Identification of Transcriptional Networks Involved in De Novo Organ Formation in Tomato Hypocotyl Explants
暂无分享,去创建一个
[1] Toshiaki Tameshige,et al. Auxin-induced WUSCHEL-RELATED HOMEOBOX13 Mediates Asymmetric Activity of Callus Formation upon Cutting. , 2022, Plant & cell physiology.
[2] Charles W. Melnyk,et al. The regeneration factors ERF114 and ERF115 regulate auxin-mediated lateral root development in response to mechanical cues. , 2022, Molecular plant.
[3] Y. Noh,et al. REGENOMICS: A web-based application for plant REGENeration-associated transcriptOMICS analyses , 2022, Computational and structural biotechnology journal.
[4] S. E. Perry,et al. AGL15 Promotion of Somatic Embryogenesis: Role and Molecular Mechanism , 2022, Frontiers in Plant Science.
[5] J. Trontin,et al. Constitutive Overexpression of a Conifer WOX2 Homolog Affects Somatic Embryo Development in Pinus pinaster and Promotes Somatic Embryogenesis and Organogenesis in Arabidopsis Seedlings , 2022, Frontiers in Plant Science.
[6] OUP accepted manuscript , 2022, Journal Of Experimental Botany.
[7] Y. Ren,et al. Genome-wide investigation of the AP2/ERF gene family in ginger: evolution and expression profiling during development and abiotic stresses , 2021, BMC plant biology.
[8] Nobutaka Mitsuda,et al. Wound-inducible WUSCHEL-RELATED HOMEOBOX 13 is required for callus growth and organ reconnection , 2021, Plant physiology.
[9] Lin Xu,et al. Pluripotency acquisition in the middle cell layer of callus is required for organ regeneration , 2021, Nature Plants.
[10] A. Sánchez-García,et al. Dynamic Hormone Gradients Regulate Wound-Induced de novo Organ Formation in Tomato Hypocotyl Explants , 2021, International journal of molecular sciences.
[11] A. Sánchez-García,et al. Tissue-Specific Metabolic Reprogramming during Wound-Induced Organ Formation in Tomato Hypocotyl Explants , 2021, International journal of molecular sciences.
[12] K. Shirasu,et al. WIND transcription factors orchestrate wound‐induced callus formation, vascular reconnection and defense response in Arabidopsis , 2021, The New phytologist.
[13] L. De Veylder,et al. Transcriptional activation of auxin biosynthesis drives developmental reprogramming of differentiated cells , 2021, bioRxiv.
[14] Y. Matsukura,et al. Wound-inducible ANAC071 and ANAC096 transcription factors promote cambial cell formation in incised Arabidopsis flowering stems , 2021, Communications biology.
[15] Kalika Prasad,et al. Model systems for regeneration: Arabidopsis , 2021, Development.
[16] Z. Lippman,et al. Conserved pleiotropy of an ancient plant homeobox gene uncovered by cis-regulatory dissection , 2021, Cell.
[17] P. Perata,et al. The Oxidative Paradox in Low Oxygen Stress in Plants , 2021, Antioxidants.
[18] A. Sánchez-García,et al. An Auxin-Mediated Regulatory Framework for Wound-Induced Adventitious Root Formation in Tomato Shoot Explants. , 2021, Plant, cell & environment.
[19] F. Cejudo,et al. Redox regulation of chloroplast metabolism , 2020, Plant physiology.
[20] Junhong Zhang,et al. Genome-Wide Identification and Molecular Characterization of the Growth-Regulating Factors-Interacting Factor Gene Family in Tomato , 2020, Genes.
[21] J. Medina,et al. The Arabidopsis Transcription Factor CDF3 Is Involved in Nitrogen Responses and Improves Nitrogen Use Efficiency in Tomato , 2020, Frontiers in Plant Science.
[22] I. Efroni,et al. A conserved superlocus regulates above- and belowground root initiation , 2020, bioRxiv.
[23] X. Zhang,et al. ARF4 regulates shoot regeneration through coordination with ARF5 and IAA12 , 2020, Plant Cell Reports.
