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Showing 1 to 12 of 104 entries
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Increased Glucose Transport into Neurons Rescues Aβ Toxicity in Drosophila.

Current biology : CB

Niccoli T, Cabecinha M, Tillmann A, Kerr F, Wong CT, Cardenes D, Vincent AJ, Bettedi L, Li L, Grönke S, Dols J, Partridge L.
PMID: 27676294
Curr Biol. 2016 Sep 26;26(18):2550. doi: 10.1016/j.cub.2016.09.018. Epub 2016 Sep 26.

No abstract available.

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Niccoli T, Cabecinha M, Tillmann A, et al. Increased Glucose Transport into Neurons Rescues Aβ Toxicity in Drosophila. Curr Biol. 2016;26(18):2550doi: 10.1016/j.cub.2016.09.018.
Niccoli, T., Cabecinha, M., Tillmann, A., Kerr, F., Wong, C. T., Cardenes, D., Vincent, A. J., Bettedi, L., Li, L., Grönke, S., Dols, J., & Partridge, L. (2016). Increased Glucose Transport into Neurons Rescues Aβ Toxicity in Drosophila. Current biology : CB, 26(18), 2550. https://doi.org/10.1016/j.cub.2016.09.018
Niccoli, Teresa, et al. "Increased Glucose Transport into Neurons Rescues Aβ Toxicity in Drosophila." Current biology : CB vol. 26,18 (2016): 2550. doi: https://doi.org/10.1016/j.cub.2016.09.018
Niccoli T, Cabecinha M, Tillmann A, Kerr F, Wong CT, Cardenes D, Vincent AJ, Bettedi L, Li L, Grönke S, Dols J, Partridge L. Increased Glucose Transport into Neurons Rescues Aβ Toxicity in Drosophila. Curr Biol. 2016 Sep 26;26(18):2550. doi: 10.1016/j.cub.2016.09.018. Epub 2016 Sep 26. PMID: 27676294; PMCID: PMC5628945.
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Sub-cellular Electrical Heterogeneity Revealed by Loose Patch Recording Reflects Differential Localization of Sarcolemmal Ion Channels in Intact Rat Hearts.

Frontiers in physiology

Kubasov IV, Stepanov A, Bobkov D, Radwanski PB, Terpilowski MA, Dobretsov M, Gyorke S.
PMID: 29487533
Front Physiol. 2018 Feb 13;9:61. doi: 10.3389/fphys.2018.00061. eCollection 2018.

The cardiac action potential (AP) is commonly recoded as an integral signal from isolated myocytes or ensembles of myocytes (with intracellular microelectrodes and extracellular macroelectrodes, respectively). These signals, however, do not provide a direct measure of activity of ion...

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Kubasov IV, Stepanov A, Bobkov D, et al. Sub-cellular Electrical Heterogeneity Revealed by Loose Patch Recording Reflects Differential Localization of Sarcolemmal Ion Channels in Intact Rat Hearts. Front Physiol. 2018;9:61doi: 10.3389/fphys.2018.00061.
Kubasov, I. V., Stepanov, A., Bobkov, D., Radwanski, P. B., Terpilowski, M. A., Dobretsov, M., & Gyorke, S. (2018). Sub-cellular Electrical Heterogeneity Revealed by Loose Patch Recording Reflects Differential Localization of Sarcolemmal Ion Channels in Intact Rat Hearts. Frontiers in physiology, 961. https://doi.org/10.3389/fphys.2018.00061
Kubasov, Igor V, et al. "Sub-cellular Electrical Heterogeneity Revealed by Loose Patch Recording Reflects Differential Localization of Sarcolemmal Ion Channels in Intact Rat Hearts." Frontiers in physiology vol. 9 (2018): 61. doi: https://doi.org/10.3389/fphys.2018.00061
Kubasov IV, Stepanov A, Bobkov D, Radwanski PB, Terpilowski MA, Dobretsov M, Gyorke S. Sub-cellular Electrical Heterogeneity Revealed by Loose Patch Recording Reflects Differential Localization of Sarcolemmal Ion Channels in Intact Rat Hearts. Front Physiol. 2018 Feb 13;9:61. doi: 10.3389/fphys.2018.00061. eCollection 2018. PMID: 29487533; PMCID: PMC5816904.
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Are There Carbenes in N-Heterocyclic Carbene Organocatalysis?.

