scholarly article | Q13442814 |
P356 | DOI | 10.3389/FENVS.2015.00013 |
P2093 | author name string | Harpreet Kaur | |
Renu Bhardwaj | |||
Poonam Yadav | |||
Vandana Gautam | |||
Ravdeep Kaur | |||
Neha Handa | |||
Amandeep Rattan | |||
Dhriti Kapoor | |||
Resham Sharma | |||
P2860 | cites work | Peroxiredoxin Q of Arabidopsis thaliana is attached to the thylakoids and functions in context of photosynthesis. | Q46968036 |
Overexpression in tobacco of a tomato GMPase gene improves tolerance to both low and high temperature stress by enhancing antioxidation capacity | Q48060245 | ||
A peroxiredoxin antioxidant is encoded by a dormancy-related gene, Per1, expressed during late development in the aleurone and embryo of barley grains. | Q48060354 | ||
Plant glutathione peroxidases are functional peroxiredoxins distributed in several subcellular compartments and regulated during biotic and abiotic stresses. | Q50710002 | ||
Redox homeostasis: Opening up ascorbate transport. | Q52838104 | ||
On the quenching of singlet oxygen by alpha-tocopherol. | Q52888260 | ||
Ectopic expression of Arabidopsis glutaredoxin AtGRXS17 enhances thermotolerance in tomato. | Q53369410 | ||
A thioredoxin--thioredoxin reductase system from rat tumor. | Q53778193 | ||
Hydroperoxide reduction by thioredoxin-specific glutathione peroxidase isoenzymes of Arabidopsis thaliana. | Q54452175 | ||
Enhanced tolerance of transgenic potato plants expressing both superoxide dismutase and ascorbate peroxidase in chloroplasts against oxidative stress and high temperature. | Q54592230 | ||
Stress induces the expression of AtNADK-1, a gene encoding a NAD(H) kinase in Arabidopsis thaliana. | Q54680633 | ||
Nonenzymatic lipid peroxidation reprograms gene expression and activates defense markers in Arabidopsis tocopherol-deficient mutants | Q55113319 | ||
Reactive oxygen species generation and antioxidant systems in plant mitochondria | Q58382531 | ||
Plant peroxiredoxins: alternative hydroperoxide scavenging enzymes | Q58382836 | ||
Proteomic analysis of copper stress responses in the roots of two rice (Oryza sativa L.) varieties differing in Cu tolerance | Q59106722 | ||
Phytochelatin synthase genes from Arabidopsis and the yeast Schizosaccharomyces pombe | Q24543974 | ||
Role of the ascorbate-glutathione cycle of mitochondria and peroxisomes in the senescence of pea leaves | Q24628436 | ||
Ascorbate as seen through plant evolution: the rise of a successful molecule? | Q26828982 | ||
The ascorbate-glutathione-α-tocopherol triad in abiotic stress response | Q27027101 | ||
Role of the glutathione/glutaredoxin and thioredoxin systems in yeast growth and response to stress conditions. | Q27937765 | ||
Glutathione-mediated detoxification systems in plants | Q28138205 | ||
Prestin is the motor protein of cochlear outer hair cells | Q28144919 | ||
Poly(ADP-ribose) polymerase in plants affects energy homeostasis, cell death and stress tolerance | Q28212063 | ||
Glutaredoxins: glutathione-dependent redox enzymes with functions far beyond a simple thioredoxin backup system | Q28237878 | ||
Evidence that feedback inhibition of NAD kinase controls responses to oxidative stress | Q28238987 | ||
The chemistry and antioxidant properties of tocopherols and tocotrienols | Q28291396 | ||
Thioredoxin and glutaredoxin: small multi-functional redox proteins with active-site disulphide bonds | Q28294864 | ||
PARP-2, A novel mammalian DNA damage-dependent poly(ADP-ribose) polymerase | Q28511873 | ||
Redox environment of the cell as viewed through the redox state of the glutathione disulfide/glutathione couple | Q29615232 | ||
Evolution and function of phytochelatin synthases | Q30320106 | ||
Cell proliferation and hair tip growth in the Arabidopsis root are under mechanistically different forms of redox control. | Q30945594 | ||
Vitamin C degradation in plant cells via enzymatic hydrolysis of 4-O-oxalyl-L-threonate | Q33210164 | ||
Ascorbate as a biosynthetic precursor in plants | Q33576728 | ||
Modulation of redox homeostasis under suboptimal conditions by Arabidopsis nudix hydrolase 7 | Q33655600 | ||
Tropospheric ozone and plants: absorption, responses, and consequences | Q33854122 | ||
A cysteine-sulfinic acid in peroxiredoxin regulates H2O2-sensing by the antioxidant Pap1 pathway | Q33863247 | ||
Molecular physiology of plant sulfur metabolism | Q34064806 | ||
Whole-genome transcriptional analysis of heavy metal stresses in Caulobacter crescentus | Q34231030 | ||
Phytochelatins, the heavy-metal-binding peptides of plants, are synthesized from glutathione by a specific gamma-glutamylcysteine dipeptidyl transpeptidase (phytochelatin synthase). | Q34302487 | ||
