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Referencias:

• Andersen, M.N., Asch, F., Wu, Y., Jensen, C.R., Naested, H., Mogensen, V.O., Koch, K.E., Soluble invertase expression is an early target of drought stress during the critical, abortion-sensitive phase of young ovary development in maize (2002) Plant Physiology, 130, pp. 591-604
• Andriotis, V.M.E., Pike, M.J., Bunnewell, S., Hills, M.J., Smith, A.M., The plastidial glucose-6-phosphate/phosphate antiporter GPT1 is essential for morphogenesis in Arabidopsis embryos (2010) The Plant Journal, 64, pp. 128-139
• Asch, F., Andersen, M.N., Jensen, C.R., Mogensen, V.O., Ovary abscisic acid concentration does not induce kernel abortion in field-grown maize subjected to drought (2001) European Journal of Agronomy, 15, pp. 119-129
• Bassetti, P., Westgate, M.E., Emergence, elongation, and senescence of maize silks (1993) Crop Science, 33, pp. 271-275
• Becerra, C., Puigdomenech, P., Vicient, C.M., Computational and experimental analysis identifies Arabidopsis genes specifically expressed during early seed development (2006) BMC Genomics, 7, p. 38
• Borderies, G., le Béchec, M., Rossignol, M., Lafitte, C., Le Deunff, E., Beckert, M., Matthys-Rochon, E., Characterization of proteins secreted during maize microspore culture: Arabinogalactan proteins (AGPs) stimulate embryo development (2004) European Journal of Cell Biology, 83, pp. 205-212
• Borrás, L., Slafer, G.A., Otegui, M.E., Seed dry weight response to source-sink manipulations in wheat, maize and soybean: A quantitative reappraisal (2004) Field Crops Research, 86, pp. 131-146
• Boyer, J.S., McLaughlin, J.E., Functional reversion to identify controlling genes in multigenic responses: Analysis of floral abortion (2007) Journal of Experimental Botany, 58, pp. 267-277
• Boyer, J.S., Westgate, M.E., Grain yields with limited water (2004) Journal of Experimental Botany, 55, pp. 2385-2394
• Boyle, M.G., Boyer, J.S., Morgan, P.W., Stem infusion of liquid culture medium prevents reproductive failure of maize at low water potential (1991) Crop Science, 31, pp. 1246-1252
• Cárcova, J., Otegui, M.E., Ear temperature and pollination timing effects on maize kernel set (2001) Crop Science, 41, pp. 1809-1815
• Cárcova, J., Otegui, M.E., Ovary growth and maize kernel set (2007) Crop Science, 47, pp. 1104-1110
• Cárcova, J., Uribelarrea, M., Borrás, L., Otegui, M.E., Westgate, M.E., Synchronous pollination within and between ears improves kernel set in maize (2000) Crop Science, 40, pp. 1056-1061
• Cheng, C.Y., Lur, H.S., Ethylene may be involved in abortion of the maize caryopsis (1996) Physiologia Plantarum, 98, pp. 245-252
• Chimenti, C.A., Marcantonio, M., Hall, A.J., Divergent selection for osmotic adjustment results in improved drought tolerance in maize (Zea mays L.) in both early growth and flowering phases (2006) Field Crops Research, 95, pp. 305-315
• Coimbra, S., Almeida, J., Junqueira, V., Costa, M.L., Pereira, L.G., Arabinogalactan proteins as molecular markers in Arabidopsis thaliana sexual reproduction (2007) Journal of Experimental Botany, 58, pp. 4027-4035
• Elkins, T., Zinn, K., McAllister, L., Hoffmann, F.M., Goodman, C.S., Genetic analysis of a Drosophila neural cell adhesion molecule: Interaction of fasciclin I and Abelson tyrosine kinase mutations (1990) Cell, 60, pp. 565-575
• Ellis, M., Egelund, J., Schultz, C.J., Bacic, A., Arabinogalactan-proteins: Key regulators at the cell surface? (2010) Plant Physiology, 153, pp. 403-419
