Adjebeng-Danquah, J., Gracen, V.E., Offei, S.K., Asante, I.K., Manu-Aduening, J., Genetic variability in storage root bulking of cassava genotypes under irrigation and no irrigation. Agriculture & Food Security, 2016, 1–12, 10.1186/s40066-016-0055-7.
Aina, O.O., Dixon, A.G.O., Akinrinde, E.A., Effect of soil moisture stress on growth and yield of cassava in Nigeria. Pakistan Journal Biological Science 10:18 (2007), 3085–3090.
Alves, A.A.C., Setter, T.L., Abscisic acid accumulation and osmotic adjustment in cassava under water deficit. Environ. & Exp. Botany 51 (2004), 259–271.
Alves, A.A.C., Setter, T.L., The Response of Cassava Leaf Area Expansion to Water Deficit: Cell Proliferation, Cell Expansion and Delayed Development. Annals of Botany 94 (2004), 605–613.
Alves, A.A.C., Cassava Botany and Physiology. Hillocks, R.J., Thresh, J.M., Bellotti, A.C., (eds.) Cassava: Biology, Production and Utilization, 2002, CABI Pub, 67–89.
Alves, A.A.C., Setter, T.L., Response of Cassava to Water Deficit: Leaf Area Growth and Abscisic Acid. Crop Science 40 (2000), 131–137.
Aubert, A., Vile, D., Pervent, M., Aldon, D., Ranty, B., Simonneau, T., Vavasseur, A., Galaud, J.P., RD20, a Stress-Inducible Caleosin, Participates in Stomatal Control, Transpiration and Drought Tolerance in Arabidopsis thaliana. Plant Cell Physiology 51:12 (2010), 1975–1987.
Belin, C., Franco, P., Bourbousse, C., Chaignepain, S., Schmitter, J., Vavasseur, A., Giraudat, J., Barbier-Brygoo, H., Thomine, S., Identification of Features Regulating OST1 Kinase Activity and OST1 Function in Guard Cells. Plant Physiology 141 (2006), 1316–1327.
Bergantin, V.R., Yamauchi, A., Pardales, J.R Jr., Bolatete, D.M., Screening cassava genotypes for resistance to water deficit during crop establishment. Journal of Crop Science 29:1 (2004), 29–39.
Bio-Rad Laboratories, Reagent comparison guide for Real-Time PCR. 2013 https://www.bio-rad.com/webroot/web/pdf/lsr/literature/Bulletin_6252.pdf.
Biratu, G.K., Elias, E., Ntawuruhunga, P., Sileshi, G.W., 2018. Cassava response to the integrated use of manure and NPK fertilizer in Zambia. Heliyon 4 e00759 1–23.
Budak, H., Kantar, M., Kurtoglu, K.Y., Drought Tolerance in Modern and Wild Wheat. The Scientific World Journal, 2013, 1–16.
Burns, A., Gleadow, R., Cliff, J., Zacarias, A., Cavagnaro, T., Cassava: The drought, war and famine crop in a changing world. Sustainability 2 (2010), 3572–3607.
Chang, S., Puryear, J., Cairney, J., A Simple and Efficient Method for Isolating RNA from Pine Trees. Plant Molecular Biology Reporter 11 (1993), 113–116.
Chinnusamy, V., Schumaker, K., Zhu, J.K., Molecular genetics perspectives on cross talk and specificity in abiotic stress signaling in plants. Journal of Experimental Botany 55 (2004), 225–236.
Connor, D.J., Cock, J.H., Parpa, G.E., Response of cassava to water shortage. I. Growth and Yield. Field Crops Research 4 (1981), 181–200.
Czechowski, T., Stitt, M., Altmann, T., Udvardi, M.K., Scheible, W.R., Genome-wide identification and testing of superior reference genes for transcript normalization in Arabidopsis. Plant Physiology 139 (2005), 5–17.
