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Modelling human Puumala hantavirus infection in relation to bank vole abundance and masting intensity in the Netherlands.

Infection ecology & epidemiology

Swart A, Bekker DL, Maas M, de Vries A, Pijnacker R, Reusken CBEM, van der Giessen JWB.
PMID: 28567209
Infect Ecol Epidemiol. 2017 Mar 24;7(1):1287986. doi: 10.1080/20008686.2017.1287986. eCollection 2017.

This paper deals with modelling the relationship between human Puumala hantavirus (PUUV) infection, the abundance and prevalence of infection of the host (the bank vole), mast, and temperature. These data were used to build and parametrise generalised regression models,...

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Swart A, Bekker DL, Maas M, et al. Modelling human Puumala hantavirus infection in relation to bank vole abundance and masting intensity in the Netherlands. Infect Ecol Epidemiol. 2017;7(1):1287986doi: 10.1080/20008686.2017.1287986.
Swart, A., Bekker, D. L., Maas, M., de Vries, A., Pijnacker, R., Reusken, C. B. E. M., & van der Giessen, J. W. B. (2017). Modelling human Puumala hantavirus infection in relation to bank vole abundance and masting intensity in the Netherlands. Infection ecology & epidemiology, 7(1), 1287986. https://doi.org/10.1080/20008686.2017.1287986
Swart, Arno, et al. "Modelling human Puumala hantavirus infection in relation to bank vole abundance and masting intensity in the Netherlands." Infection ecology & epidemiology vol. 7,1 (2017): 1287986. doi: https://doi.org/10.1080/20008686.2017.1287986
Swart A, Bekker DL, Maas M, de Vries A, Pijnacker R, Reusken CBEM, van der Giessen JWB. Modelling human Puumala hantavirus infection in relation to bank vole abundance and masting intensity in the Netherlands. Infect Ecol Epidemiol. 2017 Mar 24;7(1):1287986. doi: 10.1080/20008686.2017.1287986. eCollection 2017. PMID: 28567209; PMCID: PMC5443058.
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The effects of the prevention program 'New Perspectives' (NP) on juvenile delinquency and other life domains: study protocol for a randomized controlled trial.

BMC psychology

de Vries SL, Hoeve M, Asscher JJ, Stams GJ.
PMID: 25566382
BMC Psychol. 2014 Apr 16;2(1):10. doi: 10.1186/2050-7283-2-10. eCollection 2014.

BACKGROUND: New Perspectives (NP) is a prevention program aiming to prevent that youth at onset of a criminal career will develop a persistent criminal behaviour pattern. The effects of NP on juvenile delinquency and other life domains are investigated,...

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de Vries SL, Hoeve M, Asscher JJ, et al. The effects of the prevention program 'New Perspectives' (NP) on juvenile delinquency and other life domains: study protocol for a randomized controlled trial. BMC Psychol. 2014;2(1):10doi: 10.1186/2050-7283-2-10.
de Vries, S. L., Hoeve, M., Asscher, J. J., & Stams, G. J. (2014). The effects of the prevention program 'New Perspectives' (NP) on juvenile delinquency and other life domains: study protocol for a randomized controlled trial. BMC psychology, 2(1), 10. https://doi.org/10.1186/2050-7283-2-10
de Vries, Sanne L A, et al. "The effects of the prevention program 'New Perspectives' (NP) on juvenile delinquency and other life domains: study protocol for a randomized controlled trial." BMC psychology vol. 2,1 (2014): 10. doi: https://doi.org/10.1186/2050-7283-2-10
de Vries SL, Hoeve M, Asscher JJ, Stams GJ. The effects of the prevention program 'New Perspectives' (NP) on juvenile delinquency and other life domains: study protocol for a randomized controlled trial. BMC Psychol. 2014 Apr 16;2(1):10. doi: 10.1186/2050-7283-2-10. eCollection 2014. PMID: 25566382; PMCID: PMC4269998.
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Simulating the Transition between Gel and Liquid-Crystal Phases of Lipid Bilayers: Dependence of the Transition Temperature on the Hydration Level.

Journal of chemical theory and computation

Horta BA, de Vries AH, Hünenberger PH.
PMID: 26613501
J Chem Theory Comput. 2010 Aug 10;6(8):2488-500. doi: 10.1021/ct100200w.

Explicit-solvent molecular dynamics (MD) simulations of the monoglyceride glycerol-1-monopalmitin (GMP; bilayer patch of 2 × 6 × 6 lipids) at different hydration levels (full, half, or quarter hydration) and at different temperatures (318 to 338 K) are reported. The...