• Eshed, Y., Izhaki, A., Baum, S.F., Floyd, S.K., Bowman, J.L., Asymmetric leaf development and blade expansion in Arabidopsis are mediated by KANADI and YABBY activities (2004) Development, 131, pp. 2997-3006
• Freier, G., Vilella, F., Hall, A.J., Within-ear pollination synchrony and kernel set in maize (1984) Maydica, 29, pp. 317-324
• Gao, M., Showalter, A.M., Immunolocalization of LeAGP-1, a modular arabinogalactan-protein, reveals its developmentally regulated expression in tomato (2000) Planta, 210, pp. 865-874
• Gómez, L.D., Baud, S., Gilday, A., Li, Y., Graham, I.A., Delayed embryo development in the ARABIDOPSIS TREHALOSE-6-PHOSPHATE SYNTHASE 1 mutant is associated with altered cell wall structure, decreased cell division and starch accumulation (2006) Plant Journal, 46, pp. 69-84
• Griffiths, J.S., Tsai, A.Y.-L., Xue, H., At Alin Voiniciuc, C., Šola, K., Seifert, G.J., Haughn, G.W., SALT-OVERLY SENSITIVE5 mediates Arabidopsis seed coat mucilage adherence and organization through pectins 1[W][OPEN] (2014) Plant Physiology, 165, pp. 991-1004
• Hall, A.J., Lemcoff, J.H., Trápani, N., Water stress before and during flowering in maize and its effects on yield, its components, and their determinants (1981) Maydica, 26, pp. 19-38
• Harpaz-Saad, S., McFarlane, H.E., Xu, S., Divi, U.K., Forward, B., Western, T.L., Kieber, J.J., Cellulose synthesis via the FEI2 RLK/SOS5 pathway and CELLULOSE SYNTHASE 5 is required for the structure of seed coat mucilage in Arabidopsis (2011) Plant Journal, 68, pp. 941-953
• Hiyane, R., Hiyane, S., Tang, A.C., Boyer, J.S., Sucrose feeding reverses shade-induced kernel losses in maize (2010) Annals of Botany, 106, pp. 395-403
• Huang, D., Wu, W., Abrams, S.R., Cutler, A.J., The relationship of drought-related gene expression in Arabidopsis thaliana to hormonal and environmental factors (2008) Journal of Experimental Botany, 59, pp. 2991-3007
• Huang, G.Q., Gong, S.Y., Xu, W.L., Li, W., Li, P., Zhang, C.J., Li, X.B., A fasciclin-like arabinogalactan protein, GhFLA1, is involved in fiber initiation and elongation of cotton (2013) Plant Physiology, 161, pp. 1278-1290
• Johnson, K.L., Jones, B.J., Bacic, A., Schultz, C.J., The fasciclin-like arabinogalactan proteins of Arabidopsis. A multigene family of putative cell adhesion molecules (2003) Plant Physiology, 133, pp. 1911-1925
• Johnson, K.L., Kibble, N.A.J., Bacic, A., Schultz, C.J., Pu, Z.-Y., A Fasciclin-like arabinogalactan-protein (FLA) mutant of Arabidopsis thaliana, fla1, shows defects in shoot regeneration (2011) PLoS One, 6
• Kakumanu, A., Ambavaram, M.M.R., Klumas, C., Krishnan, A., Batlang, U., Myers, E., Pereira, A., Effects of drought on gene expression in maize reproductive and leaf meristem tissue revealed by RNA-Seq (2012) Plant Physiology, 160, pp. 846-867
• Kitazawa, K., Tryfona, T., Yoshimi, Y., Hayashi, Y., Kawauchi, S., Antonov, L., Kotake, T., β-galactosyl Yariv reagent binds to the β-1,3-galactan of arabinogalactan proteins (2013) Plant Physiology, 161, pp. 1117-1126
• Knox, J.P., Linstead, P.J., Cooper, J.P., Roberts, K., Developmentally regulated epitopes of cell surface arabinogalactan proteins and their relation to root tissue pattern formation (2001) The Plant Journal, 1, pp. 317-326
• Levitin, B., Richter, D., Markovich, I., Zik, M., Arabinogalactan proteins 6 and 11 are required for stamen and pollen function in Arabidopsis (2008) Plant Journal, 56, pp. 351-363
