[{"publisher":"BioMed Central","quality_controlled":0,"month":"10","intvolume":" 1","abstract":[{"text":"Background: The glyoxylate cycle is thought to be present in bacteria, protists, plants, fungi, and nematodes, but not in other Metazoa. However, activity of the glyoxylate cycle enzymes, malate synthase (MS) and isocitrate lyase (ICL), in animal tissues has been reported. In order to clarify the status of the MS and ICL genes in animals and get an insight into their evolution, we undertook a comparative-genomic study. Results: Using sequence similarity searches, we identified MS genes in arthropods, echinoderms, and vertebrates, including platypus and opossum, but not in the numerous sequenced genomes of placental mammals. The regions of the placental mammals' genomes expected to code for malate synthase, as determined by comparison of the gene orders in vertebrate genomes, show clear similarity to the opossum MS sequence but contain stop codons, indicating that the MS gene became a pseudogene in placental mammals. By contrast, the ICL gene is undetectable in animals other than the nematodes that possess a bifunctional, fused ICL-MS gene. Examination of phylogenetic trees of MS and ICL suggests multiple horizontal gene transfer events that probably went in both directions between several bacterial and eukaryotic lineages. The strongest evidence was obtained for the acquisition of the bifunctional ICL-MS gene from an as yet unknown bacterial source with the corresponding operonic organization by the common ancestor of the nematodes. Conclusion: The distribution of the MS and ICL genes in animals suggests that either they encode alternative enzymes of the glyoxylate cycle that are not orthologous to the known MS and ICL or the animal MS acquired a new function that remains to be characterized. Regardless of the ultimate solution to this conundrum, the genes for the glyoxylate cycle enzymes present a remarkable variety of evolutionary events including unusual horizontal gene transfer from bacteria to animals.","lang":"eng"}],"acknowledgement":"The authors thank Alexey Kondrashov for suggesting the possibility of non- orthologous gene displacement in glyoxylate cycle specific enzymes and for critical reading of this manuscript. FAK is a National Science Foundation Graduate Fellow.","doi":"10.1186/1745-6150-1-31","date_published":"2006-10-23T00:00:00Z","volume":1,"date_created":"2018-12-11T11:48:56Z","year":"2006","publication_status":"published","day":"23","publication":"Biology Direct","type":"journal_article","tmp":{"legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode","image":"/images/cc_by.png","name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","short":"CC BY (4.0)"},"status":"public","_id":"868","author":[{"orcid":"0000-0001-8243-4694","full_name":"Fyodor Kondrashov","last_name":"Kondrashov","first_name":"Fyodor","id":"44FDEF62-F248-11E8-B48F-1D18A9856A87"},{"first_name":"Eugene","full_name":"Koonin, Eugene V","last_name":"Koonin"},{"last_name":"Morgunov","full_name":"Morgunov, Igor G","first_name":"Igor"},{"first_name":"Tatiana","full_name":"Finogenova, Tatiana V","last_name":"Finogenova"},{"first_name":"Marie","last_name":"Kondrashova","full_name":"Kondrashova, Marie N"}],"publist_id":"6778","title":"Evolution of glyoxylate cycle enzymes in Metazoa Evidence of multiple horizontal transfer events and pseudogene formation","citation":{"short":"F. Kondrashov, E. Koonin, I. Morgunov, T. Finogenova, M. Kondrashova, Biology Direct 1 (2006).","ieee":"F. Kondrashov, E. Koonin, I. Morgunov, T. Finogenova, and M. Kondrashova, “Evolution of glyoxylate cycle enzymes in Metazoa Evidence of multiple horizontal transfer events and pseudogene formation,” Biology Direct, vol. 1. BioMed Central, 2006.","ama":"Kondrashov F, Koonin E, Morgunov I, Finogenova T, Kondrashova M. Evolution of glyoxylate cycle enzymes in Metazoa Evidence of multiple horizontal transfer events and pseudogene formation. Biology Direct. 2006;1. doi:10.1186/1745-6150-1-31","apa":"Kondrashov, F., Koonin, E., Morgunov, I., Finogenova, T., & Kondrashova, M. (2006). Evolution of glyoxylate cycle enzymes in Metazoa Evidence of multiple horizontal transfer events and pseudogene formation. Biology Direct. BioMed Central. https://doi.org/10.1186/1745-6150-1-31","mla":"Kondrashov, Fyodor, et al. “Evolution of Glyoxylate Cycle Enzymes in Metazoa Evidence of Multiple Horizontal Transfer Events and Pseudogene Formation.” Biology Direct, vol. 1, BioMed Central, 2006, doi:10.1186/1745-6150-1-31.","ista":"Kondrashov F, Koonin E, Morgunov I, Finogenova T, Kondrashova M. 2006. Evolution of glyoxylate cycle enzymes in Metazoa Evidence of multiple horizontal transfer events and pseudogene formation. Biology Direct. 1.","chicago":"Kondrashov, Fyodor, Eugene Koonin, Igor Morgunov, Tatiana Finogenova, and Marie Kondrashova. “Evolution of Glyoxylate Cycle Enzymes in Metazoa Evidence of Multiple Horizontal Transfer Events and Pseudogene Formation.” Biology Direct. BioMed Central, 2006. https://doi.org/10.1186/1745-6150-1-31."},"date_updated":"2021-01-12T08:20:31Z","extern":1},{"page":"141 - 151","volume":239,"date_published":"2006-03-21T00:00:00Z","issue":"2","doi":"10.1016/j.jtbi.2005.08.033","date_created":"2018-12-11T11:48:57Z","year":"2006","publication_status":"published","day":"21","publication":"Journal of Theoretical Biology","quality_controlled":0,"publisher":"Elsevier","month":"03","intvolume":" 239","abstract":[{"text":"New genes commonly appear through complete or partial duplications of pre-existing genes. Duplications of long DNA segments are constantly produced by rare mutations, may become fixed in a population by selection or random drift, and are subject to divergent evolution of the paralogous sequences after fixation, although gene conversion can impede this process. New data shed some light on each of these processes. Mutations which involve duplications can occur through at least two different mechanisms, backward strand slippage during DNA replication and unequal crossing-over. The background rate of duplication of a complete gene in humans is 10-9-10-10 per generation, although many genes located within hot-spots of large-scale mutation are duplicated much more often. Many gene duplications affect fitness strongly, and are responsible, through gene dosage effects, for a number of genetic diseases. However, high levels of intrapopulation polymorphism caused by presence or absence of long, gene-containing DNA segments imply that some duplications are not under strong selection. The polymorphism to fixation ratios appear to be approximately the same for gene duplications