F. Tardieu, C. Granier, and B. Muller, Water deficit and growth. Coordinating processes without an orchestrator? Current opinion in plant biology, 2011.
URL : https://hal.archives-ouvertes.fr/hal-02639376

P. Bhatnagar-mathur, V. Vadez, and K. K. Sharma, Transgenic approaches for abiotic stress tolerance in plants: retrospect and prospects, Plant cell reports, vol.27, pp.411-424, 2008.

W. A. Jury and H. Vaux, The role of science in solving the world's emerging water problems, Proceedings of the National Academy of Sciences of the United States of America, vol.102, p.15715, 2005.

A. V. Harter, K. A. Gardner, D. Falush, D. L. Lentz, and R. A. Bye, Origin of extant domesticated sunflowers in eastern North America, Nature, vol.430, pp.201-205, 2004.

G. J. Seiler and T. J. Gulya, Exploration for wild Helianthus species in North America: challenges and opportunities in the search for global treasures, 2004.

N. C. Kane, M. G. King, M. S. Barker, A. Raduski, and S. Karrenberg, Comparative genomic and population genetic analyses indicate highly porous genomes and high levels of gene flow between divergent Helianthus species, Evolution, vol.63, pp.2061-2075, 2009.

A. Merrien, R. Blanchet, N. Gelfi, and J. Laurent, Relationships between water supply, leaf area development and survival, and production in sunflower, Helianthus annuus L.). Agronomie, vol.1, pp.917-922, 1981.
URL : https://hal.archives-ouvertes.fr/hal-00884212

P. Casadebaig, P. Debaeke, and J. Lecoeur, Thresholds for leaf expansion and transpiration response to soil water deficit in a range of sunflower genotypes, European Journal of Agronomy, vol.28, pp.646-654, 2008.
URL : https://hal.archives-ouvertes.fr/hal-02664920

G. Kerstiens, Cuticular water permeability and its physiological significance, Journal of Experimental Botany, vol.47, pp.1813-1832, 1996.

F. Mojayad and C. Planchon, Stomatal and photosynthetic adjustment to water deficit as the expression of heterosis in sunflower, Crop science, vol.34, pp.103-107, 1994.

J. Morizet and A. Merrien, Principaux traits du comportement hydrique du tournesol, Le tournesol et l'eau. Paris: CETIOM, pp.7-20, 1990.

K. J. Mccree, C. E. Kallsen, and S. G. Richardson, Carbon Balance of Sorghum Plants during Osmotic Adjustment to Water Stress, Plant Physiol, vol.76, pp.898-902, 1984.

D. J. Cosgrove, How do plant cell walls extend?, Plant physiology, vol.102, p.1, 1993.

P. Maury, M. Berger, F. Mojayad, and C. Planchon, Leaf water characteristics and drought acclimation in sunflower genotypes, Plant and Soil, vol.223, pp.155-162, 2000.

J. P. Conroy, J. M. Virgona, R. M. Smillie, and E. W. Barlow, Influence of drought acclimation and CO2 enrichment on osmotic adjustment and chlorophyll a fluorescence of sunflower during drought, Plant physiology, vol.86, p.1108, 1988.

C. A. Chimenti and A. J. Hall, Genetic variation and changes with ontogeny of osmotic adjustment in sunflower (Helianthus annuus L.), Euphytica, vol.71, pp.201-210, 1993.

C. A. Chimenti and A. J. Hall, Responses to water stress of apoplastic water fraction and bulk modulus of elasticity in sunflower (Helianthus annuus L.) genotypes of contrasting capacity for osmotic adjustment, Plant and soil, vol.166, pp.101-107, 1994.

M. M. Jones and N. C. Turner, Osmotic adjustment in expanding and fully expanded leaves of sunflower in response to water deficits, Functional Plant Biology, vol.7, pp.181-192, 1980.

V. O. Sadras, D. J. Connor, and D. M. Whitfield, Yield, yield components and source-sink relationships in water-stressed sunflower, Field Crops Research, vol.31, pp.27-39, 1993.

M. Geisler, Transcription and Signaling Factors in the Drought Response Regulatory Network, Genes for Plant Abiotic Stress, pp.55-79, 2009.

A. Harb, A. Krishnan, M. Ambavaram, and A. Pereira, Molecular and Physiological Analysis of Drought Stress in Arabidopsis Reveals Early Responses Leading to Acclimation in Plant Growth, Plant Physiology, vol.154, issue.11, pp.1254-1271, 2010.