Daryanto, S., Wang, L., Jacinthe, P.-A., Global Synthesis of Drought Effects on Maize and Wheat Production. PLoS ONE 11:5 (2016), 1–15.
Datta, K., Baisakh, N., Ganguly, M., Krishnan, S., Yamaguchi, S.K., Datta, S.K., Over-expression of Arabidopsis and Rice stress genes’ inducible transcription factor confers drought and salinity tolerance to rice. Plant Biotechnology Journal 10 (2012), 579–586.
De Souza, A.P., Long, S.P., Toward improving photosynthesis in cassava: Characterizing photosynthetic limitations in four current African cultivars. Food Energy Security, 7, 2018, 10.1002/fes3.130 e00130.
Duque, L.O., Cassava Drought Tolerance Mechanisms Re-Visited: Evaluation of Drought Tolerance in Contrasting Cassava Genotypes Under Water Stressed Environments. 2012 https://core.ac.uk/download/pdf/79034745.pdf.
El-Sharkawy, M.A., Physiological characteristics of cassava tolerance to prolonged drought in the tropics: Implications for breeding cultivars adapted to seasonally dry and semiarid environments. Brazilian Journal of Plant Physiology 19:4 (2007), 257–286.
El-Sharkawy, M.A., International research on cassava photosynthesis, productivity, eco-physiology and responses to environmental stresses in the tropics. Photosynthetica 44 (2006), 481–512.
El-Sharkawy, M.A., Hernández, A., Del, P., Hershey, C., Yield stability of cassava during prolonged midseason water stress. Experimental Agriculture 28 (1992), 165–174.
El-Sharkawy, M.A., Cock, J.H., Response of cassava to water stress. Plant and Soil 100:1-3 (1987), 345–360, 10.1007/BF02370950.
El-Sharkawy, M.A., Cock, J.H., Water use efficiency of cassava. I. Effects of air humidity and water stress on stomata conductance and gas exchange. Crop Science 24 (1984), 497–502.
Estrada-Melo, A.C., Ma, C., Reid, M.S., Jiang, C.Z., Over expression of an ABA biosynthesis gene using a stress-inducible promoter enhances drought resistance in petunia. Horticulture Research 2 (2015), 1–9.
Fahad, S., Bajwa, A.A., Nazir, U., Anjum, S.A., Farooq, A., Zohaib, A., Huang, J., et al. Crop Production under Drought and Heat Stress: Plant Responses and Management Options. Frontiers in Plant Science 8 (2017), 1–16.
Fermont, A.M., Tittonell, P.A., Baguma, Y., Ntawuruhunga, P., Giller, K.E., Towards understanding factors that govern fertilizer response in cassava: lessons from East Africa. Nutr Cycl Agroecosyst 86 (2009), 133–151.
Fregene, M., Puonti-Kaerlas, J., Cassava biotechnology. Hillocks, R.J., Thresh, J.M., Bellotti, A.C., (eds.) CAB International 2002. Cassava: Biology, Production and Utilization, 2002.
Fu, L., Ding, Z., Han, B., Hu, W., Li, Y., Zhang, J., Physiological Investigation and Transcriptome Analysis of Polyethylene Glycol (PEG)-Induced Dehydration Stress in Cassava. International journal of Molecular Sciences 17:283 (2016), 1–18.
Fukuda, W.M.G., Guevara, C.L., Kawuki, R., Ferguson, M.E., Selected morphological and agronomic descriptors for the characterization of cassava. 2010, International Institute of Tropical Agriculture (IITA), Ibadan, Nigeria 19 pp.
Gosti, F., Beaudoi, N., Serizet, C., Webb, A.A.R., Vartanian, N., Giraudat, J., ABI1 Protein Phosphatase 2C Is a Negative Regulator of Abscisic Acid Signaling. The Plant Cell 11 (1999), 1897–1909.
Gray, V.M., A Comparison of Two Approaches for Modeling Cassava (Manihot esculenta Crantz) Crop Growth. Annals of Botany 85 (2000), 77–90.