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Horta BA, de Vries AH, Hünenberger PH. Simulating the Transition between Gel and Liquid-Crystal Phases of Lipid Bilayers: Dependence of the Transition Temperature on the Hydration Level. J Chem Theory Comput. 2010;6(8):2488-500doi: 10.1021/ct100200w.
Horta, B. A., de Vries, A. H., & Hünenberger, P. H. (2010). Simulating the Transition between Gel and Liquid-Crystal Phases of Lipid Bilayers: Dependence of the Transition Temperature on the Hydration Level. Journal of chemical theory and computation, 6(8), 2488-500. https://doi.org/10.1021/ct100200w
Horta, Bruno A C, et al. "Simulating the Transition between Gel and Liquid-Crystal Phases of Lipid Bilayers: Dependence of the Transition Temperature on the Hydration Level." Journal of chemical theory and computation vol. 6,8 (2010): 2488-500. doi: https://doi.org/10.1021/ct100200w
Horta BA, de Vries AH, Hünenberger PH. Simulating the Transition between Gel and Liquid-Crystal Phases of Lipid Bilayers: Dependence of the Transition Temperature on the Hydration Level. J Chem Theory Comput. 2010 Aug 10;6(8):2488-500. doi: 10.1021/ct100200w. PMID: 26613501.
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An Amphotericin B Derivative Equally Potent to Amphotericin B and with Increased Safety.

PloS one

Antillón A, de Vries AH, Espinosa-Caballero M, Falcón-González JM, Flores Romero D, González-Damián J, Jiménez-Montejo FE, León-Buitimea A, López-Ortiz M, Magaña R, Marrink SJ, Morales-Nava R, Periole X, Reyes-Esparza J, Rodríguez Lozada J, Santiago-Angelino TM, Vargas González MC, Regla I, Carrillo-Tripp M, Fernández-Zertuche M, Rodríguez-Fragoso L, Ortega-Blake I.
PMID: 27683101
PLoS One. 2016 Sep 28;11(9):e0162171. doi: 10.1371/journal.pone.0162171. eCollection 2016.

Amphotericin B is the most potent antimycotic known to date. However due to its large collateral toxicity, its use, although long standing, had been limited. Many attempts have been made to produce derivatives with reduced collateral damage. The molecular...

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Antillón A, de Vries AH, Espinosa-Caballero M, et al. An Amphotericin B Derivative Equally Potent to Amphotericin B and with Increased Safety. PLoS One. 2016;11(9):e0162171doi: 10.1371/journal.pone.0162171.
Antillón, A., de Vries, A. H., Espinosa-Caballero, M., Falcón-González, J. M., Flores Romero, D., González-Damián, J., Jiménez-Montejo, F. E., León-Buitimea, A., López-Ortiz, M., Magaña, R., Marrink, S. J., Morales-Nava, R., Periole, X., Reyes-Esparza, J., Rodríguez Lozada, J., Santiago-Angelino, T. M., Vargas González, M. C., Regla, I., Carrillo-Tripp, M., Fernández-Zertuche, M., Rodríguez-Fragoso, L., & Ortega-Blake, I. (2016). An Amphotericin B Derivative Equally Potent to Amphotericin B and with Increased Safety. PloS one, 11(9), e0162171. https://doi.org/10.1371/journal.pone.0162171
Antillón, Armando, et al. "An Amphotericin B Derivative Equally Potent to Amphotericin B and with Increased Safety." PloS one vol. 11,9 (2016): e0162171. doi: https://doi.org/10.1371/journal.pone.0162171
Antillón A, de Vries AH, Espinosa-Caballero M, Falcón-González JM, Flores Romero D, González-Damián J, Jiménez-Montejo FE, León-Buitimea A, López-Ortiz M, Magaña R, Marrink SJ, Morales-Nava R, Periole X, Reyes-Esparza J, Rodríguez Lozada J, Santiago-Angelino TM, Vargas González MC, Regla I, Carrillo-Tripp M, Fernández-Zertuche M, Rodríguez-Fragoso L, Ortega-Blake I. An Amphotericin B Derivative Equally Potent to Amphotericin B and with Increased Safety. PLoS One. 2016 Sep 28;11(9):e0162171. doi: 10.1371/journal.pone.0162171. eCollection 2016. PMID: 27683101; PMCID: PMC5040443.
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Protein content and freezing avoidance properties of the subdermal extracellular matrix and serum of the Antarctic snailfish, Paraliparis devriesi.

Fish physiology and biochemistry

Jung A, Johnson P, Eastman JT, Devries AL.
PMID: 24197273
Fish Physiol Biochem. 1995 Feb;14(1):71-80. doi: 10.1007/BF00004292.

