[{"month":"12","author":[{"last_name":"Hof","first_name":"Björn","id":"3A374330-F248-11E8-B48F-1D18A9856A87","full_name":"Björn Hof","orcid":"0000-0003-2057-2754"},{"first_name":"Anne","last_name":"Juel","full_name":"Juel, Anne"},{"full_name":"Mullin, Tom P","last_name":"Mullin","first_name":"Tom"}],"extern":1,"citation":{"mla":"Hof, Björn, et al. “Scaling of the Turbulence Transition Threshold in a Pipe.” <i>Physical Review Letters</i>, vol. 91, no. 24, American Physical Society, 2003, p. 244502/1-244502/4, doi:<a href=\"https://doi.org/10.1103/PhysRevLett.91.244502\">10.1103/PhysRevLett.91.244502</a>.","short":"B. Hof, A. Juel, T. Mullin, Physical Review Letters 91 (2003) 244502/1-244502/4.","ieee":"B. Hof, A. Juel, and T. Mullin, “Scaling of the turbulence transition threshold in a pipe,” <i>Physical Review Letters</i>, vol. 91, no. 24. American Physical Society, p. 244502/1-244502/4, 2003.","chicago":"Hof, Björn, Anne Juel, and Tom Mullin. “Scaling of the Turbulence Transition Threshold in a Pipe.” <i>Physical Review Letters</i>. American Physical Society, 2003. <a href=\"https://doi.org/10.1103/PhysRevLett.91.244502\">https://doi.org/10.1103/PhysRevLett.91.244502</a>.","apa":"Hof, B., Juel, A., &#38; Mullin, T. (2003). Scaling of the turbulence transition threshold in a pipe. <i>Physical Review Letters</i>. American Physical Society. <a href=\"https://doi.org/10.1103/PhysRevLett.91.244502\">https://doi.org/10.1103/PhysRevLett.91.244502</a>","ista":"Hof B, Juel A, Mullin T. 2003. Scaling of the turbulence transition threshold in a pipe. Physical Review Letters. 91(24), 244502/1-244502/4.","ama":"Hof B, Juel A, Mullin T. Scaling of the turbulence transition threshold in a pipe. <i>Physical Review Letters</i>. 2003;91(24):244502/1-244502/4. doi:<a href=\"https://doi.org/10.1103/PhysRevLett.91.244502\">10.1103/PhysRevLett.91.244502</a>"},"date_created":"2018-12-11T11:59:35Z","abstract":[{"lang":"eng","text":"Experimental evidence for the scaling of the finite amplitude of perturbation theory required to promote transition in Poiseuille flow was found. The exponent is -1 and was uncovered using considerable care in the design and execution of the experiment. Interestingly, this exponent was also found in experiments on transition in boundary layers."}],"page":"244502/1 - 244502/4","date_published":"2003-12-12T00:00:00Z","status":"public","publication":"Physical Review Letters","publist_id":"4104","issue":"24","_id":"2785","intvolume":"        91","title":"Scaling of the turbulence transition threshold in a pipe","doi":"10.1103/PhysRevLett.91.244502","quality_controlled":0,"publication_status":"published","day":"12","publisher":"American Physical Society","date_updated":"2021-01-12T06:59:42Z","year":"2003","volume":91,"type":"journal_article"},{"extern":"1","date_created":"2018-12-11T12:00:43Z","citation":{"ieee":"J. Friml, “Auxin transport - Shaping the plant,” <i>Current Opinion in Plant Biology</i>, vol. 6, no. 1. Elsevier, pp. 7–12, 2003.","chicago":"Friml, Jiří. “Auxin Transport - Shaping the Plant.” <i>Current Opinion in Plant Biology</i>. Elsevier, 2003. <a href=\"https://doi.org/10.1016/S1369526602000031\">https://doi.org/10.1016/S1369526602000031</a>.","short":"J. Friml, Current Opinion in Plant Biology 6 (2003) 7–12.","mla":"Friml, Jiří. “Auxin Transport - Shaping the Plant.” <i>Current Opinion in Plant Biology</i>, vol. 6, no. 1, Elsevier, 2003, pp. 7–12, doi:<a href=\"https://doi.org/10.1016/S1369526602000031\">10.1016/S1369526602000031</a>.","ama":"Friml J. Auxin transport - Shaping the plant. <i>Current Opinion in Plant Biology</i>. 2003;6(1):7-12. doi:<a href=\"https://doi.org/10.1016/S1369526602000031\">10.1016/S1369526602000031</a>","apa":"Friml, J. (2003). Auxin transport - Shaping the plant. <i>Current Opinion in Plant Biology</i>. Elsevier. <a href=\"https://doi.org/10.1016/S1369526602000031\">https://doi.org/10.1016/S1369526602000031</a>","ista":"Friml J. 2003. Auxin transport - Shaping the plant. Current Opinion in Plant Biology. 6(1), 7–12."},"month":"02","oa_version":"None","author":[{"orcid":"0000-0002-8302-7596","full_name":"Friml, Jirí","id":"4159519E-F248-11E8-B48F-1D18A9856A87","last_name":"Friml","first_name":"Jirí"}],"user_id":"3E5EF7F0-F248-11E8-B48F-1D18A9856A87","intvolume":"         6","_id":"2990","language":[{"iso":"eng"}],"abstract":[{"text":"Plant growth is marked by its adaptability to continuous changes in environment. A regulated, differential distribution of auxin underlies many adaptation processes including organogenesis, meristem patterning and tropisms. In executing its multiple roles, auxin displays some characteristics of both a hormone and a morphogen. Studies on auxin transport, as well as tracing the intracellular movement of its molecular components, have suggested a possible scenario to explain how growth plasticity is conferred at the cellular and molecular level. The plant perceives stimuli and changes the subcellular position of auxin-transport components accordingly. These changes modulate auxin fluxes, and the newly established auxin distribution triggers the corresponding developmental response.","lang":"eng"}],"page":"7 - 12","date_published":"2003-02-01T00:00:00Z","status":"public","publist_id":"3711","publication":"Current Opinion in Plant Biology","issue":"1","publication_status":"published","day":"01","publisher":"Elsevier","date_updated":"2021-01-12T07:40:17Z","title":"Auxin transport - Shaping the plant","doi":"10.1016/S1369526602000031","quality_controlled":"1","volume":6,"type":"journal_article","year":"2003"},{"date_updated":"2021-01-12T07:40:18Z","publisher":"American Society of Plant Biologists","day":"01","publication_status":"published","quality_controlled":0,"doi":"10.1105/tpc.008433","title":"Cell polarity and PIN protein positioning in Arabidopsis require STEROL METHYLTRANSFERASE1 function","type":"journal_article","volume":15,"year":"2003","date_created":"2018-12-11T12:00:44Z","citation":{"short":"V. Willemsen, J. Friml, M. Grebe, A. Van Den Toorn, K. Palme, B. Scheres, Plant Cell 15 (2003) 612–625.","mla":"Willemsen, Viola, et al. “Cell Polarity and PIN Protein Positioning in Arabidopsis Require STEROL METHYLTRANSFERASE1 Function.” <i>Plant Cell</i>, vol. 15, no. 3, American Society of Plant Biologists, 2003, pp. 612–25, doi:<a href=\"https://doi.org/10.1105/tpc.008433\">10.1105/tpc.008433</a>.","ieee":"V. Willemsen, J. Friml, M. Grebe, A. Van Den Toorn, K. Palme, and B. Scheres, “Cell polarity and PIN protein positioning in Arabidopsis require STEROL METHYLTRANSFERASE1 function,” <i>Plant Cell</i>, vol. 15, no. 3. American Society of Plant Biologists, pp. 612–625, 2003.","chicago":"Willemsen, Viola, Jiří Friml, Markus Grebe, Albert Van Den Toorn, Klaus Palme, and Ben Scheres. “Cell Polarity and PIN Protein Positioning in Arabidopsis Require STEROL METHYLTRANSFERASE1 Function.” <i>Plant Cell</i>. American Society of Plant Biologists, 2003. <a href=\"https://doi.org/10.1105/tpc.008433\">https://doi.org/10.1105/tpc.008433</a>.","apa":"Willemsen, V., Friml, J., Grebe, M., Van Den Toorn, A., Palme, K., &#38; Scheres, B. (2003). Cell polarity and PIN protein positioning in Arabidopsis require STEROL METHYLTRANSFERASE1 function. <i>Plant Cell</i>. American Society of Plant Biologists. <a href=\"https://doi.org/10.1105/tpc.008433\">https://doi.org/10.1105/tpc.008433</a>","ista":"Willemsen V, Friml J, Grebe M, Van Den Toorn A, Palme K, Scheres B. 2003. Cell polarity and PIN protein positioning in Arabidopsis require STEROL METHYLTRANSFERASE1 function. Plant Cell. 15(3), 612–625.","ama":"Willemsen V, Friml J, Grebe M, Van Den Toorn A, Palme K, Scheres B. Cell polarity and PIN protein positioning in Arabidopsis require STEROL METHYLTRANSFERASE1 function. <i>Plant Cell</i>. 