[{"quality_controlled":"1","external_id":{"isi":["000292714800011"]},"day":"01","oa_version":"None","volume":138,"article_type":"review","publication_status":"published","doi":"10.1016/j.imlet.2011.02.013","article_processing_charge":"No","publisher":"Elsevier","citation":{"apa":"Sixt, M. K. (2011). Interstitial locomotion of leukocytes. <i>Immunology Letters</i>. Elsevier. <a href=\"https://doi.org/10.1016/j.imlet.2011.02.013\">https://doi.org/10.1016/j.imlet.2011.02.013</a>","short":"M.K. Sixt, Immunology Letters 138 (2011) 32–34.","chicago":"Sixt, Michael K. “Interstitial Locomotion of Leukocytes.” <i>Immunology Letters</i>. Elsevier, 2011. <a href=\"https://doi.org/10.1016/j.imlet.2011.02.013\">https://doi.org/10.1016/j.imlet.2011.02.013</a>.","ama":"Sixt MK. Interstitial locomotion of leukocytes. <i>Immunology Letters</i>. 2011;138(1):32-34. doi:<a href=\"https://doi.org/10.1016/j.imlet.2011.02.013\">10.1016/j.imlet.2011.02.013</a>","ista":"Sixt MK. 2011. Interstitial locomotion of leukocytes. Immunology Letters. 138(1), 32–34.","mla":"Sixt, Michael K. “Interstitial Locomotion of Leukocytes.” <i>Immunology Letters</i>, vol. 138, no. 1, Elsevier, 2011, pp. 32–34, doi:<a href=\"https://doi.org/10.1016/j.imlet.2011.02.013\">10.1016/j.imlet.2011.02.013</a>.","ieee":"M. K. Sixt, “Interstitial locomotion of leukocytes,” <i>Immunology Letters</i>, vol. 138, no. 1. Elsevier, pp. 32–34, 2011."},"year":"2011","date_published":"2011-07-01T00:00:00Z","title":"Interstitial locomotion of leukocytes","isi":1,"month":"07","department":[{"_id":"MiSi"}],"date_updated":"2025-09-30T08:47:13Z","language":[{"iso":"eng"}],"publication":"Immunology Letters","scopus_import":"1","date_created":"2018-12-11T12:03:02Z","status":"public","page":"32 - 34","intvolume":"       138","publist_id":"3222","_id":"3385","type":"journal_article","user_id":"317138e5-6ab7-11ef-aa6d-ffef3953e345","author":[{"id":"41E9FBEA-F248-11E8-B48F-1D18A9856A87","full_name":"Sixt, Michael K","last_name":"Sixt","orcid":"0000-0002-6620-9179","first_name":"Michael K"}],"issue":"1","corr_author":"1"},{"date_updated":"2025-09-30T08:46:43Z","month":"04","department":[{"_id":"SyCr"}],"title":"Social influence on age and reproduction reduced lifespan and fecundity in multi queen ant colonies","isi":1,"date_published":"2011-04-21T00:00:00Z","year":"2011","citation":{"chicago":"Schrempf, Alexandra, Sylvia Cremer, and Jürgen Heinze. “Social Influence on Age and Reproduction Reduced Lifespan and Fecundity in Multi Queen Ant Colonies.” <i>Journal of Evolutionary Biology</i>. Wiley-Blackwell, 2011. <a href=\"https://doi.org/10.1111/j.1420-9101.2011.02278.x\">https://doi.org/10.1111/j.1420-9101.2011.02278.x</a>.","ama":"Schrempf A, Cremer S, Heinze J. Social influence on age and reproduction reduced lifespan and fecundity in multi queen ant colonies. <i>Journal of Evolutionary Biology</i>. 2011;24(7):1455-1461. doi:<a href=\"https://doi.org/10.1111/j.1420-9101.2011.02278.x\">10.1111/j.1420-9101.2011.02278.x</a>","apa":"Schrempf, A., Cremer, S., &#38; Heinze, J. (2011). Social influence on age and reproduction reduced lifespan and fecundity in multi queen ant colonies. <i>Journal of Evolutionary Biology</i>. Wiley-Blackwell. <a href=\"https://doi.org/10.1111/j.1420-9101.2011.02278.x\">https://doi.org/10.1111/j.1420-9101.2011.02278.x</a>","short":"A. Schrempf, S. Cremer, J. Heinze, Journal of Evolutionary Biology 24 (2011) 1455–1461.","mla":"Schrempf, Alexandra, et al. “Social Influence on Age and Reproduction Reduced Lifespan and Fecundity in Multi Queen Ant Colonies.” <i>Journal of Evolutionary Biology</i>, vol. 24, no. 7, Wiley-Blackwell, 2011, pp. 1455–61, doi:<a href=\"https://doi.org/10.1111/j.1420-9101.2011.02278.x\">10.1111/j.1420-9101.2011.02278.x</a>.","ieee":"A. Schrempf, S. Cremer, and J. Heinze, “Social influence on age and reproduction reduced lifespan and fecundity in multi queen ant colonies,” <i>Journal of Evolutionary Biology</i>, vol. 24, no. 7. Wiley-Blackwell, pp. 1455–1461, 2011.","ista":"Schrempf A, Cremer S, Heinze J. 2011. Social influence on age and reproduction reduced lifespan and fecundity in multi queen ant colonies. Journal of Evolutionary Biology. 24(7), 1455–1461."},"publication_status":"published","article_processing_charge":"No","publisher":"Wiley-Blackwell","doi":"10.1111/j.1420-9101.2011.02278.x","abstract":[{"text":"Evolutionary theories of ageing predict that life span increases with decreasing extrinsic mortality, and life span variation among queens in ant species seems to corroborate this prediction: queens, which are the only reproductive in a colony, live much longer than queens in multi-queen colonies. The latter often inhabit ephemeral nest sites and accordingly are assumed to experience a higher mortality risk. Yet, all prior studies compared queens from different single- and multi-queen species. Here, we demonstrate an effect of queen number on longevity and fecundity within a single, socially plastic species, where queens experience the similar level of extrinsic mortality. Queens from single- and two-queen colonies had significantly longer lifespan and higher fecundity than queens living in associations of eight queens. As queens also differ neither in morphology nor the mode of colony foundation, our study shows that the social environment itself strongly affects ageing rate.","lang":"eng"}],"volume":24,"day":"21","oa_version":"None","quality_controlled":"1","external_id":{"isi":["000292698700007"]},"corr_author":"1","issue":"7","author":[{"last_name":"Schrempf","full_name":"Schrempf, Alexandra","first_name":"Alexandra"},{"orcid":"0000-0002-2193-3868","first_name":"Sylvia","id":"2F64EC8C-F248-11E8-B48F-1D18A9856A87","full_name":"Cremer, Sylvia","last_name":"Cremer"},{"full_name":"Heinze, Jürgen","last_name":"Heinze","first_name":"Jürgen"}],"user_id":"317138e5-6ab7-11ef-aa6d-ffef3953e345","type":"journal_article","_id":"3386","page":"1455 - 1461","intvolume":"        24","publist_id":"3221","scopus_import":"1","date_created":"2018-12-11T12:03:02Z","status":"public","publication":"Journal of Evolutionary Biology","language":[{"iso":"eng"}]},{"title":"Split based computation of majority rule supertrees","article_number":"205","isi":1,"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)"},"month":"07","department":[{"_id":"JoBo"}],"date_updated":"2025-09-30T08:45:48Z","publication_status":"published","doi":"10.1186/1471-2148-11-205","article_processing_charge":"No","publisher":"BioMed Central","citation":{"ista":"Kupczok A. 2011. Split based computation of majority rule supertrees. BMC Evolutionary Biology. 11(205), 205.","ieee":"A. Kupczok, “Split based computation of majority rule supertrees,” <i>BMC Evolutionary Biology</i>, vol. 11, no. 205. BioMed Central, 2011.","mla":"Kupczok, Anne. “Split Based Computation of Majority Rule Supertrees.” <i>BMC Evolutionary Biology</i>, vol. 11, no. 205, 205, BioMed Central, 2011, doi:<a href=\"https://doi.org/10.1186/1471-2148-11-205\">10.1186/1471-2148-11-205</a>.","short":"A. Kupczok, BMC Evolutionary Biology 11 (2011).","apa":"Kupczok, A. (2011). Split based computation of majority rule supertrees. <i>BMC Evolutionary Biology</i>. BioMed Central. <a href=\"https://doi.org/10.1186/1471-2148-11-205\">https://doi.org/10.1186/1471-2148-11-205</a>","ama":"Kupczok A. Split based computation of majority rule supertrees. <i>BMC Evolutionary Biology</i>. 2011;11(205). doi:<a href=\"https://doi.org/10.1186/1471-2148-11-205\">10.1186/1471-2148-11-205</a>","chicago":"Kupczok, Anne. “Split Based Computation of Majority Rule Supertrees.” <i>BMC Evolutionary Biology</i>. BioMed Central, 2011. <a href=\"https://doi.org/10.1186/1471-2148-11-205\">https://doi.org/10.1186/1471-2148-11-205</a>."},"year":"2011","date_published":"2011-07-13T00:00:00Z","abstract":[{"lang":"eng","text":"Background: Supertree methods combine overlapping input trees into a larger supertree. Here, I consider split-based supertree methods that first extract the split information of the input trees and subsequently combine this split information into a phylogeny. Well known split-based supertree methods are matrix representation with parsimony and matrix representation with compatibility. Combining input trees on the same taxon set, as in the consensus setting, is a well-studied task and it is thus desirable to generalize consensus methods to supertree methods. Results: Here, three variants of majority-rule (MR) supertrees that generalize majority-rule consensus trees are investigated. I provide simple formulas for computing the respective score for bifurcating input- and supertrees. These score computations, together with a heuristic tree search minmizing the scores, were implemented in the python program PluMiST (Plus- and Minus SuperTrees) available from http://www.cibiv.at/software/ plumist. The different MR methods were tested by simulation and on real data sets. The search heuristic was successful in combining compatible input trees. When combining incompatible input trees, especially one variant, MR(-) supertrees, performed well. Conclusions: The presented framework allows for an efficient score computation of three majority-rule supertree variants and input trees. I combined the score computation with a heuristic search over the supertree space. The implementation was tested by simulation and on real data sets and showed promising results. Especially the MR(-) variant seems to be a reasonable score for supertree reconstruction. Generalizing these computations to multifurcating trees is an open problem, which may be tackled using this framework."