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Xhuveli L. Review in wheat breeding and genetic resources in Albania 2009; JARTS Supplement 92: 57-72.XhuveliLReview in wheat breeding and genetic resources in Albania2009925772Search in Google Scholar
Xhelo K, Elezi F. Stability of wheat genotypes in condition of Lushnja region. Albanian Journal of Agricultural Sciences 2014; (Special edition): 219-223.XheloKEleziFStability of wheat genotypes in condition of Lushnja region2014Special edition219223Search in Google Scholar
Bacu A, Çomashi K, Hoxhaj M, IbroV. GSTF1 Gene Expression at local Albanian wheat cultivar Dajti under salinity and heat conditions. The EuroBiotech Journal 2017; 1(Issue 3): 253-257.BacuAÇomashiKHoxhajMIbroV. GSTF1 Gene Expression at local Albanian wheat cultivar Dajti under salinity and heat conditions20171Issue 325325710.24190/ISSN2564-615X/2017/03.10Search in Google Scholar
Oyiga BC, Sharma RC, Shen J, Baum M, Ogbonnaya FC, Leon J, Ballvora A. Identification and characterization of salt tolerance of wheat germplasm using a multivariable screening. Journal of Agronomy and Crop Science2016; 472-485.OyigaBCSharmaRCShenJBaumMOgbonnayaFCLeonJBallvoraAIdentification and characterization of salt tolerance of wheat germplasm using a multivariable screening201647248510.1111/jac.12178Search in Google Scholar
Haq TU, Gorham J, Akhtar J, Akhtar N, Steele K A. Dynamic quantitative trait loci for salt stress components on chromosome 1 of rice. Functional Plant Biology 2010; 37:634-645.HaqTUGorhamJAkhtarJAkhtarNSteeleK ADynamic quantitative trait loci for salt stress components on chromosome 1 of rice20103763464510.1071/FP09247Search in Google Scholar
Lutts S, Kinet JM, Bouharmont J. Changes I plant response to NaCl during development of rice Oryza sativa L.) varieties differing in salinity resistance. Journal of Experimental Botany 1995; 46:1843-1852.LuttsSKinetJMBouharmontJChanges I plant response to NaCl during development of rice Oryza sativa L.) varieties differing in salinity resistance1995461843185210.1093/jxb/46.12.1843Search in Google Scholar
Hasegawa PM, Bressan RA, Zhu JK, Bohnert HJ. Plant cellular and molecular responses to high salinity. Annual Reviews in Plant Physiology, Plant Molecular Biology 2000; 51:463-499.HasegawaPMBressanRAZhuJKBohnertHJPlant cellular and molecular responses to high salinity. Annual Reviews in Plant Physiology20005146349910.1146/annurev.arplant.51.1.46315012199Search in Google Scholar
Annunziata M G, Ciarmiello LF, Woodrow P, Maximova E, Fuggi A, Carillo P. Durum wheat roots adapt to salinity remodeling the cellular content of nitrogen metabolites and sucrose. Frontiers in Plant Science 2017; 7(2035):1-16.AnnunziataM GCiarmielloLFWoodrowPMaximovaEFuggiACarilloPDurum wheat roots adapt to salinity remodeling the cellular content of nitrogen metabolites and sucrose2017711610.3389/fpls.2016.02035522001828119716Search in Google Scholar
Ashraf M, Harris PJC. Photosynthesis under stressful environments: An overview. Photosynthetica 2013; 51(2): 163-190.AshrafMHarrisPJCPhotosynthesis under stressful environments: An overview201351216319010.1007/s11099-013-0021-6Search in Google Scholar
Munns R, Tester M. Mechanisms of salinity tolerance. Annual Review in Plant Biology 2008; 59:651-681.MunnsRTesterMMechanisms of salinity tolerance20085965168110.1146/annurev.arplant.59.032607.09291118444910Search in Google Scholar
Gorham J, Lauchli A, Leidi EO. Plant responses to salinity. Physiology of Cotton 2010; 129-141.GorhamJLauchliALeidiEOPlant responses to salinity201012914110.1007/978-90-481-3195-2_13Search in Google Scholar
Hudson GS, Evans JR, Von Caemmerer S, Arvidsson YBC, Andrews TJ. Reduction ofribulose-1,5-biphosphate carboxylase oxygenase content by antisense RNA reduces photosynthesis in transgenic tobacco plants. Plant Physiology 1992; 98:294-302.HudsonGSEvansJRVon CaemmererSArvidssonYBCAndrewsTJReduction ofribulose-1,5-biphosphate carboxylase oxygenase content by antisense RNA reduces photosynthesis in transgenic tobacco plants19929829430210.1104/pp.98.1.294108018216668627Search in Google Scholar