2003;15(3):612-625. doi:<a href=\"https://doi.org/10.1105/tpc.008433\">10.1105/tpc.008433</a>"},"extern":1,"author":[{"last_name":"Willemsen","first_name":"Viola","full_name":"Willemsen, Viola"},{"full_name":"Jirí Friml","orcid":"0000-0002-8302-7596","id":"4159519E-F248-11E8-B48F-1D18A9856A87","last_name":"Friml","first_name":"Jirí"},{"full_name":"Grebe, Markus","first_name":"Markus","last_name":"Grebe"},{"full_name":"Van Den Toorn, Albert","last_name":"Van Den Toorn","first_name":"Albert"},{"first_name":"Klaus","last_name":"Palme","full_name":"Palme, Klaus"},{"first_name":"Ben","last_name":"Scheres","full_name":"Scheres, Ben"}],"month":"03","_id":"2992","intvolume":"        15","publication":"Plant Cell","issue":"3","publist_id":"3710","status":"public","date_published":"2003-03-01T00:00:00Z","page":"612 - 625","abstract":[{"text":"Plants have many polarized cell types, but relatively little is known about the mechanisms that establish polarity. The orc mutant was identified originally by defects in root patterning, and positional cloning revealed that the affected gene encodes STEROL METHYLTRANSFERASE1, which is required for the appropriate synthesis and composition of major membrane sterols. smt1orc mutants displayed several conspicuous cell polarity defects. Columella root cap cells revealed perturbed polar positioning of different organelles, and in the smt1orc root epidermis, polar initiation of root hairs was more randomized. Polar auxin transport and expression of the auxin reporter DR5-β-glucuronidase were aberrant in smt1orc. Patterning defects in smt1orc resembled those observed in mutants of the PIN gene family of putative auxin efflux transporters. Consistently, the membrane localization of the PIN1 and PIN3 proteins was disturbed in smt1orc, whereas polar positioning of the influx carrier AUX1 appeared normal. Our results suggest that balanced sterol composition is a major requirement for cell polarity and auxin efflux in Arabidopsis.","lang":"eng"}]},{"publication":"Plant Journal","publist_id":"3709","issue":"1","date_published":"2003-04-01T00:00:00Z","status":"public","page":"115 - 124","abstract":[{"text":"Plant biology is currently experiencing a growing demand for easy and reliable mRNA and protein localisation techniques. Here, we present novel whole mount in situ hybridisation and immunolocalisation protocols, suitable to localise mRNAs and proteins in Arabidopsis seedlings. We demonstrate that these methods can be used in different organs of Arabidopsis seedlings as well as in other plant species. In order to achieve better reproducibility and higher throughput, we modified these protocols for automation to be performed by a liquid handling robot. In addition, we show that other procedures such as reporter enzyme assays and tissue clearing can be similarly automated. We present examples of application of our protocols including mRNA localisation and proteins and epitope tag (co)localisations which demonstrate that these methods provide reliable and versatile tools for expression, localisation and anatomical studies in plants.","lang":"eng"}],"intvolume":"        34","_id":"2993","author":[{"orcid":"0000-0002-8302-7596","full_name":"Jirí Friml","first_name":"Jirí","last_name":"Friml","id":"4159519E-F248-11E8-B48F-1D18A9856A87"},{"id":"38F4F166-F248-11E8-B48F-1D18A9856A87","first_name":"Eva","last_name":"Benková","orcid":"0000-0002-8510-9739","full_name":"Eva Benková"},{"full_name":"Mayer, Ulrike","first_name":"Ulrike","last_name":"Mayer"},{"first_name":"Klaus","last_name":"Palme","full_name":"Palme, Klaus"},{"full_name":"Muster, Gerhard","first_name":"Gerhard","last_name":"Muster"}],"month":"04","date_created":"2018-12-11T12:00:44Z","citation":{"mla":"Friml, Jiří, et al. “Automated Whole Mount Localisation Techniques for Plant Seedlings.” <i>Plant Journal</i>, vol. 34, no. 1, Wiley-Blackwell, 2003, pp. 115–24, doi:<a href=\"https://doi.org/10.1046/j.1365-313X.2003.01705.x\">10.1046/j.1365-313X.2003.01705.x</a>.","short":"J. Friml, E. Benková, U. Mayer, K. Palme, G. Muster, Plant Journal 34 (2003) 115–124.","ieee":"J. Friml, E. Benková, U. Mayer, K. Palme, and G. Muster, “Automated whole mount localisation techniques for plant seedlings,” <i>Plant Journal</i>, vol. 34, no. 1. Wiley-Blackwell, pp. 115–124, 2003.","chicago":"Friml, Jiří, Eva Benková, Ulrike Mayer, Klaus Palme, and Gerhard Muster. “Automated Whole Mount Localisation Techniques for Plant Seedlings.” <i>Plant Journal</i>. Wiley-Blackwell, 2003. <a href=\"https://doi.org/10.1046/j.1365-313X.2003.01705.x\">https://doi.org/10.1046/j.1365-313X.2003.01705.x</a>.","apa":"Friml, J., Benková, E., Mayer, U., Palme, K., &#38; Muster, G. (2003). Automated whole mount localisation techniques for plant seedlings. <i>Plant Journal</i>. Wiley-Blackwell. <a href=\"https://doi.org/10.1046/j.1365-313X.2003.01705.x\">https://doi.org/10.1046/j.1365-313X.2003.01705.x</a>","ista":"Friml J, Benková E, Mayer U, Palme K, Muster G. 2003. Automated whole mount localisation techniques for plant seedlings. Plant Journal. 34(1), 115–124.","ama":"Friml J, Benková E, Mayer U, Palme K, Muster G. Automated whole mount localisation techniques for plant seedlings. <i>Plant Journal</i>. 2003;34(1):115-124. doi:<a href=\"https://doi.org/10.1046/j.1365-313X.2003.01705.x\">10.1046/j.1365-313X.2003.01705.x</a>"},"extern":1,"year":"2003","type":"journal_article","volume":34,"quality_controlled":0,"doi":"10.1046/j.1365-313X.2003.01705.x","title":"Automated whole mount localisation techniques for plant seedlings","date_updated":"2021-01-12T07:40:18Z","publisher":"Wiley-Blackwell","day":"01","publication_status":"published"},{"year":"2003","volume":426,"type":"journal_article","title":"Regulation of phyllotaxis by polar auxin transport","doi":"10.1038/nature02081","quality_controlled":0,"publication_status":"published","day":"20","publisher":"Nature Publishing Group","date_updated":"2021-01-12T07:40:18Z","abstract":[{"lang":"eng","text":"The regular arrangement of leaves around a plant's stem, called phyllotaxis, has for centuries attracted the attention of philosophers, mathematicians and natural scientists; however, to date, studies of phyllotaxis have been largely theoretical. Leaves and flowers are formed from the shoot apical meristem, triggered by the plant hormone auxin. Auxin is transported through plant tissues by specific cellular influx and efflux carrier proteins. Here we show that proteins involved in auxin transport regulate phyllotaxis. Our data indicate that auxin is transported upwards into the meristem through the epidermis and the outermost meristem cell layer. Existing leaf primordia act as sinks, redistributing auxin and creating its heterogeneous distribution in the meristem. Auxin accumulation occurs only at certain minimal distances from existing primordia, defining the position of future primordia. This model for phyllotaxis accounts for its reiterative nature, as well as its regularity and stability."}],"page":"255 - 260","date_published":"2003-11-20T00:00:00Z","status":"public","issue":"6964","publication":"Nature","publist_id":"3707","intvolume":"       426","_id":"2994","month":"11","author":[{"full_name":"Reinhardt, Didier","first_name":"Didier","last_name":"Reinhardt"},{"first_name":"Eva","last_name":"Pesce","full_name":"Pesce, Eva-Rachele"},{"first_name":"Pia","last_name":"Stieger","full_name":"Stieger, Pia"},{"first_name":"Therese","last_name":"Mandel","full_name":"Mandel, Therese"},{"last_name":"Baltensperger","first_name":"Kurt","full_name":"Baltensperger, Kurt"},{"last_name":"Bennett","first_name":"Malcolm","full_name":"Bennett, Malcolm"},{"full_name":"Traas, Jan","first_name":"Jan","last_name":"Traas"},{"id":"4159519E-F248-11E8-B48F-1D18A9856A87","last_name":"Friml","first_name":"Jirí","full_name":"Jirí Friml","orcid":"0000-0002-8302-7596"},{"full_name":"Kuhlemeier, Cris","first_name":"Cris","last_name":"Kuhlemeier"}],"extern":1,"citation":{"apa":"Reinhardt, D., Pesce, E., Stieger, P., Mandel, T., Baltensperger, K., Bennett, M., … Kuhlemeier, C. (2003). Regulation of phyllotaxis by polar auxin transport. <i>Nature</i>. Nature Publishing Group. <a href=\"https://doi.org/10.1038/nature02081\">https://doi.org/10.1038/nature02081</a>","ista":"Reinhardt D, Pesce E, Stieger P, Mandel T, Baltensperger K, Bennett M, Traas J, Friml J, Kuhlemeier C. 2003. Regulation of phyllotaxis by polar auxin transport. Nature. 426(6964), 255–260.","ama":"Reinhardt D, Pesce E, Stieger P, et al. Regulation of phyllotaxis by polar auxin transport. <i>Nature</i>. 2003;426(6964):255-260. doi:<a href=\"https://doi.org/10.1038/nature02081\">10.1038/nature02081</a>","short":"D. Reinhardt, E. Pesce, P. Stieger, T. Mandel, K. Baltensperger, M. Bennett, J. Traas, J. Friml, C. Kuhlemeier, Nature 426 (2003) 255–260.","mla":"Reinhardt, Didier, et al. “Regulation of Phyllotaxis by Polar Auxin Transport.” <i>Nature</i>, vol. 426, no. 6964, Nature Publishing Group, 2003, pp. 255–60, doi:<a href=\"https://doi.org/10.1038/nature02081\">10.1038/nature02081</a>.","ieee":"D. Reinhardt <i>et al.</i>, “Regulation of phyllotaxis by polar auxin transport,” <i>Nature</i>, vol. 426, no. 6964. Nature Publishing Group, pp. 255–260, 2003.","chicago":"Reinhardt, Didier, Eva Pesce, Pia Stieger, Therese Mandel, Kurt Baltensperger, Malcolm Bennett, Jan Traas, Jiří Friml, and Cris Kuhlemeier. “Regulation of Phyllotaxis by Polar Auxin Transport.” <i>Nature</i>. Nature Publishing Group, 2003. <a href=\"https://doi.org/10.1038/nature02081\">https://doi.org/10.1038/nature02081</a>."