and for presumably selectively neutral nucleotide substitutions, which, according to the McDonald-Kreitman test, is consistent with selective neutrality of duplications. However, this pattern can also be due to negative selection against most of segregating duplications and positive selection for at least some duplications which become fixed. Patterns in post-fixation evolution of duplicated genes do not easily reveal the causes of fixations. Many gene duplications which became fixed recently in a variety of organisms were positively selected because the increased expression of the corresponding genes was beneficial. The effects of gene dosage provide a unified framework for studying all phases of the life history of a gene duplication. Application of well-known methods of evolutionary genetics to accumulating data on new, polymorphic, and fixed duplication will enhance our understanding of the role of natural selection in the evolution by gene duplication.","lang":"eng"}],"publist_id":"6773","author":[{"first_name":"Fyodor","id":"44FDEF62-F248-11E8-B48F-1D18A9856A87","full_name":"Fyodor Kondrashov","orcid":"0000-0001-8243-4694","last_name":"Kondrashov"},{"full_name":"Kondrashov, Alexey S","last_name":"Kondrashov","first_name":"Alexey"}],"title":"Role of selection in fixation of gene duplications","date_updated":"2021-01-12T08:20:47Z","citation":{"ista":"Kondrashov F, Kondrashov A. 2006. Role of selection in fixation of gene duplications. Journal of Theoretical Biology. 239(2), 141–151.","chicago":"Kondrashov, Fyodor, and Alexey Kondrashov. “Role of Selection in Fixation of Gene Duplications.” Journal of Theoretical Biology. Elsevier, 2006. https://doi.org/10.1016/j.jtbi.2005.08.033.","short":"F. Kondrashov, A. Kondrashov, Journal of Theoretical Biology 239 (2006) 141–151.","ieee":"F. Kondrashov and A. Kondrashov, “Role of selection in fixation of gene duplications,” Journal of Theoretical Biology, vol. 239, no. 2. Elsevier, pp. 141–151, 2006.","apa":"Kondrashov, F., & Kondrashov, A. (2006). Role of selection in fixation of gene duplications. Journal of Theoretical Biology. Elsevier. https://doi.org/10.1016/j.jtbi.2005.08.033","ama":"Kondrashov F, Kondrashov A. Role of selection in fixation of gene duplications. Journal of Theoretical Biology. 2006;239(2):141-151. doi:10.1016/j.jtbi.2005.08.033","mla":"Kondrashov, Fyodor, and Alexey Kondrashov. “Role of Selection in Fixation of Gene Duplications.” Journal of Theoretical Biology, vol. 239, no. 2, Elsevier, 2006, pp. 141–51, doi:10.1016/j.jtbi.2005.08.033."},"extern":1,"type":"journal_article","status":"public","_id":"873"},{"language":[{"iso":"eng"}],"publication":"Magnetic Resonance in Chemistry","day":"06","publication_status":"published","year":"2006","publication_identifier":{"issn":["0749-1581","1097-458X"]},"date_created":"2020-09-18T10:13:42Z","issue":"S1","date_published":"2006-07-06T00:00:00Z","doi":"10.1002/mrc.1825","volume":44,"page":"S177-S184","oa_version":"None","abstract":[{"lang":"eng","text":"Structure elucidation of proteins by either NMR or X‐ray crystallography often requires the screening of a large number of samples for promising protein constructs and optimum solution conditions. For large‐scale screening of protein samples in solution, robust methods are needed that allow a rapid assessment of the folding of a polypeptide under diverse sample conditions. Here we present HET‐SOFAST NMR, a highly sensitive new method for semi‐quantitative characterization of the structural compactness and heterogeneity of polypeptide chains in solution. On the basis of one‐dimensional 1H HET‐SOFAST NMR data, obtained on well‐folded, molten globular, partially‐ and completely unfolded proteins, we define empirical thresholds that can be used as quantitative benchmarks for protein compactness. For 15N‐enriched protein samples, two‐dimensional 1H‐15N HET‐SOFAST correlation spectra provide site‐specific information about the structural heterogeneity along the polypeptide chain."}],"intvolume":" 44","month":"07","publisher":"Wiley","quality_controlled":"1","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","extern":"1","citation":{"chicago":"Schanda, Paul, Vincent Forge, and Bernhard Brutscher. “HET-SOFAST NMR for Fast Detection of Structural Compactness and Heterogeneity along Polypeptide Chains.” Magnetic Resonance in Chemistry. Wiley, 2006. https://doi.org/10.1002/mrc.1825.","ista":"Schanda P, Forge V, Brutscher B. 2006. HET-SOFAST NMR for fast detection of structural compactness and heterogeneity along polypeptide chains. Magnetic Resonance in Chemistry. 44(S1), S177–S184.","mla":"Schanda, Paul, et al. “HET-SOFAST NMR for Fast Detection of Structural Compactness and Heterogeneity along Polypeptide Chains.” Magnetic Resonance in Chemistry, vol. 44, no. S1, Wiley, 2006, pp. S177–84, doi:10.1002/mrc.1825.","short":"P. Schanda, V. Forge, B. Brutscher, Magnetic Resonance in Chemistry 44 (2006) S177–S184.","ieee":"P. Schanda, V. Forge, and B. Brutscher, “HET-SOFAST NMR for fast detection of structural compactness and heterogeneity along polypeptide chains,” Magnetic Resonance in Chemistry, vol. 44, no. S1. Wiley, pp. S177–S184, 2006.","apa":"Schanda, P., Forge, V., & Brutscher, B. (2006). HET-SOFAST NMR for fast detection of structural compactness and heterogeneity along polypeptide chains. Magnetic Resonance in Chemistry. Wiley. https://doi.org/10.1002/mrc.1825","ama":"Schanda P, Forge V, Brutscher B. HET-SOFAST NMR for fast detection of structural compactness and heterogeneity along polypeptide chains. Magnetic Resonance in Chemistry. 2006;44(S1):S177-S184. doi:10.1002/mrc.1825"},"date_updated":"2021-01-12T08:19:37Z","title":"HET-SOFAST NMR for fast detection of structural compactness and heterogeneity along polypeptide chains","article_processing_charge":"No","author":[{"first_name":"Paul","id":"7B541462-FAF6-11E9-A490-E8DFE5697425","last_name":"Schanda","orcid":"0000-0002-9350-7606","full_name":"Schanda, Paul"},{"first_name":"Vincent","last_name":"Forge","full_name":"Forge, Vincent"},{"first_name":"Bernhard","full_name":"Brutscher, Bernhard","last_name":"Brutscher"}],"_id":"8489","status":"public","type":"journal_article","article_type":"original"},{"_id":"8488","type":"journal_article","article_type":"original","status":"public","keyword":["Colloid and Surface Chemistry","Biochemistry","General Chemistry","Catalysis"],"date_updated":"2021-01-12T08:19:37Z","citation":{"mla":"Schanda, Paul, et al. “Speeding up Three-Dimensional Protein NMR Experiments to a Few Minutes.” Journal of the American Chemical Society, vol. 128, no. 28, American Chemical Society, 2006, pp. 9042–43, doi:10.1021/ja062025p.","apa":"Schanda, P., Van Melckebeke, H., & Brutscher, B. (2006). Speeding up three-dimensional protein NMR experiments to a few minutes. Journal of the American Chemical Society. American Chemical Society. https://doi.org/10.1021/ja062025p","ama":"Schanda P, Van Melckebeke H, Brutscher B. Speeding up three-dimensional protein NMR experiments to a few minutes. Journal of the American Chemical Society. 