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The developing embryo, Can J Bot, 69, 461, 10.1139\u002Fb91-063\nScheres, 1994, Embryonic origin of the Arabidopsis primary root and root meristem initials, Development, 120, 2475, 10.1242\u002Fdev.120.9.2475\nPoethig, 1986, Cell lineage patterns in maize embryogenesis: a clonal analysis, Dev Biol, 117, 392, 10.1016\u002F0012-1606(86)90308-8\nSaulsberry, 2002, The induced sector Arabidopsis apical embryonic fate map, Development, 129, 3403, 10.1242\u002Fdev.129.14.3403\nBerleth, 2002, Embryogenesis: pattern formation from a single cell, 1\nLaux, 2004, Genetic regulation of embryonic pattern formation, Plant Cell, 16, S190, 10.1105\u002Ftpc.016014\nKim, 2002, Identification of a developmental transition in plasmodesmatal function during embryogenesis in Arabidopsis thaliana, Development, 129, 1261, 10.1242\u002Fdev.129.5.1261\nKim, 2005, Cell-to-cell movement of GFP during embryogenesis and early seedling development in Arabidopsis, Proc Natl Acad Sci USA, 102, 2227, 10.1073\u002Fpnas.0409193102\nStadler R, Lauterbach C, Sauer N: Cell-to-cell movement of GFP reveals post-phloem transport in the outer integument and identifies symplastic domains in Arabidopsis seeds and embryos. Plant Physiol 2005, in press.\nKim, 2005, Sub-domains for transport via plasmodesmata corresponding to the apical–basal axis are established during Arabidopsis embryogenesis, Proc Natl Acad Sci USA, 102, 11945, 10.1073\u002Fpnas.0505622102\nTomenius, 1987, Localization by immunogold cytochemistry of the virus coded 30K protein in plasmodesmata of leaves infected with tobacco mosaic virus, Virology, 160, 363, 10.1016\u002F0042-6822(87)90007-9\nAtkins, 1991, The tobacco mosaic virus 30K movement protein in transgenic tobacco plants is localized to plasmodesmata, J Gen Virol, 72, 209, 10.1099\u002F0022-1317-72-1-209\nGhoshroy, 1997, Transport of proteins and nucleic acids through plasmodesmata, Annu Rev Plant Physiol Plant Mol Biol, 48, 27, 10.1146\u002Fannurev.arplant.48.1.27\nYeung, 1993, Embryogenesis in angiosperms: development of the suspensor, Plant Cell, 5, 1371, 10.1105\u002Ftpc.5.10.1371\nStadler, 2005, Expression of GFP-fusions in Arabidopsis companion cells reveals non-specific protein trafficking into sieve elements and identifies a novel post-phloem domain in roots, Plant J, 41, 319, 10.1111\u002Fj.1365-313X.2004.02298.x\nTilney, 1990, The distribution of plasmodesmata and its relationship to morphogenesis in fern gametophytes, Development, 110, 1209, 10.1242\u002Fdev.110.4.1209\nvan der Schoot, 1990, Mapping membrane potential differences and dye-coupling in internodal tissues of tomato (Solanum lycopersicum L), Planta, 182, 9, 10.1007\u002FBF00239977\nvan der Schoot, 1995, Establishment of a cell-to-cell communication pathway between separate carpels during gynoecium development, Planta, 195, 450, 10.1007\u002FBF00202604\nErwee, 1985, Symplast domains in extrastellar tissues of Egeria densa Planch, Planta, 163, 9, 10.1007\u002FBF00395891\nDuckett, 1994, Dye-coupling in the root epidermis of Arabidopsis is progressively reduced during development, Development, 120, 3247, 10.1242\u002Fdev.120.11.3247\nvan der Schoot, 1999, The symplastic organization of the shoot apical meristem\nKwiatkowska, 1999, Plasmodesmal coupling and cell differentiation in algae, 205\nOparka, 1999, Simple, but not branched, plasmodesmata allow the nonspecific trafficking of proteins in developing tobacco leaves, Cell, 97, 743, 10.1016\u002FS0092-8674(00)80786-2\nTurgeon, 1989, The sink–source transition in leaves, Annu Rev Plant Physiol Plant Mol Biol, 40, 119, 10.1146\u002Fannurev.pp.40.060189.001003\nRoberts, 2001, Dynamic changes in the frequency and architecture of plasmodesmata during the sink–source transition in tobacco leaves, Protoplasma, 218, 31, 10.1007\u002FBF01288358\nCrawford, 2001, Non-targeted and