The Antarctic snailfish, Paraliparis devriesi (Liparididae), occupies an epibenthic habitat at a depth of 500-650 m in the subzero waters of McMurdo Sound, Antarctica. This species has watery (97%) gelatinous subdermal extracellular matrix (SECM) comprising a mean of 33.8%...

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Jung A, Johnson P, Eastman JT, et al. Protein content and freezing avoidance properties of the subdermal extracellular matrix and serum of the Antarctic snailfish, Paraliparis devriesi. Fish Physiol Biochem. 1995;14(1):71-80doi: 10.1007/BF00004292.
Jung, A., Johnson, P., Eastman, J. T., & Devries, A. L. (1995). Protein content and freezing avoidance properties of the subdermal extracellular matrix and serum of the Antarctic snailfish, Paraliparis devriesi. Fish physiology and biochemistry, 14(1), 71-80. https://doi.org/10.1007/BF00004292
Jung, A, et al. "Protein content and freezing avoidance properties of the subdermal extracellular matrix and serum of the Antarctic snailfish, Paraliparis devriesi." Fish physiology and biochemistry vol. 14,1 (1995): 71-80. doi: https://doi.org/10.1007/BF00004292
Jung A, Johnson P, Eastman JT, Devries AL. Protein content and freezing avoidance properties of the subdermal extracellular matrix and serum of the Antarctic snailfish, Paraliparis devriesi. Fish Physiol Biochem. 1995 Feb;14(1):71-80. doi: 10.1007/BF00004292. PMID: 24197273.
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Synthesis and application in asymmetric C-C bond formation of solution phase ligand libraries of monodentate phosphoramidites.

Organic & biomolecular chemistry

Duursma A, Lefort L, Boogers JA, de Vries AH, de Vries JG, Minnaard AJ, Feringa BL.
PMID: 15188032
Org Biomol Chem. 2004 Jun 21;2(12):1682-4. doi: 10.1039/b404996a. Epub 2004 May 25.

A library of 96 unique monodentate phosphoramidite ligands has been synthesized in solution and used in the asymmetric conjugate addition of potassium vinyltrifluoroborate to enones resulting in up to 88% ee.

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Duursma A, Lefort L, Boogers JA, et al. Synthesis and application in asymmetric C-C bond formation of solution phase ligand libraries of monodentate phosphoramidites. Org Biomol Chem. 2004;2(12):1682-4doi: 10.1039/b404996a.
Duursma, A., Lefort, L., Boogers, J. A., de Vries, A. H., de Vries, J. G., Minnaard, A. J., & Feringa, B. L. (2004). Synthesis and application in asymmetric C-C bond formation of solution phase ligand libraries of monodentate phosphoramidites. Organic & biomolecular chemistry, 2(12), 1682-4. https://doi.org/10.1039/b404996a
Duursma, Ate, et al. "Synthesis and application in asymmetric C-C bond formation of solution phase ligand libraries of monodentate phosphoramidites." Organic & biomolecular chemistry vol. 2,12 (2004): 1682-4. doi: https://doi.org/10.1039/b404996a
Duursma A, Lefort L, Boogers JA, de Vries AH, de Vries JG, Minnaard AJ, Feringa BL. Synthesis and application in asymmetric C-C bond formation of solution phase ligand libraries of monodentate phosphoramidites. Org Biomol Chem. 2004 Jun 21;2(12):1682-4. doi: 10.1039/b404996a. Epub 2004 May 25. PMID: 15188032.
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Improving conversion and enantioselectivity in hydrogenation by combining different monodentate phosphoramidites; a new combinatorial approach in asymmetric catalysis.

Organic & biomolecular chemistry

Peña D, Minnaard AJ, Boogers JA, de Vries AH, de Vries JG, Feringa BL.
PMID: 12926377
Org Biomol Chem. 2003 Apr 07;1(7):1087-9. doi: 10.1039/b302097e.

The combination of monodentate ligands in the rhodium-catalysed enantioselective hydrogenation enables a new approach when searching for the optimal activity and enantioselectivity in catalysis.