Angewandte Chemie (International ed. in English)

Gehrke S, Hollóczki O.
PMID: 29072807
Angew Chem Int Ed Engl. 2017 Dec 18;56(51):16395-16398. doi: 10.1002/anie.201708305. Epub 2017 Nov 22.

Azolium cations are widely employed in organocatalysis to catalyse highly valuable synthetic processes in the presence of a base. These reactions are called "N-heterocyclic carbene catalysis", based on the assumption that they are initiated by the formation of a...

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Gehrke S, Hollóczki O. Are There Carbenes in N-Heterocyclic Carbene Organocatalysis?. Angew Chem Int Ed Engl. 2017;56(51):16395-16398doi: 10.1002/anie.201708305.
Gehrke, S., & Hollóczki, O. (2017). Are There Carbenes in N-Heterocyclic Carbene Organocatalysis?. Angewandte Chemie (International ed. in English), 56(51), 16395-16398. https://doi.org/10.1002/anie.201708305
Gehrke, Sascha, and Hollóczki, Oldamur. "Are There Carbenes in N-Heterocyclic Carbene Organocatalysis?." Angewandte Chemie (International ed. in English) vol. 56,51 (2017): 16395-16398. doi: https://doi.org/10.1002/anie.201708305
Gehrke S, Hollóczki O. Are There Carbenes in N-Heterocyclic Carbene Organocatalysis?. Angew Chem Int Ed Engl. 2017 Dec 18;56(51):16395-16398. doi: 10.1002/anie.201708305. Epub 2017 Nov 22. PMID: 29072807.
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Homogenous nucleation rates of n-propanol measured in the Laminar Flow Diffusion Chamber at different total pressures.

The Journal of chemical physics

Görke H, Neitola K, Hyvärinen AP, Lihavainen H, Wölk J, Strey R, Brus D.
PMID: 24811635
J Chem Phys. 2014 May 07;140(17):174301. doi: 10.1063/1.4872364.

Nucleation rates of n-propanol were investigated in the Laminar Flow Diffusion Chamber. Nucleation temperatures between 270 and 300 K and rates between 10(0) and 10(6) cm(-3) s(-1) were achieved. Since earlier measurements of n-butanol and n‑pentanol suggest a dependence...

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Görke H, Neitola K, Hyvärinen AP, et al. Homogenous nucleation rates of n-propanol measured in the Laminar Flow Diffusion Chamber at different total pressures. J Chem Phys. 2014;140(17):174301doi: 10.1063/1.4872364.
Görke, H., Neitola, K., Hyvärinen, A. P., Lihavainen, H., Wölk, J., Strey, R., & Brus, D. (2014). Homogenous nucleation rates of n-propanol measured in the Laminar Flow Diffusion Chamber at different total pressures. The Journal of chemical physics, 140(17), 174301. https://doi.org/10.1063/1.4872364
Görke, Hanna, et al. "Homogenous nucleation rates of n-propanol measured in the Laminar Flow Diffusion Chamber at different total pressures." The Journal of chemical physics vol. 140,17 (2014): 174301. doi: https://doi.org/10.1063/1.4872364
Görke H, Neitola K, Hyvärinen AP, Lihavainen H, Wölk J, Strey R, Brus D. Homogenous nucleation rates of n-propanol measured in the Laminar Flow Diffusion Chamber at different total pressures. J Chem Phys. 2014 May 07;140(17):174301. doi: 10.1063/1.4872364. PMID: 24811635.
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Confinement and inhomogeneous broadening effects in the quantum oscillatory magnetization of quantum dot ensembles.

