Academic literature on the topic 'Affiniteit (chemie)'

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Journal articles on the topic "Affiniteit (chemie)"

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Andersson, M. N., F. Schlyter, S. R. Hill, and T. Dekker. "What Reaches the Antenna? How to Calibrate Odor Flux and Ligand-Receptor Affinities." Chemical Senses 37, no. 5 (February 23, 2012): 403–20. http://dx.doi.org/10.1093/chemse/bjs009.

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Hérent, Marie-France, Sonia Collin, and Paolo Pelosi. "Affinities of Nutty and Green-smelling Pyrazines and Thiazoles to Odorant-binding Proteins, in Relation with their Lipophilicity." Chemical Senses 20, no. 6 (1995): 601–8. http://dx.doi.org/10.1093/chemse/20.6.601.

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Barlow, Stephen, Qing Zhang, Bilal R Kaafarani, Chad Risko, Fabrice Amy, Calvin K Chan, Benoit Domercq, et al. "Synthesis, Ionisation Potentials and Electron Affinities of Hexaazatrinaphthylene Derivatives." Chemistry - A European Journal 13, no. 12 (April 16, 2007): 3537–47. http://dx.doi.org/10.1002/chem.200601298.

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Lau, Justin Kai-Chi, Carrie Hoi Shan Wong, Po Shan Ng, Fung Ming Siu, Ngai Ling Ma, and Chun Wai Tsang. "Absolute Potassium Cation Affinities (PCAs) in the Gas Phase." Chemistry - A European Journal 9, no. 14 (July 21, 2003): 3383–96. http://dx.doi.org/10.1002/chem.200204678.

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Grauer, Andreas, Alexander Riechers, Stefan Ritter, and Burkhard König. "Synthetic Receptors for the Differentiation of Phosphorylated Peptides with Nanomolar Affinities." Chemistry - A European Journal 14, no. 29 (August 11, 2008): 8922–27. http://dx.doi.org/10.1002/chem.200800432.

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Zadmard, Reza, Arno Kraft, Thomas Schrader, and Uwe Linne. "Relative Binding Affinities of Molecular Capsules Investigated by ESI-Mass Spectrometry." Chemistry - A European Journal 10, no. 17 (September 6, 2004): 4233–39. http://dx.doi.org/10.1002/chem.200400034.

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Liu, Lan, Yu Bai, Nian Sun, Li Xia, Todd L. Lowary, and John S. Klassen. "Carbohydrate-Lipid Interactions: Affinities of Methylmannose Polysaccharides for Lipids in Aqueous Solution." Chemistry - A European Journal 18, no. 38 (August 14, 2012): 12059–67. http://dx.doi.org/10.1002/chem.201201222.

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Nakamura, Tadashi, Yoshihiro Noumi, Hiroyuki Yamakawa, Atsushi Nakamura, Durige Wen, Xing Li, Xiong Geng, Ken Sawada, and Tatsuo Iwasa. "Enhancement of the Olfactory Response by Lipocalin Cp-Lip1 in Newt Olfactory Receptor Cells: An Electrophysiological Study." Chemical Senses 44, no. 7 (July 26, 2019): 523–33. http://dx.doi.org/10.1093/chemse/bjz048.

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Abstract Previously, we have detected the expression of 2 lipocalin genes (lp1 and lp2) in the olfactory epithelium of the Japanese newt Cynops pyrrhogaster. Recombinant proteins of these genes (Cp-Lip1 and Cp-Lip2, respectively) exhibited high affinities to various odorants, suggesting that they work like the odorant-binding proteins (OBPs). However, the physiological functions of OBP generally remain inconclusive. Here, we examined the effect of Cp-Lip1 on the electrophysiological responses of newt olfactory receptor cells. We observed that the electro-olfactogram induced by the vapor of an odorant with high affinity to Cp-Lip1 appeared to increase in amplitude when a tiny drop of Cp-Lip1 solution was dispersed over the olfactory epithelium. However, the analysis was difficult because of possible interference by intrinsic components in the nasal mucus. We subsequently adopted a mucus-free condition by using suction electrode recordings from isolated olfactory cells, in which impulses were generated by puffs of odorant solution. When various concentration (0–5 µM) of Cp-Lip1 was mixed with the stimulus solution of odorants highly affinitive to Cp-Lip1, the impulse frequency increased in a concentration-dependent manner. The increase by Cp-Lip1 was seen more evidently at lower concentration ranges of stimulus odorants. These results strongly suggest that Cp-Lip1 broadens the sensitivity of the olfactory cells toward the lower concentration of odorants, by which animals can detect very low concentration of odorants.
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Baudet, Karine, Sebastiano Guerra, and Claude Piguet. "Chemical Potential of the Solvent: A Crucial Player for Rationalizing Host-Guest Affinities." Chemistry - A European Journal 23, no. 66 (September 21, 2017): 16787–98. http://dx.doi.org/10.1002/chem.201703184.