}],"external_id":{"isi":["000294663400001"]},"quality_controlled":"1","oa_version":"Published Version","day":"13","volume":11,"pubrep_id":"372","type":"journal_article","author":[{"last_name":"Kupczok","id":"2BB22BC2-F248-11E8-B48F-1D18A9856A87","full_name":"Kupczok, Anne","first_name":"Anne"}],"user_id":"317138e5-6ab7-11ef-aa6d-ffef3953e345","file_date_updated":"2020-07-14T12:46:11Z","issue":"205","corr_author":"1","_id":"3387","oa":1,"intvolume":"        11","publist_id":"3219","file":[{"relation":"main_file","file_size":465042,"access_level":"open_access","checksum":"68da8d04af1b97b4cbe8606e2f92ddd8","date_created":"2018-12-12T10:14:09Z","file_id":"5058","creator":"system","content_type":"application/pdf","file_name":"IST-2015-372-v1+1_1471-2148-11-205.pdf","date_updated":"2020-07-14T12:46:11Z"}],"ddc":["576"],"has_accepted_license":"1","language":[{"iso":"eng"}],"publication":"BMC Evolutionary Biology","scopus_import":"1","status":"public","date_created":"2018-12-11T12:03:03Z"},{"oa_version":"Published Version","day":"11","volume":11,"pubrep_id":"371","quality_controlled":"1","external_id":{"isi":["000293275300002"]},"abstract":[{"text":"Background: Fragmentation of terrestrial ecosystems has had detrimental effects on metapopulations of habitat specialists. Maculinea butterflies have been particularly affected because of their specialized lifecycles, requiring both specific food-plants and host-ants. However, the interaction between dispersal, effective population size, and long-term genetic erosion of these endangered butterflies remains unknown. Using non-destructive sampling, we investigated the genetic diversity of the last extant population of M. arion in Denmark, which experienced critically low numbers in the 1980s. Results: Using nine microsatellite markers, we show that the population is genetically impoverished compared to nearby populations in Sweden, but less so than monitoring programs suggested. Ten additional short repeat microsatellites were used to reconstruct changes in genetic diversity and population structure over the last 77 years from museum specimens. We also tested amplification efficiency in such historical samples as a function of repeat length and sample age. Low population numbers in the 1980s did not affect genetic diversity, but considerable turnover of alleles has characterized this population throughout the time-span of our analysis. Conclusions: Our results suggest that M. arion is less sensitive to genetic erosion via population bottlenecks than previously thought, and that managing clusters of high quality habitat may be key for long-term conservation.","lang":"eng"}],"year":"2011","date_published":"2011-07-11T00:00:00Z","citation":{"apa":"Ugelvig, L. V., Nielsen, P., Boomsma, J., &#38; Nash, D. (2011). Reconstructing eight decades of genetic variation in an isolated Danish population of the large blue butterfly Maculinea arion. <i>BMC Evolutionary Biology</i>. BioMed Central. <a href=\"https://doi.org/10.1186/1471-2148-11-201\">https://doi.org/10.1186/1471-2148-11-201</a>","short":"L.V. Ugelvig, P. Nielsen, J. Boomsma, D. Nash, BMC Evolutionary Biology 11 (2011).","chicago":"Ugelvig, Line V, Per Nielsen, Jacobus Boomsma, and David Nash. “Reconstructing Eight Decades of Genetic Variation in an Isolated Danish Population of the Large Blue Butterfly Maculinea Arion.” <i>BMC Evolutionary Biology</i>. BioMed Central, 2011. <a href=\"https://doi.org/10.1186/1471-2148-11-201\">https://doi.org/10.1186/1471-2148-11-201</a>.","ama":"Ugelvig LV, Nielsen P, Boomsma J, Nash D. Reconstructing eight decades of genetic variation in an isolated Danish population of the large blue butterfly Maculinea arion. <i>BMC Evolutionary Biology</i>. 2011;11(201). doi:<a href=\"https://doi.org/10.1186/1471-2148-11-201\">10.1186/1471-2148-11-201</a>","ista":"Ugelvig LV, Nielsen P, Boomsma J, Nash D. 2011. Reconstructing eight decades of genetic variation in an isolated Danish population of the large blue butterfly Maculinea arion. BMC Evolutionary Biology. 11(201), 201.","mla":"Ugelvig, Line V., et al. “Reconstructing Eight Decades of Genetic Variation in an Isolated Danish Population of the Large Blue Butterfly Maculinea Arion.” <i>BMC Evolutionary Biology</i>, vol. 11, no. 201, 201, BioMed Central, 2011, doi:<a href=\"https://doi.org/10.1186/1471-2148-11-201\">10.1186/1471-2148-11-201</a>.","ieee":"L. V. Ugelvig, P. Nielsen, J. Boomsma, and D. Nash, “Reconstructing eight decades of genetic variation in an isolated Danish population of the large blue butterfly Maculinea arion,” <i>BMC Evolutionary Biology</i>, vol. 11, no. 201. BioMed Central, 2011."},"publication_status":"published","article_processing_charge":"No","publisher":"BioMed Central","doi":"10.1186/1471-2148-11-201","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)"},"date_updated":"2025-09-30T08:46:17Z","month":"07","department":[{"_id":"SyCr"}],"title":"Reconstructing eight decades of genetic variation in an isolated Danish population of the large blue butterfly Maculinea arion","article_number":"201","isi":1,"date_created":"2018-12-11T12:03:03Z","scopus_import":"1","status":"public","has_accepted_license":"1","publication":"BMC Evolutionary Biology","language":[{"iso":"eng"}],"file":[{"access_level":"open_access","relation":"main_file","file_size":2166556,"date_created":"2018-12-12T10:14:18Z","checksum":"9ebfed0740f1fa071d02ec32c2b8c17f","file_id":"5069","creator":"system","file_name":"IST-2015-371-v1+1_1471-2148-11-201.pdf","date_updated":"2020-07-14T12:46:11Z","content_type":"application/pdf"}],"ddc":["576"],"intvolume":"        11","publist_id":"3220","oa":1,"_id":"3388","file_date_updated":"2020-07-14T12:46:11Z","corr_author":"1","issue":"201","user_id":"317138e5-6ab7-11ef-aa6d-ffef3953e345","author":[{"last_name":"Ugelvig","full_name":"Ugelvig, Line V","id":"3DC97C8E-F248-11E8-B48F-1D18A9856A87","orcid":"0000-0003-1832-8883","first_name":"Line V"},{"first_name":"Per","full_name":"Nielsen, Per","last_name":"Nielsen"},{"full_name":"Boomsma, Jacobus","last_name":"Boomsma","first_name":"Jacobus"},{"first_name":"David","full_name":"Nash, David","last_name":"Nash"}],"type":"journal_article"},{"_id":"3389","user_id":"317138e5-6ab7-11ef-aa6d-ffef3953e345","acknowledgement":"The research leading to these results has received funding from the European Research Council under the European Community’s Seventh Framework Programme (FP7/2007-2013)/ERC Grant Agreement No. 228180. This work was funded in part by the EC project CLASS, IST 027978, and the PASCAL2 network of excellence, IST 2002-506778.","author":[{"first_name":"Matthew","last_name":"Blaschko","full_name":"Blaschko, Matthew"},{"last_name":"Shelton","full_name":"Shelton, Jacquelyn","first_name":"Jacquelyn"},{"first_name":"Andreas","last_name":"Bartels","full_name":"Bartels, Andreas"},{"first_name":"Christoph","orcid":"0000-0001-8622-7887","full_name":"Lampert, Christoph","id":"40C20FD2-F248-11E8-B48F-1D18A9856A87","last_name":"Lampert"},{"first_name":"Arthur","full_name":"Gretton, Arthur","last_name":"Gretton"}],"type":"journal_article","issue":"11","publication":"Pattern Recognition Letters","language":[{"iso":"eng"}],"date_created":"2018-12-11T12:03:03Z","status":"public","scopus_import":"1","intvolume":"        32","page":"1572 - 1583","publist_id":"3218","publication_status":"published","publisher":"Elsevier","article_processing_charge":"No","doi":"10.1016/j.patrec.2011.02.011","year":"2011","date_published":"2011-08-01T00:00:00Z","citation":{"apa":"Blaschko, M., Shelton, J., Bartels, A., Lampert, C., &#38; Gretton, A. (2011). Semi supervised kernel canonical correlation analysis with application to human fMRI. <i>Pattern Recognition Letters</i>. Elsevier. <a href=\"https://doi.org/10.1016/j.patrec.2011.02.011\">https://doi.org/10.1016/j.patrec.2011.02.011</a>","short":"M. Blaschko, J. Shelton, A. Bartels, C. Lampert, A. Gretton, Pattern Recognition Letters 32 (2011) 1572–1583.","chicago":"Blaschko, Matthew, Jacquelyn Shelton, Andreas Bartels, Christoph Lampert, and Arthur Gretton. “Semi Supervised Kernel Canonical Correlation Analysis with Application to Human FMRI.” <i>Pattern Recognition Letters</i>. Elsevier, 2011. <a href=\"https://doi.org/10.1016/j.patrec.2011.02.011\">https://doi.org/10.1016/j.patrec.2011.02.011</a>.","ama":"Blaschko M, Shelton J, Bartels A, Lampert C, Gretton A. Semi supervised kernel canonical correlation analysis with application to human fMRI. <i>Pattern Recognition Letters</i>. 2011;32(11):1572-1583. doi:<a href=\"https://doi.org/10.1016/j.patrec.2011.02.011\">10.1016/j.patrec.2011.02.011</a>","ista":"Blaschko M, Shelton J, Bartels A, Lampert C, Gretton A. 2011. Semi supervised kernel canonical correlation analysis with application to human fMRI. Pattern Recognition Letters. 32(11), 1572–1583.","mla":"Blaschko, Matthew, et al. “Semi Supervised Kernel Canonical Correlation Analysis with Application to Human FMRI.” <i>Pattern Recognition Letters</i>, vol. 32, no. 11, Elsevier, 2011, pp. 1572–83, doi:<a href=\"https://doi.org/10.1016/j.patrec.2011.02.011\">10.1016/j.patrec.2011.02.011</a>.","ieee":"M. Blaschko, J. Shelton, A. Bartels, C. Lampert, and A. Gretton, “Semi supervised kernel canonical correlation analysis with application to human fMRI,” <i>Pattern Recognition Letters</i>, vol. 32, no. 11. Elsevier, pp. 1572–1583, 2011."},"title":"Semi supervised kernel canonical correlation analysis with application to human fMRI","isi":1,"date_updated":"2025-09-30T08:45:21Z","department":[{"_id":"ChLa"}],"month":"08","quality_controlled":"1","external_id":{"isi":["000293050700010"]},"day":"01","oa_version":"None","volume":32,"abstract":[{"lang":"eng","text":"Kernel canonical correlation analysis (KCCA) is a general technique for subspace learning that incorporates principal components analysis (PCA) and Fisher linear discriminant analysis (LDA) as special cases. By finding directions that maximize correlation, KCCA learns representations that are more closely tied to the underlying process that generates the data and can ignore high-variance noise directions. However, for data where acquisition in one or more modalities is expensive or otherwise limited, KCCA may suffer from small sample effects. We propose to use semi-supervised Laplacian regularization to utilize data that are present in only one modality. This approach is able to find highly correlated directions that also lie along the data manifold, resulting in a more robust estimate of correlated subspaces. Functional magnetic resonance imaging (fMRI) acquired data are naturally amenable to subspace techniques as data are well aligned. fMRI data of the human brain are a particularly interesting candidate. In this study we implemented various supervised and semi-supervised versions of KCCA on human fMRI data, with regression to single and multi-variate labels (corresponding to video content subjects viewed during the image acquisition). In each variate condition, the semi-supervised variants of KCCA performed better than the supervised variants, including a supervised variant with Laplacian regularization. We additionally analyze the weights learned by the regression in order to infer brain regions that are important to different types of visual processing."