2006;128(28):9042-9043. doi:10.1021/ja062025p","ieee":"P. Schanda, H. Van Melckebeke, and B. Brutscher, “Speeding up three-dimensional protein NMR experiments to a few minutes,” Journal of the American Chemical Society, vol. 128, no. 28. American Chemical Society, pp. 9042–9043, 2006.","short":"P. Schanda, H. Van Melckebeke, B. Brutscher, Journal of the American Chemical Society 128 (2006) 9042–9043.","chicago":"Schanda, Paul, Hélène Van Melckebeke, and Bernhard Brutscher. “Speeding up Three-Dimensional Protein NMR Experiments to a Few Minutes.” Journal of the American Chemical Society. American Chemical Society, 2006. https://doi.org/10.1021/ja062025p.","ista":"Schanda P, Van Melckebeke H, Brutscher B. 2006. Speeding up three-dimensional protein NMR experiments to a few minutes. Journal of the American Chemical Society. 128(28), 9042–9043."},"extern":"1","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","author":[{"first_name":"Paul","id":"7B541462-FAF6-11E9-A490-E8DFE5697425","last_name":"Schanda","full_name":"Schanda, Paul","orcid":"0000-0002-9350-7606"},{"first_name":"Hélène","full_name":"Van Melckebeke, Hélène","last_name":"Van Melckebeke"},{"full_name":"Brutscher, Bernhard","last_name":"Brutscher","first_name":"Bernhard"}],"article_processing_charge":"No","title":"Speeding up three-dimensional protein NMR experiments to a few minutes","abstract":[{"text":"We demonstrate for different protein samples that three-dimensional HNCO and HNCA correlation spectra may be recorded in a few minutes acquisition time using the band-selective excitation short-transient sequences presented here. This opens new perspectives for the NMR structural investigation of unstable protein samples and real-time site-resolved studies of protein kinetics.","lang":"eng"}],"oa_version":"None","publisher":"American Chemical Society","quality_controlled":"1","month":"06","intvolume":" 128","publication_identifier":{"issn":["0002-7863","1520-5126"]},"publication_status":"published","year":"2006","day":"21","language":[{"iso":"eng"}],"publication":"Journal of the American Chemical Society","page":"9042-9043","date_published":"2006-06-21T00:00:00Z","issue":"28","volume":128,"doi":"10.1021/ja062025p","date_created":"2020-09-18T10:13:36Z"},{"page":"334-339","doi":"10.1016/j.jmr.2005.10.007","date_published":"2006-02-01T00:00:00Z","volume":178,"issue":"2","date_created":"2020-09-18T10:13:51Z","publication_identifier":{"issn":["1090-7807"]},"year":"2006","publication_status":"published","day":"01","language":[{"iso":"eng"}],"publication":"Journal of Magnetic Resonance","publisher":"Elsevier","month":"02","intvolume":" 178","abstract":[{"text":"We demonstrate the feasibility of recording 1H–15N correlation spectra of proteins in only one second of acquisition time. The experiment combines recently proposed SOFAST-HMQC with Hadamard-type 15N frequency encoding. This allows site-resolved real-time NMR studies of kinetic processes in proteins with an increased time resolution. The sensitivity of the experiment is sufficient to be applicable to a wide range of molecular systems available at millimolar concentration on a high magnetic field spectrometer.","lang":"eng"}],"oa_version":"None","author":[{"last_name":"Schanda","orcid":"0000-0002-9350-7606","full_name":"Schanda, Paul","id":"7B541462-FAF6-11E9-A490-E8DFE5697425","first_name":"Paul"},{"full_name":"Brutscher, Bernhard","last_name":"Brutscher","first_name":"Bernhard"}],"article_processing_charge":"No","title":"Hadamard frequency-encoded SOFAST-HMQC for ultrafast two-dimensional protein NMR","citation":{"mla":"Schanda, Paul, and Bernhard Brutscher. “Hadamard Frequency-Encoded SOFAST-HMQC for Ultrafast Two-Dimensional Protein NMR.” Journal of Magnetic Resonance, vol. 178, no. 2, Elsevier, 2006, pp. 334–39, doi:10.1016/j.jmr.2005.10.007.","ieee":"P. Schanda and B. Brutscher, “Hadamard frequency-encoded SOFAST-HMQC for ultrafast two-dimensional protein NMR,” Journal of Magnetic Resonance, vol. 178, no. 2. Elsevier, pp. 334–339, 2006.","short":"P. Schanda, B. Brutscher, Journal of Magnetic Resonance 178 (2006) 334–339.","apa":"Schanda, P., & Brutscher, B. (2006). Hadamard frequency-encoded SOFAST-HMQC for ultrafast two-dimensional protein NMR. Journal of Magnetic Resonance. Elsevier. https://doi.org/10.1016/j.jmr.2005.10.007","ama":"Schanda P, Brutscher B. Hadamard frequency-encoded SOFAST-HMQC for ultrafast two-dimensional protein NMR. Journal of Magnetic Resonance. 2006;178(2):334-339. doi:10.1016/j.jmr.2005.10.007","chicago":"Schanda, Paul, and Bernhard Brutscher. “Hadamard Frequency-Encoded SOFAST-HMQC for Ultrafast Two-Dimensional Protein NMR.” Journal of Magnetic Resonance. Elsevier, 2006. https://doi.org/10.1016/j.jmr.2005.10.007.","ista":"Schanda P, Brutscher B. 2006. Hadamard frequency-encoded SOFAST-HMQC for ultrafast two-dimensional protein NMR. Journal of Magnetic Resonance. 178(2), 334–339."},"date_updated":"2021-01-12T08:19:38Z","extern":"1","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","article_type":"original","type":"journal_article","status":"public","keyword":["Nuclear and High Energy Physics","Biophysics","Biochemistry","Condensed Matter Physics"],"_id":"8490"},{"page":"869-891","issue":"3","volume":26,"doi":"10.1017/s0143385705000714","date_published":"2006-06-01T00:00:00Z","date_created":"2020-09-18T10:48:52Z","publication_identifier":{"issn":["0143-3857","1469-4417"]},"publication_status":"published","year":"2006","day":"01","publication":"Ergodic Theory and Dynamical Systems","language":[{"iso":"eng"}],"publisher":"Cambridge University Press","quality_controlled":"1","month":"06","intvolume":" 26","abstract":[{"lang":"eng","text":"We study the extent to which the Hausdorff dimension of a compact subset of an infinite-dimensional Banach space is affected by a typical mapping into a finite-dimensional space. It is possible that the dimension drops under all such mappings, but the amount by which it typically drops is controlled by the ‘thickness exponent’ of the set, which was defined by Hunt and Kaloshin (Nonlinearity12 (1999), 1263–1275). More precisely, let $X$ be a compact subset of a Banach space $B$ with thickness exponent $\\tau$ and Hausdorff dimension $d$. Let $M$ be any subspace of the (locally) Lipschitz functions from $B$ to $\\mathbb{R}^{m}$ that contains the space of bounded linear functions. We prove that for almost every (in the sense of prevalence) function $f \\in M$, the Hausdorff dimension of $f(X)$ is at least $\\min\\{ m, d / (1 + \\tau) \\}$. We also prove an analogous result for a certain part of the dimension spectra of Borel probability measures supported on $X$. The factor $1 / (1 + \\tau)$ can be improved to $1 / (1 + \\tau / 2)$ if $B$ is a Hilbert space. Since dimension cannot increase under a (locally) Lipschitz function, these theorems become dimension preservation results when $\\tau = 0$. We conjecture that many of the attractors associated with the evolution equations of mathematical physics have thickness exponent zero. We also discuss the sharpness of our results in the case $\\tau > 0$."