Journal of physics. Condensed matter : an Institute of Physics journal

Herzog F, Heedt S, Goerke S, Ibrahim A, Rupprecht B, Heyn Ch, Hardtdegen H, Schäpers T, Wilde MA, Grundler D.
PMID: 26740509
J Phys Condens Matter. 2016 Feb 03;28(4):045301. doi: 10.1088/0953-8984/28/4/045301. Epub 2016 Jan 07.

We report on the magnetization of ensembles of etched quantum dots with a lateral diameter of 460 nm, which we prepared from InGaAs/InP heterostructures. The quantum dots exhibit 1/B-periodic de-Haas-van-Alphen-type oscillations in the magnetization M(B) for external magnetic fields...

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Herzog F, Heedt S, Goerke S, et al. Confinement and inhomogeneous broadening effects in the quantum oscillatory magnetization of quantum dot ensembles. J Phys Condens Matter. 2016;28(4):045301doi: 10.1088/0953-8984/28/4/045301.
Herzog, F., Heedt, S., Goerke, S., Ibrahim, A., Rupprecht, B., Heyn, C. h., Hardtdegen, H., Schäpers, T., Wilde, M. A., & Grundler, D. (2016). Confinement and inhomogeneous broadening effects in the quantum oscillatory magnetization of quantum dot ensembles. Journal of physics. Condensed matter : an Institute of Physics journal, 28(4), 045301. https://doi.org/10.1088/0953-8984/28/4/045301
Herzog, F, et al. "Confinement and inhomogeneous broadening effects in the quantum oscillatory magnetization of quantum dot ensembles." Journal of physics. Condensed matter : an Institute of Physics journal vol. 28,4 (2016): 045301. doi: https://doi.org/10.1088/0953-8984/28/4/045301
Herzog F, Heedt S, Goerke S, Ibrahim A, Rupprecht B, Heyn Ch, Hardtdegen H, Schäpers T, Wilde MA, Grundler D. Confinement and inhomogeneous broadening effects in the quantum oscillatory magnetization of quantum dot ensembles. J Phys Condens Matter. 2016 Feb 03;28(4):045301. doi: 10.1088/0953-8984/28/4/045301. Epub 2016 Jan 07. PMID: 26740509.
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Influence of hydroxyapatite granule size, porosity, and crystallinity on tissue reaction in vivo. Part B: a comparative study with biphasic synthetic biomaterials.

Clinical oral implants research

Maté Sánchez de Val JE, Calvo-Guirado JL, Gómez-Moreno G, Gehrke S, Mazón P, De Aza PN.
PMID: 27273203
Clin Oral Implants Res. 2018 Nov;29(11):1077-1084. doi: 10.1111/clr.12880. Epub 2016 Jun 06.

OBJECTIVE: The aim of this study was to compare the influence of the physical-chemical properties of synthetic hydroxyapatite (HA) and biphasic commercial materials on the biological behavior of study materials through material characterization and SEM analysis before and after...

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Maté Sánchez de Val JE, Calvo-Guirado JL, Gómez-Moreno G, et al. Influence of hydroxyapatite granule size, porosity, and crystallinity on tissue reaction in vivo. Part B: a comparative study with biphasic synthetic biomaterials. Clin Oral Implants Res. 2016;29(11):1077-1084doi: 10.1111/clr.12880.
Maté Sánchez de Val, J. E., Calvo-Guirado, J. L., Gómez-Moreno, G., Gehrke, S., Mazón, P., & De Aza, P. N. (2018). Influence of hydroxyapatite granule size, porosity, and crystallinity on tissue reaction in vivo. Part B: a comparative study with biphasic synthetic biomaterials. Clinical oral implants research, 29(11), 1077-1084. https://doi.org/10.1111/clr.12880
Maté Sánchez de Val, José Eduardo, et al. "Influence of hydroxyapatite granule size, porosity, and crystallinity on tissue reaction in vivo. Part B: a comparative study with biphasic synthetic biomaterials." Clinical oral implants research vol. 29,11 (2018): 1077-1084. doi: https://doi.org/10.1111/clr.12880
Maté Sánchez de Val JE, Calvo-Guirado JL, Gómez-Moreno G, Gehrke S, Mazón P, De Aza PN. Influence of hydroxyapatite granule size, porosity, and crystallinity on tissue reaction in vivo. Part B: a comparative study with biphasic synthetic biomaterials. Clin Oral Implants Res. 2018 Nov;29(11):1077-1084. doi: 10.1111/clr.12880. Epub 2016 Jun 06. PMID: 27273203.
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Life-threatening asthma attack during prolonged fingolimod treatment: case report.