Guo, Y., Xiong, L., Song, C.-P., Gong, D., Halfter, U., Zhu, J.-K., A Calcium Sensor and Its Interacting Protein Kinase Are Global Regulators of Abscisic Acid Signaling in Arabidopsis. Developmental Cell 3 (2002), 233–244.
Harb, A., Krishnan, A., Ambavaram, M.R., Pereira, A., Molecular and Physiological Analysis of Drought Stress in Arabidopsis Reveals Early Responses Leading to Acclimation in Plant Growth. Plant Physiology 154:3 (2010), 1254–1271.
Hong, Y., Zheng, S., Wang, X., Dual Functions of Phospholipase Da1 in Plant Response to Drought. Molecular Plant 1:2 (2008), 262–269.
Hornetz, B., Shisanya, C.A., Gitonga, M.N., Studies on the Ecophysiology of Locally Suitable Cultivars of Food Crops and Soil Fertility Monitoring in the Semi-Arid Areas of Southeast Kenya. Verlag, Kenya. 2000.
Huang, X.-Y., Chao, D.-Y., Gao, J.-P., Zhu, M.-Z., Shi, M., Lin, H.-X., A previously unknown zinc finger protein, DST, regulates drought and salt tolerance in rice via stomatal aperture control. Genes & Development 23 (2009), 1805–1817.
Iglesias, C., Bonierbale, M., El-Sharkawy, M., Lozano, C., Bellotti, A., Wheatley, C., Howeler, R.H., (eds.) Focusing basic research for cassava varietal improvement, in Cassava Breeding, Agronomy Research and Technology Transfer in Asia - Fourth Regional Workshop, 1995, CIAT, Cali, Colombia, 40–60 Trivandrum, Kerala, India:), 2–6 November 1993.
Imai, H., Noda, Y., Tamaoki, M., Alteration of Arabidopsis SLAC1 promoter and its association with natural variation in drought tolerance. Plant Signaling & Behavior 10:3 (2015), 1–7.
Jaetzold, R., Schmidt, H., Hornet, Z.B., Shisanya, C.A., 2nd edition Farm management handbook of Kenya. Natural conditions and farm information, Vol. 11/C, 2006, Ministry of agriculture/GTZ, Nairobi (Eastern Province) http://www2.gtz.de/dokumente/bib/07-1286.pdf.
Jarvis, A., Ramirez-Villegas, J., Campo, B.V.H., Navarro-Racines, C., Is cassava the answer to African climate change adaptation?. Tropical Plant Biology 5:1 (2012), 9–29.
Jia, H., Zhang, S., Ruan, M., Wang, Y., Wang, C., Analysis and application of RD29 genes in abiotic stress response. Acta Physiologiae Plantarum 34 (2012), 1239–1250.
Jovanović, Z., Stanisavljević, N., Mikić, A., Radović, S., Maksimović, V., The expression of drought responsive element binding protein (DREB2A) related gene from pea (Pisum sativum L.) as affected by water stress. AJCS 7:10 (2013), 1590–1596.
Jung, C., Sew, J.S., Han, S.W., Koo, Y.J., Kim, C.H., Song, S.I., Nahm, B.H., Choi, Y.D., Cheong, J.J., Over-expression of MYB44 Enhances Stomatal Closure to Confer Abiotic Stress Tolerance in Transgenic Arabidopsis. Plant Physiology 146 (2008), 623–635.
Kamau, J., Melis, R., Laing, M., Derera, J., Shanahan, P., Ngugi, E., Combining the yield ability and secondary traits of selected cassava genotypes in the semi-arid areas of Eastern Kenya. Journal of Plant Breeding and Crop Science 2:7 (2010), 181–191.
Kasuga, M., Miura, S., Shinozaki, K., Yamaguchi-Shinozaki, K., A combination of the Arabidopsis DREB1A Gene and Stress-Inducible rd29A Promoter Improved Drought- and Low-Temperature Stress Tolerance in Tobacco by Gene Transfer. Plant and Cell Physiology 45:3 (2004), 346–350.