}],"oa_version":"None","author":[{"first_name":"WILLIAM","last_name":"OTT","full_name":"OTT, WILLIAM"},{"first_name":"BRIAN","full_name":"HUNT, BRIAN","last_name":"HUNT"},{"first_name":"Vadim","id":"FE553552-CDE8-11E9-B324-C0EBE5697425","last_name":"Kaloshin","full_name":"Kaloshin, Vadim","orcid":"0000-0002-6051-2628"}],"article_processing_charge":"No","title":"The effect of projections on fractal sets and measures in Banach spaces","citation":{"chicago":"OTT, WILLIAM, BRIAN HUNT, and Vadim Kaloshin. “The Effect of Projections on Fractal Sets and Measures in Banach Spaces.” Ergodic Theory and Dynamical Systems. Cambridge University Press, 2006. https://doi.org/10.1017/s0143385705000714.","ista":"OTT W, HUNT B, Kaloshin V. 2006. The effect of projections on fractal sets and measures in Banach spaces. Ergodic Theory and Dynamical Systems. 26(3), 869–891.","mla":"OTT, WILLIAM, et al. “The Effect of Projections on Fractal Sets and Measures in Banach Spaces.” Ergodic Theory and Dynamical Systems, vol. 26, no. 3, Cambridge University Press, 2006, pp. 869–91, doi:10.1017/s0143385705000714.","apa":"OTT, W., HUNT, B., & Kaloshin, V. (2006). The effect of projections on fractal sets and measures in Banach spaces. Ergodic Theory and Dynamical Systems. Cambridge University Press. https://doi.org/10.1017/s0143385705000714","ama":"OTT W, HUNT B, Kaloshin V. The effect of projections on fractal sets and measures in Banach spaces. Ergodic Theory and Dynamical Systems. 2006;26(3):869-891. doi:10.1017/s0143385705000714","short":"W. OTT, B. HUNT, V. Kaloshin, Ergodic Theory and Dynamical Systems 26 (2006) 869–891.","ieee":"W. OTT, B. HUNT, and V. Kaloshin, “The effect of projections on fractal sets and measures in Banach spaces,” Ergodic Theory and Dynamical Systems, vol. 26, no. 3. Cambridge University Press, pp. 869–891, 2006."},"date_updated":"2021-01-12T08:19:48Z","extern":"1","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","type":"journal_article","article_type":"original","status":"public","_id":"8514"},{"abstract":[{"lang":"eng","text":"We consider the evolution of a set carried by a space periodic incompressible stochastic flow in a Euclidean space. We\r\nreport on three main results obtained in [8, 9, 10] concerning long time behaviour for a typical realization of the stochastic flow. First, at time t most of the particles are at a distance of order √t away from the origin. Moreover, we prove a Central Limit Theorem for the evolution of a measure carried by the flow, which holds for almost every realization of the flow. Second, we show the existence of a zero measure full Hausdorff dimension set of points, which\r\nescape to infinity at a linear rate. Third, in the 2-dimensional case, we study the set of points visited by the original set by time t. Such a set, when scaled down by the factor of t, has a limiting non random shape."}],"oa_version":"None","publisher":"World Scientific","quality_controlled":"1","month":"03","publication_identifier":{"isbn":["9789812562012","9789812704016"]},"year":"2006","publication_status":"published","day":"01","publication":"XIVth International Congress on Mathematical Physics","language":[{"iso":"eng"}],"page":"290-295","date_published":"2006-03-01T00:00:00Z","doi":"10.1142/9789812704016_0026","date_created":"2020-09-18T10:48:59Z","_id":"8515","type":"conference","conference":{"start_date":"2003-07-28","location":"Lisbon, Portugal","end_date":"2003-08-02","name":"International Congress on Mathematical Physics"},"status":"public","citation":{"chicago":"Kaloshin, Vadim, D. DOLGOPYAT, and L. KORALOV. “Long Time Behaviour of Periodic Stochastic Flows.” In XIVth International Congress on Mathematical Physics, 290–95. World Scientific, 2006. https://doi.org/10.1142/9789812704016_0026.","ista":"Kaloshin V, DOLGOPYAT D, KORALOV L. 2006. Long time behaviour of periodic stochastic flows. XIVth International Congress on Mathematical Physics. International Congress on Mathematical Physics, 290–295.","mla":"Kaloshin, Vadim, et al. “Long Time Behaviour of Periodic Stochastic Flows.” XIVth International Congress on Mathematical Physics, World Scientific, 2006, pp. 290–95, doi:10.1142/9789812704016_0026.","ama":"Kaloshin V, DOLGOPYAT D, KORALOV L. Long time behaviour of periodic stochastic flows. In: XIVth International Congress on Mathematical Physics. World Scientific; 2006:290-295. doi:10.1142/9789812704016_0026","apa":"Kaloshin, V., DOLGOPYAT, D., & KORALOV, L. (2006). Long time behaviour of periodic stochastic flows. In XIVth International Congress on Mathematical Physics (pp. 290–295). Lisbon, Portugal: World Scientific. https://doi.org/10.1142/9789812704016_0026","short":"V. Kaloshin, D. DOLGOPYAT, L. KORALOV, in:, XIVth International Congress on Mathematical Physics, World Scientific, 2006, pp. 290–295.","ieee":"V. Kaloshin, D. DOLGOPYAT, and L. KORALOV, “Long time behaviour of periodic stochastic flows,” in XIVth International Congress on Mathematical Physics, Lisbon, Portugal, 2006, pp. 290–295."},"date_updated":"2021-01-12T08:19:49Z","extern":"1","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","author":[{"first_name":"Vadim","id":"FE553552-CDE8-11E9-B324-C0EBE5697425","last_name":"Kaloshin","orcid":"0000-0002-6051-2628","full_name":"Kaloshin, Vadim"},{"last_name":"DOLGOPYAT","full_name":"DOLGOPYAT, D.","first_name":"D."},{"last_name":"KORALOV","full_name":"KORALOV, L.","first_name":"L."