[24] J. Pérez-Pérez,et al. Understanding of Adventitious Root Formation: What Can We Learn From Comparative Genetics? , 2020, Frontiers in Plant Science.
[25] R. Mittler,et al. Integration of ROS and hormone signaling during abiotic stress. , 2020, The Plant journal : for cell and molecular biology.
[26] Javier F. Palatnik,et al. A GRF-GIF chimeric protein improves the regeneration efficiency of transgenic plants , 2020, Nature Biotechnology.
[27] Tingting Zhu,et al. The Cyclin CYCA3;4 Is a Postprophase Target of the APC/CCCS52A2 E3-Ligase Controlling Formative Cell Divisions in Arabidopsis , 2020, Plant Cell.
[28] Ronita Nag Chaudhuri,et al. ABI3 plays a role in de-novo root regeneration from Arabidopsis thaliana callus cells , 2020, Plant signaling & behavior.
[29] Y. Noh,et al. De novo shoot regeneration controlled by HEN1 and TCP3/4 in Arabidopsis. , 2020, Plant & cell physiology.
[30] Qi He,et al. Genome-wide identification and expression analysis of the NAC transcription factor family in tomato (Solanum lycopersicum) during aluminum stress , 2020, BMC Genomics.
[31] Juan Li,et al. MYB94 and MYB96 additively inhibit callus formation via directly repressing LBD29 expression in Arabidopsis thaliana. , 2020, Plant science : an international journal of experimental plant biology.
[32] J. Medina,et al. CDF transcription factors: plant regulators to deal with extreme environmental conditions. , 2020, Journal of experimental botany.
[33] Dazhong Zhao,et al. Arabidopsis ZINC FINGER PROTEIN1 Acts Downstream of GL2 to Repress Root Hair Initiation and Elongation by Directly Suppressing bHLH Genes[OPEN]. , 2020, The Plant cell.
[34] Runan Yao,et al. ShinyGO: a graphical gene-set enrichment tool for animals and plants , 2019, Bioinform..
[35] Jinpu Jin,et al. PlantRegMap: charting functional regulatory maps in plants , 2019, Nucleic Acids Res..
[36] Xin Hu,et al. Genome-wide identification of C2H2 zinc-finger genes and their expression patterns under heat stress in tomato (Solanum lycopersicum L.) , 2019, PeerJ.
[37] Dazhong Zhao,et al. Arabidopsis ZINC FINGER PROTEIN1 Acts Downstream of GL2 to Repress Root Hair Initiation and Elongation by Directly Suppressing bHLH Genes[OPEN] , 2019, Plant Cell.
[38] Jia-Wei Wang,et al. AP2/ERF Transcription Factors Integrate Age and Wound Signals for Root Regeneration[OPEN] , 2019, Plant Cell.
[39] Ari Pekka Mähönen,et al. Gradient Expression of Transcription Factor Imposes a Boundary on Organ Regeneration Potential in Plants. , 2019, Cell reports.
[40] Nobutoshi Yamaguchi,et al. Lateral root initiation requires the sequential induction of transcription factors LBD16 and PUCHI in Arabidopsis thaliana. , 2019, The New phytologist.
[41] Qiang Li,et al. RedoxiBase: A database for ROS homeostasis regulated proteins , 2019, Redox biology.
[42] Zongli Hu,et al. Genome-Wide Analysis of the MADS-Box Transcription Factor Family in Solanum lycopersicum , 2019, International journal of molecular sciences.
[43] I. Blilou,et al. A Jasmonate Signaling Network Activates Root Stem Cells and Promotes Regeneration , 2019, Cell.
[44] A. Iwase,et al. Molecular Mechanisms of Plant Regeneration. , 2019, Annual review of plant biology.
[45] Li Yang,et al. Jasmonate-mediated wound signalling promotes plant regeneration , 2019, Nature Plants.
[46] Ji-Young Lee,et al. Reprogramming of the cambium regulators during adventitious root development upon wounding of storage tap roots in radish (Raphanus sativus L.) , 2019, Biology Open.
[47] K. Lowe,et al. Using Morphogenic Genes to Improve Recovery and Regeneration of Transgenic Plants , 2019, Plants.