G. Huang, S. Ma, L. Bai, L. Zhang, and H. Ma, Signal transduction during cold, salt, and drought stresses in plants, Mol Biol Rep, vol.39, pp.969-987, 2012.

J. Zhu, Salt and drought stress signal transduction in plants, Annu Rev Plant Biol, vol.53, pp.247-273, 2002.

E. A. Bray, Classification of Genes Differentially Expressed during Waterdeficit Stress in Arabidopsis thaliana: an Analysis using Microarray and Differential Expression Data, Annals of Botany, vol.89, pp.803-811, 2002.

S. Ramanjulu and D. Bartels, Drought-and desiccation-induced modulation of gene expression in plants, Plant, cell & environment, vol.25, pp.141-151, 2002.

M. Yasuda, A. Ishikawa, Y. Jikumaru, M. Seki, and T. Umezawa, Antagonistic interaction between systemic acquired resistance and the abscisic acid-mediated abiotic stress response in Arabidopsis, The Plant Cell Online, vol.20, pp.1678-1692, 2008.

T. Umezawa, K. Nakashima, T. Miyakawa, T. Kuromori, and M. Tanokura, Molecular basis of the core regulatory network in ABA responses: sensing, signaling and transport, Plant and cell physiology, vol.51, pp.1821-1839, 2010.

T. Yoshida, Y. Fujita, H. Sayama, S. Kidokoro, and K. Maruyama, AREB1, AREB2, and ABF3 are master transcription factors that cooperatively regulate ABRE-dependent ABA signaling involved in drought stress tolerance and require ABA for full activation, The Plant Journal, vol.61, pp.672-685, 2010.

D. Golldack, I. Lüking, and O. Yang, Plant tolerance to drought and salinity: stress regulating transcription factors and their functional significance in the cellular transcriptional network, Plant cell reports, pp.1-9, 2011.

P. A. Manavella, A. L. Arce, C. A. Dezar, F. Bitton, and J. P. Renou, Cross-talk between ethylene and drought signalling pathways is mediated by the sunflower Hahb-4 transcription factor, The Plant Journal, vol.48, pp.125-137, 2006.
URL : https://hal.archives-ouvertes.fr/hal-00123714

M. Newman, The structure and function of complex networks, SIAM review, pp.167-256, 2003.

E. Villar, C. Klopp, C. Noirot, E. Novaes, and M. Kirst, RNA-Seq reveals genotype-specific molecular responses to water deficit in eucalyptus, BMC genomics, vol.12, p.538, 2011.
URL : https://hal.archives-ouvertes.fr/hal-02645044

W. W. Lorenz, R. Alba, Y. S. Yu, J. Bordeaux, and M. Simões, Microarray analysis and scale-free gene networks identify candidate regulators in droughtstressed roots of loblolly pine (P. taeda L.), BMC genomics, vol.12, p.264, 2011.

F. A. Cubillos, J. Yansouni, H. Khalili, S. Balzergue, and S. Elftieh, Expression variation in connected recombinant populations of Arabidopsis thaliana highlights distinct transcriptome architectures, BMC Genomics, vol.13, p.117, 2012.
URL : https://hal.archives-ouvertes.fr/hal-01189696

L. Cao, K. González, I. Déjean, and S. , integrOmics: an R package to unravel relationships between two omics datasets, Bioinformatics, vol.25, issue.2, pp.2855-2856, 2009.

R. Schafleitner, G. Rosales, R. O. Gaudin, A. Alvarado-aliaga, C. A. Martinez et al., Capturing candidate drought tolerance traits in two native Andean potato clones by transcription profiling of field grown plants under water stress, Plant Physiology and Biochemistry, vol.45, pp.673-690, 2007.

Y. Sato, B. Antonio, N. Namiki, R. Motoyama, and K. Sugimoto, Field transcriptome revealed critical developmental and physiological transitions involved in the expression of growth potential in japonica rice, BMC plant biology, vol.11, p.10, 2011.

M. Coque, S. Mesnildrey, M. Romestant, B. Grezes-besset, and F. Vear, Sunflower line core collections for association studies and phenomics, Proc. 17th Int Sunflower Conf, pp.725-733, 2008.