}]},{"main_file_link":[{"url":"http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3176105/","open_access":"1"}],"abstract":[{"text":"What determines the genetic contribution that an individual makes to future generations? With biparental reproduction, each individual leaves a 'pedigree' of descendants, determined by the biparental relationships in the population. The pedigree of an individual constrains the lines of descent of each of its genes. An individual's reproductive value is the expected number of copies of each of its genes that is passed on to distant generations conditional on its pedigree. For the simplest model of biparental reproduction analogous to the Wright-Fisher model, an individual's reproductive value is determined within ~10 generations, independent of population size. Partial selfing and subdivision do not greatly slow this convergence. Our central result is that the probability that a gene will survive is proportional to the reproductive value of the individual that carries it, and that conditional on survival, after a few tens of generations, the distribution of the number of surviving copies is the same for all individuals, whatever their reproductive value. These results can be generalized to the joint distribution of surviving blocks of ancestral genome. Selection on unlinked loci in the genetic background may greatly increase the variance in reproductive value, but the above results nevertheless still hold. The almost linear relationship between survival probability and reproductive value also holds for weakly favored alleles. Thus, the influence of the complex pedigree of descendants on an individual's genetic contribution to the population can be summarized through a single number: its reproductive value.","lang":"eng"}],"project":[{"_id":"25B07788-B435-11E9-9278-68D0E5697425","call_identifier":"FP7","name":"Limits to selection in biology and in evolutionary computation","grant_number":"250152"}],"quality_controlled":"1","external_id":{"isi":["000293700000018"]},"day":"01","oa_version":"Submitted Version","volume":188,"ec_funded":1,"title":"The relation between reproductive value and genetic contribution","isi":1,"department":[{"_id":"NiBa"}],"month":"08","date_updated":"2025-09-30T08:44:55Z","publication_status":"published","doi":"10.1534/genetics.111.127555","publisher":"Genetics Society of America","article_processing_charge":"No","citation":{"ista":"Barton NH, Etheridge A. 2011. The relation between reproductive value and genetic contribution. Genetics. 188(4), 953–973.","mla":"Barton, Nicholas H., and Alison Etheridge. “The Relation between Reproductive Value and Genetic Contribution.” <i>Genetics</i>, vol. 188, no. 4, Genetics Society of America, 2011, pp. 953–73, doi:<a href=\"https://doi.org/10.1534/genetics.111.127555\">10.1534/genetics.111.127555</a>.","ieee":"N. H. Barton and A. Etheridge, “The relation between reproductive value and genetic contribution,” <i>Genetics</i>, vol. 188, no. 4. Genetics Society of America, pp. 953–973, 2011.","apa":"Barton, N. H., &#38; Etheridge, A. (2011). The relation between reproductive value and genetic contribution. <i>Genetics</i>. Genetics Society of America. <a href=\"https://doi.org/10.1534/genetics.111.127555\">https://doi.org/10.1534/genetics.111.127555</a>","short":"N.H. Barton, A. Etheridge, Genetics 188 (2011) 953–973.","chicago":"Barton, Nicholas H, and Alison Etheridge. “The Relation between Reproductive Value and Genetic Contribution.” <i>Genetics</i>. Genetics Society of America, 2011. <a href=\"https://doi.org/10.1534/genetics.111.127555\">https://doi.org/10.1534/genetics.111.127555</a>.","ama":"Barton NH, Etheridge A. The relation between reproductive value and genetic contribution. <i>Genetics</i>. 2011;188(4):953-973. doi:<a href=\"https://doi.org/10.1534/genetics.111.127555\">10.1534/genetics.111.127555</a>"},"year":"2011","date_published":"2011-08-01T00:00:00Z","intvolume":"       188","page":"953 - 973","publist_id":"3217","language":[{"iso":"eng"}],"publication":"Genetics","date_created":"2018-12-11T12:03:04Z","scopus_import":"1","status":"public","type":"journal_article","author":[{"id":"4880FE40-F248-11E8-B48F-1D18A9856A87","full_name":"Barton, Nicholas H","last_name":"Barton","first_name":"Nicholas H","orcid":"0000-0002-8548-5240"},{"first_name":"Alison","last_name":"Etheridge","full_name":"Etheridge, Alison"}],"user_id":"317138e5-6ab7-11ef-aa6d-ffef3953e345","issue":"4","corr_author":"1","_id":"3390","oa":1},{"date_updated":"2025-09-30T08:44:25Z","department":[{"_id":"NiBa"}],"month":"08","title":"The contribution of statistical physics to evolutionary biology","isi":1,"date_published":"2011-08-01T00:00:00Z","year":"2011","citation":{"ieee":"H. de Vladar and N. H. Barton, “The contribution of statistical physics to evolutionary biology,” <i>Trends in Ecology and Evolution</i>, vol. 26, no. 8. Cell Press, pp. 424–432, 2011.","mla":"de Vladar, Harold, and Nicholas H. Barton. “The Contribution of Statistical Physics to Evolutionary Biology.” <i>Trends in Ecology and Evolution</i>, vol. 26, no. 8, Cell Press, 2011, pp. 424–32, doi:<a href=\"https://doi.org/10.1016/j.tree.2011.04.002\">10.1016/j.tree.2011.04.002</a>.","ista":"de Vladar H, Barton NH. 2011. The contribution of statistical physics to evolutionary biology. Trends in Ecology and Evolution. 26(8), 424–432.","ama":"de Vladar H, Barton NH. The contribution of statistical physics to evolutionary biology. <i>Trends in Ecology and Evolution</i>. 2011;26(8):424-432. doi:<a href=\"https://doi.org/10.1016/j.tree.2011.04.002\">10.1016/j.tree.2011.04.002</a>","chicago":"Vladar, Harold de, and Nicholas H Barton. “The Contribution of Statistical Physics to Evolutionary Biology.” <i>Trends in Ecology and Evolution</i>. Cell Press, 2011. <a href=\"https://doi.org/10.1016/j.tree.2011.04.002\">https://doi.org/10.1016/j.tree.2011.04.002</a>.","short":"H. de Vladar, N.H. Barton, Trends in Ecology and Evolution 26 (2011) 424–432.","apa":"de Vladar, H., &#38; Barton, N. H. (2011). The contribution of statistical physics to evolutionary biology. <i>Trends in Ecology and Evolution</i>. Cell Press. <a href=\"https://doi.org/10.1016/j.tree.2011.04.002\">https://doi.org/10.1016/j.tree.2011.04.002</a>"},"publication_status":"published","publisher":"Cell Press","article_processing_charge":"No","doi":"10.1016/j.tree.2011.04.002","abstract":[{"lang":"eng","text":"Evolutionary biology shares many concepts with statistical physics: both deal with populations, whether of molecules or organisms, and both seek to simplify evolution in very many dimensions. Often, methodologies have undergone parallel and independent development, as with stochastic methods in population genetics. Here, we discuss aspects of population genetics that have embraced methods from physics: non-equilibrium statistical mechanics, travelling waves and Monte-Carlo methods, among others, have been used to study polygenic evolution, rates of adaptation and range expansions. These applications indicate that evolutionary biology can further benefit from interactions with other areas of statistical physics; for example, by following the distribution of paths taken by a population through time"}],"main_file_link":[{"url":"http://arxiv.org/abs/1104.2854","open_access":"1"}],"volume":26,"oa_version":"Submitted Version","day":"01","ec_funded":1,"quality_controlled":"1","external_id":{"isi":["000293940800010"],"arxiv":["1104.2854"]},"project":[{"_id":"25B07788-B435-11E9-9278-68D0E5697425","call_identifier":"FP7","name":"Limits to selection in biology and in evolutionary computation","grant_number":"250152"}],"corr_author":"1","issue":"8","user_id":"317138e5-6ab7-11ef-aa6d-ffef3953e345","author":[{"orcid":"0000-0002-5985-7653","first_name":"Harold","last_name":"de Vladar","id":"2A181218-F248-11E8-B48F-1D18A9856A87","full_name":"de Vladar, Harold"},{"full_name":"Barton, Nicholas H","id":"4880FE40-F248-11E8-B48F-1D18A9856A87","last_name":"Barton","orcid":"0000-0002-8548-5240","first_name":"Nicholas H"}],"type":"journal_article","oa":1,"_id":"3391","arxiv":1,"intvolume":"        26","page":"424 - 432","publist_id":"3216","status":"public","date_created":"2018-12-11T12:03:04Z","scopus_import":"1","publication":"Trends in Ecology and Evolution","language":[{"iso":"eng"}]},{"isi":1,"title":"In vivo analysis of uropod function during physiological T cell trafficking","month":"09","department":[{"_id":"MiSi"}],"date_updated":"2025-09-30T08:43:55Z","doi":"10.4049/jimmunol.1100935","publication_identifier":{"issn":["0022-1767"],"eissn":["1550-6606"]},"publisher":"American Association of Immunologists","article_processing_charge":"No","publication_status":"published","citation":{"short":"S. Soriano, M. Hons, K. Schumann, V. Kumar, T. Dennier, R. Lyck, M.K. Sixt, J. Stein, Journal of Immunology 187 (2011) 2356–2364.","apa":"Soriano, S., Hons, M., Schumann, K., Kumar, V., Dennier, T., Lyck, R., … Stein, J. (2011). In vivo analysis of uropod function during physiological T cell trafficking. <i>Journal of Immunology</i>. American Association of Immunologists. <a href=\"https://doi.org/10.4049/jimmunol.1100935\">https://doi.org/10.4049/jimmunol.1100935</a>","ama":"Soriano S, Hons M, Schumann K, et al. In vivo analysis of uropod function during physiological T cell trafficking. <i>Journal of Immunology</i>. 2011;187(5):2356-2364. doi:<a href=\"https://doi.org/10.4049/jimmunol.1100935\">10.4049/jimmunol.1100935</a>","chicago":"Soriano, Silvia, Miroslav Hons, Kathrin Schumann, Varsha Kumar, Timo Dennier, Ruth Lyck, Michael K Sixt, and Jens Stein. “In Vivo Analysis of Uropod Function during Physiological T Cell Trafficking.” <i>Journal of Immunology</i>. American Association of Immunologists, 2011. <a href=\"https://doi.org/10.4049/jimmunol.1100935\">https://doi.org/10.4049/jimmunol.1100935</a>.","ista":"Soriano S, Hons M, Schumann K, Kumar V, Dennier T, Lyck R, Sixt MK, Stein J. 2011. In vivo analysis of uropod function during physiological T cell trafficking. Journal of Immunology. 187(5), 2356–2364.","ieee":"S. Soriano <i>et al.</i>, “In vivo analysis of uropod function during physiological T cell trafficking,” <i>Journal of Immunology</i>, vol. 187, no. 5. American Association of Immunologists, pp. 2356–2364, 2011.","mla":"Soriano, Silvia, et al. “In Vivo Analysis of Uropod Function during Physiological T Cell Trafficking.” <i>Journal of Immunology</i>, vol. 187, no. 5, American Association of Immunologists, 2011, pp. 2356–64, doi:<a href=\"https://doi.org/10.4049/jimmunol.1100935\">10.4049/jimmunol.1100935</a>."