[48] H. Harada,et al. HIF-1-Dependent Reprogramming of Glucose Metabolic Pathway of Cancer Cells and Its Therapeutic Significance , 2019, International journal of molecular sciences.
[49] Eun Woo Son,et al. iDEP: an integrated web application for differential expression and pathway analysis of RNA-Seq data , 2018, BMC Bioinformatics.
[50] C. Liu,et al. Correction: Li, X.; et al. Identification and Characterization of the WOX Family Genes in Five Solanaceae Species Reveal Their Conserved Roles in Peptide Signaling. Genes 2018, 9, 260. , 2018, Genes.
[51] A. Salman,et al. Identification and Characterization of the WOX Family Genes in Five Solanaceae Species Reveal Their Conserved Roles in Peptide Signaling , 2018, Genes.
[52] Yuxin Hu,et al. Genome-Wide Identification of Arabidopsis LBD29 Target Genes Reveals the Molecular Events behind Auxin-Induced Cell Reprogramming during Callus Formation , 2018, Plant & cell physiology.
[53] Siobhan M Brady,et al. A Gene Regulatory Network for Cellular Reprogramming in Plant Regeneration , 2018, Plant & cell physiology.
[54] Hui Zhang,et al. Thioredoxin-Mediated ROS Homeostasis Explains Natural Variation in Plant Regeneration1[OPEN] , 2018, Plant Physiology.
[55] J. Chandler. Class VIIIb APETALA2 Ethylene Response Factors in Plant Development. , 2017, Trends in plant science.
[56] Thomas J. Hardcastle,et al. Transcriptome dynamics at Arabidopsis graft junctions reveal an intertissue recognition mechanism that activates vascular regeneration , 2017, Proceedings of the National Academy of Sciences.
[57] T. Zhao,et al. A Genome-Wide Analysis of GATA Transcription Factor Family in Tomato and Analysis of Expression Patterns , 2018 .
[58] T. Zhao,et al. Genome-wide identification and characterization of GRAS transcription factors in tomato (Solanum lycopersicum) , 2017, PeerJ.
[59] Zachary B. Lippman,et al. Engineering Quantitative Trait Variation for Crop Improvement by Genome Editing , 2017, Cell.
[60] A. Chini,et al. Identification of TIFY/JAZ family genes in Solanum lycopersicum and their regulation in response to abiotic stresses , 2017, PloS one.
[61] J. Flexas,et al. Ectopic Expression of CDF3 Genes in Tomato Enhances Biomass Production and Yield under Salinity Stress Conditions , 2017, Front. Plant Sci..
[62] C. K. Kim,et al. Molecular Characterization and Expression Profiling of Tomato GRF Transcription Factor Family Genes in Response to Abiotic Stresses and Phytohormones , 2017, International journal of molecular sciences.
[63] Y. Eshed,et al. Coordination of auxin-triggered leaf initiation by tomato LEAFLESS , 2017, Proceedings of the National Academy of Sciences.
[64] M. A. Moreno-Risueno,et al. The transcription factor OBP4 controls root growth and promotes callus formation. , 2017, The New phytologist.
[65] Chao Zhou,et al. FUSCA3 interacting with LEAFY COTYLEDON2 controls lateral root formation through regulating YUCCA4 gene expression in Arabidopsis thaliana. , 2017, The New phytologist.
[66] Ge Gao,et al. PlantTFDB 4.0: toward a central hub for transcription factors and regulatory interactions in plants , 2016, Nucleic Acids Res..
[67] P. Benfey,et al. Control of Arabidopsis lateral root primordium boundaries by MYB36. , 2017, The New phytologist.
[68] T. Schmülling,et al. ERF105 is a transcription factor gene of Arabidopsis thaliana required for freezing tolerance and cold acclimation. , 2017, Plant, cell & environment.
[69] K. Morohashi,et al. WIND1 Promotes Shoot Regeneration through Transcriptional Activation of ENHANCER OF SHOOT REGENERATION1 in Arabidopsis[OPEN] , 2016, Plant Cell.
[70] G. Martin,et al. iTAK: A Program for Genome-wide Prediction and Classification of Plant Transcription Factors, Transcriptional Regulators, and Protein Kinases. , 2016, Molecular plant.