Kelly, V.A., Factors affecting demand for fertilizers in Sub-Saharan Africa. Agriculture and rural development discussion paper 23. 2006, The World Bank, Washington, DC.
Klingler, J.P., Batelli, G., Zhu, J., ABA receptors: the START of a new paradigm in phytohormone signaling. Journal of Experimental Botany 61:12 (2010), 3199–3210.
Kovacs, D., Kalmar, E., Torok, Z., Tompa, P., Chaperone Activity of ERD10 and ERD14, Two Disordered Stress-Related Plant Proteins. Plant Physiology 147 (2008), 381–390.
Kusumi, K., Hirotsuka, S., Kumamaru, T., Iba, K., Increased leaf photosynthesis caused by elevated stomatal conductance in a rice mutant deficient in SLAC1, a guard cell anion channel protein. Journal of Experimental Botany 63:15 (2012), 5635–5644.
Lamaoui, M., Jemo, M., Datla, R., Bekkaoui, F., Heat and Drought Stresses in Crops and Approaches for Their Mitigation. Frontiers in Chemistry 6:26 (2018), 1–14.
Lamesch, P., Berardini, T.Z., Li, D., Swarbreck, D., Wilks, C., Sasidharan, R., Muller, R., Huala, E., et al. The Arabidopsis Information Resource (TAIR): Improved gene annotation and new tools. Nucleic Acids Research 40 (2012), 1202–1210.
Lenis, I.J., Calle, F., Jaramillo, G., Perez, J.C., Ceballos, H., Cock, J.H., Leaf retention and cassava productivity. Field Crops Research 95 (2006), 126–134.
Li, S., Yu, X., Cheng, Z., Yu, X., Ruan, M., Li, W., Peng, M., Global gene expression analysis reveals crosstalk between response mechanisms to cold and drought Stresses in cassava seedlings. Frontiers in Plant Science 8:1259 (2017), 1–18.
Li, S., Yu, X., Lei, N., Cheng, Z., Zhao, P., He, Y., Wang, W., Peng, M., Genome-wide identification and functional prediction of cold and/or drought-responsive lncRNAs in cassava. Scientific Reports, 7, 2017, 45981, 10.1038/srep45981.
Li, J.-H., Liu, Y.-Q., Lü, P., Lin, H.-F., Bai, Y., Wang, X.-C., Chen, Y.-L., A Signaling Pathway Linking Nitric Oxide Production to Heterotrimeric G Protein and Hydrogen Peroxide Regulates Extracellular Calmodulin Induction of Stomatal Closure in Arabidopsis. Plant Physiology 150:1 (2009), 114–124.
Li, W.-X., Oono, Y., Zhu, J., He, X.-J., Wu, J.-M., Iida, K., Lu, X.-Y., Cui, X., Jin, H., Zhu, J.K., The Arabidopsis NFYA5 Transcription Factor Is Regulated Transcriptionally and Post-transcriptionally to Promote Drought Resistance. The Plant Cell 20 (2008), 2238–2251.
Lian, H.-L., Yu, X., Ye, Q., Ding, X.-S., Kitagawa, Y., Kwak, S.-S., Su, W.-A., Tang, Z.-C., The role of aquaporin RWC3 in drought avoidance in rice. Plant Cell Physiol. 45:4 (2004), 481–489.
Lipiec, J., Doussan, C., Nosalewicz, A., Kondracka, K., Effect of drought and heat stresses on plant growth and yield: a review. Int. Agrophys. 27:4 (2013), 463–477.
Liu, G., Li, X., Jin, S., Liu, X., Zhu, L., Nie, Y., Zhang, X., Over expression of Rice NAC Gene SNAC1 Improves Drought and Salt Tolerance by Enhancing Root Development and Reducing Transpiration Rate in Transgenic Cotton. PLoS One 9:1 (2014), 1–10.
