{"status":1,"totalCount":25,"data":[{"reference":"Babbs C, Roberts N, Sanchez-Pulido L, McGowan S, Ahmed M, Brown J, Sabry M, Bentley D, McVean G, Donnelly P, Gileadi O, Ponting C, Higgs D, Buckle V (2013) Homozygous mutations in a predicted endonuclease are a novel cause of congenital dyserythropoietic anemia type I. Haematologica 98: 1383-1387 | doi: 10.3324\/haematol.2013.089490.","publicationStatus":"Publi\u00e9"},{"reference":"Bertrand S, Fuentealba J, Aze A, Hudson C<\/span>, Yasuo H<\/span>, Torrejon M, Escriva H, Marcellini S (2013) \r\n\r\n\r\n\r\n\r\n\r\n\r\nA dynamic evolutionary history\r\nof the SPARC gene family. Proc Biol Sci 280: 2012-2963 | doi: 10.1098\/rspb.2012.2963.","publicationStatus":"Publi\u00e9"},{"reference":"Chambon J, Touati S, Berneau S, Cladi\u00e8re D, H\u00e9bras C<\/span>, Groeme R, McDougall A<\/span>, Wassmann K (2013) The PP2A Inhibitor I2PP2A is\r\n Essential for Sister Chromatid Segregation in Oocyte Meiosis II. Curr. Biol. 23: 485-488.","publicationStatus":"Publi\u00e9"},{"reference":"Chenevert J<\/span>, Pruli\u00e8re G<\/span>, Ishii H, Sardet C, Nishikata T (2013) Purification of mitochondrial proteins HSP60 and ATP\r\nsynthase from ascidian eggs: Implications for antibody specificity. PLoS ONE 8: 52996-52999.","publicationStatus":"Publi\u00e9"},{"reference":"Chenevert J<\/span>, Pruli\u00e8re G<\/span>, Ishii H, Sardet S, Nishikata T (2013) Purification of mitochondrial proteins {HSP60} and {ATP} synthase from ascidian eggs: implications for antibody specificity. PLoS ONE 8 | doi: 10.1371\/journal.pone.0052996.","publicationStatus":"Publi\u00e9"},{"reference":"Cossins J, Belaya K, Hicks D, Salih M, Finlayson S, Carboni N, Liu W, Maxwell S, Zoltowska K, Farsani G, Laval S, Seidhamed M, Donnelly P, Bentley D, McGowan S, M\u00fcller J, Palace J, Lochm\u00fcller H, Beeson D (2013) Congenital myasthenic syndromes due to mutations in ALG2 and ALG14. Brain 136 | doi: 10.1093\/brain\/awt010.","publicationStatus":"Publi\u00e9"},{"reference":"Dumollard R<\/span>, H\u00e9bras C<\/span>, Besnardeau L<\/span>, McDougall A<\/span> (2013) Beta-catenin patterns the cell cycle during maternal-to-zygotic transition in urochordate embryos. Dev. Biol. 384: 331-342 | doi: 10.1016\/j.ydbio.2013.10.007.","publicationStatus":"Publi\u00e9"},{"reference":"Haupaix N<\/span>, Stolfi A, Sirour C<\/span>, Picco V<\/span>, Levine M, Christiaen L, Yasuo H<\/span> (2013) p120RasGAP mediates ephrin\/Eph-dependent attenuation of FGF\/ERK signals during cell fate specification in ascidian embryos. Development 140: 52-4347 | doi: 10.1242\/dev.098756.","publicationStatus":"Publi\u00e9"},{"reference":"Holland LZ, Carvalho JE<\/span>, Escriva H, Laudet V, Schubert M<\/span>, Shimeld SM, Yu JK (2013) Evolution of bilaterian central nervous systems: A single origin? EvoDevo 4: 27-27.","publicationStatus":"Publi\u00e9"},{"reference":"Hosseini M, Goodstadt L, Hughes J, Kowalczyk M, de Gobbi M, Otto G, Copley R<\/span>, Mott R, Higgs D, Flint J (2013) Causes and Consequences of Chromatin Variation between Inbred Mice. PLoS Genet. 9 | doi: 10.1371\/journal.pgen.1003570.","publicationStatus":"Publi\u00e9"},{"reference":"Hudson C<\/span>, Kawai N<\/span>, Negishi T<\/span>, Yasuo H<\/span> (2013) \r\n\r\n\r\n\r\n\r\n\r\n\r\nbeta-catenin-driven binary fate\r\nspecification segregates germ layers in ascidian embryos. Curr. Biol. 23: 491-495 | doi: 10.1016\/j.cub.2013.02.005.","publicationStatus":"Publi\u00e9"},{"reference":"Lara-Ramirez R<\/span>, Zieger E<\/span>, Schubert M<\/span> (2013) Retinoic acid signaling in spinal cord development. Int. J. Biochem. Cell Biol. 45: 1302-1313 | doi: 10.1016\/j.biocel.2013.04.002. Epub 2013 Apr 8.","publicationStatus":"Publi\u00e9"},{"reference":"Lauzon R, Brown C, Kerr L, Tiozzo S<\/span> (2013) Phagocyte dynamics in a highly regenerative urochordate: insights into development and host defense . Dev. Biol.","publicationStatus":"Publi\u00e9"},{"reference":"Lecomte S, Reverdy L, Le quement C, Masson F, Amon A, Le goff P, Michel D, Christians E<\/span>, Le drean Y (2013) Unraveling complex interplay between HSF1 and HSF2 isoforms. PLoS ONE 8.","publicationStatus":"Publi\u00e9"},{"reference":"Levasseur M, Dumollard R<\/span>, Chambon J-P<\/span>, H\u00e9bras C<\/span>, Sinclair M, Whitaker M, McDougall A<\/span> (2013) Release from meiotic arrest in ascidian eggs requires the activity of two phosphatases but not {CaMKII}. Development 140: 4583-4593 | doi: 10.1242\/dev.096578.","publicationStatus":"Publi\u00e9"},{"reference":"Li Y, Copley R<\/span> (2013) Scaffolding low quality genomes using orthologous protein sequences. Bioinformatics 29: 160-165 | doi: 10.1093\/bioinformatics\/bts661.","publicationStatus":"Publi\u00e9"},{"reference":"Limphong P, Zhang H, Christians E<\/span>, Liu Q, Riedel M, Ivey K, Cheng P, Mitzelffelt K, Taylor G, Winge D, Srivastava D, Benjamin I (2013) Modeling human protein aggregation cardiomyopathy using murine induced pluripotent stem cells. Stem Cells Trans Med 2: 6-161.","publicationStatus":"Publi\u00e9"},{"reference":"McIntyre DC, Seay NW, Croce J<\/span>, McClay DR (2013) Short-range Wnt5 signaling initiates specification of sea urchin\r\nposterior ectoderm. Development 140: 4881-4889.","publicationStatus":"Publi\u00e9"},{"reference":"Negishi T<\/span>, McDougall A<\/span>, Yasuo H<\/span> (2013) Practical tips\r\n for imaging\r\n ascidian embryos. Dev. Growth Diff. 55: 446-453.","publicationStatus":"Publi\u00e9"},{"reference":"Ouhlen N, Mori M, Dumollard R<\/span> (2013) Oocyte maturation and fertilization: lessons from canonical and emerging models. J. Cell Sci. 126: 4321-4324.","publicationStatus":"Publi\u00e9"},{"reference":"Penwill L, Batten G, Castagnetti S<\/span>, Shaw A (2013) Growth phenotype screening of Schizzosaccharomyces pombe<\/i> using a Lensless microscope. Biosens Bioelectron 54: 345-350.","publicationStatus":"Publi\u00e9"},{"reference":"Shanks M, Downes S, Copley R<\/span>, Lise S, Broxholme J, Hudspith K, Kwasniewska A, Davies W, Hankins M, Packham E, Clouston P, Seller A, Wilkie A, Taylor J, Ragoussis J, Nemeth A (2013) Next-generation sequencing (NGS) as a diagnostic tool for retinal degeneration reveals a much higher detection rate in early-onset disease. Eur. J. Hum. Genet. 21: 274-280 | doi: 10.1038\/ejhg.2012.172.","publicationStatus":"Publi\u00e9"},{"reference":"Sharma V, Fenwick A, Brockop M, McGowan S, Goos J, Hoogeboom A, Brady A, Jeelani N, Lynch S, Mulliken J, Murray D, Phipps J, Sweeney E, Tomkins S, Wilson L<\/span>, Bennett S, Cornall R, Broxholme J, Kanapin A, 500 Whole-Genome Sequences (WGS500) Consortium _<\/span>, Johnson D, Wall S, van der Spek P, Mathijssen I, Maxson R, Twigg S, Wilkie A (2013) Mutations in {TCF12}, encoding a basic helix-loop-helix partner of {TWIST1}, are a frequent cause of coronal craniosynostosis. Nat. Genet. 45 | doi: 10.1038\/ng.2531.","publicationStatus":"Publi\u00e9"},{"reference":"Sharma V, Fenwick A, Brockop M, McGowan S, Goos J, Hoogeboom A, Brady A, Jeelani N, Lynch S, Mulliken J, Murray M, Phipps J, Sweeney S, Tomkins S, Wilson L<\/span>, Bennett S, Cornall R, Broxholme J, Kanapin E, 500 Whole-Genome Sequences (WGS500) Consortium _<\/span>, Johnson D, Wall S, van der Spek P, Mathijssen I, Maxson R, Twigg S, Wilkie A (2013) Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis. Nat. Genet. 45: 304-307 | doi: 10.1038\/ng.2531.","publicationStatus":"Publi\u00e9"},{"reference":"Squires S, Christians E<\/span>, Riedel M, Timothy D, Rodesch C, Marvin J, Benjamin I (2013) \r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\nEffects\r\nof redox state on the efficient uptake of cell permeable Peptide in Mammalian\r\ncells. Open Biochem J. 7: 54-65 | doi: 10.2174\/1874091X20130531001.","publicationStatus":"Publi\u00e9"}]}