},"year":"2011","date_published":"2011-09-01T00:00:00Z","article_type":"original","abstract":[{"text":"Migrating lymphocytes acquire a polarized phenotype with a leading and a trailing edge, or uropod. Although in vitro experiments in cell lines or activated primary cell cultures have established that Rho-p160 coiled-coil kinase (ROCK)-myosin II-mediated uropod contractility is required for integrin de-adhesion on two-dimensional surfaces and nuclear propulsion through narrow pores in three-dimensional matrices, less is known about the role of these two events during the recirculation of primary, nonactivated lymphocytes. Using pharmacological antagonists of ROCK and myosin II, we report that inhibition of uropod contractility blocked integrin-independent mouse T cell migration through narrow, but not large, pores in vitro. T cell crawling on chemokine-coated endothelial cells under shear was severely impaired by ROCK inhibition, whereas transendothelial migration was only reduced through endothelial cells with high, but not low, barrier properties. Using three-dimensional thick-tissue imaging and dynamic two-photon microscopy of T cell motility in lymphoid tissue, we demonstrated a significant role for uropod contractility in intraluminal crawling and transendothelial migration through lymph node, but not bone marrow, endothelial cells. Finally, we demonstrated that ICAM-1, but not anatomical constraints or integrin-independent interactions, reduced parenchymal motility of inhibitor-treated T cells within the dense lymphoid microenvironment, thus assigning context-dependent roles for uropod contraction during lymphocyte recirculation.","lang":"eng"}],"external_id":{"isi":["000294059500040"]},"quality_controlled":"1","day":"01","volume":187,"oa_version":"None","type":"journal_article","user_id":"317138e5-6ab7-11ef-aa6d-ffef3953e345","author":[{"full_name":"Soriano, Silvia","last_name":"Soriano","first_name":"Silvia"},{"first_name":"Miroslav","orcid":"0000-0002-6625-3348","last_name":"Hons","full_name":"Hons, Miroslav"},{"first_name":"Kathrin","full_name":"Schumann, Kathrin","last_name":"Schumann"},{"full_name":"Kumar, Varsha","last_name":"Kumar","first_name":"Varsha"},{"first_name":"Timo","last_name":"Dennier","full_name":"Dennier, Timo"},{"first_name":"Ruth","full_name":"Lyck, Ruth","last_name":"Lyck"},{"orcid":"0000-0002-6620-9179","first_name":"Michael K","last_name":"Sixt","id":"41E9FBEA-F248-11E8-B48F-1D18A9856A87","full_name":"Sixt, Michael K"},{"first_name":"Jens","last_name":"Stein","full_name":"Stein, Jens"}],"issue":"5","_id":"3392","publist_id":"3215","intvolume":"       187","page":"2356 - 2364","language":[{"iso":"eng"}],"publication":"Journal of Immunology","scopus_import":"1","date_created":"2018-12-11T12:03:04Z","status":"public"},{"oa":1,"_id":"3393","issue":"3","file_date_updated":"2020-07-14T12:46:11Z","user_id":"317138e5-6ab7-11ef-aa6d-ffef3953e345","author":[{"first_name":"Nicholas H","orcid":"0000-0002-8548-5240","last_name":"Barton","full_name":"Barton, Nicholas H","id":"4880FE40-F248-11E8-B48F-1D18A9856A87"},{"first_name":"Michael","last_name":"Turelli","full_name":"Turelli, Michael"}],"type":"journal_article","date_created":"2018-12-11T12:03:05Z","status":"public","scopus_import":"1","publication":"American Naturalist","language":[{"iso":"eng"}],"has_accepted_license":"1","ddc":["570"],"file":[{"date_updated":"2020-07-14T12:46:11Z","file_name":"IST-2016-554-v1+1_BartonTurelli2011_copy.pdf","content_type":"application/pdf","creator":"system","file_id":"4692","date_created":"2018-12-12T10:08:31Z","checksum":"7fd22a2ef3321a6fca6a439b3be5d8f4","access_level":"open_access","relation":"main_file","file_size":629130}],"publist_id":"3214","page":"E48 - E75","intvolume":"       178","date_published":"2011-09-01T00:00:00Z","year":"2011","citation":{"ista":"Barton NH, Turelli M. 2011. Spatial waves of advance with bistable dynamics: Cytoplasmic and genetic analogues of Allee effects. American Naturalist. 178(3), E48–E75.","ieee":"N. H. Barton and M. Turelli, “Spatial waves of advance with bistable dynamics: Cytoplasmic and genetic analogues of Allee effects,” <i>American Naturalist</i>, vol. 178, no. 3. The University of Chicago Press, pp. E48–E75, 2011.","mla":"Barton, Nicholas H., and Michael Turelli. “Spatial Waves of Advance with Bistable Dynamics: Cytoplasmic and Genetic Analogues of Allee Effects.” <i>American Naturalist</i>, vol. 178, no. 3, The University of Chicago Press, 2011, pp. E48–75, doi:<a href=\"https://doi.org/10.1086/661246\">10.1086/661246</a>.","short":"N.H. Barton, M. Turelli, American Naturalist 178 (2011) E48–E75.","apa":"Barton, N. H., &#38; Turelli, M. (2011). Spatial waves of advance with bistable dynamics: Cytoplasmic and genetic analogues of Allee effects. <i>American Naturalist</i>. The University of Chicago Press. <a href=\"https://doi.org/10.1086/661246\">https://doi.org/10.1086/661246</a>","ama":"Barton NH, Turelli M. Spatial waves of advance with bistable dynamics: Cytoplasmic and genetic analogues of Allee effects. <i>American Naturalist</i>. 2011;178(3):E48-E75. doi:<a href=\"https://doi.org/10.1086/661246\">10.1086/661246</a>","chicago":"Barton, Nicholas H, and Michael Turelli. “Spatial Waves of Advance with Bistable Dynamics: Cytoplasmic and Genetic Analogues of Allee Effects.” <i>American Naturalist</i>. The University of Chicago Press, 2011. <a href=\"https://doi.org/10.1086/661246\">https://doi.org/10.1086/661246</a>."},"publication_identifier":{"issn":["0003-0147"],"eissn":["1537-5323"]},"publisher":"The University of Chicago Press","article_processing_charge":"No","doi":"10.1086/661246","publication_status":"published","date_updated":"2025-09-30T08:43:28Z","department":[{"_id":"NiBa"}],"month":"09","isi":1,"title":"Spatial waves of advance with bistable dynamics: Cytoplasmic and genetic analogues of Allee effects","pubrep_id":"554","day":"01","volume":178,"oa_version":"Submitted Version","quality_controlled":"1","external_id":{"isi":["000294256800001"]},"article_type":"original","abstract":[{"lang":"eng","text":"Unlike unconditionally advantageous “Fisherian” variants that tend to spread throughout a species range once introduced anywhere, “bistable” variants, such as chromosome translocations, have two alternative stable frequencies, absence and (near) fixation. Analogous to populations with Allee effects, bistable variants tend to increase locally only once they become sufficiently common, and their spread depends on their rate of increase averaged over all frequencies. Several proposed manipulations of insect populations, such as using Wolbachia or “engineered underdominance” to suppress vector-borne diseases, produce bistable rather than Fisherian dynamics. We synthesize and extend theoretical analyses concerning three features of their spatial behavior: rate of spread, conditions to initiate spread from a localized introduction, and wave stopping caused by variation in population densities or dispersal rates. Unlike Fisherian variants, bistable variants tend to spread spatially only for particular parameter combinations and initial conditions. Wave initiation requires introduction over an extended region, while subsequent spatial spread is slower than for Fisherian waves and can easily be halted by local spatial inhomogeneities. We present several new results, including robust sufficient conditions to initiate (and stop) spread, using a one-parameter cubic approximation applicable to several models. The results have both basic and applied implications."}]},{"ec_funded":1,"volume":189,"oa_version":"Submitted Version","day":"01","project":[{"_id":"25B07788-B435-11E9-9278-68D0E5697425","call_identifier":"FP7","name":"Limits to selection in biology and in evolutionary computation","grant_number":"250152"}],"quality_controlled":"1","external_id":{"isi":["000294721600018"]},"abstract":[{"text":"Random genetic drift shifts clines in space, alters their width, and distorts their shape. Such random fluctuations complicate inferences from cline width and position. Notably, the effect of genetic drift on the expected shape of the cline is opposite to the naive (but quite common) misinterpretation of classic results on the expected cline. While random drift on average broadens the overall cline in expected allele frequency, it narrows the width of any particular cline. The opposing effects arise because locally, drift drives alleles to fixation—but fluctuations in position widen the expected cline. The effect of genetic drift can be predicted from standardized variance in allele frequencies, averaged across the habitat: 〈F〉. A cline maintained by spatially varying selection (step change) is expected to be narrower by a factor of  relative to the cline in the absence of drift. The expected cline is broader by the inverse of this factor. In a tension zone maintained by underdominance, the expected cline width is narrower by about 1 – 〈F〉relative to the width in the absence of drift. Individual clines can differ substantially from the expectation, and we give quantitative predictions for the variance in cline position and width. The predictions apply to clines in almost one-dimensional circumstances such as hybrid zones in rivers, deep valleys, or along a coast line and give a guide to what patterns to expect in two dimensions.","lang":"eng"}],"main_file_link":[{"url":"http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3176109/","open_access":"1"}],"citation":{"ama":"Polechova J, Barton NH. Genetic drift widens the expected cline but narrows the expected cline width. <i>Genetics</i>. 2011;189(1):227-235. doi:<a href=\"https://doi.org/10.1534/genetics.111.129817\">10.1534/genetics.111.129817</a>","chicago":"Polechova, Jitka, and Nicholas H Barton. “Genetic Drift Widens the Expected Cline but Narrows the Expected Cline Width.” <i>Genetics</i>. Genetics Society of America, 2011. <a href=\"https://doi.org/10.1534/genetics.111.129817\">https://doi.org/10.1534/genetics.111.129817</a>.","short":"J. Polechova, N.H. Barton, Genetics 189 (2011) 227–235.","apa":"Polechova, J., &#38; Barton, N. H. (2011). Genetic drift widens the expected cline but narrows the expected cline width. <i>Genetics</i>. Genetics Society of America. <a href=\"https://doi.org/10.1534/genetics.111.129817\">https://doi.org/10.1534/genetics.111.129817</a>","ieee":"J. Polechova and N. H. Barton, “Genetic drift widens the expected cline but narrows the expected cline width,” <i>Genetics</i>, vol. 189, no. 1. Genetics Society of America, pp. 227–235, 2011.","mla":"Polechova, Jitka, and Nicholas H. Barton. “Genetic Drift Widens the Expected Cline but Narrows the Expected Cline Width.” <i>Genetics</i>, vol. 189, no. 1, Genetics Society of America, 2011, pp. 227–35, doi:<a href=\"https://doi.org/10.1534/genetics.111.129817\">10.1534/genetics.111.129817</a>.","ista":"Polechova J, Barton NH. 2011. Genetic drift widens the expected cline but narrows the expected cline width. Genetics. 189(1), 227–235."},"year":"2011","date_published":"2011-09-01T00:00:00Z","doi":"10.1534/genetics.111.129817","publisher":"Genetics Society of America","article_processing_charge":"No","publication_status":"published","department":[{"_id":"NiBa"}],"month":"09","date_updated":"2025-09-30T08:42:59Z","isi":1,"title":"Genetic drift widens the expected cline but narrows the expected cline width","scopus_import":"1","status":"public","date_created":"2018-12-11T12:03:05Z","language":[{"iso":"eng"}],"publication":"Genetics","publist_id":"3213","page":"227 - 235","intvolume":"       189","oa":1,"_id":"3394","issue":"1","corr_author":"1","type":"journal_article","author":[{"full_name":"Polechova, Jitka","id":"3BBFB084-F248-11E8-B48F-1D18A9856A87","last_name":"Polechova","first_name":"Jitka","orcid":"0000-0003-0951-3112"},{"orcid":"0000-0002-8548-5240","first_name":"Nicholas H","id":"4880FE40-F248-11E8-B48F-1D18A9856A87","full_name":"Barton, Nicholas H","last_name":"Barton"}],"user_id":"317138e5-6ab7-11ef-aa6d-ffef3953e345"},{"publication":"Biological Journal of the Linnean Society","language":[{"iso":"eng"}],"date_created":"2018-12-11T12:03:06Z","scopus_import":"1","status":"public","page":"407 - 418","intvolume":"       104","publist_id":"3212","_id":"3395","related_material":{"record":[{"relation":"research_data","status":"public","id":"9762"}]},"user_id":"317138e5-6ab7-11ef-aa6d-ffef3953e345","acknowledgement":"This work was supported by a pre-doctoral fellowship awarded by the Autonomous Government of Catalonia to F.P. (2006FIC-00082). Research was funded by projects FBBVA-BIOCON 08-187/09, CGL2006-13423, and CTM2007-66635. The authors are part of the research group 