}],"article_processing_charge":"No","title":"Long time behaviour of periodic stochastic flows"},{"day":"01","publication":"Discrete & Continuous Dynamical Systems - A","language":[{"iso":"eng"}],"publication_identifier":{"issn":["1553-5231"]},"publication_status":"published","year":"2006","doi":"10.3934/dcds.2006.15.611","volume":15,"issue":"2","date_published":"2006-05-01T00:00:00Z","date_created":"2020-09-18T10:48:43Z","page":"611-640","oa_version":"None","month":"05","intvolume":" 15","quality_controlled":"1","publisher":"American Institute of Mathematical Sciences (AIMS)","extern":"1","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","citation":{"mla":"Kaloshin, Vadim, and Maria Saprykina. “Generic 3-Dimensional Volume-Preserving Diffeomorphisms with Superexponential Growth of Number of Periodic Orbits.” Discrete & Continuous Dynamical Systems - A, vol. 15, no. 2, American Institute of Mathematical Sciences (AIMS), 2006, pp. 611–40, doi:10.3934/dcds.2006.15.611.","short":"V. Kaloshin, M. Saprykina, Discrete & Continuous Dynamical Systems - A 15 (2006) 611–640.","ieee":"V. Kaloshin and M. Saprykina, “Generic 3-dimensional volume-preserving diffeomorphisms with superexponential growth of number of periodic orbits,” Discrete & Continuous Dynamical Systems - A, vol. 15, no. 2. American Institute of Mathematical Sciences (AIMS), pp. 611–640, 2006.","apa":"Kaloshin, V., & Saprykina, M. (2006). Generic 3-dimensional volume-preserving diffeomorphisms with superexponential growth of number of periodic orbits. Discrete & Continuous Dynamical Systems - A. American Institute of Mathematical Sciences (AIMS). https://doi.org/10.3934/dcds.2006.15.611","ama":"Kaloshin V, Saprykina M. Generic 3-dimensional volume-preserving diffeomorphisms with superexponential growth of number of periodic orbits. Discrete & Continuous Dynamical Systems - A. 2006;15(2):611-640. doi:10.3934/dcds.2006.15.611","chicago":"Kaloshin, Vadim, and Maria Saprykina. “Generic 3-Dimensional Volume-Preserving Diffeomorphisms with Superexponential Growth of Number of Periodic Orbits.” Discrete & Continuous Dynamical Systems - A. American Institute of Mathematical Sciences (AIMS), 2006. https://doi.org/10.3934/dcds.2006.15.611.","ista":"Kaloshin V, Saprykina M. 2006. Generic 3-dimensional volume-preserving diffeomorphisms with superexponential growth of number of periodic orbits. Discrete & Continuous Dynamical Systems - A. 15(2), 611–640."},"date_updated":"2021-01-12T08:19:48Z","title":"Generic 3-dimensional volume-preserving diffeomorphisms with superexponential growth of number of periodic orbits","author":[{"last_name":"Kaloshin","orcid":"0000-0002-6051-2628","full_name":"Kaloshin, Vadim","id":"FE553552-CDE8-11E9-B324-C0EBE5697425","first_name":"Vadim"},{"last_name":"Saprykina","full_name":"Saprykina, Maria","first_name":"Maria"}],"article_processing_charge":"No","_id":"8513","status":"public","article_type":"original","type":"journal_article"},{"_id":"869","type":"journal_article","status":"public","date_updated":"2021-01-12T08:20:33Z","citation":{"ista":"Kondrashov F, Ogurtsov A, Kondrashov A. 2006. Selection in favor of nucleotides G and C diversifies evolution rates and levels of polymorphism at mammalian synonymous sites. Journal of Theoretical Biology. 240(4), 616–626.","chicago":"Kondrashov, Fyodor, Aleksey Ogurtsov, and Alexey Kondrashov. “Selection in Favor of Nucleotides G and C Diversifies Evolution Rates and Levels of Polymorphism at Mammalian Synonymous Sites.” Journal of Theoretical Biology. Elsevier, 2006. https://doi.org/10.1016/j.jtbi.2005.10.020.","ieee":"F. Kondrashov, A. Ogurtsov, and A. Kondrashov, “Selection in favor of nucleotides G and C diversifies evolution rates and levels of polymorphism at mammalian synonymous sites,” Journal of Theoretical Biology, vol. 240, no. 4. Elsevier, pp. 616–626, 2006.","short":"F. Kondrashov, A. Ogurtsov, A. Kondrashov, Journal of Theoretical Biology 240 (2006) 616–626.","ama":"Kondrashov F, Ogurtsov A, Kondrashov A. Selection in favor of nucleotides G and C diversifies evolution rates and levels of polymorphism at mammalian synonymous sites. Journal of Theoretical Biology. 2006;240(4):616-626. doi:10.1016/j.jtbi.2005.10.020","apa":"Kondrashov, F., Ogurtsov, A., & Kondrashov, A. (2006). Selection in favor of nucleotides G and C diversifies evolution rates and levels of polymorphism at mammalian synonymous sites. Journal of Theoretical Biology. Elsevier. https://doi.org/10.1016/j.jtbi.2005.10.020","mla":"Kondrashov, Fyodor, et al. “Selection in Favor of Nucleotides G and C Diversifies Evolution Rates and Levels of Polymorphism at Mammalian Synonymous Sites.” Journal of Theoretical Biology, vol. 240, no. 4, Elsevier, 2006, pp. 616–26, doi:10.1016/j.jtbi.2005.10.020."},"extern":1,"publist_id":"6779","author":[{"last_name":"Kondrashov","orcid":"0000-0001-8243-4694","full_name":"Fyodor Kondrashov","first_name":"Fyodor","id":"44FDEF62-F248-11E8-B48F-1D18A9856A87"},{"first_name":"Aleksey","full_name":"Ogurtsov, Aleksey Yu","last_name":"Ogurtsov"},{"last_name":"Kondrashov","full_name":"Kondrashov, Alexey S","first_name":"Alexey"}],"title":"Selection in favor of nucleotides G and C diversifies evolution rates and levels of polymorphism at mammalian synonymous sites","abstract":[{"text":"The impact of synonymous nucleotide substitutions on fitness in mammals remains controversial. Despite some indications of selective constraint, synonymous sites are often assumed to be neutral, and the rate of their evolution is used as a proxy for mutation rate. We subdivide all sites into four classes in terms of the mutable CpG context, nonCpG, postC, preG, and postCpreG, and compare four-fold synonymous sites and intron sites residing outside transposable elements. The distribution of the rate of evolution across all synonymous sites is trimodal. Rate of evolution at nonCpG synonymous sites, not preceded by C and not followed by G, is ∼10% below that at such intron sites. In contrast, rate of evolution at postCpreG synonymous sites is ∼30% above that at such intron sites. Finally, synonymous and intron postC and preG sites evolve at similar rates. The relationship between the levels of polymorphism at the corresponding synonymous and intron sites is very similar to that between their rates of evolution. Within every class, synonymous sites are occupied by G or C much more often than intron sites, whose nucleotide composition is consistent with neutral mutation-drift equilibrium. These patterns suggest that synonymous sites are under weak selection in favor of G and C, with the average coefficient s∼0.25/Ne∼10-5, where Ne is the effective population size. Such selection decelerates evolution and reduces variability at sites with symmetric mutation, but has the opposite effects at sites where the favored nucleotides are more mutable. The amino-acid composition of proteins dictates that many synonymous sites are CpGprone, which causes them, on average, to evolve faster and to be more polymorphic than intron sites. An average genotype carries ∼107 