The Agony of Choice: How Plants Balance Growth and Survival under Water-Limiting Conditions1
暂无分享,去创建一个
[1] J. Boyer. Plant Productivity and Environment , 1982, Science.
[2] J. Boyer,et al. Complete turgor maintenance at low water potentials in the elongating region of maize leaves. , 1982, Plant physiology.
[3] P. M. Neumann,et al. Hydraulic Signals from the Roots and Rapid Cell-Wall Hardening in Growing Maize (Zea mays L.) Leaves Are Primary Responses to Polyethylene Glycol-Induced Water Deficits , 1994, Plant physiology.
[4] S. Mackenzie,et al. Nucleotide Sequence of a cDNA from Limnanthes douglasii L. Encoding a [delta]-15 Linoleic Acid Desaturase , 1995, Plant physiology.
[5] F. Tardieu,et al. Temperature Affects Expansion Rate of Maize Leaves without Change in Spatial Distribution of Cell Length (Analysis of the Coordination between Cell Division and Cell Expansion) , 1995, Plant physiology.
[6] J. Boyer,et al. Decreased Growth-Induced Water Potential (A Primary Cause of Growth Inhibition at Low Water Potentials) , 1997, Plant physiology.
[7] P. Schnable,et al. Sequence Analysis of the Cloned glossy8 Gene of Maize Suggests That It May Code for a [beta]-Ketoacyl Reductase Required for the Biosynthesis of Cuticular Waxes , 1997, Plant physiology.
[8] R. Munns,et al. Effect of water stress on cell division and cell-division-cycle 2-like cell-cycle kinase activity in wheat leaves , 1998, Plant physiology.
[9] M. Zivy,et al. Protein changes in response to progressive water deficit in maize . Quantitative variation and polypeptide identification , 1998, Plant physiology.
[10] F. Tardieu,et al. Spatial distributions of expansion rate, cell division rate and cell size in maize leaves: a synthesis of the effects of soil water status, evaporative demand and temperature. , 2000, Journal of experimental botany.
[11] D. Inzé,et al. Spatial distribution of cell division rate can be deduced from that of p34(cdc2) kinase activity in maize leaves grown at contrasting temperatures and soil water conditions. , 2000, Plant physiology.
[12] M. Geisler,et al. Oriented Asymmetric Divisions That Generate the Stomatal Spacing Pattern in Arabidopsis Are Disrupted by the too many mouths Mutation , 2000, Plant Cell.
[13] D. Inzé,et al. Expression of cell cycle regulatory genes and morphological alterations in response to salt stress in Arabidopsis thaliana , 2000, Planta.
[14] J. Araus,et al. Plant breeding and drought in C3 cereals: what should we breed for? , 2002, Annals of botany.
[15] Alcalde Rovira Roure. Plant Breeding and Drought in C 3 Cereals: What Should We Breed For? , 2002 .
[16] Alain Charcosset,et al. Combining Quantitative Trait Loci Analysis and an Ecophysiological Model to Analyze the Genetic Variability of the Responses of Maize Leaf Growth to Temperature and Water Deficit1 , 2003, Plant Physiology.
[17] J. Kim,et al. The AtGRF family of putative transcription factors is involved in leaf and cotyledon growth in Arabidopsis. , 2003, The Plant journal : for cell and molecular biology.
[18] J. Boyer,et al. Change in XET activities, cell wall extensibility and hypocotyl elongation of soybean seedlings at low water potential , 2005, Planta.
[19] G. Kudoyarova,et al. Effect of PEG-treatment on the leaf growth response and auxin content in shoots of wheat seedlings , 2002, Plant Growth Regulation.
[20] V. Shulaev,et al. When Defense Pathways Collide. The Response of Arabidopsis to a Combination of Drought and Heat Stress1[w] , 2004, Plant Physiology.
[21] Robert Ascenzi,et al. Molecular genetic analysis of the drought-inducible linker histone variant in Arabidopsis thaliana , 1999, Plant Molecular Biology.