},"date_created":"2018-12-11T12:00:45Z"},{"month":"11","author":[{"orcid":"0000-0002-8302-7596","full_name":"Jirí Friml","last_name":"Friml","first_name":"Jirí","id":"4159519E-F248-11E8-B48F-1D18A9856A87"},{"first_name":"Anne","last_name":"Vieten","full_name":"Vieten, Anne"},{"full_name":"Sauer, Michael","first_name":"Michael","last_name":"Sauer"},{"first_name":"Dolf","last_name":"Weijers","full_name":"Weijers, Dolf"},{"full_name":"Schwarz, Heinz","last_name":"Schwarz","first_name":"Heinz"},{"full_name":"Hamann, Thorsten","first_name":"Thorsten","last_name":"Hamann"},{"full_name":"Offringa, Remko","first_name":"Remko","last_name":"Offringa"},{"full_name":"Jürgens, Gerd","last_name":"Jürgens","first_name":"Gerd"}],"citation":{"ieee":"J. Friml <i>et al.</i>, “Efflux dependent auxin gradients establish the apical basal axis of Arabidopsis,” <i>Nature</i>, vol. 426, no. 6963. Nature Publishing Group, pp. 147–153, 2003.","chicago":"Friml, Jiří, Anne Vieten, Michael Sauer, Dolf Weijers, Heinz Schwarz, Thorsten Hamann, Remko Offringa, and Gerd Jürgens. “Efflux Dependent Auxin Gradients Establish the Apical Basal Axis of Arabidopsis.” <i>Nature</i>. Nature Publishing Group, 2003. <a href=\"https://doi.org/10.1038/nature02085\">https://doi.org/10.1038/nature02085</a>.","mla":"Friml, Jiří, et al. “Efflux Dependent Auxin Gradients Establish the Apical Basal Axis of Arabidopsis.” <i>Nature</i>, vol. 426, no. 6963, Nature Publishing Group, 2003, pp. 147–53, doi:<a href=\"https://doi.org/10.1038/nature02085\">10.1038/nature02085</a>.","short":"J. Friml, A. Vieten, M. Sauer, D. Weijers, H. Schwarz, T. Hamann, R. Offringa, G. Jürgens, Nature 426 (2003) 147–153.","ama":"Friml J, Vieten A, Sauer M, et al. Efflux dependent auxin gradients establish the apical basal axis of Arabidopsis. <i>Nature</i>. 2003;426(6963):147-153. doi:<a href=\"https://doi.org/10.1038/nature02085\">10.1038/nature02085</a>","apa":"Friml, J., Vieten, A., Sauer, M., Weijers, D., Schwarz, H., Hamann, T., … Jürgens, G. (2003). Efflux dependent auxin gradients establish the apical basal axis of Arabidopsis. <i>Nature</i>. Nature Publishing Group. <a href=\"https://doi.org/10.1038/nature02085\">https://doi.org/10.1038/nature02085</a>","ista":"Friml J, Vieten A, Sauer M, Weijers D, Schwarz H, Hamann T, Offringa R, Jürgens G. 2003. Efflux dependent auxin gradients establish the apical basal axis of Arabidopsis. Nature. 426(6963), 147–153."},"date_created":"2018-12-11T12:00:45Z","extern":1,"status":"public","date_published":"2003-11-13T00:00:00Z","issue":"6963","publication":"Nature","publist_id":"3708","abstract":[{"text":"Axis formation occurs in plants, as in animals, during early embryogenesis. However, the underlying mechanism is not known. Here we show that the first manifestation of the apical-basal axis in plants, the asymmetric division of the zygote, produces a basal cell that transports and an apical cell that responds to the signalling molecule auxin. This apical-basal auxin activity gradient triggers the specification of apical embryo structures and is actively maintained by a novel component of auxin efflux, PIN7, which is located apically in the basal cell. Later, the developmentally regulated reversal of PIN7 and onset of PIN1 polar localization reorganize the auxin gradient for specification of the basal root pole. An analysis of pin quadruple mutants identifies PIN-dependent transport as an essential part of the mechanism for embryo axis formation. Our results indicate how the establishment of cell polarity, polar auxin efflux and local auxin response result in apical-basal axis formation of the embryo, and thus determine the axiality of the adult plant.\n","lang":"eng"}],"page":"147 - 153","_id":"2995","intvolume":"       426","quality_controlled":0,"title":"Efflux dependent auxin gradients establish the apical basal axis of Arabidopsis","doi":"10.1038/nature02085","publisher":"Nature Publishing Group","date_updated":"2021-01-12T07:40:19Z","publication_status":"published","day":"13","year":"2003","volume":426,"type":"journal_article"},{"month":"11","author":[{"first_name":"Eva","last_name":"Benková","id":"38F4F166-F248-11E8-B48F-1D18A9856A87","orcid":"0000-0002-8510-9739","full_name":"Eva Benková"},{"full_name":"Michniewicz, Marta","first_name":"Marta","last_name":"Michniewicz"},{"last_name":"Sauer","first_name":"Michael","full_name":"Sauer, Michael"},{"full_name":"Teichmann, Thomas","first_name":"Thomas","last_name":"Teichmann"},{"first_name":"Daniela","last_name":"Seifertová","full_name":"Seifertová, Daniela"},{"full_name":"Jürgens, Gerd","first_name":"Gerd","last_name":"Jürgens"},{"id":"4159519E-F248-11E8-B48F-1D18A9856A87","first_name":"Jirí","last_name":"Friml","orcid":"0000-0002-8302-7596","full_name":"Jirí Friml"}],"date_created":"2018-12-11T12:00:46Z","citation":{"chicago":"Benková, Eva, Marta Michniewicz, Michael Sauer, Thomas Teichmann, Daniela Seifertová, Gerd Jürgens, and Jiří Friml. “Local, Efflux-Dependent Auxin Gradients as a Common Module for Plant Organ Formation.” <i>Cell</i>. Cell Press, 2003. <a href=\"https://doi.org/10.1016/S0092-8674(03)00924-3\">https://doi.org/10.1016/S0092-8674(03)00924-3</a>.","ieee":"E. Benková <i>et al.</i>, “Local, efflux-dependent auxin gradients as a common module for plant organ formation,” <i>Cell</i>, vol. 115, no. 5. Cell Press, pp. 591–602, 2003.","short":"E. Benková, M. Michniewicz, M. Sauer, T. Teichmann, D. Seifertová, G. Jürgens, J. Friml, Cell 115 (2003) 591–602.","mla":"Benková, Eva, et al. “Local, Efflux-Dependent Auxin Gradients as a Common Module for Plant Organ Formation.” <i>Cell</i>, vol. 115, no. 5, Cell Press, 2003, pp. 591–602, doi:<a href=\"https://doi.org/10.1016/S0092-8674(03)00924-3\">10.1016/S0092-8674(03)00924-3</a>.","ama":"Benková E, Michniewicz M, Sauer M, et al. Local, efflux-dependent auxin gradients as a common module for plant organ formation. <i>Cell</i>. 2003;115(5):591-602. doi:<a href=\"https://doi.org/10.1016/S0092-8674(03)00924-3\">10.1016/S0092-8674(03)00924-3</a>","ista":"Benková E, Michniewicz M, Sauer M, Teichmann T, Seifertová D, Jürgens G, Friml J. 2003. Local, efflux-dependent auxin gradients as a common module for plant organ formation. Cell. 115(5), 591–602.","apa":"Benková, E., Michniewicz, M., Sauer, M., Teichmann, T., Seifertová, D., Jürgens, G., &#38; Friml, J. (2003). Local, efflux-dependent auxin gradients as a common module for plant organ formation. <i>Cell</i>. Cell Press. <a href=\"https://doi.org/10.1016/S0092-8674(03)00924-3\">https://doi.org/10.1016/S0092-8674(03)00924-3</a>"},"extern":1,"status":"public","date_published":"2003-11-26T00:00:00Z","publication":"Cell","issue":"5","publist_id":"3706","abstract":[{"text":"Plants, compared to animals, exhibit an amazing adaptability and plasticity in their development. This is largely dependent on the ability of plants to form new organs, such as lateral roots, leaves, and flowers during postembryonic development. Organ primordia develop from founder cell populations into organs by coordinated cell division and differentiation. Here, we show that organ formation in Arabidopsis involves dynamic gradients of the signaling molecule auxin with maxima at the primordia tips. These gradients are mediated by cellular efflux requiring asymmetrically localized PIN proteins, which represent a functionally redundant network for auxin distribution in both aerial and underground organs. PIN1 polar localization undergoes a dynamic rearrangement, which correlates with establishment of auxin gradients and primordium development. Our results suggest that PIN-dependent, local auxin gradients represent a common module for formation of all plant organs, regardless of their mature morphology or developmental origin.\n","lang":"eng"}],"page":"591 - 602","_id":"2996","intvolume":"       115","quality_controlled":0,"title":"Local, efflux-dependent auxin gradients as a common module for plant organ formation","doi":"10.1016/S0092-8674(03)00924-3","publisher":"Cell Press","date_updated":"2021-01-12T07:40:19Z","publication_status":"published","day":"26","year":"2003","volume":115,"type":"journal_article"},{"extern":1,"date_created":"2018-12-11T12:01:37Z","citation":{"ista":"Chen H, Hippenmeyer S, Arber S, Frank E. 2003. Development of the monosynaptic stretch reflex circuit. Current Opinion in Neurobiology. 13(1), 96–102.","apa":"Chen, H., Hippenmeyer, S., Arber, S., &#38; Frank, E. (2003). Development of the monosynaptic stretch reflex circuit. <i>Current Opinion in Neurobiology</i>. Elsevier. <a href=\"https://doi.org/10.1016/S0959-4388(03)00006-0\">https://doi.org/10.1016/S0959-4388(03)00006-0</a>","ama":"Chen H, Hippenmeyer S, Arber S, Frank E. Development of the monosynaptic stretch reflex circuit. <i>Current Opinion in Neurobiology</i>. 