suboptimal nucleotides at synonymous sites, implying synergistic epistasis in selection against them.","lang":"eng"}],"acknowledgement":"This research was supported in part by the Intramural Research Program of the NIH, National Library of Medicine.","quality_controlled":0,"publisher":"Elsevier","month":"06","intvolume":" 240","publication_status":"published","year":"2006","day":"21","publication":"Journal of Theoretical Biology","page":"616 - 626","date_published":"2006-06-21T00:00:00Z","doi":"10.1016/j.jtbi.2005.10.020","issue":"4","volume":240,"date_created":"2018-12-11T11:48:56Z"},{"publication_status":"published","year":"2006","day":"09","publication":"BMC Cancer","volume":6,"date_published":"2006-02-09T00:00:00Z","doi":"10.1186/1471-2407-6-36","date_created":"2018-12-11T11:49:07Z","abstract":[{"lang":"eng","text":"Background: Carcinogenesis typically involves multiple somatic mutations in caretaker (DNA repair) and gatekeeper (tumor suppressors and oncogenes) genes. Analysis of mutation spectra of the tumor suppressor that is most commonly mutated in human cancers, p53, unexpectedly suggested that somatic evolution of the p53 gene during tumorigenesis is dominated by positive selection for gain of function. This conclusion is supported by accumulating experimental evidence of evolution of new functions of p53 in tumors. These findings prompted a genome-wide analysis of possible positive selection during tumor evolution. Methods: A comprehensive analysis of probable somatic mutations in the sequences of Expressed Sequence Tags (ESTs) from malignant tumors and normal tissues was performed in order to access the prevalence of positive selection in cancer evolution. For each EST, the numbers of synonymous and non-synonymous substitutions were calculated. In order to identify genes with a signature of positive selection in cancers, these numbers were compared to: i) expected numbers and ii) the numbers for the respective genes in the ESTs from normal tissues. Results: We identified 112 genes with a signature of positive selection in cancers, i.e., a significantly elevated ratio of non-synonymous to synonymous substitutions, in tumors as compared to 37 such genes in an approximately equal-sized EST collection from normal tissues. A substantial fraction of the tumor-specific positive-selection candidates have experimentally demonstrated or strongly predicted links to cancer. Conclusion: The results of EST analysis should be interpreted with extreme caution given the noise introduced by sequencing errors and undetected polymorphisms. Furthermore, an inherent limitation of EST analysis is that multiple mutations amenable to statistical analysis can be detected only in relatively highly expressed genes. Nevertheless, the present results suggest that positive selection might affect a substantial number of genes during tumorigenic somatic evolution."}],"acknowledgement":"This work was supported by the Intramural Research Program of the National Library of Medicine at the National Institutes of Health/DHHS. FAK is an NSF Graduate Fellow. We thank Yuri Pavlov for helpful discussions.","publisher":"BioMed Central","quality_controlled":0,"month":"02","intvolume":" 6","date_updated":"2021-01-12T08:21:47Z","citation":{"short":"V. Babenko, M. Basu, F. Kondrashov, I. Rogozin, E. Koonin, BMC Cancer 6 (2006).","ieee":"V. Babenko, M. Basu, F. Kondrashov, I. Rogozin, and E. Koonin, “Signs of positive selection of somatic mutations in human cancers detected by EST sequence analysis,” BMC Cancer, vol. 6. BioMed Central, 2006.","apa":"Babenko, V., Basu, M., Kondrashov, F., Rogozin, I., & Koonin, E. (2006). Signs of positive selection of somatic mutations in human cancers detected by EST sequence analysis. BMC Cancer. BioMed Central. https://doi.org/10.1186/1471-2407-6-36","ama":"Babenko V, Basu M, Kondrashov F, Rogozin I, Koonin E. Signs of positive selection of somatic mutations in human cancers detected by EST sequence analysis. BMC Cancer. 2006;6. doi:10.1186/1471-2407-6-36","mla":"Babenko, Vladimir, et al. “Signs of Positive Selection of Somatic Mutations in Human Cancers Detected by EST Sequence Analysis.” BMC Cancer, vol. 6, BioMed Central, 2006, doi:10.1186/1471-2407-6-36.","ista":"Babenko V, Basu M, Kondrashov F, Rogozin I, Koonin E. 2006. Signs of positive selection of somatic mutations in human cancers detected by EST sequence analysis. BMC Cancer. 6.","chicago":"Babenko, Vladimir, Malay Basu, Fyodor Kondrashov, Igor Rogozin, and Eugene Koonin. “Signs of Positive Selection of Somatic Mutations in Human Cancers Detected by EST Sequence Analysis.” BMC Cancer. BioMed Central, 2006. https://doi.org/10.1186/1471-2407-6-36."},"extern":1,"publist_id":"6744","author":[{"last_name":"Babenko","full_name":"Babenko, Vladimir N","first_name":"Vladimir"},{"first_name":"Malay","full_name":"Basu, Malay K","last_name":"Basu"},{"orcid":"0000-0001-8243-4694","full_name":"Fyodor Kondrashov","last_name":"Kondrashov","id":"44FDEF62-F248-11E8-B48F-1D18A9856A87","first_name":"Fyodor"},{"first_name":"Igor","full_name":"Rogozin, Igor B","last_name":"Rogozin"},{"full_name":"Koonin, Eugene V","last_name":"Koonin","first_name":"Eugene"}],"title":"Signs of positive selection of somatic mutations in human cancers detected by EST sequence analysis","_id":"903","type":"journal_article","tmp":{"legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode","image":"/images/cc_by.png","name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","short":"CC BY (4.0)"},"status":"public"},{"oa_version":"None","pmid":1,"abstract":[{"text":"Cytosine methylation, a common form of DNA modification that antagonizes transcription, is found at transposons and repeats in vertebrates, plants and fungi. Here we have mapped DNA methylation in the entire Arabidopsis thaliana genome at high resolution. DNA methylation covers transposons and is present within a large fraction of A. thaliana genes. Methylation within genes is conspicuously biased away from gene ends, suggesting a dependence on RNA polymerase transit. Genic methylation is strongly influenced by transcription: moderately transcribed genes are most likely to be methylated, whereas genes at either extreme are least likely. In turn, transcription is influenced by methylation: short methylated genes are poorly expressed, and loss of methylation in the body of a gene leads to enhanced transcription. Our results indicate that genic transcription and DNA methylation are closely interwoven processes.","lang":"eng"}],"intvolume":" 39","month":"11","scopus_import":"1","language":[{"iso":"eng"}],"publication_status":"published","publication_identifier":{"issn":["1061-4036"],"eissn":["1546-1718"]},"issue":"1","volume":39,"_id":"9505","status":"public","article_type":"original","type":"journal_article","extern":"1","date_updated":"2021-12-14T09:02:51Z","department":[{"_id":"DaZi"}],"quality_controlled":"1","publisher":"Nature Publishing Group","publication":"Nature Genetics","day":"26","year":"2006","date_created":"2021-06-07T12:19:31Z","doi":"10.1038/ng1929","date_published":"2006-11-26T00:00:00Z","page":"61-69","user_id":"8b945eb4-e2f2-11eb-945a-df72226e66a9","citation":{"ista":"Zilberman D, Gehring M, Tran RK, Ballinger T, Henikoff S. 2006. Genome-wide analysis of Arabidopsis thaliana DNA methylation uncovers an interdependence between methylation and transcription. Nature Genetics. 