F. Vear, F. Serre, I. Jouan-dufournel, P. Bert, and S. Roche, Inheritance of quantitative resistance to downy mildew (Plasmopara halstedii) in sunflower (Helianthus annuus L.), Euphytica, vol.164, pp.561-570, 2008.
URL : https://hal.archives-ouvertes.fr/hal-00528103

J. Gouzy, S. Carrere, and T. Schiex, FrameDP: sensitive peptide detection on noisy matured sequences, Bioinformatics, vol.25, pp.670-671, 2009.
URL : https://hal.archives-ouvertes.fr/hal-02665259

J. P. Shaffer, Multiple hypothesis testing, Annual review of psychology, vol.46, pp.561-584, 1995.

A. Schweighofer, H. Hirt, and I. Meskiene, Plant PP2C phosphatases: emerging functions in stress signaling, Trends in plant science, vol.9, pp.236-243, 2004.

T. Yoshida, N. Nishimura, N. Kitahata, T. Kuromori, and T. Ito, ABA-Hypersensitive Germination3 Encodes a Protein Phosphatase 2C (AtPP2CA) That Strongly Regulates Abscisic Acid Signaling During Germination Among Arabidopsis Protein Phosphatase 2Cs, Plant Physiol, vol.140, pp.115-126, 2006.

I. Chérel, E. Michard, N. Platet, K. Mouline, and C. Alcon, Physical and functional interaction of the Arabidopsis K+ channel AKT2 and phosphatase AtPP2CA, The Plant Cell Online, vol.14, pp.1133-1146, 2002.

J. M. Kuhn, A. Boisson-dernier, M. B. Dizon, M. H. Maktabi, and J. I. Schroeder, The Protein Phosphatase AtPP2CA Negatively Regulates Abscisic Acid Signal Transduction in Arabidopsis, and Effects of Abh1 on AtPP2CA mRNA, Plant Physiol, vol.140, pp.127-139, 2006.

S. Tä-htiharju and T. Palva, Antisense inhibition of protein phosphatase 2C accelerates cold acclimation in Arabidopsis thaliana, The Plant Journal, vol.26, pp.461-470, 2001.

E. Vranová, C. Langebartels, M. Van-montagu, D. Inzé, V. Camp et al., Oxidative Stress, Heat Shock and Drought Differentially Affect Expression of a Tobacco Protein Phosphatase 2C, J Exp Bot, vol.51, pp.1763-1764, 2000.

E. Bell, R. A. Creelman, and J. E. Mullet, A Chloroplast Lipoxygenase Is Required for Wound-Induced Jasmonic Acid Accumulation in Arabidopsis, PNAS, vol.92, pp.8675-8679, 1995.

J. G. Turner, C. Ellis, and A. Devoto, The jasmonate signal pathway, The Plant Cell Online, vol.14, pp.153-164, 2002.

Y. He, H. Fukushige, D. F. Hildebrand, and S. Gan, Evidence supporting a role of jasmonic acid in Arabidopsis leaf senescence, Plant Physiology, vol.128, pp.876-884, 2002.

A. Gigon, A. R. Matos, D. Laffray, Y. Zuily-fodil, and A. T. Pham-thi, Effect of drought stress on lipid metabolism in the leaves of Arabidopsis thaliana (ecotype Columbia), Annals of botany, vol.94, pp.345-351, 2004.

C. Wang, C. A. Zien, M. Afitlhile, R. Welti, and D. F. Hildebrand, Involvement of phospholipase D in wound-induced accumulation of jasmonic acid in Arabidopsis, The Plant Cell Online, vol.12, pp.2237-2246, 2000.

L. M. Weaver, S. Gan, B. Quirino, and R. M. Amasino, A comparison of the expression patterns of several senescence-associated genes in response to stress and hormone treatment, Plant molecular biology, vol.37, pp.455-469, 1998.

R. Wang, K. Guegler, S. T. Labrie, and N. M. Crawford, Genomic analysis of a nutrient response in Arabidopsis reveals diverse expression patterns and novel metabolic and potential regulatory genes induced by nitrate, The Plant Cell Online, vol.12, pp.1491-1510, 2000.

M. H. De-carvalho, Drought stress and reactive oxygen species: production, scavenging and signaling, Plant Signaling & Behavior, vol.3, p.156, 2008.
URL : https://hal.archives-ouvertes.fr/bioemco-00370490

G. Krouk, B. Lacombe, A. Bielach, F. Perrine-walker, and K. Malinska, Nitrate-regulated auxin transport by NRT1. 1 defines a mechanism for nutrient sensing in plants, Developmental cell, vol.18, pp.927-937, 2010.
URL : https://hal.archives-ouvertes.fr/hal-00508268

Y. F. Tsay, C. H. Ho, H. Y. Chen, and S. H. Lin, Integration of Nitrogen and Potassium Signaling, Annual Review of Plant Biology, vol.62, pp.207-226, 2011.