Parry MAJ, Keys AJ, Madgwick PJ, Carmo-Silva AE, Andralojc PJ. Rubisco regulation: a role for inhibitors. Journal of Experimental Botany 2008; 59(7):1569-1580.ParryMAJKeysAJMadgwickPJCarmo-SilvaAEAndralojcPJRubisco regulation: a role for inhibitors20085971569158010.1093/jxb/ern084Search in Google Scholar
Eckardt NA. A new chlorophyll degradation pathway. Plant Cell 2009: 21:700.EckardtNAA new chlorophyll degradation pathway20092170010.1105/tpc.109.210313Search in Google Scholar
Khan MA, Shirazi MU, Khan MA. Role of proline, K/Na ratio and chlorophyll content in salt tolerance of wheat Triticum aestivum L.). Journal of Botany 2009; 41: 633-638.KhanMAShiraziMUKhanMARole of proline, K/Na ratio and chlorophyll content in salt tolerance of wheat Triticum aestivum L.)200941633638Search in Google Scholar
Akram NA, Ashraf M. Improvement in growth, chlorophyll pigments and photosynthetic performance in salt-stressed pants of sunflower Helianthus annuus L.) by foliar application of 5-aminolevunilic acid. Agrochimica 2011; 55: 94-104.AkramNAAshrafMImprovement in growth, chlorophyll pigments and photosynthetic performance in salt-stressed pants of sunflower Helianthus annuus L.) by foliar application of 5-aminolevunilic acid20115594104Search in Google Scholar
Davison PA, Hunter CN, Horton P. Overexpression of β-carotene hydroxylase enhances stress tolerance in Arabidopsis. Nature 2002; 418:203-206.DavisonPAHunterCNHortonPOverexpression of β-carotene hydroxylase enhances stress tolerance in Arabidopsis200241820320610.1038/nature00861Search in Google Scholar
Verma S, Mishra SN. Putrescine alleviation of growth in salt stressed Brassica juncea by inducing antioxidative defence system. Journal of Plant Physiology 2005; 162: 669-677.VermaSMishraSNPutrescine alleviation of growth in salt stressed Brassica juncea by inducing antioxidative defence system200516266967710.1016/j.jplph.2004.08.008Search in Google Scholar
Puniran-Hartley N, Hartley J, Shabala L, and Shabala S. Salinity induced accumulation of organic osmolytes in barley and wheat laves correlates with increased oxidative stress tolerance in plants evidence for cross tolerance. Plant Physiology and Biochemistry 2014; 83: 32-39.Puniran-HartleyNHartleyJShabalaLShabalaSSalinity induced accumulation of organic osmolytes in barley and wheat laves correlates with increased oxidative stress tolerance in plants evidence for cross tolerance201483323910.1016/j.plaphy.2014.07.005Search in Google Scholar
Gao R, Curtis TY, Powers SJ, Xu H, Huang J, and Halford NG. Food safety: structure and expression of the asparagines synthetase gene family of wheat. Journal of Cereals Science 2016; 68: 122-131.GaoRCurtisTYPowersSJXuHHuangJHalfordNGFood safety: structure and expression of the asparagines synthetase gene family of wheat20166812213110.1016/j.jcs.2016.01.010Search in Google Scholar
Silveira JAG, Melo ARB, Martins MO, Ferreira-Silva SL, Aragao RM, Silva EN, et al. Salinity affexcts indirectly nitrate acquisition associated with glutamine accumulation in cowpea roots.Plant Biology 2012; 56: 575-580.SilveiraJAGMeloARBMartinsMOFerreira-SilvaSLAragaoRMSilvaENet alSalinity affexcts indirectly nitrate acquisition associated with glutamine accumulation in cowpea roots20125657558010.1007/s10535-012-0065-7Search in Google Scholar
Sanders D, Plant biology: The salty tale of Arabidopsis. Current Biology 2000; 10:486-488.SandersDPlant biology: The salty tale of Arabidopsis20001048648810.1016/S0960-9822(00)00554-6Search in Google Scholar
Zhu JK. Genetic analysis of plant salt tolerance using Arabidopsis Plant Physiology 2000; 124:941-948.ZhuJKGenetic analysis of plant salt tolerance using Arabidopsis200012494194810.1104/pp.124.3.941Search in Google Scholar
Yokoi S, Brassan RA, Hasegawa PM. Salt stress tolerance of plants. JIRCAS Working Report 2002; 25-33.YokoiSBrassanRAHasegawaPMSalt stress tolerance of plants20022533Search in Google Scholar
Zhu JK. Plant salt tolerance. Trends in Plant Science 2001; 6: 66-71.ZhuJKPlant salt tolerance20016667110.1016/S1360-1385(00)01838-0Search in Google Scholar