39(1), 61–69.","chicago":"Zilberman, Daniel, Mary Gehring, Robert K. Tran, Tracy Ballinger, and Steven Henikoff. “Genome-Wide Analysis of Arabidopsis Thaliana DNA Methylation Uncovers an Interdependence between Methylation and Transcription.” Nature Genetics. Nature Publishing Group, 2006. https://doi.org/10.1038/ng1929.","ama":"Zilberman D, Gehring M, Tran RK, Ballinger T, Henikoff S. Genome-wide analysis of Arabidopsis thaliana DNA methylation uncovers an interdependence between methylation and transcription. Nature Genetics. 2006;39(1):61-69. doi:10.1038/ng1929","apa":"Zilberman, D., Gehring, M., Tran, R. K., Ballinger, T., & Henikoff, S. (2006). Genome-wide analysis of Arabidopsis thaliana DNA methylation uncovers an interdependence between methylation and transcription. Nature Genetics. Nature Publishing Group. https://doi.org/10.1038/ng1929","short":"D. Zilberman, M. Gehring, R.K. Tran, T. Ballinger, S. Henikoff, Nature Genetics 39 (2006) 61–69.","ieee":"D. Zilberman, M. Gehring, R. K. Tran, T. Ballinger, and S. Henikoff, “Genome-wide analysis of Arabidopsis thaliana DNA methylation uncovers an interdependence between methylation and transcription,” Nature Genetics, vol. 39, no. 1. Nature Publishing Group, pp. 61–69, 2006.","mla":"Zilberman, Daniel, et al. “Genome-Wide Analysis of Arabidopsis Thaliana DNA Methylation Uncovers an Interdependence between Methylation and Transcription.” Nature Genetics, vol. 39, no. 1, Nature Publishing Group, 2006, pp. 61–69, doi:10.1038/ng1929."},"title":"Genome-wide analysis of Arabidopsis thaliana DNA methylation uncovers an interdependence between methylation and transcription","article_processing_charge":"No","external_id":{"pmid":["17128275"]},"author":[{"first_name":"Daniel","id":"6973db13-dd5f-11ea-814e-b3e5455e9ed1","orcid":"0000-0002-0123-8649","full_name":"Zilberman, Daniel","last_name":"Zilberman"},{"last_name":"Gehring","full_name":"Gehring, Mary","first_name":"Mary"},{"first_name":"Robert K.","last_name":"Tran","full_name":"Tran, Robert K."},{"last_name":"Ballinger","full_name":"Ballinger, Tracy","first_name":"Tracy"},{"first_name":"Steven","full_name":"Henikoff, Steven","last_name":"Henikoff"}]},{"pmid":1,"oa_version":"None","abstract":[{"text":"Dynamic self-assembly (DySA) processes occurring outside of thermodynamic equilibrium underlie many forms of adaptive and intellligent behaviors in natural systems. Relatively little, however, is known about the principles that govern DySA and the ways in which it can be extended to artificial ensembles. This article discusses recent advances in both the theory and the practice of nonequilibrium self-assembly. It is argued that a union of ideas from thermodynamics and dynamic systems' theory can provide a general description of DySA. In parallel, heuristic design rules can be used to construct DySA systems of increasing complexities based on a variety of suitable interactions/potentials on length scales from nanoscopic to macroscopic. Applications of these rules to magnetohydrodynamic DySA are also discussed.","lang":"eng"}],"month":"01","intvolume":" 110","scopus_import":"1","language":[{"iso":"eng"}],"publication_identifier":{"issn":["1520-6106","1520-5207"]},"publication_status":"published","volume":110,"issue":"6","_id":"13430","status":"public","keyword":["Materials Chemistry","Surfaces","Coatings and Films","Physical and Theoretical Chemistry"],"type":"journal_article","article_type":"original","extern":"1","date_updated":"2023-08-08T11:33:08Z","quality_controlled":"1","publisher":"American Chemical Society","day":"25","publication":"The Journal of Physical Chemistry B","year":"2006","date_published":"2006-01-25T00:00:00Z","doi":"10.1021/jp054153q","date_created":"2023-08-01T10:37:35Z","page":"2482-2496","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","citation":{"ista":"Fialkowski M, Bishop KJM, Klajn R, Smoukov SK, Campbell CJ, Grzybowski BA. 2006. Principles and implementations of dissipative (dynamic) self-assembly. The Journal of Physical Chemistry B. 110(6), 2482–2496.","chicago":"Fialkowski, Marcin, Kyle J. M. Bishop, Rafal Klajn, Stoyan K. Smoukov, Christopher J. Campbell, and Bartosz A. Grzybowski. “Principles and Implementations of Dissipative (Dynamic) Self-Assembly.” The Journal of Physical Chemistry B. American Chemical Society, 2006. https://doi.org/10.1021/jp054153q.","ama":"Fialkowski M, Bishop KJM, Klajn R, Smoukov SK, Campbell CJ, Grzybowski BA. Principles and implementations of dissipative (dynamic) self-assembly. The Journal of Physical Chemistry B. 2006;110(6):2482-2496. doi:10.1021/jp054153q","apa":"Fialkowski, M., Bishop, K. J. M., Klajn, R., Smoukov, S. K., Campbell, C. J., & Grzybowski, B. A. (2006). Principles and implementations of dissipative (dynamic) self-assembly. The Journal of Physical Chemistry B. American Chemical Society. https://doi.org/10.1021/jp054153q","ieee":"M. Fialkowski, K. J. M. Bishop, R. Klajn, S. K. Smoukov, C. J. Campbell, and B. A. Grzybowski, “Principles and implementations of dissipative (dynamic) self-assembly,” The Journal of Physical Chemistry B, vol. 110, no. 6. American Chemical Society, pp. 2482–2496, 2006.","short":"M. Fialkowski, K.J.M. Bishop, R. Klajn, S.K. Smoukov, C.J. Campbell, B.A. Grzybowski, The Journal of Physical Chemistry B 110 (2006) 2482–2496.","mla":"Fialkowski, Marcin, et al. “Principles and Implementations of Dissipative (Dynamic) Self-Assembly.” The Journal of Physical Chemistry B, vol. 110, no. 6, American Chemical Society, 2006, pp. 2482–96, doi:10.1021/jp054153q."},"title":"Principles and implementations of dissipative (dynamic) self-assembly","author":[{"first_name":"Marcin","last_name":"Fialkowski","full_name":"Fialkowski, Marcin"},{"first_name":"Kyle J. M.","full_name":"Bishop, Kyle J. M.","last_name":"Bishop"},{"id":"8e84690e-1e48-11ed-a02b-a1e6fb8bb53b","first_name":"Rafal","last_name":"Klajn","full_name":"Klajn, Rafal"},{"first_name":"Stoyan K.","last_name":"Smoukov","full_name":"Smoukov, Stoyan K."