F. Q. Guo, J. Young, and N. M. Crawford, The nitrate transporter AtNRT1. 1 (CHL1) functions in stomatal opening and contributes to drought susceptibility in Arabidopsis, The Plant Cell Online, vol.15, pp.107-117, 2003.

M. Fujita, Y. Fujita, K. Maruyama, M. Seki, and K. Hiratsu, A dehydration-induced NAC protein, RD26, is involved in a novel ABAdependent stress-signaling pathway, The Plant Journal, vol.39, pp.863-876, 2004.

R. D. Isokpehi, S. S. Simmons, H. Cohly, S. Ekunwe, and G. B. Begonia, Identification of drought-responsive universal stress proteins in viridiplantae, Bioinformatics and biology insights, vol.5, 2011.

J. Gimeno, J. Gadea, J. Forment, J. Perez-valle, and J. Santiago, Shared and novel molecular responses of mandarin to drought, Plant Mol Biol, vol.70, pp.403-420, 2009.

F. J. Sánchez, M. Manzanares, E. F. De-andres, J. L. Tenorio, and L. Ayerbe, Turgor maintenance, osmotic adjustment and soluble sugar and proline accumulation in 49 pea cultivars in response to water stress, Field crops research, vol.59, pp.225-235, 1998.

A. Sofo, B. Dichio, C. Xiloyannis, and A. Masia, Lipoxygenase activity and proline accumulation in leaves and roots of olive trees in response to drought stress, Physiologia Plantarum, vol.121, pp.58-65, 2004.

I. Cechin, S. C. Rossi, V. C. Oliveira, and T. F. Fumis, Photosynthetic responses and proline content of mature and young leaves of sunflower plants under water deficit, Photosynthetica, vol.44, pp.143-146, 2006.

D. Bartels and R. Sunkar, Drought and salt tolerance in plants, Critical Reviews in Plant Sciences, vol.24, pp.23-58, 2005.

D. Posé, I. Castanedo, O. Borsani, B. Nieto, and A. Rosado, Identification of the Arabidopsis dry2/sqe1-5 mutant reveals a central role for sterols in drought tolerance and regulation of reactive oxygen species, The Plant Journal, vol.59, pp.63-76, 2009.

R. A. Gaxiola, J. Li, S. Undurraga, L. M. Dang, and G. J. Allen, Drought-and salt-tolerant plants result from overexpression of the AVP1 H+-pump, Proceedings of the National Academy of Sciences, vol.98, p.11444, 2001.

S. Park, J. Li, J. K. Pittman, G. A. Berkowitz, and H. Yang, Up-regulation of a H+-pyrophosphatase (H+-PPase) as a strategy to engineer drought-resistant crop plants, Proceedings of the National Academy of Sciences of the United States of America, vol.102, p.18830, 2005.

Q. Gong, P. Li, S. Ma, S. Indu-rupassara, and H. J. Bohnert, Salinity stress adaptation competence in the extremophile Thellungiella halophila in comparison with its relative Arabidopsis thaliana, The Plant Journal, vol.44, pp.826-839, 2005.

C. E. Wong, Y. Li, A. Labbe, D. Guevara, and P. Nuin, Transcriptional profiling implicates novel interactions between abiotic stress and hormonal responses in Thellungiella, a close relative of Arabidopsis, Plant Physiology, vol.140, pp.1437-1450, 2006.

Y. Guan and E. A. Nothnagel, Binding of Arabinogalactan Proteins by Yariv Phenylglycoside Triggers Wound-Like Responses in Arabidopsis Cell Cultures, Plant Physiol, vol.135, pp.1346-1366, 2004.

D. Huang, W. Wu, S. R. Abrams, and A. J. Cutler, The relationship of droughtrelated gene expression in Arabidopsis thaliana to hormonal and environmental factors, Journal of experimental Botany, vol.59, pp.2991-3007, 2008.

T. D. Missihoun, J. Schmitz, R. Klug, H. H. Kirch, and D. Bartels, Betaine aldehyde dehydrogenase genes from Arabidopsis with different sub-cellular localization affect stress responses, Planta, vol.233, pp.369-382, 2011.