Lobell, D.B., Schlenker, W., Costa-Roberts, J., Climate trends and global crop production since 1980. Science 333 (2011), 616–620.
Lokko, Y., Anderson, J., Rudd, S., Raji, A., Horvath, D., Mikel, M.A., Ingelbrecht, I.L., Characterization of an 18,166 EST dataset for cassava (Manihot esculenta Crantz) enriched for drought-responsive genes. Plant Cell Reporter 26 (2007), 1605–1618.
Lu, S., Bahn, S.C., Qu, G., Qin, H., Hong, Y., Xu, Q., Zhou, Y., Hong, Y., Wang, X., Increased expression of phospholipase Da1 in guard cells decreases water loss with improved seed production under drought in Brassica napus. Plant Biotechnology Journal 11 (2013), 380–389.
Lu, P.L., Chen, N.-Z., An, R., Su, Z., Qi, B.-S., Ren, F., Wang, X.-C., A novel drought-inducible gene, ATAF1, encodes a NAC family protein that negatively regulates the expression of stress-responsive genes in Arabidopsis. Plant Molecular Biology 63 (2007), 289–305.
Maingi, J., Shisanya, C., Gitonga, N.M., Hornetz, B., Nitrogen fixation by common bean (Phaseolus vulgare L.) in pure and mixed stands in semi-arid southeast Kenya. European Journal of Agronomy 14 (2001), 1–12.
Marshall, O.J., Perlprimer: cross-platform, graphical primers design for standard, bisulphite and real-time PCR. Bioinformatics 20:15 (2004), 2471–2472.
Merlot, S., Gosti, F., Guerrier, D., Vavasseur, A., Giraudat, J., The ABI1 and ABI2 protein phosphatases 2C act in a negative feedback regulatory loop of the abscisic acid signaling pathway. The Plant Journal 25:3 (2001), 295–303.
Mganga, K.Z., Musimba, N.K.R., Nyangito, M.M., Nyariki, D.M., Mwangombe, A.W., Ekaya, W.N., Verhagen, J., The role of moisture in the successfully rehabilitation of denuded patches of a semi-arid environment in Kenya. Journal of Environmental Science & Technology 3:4 (2010), 195–207.
Mganga, K.Z., Musimba, N.K.R., Nyariki, D.M., Nyangito, M.M., Mwangombe, A.W., Ekaya, W.N., Muiru, W.M., Dry matter yields and hydrological properties of three perennial grasses of a semi-arid environment in east Africa. African Journal of Plant Science 4:5 (2010), 138–144.
Mishra, G., Zhang, W., Deng, F., Zhao, J., Wang, X., A bifurcating pathway directs abscisic acid effects on stomatal closure and opening in Arabidopsis. Science 312 (2006), 264–266.
Movahedi, S., Tabatabaei, S., Alizade, H., Ghobadi, C., Yamchi, A., Khaksar, G., Constitutive expression of Arabidopsis DREB1B in transgenic potato enhances drought and freezing tolerance. Biologia Plantarum 56:1 (2012), 37–42.
Moreno, I., Gruissem, W., Vanderschuren, H., Reference genes for reliable potyvirus quantitation in cassava and analysis of Cassava brown streak virus load in host varieties. Journal of Virological Methods 177 (2011), 49–54.
Mustilli, A.C., Merlot, S., Vavasseur, A., Fenzi, F., Giraudat, J., Arabidopsis OST1 Protein Kinase Mediates the Regulation of Stomatal Aperture by Abscisic Acid and Acts Upstream of Reactive Oxygen Species Production. The Plant Cell 14:12 (2002), 3089–3099.
Msanne, J., Lin, J., Stone, J.M., Awada, T., Characterization of abiotic stress-responsive Arabidopsis thaliana RD29A and RD29B genes and evaluation of transgenes. Planta 234 (2011), 97–107.