2003;13(1):96-102. doi:<a href=\"https://doi.org/10.1016/S0959-4388(03)00006-0\">10.1016/S0959-4388(03)00006-0</a>","mla":"Chen, Hsiao, et al. “Development of the Monosynaptic Stretch Reflex Circuit.” <i>Current Opinion in Neurobiology</i>, vol. 13, no. 1, Elsevier, 2003, pp. 96–102, doi:<a href=\"https://doi.org/10.1016/S0959-4388(03)00006-0\">10.1016/S0959-4388(03)00006-0</a>.","short":"H. Chen, S. Hippenmeyer, S. Arber, E. Frank, Current Opinion in Neurobiology 13 (2003) 96–102.","chicago":"Chen, Hsiao, Simon Hippenmeyer, Silvia Arber, and Eric Frank. “Development of the Monosynaptic Stretch Reflex Circuit.” <i>Current Opinion in Neurobiology</i>. Elsevier, 2003. <a href=\"https://doi.org/10.1016/S0959-4388(03)00006-0\">https://doi.org/10.1016/S0959-4388(03)00006-0</a>.","ieee":"H. Chen, S. Hippenmeyer, S. Arber, and E. Frank, “Development of the monosynaptic stretch reflex circuit,” <i>Current Opinion in Neurobiology</i>, vol. 13, no. 1. Elsevier, pp. 96–102, 2003."},"month":"02","author":[{"last_name":"Chen","first_name":"Hsiao","full_name":"Chen, Hsiao Huei"},{"orcid":"0000-0003-2279-1061","full_name":"Simon Hippenmeyer","last_name":"Hippenmeyer","first_name":"Simon","id":"37B36620-F248-11E8-B48F-1D18A9856A87"},{"full_name":"Arber, Silvia","last_name":"Arber","first_name":"Silvia"},{"last_name":"Frank","first_name":"Eric","full_name":"Frank, Eric"}],"intvolume":"        13","_id":"3139","abstract":[{"lang":"eng","text":"Significant advances have been made during the past few years in our understanding of how the spinal monosynaptic reflex develops. Transcription factors in the Neurogenin, Runt, ETS, and LIM families control sequential steps of the specification of various subtypes of dorsal root ganglia sensory neurons. The initiation of muscle spindle differentiation requires neuregulin 1, derived from Ia afferent sensory neurons, and signaling through ErbB receptors in intrafusal muscle fibers. Several retrograde signals from the periphery are important for the establishment of late connectivity in the reflex circuit. Finally, neurotrophin 3 released from muscle spindles regulates the strength of sensory-motor connections within the spinal cord postnatally."}],"page":"96 - 102","date_published":"2003-02-01T00:00:00Z","status":"public","issue":"1","publist_id":"3557","publication":"Current Opinion in Neurobiology","publication_status":"published","day":"01","publisher":"Elsevier","date_updated":"2019-04-26T07:22:24Z","title":"Development of the monosynaptic stretch reflex circuit","doi":"10.1016/S0959-4388(03)00006-0","quality_controlled":0,"volume":13,"type":"review","year":"2003"},{"year":"2003","volume":5,"type":"journal_article","quality_controlled":0,"title":"Spontaneous receptor-independent heterotrimeric G-protein signalling in an RGS mutant","doi":"10.1038/ncb941","publisher":"Nature Publishing Group","date_updated":"2021-01-12T07:41:24Z","publication_status":"published","day":"01","date_published":"2003-03-01T00:00:00Z","status":"public","publication":"Nature Cell Biology","issue":"3","publist_id":"3544","abstract":[{"lang":"eng","text":"Tripartite G-protein-coupled receptors (GPCRs) represent one of the largest groups of signal transducers, transmitting signals from hormones, neuropeptides, odorants, food and light. Ligand-bound receptors catalyse GDP/GTP exchange on the G-protein α-subunit (Gα), leading to α-GTP separation from the βγ subunits and pathway activation. Activating mutations in the receptors or G proteins underlie many human diseases, including some cancers, dwarfism and premature puberty. Regulators of G-protein signalling (RGS proteins) are known to modulate the level and duration of ligand-induced signalling by accelerating the intrinsic GTPase activity of the Gα subunit, and thus reformation of the inactive GDP-bound Gα. Here we find that even in the absence of receptor, mutation of the RGS family member Sst2 (refs 6-9) permits spontaneous activation of the G-protein-coupled mating pathway in Saccharomyces cerevisiae at levels normally seen only in the presence of ligand. Our work demonstrates the occurence of spontaneous tripartite G-protein signalling in vivo and identifies a requirement for RGS proteins in preventing such receptor-independent activation."}],"page":"231 - 235","intvolume":"         5","_id":"3150","month":"03","author":[{"full_name":"Daria Siekhaus","orcid":"0000-0001-8323-8353","id":"3D224B9E-F248-11E8-B48F-1D18A9856A87","first_name":"Daria E","last_name":"Siekhaus"},{"full_name":"Drubin, David G","last_name":"Drubin","first_name":"David"}],"citation":{"ista":"Siekhaus DE, Drubin D. 2003. Spontaneous receptor-independent heterotrimeric G-protein signalling in an RGS mutant. Nature Cell Biology. 5(3), 231–235.","apa":"Siekhaus, D. E., &#38; Drubin, D. (2003). Spontaneous receptor-independent heterotrimeric G-protein signalling in an RGS mutant. <i>Nature Cell Biology</i>. Nature Publishing Group. <a href=\"https://doi.org/10.1038/ncb941\">https://doi.org/10.1038/ncb941</a>","ama":"Siekhaus DE, Drubin D. Spontaneous receptor-independent heterotrimeric G-protein signalling in an RGS mutant. <i>Nature Cell Biology</i>. 2003;5(3):231-235. doi:<a href=\"https://doi.org/10.1038/ncb941\">10.1038/ncb941</a>","short":"D.E. Siekhaus, D. Drubin, Nature Cell Biology 5 (2003) 231–235.","mla":"Siekhaus, Daria E., and David Drubin. “Spontaneous Receptor-Independent Heterotrimeric G-Protein Signalling in an RGS Mutant.” <i>Nature Cell Biology</i>, vol. 5, no. 3, Nature Publishing Group, 2003, pp. 231–35, doi:<a href=\"https://doi.org/10.1038/ncb941\">10.1038/ncb941</a>.","chicago":"Siekhaus, Daria E, and David Drubin. “Spontaneous Receptor-Independent Heterotrimeric G-Protein Signalling in an RGS Mutant.” <i>Nature Cell Biology</i>. Nature Publishing Group, 2003. <a href=\"https://doi.org/10.1038/ncb941\">https://doi.org/10.1038/ncb941</a>.","ieee":"D. E. Siekhaus and D. Drubin, “Spontaneous receptor-independent heterotrimeric G-protein signalling in an RGS mutant,” <i>Nature Cell Biology</i>, vol. 5, no. 3. Nature Publishing Group, pp. 231–235, 2003."},"date_created":"2018-12-11T12:01:41Z","extern":1},{"month":"01","author":[{"full_name":"Rayburn, Lowell Y","first_name":"Lowell","last_name":"Rayburn"},{"last_name":"Gooding","first_name":"Holly","full_name":"Gooding, Holly C"},{"last_name":"Choksi","first_name":"Semil","full_name":"Choksi, Semil P"},{"full_name":"Maloney, Dhea","last_name":"Maloney","first_name":"Dhea"},{"full_name":"Kidd, Ambrose R","last_name":"Kidd","first_name":"Ambrose"},{"orcid":"0000-0001-8323-8353","full_name":"Daria Siekhaus","id":"3D224B9E-F248-11E8-B48F-1D18A9856A87","last_name":"Siekhaus","first_name":"Daria E"},{"last_name":"Bender","first_name":"Michael","full_name":"Bender, Michael"}],"extern":1,"citation":{"ieee":"L. Rayburn <i>et al.</i>, “Amontillado, the Drosophila homolog of the prohormone processing protease PC2, is required during embryogenesis and early larval development,” <i>Genetics</i>, vol. 163, no. 1. Genetics Society of America, pp. 227–237, 2003.","chicago":"Rayburn, Lowell, Holly Gooding, Semil Choksi, Dhea Maloney, Ambrose Kidd, Daria E Siekhaus, and Michael Bender. “Amontillado, the Drosophila Homolog of the Prohormone Processing Protease PC2, Is Required during Embryogenesis and Early Larval Development.” <i>Genetics</i>. Genetics Society of America, 2003.","short":"L. Rayburn, H. Gooding, S. Choksi, D. Maloney, A. Kidd, D.E. Siekhaus, M. Bender, Genetics 163 (2003) 227–237.","mla":"Rayburn, Lowell, et al. “Amontillado, the Drosophila Homolog of the Prohormone Processing Protease PC2, Is Required during Embryogenesis and Early Larval Development.” <i>Genetics</i>, vol. 163, no. 1, Genetics Society of America, 2003, pp. 227–37.","ama":"Rayburn L, Gooding H, Choksi S, et al. Amontillado, the Drosophila homolog of the prohormone processing protease PC2, is required during embryogenesis and early larval development. <i>Genetics</i>. 2003;163(1):227-237.","apa":"Rayburn, L., Gooding, H., Choksi, S., Maloney, D., Kidd, A., Siekhaus, D. E., &#38; Bender, M. (2003). Amontillado, the Drosophila homolog of the prohormone processing protease PC2, is required during embryogenesis and early larval development. <i>Genetics</i>. Genetics Society of America.","ista":"Rayburn L, Gooding H, Choksi S, Maloney D, Kidd A, Siekhaus DE, Bender M. 2003. Amontillado, the Drosophila homolog of the prohormone processing protease PC2, is required during embryogenesis and early larval development. Genetics. 163(1), 227–237."