Thioredoxin structure and mechanism: conformational changes on oxidation of the active-site sulfhydryls to a disulfide | Q34313529 | ||
Transgenic barley grain overexpressing thioredoxin shows evidence that the starchy endosperm communicates with the embryo and the aleurone | Q34416354 | ||
The origin of atmospheric oxygen on Earth: the innovation of oxygenic photosynthesis | Q34444656 | ||
Plant thioredoxins are key actors in the oxidative stress response | Q34539514 | ||
PLANT THIOREDOXIN SYSTEMS REVISITED. | Q34546213 | ||
An expression analysis of the ascorbate biosynthesis enzyme VTC2. | Q34783450 | ||
Phytochelatins and metallothioneins: roles in heavy metal detoxification and homeostasis | Q34833561 | ||
Arabidopsis monothiol glutaredoxin, AtGRXS17, is critical for temperature-dependent postembryonic growth and development via modulating auxin response | Q35063470 | ||
Plant Peroxiredoxins | Q35540286 | ||
Glutaredoxin GRXS13 plays a key role in protection against photooxidative stress in Arabidopsis | Q35632271 | ||
The thioredoxin h system of higher plants | Q35761482 | ||
Expression analysis of four peroxiredoxin genes from Tamarix hispida in response to different abiotic stresses and Exogenous Abscisic Acid (ABA). | Q35866091 | ||
Comprehensive gene expression analysis of the NAC gene family under normal growth conditions, hormone treatment, and drought stress conditions in rice using near-isogenic lines (NILs) generated from crossing Aday Selection (drought tolerant) and IR6 | Q35911629 | ||
The plant thioredoxin system. | Q35993549 | ||
Silencing of poly(ADP-ribose) polymerase in plants alters abiotic stress signal transduction | Q36002679 | ||
The plant multigenic family of thiol peroxidases | Q36125293 | ||
Oxidative stress: molecular perception and transduction of signals triggering antioxidant gene defenses | Q36188746 | ||
The role of alpha-tocopherol in plant stress tolerance. | Q36189126 | ||
AtPCS1, a phytochelatin synthase from Arabidopsis: isolation and in vitro reconstitution | Q36393732 | ||
NAD(P) synthesis and pyridine nucleotide cycling in plants and their potential importance in stress conditions. | Q36484213 | ||
Thioredoxin links redox to the regulation of fundamental processes of plant mitochondria | Q36603278 | ||
Poly(ADP-ribose) polymerase is a mediator of necrotic cell death by ATP depletion | Q36704795 | ||
Oxidative modifications to cellular components in plants | Q36731443 | ||
Redox based anti-oxidant systems in plants: biochemical and structural analyses | Q37060622 | ||
Enzyme activities and subcellular localization of members of the Arabidopsis glutathione transferase superfamily | Q37133113 | ||
Regeneration mechanisms of Arabidopsis thaliana methionine sulfoxide reductases B by glutaredoxins and thioredoxins. | Q37254011 | ||
The role of NAD biosynthesis in plant development and stress responses | Q37388246 | ||
Peroxiredoxins: a less studied component of hydrogen peroxide detoxification in photosynthetic organisms | Q37393904 | ||
From proteomics to structural studies of cytosolic/mitochondrial-type thioredoxin systems in barley seeds | Q37613980 | ||
Structure, function, and mechanism of thioredoxin proteins | Q37688111 | ||
Roles of enzymatic and nonenzymatic antioxidants in plants during abiotic stress | Q37705371 | ||
Tocochromanol functions in plants: antioxidation and beyond. | Q37729524 | ||
Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants | Q37792599 | ||
Glutathione in plants: an integrated overview. | Q37903382 | ||
The role of L-ascorbic acid recycling in responding to environmental stress and in promoting plant growth | Q38060699 | ||
Role of glutaredoxin in metabolic oxidative stress. Glutaredoxin as a sensor of oxidative stress mediated by H2O2. | Q38362754 | ||
NADK2, an Arabidopsis chloroplastic NAD kinase, plays a vital role in both chlorophyll synthesis and chloroplast protection | Q38936863 | ||
A tomato glutaredoxin gene SlGRX1 regulates plant responses to oxidative, drought and salt stresses. | Q39037056 | ||
Ascorbate peroxidase 1 plays a key role in the response of Arabidopsis thaliana to stress combination | Q39146877 | ||
Ascorbate peroxidase-related (APx-R) is a new heme-containing protein functionally associated with ascorbate peroxidase but evolutionarily divergent | Q39164079 | ||
Role of L-ascorbate in alleviating abiotic stresses in crop plants | Q39311426 | ||
A novel NADPH thioredoxin reductase, localized in the chloroplast, which deficiency causes hypersensitivity to abiotic stress in Arabidopsis thaliana. | Q39447235 | ||
