and Fatty Acid composition of chloroplast thylakoid membranes in two wheat varieties of contrasting hardiness. Plant Physiol. 1985;79(3):756-9doi: 10.1104/pp.79.3.756.
Vigh, L., Horvàth, I., van Hasselt, P. R., & Kuiper, P. J. (1985). Effect of frost hardening on lipid and Fatty Acid composition of chloroplast thylakoid membranes in two wheat varieties of contrasting hardiness. Plant physiology, 79(3), 756-9. https://doi.org/10.1104/pp.79.3.756
Vigh, L, et al. "Effect of frost hardening on lipid and Fatty Acid composition of chloroplast thylakoid membranes in two wheat varieties of contrasting hardiness." Plant physiology vol. 79,3 (1985): 756-9. doi: https://doi.org/10.1104/pp.79.3.756
Vigh L, Horvàth I, van Hasselt PR, Kuiper PJ. Effect of frost hardening on lipid and Fatty Acid composition of chloroplast thylakoid membranes in two wheat varieties of contrasting hardiness. Plant Physiol. 1985 Nov;79(3):756-9. doi: 10.1104/pp.79.3.756. PMID: 16664487; PMCID: PMC1074966.
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Prophylactic implantable cardioverter-defibrillators increased life expectancy with an acceptable cost-effectiveness ratio.

ACP journal club

Hillegass WB, McElderry HT.
PMID: 16539367
ACP J Club. 2006 Mar-Apr;144(2):52.

No abstract available.

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Hillegass WB, McElderry HT. Prophylactic implantable cardioverter-defibrillators increased life expectancy with an acceptable cost-effectiveness ratio. ACP J Club. 2006;144(2):52
Hillegass, W. B., & McElderry, H. T. (2006). Prophylactic implantable cardioverter-defibrillators increased life expectancy with an acceptable cost-effectiveness ratio. ACP journal club, 144(2), 52.
Hillegass, William B, and McElderry, Hugh T. "Prophylactic implantable cardioverter-defibrillators increased life expectancy with an acceptable cost-effectiveness ratio." ACP journal club vol. 144,2 (2006): 52.
Hillegass WB, McElderry HT. Prophylactic implantable cardioverter-defibrillators increased life expectancy with an acceptable cost-effectiveness ratio. ACP J Club. 2006 Mar-Apr;144(2):52. PMID: 16539367.
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A Family of Single-Isomer Chiral Resolving Agents for Capillary Electrophoresis. 2. Hepta-6-sulfato-β-cyclodextrin.

Analytical chemistry

Vincent JB, Kirby DM, Nguyen TV, Vigh G.
PMID: 21639174
Anal Chem. 1997 Nov 01;69(21):4419-28. doi: 10.1021/ac970418o.

A new, hydrophilic, single-isomer charged cyclodextrin, the sodium salt of hepta-6-sulfato-β-cyclodextrin has been synthesized, characterized, and used for the capillary electrophoretic separation of the enantiomers of numerous noncharged, acidic, basic, and zwitterionic analytes. Hepta-6-sulfato-β-cyclodextrin proved to be a much...

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Vincent JB, Kirby DM, Nguyen TV, et al. A Family of Single-Isomer Chiral Resolving Agents for Capillary Electrophoresis. 2. Hepta-6-sulfato-β-cyclodextrin. Anal Chem. 1997;69(21):4419-28doi: 10.1021/ac970418o.
Vincent, J. B., Kirby, D. M., Nguyen, T. V., & Vigh, G. (1997). A Family of Single-Isomer Chiral Resolving Agents for Capillary Electrophoresis. 2. Hepta-6-sulfato-β-cyclodextrin. Analytical chemistry, 69(21), 4419-28. https://doi.org/10.1021/ac970418o
Vincent, J B, et al. "A Family of Single-Isomer Chiral Resolving Agents for Capillary Electrophoresis. 2. Hepta-6-sulfato-β-cyclodextrin." Analytical chemistry vol. 69,21 (1997): 4419-28. doi: https://doi.org/10.1021/ac970418o
Vincent JB, Kirby DM, Nguyen TV, Vigh G. A Family of Single-Isomer Chiral Resolving Agents for Capillary Electrophoresis. 2. Hepta-6-sulfato-β-cyclodextrin. Anal Chem. 1997 Nov 01;69(21):4419-28. doi: 10.1021/ac970418o. PMID: 21639174.
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Peak shape distortions in the capillary electrophoretic separations of strong electrolytes when the background electrolyte contains two strong electrolyte co-ions.

Analytical chemistry

Williams RL, Childs B, Dose EV, Guiochon G, Vigh G.
PMID: 21639342
Anal Chem. 1997 Apr 01;69(7):1347-54. doi: 10.1021/ac9609337.

A series of 25 mM phosphate buffer background electrolytes were prepared from phosphoric acid and mixtures of lithium hydroxide and tetrabutylammonium hydroxide as pH adjusters and sources of background electrolyte co-ions. These background electrolytes were used for the capillary...

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Williams RL, Childs B, Dose EV, et al. Peak shape distortions in the capillary electrophoretic separations of strong electrolytes when the background electrolyte contains two strong electrolyte co-ions. Anal Chem. 1997;69(7):1347-54doi: 10.1021/ac9609337.
Williams, R. L., Childs, B., Dose, E. V., Guiochon, G., & Vigh, G. (1997). Peak shape distortions in the capillary electrophoretic separations of strong electrolytes when the background electrolyte contains two strong electrolyte co-ions. Analytical chemistry, 69(7), 1347-54. https://doi.org/10.1021/ac9609337
Williams, R L, et al. "Peak shape distortions in the capillary electrophoretic separations of strong electrolytes when the background electrolyte contains two strong electrolyte co-ions." Analytical chemistry vol. 69,7 (1997): 1347-54. doi: https://doi.org/10.1021/ac9609337
Williams RL, Childs B, Dose EV, Guiochon G, Vigh G. Peak shape distortions in the capillary electrophoretic separations of strong electrolytes when the background electrolyte contains two strong electrolyte co-ions. Anal Chem. 1997 Apr 01;69(7):1347-54. doi: 10.1021/ac9609337. PMID: 21639342.
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Showing 1 to 12 of 227 entries