[22] W. Jury,et al. The role of science in solving the world's emerging water problems. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[23] D. Inzé,et al. The elongata mutants identify a functional Elongator complex in plants with a role in cell proliferation during organ growth. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[24] D. Cosgrove. Growth of the plant cell wall , 2005, Nature Reviews Molecular Cell Biology.
[25] C. Granier,et al. Plasticity to soil water deficit in Arabidopsis thaliana: dissection of leaf development into underlying growth dynamic and cellular variables reveals invisible phenotypes. , 2006, Plant, cell & environment.
[26] T. Mészáros,et al. Activation of an alfalfa cyclin-dependent kinase inhibitor by calmodulin-like domain protein kinase. , 2006, The Plant journal : for cell and molecular biology.
[27] Patrick Achard,et al. Integration of Plant Responses to Environmentally Activated Phytohormonal Signals , 2006, Science.
[28] K. Chenu,et al. PHENOPSIS, an automated platform for reproducible phenotyping of plant responses to soil water deficit in Arabidopsis thaliana permitted the identification of an accession with low sensitivity to soil water deficit. , 2006, The New phytologist.
[29] Jianhua Zhu,et al. Methods and concepts in quantifying resistance to drought, salt and freezing, abiotic stresses that affect plant water status. , 2006, The Plant journal : for cell and molecular biology.
[30] L. Schreiber,et al. The short-term growth response to salt of the developing barley leaf. , 2006, Journal of experimental botany.
[31] J. H. Costa,et al. AOX--a functional marker for efficient cell reprogramming under stress? , 2006, Trends in plant science.
[32] F. Tardieu,et al. Association of Specific Expansins with Growth in Maize Leaves Is Maintained under Environmental, Genetic, and Developmental Sources of Variation1[C][W][OA] , 2006, Plant Physiology.
[33] J. Nap,et al. The SWI/SNF chromatin-remodeling gene AtCHR12 mediates temporary growth arrest in Arabidopsis thaliana upon perceiving environmental stress. , 2007, The Plant journal : for cell and molecular biology.
[34] M. Foolad,et al. Roles of glycine betaine and proline in improving plant abiotic stress resistance , 2007 .
[35] J. Avice,et al. Peroxidases and lignification in relation to the intensity of water-deficit stress in white clover (Trifolium repens L.). , 2007, Journal of experimental botany.
[36] D. Bergmann,et al. Stomatal development. , 2007, Annual review of plant biology.
[37] D. Inzé,et al. Novel Plant-specific Cyclin-dependent Kinase Inhibitors Induced by Biotic and Abiotic Stresses* , 2007, Journal of Biological Chemistry.
[38] Dirk Inzé,et al. The ins and outs of the plant cell cycle , 2007, Nature Reviews Molecular Cell Biology.
[39] Dirk Inzé,et al. Mitochondrial type-I prohibitins of Arabidopsis thaliana are required for supporting proficient meristem development. , 2007, The Plant journal : for cell and molecular biology.
[40] P. Achard,et al. Plant DELLAs Restrain Growth and Promote Survival of Adversity by Reducing the Levels of Reactive Oxygen Species , 2008, Current Biology.
[41] Stuart A. Casson,et al. Influence of environmental factors on stomatal development. , 2008, The New phytologist.
[42] C. Tonelli,et al. Over-expression of the Arabidopsis AtMYB41 gene alters cell expansion and leaf surface permeability. , 2008, The Plant journal : for cell and molecular biology.
[43] E. Mazzucotelli,et al. Drought tolerance improvement in crop plants: An integrated view from breeding to genomics , 2008 .
[44] Daniel L. Mace,et al. Cell Identity Mediates the Response of Arabidopsis Roots to Abiotic Stress , 2008, Science.
[45] Elizabeth Pennisi,et al. The Blue Revolution, Drop by Drop, Gene by Gene , 2008, Science.
[46] C. Granier,et al. Rewatering plants after a long water-deficit treatment reveals that leaf epidermal cells retain their ability to expand after the leaf has apparently reached its final size. , 2008, Annals of botany.