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Peña D, Minnaard AJ, Boogers JA, et al. Improving conversion and enantioselectivity in hydrogenation by combining different monodentate phosphoramidites; a new combinatorial approach in asymmetric catalysis. Org Biomol Chem. 2003;1(7):1087-9doi: 10.1039/b302097e.
Peña, D., Minnaard, A. J., Boogers, J. A., de Vries, A. H., de Vries, J. G., & Feringa, B. L. (2003). Improving conversion and enantioselectivity in hydrogenation by combining different monodentate phosphoramidites; a new combinatorial approach in asymmetric catalysis. Organic & biomolecular chemistry, 1(7), 1087-9. https://doi.org/10.1039/b302097e
Peña, Diego, et al. "Improving conversion and enantioselectivity in hydrogenation by combining different monodentate phosphoramidites; a new combinatorial approach in asymmetric catalysis." Organic & biomolecular chemistry vol. 1,7 (2003): 1087-9. doi: https://doi.org/10.1039/b302097e
Peña D, Minnaard AJ, Boogers JA, de Vries AH, de Vries JG, Feringa BL. Improving conversion and enantioselectivity in hydrogenation by combining different monodentate phosphoramidites; a new combinatorial approach in asymmetric catalysis. Org Biomol Chem. 2003 Apr 07;1(7):1087-9. doi: 10.1039/b302097e. PMID: 12926377.
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Selective Pd-catalyzed oxidative coupling of anilides with olefins through C-H bond activation at room temperature.

Journal of the American Chemical Society

Boele MD, van Strijdonck GP, de Vries AH, Kamer PC, de Vries JG, van Leeuwen PW.
PMID: 11853427
J Am Chem Soc. 2002 Feb 27;124(8):1586-7. doi: 10.1021/ja0176907.

Using a high-throughput experimentation approach we found a selective and mild Pd-catalyzed oxidative coupling reaction between anilide derivatives and acrylates that occurs through ortho C-H bond activation. The reaction is carried out in an acidic environment and occurs even...

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Boele MD, van Strijdonck GP, de Vries AH, et al. Selective Pd-catalyzed oxidative coupling of anilides with olefins through C-H bond activation at room temperature. J Am Chem Soc. 2002;124(8):1586-7doi: 10.1021/ja0176907.
Boele, M. D., van Strijdonck, G. P., de Vries, A. H., Kamer, P. C., de Vries, J. G., & van Leeuwen, P. W. (2002). Selective Pd-catalyzed oxidative coupling of anilides with olefins through C-H bond activation at room temperature. Journal of the American Chemical Society, 124(8), 1586-7. https://doi.org/10.1021/ja0176907
Boele, Maarten D K, et al. "Selective Pd-catalyzed oxidative coupling of anilides with olefins through C-H bond activation at room temperature." Journal of the American Chemical Society vol. 124,8 (2002): 1586-7. doi: https://doi.org/10.1021/ja0176907
Boele MD, van Strijdonck GP, de Vries AH, Kamer PC, de Vries JG, van Leeuwen PW. Selective Pd-catalyzed oxidative coupling of anilides with olefins through C-H bond activation at room temperature. J Am Chem Soc. 2002 Feb 27;124(8):1586-7. doi: 10.1021/ja0176907. PMID: 11853427.
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Fusion of SV40 Tumor Cells and Indicator Cells.

Science (New York, N.Y.)

Payne FE, de Vries L.
PMID: 17749108
Science. 1967 Oct 27;158(3800):533-4. doi: 10.1126/science.158.3800.533-b.

No abstract available.

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Payne FE, de Vries L. Fusion of SV40 Tumor Cells and Indicator Cells. Science. 1967;158(3800):533-4doi: 10.1126/science.158.3800.533-b.
Payne, F. E., & de Vries, L. (1967). Fusion of SV40 Tumor Cells and Indicator Cells. Science (New York, N.Y.), 158(3800), 533-4. https://doi.org/10.1126/science.158.3800.533-b
Payne, F E, and de Vries, L. "Fusion of SV40 Tumor Cells and Indicator Cells." Science (New York, N.Y.) vol. 158,3800 (1967): 533-4. doi: https://doi.org/10.1126/science.158.3800.533-b
Payne FE, de Vries L. Fusion of SV40 Tumor Cells and Indicator Cells. Science. 1967 Oct 27;158(3800):533-4. doi: 10.1126/science.158.3800.533-b. PMID: 17749108.
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Equine arteritis virus.

Theriogenology

Glaser AL, Chirnside ED, Horzinek MC, de Vries AA.
PMID: 16728076
Theriogenology. 1997 Apr 15;47(6):1275-95. doi: 10.1016/s0093-691x(97)00107-6.

Equine arteritis virus (EAV) is a small, enveloped, positive-stranded RNA virus, in the family Arteriviridae , W.H.ich can infect both horses and donkeys. While the majority of EAV infections are asymptomatic, acutely infected animals may develop a wide range...