},"date_created":"2018-12-11T12:01:41Z","abstract":[{"lang":"eng","text":"Biosynthesis of most peptide hormones and neuropeptides requires proteolytic excision of the active peptide from inactive proprotein precursors, an activity carried out by subtilisin-like proprotein convertases (SPCs) in constitutive or regulated secretory pathways. The Drosophila amontillado (amon) gene encodes a homolog of the mammalian PC2 protein, an SPC that functions in the regulated secretory pathway in neuroendocrine tissues. We have identified amon mutants by isolating ethylmethanesulfonate (EMS)-induced lethal and visible mutations that define two complementation groups in the amon interval at 97D1 of the third chromosome. DNA sequencing identified the amon complementation group and the DNA sequence change for each of the nine amon alleles isolated. amon mutants display partial embryonic lethality, are defective in larval growth, and arrest during the first to second instar larval molt. Mutant larvae can be rescued by heat-shock-induced expression of the amon protein. Rescued larvae arrest at the subsequent larval molt, suggesting that amon is also required for the second to third instar larval molt. Our data indicate that the amon proprotein convertase is required during embryogenesis and larval development in Drosophila and support the hypothesis that AMON acts to proteolytically process peptide hormones that regulate hatching, larval growth, and larval ecdysis."}],"page":"227 - 237","status":"public","date_published":"2003-01-01T00:00:00Z","publist_id":"3545","issue":"1","publication":"Genetics","_id":"3151","intvolume":"       163","title":"Amontillado, the Drosophila homolog of the prohormone processing protease PC2, is required during embryogenesis and early larval development","quality_controlled":0,"publication_status":"published","day":"01","publisher":"Genetics Society of America","date_updated":"2021-01-12T07:41:25Z","year":"2003","volume":163,"type":"journal_article"},{"publication_status":"published","day":"30","publisher":"IEEE","date_updated":"2021-01-12T07:41:33Z","title":"Computing geodesics and minimal surfaces via graph cuts","doi":"10.1109/ICCV.2003.1238310","quality_controlled":0,"volume":1,"type":"conference","conference":{"name":"ICCV: International Conference on Computer Vision"},"year":"2003","extern":1,"citation":{"mla":"Boykov, Yuri, and Vladimir Kolmogorov. <i>Computing Geodesics and Minimal Surfaces via Graph Cuts</i>. Vol. 1, IEEE, 2003, pp. 26–33, doi:<a href=\"https://doi.org/10.1109/ICCV.2003.1238310\">10.1109/ICCV.2003.1238310</a>.","short":"Y. Boykov, V. Kolmogorov, in:, IEEE, 2003, pp. 26–33.","ieee":"Y. Boykov and V. Kolmogorov, “Computing geodesics and minimal surfaces via graph cuts,” presented at the ICCV: International Conference on Computer Vision, 2003, vol. 1, pp. 26–33.","chicago":"Boykov, Yuri, and Vladimir Kolmogorov. “Computing Geodesics and Minimal Surfaces via Graph Cuts,” 1:26–33. IEEE, 2003. <a href=\"https://doi.org/10.1109/ICCV.2003.1238310\">https://doi.org/10.1109/ICCV.2003.1238310</a>.","apa":"Boykov, Y., &#38; Kolmogorov, V. (2003). Computing geodesics and minimal surfaces via graph cuts (Vol. 1, pp. 26–33). Presented at the ICCV: International Conference on Computer Vision, IEEE. <a href=\"https://doi.org/10.1109/ICCV.2003.1238310\">https://doi.org/10.1109/ICCV.2003.1238310</a>","ista":"Boykov Y, Kolmogorov V. 2003. Computing geodesics and minimal surfaces via graph cuts. ICCV: International Conference on Computer Vision vol. 1, 26–33.","ama":"Boykov Y, Kolmogorov V. Computing geodesics and minimal surfaces via graph cuts. In: Vol 1. IEEE; 2003:26-33. doi:<a href=\"https://doi.org/10.1109/ICCV.2003.1238310\">10.1109/ICCV.2003.1238310</a>"},"date_created":"2018-12-11T12:01:48Z","month":"09","author":[{"last_name":"Boykov","first_name":"Yuri","full_name":"Boykov, Yuri"},{"id":"3D50B0BA-F248-11E8-B48F-1D18A9856A87","first_name":"Vladimir","last_name":"Kolmogorov","full_name":"Vladimir Kolmogorov"}],"intvolume":"         1","_id":"3170","abstract":[{"text":"Geodesic active contours and graph cuts are two standard image segmentation techniques. We introduce a new segmentation method combining some of their benefits. Our main intuition is that any cut on a graph embedded in some continuous space can be interpreted as a contour (in 2D) or a surface (in 3D). We show how to build a grid graph and set its edge weights so that the cost of cuts is arbitrarily close to the length (area) of the corresponding contours (surfaces) for any anisotropic Riemannian metric. There are two interesting consequences of this technical result. First, graph cut algorithms can be used to find globally minimum geodesic contours (minimal surfaces in 3D) under arbitrary Riemannian metric for a given set of boundary conditions. Second, we show how to minimize metrication artifacts in existing graph-cut based methods in vision. Theoretically speaking, our work provides an interesting link between several branches of mathematics -differential geometry, integral geometry, and combinatorial optimization. The main technical problem is solved using Cauchy-Crofton formula from integral geometry.","lang":"eng"}],"page":"26 - 33","status":"public","date_published":"2003-09-30T00:00:00Z","publist_id":"3511"},{"publication_status":"published","day":"26","publisher":"Springer","date_updated":"2021-01-12T07:41:34Z","title":"Generalized multi camera scene reconstruction using graph cuts","doi":"10.1007/978-3-540-45063-4_32","quality_controlled":0,"volume":2683,"type":"conference","conference":{"name":"EMMCVPR: Energy Minimization Methods in Computer Vision and Pattern Recognition"},"year":"2003","alternative_title":["LNCS"],"extern":1,"date_created":"2018-12-11T12:01:48Z","citation":{"apa":"Kolmogorov, V., Zabih, R., &#38; Gortler, S. (2003). Generalized multi camera scene reconstruction using graph cuts (Vol. 2683, pp. 501–516). Presented at the EMMCVPR: Energy Minimization Methods in Computer Vision and Pattern Recognition, Springer. <a href=\"https://doi.org/10.1007/978-3-540-45063-4_32\">https://doi.org/10.1007/978-3-540-45063-4_32</a>","ista":"Kolmogorov V, Zabih R, Gortler S. 2003. Generalized multi camera scene reconstruction using graph cuts. EMMCVPR: Energy Minimization Methods in Computer Vision and Pattern Recognition, LNCS, vol. 2683, 501–516.","ama":"Kolmogorov V, Zabih R, Gortler S. Generalized multi camera scene reconstruction using graph cuts. In: Vol 2683. Springer; 2003:501-516. doi:<a href=\"https://doi.org/10.1007/978-3-540-45063-4_32\">10.1007/978-3-540-45063-4_32</a>","short":"V. Kolmogorov, R. Zabih, S. Gortler, in:, Springer, 2003, pp. 501–516.","mla":"Kolmogorov, Vladimir, et al. <i>Generalized Multi Camera Scene Reconstruction Using Graph Cuts</i>. Vol. 2683, Springer, 2003, pp. 501–16, doi:<a href=\"https://doi.org/10.1007/978-3-540-45063-4_32\">10.1007/978-3-540-45063-4_32</a>.","ieee":"V. Kolmogorov, R. Zabih, and S. Gortler, “Generalized multi camera scene reconstruction using graph cuts,” presented at the EMMCVPR: Energy Minimization Methods in Computer Vision and Pattern Recognition, 2003, vol. 2683, pp. 501–516.","chicago":"Kolmogorov, Vladimir, Ramin Zabih, and Steven Gortler. “Generalized Multi Camera Scene Reconstruction Using Graph Cuts,” 2683:501–16. Springer, 2003. <a href=\"https://doi.org/10.1007/978-3-540-45063-4_32\">https://doi.org/10.1007/978-3-540-45063-4_32</a>."},"month":"06","author":[{"full_name":"Vladimir Kolmogorov","last_name":"Kolmogorov","first_name":"Vladimir","id":"3D50B0BA-F248-11E8-B48F-1D18A9856A87"},{"last_name":"Zabih","first_name":"Ramin","full_name":"Zabih, Ramin"},{"first_name":"Steven","last_name":"Gortler","full_name":"Gortler, Steven"}],"_id":"3171","intvolume":"      2683","abstract":[{"lang":"eng","text":"Reconstructing a 3-D scene from more than one camera is a classical problem in computer vision. One of the major sources of difficulty is the fact that not all scene elements are visible from all cameras. In the last few years, two promising approaches have been developed 11,12 that formulate the scene reconstruction problem in terms of energy minimization, and minimize the energy using graph cuts. These energy minimization approaches treat the input images symmetrically, handle visibility constraints correctly, and allow spatial smoothness to be enforced. However, these algorithm propose different problem formulations, and handle a limited class of smoothness terms. One algorithm 11 uses a problem formulation that is restricted to two-camera stereo, and imposes smoothness between a pair of cameras. The other algorithm 12 can handle an arbitrary number of cameras, but imposes smoothness only with respect to a single camera. In this paper we give a more general energy minimization formulation for the problem, which allows a larger class of spatial smoothness constraints. We show that our formulation includes both of the previous approaches as special cases, as well as permitting new energy functions. Experimental results on real data with ground truth are also included. "}],"page":"501 - 516","date_published":"2003-06-26T00:00:00Z","status":"public","publist_id":"3512"},{"type":"conference","volume":2,"conference":{"name":"ICCV: International Conference on Computer Vision"},"year":"2003","day":"30","publication_status":"published","date_updated":"2021-01-12T07:41:35Z","publisher":"IEEE","doi":"10.1109/ICCV.2003.1238463","title":"Visual