[47] P. Hedden,et al. The Cold-Inducible CBF1 Factor–Dependent Signaling Pathway Modulates the Accumulation of the Growth-Repressing DELLA Proteins via Its Effect on Gibberellin Metabolism[W] , 2008, The Plant Cell Online.
[48] Adam J. Carroll,et al. The Absence of ALTERNATIVE OXIDASE1a in Arabidopsis Results in Acute Sensitivity to Combined Light and Drought Stress[W][OA] , 2008, Plant Physiology.
[49] K. Yamaguchi-Shinozaki,et al. Update on Abiotic Stresses in Arabidopsis and Grasses Transcriptional Regulatory Networks in Response to Abiotic Stresses in Arabidopsis and Grasses , 2008 .
[50] K. Oda,et al. The DDF1 transcriptional activator upregulates expression of a gibberellin-deactivating gene, GA2ox7, under high-salinity stress in Arabidopsis. , 2008, The Plant journal : for cell and molecular biology.
[51] Christopher P. Bonin,et al. ’ s Choice Series on the Next Generation of Biotech Crops Bacterial RNA Chaperones Confer Abiotic Stress Tolerance in Plants and Improved Grain Yield in Maize under Water-Limited Conditions [ W ] , 2008 .
[52] I. Sabirzhanova,et al. Changes in expansin gene expression, IAA content, and extension growth of leaf cells in maize plants subjected to salinity , 2008, Russian Journal of Plant Physiology.
[53] L. Aguirrezábal,et al. Genetic variability for leaf growth rate and duration under water deficit in sunflower: analysis of responses at cell, organ, and plant level. , 2008, Journal of experimental botany.
[54] S. Dhondt,et al. Gibberellin Signaling Controls Cell Proliferation Rate in Arabidopsis , 2009, Current Biology.
[55] Abraham Blum,et al. Effective use of water (EUW) and not water-use efficiency (WUE) is the target of crop yield improvement under drought stress , 2009 .
[56] D. Inzé,et al. Developmental Stage Specificity and the Role of Mitochondrial Metabolism in the Response of Arabidopsis Leaves to Prolonged Mild Osmotic Stress1[C][W][OA] , 2009, Plant Physiology.
[57] S. Wilkinson,et al. Drought, ozone, ABA and ethylene: new insights from cell to plant to community. , 2010, Plant, cell & environment.
[58] Magalie Uyttewaal,et al. Integrating physical stress, growth, and development. , 2010, Current opinion in plant biology.
[59] R. Richards,et al. Breeding for improved water productivity in temperate cereals: phenotyping, quantitative trait loci, markers and the selection environment , 2010 .
[60] F. Tardieu,et al. Rice leaf growth and water potential are resilient to evaporative demand and soil water deficit once the effects of root system are neutralized. , 2010, Plant, cell & environment.
[61] D. Inzé,et al. More from less: plant growth under limited water. , 2010, Current opinion in biotechnology.
[62] Martin Kuiper,et al. Targeted interactomics reveals a complex core cell cycle machinery in Arabidopsis thaliana , 2010, Molecular systems biology.
[63] F. Tardieu,et al. Control of leaf growth by abscisic acid: hydraulic or non-hydraulic processes? , 2010, Plant, cell & environment.
[64] M. Seki,et al. Chromatin regulation functions in plant abiotic stress responses. , 2010, Plant, cell & environment.
[65] A. Savouré,et al. Proline: a multifunctional amino acid. , 2010, Trends in plant science.
[66] Yafan Huang,et al. Narrowing down the targets: towards successful genetic engineering of drought-tolerant crops. , 2010, Molecular plant.
[67] Nobuhiro Suzuki,et al. Reactive oxygen species homeostasis and signalling during drought and salinity stresses. , 2010, Plant, cell & environment.
[68] S. Chen,et al. NIMA-related kinase NEK6 affects plant growth and stress response in Arabidopsis. , 2011, The Plant journal : for cell and molecular biology.