targeted protein movement through plasmodesmata in leaves in different developmental and physiological states, Plant Physiol, 125, 1802, 10.1104\u002Fpp.125.4.1802",{"VOID":181},"10.1016\u002Fj.pbi.2005.09.013","PUBLICATION","VERIFIED","2024-09-04T17:09:43.211+00:00","Auto 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recombination and genome evolution in plants",{"VOID":283},"[\"13766688707050359881\"]",{"VOID":285},"Bhullar, 2014, Silencing of a metaphase I-specific gene results in a phenotype similar to that of the Pairing homeologous 1 (Ph1) gene mutations, Proc Natl Acad Sci U S A, 111, 14187, 10.1073\u002Fpnas.1416241111\nRobbins, 1991, Meiotic instability of the R-r complex arising from displaced intragenic exchange and intrachromosomal rearrangement, Genetics, 129, 271, 10.1093\u002Fgenetics\u002F129.1.271\nde Massy, 2013, Initiation of meiotic recombination: how and where? Conservation and specificities among eukaryotes, Annu Rev Genet, 47, 563, 10.1146\u002Fannurev-genet-110711-155423\nHartung, 2013, Molecular characterization of two paralogous SPO11 homologues in Arabidopsis thaliana, Nucleic Acids Res, 28, 1548, 10.1093\u002Fnar\u002F28.7.1548\nSprink, 2014, The splicing fate of plant SPO11 genes, Front Plant Sci, 5, 214, 10.3389\u002Ffpls.2014.00214\nThacker, 2014, Homologue engagement controls meiotic DNA break number and distribution, Nature, 510, 241, 10.1038\u002Fnature13120\nPawlowski, 2003, Altered nuclear distribution of recombination protein RAD51 in maize mutants suggests the involvement of RAD51 in meiotic homology recognition, Plant Cell, 15, 1807, 10.1105\u002Ftpc.012898\nAnderson, 2003, High-resolution crossover maps for each bivalent of Zea mays using recombination nodules, Genetics, 165, 849, 10.1093\u002Fgenetics\u002F165.2.849\nSanchez-Moran, 2007, ASY1 mediates AtDMC1-dependent interhomolog recombination during meiosis in Arabidopsis, Genes Dev, 21, 2220, 10.1101\u002Fgad.439007\nVaras, 2015, Analysis of the relationships between DNA double-strand breaks, synaptonemal complex and crossovers using the Atfas1-4 mutant, PLoS Genet, 11, e1005301, 10.1371\u002Fjournal.pgen.1005301\nMercier, 2015, The molecular biology of meiosis in plants, Annu Rev Plant Biol, 66, 297, 10.1146\u002Fannurev-arplant-050213-035923\nChoulet, 2014, Structural and functional partitioning of bread wheat chromosome 3B, Science, 345, 1249721, 10.1126\u002Fscience.1249721\nThe International Barley Genome Sequencing Consortium, 2012, A physical, genetic and functional sequence assembly of the barley genome, Nature, 491, 711, 10.1038\u002Fnature11543\nPaterson, 2009, The Sorghum bicolor genome and the diversification of grasses, Nature, 457, 551, 10.1038\u002Fnature07723\nSi, 2015, Widely distributed hot and cold spots in meiotic recombination as shown by the sequencing of rice F2 plants, New Phytol, 206, 1491, 10.1111\u002Fnph.13319\nMcMullen, 2009, Genetic properties of the maize nested association mapping population, Science, 325, 737, 10.1126\u002Fscience.1174320\nRodgers-Melnick, 2015, Recombination in diverse maize is stable, predictable, and associated with genetic load, Proc Natl Acad Sci U S A, 112, 3823, 10.1073\u002Fpnas.1413864112\nGore, 2009, A first-generation haplotype map of maize, Science, 326, 1115, 10.1126\u002Fscience.1177837\nGiraut, 2011, Genome-wide crossover distribution in Arabidopsis thaliana meiosis reveals sex-specific patterns along chromosomes, PLoS Genet, 7, e1002354, 10.1371\u002Fjournal.pgen.1002354\nHorton, 2012, Genome-wide patterns of genetic variation in worldwide Arabidopsis thaliana accessions from the RegMap panel, Nat Genet, 44, 212, 10.1038\u002Fng.1042\nChoi, 2013, Arabidopsis meiotic crossover hot spots overlap with H2A.Z. nucleosomes at gene promoters, Nat Genet, 45, 1327, 10.1038\u002Fng.2766\nPaape, 2012, Fine-scale population recombination 