Nadeem, M., Li, J., Yahya, M., Sher, A., Ma, C., Wang, X., Qiu, L., Research Progress and Perspective on Drought Stress in Legumes: A Review. International journal of molecular sciences 20:10 (2019), 1–32.
Nduwumuremyi, A., Melis, R., Shanahan, P., Theodore, A., Interaction of genotype and environment effects on important traits of cassava (Manihot esculenta Crantz). The Crop Journal 5 (2017), 373–386.
Ng, N.Q., Ng, S.Y.C., Genetic resources and conservation. Hillocks, R.J., Thresh, J.M., Bellotti, A.C., (eds.) @CAB International 2002. Cassava: Biology, Production and Utilization, 2002.
Nishimura, N., Sarkeshik, A., Nito, K., Park, S.Y., Wang, A., Carvalho, P.C., Lee, S., Caddell, D.F., Cutler, S.R., Chory, J., Yates, J.R., Schroeder, J.I., PYR/PYL/RCAR family members are major in-vivo ABI1 protein phosphatase 2C-interacting proteins in Arabidopsis. The Plant Journal 61 (2010), 290–299.
Okamoto, A., Peterson, F.C., Defries, A., Park, S.Y., Endo, A., Nambara, E., Volkman, B.F., Cutler, S.R., Activation of dimeric ABA receptors elicits guard cell closure, ABA-regulated gene expression, and drought tolerance. Proc Natl Acad Sci U S A 110:29 (2013), 12132–12137.
Okogbenin, E., Setter, T.L., Ferguson, M.E., Fregene, M., Phenotypic approaches to drought in cassava: review. Frontiers in Physiology 4:93 (2013), 1–15.
Pfaffl, M.W., Tichopad, A., Prgomet, C., Neuvians, T.P., Determination of stable housekeeping genes, differentially regulated target genes and sample integrity: BestKeeper–Excel-based tool using pair-wise correlations. Biotechnology Letters 26 (2004), 509–515.
Pfaffl, M.W., A new mathematical model for relative quantification in real-time RT–PCR. Nucleic Acids Research 29:9 (2001), 2003–2007.
Pellet, D.M., EL-Sharkawy, M.A., Sink-source relations in cassava: effects of reciprocal grafting on yield and leaf photosynthesis. Experimental Agriculture 30 (1994), 359–367.
Prochnik, S., Pradeep, R.M., Desany, B., Pablo, D.R., Kodira, C., Mohammed, M., Rounsley, S., The Cassava Genome: Current Progress, Future Directions. Tropical Plant Biology 5 (2012), 88–94.
Raven, J.A., Speedy small stomata?. Journal of Experimental Botany 65:6 (2014), 1415–1424.
Raza, A., Razzaq, A., Mehmood, S.S., Zou, X., Zhang, X., Lv, Y., Xu, J., Impact of Climate Change on Crops Adaptation and Strategies to Tackle Its Outcome: A Review. Plants (Basel) 8:2 (2019), 1–29.
Reddy, S.P., Srinivas, R.D., Sivasakthi, K., Bhatnagar-Mathur, P., Vadez, V., Sharma, K.K., Evaluation of Sorghum [Sorghum bicolor (L.)] reference Genes in Various Tissues and under Abiotic Stress Conditions for Quantitative Real-Time PCR Data Normalization. Frontiers in Plant Science, 7(529), 2016.
Rosenthal, D.M., Slattery, R.A., Miller, R.E., Grennan, A.K., Cavagnaro, T.R., Fauquet, C.M., Ort, D.R., Cassava about-FACE: Greater than expected yield stimulation of Cassava (Manihot esculenta) by future CO2 levels. Global Change Biology 18 (2012), 2661–2675.
Rosenthal, D.M., Ort, D.R., Examining Cassava's Potential to Enhance Food Security under Climate Change. Tropical Plant Biology 5:1 (2012), 30–38.