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Eckert-Maksik, Mirjana, Martin Klessinger, and Zvonimir B. Maksii. "A Theoretical Study of the Additivity of Proton Affinities in Aromatics: Polysubstituted Benzenes." Chemistry - A European Journal 2, no. 10 (October 1996): 1251–57. http://dx.doi.org/10.1002/chem.19960021011.

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Dissertations / Theses on the topic "Affiniteit (chemie)"

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Klein, Ursula. "Verbindung und Affinität : die Grundlegung der neuzeitlichen Chemie an der Wende vom 17 zum 18 Jahrhundert /." Basel : Birkauser, 1994. http://catalogue.bnf.fr/ark:/12148/cb391668100.

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Berger, Jutta. "Affinität und Reaktion : über die Entstehung der Reaktionskinetik in der Chemie des 19. Jahrhunderts /." Berlin : Verl. für Wiss.- und Regionalgeschichte, 2000. http://www.gbv.de/dms/ilmenau/toc/317925458.PDF.

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Wasserthal, Lennard [Verfasser], and Andreas [Akademischer Betreuer] Hirsch. "Regioselective synthesis of multifullerenes with tuneable solvent affinities / Lennard Wasserthal. Gutachter: Andreas Hirsch." Erlangen : Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 2014. http://d-nb.info/1065004982/34.

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Nockemann, Peter [Verfasser]. "Zur Affinität von Quecksilber zu Stickstoff-Donorliganden / vorgelegt von Peter Nockemann." 2002. http://d-nb.info/964991632/34.

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Books on the topic "Affiniteit (chemie)"

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Affinity and matter: Elements of chemical philosophy, 1800-1865. Yverdon, Switzerland: Gordon and Breach Science Publishers, 1993.

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Klein, Ursula. Verbindung und Affinität: Die Grundlegung der neuzeitlichen Chemie an der Wende vom 17. zum 18. Jahrhundert (Science Networks. Historical Studies). Birkhäuser Basel, 1994.

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Gmelin, Leopold. Handbuch der theoretischen Chemie: Band 1: Welcher die Lehre von der Cohäsion und Adhäsion, von der Affinität im Allgemeinen, von den unwägbaren Stoffen ... Welcher die Lehre vonden unorganischen Ver. Springer, 1988.

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Book chapters on the topic "Affiniteit (chemie)"

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Weyer, Jost. "Affinität der Stoffe." In Geschichte der Chemie Band 1 – Altertum, Mittelalter, 16. bis 18. Jahrhundert, 531–45. Berlin, Heidelberg: Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-55798-3_18.

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2

"8 Chemische Affinität." In Physikalische Chemie, 324–76. De Gruyter, 1986. http://dx.doi.org/10.1515/9783110849684.324.

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Conference papers on the topic "Affiniteit (chemie)"

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Steven, I., L. Wagner, W. E. van Nostrand, and D. D. Cunningham. "PREPARATION AND CHARACTERIZATION OF MONOCLONAL ANTIBODIES TO PROTEASE NEXIN." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644447.

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Protease nexin I (PN-1) is a cell-secreted protease inhibitor which modulates the activity of certain serine proteases in the extracellular environment. To probe PN-1 functions, we prepared a panel of monoclonal antibodies (mAbs) against it and studied their effects on a variety of PN-1 activities. Three highly potent inhibitors of PN-1 activity have been characterized. MAbs pl-6 and pl-9 stoichiometri-cally block PN-l-mediated anti-thrombin and anti-urokinase activity. These mAbs block PN-l-mediated anti-trypsin activity less effectively. MAb pl-18 stoichiometrically blocks all PN-1 antiprotease activities tested including anti-trypsin activity and therefore appears to bind at the reactive center of PN-1. Heparin, which greatly accelerates PN-1 anti-thrombin activity, does not compete with the binding of these blocking mAbs. None of these blocking mAbs could bind to thrombin-PN-1 complexes. A mAb (pl-1) which did not block PN-1 activity was capable of binding to these complexes. MAbs pl-9 and pl-18 were used to immunopurify two forms of PN-1 which have different affinities for heparin-Sepharose. These have been referred to as the low heparin affinity and high heparin affinity forms of PN-1 (Scott et al., J. Biol. Chem. 260,7029-7034 [1985]). MAb pl-18 binds only to the high heparin affinity form while mAb pl-9 binds to both forms. Preliminary characterization of this low heparin affinity form reveals no major differences between it and the well characterized high heparin affinity form.
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