References
- Salt tolerance;The Arabidopsis Book Xiong, L.;Zhu, J.K.;Somerville, C.R.(ed.);Meyerowitz, E.M.(ed.) https://doi.org/10.1199/tab.0048
- Biochem. Soc. Trans. v.24 Oxidative stress and responses in Arabidopsis thaliana and Oryza sativa subjected to chilling and salinity stress Burdon, R.H.;O'Kane, D.;Fadzillah, N.;Gill, V.;Boyd, P.A.;Finch, R.R. https://doi.org/10.1042/bst0240469
- Plant Physiol. v.113 Increased resistance to oxidative stress in transgenic plants by targeting mannitol biosynthesis to chloroplasts Shen, B.;Jensen, R.G.;Bohnert, H. https://doi.org/10.1104/pp.113.4.1177
- Plant Cell v.11 A recessive Arabidopsis mutant that grows photoautotrophically under salt stress shows enhanced active oxygen detoxification Tsugane, K.;Kobayashi, K.;Niwa, Y.;Ohba, Y.;Wada, K.;Kobayashi, H. https://doi.org/10.1105/tpc.11.7.1195
- Plant Physiol. v.122 Removal of feedback inhibition of D1-pyrroline-5-carboxylate synthetase results in increased proline accumulation and protection of plants from osmotic stress Hong, Z.;Lakkineni, K.;Zhang, Z.;Verma, D.P.S. https://doi.org/10.1104/pp.122.4.1129
- Trends Plant Sci. v.6 Plant salt tolerance Zhu, J.K. https://doi.org/10.1016/S1360-1385(00)01838-0
- Curr. Opin. Plant Biol. v.1 Plant stress adaptations, making metabolism move Bohnert, H.J.;Sheveleva, E. https://doi.org/10.1016/S1369-5266(98)80115-5
- Plant Sci. v.135 Antioxidant responses of rice seedlings to salinity stress Dionisio-Sese, M.L.;Tobita, S. https://doi.org/10.1016/S0168-9452(98)00025-9
- Plant Sci. v.165 Scavenging of reactive oxygen species in NaCl-stressed rice (Oryza sativa L.) - differential response in salt-tolerant and sensitive varieties Vaidyanathan, H.;Sivakumar, P.;Chakrabarty, R.;Thomas, G. https://doi.org/10.1016/j.plantsci.2003.08.005
- Plant Sci. v.164 The effect of salt stress on lipid peroxidation and antioxidants in leaves of sugar beet Beta vulgaris L. and wild beet Beta maritime L. Bor, M.;Ozdemir, F.;Turkan, I. https://doi.org/10.1016/S0168-9452(02)00338-2
-
Science
v.285
Salt tolerance conferred by overexpression of a vacuolar
$Na^+/H^+$ antiport in Arabidopsis Apse, M.P.;Aharon, G.S.;Snedden, W.A.;Blumwald, E. https://doi.org/10.1126/science.285.5431.1256 -
Biochim. Biophys. Acta
v.1446
Molecular cloning and expression of the
$Na^+/H^+$ exchanger gene in Oryza sativa Fukuda, A.;Nakamura, A.;Tanaka, Y. https://doi.org/10.1016/S0167-4781(99)00065-2 -
Plant J.
v.30
Differential expression and function of Arabidopsis thaliana NHX
$Na^+/H^+$ antiporters in the salt stress response Yokoi, S.;Quintero, F.J.;Cubero, B.;Ruiz, M.T.;Bressan, R.A.;Hasegawa, P.M.;Pardo, J.M. https://doi.org/10.1046/j.1365-313X.2002.01309.x -
Plant Soil
v.253
Characterization of a family of vacuolar
$Na^+/H^+$ antiporters in Arabidopsis thaliana Aharon, G.S.;Apse, M.P.;Duan, S.;Hua, X.;Blumwald, E. https://doi.org/10.1023/A:1024577205697 - J. Plant Biol. v.46 Differences in photosynthetic characterization of salt tolerance for two rice (Oryza sativa) cultivars Oh, M.J.;Chun, H.S.;Lee, C.B. https://doi.org/10.1007/BF03030296
-
Plant Physiol.