2009SGR-636, 2009SGR-655, and 2009SGR-1364 of the Generalitat de Catalunya. F.P. acknowledges EU-Synthesys grant (GB-TAF-4474).","author":[{"first_name":"Ferran","orcid":"0000-0002-0343-8329","id":"3F0E2A22-F248-11E8-B48F-1D18A9856A87","full_name":"Palero, Ferran","last_name":"Palero"},{"first_name":"Pere","full_name":"Abello, Pere","last_name":"Abello"},{"first_name":"Enrique","full_name":"Macpherson, Enrique","last_name":"Macpherson"},{"full_name":"Beaumont, Mark","last_name":"Beaumont","first_name":"Mark"},{"first_name":"Marta","last_name":"Pascual","full_name":"Pascual, Marta"}],"type":"journal_article","corr_author":"1","issue":"2","quality_controlled":"1","external_id":{"isi":["000294902700013"]},"oa_version":"None","volume":104,"day":"14","abstract":[{"text":"Defining population structure and genetic diversity levels is of the utmost importance for developing efficient conservation strategies. Overfishing has caused mean annual catches of the European spiny lobster (Palinurus elephas) to decrease alarmingly along its distribution area. In this context, there is a need for comprehensive studies aiming to evaluate the genetic health of the exploited populations. The present study is based on a set of ten nuclear markers amplified in 331 individuals from ten different localities covering most of P. elephas distribution area. Samples from Atlantic and Mediterranean basins showed small but significant differences, indicating that P. elephas populations do not behave as a single panmictic unit but form two partially-overlapping groups. Despite intense overfishing, our dataset did not recover a recent bottleneck signal, and instead showed a large and stable historical effective size. This result could be accounted for by specific life-history traits (reproduction and longevity) and the limitations of molecular markers in covering recent timescales for nontemporal samples. The findings of the present study emphasize the need to integrate information on effective population sizes and life-history parameters when evaluating population connectivity levels from genetic data.","lang":"eng"}],"publication_status":"published","article_processing_charge":"No","publisher":"Wiley-Blackwell","doi":"10.1111/j.1095-8312.2011.01728.x","year":"2011","date_published":"2011-09-14T00:00:00Z","citation":{"ista":"Palero F, Abello P, Macpherson E, Beaumont M, Pascual M. 2011. Effect of oceanographic barriers and overfishing on the population genetic structure of the European spiny lobster Palinurus elephas. Biological Journal of the Linnean Society. 104(2), 407–418.","mla":"Palero, Ferran, et al. “Effect of Oceanographic Barriers and Overfishing on the Population Genetic Structure of the European Spiny Lobster Palinurus Elephas.” <i>Biological Journal of the Linnean Society</i>, vol. 104, no. 2, Wiley-Blackwell, 2011, pp. 407–18, doi:<a href=\"https://doi.org/10.1111/j.1095-8312.2011.01728.x\">10.1111/j.1095-8312.2011.01728.x</a>.","ieee":"F. Palero, P. Abello, E. Macpherson, M. Beaumont, and M. Pascual, “Effect of oceanographic barriers and overfishing on the population genetic structure of the European spiny lobster Palinurus elephas,” <i>Biological Journal of the Linnean Society</i>, vol. 104, no. 2. Wiley-Blackwell, pp. 407–418, 2011.","apa":"Palero, F., Abello, P., Macpherson, E., Beaumont, M., &#38; Pascual, M. (2011). Effect of oceanographic barriers and overfishing on the population genetic structure of the European spiny lobster Palinurus elephas. <i>Biological Journal of the Linnean Society</i>. Wiley-Blackwell. <a href=\"https://doi.org/10.1111/j.1095-8312.2011.01728.x\">https://doi.org/10.1111/j.1095-8312.2011.01728.x</a>","short":"F. Palero, P. Abello, E. Macpherson, M. Beaumont, M. Pascual, Biological Journal of the Linnean Society 104 (2011) 407–418.","chicago":"Palero, Ferran, Pere Abello, Enrique Macpherson, Mark Beaumont, and Marta Pascual. “Effect of Oceanographic Barriers and Overfishing on the Population Genetic Structure of the European Spiny Lobster Palinurus Elephas.” <i>Biological Journal of the Linnean Society</i>. Wiley-Blackwell, 2011. <a href=\"https://doi.org/10.1111/j.1095-8312.2011.01728.x\">https://doi.org/10.1111/j.1095-8312.2011.01728.x</a>.","ama":"Palero F, Abello P, Macpherson E, Beaumont M, Pascual M. Effect of oceanographic barriers and overfishing on the population genetic structure of the European spiny lobster Palinurus elephas. <i>Biological Journal of the Linnean Society</i>. 2011;104(2):407-418. doi:<a href=\"https://doi.org/10.1111/j.1095-8312.2011.01728.x\">10.1111/j.1095-8312.2011.01728.x</a>"},"title":"Effect of oceanographic barriers and overfishing on the population genetic structure of the European spiny lobster Palinurus elephas","isi":1,"date_updated":"2025-09-30T08:42:31Z","month":"09","department":[{"_id":"NiBa"}]},{"abstract":[{"text":"Facial branchiomotor neurons (FBMNs) in zebrafish and mouse embryonic hindbrain undergo a characteristic tangential migration from rhombomere (r) 4, where they are born, to r6/7. Cohesion among neuroepithelial cells (NCs) has been suggested to function in FBMN migration by inhibiting FBMNs positioned in the basal neuroepithelium such that they move apically between NCs towards the midline of the neuroepithelium instead of tangentially along the basal side of the neuroepithelium towards r6/7. However, direct experimental evaluation of this hypothesis is still lacking. Here, we have used a combination of biophysical cell adhesion measurements and high-resolution time-lapse microscopy to determine the role of NC cohesion in FBMN migration. We show that reducing NC cohesion by interfering with Cadherin 2 (Cdh2) activity results in FBMNs positioned at the basal side of the neuroepithelium moving apically towards the neural tube midline instead of tangentially towards r6/7. In embryos with strongly reduced NC cohesion, ectopic apical FBMN movement frequently results in fusion of the bilateral FBMN clusters over the apical midline of the neural tube. By contrast, reducing cohesion among FBMNs by interfering with Contactin 2 (Cntn2) expression in these cells has little effect on apical FBMN movement, but reduces the fusion of the bilateral FBMN clusters in embryos with strongly diminished NC cohesion. These data provide direct experimental evidence that NC cohesion functions in tangential FBMN migration by restricting their apical movement.","lang":"eng"}],"article_type":"original","volume":138,"day":"28","oa_version":"Published Version","external_id":{"isi":["000296060100011"]},"quality_controlled":"1","month":"09","department":[{"_id":"CaHe"}],"date_updated":"2025-09-30T08:41:19Z","title":"Defective neuroepithelial cell cohesion affects tangential branchiomotor neuron migration in the zebrafish neural tube","isi":1,"citation":{"apa":"Stockinger, P., Heisenberg, C.-P. J., &#38; Maître, J.-L. (2011). Defective neuroepithelial cell cohesion affects tangential branchiomotor neuron migration in the zebrafish neural tube. <i>Development</i>. Company of Biologists. <a href=\"https://doi.org/10.1242/dev.071233\">https://doi.org/10.1242/dev.071233</a>","short":"P. Stockinger, C.-P.J. Heisenberg, J.-L. Maître, Development 138 (2011) 4673–4683.","chicago":"Stockinger, Petra, Carl-Philipp J Heisenberg, and Jean-Léon Maître. “Defective Neuroepithelial Cell Cohesion Affects Tangential Branchiomotor Neuron Migration in the Zebrafish Neural Tube.” <i>Development</i>. Company of Biologists, 2011. <a href=\"https://doi.org/10.1242/dev.071233\">https://doi.org/10.1242/dev.071233</a>.","ama":"Stockinger P, Heisenberg C-PJ, Maître J-L. Defective neuroepithelial cell cohesion affects tangential branchiomotor neuron migration in the zebrafish neural tube. <i>Development</i>. 2011;138(21):4673-4683. doi:<a href=\"https://doi.org/10.1242/dev.071233\">10.1242/dev.071233</a>","ista":"Stockinger P, Heisenberg C-PJ, Maître J-L. 2011. Defective neuroepithelial cell cohesion affects tangential branchiomotor neuron migration in the zebrafish neural tube. Development. 138(21), 4673–4683.","mla":"Stockinger, Petra, et al. “Defective Neuroepithelial Cell Cohesion Affects Tangential Branchiomotor Neuron Migration in the Zebrafish Neural Tube.” <i>Development</i>, vol. 138, no. 21, Company of Biologists, 2011, pp. 4673–83, doi:<a href=\"https://doi.org/10.1242/dev.071233\">10.1242/dev.071233</a>.","ieee":"P. Stockinger, C.-P. J. Heisenberg, and J.-L. Maître, “Defective neuroepithelial cell cohesion affects tangential branchiomotor neuron migration in the zebrafish neural tube,” <i>Development</i>, vol. 138, no. 21. Company of Biologists, pp. 4673–4683, 2011."},"year":"2011","date_published":"2011-09-28T00:00:00Z","publication_status":"published","doi":"10.1242/dev.071233","article_processing_charge":"No","publisher":"Company of Biologists","file":[{"date_created":"2019-10-07T14:19:42Z","checksum":"ca12b79e01ef36c1ef1aea31cf7e7139","access_level":"open_access","relation":"main_file","file_size":4672439,"date_updated":"2020-07-14T12:46:12Z","file_name":"2011_Development_Stockinger.pdf","content_type":"application/pdf","creator":"dernst","file_id":"6930"}],"ddc":["570"],"page":"4673 - 4683","intvolume":"       138","publist_id":"3210","scopus_import":"1","date_created":"2018-12-11T12:03:06Z","status":"public","has_accepted_license":"1","acknowledged_ssus":[{"_id":"Bio"},{"_id":"PreCl"}],"language":[{"iso":"eng"}],"publication":"Development","file_date_updated":"2020-07-14T12:46:12Z","issue":"21","corr_author":"1","type":"journal_article","author":[{"first_name":"Petra","last_name":"Stockinger","id":"261CB030-E90D-11E9-B182-F697D44B663C","full_name":"Stockinger, Petra"},{"first_name":"Carl-Philipp J","orcid":"0000-0002-0912-4566","last_name":"Heisenberg","full_name":"Heisenberg, Carl-Philipp J","id":"39427864-F248-11E8-B48F-1D18A9856A87"},{"id":"48F1E0D8-F248-11E8-B48F-1D18A9856A87","full_name":"Maître, Jean-Léon","last_name":"Maître","orcid":"0000-0002-3688-1474","first_name":"Jean-Léon"}],"user_id":"317138e5-6ab7-11ef-aa6d-ffef3953e345","oa":1,"_id":"3396"},{"language":[{"iso":"eng"}],"publication":"Current Opinion in Cell Biology","date_created":"2018-12-11T12:03:06Z","scopus_import":"1","status":"public","publist_id":"3211","intvolume":"        23","page":"508 - 514","_id":"3397","oa":1,"type":"journal_article","author":[{"first_name":"Jean-Léon","orcid":"0000-0002-3688-1474","id":"48F1E0D8-F248-11E8-B48F-1D18A9856A87","full_name":"Maître, Jean-Léon","last_name":"Maître"},{"last_name":"Heisenberg","full_name":"Heisenberg, Carl-Philipp J","id":"39427864-F248-11E8-B48F-1D18A9856A87","orcid":"0000-0002-0912-4566","first_name":"Carl-Philipp J"}],"user_id":"317138e5-6ab7-11ef-aa6d-ffef3953e345","issue":"5","corr_author":"1","external_id":{"isi":["000296040800002"]},"quality_controlled":"1","volume":23,"day":"01","oa_version":"Submitted Version","abstract":[{"text":"Recent advances in microscopy techniques and biophysical measurements have provided novel insight into the molecular, cellular and biophysical basis of cell adhesion. However, comparably little is known about a core element of cell–cell adhesion—the energy of adhesion at the cell–cell contact. In this review, we discuss approaches to understand the nature and regulation of adhesion energy, and propose strategies to determine adhesion energy between cells in vitro and in vivo.","lang":"eng"}],"main_file_link":[{"open_access":"1","url":"http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3188705/"}],"doi":"10.1016/j.ceb.2011.07.004","publisher":"Elsevier","article_processing_charge":"No","publication_status":"published","citation":{"ista":"Maître J-L, Heisenberg C-PJ. 2011. The role of adhesion energy in controlling cell-cell contacts. Current Opinion in Cell Biology. 