Roychoudhury, A., Paul, S., Basu, S., Cross-talk between abscisic acid-dependent and abscisic acid-independent pathways during abiotic stress. Plant Cell Rep 32 (2013), 985–1006.
Ruijter, J.M., Ramakers, C., Hoogaars, W., Bakker, O., van den Hoff, M.J., Karlen, Y., Moorman, A.F., Amplification efficiency: linking baseline and bias in the analysis of quantitative PCR data. Nucleic Acids Research 37:6 (2009), 2–12.
Rymaszewski, W., Vile, D., Bediee, A., Dauzat, M., Luchaire, N., Kamrowska, D., Granier, C., Jacek Henniga, J., Stress-Related Gene Expression Reflects Morpho-physiological Responses to Water Deficit. Plant Physiology 174 (2017), 1913–1930.
Sang, J., Han, X., Liu, M., Qiao, G., Jiang, J., Zhuo, R., Selection and validation of reference genes for real-time quantitative PCR in hyper-accumulating ecotype of Sedum alfredii under different heavy metals stresses. PLoS ONE, 8, 2013, 10.1371/journal.pone.0082927 e82927.
Sakuma, Y., Maruyama, K., Osakabe, Y., Qin, F., Seki, M., Shinozaki, K., Yamaguchi-Shinozaki, K., Functional Analysis of an Arabidopsis Transcription Factor, DREB2A, Involved in Drought-Responsive Gene Expression. The Plant Cell 18 (2006), 1292–1309.
Schneider, D.N., Freitag, N.M., Liedgens, M., Feil, B., Stamp, P., Early growth of field-grown Swiss flint maize landraces. Maydica 56 (2011), 1–9.
Seki, M., Kamei, A., Yamaguchi-Shinozaki, K., Shinozaki, K., Molecular responses to drought, salinity and frost: common and different paths for plant protection. Current Opinion in Biotechnology 14 (2003), 194–199.
Shan, Z., Luo, X., Wei, M., Huang, T., Khan, A., Zhu, Y., Physiological and proteomic analysis on long-term drought resistance of cassava (Manihot esculenta Crantz). Scientific Reports 8 (2018), 1–12 17982.
Shinozaki, K., Yamaguchi-Shinozaki, K., Gene networks involved in drought stress response and tolerance. Journal of Experimental Botany 58:2 (2007), 221–227.
Shinozaki, K., Yamaguchi-Shinozaki, K., Molecular responses to dehydration and low temperature: Differences and cross talk between two stress-signaling pathways. Curr. Opin. Plant Biol. 3 (2000), 217–223.
Shinozaki, K., Yamaguchi-Shinozaki, K., Gene expression and signal transduction in water-stress response. Plant Physiol. 11:5 (1997), 327–334.
Shisanya, C.A., Recha, C., Anyamba, A., Rainfall Variability and Its Impact on Normalized Difference Vegetation Index in Arid and Semi-Arid Lands of Kenya. International Journal of Geosciences 2 (2011), 36–47.
Sombroek, W.G., Braun, H.M.H., Van der Pour, B.J.A., Exploratory soil map and agro-climatic zones map of Kenya. Scale: 1:1,000,000. Report in Kenya Soil Survey, 1982 Nairobi, Kenya.
SPSS Inc, IBM_SPSS_Node_21.0.0.0_Mac_ML for Mac User's Guide. 2012, SPSS Inc, Chicago, IL.
Stevanović, M., Popp, A., Lotze-Campen, H., Dietrich, J.P., Müller, C., Bonsch, M., Schmitz, C., Weindl, I., et al. The impact of high-end climate change on agricultural welfare. Science Advances 2:8 (2016), 1–9.
Stitt, M., Rising CO2 levels and their potential significance for carbon flow in photosynthetic cells. Plant, Cell & Environment 14 (1991), 741–762.