},{"first_name":"Christopher J.","full_name":"Campbell, Christopher J.","last_name":"Campbell"},{"first_name":"Bartosz A.","last_name":"Grzybowski","full_name":"Grzybowski, Bartosz A."}],"external_id":{"pmid":["16471845"]},"article_processing_charge":"No"},{"page":"15046-15047","date_created":"2023-08-01T10:36:27Z","date_published":"2006-11-29T00:00:00Z","doi":"10.1021/ja0642966","year":"2006","publication":"Journal of the American Chemical Society","day":"29","publisher":"American Chemical Society","quality_controlled":"1","article_processing_charge":"No","external_id":{"pmid":["17117829"]},"author":[{"full_name":"Kalsin, Alexander M.","last_name":"Kalsin","first_name":"Alexander M."},{"first_name":"Bartlomiej","last_name":"Kowalczyk","full_name":"Kowalczyk, Bartlomiej"},{"full_name":"Smoukov, Stoyan K.","last_name":"Smoukov","first_name":"Stoyan K."},{"last_name":"Klajn","full_name":"Klajn, Rafal","id":"8e84690e-1e48-11ed-a02b-a1e6fb8bb53b","first_name":"Rafal"},{"full_name":"Grzybowski, Bartosz A.","last_name":"Grzybowski","first_name":"Bartosz A."}],"title":"Ionic-like behavior of oppositely charged nanoparticles","citation":{"chicago":"Kalsin, Alexander M., Bartlomiej Kowalczyk, Stoyan K. Smoukov, Rafal Klajn, and Bartosz A. Grzybowski. “Ionic-like Behavior of Oppositely Charged Nanoparticles.” Journal of the American Chemical Society. American Chemical Society, 2006. https://doi.org/10.1021/ja0642966.","ista":"Kalsin AM, Kowalczyk B, Smoukov SK, Klajn R, Grzybowski BA. 2006. Ionic-like behavior of oppositely charged nanoparticles. Journal of the American Chemical Society. 128(47), 15046–15047.","mla":"Kalsin, Alexander M., et al. “Ionic-like Behavior of Oppositely Charged Nanoparticles.” Journal of the American Chemical Society, vol. 128, no. 47, American Chemical Society, 2006, pp. 15046–47, doi:10.1021/ja0642966.","ama":"Kalsin AM, Kowalczyk B, Smoukov SK, Klajn R, Grzybowski BA. Ionic-like behavior of oppositely charged nanoparticles. Journal of the American Chemical Society. 2006;128(47):15046-15047. doi:10.1021/ja0642966","apa":"Kalsin, A. M., Kowalczyk, B., Smoukov, S. K., Klajn, R., & Grzybowski, B. A. (2006). Ionic-like behavior of oppositely charged nanoparticles. Journal of the American Chemical Society. American Chemical Society. https://doi.org/10.1021/ja0642966","short":"A.M. Kalsin, B. Kowalczyk, S.K. Smoukov, R. Klajn, B.A. Grzybowski, Journal of the American Chemical Society 128 (2006) 15046–15047.","ieee":"A. M. Kalsin, B. Kowalczyk, S. K. Smoukov, R. Klajn, and B. A. Grzybowski, “Ionic-like behavior of oppositely charged nanoparticles,” Journal of the American Chemical Society, vol. 128, no. 47. American Chemical Society, pp. 15046–15047, 2006."},"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","volume":128,"issue":"47","publication_status":"published","publication_identifier":{"issn":["0002-7863"],"eissn":["1520-5126"]},"language":[{"iso":"eng"}],"scopus_import":"1","intvolume":" 128","month":"11","abstract":[{"lang":"eng","text":"Mixtures of oppositely charged nanoparticles of various sizes and charge ratios precipitate only at the point of electroneutrality. This phenomenonspecific to the nanoscale and reminiscent of threshold precipitation of ionsis a consequence of the formation of core-and-shell nanoparticle aggregates, in which the shells are composed of like-charged particles and are stabilized by efficient electrostatic screening."}],"oa_version":"None","pmid":1,"date_updated":"2023-08-08T11:30:06Z","extern":"1","article_type":"original","type":"journal_article","keyword":["Colloid and Surface Chemistry","Biochemistry","General Chemistry","Catalysis"],"status":"public","_id":"13428"},{"scopus_import":"1","intvolume":" 45","month":"08","abstract":[{"text":"The fruitful core: Organic syntheses reported in the literature from 1850 to 2004 are analyzed with mathematical tools from network theory and statistical physics. There is a set of substances (the core) from which the majority of other organic compounds can be made (see picture; red: core, blue: periphery, green: islands). Search algorithms are used to identify small optimal sets of maximally useful chemicals.","lang":"eng"}],"pmid":1,"oa_version":"None","issue":"32","volume":45,"publication_status":"published","publication_identifier":{"eissn":["1521-3773"],"issn":["1433-7851"]},"language":[{"iso":"eng"}],"type":"journal_article","article_type":"original","keyword":["General Chemistry","Catalysis"],"status":"public","_id":"13429","date_updated":"2023-08-08T11:31:27Z","extern":"1","quality_controlled":"1","publisher":"Wiley","page":"5348-5354","date_created":"2023-08-01T10:37:16Z","date_published":"2006-08-11T00:00:00Z","doi":"10.1002/anie.200600881","year":"2006","publication":"Angewandte Chemie International Edition","day":"11","external_id":{"pmid":["16835857"]},"article_processing_charge":"No","author":[{"first_name":"Kyle J. M.","full_name":"Bishop, Kyle J. M.","last_name":"Bishop"},{"id":"8e84690e-1e48-11ed-a02b-a1e6fb8bb53b","first_name":"Rafal","full_name":"Klajn, Rafal","last_name":"Klajn"},{"first_name":"Bartosz A.","last_name":"Grzybowski","full_name":"Grzybowski, Bartosz A."}],"title":"The core and most useful molecules in organic chemistry","citation":{"mla":"Bishop, Kyle J. M., et al. “The Core and Most Useful Molecules in Organic Chemistry.” Angewandte Chemie International Edition, vol. 45, no. 32, Wiley, 2006, pp. 5348–54, doi:10.1002/anie.200600881.","apa":"Bishop, K. J. M., Klajn, R., & Grzybowski, B. A. (2006). The core and most useful molecules in organic chemistry. Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.200600881","ama":"Bishop KJM, Klajn R, Grzybowski BA. The core and most useful molecules in organic chemistry. Angewandte Chemie International Edition. 2006;45(32):5348-5354. doi:10.1002/anie.200600881","short":"K.J.M. Bishop, R. Klajn, B.A. Grzybowski, Angewandte Chemie International Edition 45 (2006) 5348–5354.","ieee":"K. J. M. Bishop, R. Klajn, and B. A. Grzybowski, “The core and most useful molecules in organic chemistry,” Angewandte Chemie International Edition, vol. 45, no. 32. Wiley, pp. 5348–5354, 2006.","chicago":"Bishop, Kyle J. M., Rafal Klajn, and Bartosz A. Grzybowski. “The Core and Most Useful Molecules in Organic Chemistry.” Angewandte Chemie International Edition. Wiley, 2006. https://doi.org/10.1002/anie.200600881.","ista":"Bishop KJM, Klajn R, Grzybowski BA. 2006. The core and most useful molecules in organic chemistry. Angewandte Chemie International Edition. 45(32), 5348–5354."},"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87"}]