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10.1073\u002Fpnas.0409227102",{"VOID":888},"10.1016\u002Fj.pbi.2005.05.010","2024-05-17T00:18:12.424+00:00","https:\u002F\u002Fwww.sciencedirect.com\u002Fscience\u002Farticle\u002Fpii\u002FS1369526605000713",[892,907,922],{"id":893,"sortIndex":85,"researcher":24,"roles":894,"affiliations":895,"properties":904,"displayName":906,"givenName":24,"familyName":24},"43e58aa9-8e2e-42bc-9742-c448d130291f",[191],[896],{"id":897,"sortIndex":85,"affiliation":898,"properties":24},"8286fda1-da34-4001-8382-7ebc06d995e4",{"id":897,"createTime":24,"updateTime":24,"relativeEntities":899,"slug":24,"properties":900,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":903,"statistic":24},[],{"title":901},{"VI":902},"Max Planck Institute for Plant Breeding Research, Department of Plant–Microbe Interactions, Carl-von-Linné-Weg 10, D-50829 Cologne, Germany",[],{"title":905},{"VI":906},"Marcel 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10.1093\u002Fjxb\u002Fers124\nSmidansky, 2002, Enhanced ADP-glucose pyrophosphorylase activity in wheat endosperm increases seed yield, Proc Natl Acad Sci USA, 99, 1724, 10.1073\u002Fpnas.022635299\nNuccio, 2015, Expression of trehalose-6-phosphate phosphatase in maize ears improves yield in well-watered and drought conditions, Nat Biotechnol, 33, 10.1038\u002Fnbt.3277\nGriffiths, 2016, Chemical intervention in plant sugar signalling increases yield and resilience, Nature, 540, 10.1038\u002Fnature20591\nJung, 2015, Identification of the transporter responsible for sucrose accumulation in sugar beet taproots, Nat Plants, 1\nKoerner, 2015, Paradigm shift in plant growth control, Curr Opin Plant Biol, 25, 107, 10.1016\u002Fj.pbi.2015.05.003\nFarrar, 2000, The control of carbon acquisition by roots, New Phytol, 147, 43, 10.1046\u002Fj.1469-8137.2000.00688.x\nEom, 2015, SWEETs, transporters for intracellular and intercellular sugar translocation, Curr Opin Plant Biol, 25, 53, 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quantitative trait for tomato yield using interspecific introgressions, Science, 305, 1786, 10.1126\u002Fscience.1101666\nBermudez, 2014, Silencing of the tomato sugar partitioning affecting protein (SPA) modifies sink strength through a shift in leaf sugar metabolism, Plant J, 77, 676, 10.1111\u002Ftpj.12418\nSoyk, 2017, Bypassing negative epistasis on yield in tomato imposed by a domestication gene, Cell, 169, 10.1016\u002Fj.cell.2017.04.032\nSoyk, 2017, Variation in the flowering gene SELF PRUNING 5G promotes day-neutrality and early yield in tomato, Nat Genet, 49, 162, 10.1038\u002Fng.3733\nPark, 2014, Optimization of crop productivity in tomato using induced mutations in the florigen pathway, Nat Genet, 46, 1337, 10.1038\u002Fng.3131\nArnold, 2011, A quantitative comparison of Calvin–Benson cycle models, Trends Plant Sci, 16, 676, 10.1016\u002Fj.tplants.2011.09.004\nNikoloski, 2015, Inference and prediction of metabolic network fluxes, Plant Physiol, 169, 1443\nDal’Molin, 2013, 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149, 10.1104\u002Fpp.107.111674\nSzemenyei, 2008, TOPLESS mediates auxin-dependent transcriptional repression during Arabidopsis embryogenesis, Science, 319, 1384, 10.1126\u002Fscience.1151461\nLong, 2006, TOPLESS regulates apical embryonic fate in Arabidopsis, Science, 312, 1520, 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motors in plants: from subcellular dynamics to motility regulation",{"VOID":1307},"[\"382893827148796868\"]",{"VOID":1309},"Vicente, 2015, Mitosis, microtubule dynamics and the evolution of kinesins, Exp Cell Res, 334, 61, 10.1016\u002Fj.yexcr.2015.02.010\nMiki, 2014, Endogenous localizome identifies 43 mitotic kinesins in a plant cell, Proc Natl Acad Sci U S A, 111, E1053, 10.1073\u002Fpnas.1311243111\nShen, 2012, Phylogenetic analysis of the kinesin superfamily from Physcomitrella, Front Plant Sci, 3, 230, 