[71] G. Persiau,et al. The heterodimeric transcription factor complex ERF115–PAT1 grants regeneration competence , 2016, Nature Plants.
[72] S. Brady,et al. Transcriptional Regulation of Arabidopsis Polycomb Repressive Complex 2 Coordinates Cell-Type Proliferation and Differentiation[OPEN] , 2016, Plant Cell.
[73] R. Peng,et al. Genome-Wide Identification and Analysis of the MYB Transcription Factor Superfamily in Solanum lycopersicum. , 2016, Plant & cell physiology.
[74] R. Satija,et al. Root Regeneration Triggers an Embryo-like Sequence Guided by Hormonal Interactions , 2016, Cell.
[75] A. Iwase,et al. Plant regeneration: cellular origins and molecular mechanisms , 2016, Development.
[76] Y. Tsutsumi,et al. Diverse functions and reactions of class III peroxidases. , 2016, The New phytologist.
[77] P. J. King,et al. NRF2 Orchestrates the Metabolic Shift during Induced Pluripotent Stem Cell Reprogramming , 2016, Cell reports.
[78] Quirin L Ranftl,et al. LLM-Domain Containing B-GATA Factors Control Different Aspects of Cytokinin-Regulated Development in Arabidopsis thaliana1[OPEN] , 2016, Plant Physiology.
[79] Yunbo Luo,et al. Genome-wide analysis of tomato NF-Y factors and their role in fruit ripening , 2016, BMC Genomics.
[80] Z. Ye,et al. Genome-wide identification and expression profiling analysis of trihelix gene family in tomato. , 2015, Biochemical and biophysical research communications.
[81] M. Blázquez,et al. A bHLH-Based Feedback Loop Restricts Vascular Cell Proliferation in Plants. , 2015, Developmental cell.
[82] Z. Ye,et al. Comprehensive analysis and expression profile of the homeodomain leucine zipper IV transcription factor family in tomato. , 2015, Plant physiology and biochemistry : PPB.
[83] F. Fu,et al. Genome-wide systematic characterization of the bZIP transcriptional factor family in tomato (Solanum lycopersicum L.) , 2015, BMC Genomics.
[84] T. Demura,et al. Transcriptional repression by MYB3R proteins regulates plant organ growth , 2015, The EMBO journal.
[85] E. Meyerowitz,et al. PLETHORA Genes Control Regeneration by a Two-Step Mechanism , 2015, Current Biology.
[86] R. Beckett,et al. Roles of apoplastic peroxidases in plant response to wounding. , 2015, Phytochemistry.
[87] H. Ezura,et al. WIND1-based acquisition of regeneration competency in Arabidopsis and rapeseed , 2015, Journal of Plant Research.
[88] Jinyan Wang,et al. Genome-wide analysis of bHLH transcription factor and involvement in the infection by yellow leaf curl virus in tomato (Solanum lycopersicum) , 2015, BMC Genomics.
[89] H. Fukuda,et al. A bHLH Complex Activates Vascular Cell Division via Cytokinin Action in Root Apical Meristem , 2014, Current Biology.
[90] P. L. Chang,et al. CYCP2;1 integrates genetic and nutritional information to promote meristem cell division in Arabidopsis. , 2014, Developmental biology.
[91] Ruirui Xu. Genome-wide analysis and identification of stress-responsive genes of the CCCH zinc finger family in Solanum lycopersicum , 2014, Molecular Genetics and Genomics.
[92] T. Laux,et al. WOX13-like genes are required for reprogramming of leaf and protoplast cells into stem cells in the moss Physcomitrella patens , 2014, Development.
[93] R. Sablowski,et al. Arabidopsis JAGGED links floral organ patterning to tissue growth by repressing Kip-related cell cycle inhibitors , 2014, Proceedings of the National Academy of Sciences.
[94] Hai Huang,et al. Genetic and epigenetic controls of plant regeneration. , 2014, Current topics in developmental biology.
[95] Nobutaka Mitsuda,et al. Arabidopsis WIND1 induces callus formation in rapeseed, tomato, and tobacco , 2013, Plant signaling & behavior.