Patient preference and adherence

Zecca C, Caporro M, Györik S, Gobbi C.
PMID: 25053881
Patient Prefer Adherence. 2014 Jul 14;8:987-9. doi: 10.2147/PPA.S65708. eCollection 2014.

BACKGROUND: Fingolimod (FTY) mediates bronchoconstriction by interacting with sphingosine-1-phosphate receptors. The majority of the reported adverse respiratory events occur during the first weeks of treatment.CASE PRESENTATION: A 49-year-old woman developed a life-threatening asthma attack after 6 months of continuous...

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Zecca C, Caporro M, Györik S, et al. Life-threatening asthma attack during prolonged fingolimod treatment: case report. Patient Prefer Adherence. 2014;8:987-9doi: 10.2147/PPA.S65708.
Zecca, C., Caporro, M., Györik, S., & Gobbi, C. (2014). Life-threatening asthma attack during prolonged fingolimod treatment: case report. Patient preference and adherence, 8987-9. https://doi.org/10.2147/PPA.S65708
Zecca, Chiara, et al. "Life-threatening asthma attack during prolonged fingolimod treatment: case report." Patient preference and adherence vol. 8 (2014): 987-9. doi: https://doi.org/10.2147/PPA.S65708
Zecca C, Caporro M, Györik S, Gobbi C. Life-threatening asthma attack during prolonged fingolimod treatment: case report. Patient Prefer Adherence. 2014 Jul 14;8:987-9. doi: 10.2147/PPA.S65708. eCollection 2014. PMID: 25053881; PMCID: PMC4105229.
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Correction: Hormonal Neuroendocrine and Vasoconstrictor Peptide Responses of Ball Game and Cyclic Sport Elite Athletes by Treadmill Test.

PloS one

Protzner A, Szmodis M, Udvardy A, Bosnyák E, Trájer E, Komka Z, Györe I, Tóth M.
PMID: 27074022
PLoS One. 2016 Apr 13;11(4):e0153905. doi: 10.1371/journal.pone.0153905. eCollection 2016.

No abstract available.

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Protzner A, Szmodis M, Udvardy A, et al. Correction: Hormonal Neuroendocrine and Vasoconstrictor Peptide Responses of Ball Game and Cyclic Sport Elite Athletes by Treadmill Test. PLoS One. 2016;11(4):e0153905doi: 10.1371/journal.pone.0153905.
Protzner, A., Szmodis, M., Udvardy, A., Bosnyák, E., Trájer, E., Komka, Z., Györe, I., & Tóth, M. (2016). Correction: Hormonal Neuroendocrine and Vasoconstrictor Peptide Responses of Ball Game and Cyclic Sport Elite Athletes by Treadmill Test. PloS one, 11(4), e0153905. https://doi.org/10.1371/journal.pone.0153905
Protzner, Anna, et al. "Correction: Hormonal Neuroendocrine and Vasoconstrictor Peptide Responses of Ball Game and Cyclic Sport Elite Athletes by Treadmill Test." PloS one vol. 11,4 (2016): e0153905. doi: https://doi.org/10.1371/journal.pone.0153905
Protzner A, Szmodis M, Udvardy A, Bosnyák E, Trájer E, Komka Z, Györe I, Tóth M. Correction: Hormonal Neuroendocrine and Vasoconstrictor Peptide Responses of Ball Game and Cyclic Sport Elite Athletes by Treadmill Test. PLoS One. 2016 Apr 13;11(4):e0153905. doi: 10.1371/journal.pone.0153905. eCollection 2016. PMID: 27074022; PMCID: PMC4830537.
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Two Small RNAs Conserved in Enterobacteriaceae Provide Intrinsic Resistance to Antibiotics Targeting the Cell Wall Biosynthesis Enzyme Glucosamine-6-Phosphate Synthase.