F. Liu, H. Jiang, S. Ye, W. P. Chen, and W. Liang, The Arabidopsis P450 protein CYP82C2 modulates jasmonate-induced root growth inhibition, defense gene expression and indole glucosinolate biosynthesis, Cell research, vol.20, pp.539-552, 2010.

Y. Sasaki-sekimoto, N. Taki, T. Obayashi, M. Aono, and F. Matsumoto, Coordinated activation of metabolic pathways for antioxidants and defence compounds by jasmonates and their roles in stress tolerance in Arabidopsis, The Plant Journal, vol.44, pp.653-668, 2005.

B. Dombrecht, G. P. Xue, S. J. Sprague, J. A. Kirkegaard, and J. J. Ross, MYC2 differentially modulates diverse jasmonate-dependent functions in Arabidopsis, The Plant Cell Online, vol.19, pp.2225-2245, 2007.

C. Jung, S. H. Lyou, S. Y. Yeu, M. A. Kim, and S. Rhee, Microarray-based screening of jasmonate-responsive genes in Arabidopsis thaliana, Plant cell reports, vol.26, pp.1053-1063, 2007.

A. Devoto, C. Ellis, A. Magusin, H. S. Chang, and C. Chilcott, Expression profiling reveals COI1 to be a key regulator of genes involved in wound-and methyl jasmonate-induced secondary metabolism, defence, and hormone interactions, Plant molecular biology, vol.58, pp.497-513, 2005.

L. Cao, K. Boitard, S. Besse, and P. , Sparse PLS discriminant analysis: biologically relevant feature selection and graphical displays for multiclass problems, BMC Bioinformatics, vol.12, p.253, 2011.
URL : https://hal.archives-ouvertes.fr/hal-00959981

D. Rossouw, C. Robert-granié, and P. Besse, A sparse PLS for variable selection when integrating omics data, Genetics and Molecular Biology, vol.7, p.35, 2008.
URL : https://hal.archives-ouvertes.fr/hal-02663938

P. Casadebaig, L. Guilioni, J. Lecoeur, C. A. Champolivier, and L. , SUNFLO, a model to simulate genotype-specific performance of the sunflower crop in contrasting environments, Agricultural and Forest Meteorology, vol.151, pp.163-178, 2011.
URL : https://hal.archives-ouvertes.fr/hal-01506231

G. D. Farquhar, J. R. Ehleringer, and K. T. Hubick, Carbon Isotope Discrimination and Photosynthesis, Annual Review of Plant Physiology and Plant Molecular Biology, vol.40, pp.503-537, 1989.

J. S. Boyer, Relationship of water potential to growth of leaves, Plant Physiology, vol.43, p.1056, 1968.

S. J. Conn, M. Gilliham, A. Athman, A. W. Schreiber, and U. Baumann, Cell-specific vacuolar calcium storage mediated by CAX1 regulates apoplastic calcium concentration, gas exchange, and plant productivity in Arabidopsis, The Plant Cell Online, vol.23, pp.240-257, 2011.

J. Guo, J. Wang, L. Xi, W. D. Huang, and J. Liang, RACK1 is a negative regulator of ABA responses in Arabidopsis, Journal of experimental botany, vol.60, pp.3819-3833, 2009.

J. Guo, S. Wang, O. Valerius, H. Hall, and Q. Zeng, Involvement of Arabidopsis RACK1 in protein translation and its regulation by abscisic acid, Plant physiology, vol.155, pp.370-383, 2011.

J. H. Ko, S. H. Yang, and K. H. Han, Upregulation of an Arabidopsis RING-H2 gene, XERICO, confers drought tolerance through increased abscisic acid biosynthesis, The Plant Journal, vol.47, pp.343-355, 2006.

Y. Y. Zhang and Q. Xie, Ubiquitination in Abscisic Acid-Related Pathway, Journal of Integrative Plant Biology, vol.49, pp.87-93, 2007.

C. Hernández-blanco, D. X. Feng, J. Hu, A. Sánchez-vallet, and L. Deslandes, Impairment of cellulose synthases required for Arabidopsis secondary cell wall formation enhances disease resistance, The Plant Cell Online, vol.19, pp.890-903, 2007.

P. J. Seo, S. B. Lee, M. C. Suh, M. J. Park, and Y. S. Go, The MYB96 transcription factor regulates cuticular wax biosynthesis under drought conditions in Arabidopsis, The Plant Cell Online, vol.23, pp.1138-1152, 2011.