Subere, J.O.Q., Bolatete, D., Bergantin, R., Pardales, A., Belmonte, J.J., Mariscal, A., Sebidos, R., Yamauchi, A., Genotypic Variation in Responses of Cassava (Manihot esculenta Crantz) to Drought and Re-watering: Root System Development. Plant Production Science 12:4 (2003), 462–474.
Taberlet, P., Gielly, L., Pautou, G., Bouvet, J., Universal primers for amplification of three non-coding regions of chloroplast DNA. Plant Molecular Biology 17 (1991), 1105–1109.
TAIR, The Arabidopsis Information Resource (TAIR). 2013 on Oct 10, 2013 www.arabidopsis.org.
Tumuhimbise, R., Melis, R., Shanahan, P., Kawuki, R., Genotype × environment interaction effects on early fresh storage root yield and related traits in cassava. The Crop J. 2 (2014), 329–337.
Turyagyenda, F.L., Elizabeth, B.K., Ferguson, M., Baguma, Y., Agaba, M., Harvey, J.W., Osiru, D.S.O., Physiological and molecular characterization of drought responses and identification of candidate tolerance genes in cassava. Annals of Botany 5 (2013), 1–17.
Udvardi, M.K., Czechowski, T., Scheible, W.R., Eleven Golden Rules of Quantitative RT-PCR. Plant Cell 20 (2008), 1736–1737.
Utsumi, Y., Tanaka, M., Morosawa, T., Kurotani, A., Yoshida, T., Mochida, K., Matsui, A., Umemura, Y., Ishitani, M., Shinozaki, K., Sakurai, T., Seki, M., Transcriptome Analysis Using a High-Density Oligo-microarray under Drought Stress in Various Genotypes of Cassava: An Important Tropical Crop. DNA Research 19:4 (2012), 335–345.
Vaseva, I., Sabotic, J., Sustar-Vozlic, J., Meglic, V., Kidric, M., Demirevska, K., Simova-Stoilova, The Response of Plants to Drought Stress: The Role or Dehydrins, Chaperones, Proteases and Protease Inhibitors in Maintaining Cellular Protein Function. Droughts: New Research, 2012, 1–45 ISBN: 978-1-62100-769-2.
Wang, X.-D., Ullah, H., Jones, A.M., Assmann, S.M., G Protein Regulation of Ion Channels and Abscisic Acid Signaling in Arabidopsis Guard Cells. Science 292 (2001), 2070–2072.
Xie, X., Wang, Y., Williamson, L., Holroyd, G.H., Tagliavia, C., Murchie, E., Theobald, J., Knight, M.R., Davies, W.J., Ottoline, L.H.M., Hetherington, A.M., The Identification of Genes Involved in the Stomatal Response to Reduced Atmospheric Relative Humidity. Current Biology 16 (2006), 882–887.
Yang, S., Vanderbeld, B., Wan, J., Huang, Y., Narrowing Down the Targets: Towards Successful Genetic Engineering of Drought-Tolerant Crops. Molecular Plant 3:3 (2010), 469–490.
You, J., Zong, W., Li, X., Ning, J., Hu, H., Li, X., Xiao, J., Xiong, L., The SNAC1-targeted gene OsSRO1c modulates stomatal closure and oxidative stress tolerance by regulating hydrogen peroxide in rice. Experimental Botany 64:2 (2013), 569–583.
Yoshida, R., Umezawa, T., Mizoguchi, T., Takahashi, S., Takahashi, F., Shinozaki, K., The Regulatory Domain of SRK2E/OST1/SnRK2.6 Interacts with ABI1 and Integrates Abscisic Acid (ABA) and Osmotic Stress Signals Controlling Stomatal Closure in Arabidopsis. Biological Chemistry 281:8 (2006), 5310–5318.
Zhang, J., Xie, W., Yu, X., Zhang, Z., Zhao, Y., Wang, N., Wang, Y., Selection of suitable reference genes for RT-qPCR gene expression analysis in Siberian Wild Rye (Elymus sibiricus) under different experimental conditions. Genes 10:451 (2019), 1–23.