[69] Y. Gibon,et al. Water deficits uncouple growth from photosynthesis, increase C content, and modify the relationships between C and growth in sink organs. , 2011, Journal of experimental botany.
[70] P. Verslues,et al. Essential Role of Tissue-Specific Proline Synthesis and Catabolism in Growth and Redox Balance at Low Water Potential1[W][OA] , 2011, Plant Physiology.
[71] C. Tonelli,et al. Survival and growth of Arabidopsis plants given limited water are not equal , 2011, Nature Biotechnology.
[72] A. Millar,et al. The role of mitochondrial respiration in salinity tolerance. , 2011, Trends in plant science.
[73] Yutaka Sato,et al. RSS1 regulates the cell cycle and maintains meristematic activity under stress conditions in rice , 2011, Nature communications.
[74] Akira Oikawa,et al. Pause-and-Stop: The Effects of Osmotic Stress on Cell Proliferation during Early Leaf Development in Arabidopsis and a Role for Ethylene Signaling in Cell Cycle Arrest[W] , 2011, Plant Cell.
[75] J. Tollefson. Drought-tolerant maize gets US debut , 2011, Nature.
[76] J. Araus,et al. Enhancing drought tolerance in C(4) crops. , 2011, Journal of experimental botany.
[77] F. Tardieu,et al. Do pH changes in the leaf apoplast contribute to rapid inhibition of leaf elongation rate by water stress? Comparison of stress responses induced by polyethylene glycol and down-regulation of root hydraulic conductivity. , 2011, Plant, cell & environment.
[78] D. Inzé,et al. A reciprocal 15N-labeling proteomic analysis of expanding Arabidopsis leaves subjected to osmotic stress indicates importance of mitochondria in preserving plastid functions. , 2011, Journal of proteome research.
[79] Mark Stitt,et al. Systems-based analysis of Arabidopsis leaf growth reveals adaptation to water deficit , 2012, Molecular systems biology.
[80] J. Heard,et al. Drought tolerance through biotechnology: improving translation from the laboratory to farmers' fields. , 2012, Current opinion in biotechnology.
[81] Zhanyuan J. Zhang,et al. Overexpression of AtDREB1A Causes a Severe Dwarf Phenotype by Decreasing Endogenous Gibberellin Levels in Soybean [Glycine max (L.) Merr.] , 2012, PloS one.
[82] B. Mueller‐Roeber,et al. ROS homeostasis during development: an evolutionary conserved strategy , 2012, Cellular and Molecular Life Sciences.
[83] Frank Van Breusegem,et al. AtWRKY15 perturbation abolishes the mitochondrial stress response that steers osmotic stress tolerance in Arabidopsis , 2012, Proceedings of the National Academy of Sciences.
[84] Simon R. Law,et al. Cyclin-dependent Kinase E1 (CDKE1) Provides a Cellular Switch in Plants between Growth and Stress Responses , 2012, The Journal of Biological Chemistry.
[85] D. Inzé,et al. DELLA Signaling Mediates Stress-Induced Cell Differentiation in Arabidopsis Leaves through Modulation of Anaphase-Promoting Complex/Cyclosome Activity1[W][OA] , 2012, Plant Physiology.
[86] François Tardieu,et al. Any trait or trait-related allele can confer drought tolerance: just design the right drought scenario. , 2012, Journal of experimental botany.
[87] Arjun Krishnan,et al. Effects of Drought on Gene Expression in Maize Reproductive and Leaf Meristem Tissue Revealed by RNA-Seq1[W][OA] , 2012, Plant Physiology.
[88] K. Shinozaki,et al. Arabidopsis GROWTH-REGULATING FACTOR7 Functions as a Transcriptional Repressor of Abscisic Acid– and Osmotic Stress–Responsive Genes, Including DREB2A[W] , 2012, Plant Cell.
[89] S. Komaki,et al. Control of the plant cell cycle by developmental and environmental cues. , 2012, Plant & cell physiology.