correspondence using energy minimization and mutual information","quality_controlled":0,"_id":"3174","intvolume":"         2","page":"1033 - 1040","abstract":[{"lang":"eng","text":"We address visual correspondence problems without assuming that scene points have similar intensities in different views. This situation is common, usually due to non-lambertian scenes or to differences between cameras. We use maximization of mutual information, a powerful technique for registering images that requires no a priori model of the relationship between scene intensities in different views. However, it has proven difficult to use mutual information to compute dense visual correspondence. Comparing fixed-size windows via mutual information suffers from the well-known problems of fixed windows, namely poor performance at discontinuities and in low-texture regions. In this paper, we show how to compute visual correspondence using mutual information without suffering from these problems. Using 'a simple approximation, mutual information can be incorporated into the standard energy minimization framework used in early vision. The energy can then be efficiently minimized using graph cuts, which preserve discontinuities and handle low-texture regions. The resulting algorithm combines the accurate disparity maps that come from graph cuts with the tolerance for intensity changes that comes from mutual information."}],"publist_id":"3510","status":"public","date_published":"2003-09-30T00:00:00Z","extern":1,"citation":{"chicago":"Kim, Junhwan, Vladimir Kolmogorov, and Ramin Zabih. “Visual Correspondence Using Energy Minimization and Mutual Information,” 2:1033–40. IEEE, 2003. <a href=\"https://doi.org/10.1109/ICCV.2003.1238463\">https://doi.org/10.1109/ICCV.2003.1238463</a>.","ieee":"J. Kim, V. Kolmogorov, and R. Zabih, “Visual correspondence using energy minimization and mutual information,” presented at the ICCV: International Conference on Computer Vision, 2003, vol. 2, pp. 1033–1040.","mla":"Kim, Junhwan, et al. <i>Visual Correspondence Using Energy Minimization and Mutual Information</i>. Vol. 2, IEEE, 2003, pp. 1033–40, doi:<a href=\"https://doi.org/10.1109/ICCV.2003.1238463\">10.1109/ICCV.2003.1238463</a>.","short":"J. Kim, V. Kolmogorov, R. Zabih, in:, IEEE, 2003, pp. 1033–1040.","ama":"Kim J, Kolmogorov V, Zabih R. Visual correspondence using energy minimization and mutual information. In: Vol 2. IEEE; 2003:1033-1040. doi:<a href=\"https://doi.org/10.1109/ICCV.2003.1238463\">10.1109/ICCV.2003.1238463</a>","ista":"Kim J, Kolmogorov V, Zabih R. 2003. Visual correspondence using energy minimization and mutual information. ICCV: International Conference on Computer Vision vol. 2, 1033–1040.","apa":"Kim, J., Kolmogorov, V., &#38; Zabih, R. (2003). Visual correspondence using energy minimization and mutual information (Vol. 2, pp. 1033–1040). Presented at the ICCV: International Conference on Computer Vision, IEEE. <a href=\"https://doi.org/10.1109/ICCV.2003.1238463\">https://doi.org/10.1109/ICCV.2003.1238463</a>"},"date_created":"2018-12-11T12:01:49Z","author":[{"full_name":"Kim, Junhwan","first_name":"Junhwan","last_name":"Kim"},{"first_name":"Vladimir","last_name":"Kolmogorov","id":"3D50B0BA-F248-11E8-B48F-1D18A9856A87","full_name":"Vladimir Kolmogorov"},{"last_name":"Zabih","first_name":"Ramin","full_name":"Zabih, Ramin"}],"month":"09"},{"year":"2003","volume":67,"type":"journal_article","title":"On the parameterized complexity of the fixed alphabet shortest common supersequence and longest common subsequence problems","doi":"10.1016/S0022-0000(03)00078-3","quality_controlled":0,"publication_status":"published","day":"01","publisher":"Elsevier","date_updated":"2021-01-12T07:41:49Z","abstract":[{"lang":"eng","text":"We show that the fixed alphabet shortest common supersequence (SCS) and the fixed alphabet longest common subsequence (LCS) problems parameterized in the number of strings are W[1]-hard. Unless W[1]=FPT, this rules out the existence of algorithms with time complexity of O(f(k)nα) for those problems. Here n is the size of the problem instance, α is constant, k is the number of strings and f is any function of k. The fixed alphabet version of the LCS problem is of particular interest considering the importance of sequence comparison (e.g. multiple sequence alignment) in the fixed length alphabet world of DNA and protein sequences."}],"page":"757 - 771","date_published":"2003-12-01T00:00:00Z","status":"public","publication":"Journal of Computer and System Sciences","publist_id":"3472","issue":"4","intvolume":"        67","_id":"3209","month":"12","author":[{"first_name":"Krzysztof Z","last_name":"Pietrzak","id":"3E04A7AA-F248-11E8-B48F-1D18A9856A87","orcid":"0000-0002-9139-1654","full_name":"Krzysztof Pietrzak"}],"extern":1,"date_created":"2018-12-11T12:02:01Z","citation":{"chicago":"Pietrzak, Krzysztof Z. “On the Parameterized Complexity of the Fixed Alphabet Shortest Common Supersequence and Longest Common Subsequence Problems.” <i>Journal of Computer and System Sciences</i>. Elsevier, 2003. <a href=\"https://doi.org/10.1016/S0022-0000(03)00078-3\">https://doi.org/10.1016/S0022-0000(03)00078-3</a>.","ieee":"K. Z. Pietrzak, “On the parameterized complexity of the fixed alphabet shortest common supersequence and longest common subsequence problems,” <i>Journal of Computer and System Sciences</i>, vol. 67, no. 4. Elsevier, pp. 757–771, 2003.","short":"K.Z. Pietrzak, Journal of Computer and System Sciences 67 (2003) 757–771.","mla":"Pietrzak, Krzysztof Z. “On the Parameterized Complexity of the Fixed Alphabet Shortest Common Supersequence and Longest Common Subsequence Problems.” <i>Journal of Computer and System Sciences</i>, vol. 67, no. 4, Elsevier, 2003, pp. 757–71, doi:<a href=\"https://doi.org/10.1016/S0022-0000(03)00078-3\">10.1016/S0022-0000(03)00078-3</a>.","ama":"Pietrzak KZ. On the parameterized complexity of the fixed alphabet shortest common supersequence and longest common subsequence problems. <i>Journal of Computer and System Sciences</i>. 2003;67(4):757-771. doi:<a href=\"https://doi.org/10.1016/S0022-0000(03)00078-3\">10.1016/S0022-0000(03)00078-3</a>","ista":"Pietrzak KZ. 2003. On the parameterized complexity of the fixed alphabet shortest common supersequence and longest common subsequence problems. Journal of Computer and System Sciences. 67(4), 757–771.","apa":"Pietrzak, K. Z. (2003). On the parameterized complexity of the fixed alphabet shortest common supersequence and longest common subsequence problems. <i>Journal of Computer and System Sciences</i>. Elsevier. <a href=\"https://doi.org/10.1016/S0022-0000(03)00078-3\">https://doi.org/10.1016/S0022-0000(03)00078-3</a>"}},{"conference":{"name":"EUROCRYPT: Theory and Applications of Cryptographic Techniques"},"year":"2003","volume":2656,"type":"conference","title":"The security of many round Luby Rackoff pseudo random permutations","doi":"10.1007/3-540-39200-9_34","quality_controlled":0,"publication_status":"published","day":"04","publisher":"Springer","date_updated":"2021-01-12T07:41:49Z","abstract":[{"text":"Luby and Rackoff showed how to construct a (super-)pseudo-random permutation {0,1}2n→ {0,1}2n from some number r of pseudo-random functions {0,1}n → {0,1}n. Their construction, motivated by DES, consists of a cascade of r Feistel permutations. A Feistel permutation 1for a pseudo-random function f is defined as (L, R) → (R,L ⊕ f (R)), where L and R are the left and right part of the input and ⊕ denotes bitwise XOR or, in this paper, any other group operation on {0,1}n. The only non-trivial step of the security proof consists of proving that the cascade of r Feistel permutations with independent uniform random functions {0,1}n → {0,1}n, denoted Ψ2nr is indistinguishable from a uniform random permutation {0,1}2n → {0,1}2n by any computationally unbounded adaptive distinguisher making at most O(2cn) combined chosen plaintext/ciphertext queries for any c &lt; α, where a is a security parameter. Luby and Rackoff proved α = 1/2 for r = 4. A natural problem, proposed by Pieprzyk is to improve on α for larger r. The best known result, α = 3/4 for r = 6, is due to Patarin. In this paper we prove a = 1 -O(1/r), i.e., the trivial upper bound α = 1 can be approached. The proof uses some new techniques that can be of independent interest. ","lang":"eng"}],"page":"544 - 561","date_published":"2003-06-04T00:00:00Z","status":"public","publist_id":"3473","intvolume":"      2656","_id":"3210","month":"06","author":[{"last_name":"Maurer","first_name":"Ueli","full_name":"Maurer, Ueli M"},{"id":"3E04A7AA-F248-11E8-B48F-1D18A9856A87","last_name":"Pietrzak","first_name":"Krzysztof Z","full_name":"Krzysztof