Frontiers in microbiology

Khan MA, Göpel Y, Milewski S, Görke B.
PMID: 27379045
Front Microbiol. 2016 Jun 15;7:908. doi: 10.3389/fmicb.2016.00908. eCollection 2016.

Formation of glucosamine-6-phosphate (GlcN6P) by enzyme GlcN6P synthase (GlmS) represents the first step in bacterial cell envelope synthesis. In Escherichia coli, expression of glmS is controlled by small RNAs (sRNAs) GlmY and GlmZ. GlmZ activates the glmS mRNA by...

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Khan MA, Göpel Y, Milewski S, et al. Two Small RNAs Conserved in Enterobacteriaceae Provide Intrinsic Resistance to Antibiotics Targeting the Cell Wall Biosynthesis Enzyme Glucosamine-6-Phosphate Synthase. Front Microbiol. 2016;7:908doi: 10.3389/fmicb.2016.00908.
Khan, M. A., Göpel, Y., Milewski, S., & Görke, B. (2016). Two Small RNAs Conserved in Enterobacteriaceae Provide Intrinsic Resistance to Antibiotics Targeting the Cell Wall Biosynthesis Enzyme Glucosamine-6-Phosphate Synthase. Frontiers in microbiology, 7908. https://doi.org/10.3389/fmicb.2016.00908
Khan, Muna A, et al. "Two Small RNAs Conserved in Enterobacteriaceae Provide Intrinsic Resistance to Antibiotics Targeting the Cell Wall Biosynthesis Enzyme Glucosamine-6-Phosphate Synthase." Frontiers in microbiology vol. 7 (2016): 908. doi: https://doi.org/10.3389/fmicb.2016.00908
Khan MA, Göpel Y, Milewski S, Görke B. Two Small RNAs Conserved in Enterobacteriaceae Provide Intrinsic Resistance to Antibiotics Targeting the Cell Wall Biosynthesis Enzyme Glucosamine-6-Phosphate Synthase. Front Microbiol. 2016 Jun 15;7:908. doi: 10.3389/fmicb.2016.00908. eCollection 2016. PMID: 27379045; PMCID: PMC4908143.
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F-FDG PET scan as follow-up tool for sarcoidosis with symptomatic cardiac conduction disturbances requiring a pacemaker.

BMJ case reports

Györik S, Ceriani L, Menafoglio A, Gallino A, Wyttenbach R.
PMID: 21687094
BMJ Case Rep. 2009;2009:bcr2006070805. doi: 10.1136/bcr.2006.070805. Epub 2009 Feb 18.

No abstract available.

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Györik S, Ceriani L, Menafoglio A, et al. F-FDG PET scan as follow-up tool for sarcoidosis with symptomatic cardiac conduction disturbances requiring a pacemaker. BMJ Case Rep. 2009;2009:bcr2006070805doi: 10.1136/bcr.2006.070805.
Györik, S., Ceriani, L., Menafoglio, A., Gallino, A., & Wyttenbach, R. (2009). F-FDG PET scan as follow-up tool for sarcoidosis with symptomatic cardiac conduction disturbances requiring a pacemaker. BMJ case reports, 2009bcr2006070805. https://doi.org/10.1136/bcr.2006.070805
Györik, S, et al. "F-FDG PET scan as follow-up tool for sarcoidosis with symptomatic cardiac conduction disturbances requiring a pacemaker." BMJ case reports vol. 2009 (2009): bcr2006070805. doi: https://doi.org/10.1136/bcr.2006.070805
Györik S, Ceriani L, Menafoglio A, Gallino A, Wyttenbach R. F-FDG PET scan as follow-up tool for sarcoidosis with symptomatic cardiac conduction disturbances requiring a pacemaker. BMJ Case Rep. 2009;2009:bcr2006070805. doi: 10.1136/bcr.2006.070805. Epub 2009 Feb 18. PMID: 21687094; PMCID: PMC3106073.
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Methacrylated gelatin/hyaluronan-based hydrogels for soft tissue engineering.