[90] J. Araus,et al. Phenotyping maize for adaptation to drought , 2012, Front. Physio..
[91] J. Bailey-Serres,et al. Waterproofing Crops: Effective Flooding Survival Strategies1 , 2012, Plant Physiology.
[92] T. Juenger,et al. Physiological Genomics of Response to Soil Drying in Diverse Arabidopsis Accessions[W][OA] , 2012, Plant Cell.
[93] D. Inzé,et al. A Local Maximum in Gibberellin Levels Regulates Maize Leaf Growth by Spatial Control of Cell Division , 2012, Current Biology.
[94] G. Kang,et al. Proteomics reveals the effects of salicylic acid on growth and tolerance to subsequent drought stress in wheat. , 2012, Journal of proteome research.
[95] James A.H. Murray,et al. A Bistable Circuit Involving SCARECROW-RETINOBLASTOMA Integrates Cues to Inform Asymmetric Stem Cell Division , 2012, Cell.
[96] H. Seo,et al. Overexpression of stress-related genes, BrERF4 and AtMYB44, in Arabidopsis thaliana alters cell expansion but not cell proliferation during leaf growth , 2012, Journal of Plant Biology.
[97] Dirk Inzé,et al. Leaf size control: complex coordination of cell division and expansion. , 2012, Trends in plant science.
[98] F. Tardieu,et al. Phosphoproteome Dynamics Upon Changes in Plant Water Status Reveal Early Events Associated With Rapid Growth Adjustment in Maize Leaves* , 2012, Molecular & Cellular Proteomics.
[99] D. Lawlor. Genetic engineering to improve plant performance under drought: physiological evaluation of achievements, limitations, and possibilities. , 2013, Journal of experimental botany.
[100] M. Bennett,et al. Endodermal ABA Signaling Promotes Lateral Root Quiescence during Salt Stress in Arabidopsis Seedlings[C][W] , 2013, Plant Cell.
[101] Dirk Inzé,et al. ETHYLENE RESPONSE FACTOR6 Acts as a Central Regulator of Leaf Growth under Water-Limiting Conditions in Arabidopsis1[C][W][OA] , 2013, Plant Physiology.
[102] Y. Kamiya,et al. ABA inhibits entry into stomatal-lineage development in Arabidopsis leaves. , 2013, The Plant journal : for cell and molecular biology.
[103] D. Inzé,et al. Addressing the Role of microRNAs in Reprogramming Leaf Growth during Drought Stress in Brachypodium distachyon , 2012, Molecular plant.
[104] K. Shinozaki,et al. Osmotic Stress Responses and Plant Growth Controlled by Potassium Transporters in Arabidopsis[C][W] , 2013, Plant Cell.
[105] Pengcheng Wang,et al. The MPK 6-ERF 6-ROS-Responsive cis-Acting Element 7 / GCC Box Complex Modulates Oxidative Gene Transcription and the Oxidative Response in Arabidopsis 1 [ W ] [ OA ] , 2013 .
[106] D. Inzé,et al. Molecular and physiological analysis of growth-limiting drought stress in Brachypodium distachyon leaves. , 2013, Molecular plant.
[107] Hongmei Yu,et al. GASA14 regulates leaf expansion and abiotic stress resistance by modulating reactive oxygen species accumulation. , 2013, Journal of experimental botany.
[108] Yanyan Du,et al. The MPK6-ERF6-ROS-Responsive cis-Acting Element7/GCC Box Complex Modulates Oxidative Gene Transcription and the Oxidative Response in Arabidopsis1[W][OA] , 2013, Plant Physiology.
[109] S. Rasmussen,et al. Transcriptome Responses to Combinations of Stresses in Arabidopsis1[W][OA] , 2013, Plant Physiology.
[110] Xiangzong Meng,et al. Phosphorylation of an ERF Transcription Factor by Arabidopsis MPK3/MPK6 Regulates Plant Defense Gene Induction and Fungal Resistance[C][W] , 2013, Plant Cell.