Pietrzak","orcid":"0000-0002-9139-1654"}],"alternative_title":["LNCS"],"extern":1,"citation":{"chicago":"Maurer, Ueli, and Krzysztof Z Pietrzak. “The Security of Many Round Luby Rackoff Pseudo Random Permutations,” 2656:544–61. Springer, 2003. <a href=\"https://doi.org/10.1007/3-540-39200-9_34\">https://doi.org/10.1007/3-540-39200-9_34</a>.","ieee":"U. Maurer and K. Z. Pietrzak, “The security of many round Luby Rackoff pseudo random permutations,” presented at the EUROCRYPT: Theory and Applications of Cryptographic Techniques, 2003, vol. 2656, pp. 544–561.","mla":"Maurer, Ueli, and Krzysztof Z. Pietrzak. <i>The Security of Many Round Luby Rackoff Pseudo Random Permutations</i>. Vol. 2656, Springer, 2003, pp. 544–61, doi:<a href=\"https://doi.org/10.1007/3-540-39200-9_34\">10.1007/3-540-39200-9_34</a>.","short":"U. Maurer, K.Z. Pietrzak, in:, Springer, 2003, pp. 544–561.","ama":"Maurer U, Pietrzak KZ. The security of many round Luby Rackoff pseudo random permutations. In: Vol 2656. Springer; 2003:544-561. doi:<a href=\"https://doi.org/10.1007/3-540-39200-9_34\">10.1007/3-540-39200-9_34</a>","ista":"Maurer U, Pietrzak KZ. 2003. The security of many round Luby Rackoff pseudo random permutations. EUROCRYPT: Theory and Applications of Cryptographic Techniques, LNCS, vol. 2656, 544–561.","apa":"Maurer, U., &#38; Pietrzak, K. Z. (2003). The security of many round Luby Rackoff pseudo random permutations (Vol. 2656, pp. 544–561). Presented at the EUROCRYPT: Theory and Applications of Cryptographic Techniques, Springer. <a href=\"https://doi.org/10.1007/3-540-39200-9_34\">https://doi.org/10.1007/3-540-39200-9_34</a>"},"date_created":"2018-12-11T12:02:02Z"},{"intvolume":"       166","_id":"3425","language":[{"iso":"eng"}],"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","date_published":"2003-01-01T00:00:00Z","status":"public","publist_id":"2976","page":"277 - 288","date_created":"2018-12-11T12:03:16Z","citation":{"ama":"Bollenbach MT, Strother T, Bauer W. 3D supernova collapse calculations. In: Vol 166. Springer; 2003:277-288. doi:<a href=\"https://doi.org/10.1007/978-1-4020-2705-5_21\">10.1007/978-1-4020-2705-5_21</a>","ista":"Bollenbach MT, Strother T, Bauer W. 2003. 3D supernova collapse calculations. NATO ASI on Structure and Dynamics of Elementary Matter, Nato Science Series II, vol. 166, 277–288.","apa":"Bollenbach, M. T., Strother, T., &#38; Bauer, W. (2003). 3D supernova collapse calculations (Vol. 166, pp. 277–288). Presented at the NATO ASI on Structure and Dynamics of Elementary Matter, Springer. <a href=\"https://doi.org/10.1007/978-1-4020-2705-5_21\">https://doi.org/10.1007/978-1-4020-2705-5_21</a>","chicago":"Bollenbach, Mark Tobias, T. Strother, and Wolfgang Bauer. “3D Supernova Collapse Calculations,” 166:277–88. Springer, 2003. <a href=\"https://doi.org/10.1007/978-1-4020-2705-5_21\">https://doi.org/10.1007/978-1-4020-2705-5_21</a>.","ieee":"M. T. Bollenbach, T. Strother, and W. Bauer, “3D supernova collapse calculations,” presented at the NATO ASI on Structure and Dynamics of Elementary Matter, 2003, vol. 166, pp. 277–288.","mla":"Bollenbach, Mark Tobias, et al. <i>3D Supernova Collapse Calculations</i>. Vol. 166, Springer, 2003, pp. 277–88, doi:<a href=\"https://doi.org/10.1007/978-1-4020-2705-5_21\">10.1007/978-1-4020-2705-5_21</a>.","short":"M.T. Bollenbach, T. Strother, W. Bauer, in:, Springer, 2003, pp. 277–288."},"alternative_title":["Nato Science Series II"],"extern":"1","month":"01","oa_version":"None","author":[{"orcid":"0000-0003-4398-476X","full_name":"Bollenbach, Mark Tobias","id":"3E6DB97A-F248-11E8-B48F-1D18A9856A87","last_name":"Bollenbach","first_name":"Mark Tobias"},{"full_name":"Strother, T.","last_name":"Strother","first_name":"T."},{"full_name":"Bauer, Wolfgang","last_name":"Bauer","first_name":"Wolfgang"}],"article_processing_charge":"No","volume":166,"type":"conference","year":"2003","conference":{"name":"NATO ASI on Structure and Dynamics of Elementary Matter"},"publisher":"Springer","date_updated":"2021-01-12T07:43:23Z","publication_status":"published","day":"01","title":"3D supernova collapse calculations","doi":"10.1007/978-1-4020-2705-5_21"},{"publisher":"Deutscher Ärzte Verlag","date_updated":"2021-01-12T07:43:35Z","publication_status":"published","day":"01","quality_controlled":0,"title":"Molekulare und zelluläre Grundlagen des Nervensystems.","editor":[{"last_name":"Schmidt","first_name":"R.","full_name":"Schmidt, R. F."}],"volume":"B","type":"book_chapter","year":"2003","date_created":"2018-12-11T12:03:26Z","citation":{"apa":"Jonas, P. M., &#38; Unsicker, K. (2003). Molekulare und zelluläre Grundlagen des Nervensystems. In R. Schmidt (Ed.), <i>Lehrbuch Vorklinik</i> (Vol. B, pp. 3–26). Deutscher Ärzte Verlag.","ista":"Jonas PM, Unsicker K. 2003.Molekulare und zelluläre Grundlagen des Nervensystems. In: Lehrbuch Vorklinik. vol. B, 3–26.","ama":"Jonas PM, Unsicker K. Molekulare und zelluläre Grundlagen des Nervensystems. In: Schmidt R, ed. <i>Lehrbuch Vorklinik</i>. Vol B. Deutscher Ärzte Verlag; 2003:3-26.","mla":"Jonas, Peter M., and Klaus Unsicker. “Molekulare Und Zelluläre Grundlagen Des Nervensystems.” <i>Lehrbuch Vorklinik</i>, edited by R. Schmidt, vol. B, Deutscher Ärzte Verlag, 2003, pp. 3–26.","short":"P.M. Jonas, K. Unsicker, in:, R. Schmidt (Ed.), Lehrbuch Vorklinik, Deutscher Ärzte Verlag, 2003, pp. 3–26.","ieee":"P. M. Jonas and K. Unsicker, “Molekulare und zelluläre Grundlagen des Nervensystems.,” in <i>Lehrbuch Vorklinik</i>, vol. B, R. Schmidt, Ed. Deutscher Ärzte Verlag, 2003, pp. 3–26.","chicago":"Jonas, Peter M, and Klaus Unsicker. “Molekulare Und Zelluläre Grundlagen Des Nervensystems.” In <i>Lehrbuch Vorklinik</i>, edited by R. Schmidt, B:3–26. Deutscher Ärzte Verlag, 2003."},"extern":1,"month":"01","author":[{"first_name":"Peter M","last_name":"Jonas","id":"353C1B58-F248-11E8-B48F-1D18A9856A87","full_name":"Peter Jonas","orcid":"0000-0001-5001-4804"},{"last_name":"Unsicker","first_name":"Klaus","full_name":"Unsicker, Klaus"}],"_id":"3458","status":"public","date_published":"2003-01-01T00:00:00Z","publist_id":"2929","publication":"Lehrbuch Vorklinik","page":"3 - 26"},{"issue":"6948","publication":"Nature","publist_id":"2859","date_published":"2003-07-31T00:00:00Z","status":"public","page":"552 - 556","abstract":[{"text":"Neurons can produce action potentials with high temporal precision(1). A fundamental issue is whether, and how, this capability is used in information processing. According to the `cell assembly' hypothesis, transient synchrony of anatomically distributed groups of neurons underlies processing of both external sensory input and internal cognitive mechanisms(2-4). Accordingly, neuron populations should be arranged into groups whose synchrony exceeds that predicted by common modulation by sensory input. Here we find that the spike times of hippocampal pyramidal cells can be predicted more accurately by using the spike times of simultaneously recorded neurons in addition to the animals location in space. This improvement remained when the spatial prediction was refined with a spatially dependent theta phase modulation(5-8). The time window in which spike times are best predicted from simultaneous peer activity is 10-30 ms, suggesting that cell assemblies are synchronized at this timescale. Because this temporal window matches the membrane time constant of pyramidal neurons(9), the period of the hippocampal gamma oscillation(10) and the time window for synaptic plasticity(11), we propose that cooperative activity at this timescale is optimal for information transmission and storage in cortical circuits.","lang":"eng"}],"_id":"3526","intvolume":"       424","author":[{"first_name":"Kenneth","last_name":"Harris","full_name":"Harris, Kenneth D"},{"full_name":"Jozsef Csicsvari","orcid":"0000-0002-5193-4036","first_name":"Jozsef L","last_name":"Csicsvari","id":"3FA14672-F248-11E8-B48F-1D18A9856A87"},{"first_name":"Hajima","last_name":"Hirase","full_name":"Hirase, Hajima"},{"full_name":"Dragoi, George","last_name":"Dragoi","first_name":"George"},{"first_name":"György","last_name":"Buzsáki","full_name":"Buzsáki, György"}],"month":"07","date_created":"2018-12-11T12:03:47Z","citation":{"ista":"Harris K, Csicsvari JL, Hirase H, Dragoi G, Buzsáki G. 2003. Organization of cell assemblies in the hippocampus. Nature. 424(6948), 552–556.","apa":"Harris, K., Csicsvari, J. L., Hirase, H., Dragoi, G., &#38; Buzsáki, G. (2003). Organization of cell assemblies in the hippocampus. <i>Nature</i>. Nature Publishing Group. <a href=\"https://doi.org/0.1038/nature01834\">https://doi.org/0.1038/nature01834</a>","ama":"Harris K, Csicsvari JL, Hirase H, Dragoi G, Buzsáki G. Organization of cell assemblies in the hippocampus. <i>Nature</i>. 