23(5), 508–514.","mla":"Maître, Jean-Léon, and Carl-Philipp J. Heisenberg. “The Role of Adhesion Energy in Controlling Cell-Cell Contacts.” <i>Current Opinion in Cell Biology</i>, vol. 23, no. 5, Elsevier, 2011, pp. 508–14, doi:<a href=\"https://doi.org/10.1016/j.ceb.2011.07.004\">10.1016/j.ceb.2011.07.004</a>.","ieee":"J.-L. Maître and C.-P. J. Heisenberg, “The role of adhesion energy in controlling cell-cell contacts,” <i>Current Opinion in Cell Biology</i>, vol. 23, no. 5. Elsevier, pp. 508–514, 2011.","apa":"Maître, J.-L., &#38; Heisenberg, C.-P. J. (2011). The role of adhesion energy in controlling cell-cell contacts. <i>Current Opinion in Cell Biology</i>. Elsevier. <a href=\"https://doi.org/10.1016/j.ceb.2011.07.004\">https://doi.org/10.1016/j.ceb.2011.07.004</a>","short":"J.-L. Maître, C.-P.J. Heisenberg, Current Opinion in Cell Biology 23 (2011) 508–514.","chicago":"Maître, Jean-Léon, and Carl-Philipp J Heisenberg. “The Role of Adhesion Energy in Controlling Cell-Cell Contacts.” <i>Current Opinion in Cell Biology</i>. Elsevier, 2011. <a href=\"https://doi.org/10.1016/j.ceb.2011.07.004\">https://doi.org/10.1016/j.ceb.2011.07.004</a>.","ama":"Maître J-L, Heisenberg C-PJ. The role of adhesion energy in controlling cell-cell contacts. <i>Current Opinion in Cell Biology</i>. 2011;23(5):508-514. doi:<a href=\"https://doi.org/10.1016/j.ceb.2011.07.004\">10.1016/j.ceb.2011.07.004</a>"},"date_published":"2011-10-01T00:00:00Z","year":"2011","isi":1,"title":"The role of adhesion energy in controlling cell-cell contacts","department":[{"_id":"CaHe"}],"month":"10","date_updated":"2025-09-30T08:42:02Z"},{"file":[{"date_created":"2018-12-12T10:15:40Z","checksum":"46f8cbde61f06fcacf8fa297cacfa0e5","access_level":"open_access","file_size":147367,"relation":"main_file","date_updated":"2020-07-14T12:46:12Z","file_name":"IST-2015-377-v1+1_journal.pone.0017323.pdf","content_type":"application/pdf","file_id":"5162","creator":"system"}],"ddc":["576"],"intvolume":"         6","publist_id":"3059","scopus_import":"1","date_created":"2018-12-11T12:03:07Z","status":"public","has_accepted_license":"1","publication":"PLoS One","language":[{"iso":"eng"}],"file_date_updated":"2020-07-14T12:46:12Z","corr_author":"1","issue":"3","acknowledgement":"This work was supported by the German Science Foundation (www.dfg.de, He 1623/23).","author":[{"first_name":"Sylvia","orcid":"0000-0002-2193-3868","id":"2F64EC8C-F248-11E8-B48F-1D18A9856A87","full_name":"Cremer, Sylvia","last_name":"Cremer"},{"first_name":"Alexandra","full_name":"Schrempf, Alexandra","last_name":"Schrempf"},{"first_name":"Jürgen","full_name":"Heinze, Jürgen","last_name":"Heinze"}],"user_id":"317138e5-6ab7-11ef-aa6d-ffef3953e345","type":"journal_article","oa":1,"_id":"3399","abstract":[{"lang":"eng","text":"Context-dependent adjustment of mating tactics can drastically increase the mating success of behaviourally flexible animals. We used the ant Cardiocondyla obscurior as a model system to study adaptive adjustment of male mating tactics. This species shows a male diphenism of wingless fighter males and peaceful winged males. Whereas the wingless males stay and exclusively mate in the maternal colony, the mating behaviour of winged males is plastic. They copulate with female sexuals in their natal nests early in life but later disperse in search for sexuals outside. In this study, we observed the nest-leaving behaviour of winged males under different conditions and found that they adaptively adjust the timing of their dispersal to the availability of mating partners, as well as the presence, and even the type of competitors in their natal nests. In colonies with virgin female queens winged males stayed longest when they were the only male in the nest. They left earlier when mating partners were not available or when other males were present. In the presence of wingless, locally mating fighter males, winged males dispersed earlier than in the presence of docile, winged competitors. This suggests that C. obscurior males are capable of estimating their local breeding chances and adaptively adjust their dispersal behaviour in both an opportunistic and a risk-sensitive way, thus showing hitherto unknown behavioural plasticity in social insect males."}],"volume":6,"day":"29","oa_version":"Published Version","pubrep_id":"377","quality_controlled":"1","external_id":{"isi":["000289054600009"]},"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)"},"date_updated":"2025-09-30T08:40:50Z","department":[{"_id":"SyCr"}],"month":"03","title":"Competition and opportunity shape the reproductive tactics of males in the ant Cardiocondyla obscurior","article_number":"e17323","isi":1,"date_published":"2011-03-29T00:00:00Z","year":"2011","citation":{"chicago":"Cremer, Sylvia, Alexandra Schrempf, and Jürgen Heinze. “Competition and Opportunity Shape the Reproductive Tactics of Males in the Ant Cardiocondyla Obscurior.” <i>PLoS One</i>. Public Library of Science, 2011. <a href=\"https://doi.org/10.1371/journal.pone.0017323\">https://doi.org/10.1371/journal.pone.0017323</a>.","ama":"Cremer S, Schrempf A, Heinze J. Competition and opportunity shape the reproductive tactics of males in the ant Cardiocondyla obscurior. <i>PLoS One</i>. 2011;6(3). doi:<a href=\"https://doi.org/10.1371/journal.pone.0017323\">10.1371/journal.pone.0017323</a>","apa":"Cremer, S., Schrempf, A., &#38; Heinze, J. (2011). Competition and opportunity shape the reproductive tactics of males in the ant Cardiocondyla obscurior. <i>PLoS One</i>. Public Library of Science. <a href=\"https://doi.org/10.1371/journal.pone.0017323\">https://doi.org/10.1371/journal.pone.0017323</a>","short":"S. Cremer, A. Schrempf, J. Heinze, PLoS One 6 (2011).","mla":"Cremer, Sylvia, et al. “Competition and Opportunity Shape the Reproductive Tactics of Males in the Ant Cardiocondyla Obscurior.” <i>PLoS One</i>, vol. 6, no. 3, e17323, Public Library of Science, 2011, doi:<a href=\"https://doi.org/10.1371/journal.pone.0017323\">10.1371/journal.pone.0017323</a>.","ieee":"S. Cremer, A. Schrempf, and J. Heinze, “Competition and opportunity shape the reproductive tactics of males in the ant Cardiocondyla obscurior,” <i>PLoS One</i>, vol. 6, no. 3. Public Library of Science, 2011.","ista":"Cremer S, Schrempf A, Heinze J. 2011. Competition and opportunity shape the reproductive tactics of males in the ant Cardiocondyla obscurior. PLoS One. 6(3), e17323."},"publication_status":"published","article_processing_charge":"No","publisher":"Public Library of Science","doi":"10.1371/journal.pone.0017323"},{"author":[{"id":"33BA6C30-F248-11E8-B48F-1D18A9856A87","full_name":"Janovjak, Harald L","last_name":"Janovjak","first_name":"Harald L","orcid":"0000-0002-8023-9315"},{"last_name":"Sandoz","full_name":"Sandoz, Guillaume","first_name":"Guillaume"},{"first_name":"Ehud","full_name":"Isacoff, Ehud","last_name":"Isacoff"}],"user_id":"317138e5-6ab7-11ef-aa6d-ffef3953e345","type":"journal_article","corr_author":"1","issue":"232","file_date_updated":"2020-07-14T12:46:12Z","_id":"3405","oa":1,"publist_id":"2997","page":"1 - 6","intvolume":"         2","ddc":["570","571"],"file":[{"file_id":"4891","creator":"system","file_name":"IST-2017-832-v1+1_janovjak.pdf","date_updated":"2020-07-14T12:46:12Z","content_type":"application/pdf","access_level":"open_access","relation":"main_file","file_size":387654,"date_created":"2018-12-12T10:11:36Z","checksum":"6b68d65aadd97c18d663eb117a0a9d35"}],"publication":"Nature Communications","language":[{"iso":"eng"}],"has_accepted_license":"1","scopus_import":"1","status":"public","date_created":"2018-12-11T12:03:09Z","isi":1,"title":"Modern ionotropic glutamate receptor with a K+ selectivity signature sequence","date_updated":"2025-09-30T08:40:22Z","department":[{"_id":"HaJa"}],"month":"03","article_processing_charge":"No","publisher":"Nature Publishing Group","doi":"10.1038/ncomms1231","publication_status":"published","year":"2011","date_published":"2011-03-08T00:00:00Z","citation":{"ista":"Janovjak HL, Sandoz G, Isacoff E. 2011. Modern ionotropic glutamate receptor with a K+ selectivity signature sequence. Nature Communications. 2(232), 1–6.","mla":"Janovjak, Harald L., et al. “Modern Ionotropic Glutamate Receptor with a K+ Selectivity Signature Sequence.” <i>Nature Communications</i>, vol. 2, no. 232, Nature Publishing Group, 2011, pp. 1–6, doi:<a href=\"https://doi.org/10.1038/ncomms1231\">10.1038/ncomms1231</a>.","ieee":"H. L. Janovjak, G. Sandoz, and E. Isacoff, “Modern ionotropic glutamate receptor with a K+ selectivity signature sequence,” <i>Nature Communications</i>, vol. 2, no. 232. Nature Publishing Group, pp. 1–6, 2011.","apa":"Janovjak, H. L., Sandoz, G., &#38; Isacoff, E. (2011). Modern ionotropic glutamate receptor with a K+ selectivity signature sequence. <i>Nature Communications</i>. Nature Publishing Group. <a href=\"https://doi.org/10.1038/ncomms1231\">https://doi.org/10.1038/ncomms1231</a>","short":"H.L. Janovjak, G. Sandoz, E. Isacoff, Nature Communications 2 (2011) 1–6.","chicago":"Janovjak, Harald L, Guillaume Sandoz, and Ehud Isacoff. “Modern Ionotropic Glutamate Receptor with a K+ Selectivity Signature Sequence.” <i>Nature Communications</i>. Nature Publishing Group, 2011. <a href=\"https://doi.org/10.1038/ncomms1231\">https://doi.org/10.1038/ncomms1231</a>.","ama":"Janovjak HL, Sandoz G, Isacoff E. Modern ionotropic glutamate receptor with a K+ selectivity signature sequence. <i>Nature Communications</i>. 2011;2(232):1-6. doi:<a href=\"https://doi.org/10.1038/ncomms1231\">10.1038/ncomms1231</a>"},"abstract":[{"text":"Glutamate is the major excitatory neurotransmitter in the mammalian central nervous system and gates non-selective cation channels. The origins of glutamate receptors are not well understood as they differ structurally and functionally from simple bacterial ligand-gated ion channels. Here we report the discovery of an ionotropic glutamate receptor that combines the typical eukaryotic domain architecture with the 'TXVGYG' signature sequence of the selectivity filter found in K+ channels. This receptor exhibits functional properties intermediate between bacterial and eukaryotic glutamate-gated ion channels, suggesting a link in the evolution of ionotropic glutamate receptors.","lang":"eng"}],"quality_controlled":"1","external_id":{"isi":["000289982600022"]},"pubrep_id":"832","volume":2,"day":"08","oa_version":"Submitted Version"},{"conference":{"name":"GbRPR: Graph-based Representations in Pattern Recognition","end_date":"2011-05-20","location":"Münster, Germany","start_date":"2011-05-18"},"abstract":[{"lang":"eng","text":"This paper presents a method to create a model of an articulated object using the planar motion in an initialization video. The model consists of rigid parts connected by points of articulation. The rigid parts are described by the positions of salient feature-points tracked throughout the video. Following a filtering step that identifies points that belong to different objects, rigid parts are found by a grouping process in a graph pyramid. Valid articulation points are selected by verifying multiple hypotheses for each pair of parts."