Noctor G, Mhamdi A, Chaouch S, Han Y, Neukermans J, Garcia BM, Queval G, Foyer C. Glutathione in plants: an integrated overview Plant, Cell& Environment 2012; 35:454-484.NoctorGMhamdiAChaouchSHanYNeukermansJGarciaBMQuevalGFoyerCGlutathione in plants: an integrated overview Plant20123545448410.1111/j.1365-3040.2011.02400.xSearch in Google Scholar
Komatsu S, Kamal AHM, Hossain Z. Wheat proteomics: proteome modulation and abiotic stress acclimation. Frontiers in Plant Science 2014; 5: art 684.KomatsuSKamalAHMHossainZWheat proteomics: proteome modulation and abiotic stress acclimation20145art 68410.3389/fpls.2014.00684425912425538718Search in Google Scholar
Niazi A, Ramezani A, Dinari A. GSTF1 gene expression analysis in cultivated wheat plants under salinity and ABA treatments. Molecular Biology Research Communications 2014; 3(1):9-19.NiaziARamezaniADinariAGSTF1 gene expression analysis in cultivated wheat plants under salinity and ABA treatments201431919Search in Google Scholar
Hoagland, D.R. and Arnon, D.I. (1950) The Water-Culture Method for Growing Plants without Soil. California Agricultural Experiment Station, Berkeley.HoaglandD.R.ArnonD.I.1950California Agricultural Experiment StationBerkeleySearch in Google Scholar
Hiscox JD, Israelstam GF. A method for the extraction of chlorophyll from leaf tissue without maceration. Canadian Journal of Botany 1979; 57: 1332-1334.HiscoxJDIsraelstamGFA method for the extraction of chlorophyll from leaf tissue without maceration1979571332133410.1139/b79-163Search in Google Scholar
Richardson AD, Duigan SP & Berlyn GP. An evaluation of noninvasive methods to estimate foliar chlorophyll content. New Phytologist 2002; 153: 185-194.RichardsonADDuiganSP&BerlynGP.An evaluation of noninvasive methods to estimate foliar chlorophyll content200215318519410.1046/j.0028-646X.2001.00289.xSearch in Google Scholar
Arnon DI. Copper enzymes in isolated chloroplasts polyphenol oxidase in Beta vulgari. Plant Physiology 1949; 24: 1-15.ArnonDICopper enzymes in isolated chloroplasts polyphenol oxidase in Beta vulgari19492411510.1104/pp.24.1.1Search in Google Scholar
Van Horn JD, Bulaj G, Goldenberg DP, Burrows CJ. The cys-xaa-his metal-binding motif. {n} versus {s} coordination and nickel mediated formation of cysteinyl sulfinic acid. J. Biol. Inorg. Chem. 2003; 8: 601-610.Van HornJDBulajGGoldenbergDPBurrowsCJThe cys-xaa-his metal-binding motif. {n} versus {s} coordination and nickel mediated formation of cysteinyl sulfinic acid2003860161010.1007/s00775-003-0454-7Search in Google Scholar
Ellman GL. Arch.Biochem.Biophys 1959; 82:70-77.EllmanGL195982707710.1016/0003-9861(59)90090-6Search in Google Scholar
Komatsu S, Kamal HM, Hossain Z. Wheat proteomics: proteome modulation and abiotic stress acclimation. Frontiers in Plant Science 2014; 5: art 684.KomatsuSKamalHMHossainZWheat proteomics: proteome modulation and abiotic stress acclimation20145art 68410.3389/fpls.2014.00684Search in Google Scholar
Bohnert HJ, Nelson DE, Jensen DG. Adaptations to environmental stresses. Plant Cell 1995; 7: 1099-1111.BohnertHJNelsonDEJensenDGAdaptations to environmental stresses199571099111110.2307/3870060Search in Google Scholar
Wachter A, Wolf S, Steiniger H, Bogs J, Rausch T.Differential Targeting of GSH1 and GSH2 is achieved by multiple transcription initiation: Implications for the compartmentalization of glutathione biosynthesis in the Brasicaceae Plant Jl 2005; 41(1):15-30.WachterAWolfSSteinigerHBogsJRauschTDifferential Targeting of GSH1 and GSH2 is achieved by multiple transcription initiation: Implications for the compartmentalization of glutathione biosynthesis in the Brasicaceae2005411153010.1111/j.1365-313X.2004.02269.x15610346Search in Google Scholar
Bacu A, Duka D. Comparison of total plant amount and tissue distribution of glutathione at wheat cultivars grown in the absence of external stresses. Journal of Environmental Protection and Ecology 2018; 19(4): 1583-1590.BacuADukaDComparison of total plant amount and tissue distribution of glutathione at wheat cultivars grown in the absence of external stresses201819415831590Search in Google Scholar