2003;424(6948):552-556. doi:<a href=\"https://doi.org/0.1038/nature01834\">0.1038/nature01834</a>","mla":"Harris, Kenneth, et al. “Organization of Cell Assemblies in the Hippocampus.” <i>Nature</i>, vol. 424, no. 6948, Nature Publishing Group, 2003, pp. 552–56, doi:<a href=\"https://doi.org/0.1038/nature01834\">0.1038/nature01834</a>.","short":"K. Harris, J.L. Csicsvari, H. Hirase, G. Dragoi, G. Buzsáki, Nature 424 (2003) 552–556.","chicago":"Harris, Kenneth, Jozsef L Csicsvari, Hajima Hirase, George Dragoi, and György Buzsáki. “Organization of Cell Assemblies in the Hippocampus.” <i>Nature</i>. Nature Publishing Group, 2003. <a href=\"https://doi.org/0.1038/nature01834\">https://doi.org/0.1038/nature01834</a>.","ieee":"K. Harris, J. L. Csicsvari, H. Hirase, G. Dragoi, and G. Buzsáki, “Organization of cell assemblies in the hippocampus,” <i>Nature</i>, vol. 424, no. 6948. Nature Publishing Group, pp. 552–556, 2003."},"extern":1,"year":"2003","type":"journal_article","volume":424,"quality_controlled":0,"doi":"0.1038/nature01834","title":"Organization of cell assemblies in the hippocampus","date_updated":"2021-01-12T07:44:04Z","publisher":"Nature Publishing Group","day":"31","publication_status":"published"},{"month":"01","author":[{"full_name":"Jozsef Csicsvari","orcid":"0000-0002-5193-4036","last_name":"Csicsvari","first_name":"Jozsef L","id":"3FA14672-F248-11E8-B48F-1D18A9856A87"},{"last_name":"Jamieson","first_name":"Brian","full_name":"Jamieson, Brian G"},{"first_name":"Kensall","last_name":"Wise","full_name":"Wise, Kensall D"},{"full_name":"Buzsáki, György","first_name":"György","last_name":"Buzsáki"}],"extern":1,"date_created":"2018-12-11T12:03:48Z","citation":{"short":"J.L. Csicsvari, B. Jamieson, K. Wise, G. Buzsáki, Neuron 37 (2003) 311–322.","mla":"Csicsvari, Jozsef L., et al. “Mechanisms of Gamma Oscillations in the Hippocampus of the Behaving Rat.” <i>Neuron</i>, vol. 37, no. 2, Elsevier, 2003, pp. 311–22, doi:<a href=\"https://doi.org/10.1016/S0896-6273(02)01169-8\">10.1016/S0896-6273(02)01169-8</a>.","ieee":"J. L. Csicsvari, B. Jamieson, K. Wise, and G. Buzsáki, “Mechanisms of gamma oscillations in the hippocampus of the behaving rat,” <i>Neuron</i>, vol. 37, no. 2. Elsevier, pp. 311–322, 2003.","chicago":"Csicsvari, Jozsef L, Brian Jamieson, Kensall Wise, and György Buzsáki. “Mechanisms of Gamma Oscillations in the Hippocampus of the Behaving Rat.” <i>Neuron</i>. Elsevier, 2003. <a href=\"https://doi.org/10.1016/S0896-6273(02)01169-8\">https://doi.org/10.1016/S0896-6273(02)01169-8</a>.","apa":"Csicsvari, J. L., Jamieson, B., Wise, K., &#38; Buzsáki, G. (2003). Mechanisms of gamma oscillations in the hippocampus of the behaving rat. <i>Neuron</i>. Elsevier. <a href=\"https://doi.org/10.1016/S0896-6273(02)01169-8\">https://doi.org/10.1016/S0896-6273(02)01169-8</a>","ista":"Csicsvari JL, Jamieson B, Wise K, Buzsáki G. 2003. Mechanisms of gamma oscillations in the hippocampus of the behaving rat. Neuron. 37(2), 311–322.","ama":"Csicsvari JL, Jamieson B, Wise K, Buzsáki G. Mechanisms of gamma oscillations in the hippocampus of the behaving rat. <i>Neuron</i>. 2003;37(2):311-322. doi:<a href=\"https://doi.org/10.1016/S0896-6273(02)01169-8\">10.1016/S0896-6273(02)01169-8</a>"},"abstract":[{"text":"Gamma frequency oscillations (30-100 Hz) have been suggested to underlie various cognitive and motor functions. Here, we examine the generation of gamma oscillation currents in the hippocampus, using two-dimensional, 96-site silicon probes. Two gamma generators were identified, one in the dentate gyrus and another in the CA3-CA1 regions. The coupling strength between the two oscillators varied during both theta and nontheta states. Both pyramidal cells and interneurons were phase-locked to gamma waves. Anatomical connectivity, rather than physical distance, determined the coupling strength of the oscillating neurons. CA3 pyramidal neurons discharged CA3 and CA1 interneurons at latencies indicative of monosynaptic connections. Intrahippocampal gamma oscillation emerges in the CA3 recurrent system, which entrains the CA1 region via its interneurons.","lang":"eng"}],"page":"311 - 322","status":"public","date_published":"2003-01-01T00:00:00Z","publist_id":"2857","publication":"Neuron","issue":"2","_id":"3528","intvolume":"        37","title":"Mechanisms of gamma oscillations in the hippocampus of the behaving rat","doi":"10.1016/S0896-6273(02)01169-8","quality_controlled":0,"publication_status":"published","day":"01","publisher":"Elsevier","date_updated":"2021-01-12T07:44:05Z","year":"2003","volume":37,"type":"journal_article"},{"publication":"Journal of Neurophysiology","publist_id":"2856","issue":"2","date_published":"2003-08-01T00:00:00Z","status":"public","page":"1314 - 1323","abstract":[{"lang":"eng","text":"Parallel recording of neuronal activity in the behaving animal is a prerequisite for our understanding of neuronal representation and storage of information. Here we describe the development of micro-machined silicon microelectrode arrays for unit and local field recordings. The two-dimensional probes with 96 or 64 recording sites provided high-density recording of unit and field activity with minimal tissue displacement or damage. The on-chip active circuit eliminated movement and other artifacts and greatly reduced the weight of the headgear. The precise geometry of the recording tips allowed for the estimation of the spatial location of the recorded neurons and for high-resolution estimation of extracellular current source density. Action potentials could be simultaneously recorded from the soma and dendrites of the same neurons. Silicon technology is a promising approach for high-density, high-resolution sampling of neuronal activity in both basic research and prosthetic devices."}],"_id":"3529","intvolume":"        90","author":[{"id":"3FA14672-F248-11E8-B48F-1D18A9856A87","last_name":"Csicsvari","first_name":"Jozsef L","orcid":"0000-0002-5193-4036","full_name":"Jozsef Csicsvari"},{"last_name":"Henze","first_name":"Darrell","full_name":"Henze, Darrell A"},{"full_name":"Jamieson, Brian G","last_name":"Jamieson","first_name":"Brian"},{"full_name":"Harris, Kenneth D","last_name":"Harris","first_name":"Kenneth"},{"full_name":"Sirota, Anton M","last_name":"Sirota","first_name":"Anton"},{"last_name":"Bartho","first_name":"Peter","full_name":"Bartho, Peter"},{"last_name":"Wise","first_name":"Kensall","full_name":"Wise, Kensall D"},{"first_name":"György","last_name":"Buzsáki","full_name":"Buzsáki, György"}],"month":"08","date_created":"2018-12-11T12:03:48Z","citation":{"chicago":"Csicsvari, Jozsef L, Darrell Henze, Brian Jamieson, Kenneth Harris, Anton Sirota, Peter Bartho, Kensall Wise, and György Buzsáki. “Massively Parallel Recording of Unit and Local Field Potentials with Silicon-Based Electrodes.” <i>Journal of Neurophysiology</i>. American Physiological Society, 2003. <a href=\"https://doi.org/10.1152/jn.00116.2003\">https://doi.org/10.1152/jn.00116.2003</a>.","ieee":"J. L. Csicsvari <i>et al.</i>, “Massively parallel recording of unit and local field potentials with silicon-based electrodes,” <i>Journal of Neurophysiology</i>, vol. 90, no. 2. American Physiological Society, pp. 1314–1323, 2003.","short":"J.L. Csicsvari, D. Henze, B. Jamieson, K. Harris, A. Sirota, P. Bartho, K. Wise, G. Buzsáki, Journal of Neurophysiology 90 (2003) 1314–1323.","mla":"Csicsvari, Jozsef L., et al. “Massively Parallel Recording of Unit and Local Field Potentials with Silicon-Based Electrodes.” <i>Journal of Neurophysiology</i>, vol. 90, no. 2, American Physiological Society, 2003, pp. 1314–23, doi:<a href=\"https://doi.org/10.1152/jn.00116.2003\">10.1152/jn.00116.2003</a>.","ama":"Csicsvari JL, Henze D, Jamieson B, et al. Massively parallel recording of unit and local field potentials with silicon-based electrodes. <i>Journal of Neurophysiology</i>. 2003;90(2):1314-1323. doi:<a href=\"https://doi.org/10.1152/jn.00116.2003\">10.1152/jn.00116.2003</a>","ista":"Csicsvari JL, Henze D, Jamieson B, Harris K, Sirota A, Bartho P, Wise K, Buzsáki G. 2003. Massively parallel recording of unit and local field potentials with silicon-based electrodes. Journal of Neurophysiology. 90(2), 1314–1323.","apa":"Csicsvari, J. L., Henze, D., Jamieson, B., Harris, K., Sirota, A., Bartho, P., … Buzsáki, G. (2003). Massively parallel recording of unit and local field potentials with silicon-based electrodes. <i>Journal of Neurophysiology</i>. American Physiological Society. <a href=\"https://doi.org/10.1152/jn.00116.2003\">https://doi.org/10.1152/jn.00116.2003</a>"},"extern":1,"year":"2003","type":"journal_article","volume":90,"quality_controlled":0,"doi":"10.1152/jn.00116.2003","title":"Massively parallel recording of unit and local field potentials with silicon-based electrodes","date_updated":"2021-01-12T07:44:05Z","publisher":"American Physiological Society","day":"01","publication_status":"published"}]