}],"quality_controlled":"1","alternative_title":["LNCS"],"day":"01","oa_version":"None","volume":6658,"title":"Spatio-temporal extraction of articulated models in a graph pyramid","date_updated":"2024-10-09T21:02:32Z","department":[{"_id":"HeEd"}],"month":"06","publication_status":"published","publisher":"Springer","article_processing_charge":"No","publication_identifier":{"isbn":["9783642208430"],"eissn":["1611-3349"],"issn":["0302-9743"],"eisbn":["9783642208447"]},"doi":"10.1007/978-3-642-20844-7_22","date_published":"2011-06-01T00:00:00Z","year":"2011","citation":{"ama":"Artner NM, Ion A, Kropatsch WG. Spatio-temporal extraction of articulated models in a graph pyramid. In: Jiang X, Ferrer M, Torsello A, eds. <i>Graph-Based Representations in Pattern Recognition</i>. Vol 6658. LNIP. Berlin, Heidelberg: Springer; 2011:215-224. doi:<a href=\"https://doi.org/10.1007/978-3-642-20844-7_22\">10.1007/978-3-642-20844-7_22</a>","chicago":"Artner, Nicole M., Adrian Ion, and Walter G. Kropatsch. “Spatio-Temporal Extraction of Articulated Models in a Graph Pyramid.” In <i>Graph-Based Representations in Pattern Recognition</i>, edited by Xiaoyi Jiang, Miquel Ferrer, and Andrea Torsello, 6658:215–24. LNIP. Berlin, Heidelberg: Springer, 2011. <a href=\"https://doi.org/10.1007/978-3-642-20844-7_22\">https://doi.org/10.1007/978-3-642-20844-7_22</a>.","short":"N.M. Artner, A. Ion, W.G. Kropatsch, in:, X. Jiang, M. Ferrer, A. Torsello (Eds.), Graph-Based Representations in Pattern Recognition, Springer, Berlin, Heidelberg, 2011, pp. 215–224.","apa":"Artner, N. M., Ion, A., &#38; Kropatsch, W. G. (2011). Spatio-temporal extraction of articulated models in a graph pyramid. In X. Jiang, M. Ferrer, &#38; A. Torsello (Eds.), <i>Graph-Based Representations in Pattern Recognition</i> (Vol. 6658, pp. 215–224). Berlin, Heidelberg: Springer. <a href=\"https://doi.org/10.1007/978-3-642-20844-7_22\">https://doi.org/10.1007/978-3-642-20844-7_22</a>","ieee":"N. M. Artner, A. Ion, and W. G. Kropatsch, “Spatio-temporal extraction of articulated models in a graph pyramid,” in <i>Graph-Based Representations in Pattern Recognition</i>, Münster, Germany, 2011, vol. 6658, pp. 215–224.","mla":"Artner, Nicole M., et al. “Spatio-Temporal Extraction of Articulated Models in a Graph Pyramid.” <i>Graph-Based Representations in Pattern Recognition</i>, edited by Xiaoyi Jiang et al., vol. 6658, Springer, 2011, pp. 215–24, doi:<a href=\"https://doi.org/10.1007/978-3-642-20844-7_22\">10.1007/978-3-642-20844-7_22</a>.","ista":"Artner NM, Ion A, Kropatsch WG. 2011. Spatio-temporal extraction of articulated models in a graph pyramid. Graph-Based Representations in Pattern Recognition. GbRPR: Graph-based Representations in Pattern RecognitionLNIP, LNCS, vol. 6658, 215–224."},"intvolume":"      6658","page":"215-224","series_title":"LNIP","publication":"Graph-Based Representations in Pattern Recognition","language":[{"iso":"eng"}],"status":"public","scopus_import":"1","date_created":"2022-03-21T08:08:35Z","acknowledgement":"This work has been partially supported by the Austrian Science Fund under grants S9103-N13 and P18716-N13.","author":[{"first_name":"Nicole M.","last_name":"Artner","full_name":"Artner, Nicole M."},{"id":"29F89302-F248-11E8-B48F-1D18A9856A87","full_name":"Ion, Adrian","last_name":"Ion","first_name":"Adrian"},{"full_name":"Kropatsch, Walter G.","last_name":"Kropatsch","first_name":"Walter G."}],"user_id":"c635000d-4b10-11ee-a964-aac5a93f6ac1","type":"conference","corr_author":"1","_id":"10907","place":"Berlin, Heidelberg","editor":[{"first_name":"Xiaoyi","last_name":"Jiang","full_name":"Jiang, Xiaoyi"},{"full_name":"Ferrer, Miquel","last_name":"Ferrer","first_name":"Miquel"},{"full_name":"Torsello, Andrea","last_name":"Torsello","first_name":"Andrea"}]},{"external_id":{"pmid":["21257907"]},"quality_controlled":"1","oa_version":"Published Version","day":"01","volume":108,"main_file_link":[{"open_access":"1","url":"https://doi.org/10.1073/pnas.1019273108"}],"abstract":[{"lang":"eng","text":"Imprinted genes are expressed primarily or exclusively from either the maternal or paternal allele, a phenomenon that occurs in flowering plants and mammals. Flowering plant imprinted gene expression has been described primarily in endosperm, a terminal nutritive tissue consumed by the embryo during seed development or after germination. Imprinted expression in Arabidopsis thaliana endosperm is orchestrated by differences in cytosine DNA methylation between the paternal and maternal genomes as well as by Polycomb group proteins. Currently, only 11 imprinted A. thaliana genes are known. Here, we use extensive sequencing of cDNA libraries to identify 9 paternally expressed and 34 maternally expressed imprinted genes in A. thaliana endosperm that are regulated by the DNA-demethylating glycosylase DEMETER, the DNA methyltransferase MET1, and/or the core Polycomb group protein FIE. These genes encode transcription factors, proteins involved in hormone signaling, components of the ubiquitin protein degradation pathway, regulators of histone and DNA methylation, and small RNA pathway proteins. We also identify maternally expressed genes that may be regulated by unknown mechanisms or deposited from maternal tissues. We did not detect any imprinted genes in the embryo. Our results show that imprinted gene expression is an extensive mechanistically complex phenomenon that likely affects multiple aspects of seed development."}],"article_type":"original","publication_status":"published","publication_identifier":{"eissn":["1091-6490"],"issn":["0027-8424"]},"publisher":"National Academy of Sciences","article_processing_charge":"No","doi":"10.1073/pnas.1019273108","date_published":"2011-02-01T00:00:00Z","year":"2011","citation":{"ama":"Hsieh T-F, Shin J, Uzawa R, et al. Regulation of imprinted gene expression in Arabidopsis endosperm. <i>Proceedings of the National Academy of Sciences</i>. 2011;108(5):1755-1762. doi:<a href=\"https://doi.org/10.1073/pnas.1019273108\">10.1073/pnas.1019273108</a>","chicago":"Hsieh, Tzung-Fu, Juhyun Shin, Rie Uzawa, Pedro Silva, Stephanie Cohen, Matthew J. Bauer, Meryl Hashimoto, et al. “Regulation of Imprinted Gene Expression in Arabidopsis Endosperm.” <i>Proceedings of the National Academy of Sciences</i>. National Academy of Sciences, 2011. <a href=\"https://doi.org/10.1073/pnas.1019273108\">https://doi.org/10.1073/pnas.1019273108</a>.","short":"T.-F. Hsieh, J. Shin, R. Uzawa, P. Silva, S. Cohen, M.J. Bauer, M. Hashimoto, R.C. Kirkbride, J.J. Harada, D. Zilberman, R.L. Fischer, Proceedings of the National Academy of Sciences 108 (2011) 1755–1762.","apa":"Hsieh, T.-F., Shin, J., Uzawa, R., Silva, P., Cohen, S., Bauer, M. J., … Fischer, R. L. (2011). Regulation of imprinted gene expression in Arabidopsis endosperm. <i>Proceedings of the National Academy of Sciences</i>. National Academy of Sciences. <a href=\"https://doi.org/10.1073/pnas.1019273108\">https://doi.org/10.1073/pnas.1019273108</a>","ieee":"T.-F. Hsieh <i>et al.</i>, “Regulation of imprinted gene expression in Arabidopsis endosperm,” <i>Proceedings of the National Academy of Sciences</i>, vol. 108, no. 5. National Academy of Sciences, pp. 1755–1762, 2011.","mla":"Hsieh, Tzung-Fu, et al. “Regulation of Imprinted Gene Expression in Arabidopsis Endosperm.” <i>Proceedings of the National Academy of Sciences</i>, vol. 108, no. 5, National Academy of Sciences, 2011, pp. 1755–62, doi:<a href=\"https://doi.org/10.1073/pnas.1019273108\">10.1073/pnas.1019273108</a>.","ista":"Hsieh T-F, Shin J, Uzawa R, Silva P, Cohen S, Bauer MJ, Hashimoto M, Kirkbride RC, Harada JJ, Zilberman D, Fischer RL. 2011. Regulation of imprinted gene expression in Arabidopsis endosperm. Proceedings of the National Academy of Sciences. 108(5), 1755–1762."},"title":"Regulation of imprinted gene expression in Arabidopsis endosperm","date_updated":"2021-12-14T08:33:49Z","month":"02","department":[{"_id":"DaZi"}],"publication":"Proceedings of the National Academy of Sciences","language":[{"iso":"eng"}],"scopus_import":"1","date_created":"2021-06-07T07:40:38Z","status":"public","intvolume":"       108","page":"1755-1762","pmid":1,"_id":"9483","oa":1,"extern":"1","user_id":"8b945eb4-e2f2-11eb-945a-df72226e66a9","author":[{"last_name":"Hsieh","full_name":"Hsieh, Tzung-Fu","first_name":"Tzung-Fu"},{"first_name":"Juhyun","last_name":"Shin","full_name":"Shin, Juhyun"},{"last_name":"Uzawa","full_name":"Uzawa, Rie","first_name":"Rie"},{"last_name":"Silva","full_name":"Silva, Pedro","first_name":"Pedro"},{"full_name":"Cohen, Stephanie","last_name":"Cohen","first_name":"Stephanie"},{"full_name":"Bauer, Matthew J.","last_name":"Bauer","first_name":"Matthew J."},{"full_name":"Hashimoto, Meryl","last_name":"Hashimoto","first_name":"Meryl"},{"last_name":"Kirkbride","full_name":"Kirkbride, Ryan C.","first_name":"Ryan C."},{"last_name":"Harada","full_name":"Harada, John J.","first_name":"John J."},{"last_name":"Zilberman","full_name":"Zilberman, Daniel","id":"6973db13-dd5f-11ea-814e-b3e5455e9ed1","orcid":"0000-0002-0123-8649","first_name":"Daniel"},{"full_name":"Fischer, Robert L.","last_name":"Fischer","first_name":"Robert L."