10.3389\u002Ffpls.2012.00230\nScholey, 2013, Kinesin-2: a family of heterotrimeric and homodimeric motors with diverse intracellular transport functions, Annu Rev Cell Dev Biol, 29, 443, 10.1146\u002Fannurev-cellbio-101512-122335\nVerhey, 2011, Kinesin motors and primary cilia, Biochem Soc Trans, 39, 1120, 10.1042\u002FBST0391120\nGuo, 2009, Evaluating the microtubule cytoskeleton and its interacting proteins in monocots by mining the rice genome, Ann Bot, 103, 387, 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class proteins translate the positional Information of the preprophase band to establish the cortical division zone in Arabidopsis thaliana, Plant Cell, 26, 2617, 10.1105\u002Ftpc.114.124933\nLipka, 2012, Potential roles for Kinesins at the cortical division site, Front. 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positioning in Physcomitrella patens, Plant Cell Physiol, 56, 737, 10.1093\u002Fpcp\u002Fpcv002\nEng, 2014, The microtubule plus-end tracking protein ARMADILLO-REPEAT KINESIN1 promotes microtubule catastrophe in Arabidopsis, Plant Cell, 26, 3372, 10.1105\u002Ftpc.114.126789\nCross, 2014, Prime movers: the mechanochemistry of mitotic kinesins, Nat Rev Mol Cell Biol, 15, 257, 10.1038\u002Fnrm3768\nWalczak, 2013, Microtubule-depolymerizing kinesins, Annu Rev Cell Dev Biol, 29, 417, 10.1146\u002Fannurev-cellbio-101512-122345\nLu, 2005, An internal motor kinesin is associated with the Golgi apparatus and plays a role in trichome morphogenesis in Arabidopsis, Mol Biol Cell, 16, 811, 10.1091\u002Fmbc.e04-05-0400\nOda, 2013, Rho of plant GTPase signaling regulates the behavior of Arabidopsis kinesin-13A to establish secondary cell wall patterns, Plant Cell, 25, 4439, 10.1105\u002Ftpc.113.117853\nAmbrose, 2007, The kinesin ATK5 functions in early spindle assembly in Arabidopsis, Plant Cell, 19, 226, 10.1105\u002Ftpc.106.047613\nAmbrose, 2005, A minus-end-directed kinesin with plus-end tracking protein activity is involved in spindle morphogenesis, Mol Biol Cell, 16, 1584, 10.1091\u002Fmbc.e04-10-0935\nLiu, 1996, A kinesin-like protein, KatAp, in the cells of Arabidopsis and other plants, Plant Cell, 8, 119\nLee, 2013, The rise and fall of the phragmoplast microtubule array, Curr Opin Plant Biol, 16, 757, 10.1016\u002Fj.pbi.2013.10.008\nHiwatashi, 2008, Kinesins are indispensable for interdigitation of phragmoplast microtubules in the moss Physcomitrella patens, Plant Cell, 20, 3094, 10.1105\u002Ftpc.108.061705\nHiwatashi, 2014, Kinesins have a dual function in organizing microtubules during both tip growth and cytokinesis in Physcomitrella patens, Plant Cell, 26, 1256, 10.1105\u002Ftpc.113.121723\nSasabe, 2012, Regulation of organization and function of microtubules by the mitogen-activated protein kinase cascade during plant cytokinesis, Cytoskeleton (Hoboken), 69, 913, 10.1002\u002Fcm.21072\nVerhey, 2009, Traffic control: regulation of kinesin motors, Nat Rev Mol Cell Biol, 10, 765, 10.1038\u002Fnrm2782\nKong, 2015, Kinesin-4 functions in vesicular transport on cortical microtubules and regulates cell wall mechanics during cell elongation in plants, Mol Plant, 8, 1011, 10.1016\u002Fj.molp.2015.01.004\nZhu, 2015, The fragile Fiber1 kinesin contributes to cortical microtubule-mediated trafficking of cell wall components, Plant Physiol, 167, 780, 10.1104\u002Fpp.114.251462\nWalter, 2015, The non-processive rice kinesin-14 OsKCH1 transports actin filaments along microtubules with two distinct velocities, Nat Plants, 1, 10.1038\u002Fnplants.2015.111\nZhu, 2011, Single molecule analysis of the Arabidopsis FRA1 kinesin shows that it is a functional motor protein with unusually high processivity, Mol Plant, 4, 879, 10.1093\u002Fmp\u002Fssr077\nStraube, 2006, Conventional kinesin mediates microtubule-microtubule interactions in vivo, Mol Biol Cell, 17, 907, 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