The role of metabolism in the antioxidant function of vitamin E. | Q40824354 | ||
Functional analysis of the pathways for 2-Cys peroxiredoxin reduction in Arabidopsis thaliana chloroplasts. | Q42429663 | ||
The genetic basis of singlet oxygen-induced stress responses of Arabidopsis thaliana | Q42640428 | ||
A novel monothiol glutaredoxin (Grx4) from Escherichia coli can serve as a substrate for thioredoxin reductase. | Q42653676 | ||
Response of mitochondrial thioredoxin PsTrxo1, antioxidant enzymes, and respiration to salinity in pea (Pisum sativum L.) leaves. | Q42795803 | ||
Apoplastic ascorbate contributes to the differential ozone sensitivity in two varieties of winter wheat under fully open-air field conditions | Q42882866 | ||
Arabidopsis GLUTATHIONE REDUCTASE1 plays a crucial role in leaf responses to intracellular hydrogen peroxide and in ensuring appropriate gene expression through both salicylic acid and jasmonic acid signaling pathways. | Q43057979 | ||
Overexpression of chloroplastic monodehydroascorbate reductase enhanced tolerance to temperature and methyl viologen-mediated oxidative stresses. | Q43129341 | ||
Metabolome and photochemical analysis of rice plants overexpressing Arabidopsis NAD kinase gene | Q43162716 | ||
The cellular redox state in plant stress biology--a charging concept. | Q43170747 | ||
The role of AtNUDT7, a Nudix hydrolase, in the plant defense response | Q43190023 | ||
Enhanced tolerance of transgenic tall fescue plants overexpressing 2-Cys peroxiredoxin against methyl viologen and heat stresses. | Q43219614 | ||
Overexpression of dehydroascorbate reductase, but not monodehydroascorbate reductase, confers tolerance to aluminum stress in transgenic tobacco | Q43230146 | ||
Transgenic expression of fern Pteris vittata glutaredoxin PvGrx5 in Arabidopsis thaliana increases plant tolerance to high temperature stress and reduces oxidative damage to proteins | Q43236136 | ||
Modulation of the poly(ADP-ribosyl)ation reaction via the Arabidopsis ADP-ribose/NADH pyrophosphohydrolase, AtNUDX7, is involved in the response to oxidative stress | Q43298134 | ||
Induction of thioredoxin is required for nodule development to reduce reactive oxygen species levels in soybean roots | Q43442339 | ||
A specific role for tocopherol and of chemical singlet oxygen quenchers in the maintenance of photosystem II structure and function in Chlamydomonas reinhardtii | Q43962965 | ||
Probing the diversity of the Arabidopsis glutathione S-transferase gene family | Q44045440 | ||
Double antisense plants lacking ascorbate peroxidase and catalase are less sensitive to oxidative stress than single antisense plants lacking ascorbate peroxidase or catalase | Q44201177 | ||
Analysis of the molecular evolutionary history of the ascorbate peroxidase gene family: inferences from the rice genome | Q45187701 | ||
Alterations in tocopherol cyclase activity in transgenic and mutant plants of Arabidopsis affect tocopherol content, tocopherol composition, and oxidative stress. | Q45234546 | ||
Hydroponically cultivated radish fed L-galactono-1,4-lactone exhibit increased tolerance to ozone | Q45713275 | ||
Increasing tolerance to ozone by elevating foliar ascorbic acid confers greater protection against ozone than increasing avoidance | Q46053716 | ||
Tocopherol deficiency in transgenic tobacco (Nicotiana tabacum L.) plants leads to accelerated senescence | Q46236172 | ||
Overexpression of an ADP-ribose pyrophosphatase, AtNUDX2, confers enhanced tolerance to oxidative stress in Arabidopsis plants | Q46361988 | ||
A peroxiredoxin Q homolog from gentians is involved in both resistance against fungal disease and oxidative stress | Q46445905 | ||
Purification and cDNA cloning of chloroplastic monodehydroascorbate reductase from spinach | Q46453676 | ||
Tocopherol metabolism, oxidation and recycling under high light stress in Arabidopsis | Q46614829 | ||
Vitamin E protects against photoinhibition and photooxidative stress in Arabidopsis thaliana | Q46781709 | ||
Ascorbate peroxidase gene family in tomato: its identification and characterization | Q46890553 | ||
Vitamin E is essential for the tolerance of Arabidopsis thaliana to metal-induced oxidative stress | Q46905212 | ||
P921 | main subject | abiotic stress | Q4667893 |
P577 | publication date | 2015-03-04 | |
P1433 | published in | Frontiers in environmental science | Q27727391 |
P1476 | title | Redox homeostasis in plants under abiotic stress: role of electron carriers, energy metabolism mediators and proteinaceous thiols | |
P478 | volume | 3 |
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