• Li, J., Yu, M., Geng, L.L., Zhao, J., The fasciclin-like arabinogalactan protein gene, FLA3, is involved in microspore development of Arabidopsis (2010) Plant Journal, 64, pp. 482-497
• Li, S., Smaj, J., Franklin-Tong, V.E., A mitogen-activated protein kinase signals to programmed cell death induced by self-incompatibility in Papaver pollen (2007) Plant Physiology, 145, pp. 236-245
• Luo, M., Liu, J., Lee, R.D., Scully, B.T., Guo, B., Monitoring the expression of maize genes in developing kernels under drought stress using oligo-microarray (2010) Journal of Integrative Plant Biology, 52, pp. 1059-1074
• MacMillan, C.P., Mansfield, S.D., Stachurski, Z.H., Evans, R., Southerton, S.G., Fasciclin-like arabinogalactan proteins: Specialization for stem biomechanics and cell wall architecture in Arabidopsis and eucalyptus (2010) Plant Journal, 62, pp. 689-703
• Marino, R., Ponnaiah, M., Krajewski, P., Frova, C., Gianfranceschi, L., Pé, M.E., Sari-Gorla, M., Addressing drought tolerance in maize by transcriptional profiling and mapping (2009) Molecular Genetics and Genomics, 281, pp. 163-179
• Martin, A., Lee, J., Kichey, T., Gerentes, D., Zivy, M., Tatout, C., Hirel, B., Two cytosolic glutamine synthetase isoforms of maize are specifically involved in the control of grain production (2006) Plant Cell, 18, pp. 3252-3274
• McLaughlin, J.E., Boyer, J.S., Glucose localization in maize ovaries when kernel number decreases at low water potential and sucrose is fed to the stems (2004) Annals of Botany, 94, pp. 75-86
• McLaughlin, J.E., Boyer, J.S., Sugar-responsive gene expression, invertase activity, and senescence in aborting maize ovaries at low water potentials (2004) Annals of Botany, 94, pp. 675-689
• Miller, J.D., Arteca, R.N., Pell, E.J., Senescence-associated gene expression during ozone-induced leaf senescence in Arabidopsis (1999) Plant Physiology, 120, pp. 1015-1024
• Nielsen, R.L.B., (2016) A Fast & Accurate “pregnancy ” test for corn. 14–17
• Otegui, M.E., Kernel set and flower synchrony within the ear of maize: II. Plant population effects (1997) Crop Science, 37, pp. 448-455
• Otegui, M.E., Andrade, F.H., Suero, E.E., Growth, water use, and kernel abortion of maize subjected to drought at silking (1995) Field Crops Research, 40, pp. 87-94
• Otegui, M.E., Bonhomme, R., Grain yield components in maize. I—Ear growth and kernel set (1998) Field Crops Research, 56, pp. 247-256
• Oury, V., Caldeira, C.F., Prodhomme, D., Pichon, J.-P., Gibon, Y., Tardieu, F., Turc, O., Is change in ovary carbon status a cause or a consequence of maize ovary abortion in water deficit during flowering? (2016) Plant Physiology, 171, pp. 997-1008
• Oury, V., Tardieu, F., Turc, O., Ovary apical abortion under water deficit is caused by changes in sequential development of ovaries and in silk growth rate in maize (2016) Plant Physiology, 171, pp. 986-996
• Patton, D.A., Schetter, A.L., Franzmann, L.H., Nelson, K., Ward, E.R., Meinke, D.W., An embryo-defective mutant of Arabidopsis disrupted in the final step of biotin synthesis (1998) Plant Physiology, 116, pp. 935-946
• Paul, M.J., Primavesi, L.F., Jhurreea, D., Zhang, Y., Trehalose metabolism and signaling (2008) Annual Review of Plant Biology, 59, pp. 417-441
• Poon, S., Heath, R.L., Clarke, A.E., A chimeric arabinogalactan protein promotes somatic embryogenesis in cotton cell culture (2012) Plant Physiology, 160, pp. 684-695