H. Sakamoto, O. Matsuda, and K. Iba, ITN1, a novel gene encoding an ankyrin-repeat protein that affects the ABA-mediated production of reactive oxygen species and is involved in salt-stress tolerance in Arabidopsis thaliana, The Plant Journal, vol.56, pp.411-422, 2008.

K. P. Lee, C. Kim, F. Landgraf, and K. Apel, EXECUTER1-and EXE-CUTER2-dependent transfer of stress-related signals from the plastid to the nucleus of Arabidopsis thaliana, Proceedings of the National Academy of Sciences, vol.104, p.10270, 2007.

D. Przybyla, C. Göbel, A. Imboden, M. Hamberg, and I. Feussner, Enzymatic, but not non-enzymatic, 1O2-mediated peroxidation of polyunsaturated fatty acids forms part of the EXECUTER1-dependent stress response program in the flu mutant of Arabidopsis thaliana, The Plant Journal, vol.54, pp.236-248, 2008.

T. A. Cuin and S. Shabala, Compatible solutes reduce ROS-induced potassium efflux in Arabidopsis roots, Plant, cell & environment, vol.30, pp.875-885, 2007.

T. A. Cuin and S. Shabala, Compatible solutes mitigate damaging effects of salt stress by reducing the impact of stress-induced reactive oxygen species, Plant signaling & behavior, vol.3, p.207, 2008.

P. A. Manavella, C. A. Dezar, G. Bonaventure, I. T. Baldwin, and R. L. Chan, HAHB4, a sunflower HD-Zip protein, integrates signals from the jasmonic acid and ethylene pathways during wounding and biotic stress responses, The Plant Journal, vol.56, pp.376-388, 2008.

P. Kiani, S. Grieu, P. Maury, P. Hewezi, T. Gentzbittel et al., Genetic variability for physiological traits under drought conditions and differential expression of water stress-associated genes in sunflower, Helianthus annuus L.). TAG Theoretical and Applied Genetics, vol.114, pp.193-207, 2007.
URL : https://hal.archives-ouvertes.fr/hal-02656893

J. Roche, T. Hewezi, A. Bouniols, and L. Gentzbittel, Transcriptional profiles of primary metabolism and signal transduction-related genes in response to water stress in field-grown sunflower genotypes using a thematic cDNA microarray, Planta, vol.226, pp.601-617, 2007.

S. Jozefczuk, S. Klie, G. Catchpole, J. Szymanski, and A. Cuadros-inostroza, Metabolomic and transcriptomic stress response of Escherichia coli, Molecular Systems Biology, vol.6, 2010.

J. M. Buescher, W. Liebermeister, J. M. Uhr, M. Muntel, and J. , Global Network Reorganization During Dynamic Adaptations of Bacillus subtilis Metabolism, Science, vol.335, pp.1099-1103, 2012.
URL : https://hal.archives-ouvertes.fr/hal-01000240

T. R. Sinclair, Theoretical analysis of soil and plant traits influencing daily plant water flux on drying soils, Agronomy Journal, vol.97, pp.1148-1152, 2005.

R. C. Gentleman, V. J. Carey, D. M. Bates, B. Bolstad, and M. Dettling, Bioconductor: open software development for computational biology and bioinformatics, Genome biology, vol.5, p.80, 2004.

S. Gagnot, J. P. Tamby, M. L. Martin-magniette, F. Bitton, and L. Taconnat, CATdb: a public access to Arabidopsis transcriptome data from the URGV-CATMA platform, Nucleic Acids Research, vol.36, pp.986-990, 2008.
URL : https://hal.archives-ouvertes.fr/hal-01203869

T. Barrett, D. B. Troup, S. E. Wilhite, P. Ledoux, and D. Rudnev, NCBI GEO: mining tens of millions of expression profiles-database and tools update, Nucleic acids research, vol.35, pp.760-765, 2007.

Z. Du, X. Zhou, Y. Ling, Z. Zhang, and Z. Su, agriGO: a GO analysis toolkit for the agricultural community, Nucleic Acids Research, vol.38, pp.64-70, 2010.

S. L. Spurgeon, R. C. Jones, and R. Ramakrishnan, High throughput gene expression measurement with real time PCR in a microfluidic dynamic array, PloS one, vol.3, p.1662, 2008.

J. Nolot and P. Debaeke, Principles and tools for the design, management and evaluation of cropping systems, Cahiers Agricultures, vol.12, pp.387-400, 2003.
URL : https://hal.archives-ouvertes.fr/hal-02671749