}],"type":"journal_article","issue":"5"},{"abstract":[{"text":"Little is known about chromatin remodeling events immediately after fertilization. A recent report by Autran et al. (2011) in Cell now shows that chromatin regulatory pathways that silence transposable elements are responsible for global delayed activation of gene expression in the early Arabidopsis embryo.","lang":"eng"}],"main_file_link":[{"url":"https://doi.org/10.1016/j.devcel.2011.05.018","open_access":"1"}],"volume":20,"day":"14","oa_version":"Published Version","external_id":{"pmid":["21664571"]},"quality_controlled":"1","month":"06","department":[{"_id":"DaZi"}],"date_updated":"2021-12-14T08:34:37Z","title":"Balancing parental contributions in plant embryonic gene activation","citation":{"short":"D. Zilberman, Balancing Parental Contributions in Plant Embryonic Gene Activation, Elsevier, 2011.","apa":"Zilberman, D. (2011). <i>Balancing parental contributions in plant embryonic gene activation</i>. <i>Developmental Cell</i> (Vol. 20, pp. 735–736). Elsevier. <a href=\"https://doi.org/10.1016/j.devcel.2011.05.018\">https://doi.org/10.1016/j.devcel.2011.05.018</a>","ama":"Zilberman D. <i>Balancing Parental Contributions in Plant Embryonic Gene Activation</i>. Vol 20. Elsevier; 2011:735-736. doi:<a href=\"https://doi.org/10.1016/j.devcel.2011.05.018\">10.1016/j.devcel.2011.05.018</a>","chicago":"Zilberman, Daniel. <i>Balancing Parental Contributions in Plant Embryonic Gene Activation</i>. <i>Developmental Cell</i>. Vol. 20. Elsevier, 2011. <a href=\"https://doi.org/10.1016/j.devcel.2011.05.018\">https://doi.org/10.1016/j.devcel.2011.05.018</a>.","ista":"Zilberman D. 2011. Balancing parental contributions in plant embryonic gene activation, Elsevier,p.","ieee":"D. Zilberman, <i>Balancing parental contributions in plant embryonic gene activation</i>, vol. 20, no. 6. Elsevier, 2011, pp. 735–736.","mla":"Zilberman, Daniel. “Balancing Parental Contributions in Plant Embryonic Gene Activation.” <i>Developmental Cell</i>, vol. 20, no. 6, Elsevier, 2011, pp. 735–36, doi:<a href=\"https://doi.org/10.1016/j.devcel.2011.05.018\">10.1016/j.devcel.2011.05.018</a>."},"date_published":"2011-06-14T00:00:00Z","year":"2011","publication_status":"published","doi":"10.1016/j.devcel.2011.05.018","publication_identifier":{"issn":["1534-5807"],"eissn":["1878-1551"]},"publisher":"Elsevier","article_processing_charge":"No","pmid":1,"intvolume":"        20","page":"735-736","date_created":"2021-06-08T06:23:39Z","status":"public","language":[{"iso":"eng"}],"publication":"Developmental Cell","issue":"6","extern":"1","type":"other_academic_publication","user_id":"8b945eb4-e2f2-11eb-945a-df72226e66a9","author":[{"first_name":"Daniel","orcid":"0000-0002-0123-8649","last_name":"Zilberman","id":"6973db13-dd5f-11ea-814e-b3e5455e9ed1","full_name":"Zilberman, Daniel"}],"oa":1,"_id":"9522"},{"title":"Data from: Effect of oceanographic barriers and overfishing on the population genetic structure of the European spiny lobster (Palinurus elephas)","author":[{"last_name":"Palero","id":"3F0E2A22-F248-11E8-B48F-1D18A9856A87","full_name":"Palero, Ferran","orcid":"0000-0002-0343-8329","first_name":"Ferran"},{"full_name":"Abello, Pere","last_name":"Abello","first_name":"Pere"},{"first_name":"Enrique","full_name":"Macpherson, Enrique","last_name":"Macpherson"},{"full_name":"Beaumont, Mark","last_name":"Beaumont","first_name":"Mark"},{"first_name":"Marta","last_name":"Pascual","full_name":"Pascual, Marta"}],"user_id":"6785fbc1-c503-11eb-8a32-93094b40e1cf","type":"research_data_reference","date_updated":"2025-09-30T08:42:31Z","department":[{"_id":"NiBa"}],"month":"05","_id":"9762","publisher":"IST Austria","article_processing_charge":"No","doi":"10.5061/dryad.299h8","oa":1,"date_published":"2011-05-12T00:00:00Z","related_material":{"record":[{"relation":"used_in_publication","id":"3395","status":"public"}]},"year":"2011","citation":{"short":"F. Palero, P. Abello, E. Macpherson, M. Beaumont, M. Pascual, (2011).","apa":"Palero, F., Abello, P., Macpherson, E., Beaumont, M., &#38; Pascual, M. (2011). Data from: Effect of oceanographic barriers and overfishing on the population genetic structure of the European spiny lobster (Palinurus elephas). IST Austria. <a href=\"https://doi.org/10.5061/dryad.299h8\">https://doi.org/10.5061/dryad.299h8</a>","ama":"Palero F, Abello P, Macpherson E, Beaumont M, Pascual M. Data from: Effect of oceanographic barriers and overfishing on the population genetic structure of the European spiny lobster (Palinurus elephas). 2011. doi:<a href=\"https://doi.org/10.5061/dryad.299h8\">10.5061/dryad.299h8</a>","chicago":"Palero, Ferran, Pere Abello, Enrique Macpherson, Mark Beaumont, and Marta Pascual. “Data from: Effect of Oceanographic Barriers and Overfishing on the Population Genetic Structure of the European Spiny Lobster (Palinurus Elephas).” IST Austria, 2011. <a href=\"https://doi.org/10.5061/dryad.299h8\">https://doi.org/10.5061/dryad.299h8</a>.","ista":"Palero F, Abello P, Macpherson E, Beaumont M, Pascual M. 2011. Data from: Effect of oceanographic barriers and overfishing on the population genetic structure of the European spiny lobster (Palinurus elephas), IST Austria, <a href=\"https://doi.org/10.5061/dryad.299h8\">10.5061/dryad.299h8</a>.","ieee":"F. Palero, P. Abello, E. Macpherson, M. Beaumont, and M. Pascual, “Data from: Effect of oceanographic barriers and overfishing on the population genetic structure of the European spiny lobster (Palinurus elephas).” IST Austria, 2011.","mla":"Palero, Ferran, et al. <i>Data from: Effect of Oceanographic Barriers and Overfishing on the Population Genetic Structure of the European Spiny Lobster (Palinurus Elephas)</i>. IST Austria, 2011, doi:<a href=\"https://doi.org/10.5061/dryad.299h8\">10.5061/dryad.299h8</a>."},"main_file_link":[{"open_access":"1","url":"https://doi.org/10.5061/dryad.299h8"}],"abstract":[{"text":"Defining population structure and genetic diversity levels is of the utmost importance for developing efficient conservation strategies. Overfishing has caused mean annual catches of the European spiny lobster (Palinurus elephas) to decrease alarmingly along its distribution area. In this context, there is a need for comprehensive studies to evaluate the genetic health of the exploited populations. The present work is based on a set of 10 nuclear markers amplified in 331 individuals from 10 different localities covering most of P. elephas distribution area. Samples from Atlantic and Mediterranean basins showed small but significant differences, indicating that P. elephas populations do not behave as a single panmictic unit but form two partially-overlapping groups. Despite intense overfishing, our dataset did not recover a recent bottleneck signal, and showed a large and stable historical effective size instead. This result could be accounted for by specific life history traits (reproduction and longevity) and the limitations of molecular markers in covering very recent timescales for non temporal samples. Our study emphasizes the necessity of integrating information on effective population sizes and life history parameters when evaluating population connectivity levels from genetic data.","lang":"eng"}],"day":"12","oa_version":"Published Version","date_created":"2021-08-02T07:11:19Z","status":"public"},{"department":[{"_id":"PeJo"}],"month":"03","date_updated":"2025-09-30T09:25:10Z","isi":1,"title":"Spontaneous glutamate release is independent of calcium influx and tonically activated by the calcium-sensing receptor","citation":{"short":"N. Vyleta, S. Smith, European Journal of Neuroscience 31 (2011) 4593–4606.","apa":"Vyleta, N., &#38; Smith, S. (2011). Spontaneous glutamate release is independent of calcium influx and tonically activated by the calcium-sensing receptor. <i>European Journal of Neuroscience</i>. Wiley-Blackwell. <a href=\"https://doi.org/10.1523/JNEUROSCI.6398-10.2011\">https://doi.org/10.1523/JNEUROSCI.6398-10.2011</a>","ama":"Vyleta N, Smith S. Spontaneous glutamate release is independent of calcium influx and tonically activated by the calcium-sensing receptor. <i>European Journal of Neuroscience</i>. 2011;31(12):4593-4606. doi:<a href=\"https://doi.org/10.1523/JNEUROSCI.6398-10.2011\">10.1523/JNEUROSCI.6398-10.2011</a>","chicago":"Vyleta, Nicholas, and Stephen Smith. “Spontaneous Glutamate Release Is Independent of Calcium Influx and Tonically Activated by the Calcium-Sensing Receptor.” <i>European Journal of Neuroscience</i>. Wiley-Blackwell, 2011. <a href=\"https://doi.org/10.1523/JNEUROSCI.6398-10.2011\">https://doi.org/10.1523/JNEUROSCI.6398-10.2011</a>.","ista":"Vyleta N, Smith S. 2011. Spontaneous glutamate release is independent of calcium influx and tonically activated by the calcium-sensing receptor. European Journal of Neuroscience. 31(12), 4593–4606.","ieee":"N. Vyleta and S. Smith, “Spontaneous glutamate release is independent of calcium influx and tonically activated by the calcium-sensing receptor,” <i>European Journal of Neuroscience</i>, vol. 31, no. 12. Wiley-Blackwell, pp. 4593–4606, 2011.","mla":"Vyleta, Nicholas, and Stephen Smith. “Spontaneous Glutamate Release Is Independent of Calcium Influx and Tonically Activated by the Calcium-Sensing Receptor.” <i>European Journal of Neuroscience</i>, vol. 31, no. 12, Wiley-Blackwell, 2011, pp. 4593–606, doi:<a href=\"https://doi.org/10.1523/JNEUROSCI.6398-10.2011\">10.1523/JNEUROSCI.6398-10.2011</a>."},"year":"2011","date_published":"2011-03-23T00:00:00Z","doi":"10.1523/JNEUROSCI.6398-10.2011","article_processing_charge":"No","publisher":"Wiley-Blackwell","publication_status":"published","abstract":[{"lang":"eng","text":"Spontaneous release of glutamate is important for maintaining synaptic strength and controlling spike timing in the brain. Mechanisms regulating spontaneous exocytosis remain poorly understood. Extracellular calcium concentration ([Ca2+]o) regulates Ca2+ entry through voltage-activated calcium channels (VACCs) and consequently is a pivotal determinant of action potential-evoked vesicle fusion. Extracellular Ca 2+ also enhances spontaneous release, but via unknown mechanisms. Here we report that external Ca2+ triggers spontaneous glutamate release more weakly than evoked release in mouse neocortical neurons. Blockade of VACCs has no effect on the spontaneous release rate or its dependence on [Ca2+]o. Intracellular [Ca2+] slowly increases in a minority of neurons following increases in [Ca2+]o. Furthermore, the enhancement of spontaneous release by extracellular calcium is insensitive to chelation of intracellular calcium by BAPTA. Activation of the calcium-sensing receptor (CaSR), a G-protein-coupled receptor present in nerve terminals, by several specific agonists increased spontaneous glutamate release. The frequency of spontaneous synaptic transmission was decreased in CaSR mutant neurons. The concentration-effect relationship for extracellular calcium regulation of spontaneous release was well described by a combination of CaSR-dependent and CaSR-independent mechanisms. Overall these results indicate that extracellular Ca2+ does not trigger spontaneous glutamate release by simply increasing calcium influx but stimulates CaSR and thereby promotes resting spontaneous glutamate release. "}],"main_file_link":[{"url":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3097128/","open_access":"1"}],"oa_version":"Submitted Version","volume":31,"day":"23","quality_controlled":"1","external_id":{"isi":["000288750700025"]},"issue":"12","type":"journal_article","user_id":"317138e5-6ab7-11ef-aa6d-ffef3953e345","author":[{"first_name":"Nicholas","last_name":"Vyleta","id":"36C4978E-F248-11E8-B48F-1D18A9856A87","full_name":"Vyleta, Nicholas"},{"last_name":"Smith","full_name":"Smith, Stephen","first_name":"Stephen"}],"oa":1,"_id":"469","publist_id":"7353","intvolume":"        31","page":"4593 - 4606","status":"public","scopus_import":"1","date_created":"2018-12-11T11:46:39Z","language":[{"iso":"eng"}],"publication":"European Journal of Neuroscience"}]