• Qin, L., Trouverie, J., Chateau-Joubert, S., Simond-Côte, E., Thévenot, C., Prioul, J.L., Involvement of the Ivr2-invertase in the perianth during maize kernel development under water stress (2004) Plant Science, 166, pp. 371-379
• Quaggiotti, S., Trentin, A.R., Dalla Vecchia, F., Ghisi, R., Response of maize (Zea mays L.) nitrate reductase to UV-B radiation (2004) Plant Science, 167, pp. 107-116
• Reed, A.J., Singletary, G.W., Roles of carbohydrate supply and phytohormones in maize kernel abortion (1989) Plant Physiology, 91, pp. 986-992
• Ritchie, S.W., Hanway, J.J., Benson, G.O., Herman, J.C., (1993) How a corn plant develops. Iowa State University cooperative extension service. Special Report 48
• Roach, M.J., Deyholos, M.K., Microarray analysis of flax (Linum usitatissimum L.) stems identifies transcripts enriched in fibre-bearing phloem tissues (2007) Molecular Genetics and Genomics, 278, pp. 149-165
• Ruan, Y.L., Jin, Y., Yang, Y.J., Li, G.J., Boyer, J.S., Sugar input, metabolism, and signaling mediated by invertase: Roles in development, yield potential, and response to drought and heat (2010) Molecular Plant, 3, pp. 942-955
• Ruan, Y.L., Patrick, J.W., Bouzayen, M., Osorio, S., Fernie, A.R., Molecular regulation of seed and fruit set (2012) Trends in Plant Science, 17, pp. 656-665
• Schultz, C.J., Johnson, K.L., Currie, G., Bacic, A., The classical arabinogalactan protein gene family of Arabidopsis (2000) The Plant Cell, 12, pp. 1751-1767
• Schultz, C.J., Rumsewicz, M.P., Johnson, K.L., Jones, B.J., Gaspar, Y.M., Bacic, A., Using genomic resources to guide research directions (2002) The arabinogalactan protein gene family as a test case. Plant physiology, 129, pp. 1448-1463
• Schussler, J.R., Westgate, M.E., Maize kernel set at low water potential: II. Sensitivity to reduced assimilates at pollination (1991) Crop Science, 31, pp. 1196-1203
• Schussler, J.R., Westgate, M.E., Maize kernel set at low water potential: I. Sensitivity to reduced assimilates during early kernel growth (1991) Crop Science, 31, pp. 1189-1195
• Schussler, J.R., Westgate, M.E., Assimilate flux determines kernel set at low water potential in maize (1995) Crop Science, 35, pp. 1074-1080
• Seifert, G.J., Barber, C., Wells, B., Dolan, L., Roberts, K., Galactose biosynthesis in Arabidopsis: Genetic evidence for substrate channeling from UDP-D-galactose into cell wall polymers (2002) Current Biology, 12, pp. 1840-1845
• Seifert, G.J., Roberts, K., The biology of arabinogalactan proteins (2007) Annual Review of Plant Biology, 58, pp. 137-161
• Seifert, G.J., Xue, H., Acet, T., The Arabidopsis thaliana FASCICLIN LIKE ARABINOGALACTAN PROTEIN 4 gene acts synergistically with abscisic acid signalling to control root growth (2014) Annals of Botany, 114, pp. 1125-1133
• Sekhon, R.S., Lin, H., Childs, K.L., Hansey, C.N., Robin, B.C., De Leon, N., Kaeppler, S.M., Genome-wide atlas of transcription during maize development (2011) Plant Journal, 66, pp. 553-563
• Setter, T.L., Flannigan, B.A., Melkonian, J., Loss of kernel set due to water deficit and shade in maize: Carbohydrate supplies, abscisic acid, and cytokinins (2001) Crop Science, 41, pp. 1530-1540
• Shi, H., Kim, Y., Guo, Y., Stevenson, B., Zhu, J.K., The Arabidopsis SOS5 locus encodes a putative cell surface adhesion protein and is required for normal cell expansion (2003) Plant Cell, 15, pp. 19-32
• Showalter, A.M., Keppler, B., Lichtenberg, J., Gu, D., Welch, L.R., A bioinformatics approach to the identification, classification, and analysis of hydroxyproline-rich glycoproteins (2010) Plant Physiology, 153, pp. 485-513
