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Referencias:

• Menand, B., An ancient mechanism controls the development of cells with a rooting function in land plants (2007) Science, 316, pp. 1477-1480
• Datta, S., Prescott, H., Dolan, L., Intensity of a pulse of rsl4 transcription factor synthesis determines arabidopsis root hair cell size (2015) Nat Plants, 1, p. 15138
• Slabaugh, E., Held, M., Brandizzi, F., Control of root hair development in arabidopsis thaliana by an endoplasmic reticulum anchored member of the r2r3-myb transcription factor family (2011) Plant J, 67, pp. 395-405
• Xu, P., Hdg11 upregulates cell-wall-loosening protein genes to promote root elongation in arabidopsis (2014) J Exp Bot, 65, pp. 4285-4295
• Yi, K., Menand, B., Bell, E., Dolan, L., A basic helix-loop-helix transcription factor controls cell growth and size in root hairs (2010) Nat Genet, 42, pp. 264-267
• Salazar-Henao, J.E., Schmidt, W., An inventory of nutrient-responsive genes in arabidopsis root hairs (2016) Front Plant Sci, 7, p. 237
• Song, L., The molecular mechanism of ethylene-mediated root hair development induced by phosphate starvation (2016) PLoS Genet, 12, p. e1006194
• Guilfoyle, T., Hagen, G., Ulmasov, T., Murfett, J., How does auxin turn on genes? (1998) Plant Physiol, 118, pp. 341-347
• Fukaki, H., Tameda, S., Masuda, H., Tasaka, M., Lateral root formation is blocked by a gain-of-function mutation in the solitary-root/iaa14 gene of arabidopsis (2002) Plant J, 29, pp. 153-168
• Bargmann, B.O.R., A map of cell type-specific auxin responses (2013) Mol Syst Biol, 9, p. 688
• Okushima, Y., Functional genomic analysis of the auxin response factor gene family members in arabidopsis thaliana: Unique and overlapping functions of arf7 and arf19 (2005) Plant Cell, 17, pp. 444-463
• Foreman, J., Reactive oxygen species produced by nadph oxidase regulate plant cell growth (2003) Nature, 422, pp. 442-446
• Wu, J., Spermidine oxidase-derived h2o2 regulates pollen plasma membrane hyperpolarization-Activated ca2+-permeable channels and pollen tube growth (2010) Plant J, 63, pp. 1042-1053
• Lee, Y., Rubio, M.C., Alassimone, J., Geldner, N., A mechanism for localized lignin deposition in the endodermis (2013) Cell, 153, pp. 402-412
• Xie, H.-T., Wan, Z.-Y., Li, S., Zhang, Y., Spatiotemporal production of reactive oxygen species by nadph oxidase is critical for tapetal programmed cell death and pollen development in arabidopsis (2014) Plant Cell, 26, pp. 2007-2023
• Orman-Ligeza, B., Rboh-mediated ros production facilitates lateral root emergence in arabidopsis (2016) Development, 143, pp. 3328-3339
• Monshausen, G.B., Bibikova, T.N., Messerli, M.A., Shi, C., Gilroy, S., Oscillations in extracellular ph and reactive oxygen species modulate tip growth of arabidopsis root hairs (2007) Proc Natl Acad Sci USA, 104, pp. 20996-21001
• Takeda, S., Local positive feedback regulation determines cell shape in root hair cells (2008) Science, 319, pp. 1241-1244
• Boisson-Dernier, A., Anxur receptor-like kinases coordinate cell wall integrity with growth at the pollen tube tip via nadph oxidases (2013) PLoS Biol, 11, p. e1001719
• Passardi, F., Penel, C., Dunand, C., Performing the paradoxical: How plant peroxidases modify the cell wall (2004) Trends Plant Sci, 9, pp. 534-540
• Brouwer, K.S., Van Valen, T., Day, D.A., Lambers, H., Hydroxamate-stimulated o(2) uptake in roots of pisum sativum and zea mays, mediated by a peroxidase: Its consequences for respiration measurements (1986) Plant Physiol, 82, pp. 236-240
• Schlereth, A., Monopteros controls embryonic root initiation by regulating a mobile transcription factor (2010) Nature, 464, pp. 913-916
• Galli, M., Auxin signaling modules regulate maize inflorescence architecture (2015) Proc Natl Acad Sci USA, 112, pp. 13372-13377
• Lee, M.-S., An, J.-H., Cho, H.-T., Biological and molecular functions of two ear motifs of arabidopsis iaa7 (2016) J Plant Biol, 59, pp. 24-32
• Tsukagoshi, H., Busch, W., Benfey, P.N., Transcriptional regulation of ros controls transition from proliferation to differentiation in the root (2010) Cell, 143, pp. 606-616
• Lu, D., Wang, T., Persson, S., Mueller-Roeber, B., Schippers, J.H.M., Transcriptional control of ros homeostasis by kuoda1 regulates cell expansion during leaf development (2014) Nat Commun, 5, p. 3767
• Vijayakumar, P., Datta, S., Dolan, L., Root hair defective six-like4 (rsl4) promotes root hair elongation by transcriptionally regulating the expression of genes required for cell growth (2016) New Phytol, 212, pp. 944-953
• Hwang, Y., Choi, H.S., Cho, H.M., Cho, H.T., Tracheophytes contain conserved orthologs of a basic helix-loop-helix transcription factor that modulate root hair specific genes (2017) Plant Cell, 29, pp. 39-53
• Sundaravelpandian, K., Chandrika, N.N., Schmidt, W., Pft1, a transcriptional mediator complex subunit, controls root hair differentiation through reactive oxygen species (ros) distribution in arabidopsis (2013) New Phytol, 197, pp. 151-161
• Yun, B.W., S-nitrosylation of nadph oxidase regulates cell death in plant immunity (2011) Nature, 478, pp. 264-268
• Nestler, J., Roothairless5, which functions in maize (zea mays l.) root hair initiation and elongation encodes a monocot-specific nadph oxidase (2014) Plant J, 79, pp. 729-740
• Kwon, T., Transcriptional response of arabidopsis seedlings during spaceflight reveals peroxidase and cell wall remodeling genes associated with root hair development (2015) Am J Bot, 102, pp. 21-35
• Dunand, C., Crévecoeur, M., Penel, C., Distribution of superoxide and hydrogen peroxide in arabidopsis root and their influence on root development: Possible interaction with peroxidases (2007) New Phytol, 174, pp. 332-341
• Dynowski, M., Schaaf, G., Loque, D., Moran, O., Ludewig, U., Plant plasma membrane water channels conduct the signalling molecule h2o2 (2008) Biochem J, 414, pp. 53-61
• Miller, E.W., Dickinson, B.C., Chang, C.J., Aquaporin-3 mediates hydrogen peroxide uptake to regulate downstream intracellular signaling (2010) Proc Natl Acad Sci USA, 107, pp. 15681-15686
• Tian, S., Plant aquaporin atpip1;4 links apoplastic H2O2 induction to disease immunity pathways (2016) Plant Physiol, 171, pp. 1635-1650

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