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Glaser AL, Chirnside ED, Horzinek MC, et al. Equine arteritis virus. Theriogenology. 1997;47(6):1275-95doi: 10.1016/s0093-691x(97)00107-6.
Glaser, A. L., Chirnside, E. D., Horzinek, M. C., & de Vries, A. A. (1997). Equine arteritis virus. Theriogenology, 47(6), 1275-95. https://doi.org/10.1016/s0093-691x(97)00107-6
Glaser, A L, et al. "Equine arteritis virus." Theriogenology vol. 47,6 (1997): 1275-95. doi: https://doi.org/10.1016/s0093-691x(97)00107-6
Glaser AL, Chirnside ED, Horzinek MC, de Vries AA. Equine arteritis virus. Theriogenology. 1997 Apr 15;47(6):1275-95. doi: 10.1016/s0093-691x(97)00107-6. PMID: 16728076; PMCID: PMC7127492.
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Melting inhibition and superheating of ice by an antifreeze glycopeptide.

Science (New York, N.Y.)

Knight CA, Devries AL.
PMID: 17750260
Science. 1989 Aug 04;245(4917):505-7. doi: 10.1126/science.245.4917.505.

The melting of pure ice single crystals can be inhibited by the presence of an antifreeze glycopeptide isolated from an Antarctic fish. This inhibition effect exhibits crystallographic dependence and can result in superheating of the crystal by heat conduction...

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Knight CA, Devries AL. Melting inhibition and superheating of ice by an antifreeze glycopeptide. Science. 1989;245(4917):505-7doi: 10.1126/science.245.4917.505.
Knight, C. A., & Devries, A. L. (1989). Melting inhibition and superheating of ice by an antifreeze glycopeptide. Science (New York, N.Y.), 245(4917), 505-7. https://doi.org/10.1126/science.245.4917.505
Knight, C A, and Devries, A L. "Melting inhibition and superheating of ice by an antifreeze glycopeptide." Science (New York, N.Y.) vol. 245,4917 (1989): 505-7. doi: https://doi.org/10.1126/science.245.4917.505
Knight CA, Devries AL. Melting inhibition and superheating of ice by an antifreeze glycopeptide. Science. 1989 Aug 04;245(4917):505-7. doi: 10.1126/science.245.4917.505. PMID: 17750260.
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STUDIES ON AMINO ACID METABOLISM. II. BLOOD GLYCINE AND TOTAL AMINO ACIDS IN VARIOUS PATHOLOGICAL CONDITIONS, WITH OBSERVATIONS ON THE EFFECTS OF INTRAVENOUSLY ADMINISTERED GLYCINE.

The Journal of clinical investigation

de Vries A, Alexander B, Quamo Y.
PMID: 16695586
J Clin Invest. 1948 Sep;27(5):655-64. doi: 10.1172/JCI102013.

No abstract available.

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de Vries A, Alexander B, Quamo Y. STUDIES ON AMINO ACID METABOLISM. II. BLOOD GLYCINE AND TOTAL AMINO ACIDS IN VARIOUS PATHOLOGICAL CONDITIONS, WITH OBSERVATIONS ON THE EFFECTS OF INTRAVENOUSLY ADMINISTERED GLYCINE. J Clin Invest. 1948;27(5):655-64doi: 10.1172/JCI102013.
de Vries, A., Alexander, B., & Quamo, Y. (1948). STUDIES ON AMINO ACID METABOLISM. II. BLOOD GLYCINE AND TOTAL AMINO ACIDS IN VARIOUS PATHOLOGICAL CONDITIONS, WITH OBSERVATIONS ON THE EFFECTS OF INTRAVENOUSLY ADMINISTERED GLYCINE. The Journal of clinical investigation, 27(5), 655-64. https://doi.org/10.1172/JCI102013
de Vries, A, et al. "STUDIES ON AMINO ACID METABOLISM. II. BLOOD GLYCINE AND TOTAL AMINO ACIDS IN VARIOUS PATHOLOGICAL CONDITIONS, WITH OBSERVATIONS ON THE EFFECTS OF INTRAVENOUSLY ADMINISTERED GLYCINE." The Journal of clinical investigation vol. 27,5 (1948): 655-64. doi: https://doi.org/10.1172/JCI102013
de Vries A, Alexander B, Quamo Y. STUDIES ON AMINO ACID METABOLISM. II. BLOOD GLYCINE AND TOTAL AMINO ACIDS IN VARIOUS PATHOLOGICAL CONDITIONS, WITH OBSERVATIONS ON THE EFFECTS OF INTRAVENOUSLY ADMINISTERED GLYCINE. J Clin Invest. 1948 Sep;27(5):655-64. doi: 10.1172/JCI102013. PMID: 16695586; PMCID: PMC439538.
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Showing 1 to 12 of 215 entries