[96] Pierre Barbier de Reuille,et al. A bHLH complex controls embryonic vascular tissue establishment and indeterminate growth in Arabidopsis. , 2013, Developmental cell.
[97] E. Knaap,et al. Genome-wide identification, phylogeny and expression analysis of SUN, OFP and YABBY gene family in tomato , 2013, Molecular Genetics and Genomics.
[98] Patrick Xuechun Zhao,et al. PlantTFcat: an online plant transcription factor and transcriptional regulator categorization and analysis tool , 2013, BMC Bioinformatics.
[99] Nobuhiro Suzuki,et al. Reactive oxygen species-dependent wound responses in animals and plants. , 2012, Free radical biology & medicine.
[100] Z. Fei,et al. Genome-wide analysis of WRKY transcription factors in Solanum lycopersicum , 2012, Molecular Genetics and Genomics.
[101] Yuxin Hu,et al. LATERAL ORGAN BOUNDARIES DOMAIN transcription factors direct callus formation in Arabidopsis regeneration , 2012, Cell Research.
[102] T. Goh,et al. The establishment of asymmetry in Arabidopsis lateral root founder cells is regulated by LBD16/ASL18 and related LBD/ASL proteins , 2012, Development.
[103] Y. Kamiya,et al. Spatially selective hormonal control of RAP2.6L and ANAC071 transcription factors involved in tissue reunion in Arabidopsis , 2011, Proceedings of the National Academy of Sciences.
[104] I. Verstraeten,et al. CUC2 as an early marker for regeneration competence in Arabidopsis root explants. , 2011, Journal of plant physiology.
[105] M. Seki,et al. The AP2/ERF Transcription Factor WIND1 Controls Cell Dedifferentiation in Arabidopsis , 2011, Current Biology.
[106] Sonja J. Prohaska,et al. Proteinortho: Detection of (Co-)orthologs in large-scale analysis , 2011, BMC Bioinformatics.
[107] N. Tuteja,et al. Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. , 2010, Plant physiology and biochemistry : PPB.
[108] P. Benfey,et al. Transcriptional Regulation of ROS Controls Transition from Proliferation to Differentiation in the Root , 2010, Cell.
[109] I. Takahashi,et al. Two Arabidopsis cyclin A3s possess G1 cyclin-like features , 2010, Plant Cell Reports.
[110] Daniel Koenig,et al. LYRATE Is a Key Regulator of Leaflet Initiation and Lamina Outgrowth in Tomato[C][W][OA] , 2009, The Plant Cell Online.
[111] Dominique C Bergmann,et al. Regulation of the Arabidopsis root vascular initial population by LONESOME HIGHWAY , 2007, Development.
[112] S. Ochatt. Flow cytometry (ploidy determination, cell cycle analysis, DNA content per nucleus) , 2006 .
[113] Ziv Bar-Joseph,et al. STEM: a tool for the analysis of short time series gene expression data , 2006, BMC Bioinformatics.
[114] D. Inzé,et al. The DP-E2F-like Gene DEL1 Controls the Endocycle in Arabidopsis thaliana , 2005, Current Biology.
[115] R. Amasino,et al. The PLETHORA Genes Mediate Patterning of the Arabidopsis Root Stem Cell Niche , 2004, Cell.
[116] R. Ophir,et al. Plant Respiratory Burst Oxidase Homologs Impinge on Wound Responsiveness and Development in Lycopersicon esculentum Online version contains Web-only data. , 2004, The Plant Cell Online.
[117] Martin Frenz,et al. Microsurgical and laser ablation analysis of interactions between the zones and layers of the tomato shoot apical meristem , 2003, Development.
[118] S. Sabatini,et al. SCARECROW is involved in positioning the stem cell niche in the Arabidopsis root meristem. , 2003, Genes & development.
[119] E. Weber,et al. Phänologische Entwicklungsstadien von Gemüsepflanzen II. Fruchtgemüse und Hülsenfrüchte Codierung und Beschreibung nach der erweiterten BBCH-Skala - mit Abbildungen , 1995 .
[120] D. Galbraith,et al. Rapid Flow Cytometric Analysis of the Cell Cycle in Intact Plant Tissues , 1983, Science.