v.108
Overexpression of
${\Delta}-pyrroline-5-carboxylate$ synthase increases proline production and confers osmotolerance in transgenic plants Kishor, P.B.K.;Hong, Z.;Miao, G.;Hu, C.A.;Verma, D.P.S. - Plant J. v.12 Transformation of Arabidopsis thaliana with the coda gene for choline oxidase; accumulation of glycinebetaine and enhanced tolerance to salt and cold stress Hayashi, H.;Alia, Mustardy L.;Deshnium, P.;Ida, M.;Murata, N. https://doi.org/10.1046/j.1365-313X.1997.12010133.x
- Curr. Opin. Plant Biol. v.2 Metabolic engineering of plants for osmotic sress resistance Nuccio, M.L.;Rhodes, D.;McNeil, S.D.;Hanson, A.D. https://doi.org/10.1016/S1369-5266(99)80026-0
- J. Plant Physiol. v.151 Effect of pretreatment with methyl jasmonate on the response of Pisum sativum to salt stress Fedina, I.S.;Tsonev, T.D. https://doi.org/10.1016/S0176-1617(97)80071-5
- Photosynthetica v.35 Response of photosynthesis of Pisum sativum to salt stress as affected by methyl jasmonate Velitchkova, M.;Fedina, I. https://doi.org/10.1023/A:1006878016556
- Biol. Plant. v.43 Response of Scenedesmus incrassatulus to salt stress as affected by methyl jasmonate Fedina, I.S.;Benderliev, K.M. https://doi.org/10.1023/A:1002816502941
- Annu. Rev. Plant Physiol. Plant Mol. Biol. v.42 Chlorophyll fluorescence and photosynthesis: the basics Krause, G.H.;Weis, E. https://doi.org/10.1146/annurev.pp.42.060191.001525
- Photosynth. Res. v.25 The use of chlorophyll fluorescence nomenclature in plant stress physiology van Kooten, O.;Snel, F.H. https://doi.org/10.1007/BF00033156
- Photosynth. Res. v.54 Resolving chlorophyll a fluorescence images of photosynthetic efficiency into photochemical and non-photochemical components-Calculation of qP and Fv'/Fm' without measuring Fo' Oxborough, K.;Baker, N.R. https://doi.org/10.1023/A:1005936823310
- Biochim. Biophys. Acta v.990 Relationship between the quantum yield of photosynthetic electron transport and the quenching of chlorophyll fluorescence Genty, B.;Briantais, J.M.;Baker, N.R. https://doi.org/10.1016/S0304-4165(89)80016-9
- J. Photosci. v.11 Construction of gene-specific primers of various antioxidant isoenzyme genes and their expressions in rice (Oryza sativa L.) seedlings obtained from gamma-irradiated seeds Kim, J.H.;Chung, B.Y.;Kim, J.S.;Wi, S.G.;Yang, D.H.;Lee, C.H.;Lee, M.C.
- Proc. Natl. Acad. Sci. USA v.99 A rice spotted leaf gene, Spl7, encodes a heat stress transcription factor protein Yamanouchi, U.;Yano, M.;Lin, H.;Ashikari, M.;Yamada, K.
- Plant Physiol. v.70 Salt tolerance in crop plants monitored by chlorophyll fluorescence in vivo Smille, R.M.;Nott, R. https://doi.org/10.1104/pp.70.4.1049
- J. Plant Physiol. v.157 Effects of salinity on sodium content and photosynthetic responses of rice seedlings differing in salt tolerance Dionisio-Sese, M.L.;Tobita, S. https://doi.org/10.1016/S0176-1617(00)80135-2
- Crop Sci. v.44 Sorghum and salinity ll. Gas exchange and chlorophyll fluorescence of Sorghum under salt stress Netondo, G.W.;Onyango, J.C.;Beck, E. https://doi.org/10.2135/cropsci2004.0806
- Photosynthetica v.42 Dissipation of excess energy in Mehler-peroxidase reaction in Rumex leaves during salt shock Chen, H.X.;Gao, H.Y.;An, S.Z.;Li, W.J. https://doi.org/10.1023/B:PHOT.0000040579.37842.ca
-
Func. Plant Biol.
v.29
Factors affecting
$CO_2$ assimilation, leaf injury and growth in salt-stressed durum wheat James, R.A.;Rivelli, A.R.;Munns, R.;von Caemmerer, S. https://doi.org/10.1071/FP02069 - Plant Cell Environ. v.23 Expression of dehydration-stress-related genes in the crowns of wheatgrass species [Lophopyrum elongatum (Host) A. Love and Agropyron desertorum (Fisch. Ex Link.) Schult.] having contrasting acclimation to salt, cold and drought Tabaei-Aghdaei, S.R.;Harrison, P.;Pearce, R.S. https://doi.org/10.1046/j.1365-3040.2000.00572.x
- Plant Physiol. v.131 Expression of a bifunctional fusion of the Escherichia coli genes for trehalose-6-phosphate synthase and trehalose-6-phosphate phosphatase in transgenic rice plants increases trehalose accumulation and abiotic stress tolerance without stunting growth Jang, I.C.;Oh, S.J.;Seo, J.S.;Choi, W.B.;Song, S.I.;Kim, C.H.;Kim, Y.S.;Seo, H.S.;Choi, Y.D.;Nahm, B.H.;Kim, J.K. https://doi.org/10.1104/pp.007237
- New Phytol. v.141 Response of antioxidant systems and leaf water relations to NaCl stress in pea plants Hernandez, J.A.;Campillo, A.;Jimenez, A.;Alacon, J.J.;Sevilla, F. https://doi.org/10.1046/j.1469-8137.1999.00341.x
- J. Plant Physiol. v.161 Defense potentials to NaCl in a mangrove, Bruguiera parviflora: differential changes of isoforms of some antioxidant enzymes Parida, A.K.;Das, A.B.;Mohanty, P. https://doi.org/10.1078/0176-1617-01084
- Plant Physiol. v.123 Expression of spinach ascorbate peroxidase isoenzymes in response to oxidative stress Yoshimura, K.;Yabuta, Y.;Ishikawa, T.;Shigeoka, S. https://doi.org/10.1104/pp.123.1.223
- Z. Naturforsch. v.59c Salt-stress induced alterations in protein profile and protease activity in the mangrove, Bruguiera parviflora Parida, A.K.;Das, A.B.;Mittra, B.;Mohanty, P.
- Ecotox. Environ. Safe. v.60 Salt tolerance and salinity effects on plants: a review Parida, A.K.;Das, A.B. https://doi.org/10.1016/j.ecoenv.2004.06.010
-
J. Biol. Chem.
v.279
Regulation of vacuolar
$Na^+/H^+$ exchange in Arabidopsis thaliana by the Salt-Overly-Sensitive (SOS) pathway Qiu, Q.S.;Guo, Y.;Quintero, F.J.;Pardo, J.M.;Schumaker, K.S.;Zhu, J.K. https://doi.org/10.1074/jbc.M307982200