Journal of tissue engineering

Kessler L, Gehrke S, Winnefeld M, Huber B, Hoch E, Walter T, Wyrwa R, Schnabelrauch M, Schmidt M, Kückelhaus M, Lehnhardt M, Hirsch T, Jacobsen F.
PMID: 29318000
J Tissue Eng. 2017 Dec 21;8:2041731417744157. doi: 10.1177/2041731417744157. eCollection 2017.

In vitro-generated soft tissue could provide alternate therapies for soft tissue defects. The aim of this study was to evaluate methacrylated gelatin/hyaluronan as scaffolds for soft tissue engineering and their interaction with human adipose-derived stem cells (hASCs). ASCs were...

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Kessler L, Gehrke S, Winnefeld M, et al. Methacrylated gelatin/hyaluronan-based hydrogels for soft tissue engineering. J Tissue Eng. 2017;8:2041731417744157doi: 10.1177/2041731417744157.
Kessler, L., Gehrke, S., Winnefeld, M., Huber, B., Hoch, E., Walter, T., Wyrwa, R., Schnabelrauch, M., Schmidt, M., Kückelhaus, M., Lehnhardt, M., Hirsch, T., & Jacobsen, F. (2017). Methacrylated gelatin/hyaluronan-based hydrogels for soft tissue engineering. Journal of tissue engineering, 82041731417744157. https://doi.org/10.1177/2041731417744157
Kessler, Lukas, et al. "Methacrylated gelatin/hyaluronan-based hydrogels for soft tissue engineering." Journal of tissue engineering vol. 8 (2017): 2041731417744157. doi: https://doi.org/10.1177/2041731417744157
Kessler L, Gehrke S, Winnefeld M, Huber B, Hoch E, Walter T, Wyrwa R, Schnabelrauch M, Schmidt M, Kückelhaus M, Lehnhardt M, Hirsch T, Jacobsen F. Methacrylated gelatin/hyaluronan-based hydrogels for soft tissue engineering. J Tissue Eng. 2017 Dec 21;8:2041731417744157. doi: 10.1177/2041731417744157. eCollection 2017. PMID: 29318000; PMCID: PMC5753891.
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Time Course of Metabolomic Alterations in Cerebrospinal Fluid After Aneurysmal Subarachnoid Hemorrhage.

Frontiers in neurology

Ho WM, Görke AS, Glodny B, Oberacher H, Helbok R, Thomé C, Petr O.
PMID: 32655487
Front Neurol. 2020 Jun 23;11:589. doi: 10.3389/fneur.2020.00589. eCollection 2020.

No abstract available.

Cite
Ho WM, Görke AS, Glodny B, et al. Time Course of Metabolomic Alterations in Cerebrospinal Fluid After Aneurysmal Subarachnoid Hemorrhage. Front Neurol. 2020;11:589doi: 10.3389/fneur.2020.00589.
Ho, W. M., Görke, A. S., Glodny, B., Oberacher, H., Helbok, R., Thomé, C., & Petr, O. (2020). Time Course of Metabolomic Alterations in Cerebrospinal Fluid After Aneurysmal Subarachnoid Hemorrhage. Frontiers in neurology, 11589. https://doi.org/10.3389/fneur.2020.00589
Ho, Wing Mann, et al. "Time Course of Metabolomic Alterations in Cerebrospinal Fluid After Aneurysmal Subarachnoid Hemorrhage." Frontiers in neurology vol. 11 (2020): 589. doi: https://doi.org/10.3389/fneur.2020.00589
Ho WM, Görke AS, Glodny B, Oberacher H, Helbok R, Thomé C, Petr O. Time Course of Metabolomic Alterations in Cerebrospinal Fluid After Aneurysmal Subarachnoid Hemorrhage. Front Neurol. 2020 Jun 23;11:589. doi: 10.3389/fneur.2020.00589. eCollection 2020. PMID: 32655487; PMCID: PMC7324721.
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