• Storey, J.D., Tibshirani, R., Statistical significance for genomewide studies (2003) Proceedings of the National Academy of Sciences, 100, pp. 9440-9445
• Tang, X.C., He, Y.Q., Wang, Y., Sun, M.X., The role of arabinogalactan proteins binding to Yariv reagents in the initiation, cell developmental fate, and maintenance of microspore embryogenesis in Brassica napus L. cv. Topas (2006) Journal of Experimental Botany, 57, pp. 2639-2650
• Uauy, C., Distelfeld, A., Fahima, T., Blechl, A., Dubcovsky, J., A NAC gene regulating senescence improves grain protein, zinc, and iron content in wheat (2006) Science, 314, pp. 1298-1301
• Vega, C.R.C., Andrade, F.H., Sadras, V.O., Uhart, S.A., Valentinuz, O.R., Seed number as a function of growth. A comparative study in soybean, sunflower, and maize (2001) Crop Science, 41, pp. 748-754
• Vespa, L., Vachon, G., Berger, F., Perazza, D., Faure, J.D., Herzog, M., The immunophilin-interacting protein AtFIP37 from arabidopsis is essential for plant development and is involved in trichome endoreduplication (2004) Plant Physiology, 134, pp. 1283-1292
• Wang, P., Zhang, L., Yao, J., Shi, Y., Li, P., Ding, K., An arabinogalactan from flowers of Panax notoginseng inhibits angiogenesis by BMP2/Smad/Id1 signaling (2015) Carbohydrate Polymers, 121, pp. 328-335
• Westgate, M.E., Boyer, J.S., Reproduction at low silk and pollen water potentials in maize (1986) Crop Science, 26, pp. 951-956
• Winter, D., Vinegar, B., Nahal, H., Ammar, R., Wilson, G., An “electronic fluorescent pictograph” browser for exploring and analyzing large-scale biological data sets (2007) PLoS One, 2
• Xue, H., Veit, C., Abas, L., Tryfona, T., Maresch, D., Ricardi, M.M., Seifert, G.J., Arabidopsis thaliana FLA4 functions as a glycan-stabilized soluble factor via its carboxy-proximal Fasciclin 1 domain (2017) The Plant Journal, 91, pp. 613-630
• Yariv, J., Lis, H., Katchalski, E., Precipitation of arabic acid and some seed polysaccharides by glycosylphenylazo dyes (1967) Biochemical Journal, 105, p. 1C
• Yariv, J., Rapport, M.M., Graf, L., The interaction of glycosides and saccharides with antibody to the corresponding phenylazo glycosides (1962) Biochemical Journal, 85, p. 383
• Yates, E.A., Valdor, J.-F., Haslam, S.M., Morris, H.R., Dell, A., Mackie, W., Knox, J.P., Characterization of carbohydrate structural features recognized by anti-arabinogalactan-protein monoclonal antibodies (1996) Glycobiology, 6, pp. 131-139
• Yu, L.X., Setter, T.L., Comparative transcriptional profiling of placenta and endosperm in developing maize kernels in response to water deficit (2003) Plant Physiology, 131, pp. 568-582
• Zhang, F., Wang, Z., Dong, W., Sun, C., Wang, H., Song, A., Teng, N., Transcriptomic and proteomic analysis reveals mechanisms of embryo abortion during chrysanthemum cross breeding (2014) Scientific Reports, 4, p. 6536
• Zhao, P., Zhou, X., Zhang, L., Wang, W., Ma, L., Yang, L., Sun, M., A bipartite molecular module controls cell death activation in the basal cell lineage of plant embryos (2013) PLoS Biology, 11
• Zhong, R., Burk, D.H., Morrison, W.H., Ye, Z.-H., A kinesin-like protein is essential for oriented deposition of cellulose microfibrils and cell wall strength (2002) Plant Cell, 14, pp. 3101-3117
• Zinselmeier, C., Jeong, B.R., Boyer, J.S., Starch and the control of kernel number in maize at low water potentials (1999) Plant Physiology, 121, pp. 25-35

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