Student or educator? Sign up with your school email and get 6 months of Pro free.
CoChat
Sign Up
Cited by 59

The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

RETRACTED: The interplay between reactive oxygen and nitrogen species contributes in the regulatory mechanism of the nitro-oxidative stress induced by cadmium in Arabidopsis

Liu, Shiliang, Yang, Rongjie, Tripathi, Durgesh Kumar, Li, Xi, He, Wei, Wu, Mengxi, Ali, Shafaqat, Ma, Mingdong, Cheng, Qingsu, Pan, Yuanzhi·2018·Journal of Hazardous Materials
DOI 10.1016/j.jhazmat.2017.12.004
Open this paper in CoChat — free account

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1016/j.jhazmat.2017.12.004This paper is marked retracted.

Cites

2 of 2 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Show all 2 references

Research works printed but not linked: 74

  1. Leitner, 2009, NO signals in the haze: nitric oxide signalling in plant defence, Curr. Opin. Plant Bio., 12, 451, 10.1016/j.pbi.2009.05.012 · DOI · Paper page
  2. Astier, 2012, Nitric oxide-dependent posttranslational modification in plants: an update, Int. J. Mol. Sci., 13, 15193, 10.3390/ijms131115193 · DOI · Paper page
  3. Wang, 2015, Nitric oxide negatively regulates abscisic acid signaling in guard cells by S-nitrosylation of OST1, Proc. Natl. Acad. Sci. U. S. A., 112, 613, 10.1073/pnas.1423481112 · DOI · Paper page
  4. Liu, 2016, Beneficial behavior of nitric oxide in copper-treated medicinal plants, J. Hazard. Mater., 314, 140, 10.1016/j.jhazmat.2016.04.042 · DOI
  5. Chaki, 2009, Involvement of reactive nitrogen and oxygen species (RNS and ROS) in sunflower mildew interaction, Plant Cell Physiol., 50, 265, 10.1093/pcp/pcn196 · DOI · Paper page
  6. Leterrier, 2011, Function of S-nitrosoglutathione reductase (GSNOR) in plant development and under biotic/abiotic stress, Plant Signal. Behav., 6, 789, 10.4161/psb.6.6.15161 · DOI · Paper page
  7. Corpas, 2013, Nitro-oxidative stress vs oxidative or nitrosative stress in higher plants, New Phytol., 199, 633, 10.1111/nph.12380 · DOI · Paper page
  8. Barroso, 2006, L.A. del Río, Localization of S-nitrosoglutathione and expression of S-nitrosoglutathione reductase in pea plants under cadmium stress, J. Exp. Bot., 57, 1785, 10.1093/jxb/erj175 · DOI · Paper page
  9. Yun, 2016, Nitric oxide and S-nitrosoglutathione function additively during plant immunity, New Phytol., 211, 516, 10.1111/nph.13903 · DOI
  10. Frungillo, 2014, S-nitrosothiols regulate nitric oxide production and storage in plants through the nitrogen assimilation pathway, Nat. Commun., 5, 5401, 10.1038/ncomms6401 · DOI · Paper page
  11. Lee, 2008, Modulation of nitrosative stress by S-nitrosoglutathione reductase is critical for thermotolerance and plant growth in Arabidopsis, Plant Cell, 20, 786, 10.1105/tpc.107.052647 · DOI · Paper page
  12. Smith, 2000, Kinetics and mechanism of the decomposition of S-nitrosoglutathione by L-ascorbic acid and copper ions in aqueous solution to produce nitric oxide, Nitric Oxide, 4, 57, 10.1006/niox.2000.0272 · DOI
  13. Scheler, 2013, Nitric oxide and reactive oxygen species in plant biotic interactions, Curr. Opin. Plant Bio., 16, 534, 10.1016/j.pbi.2013.06.020 · DOI · Paper page
  14. Corpas, 2017, Plant peroxisomes: a nitro-oxidative cocktail, Redox Bio., 11, 535, 10.1016/j.redox.2016.12.033 · DOI · Paper page
  15. Corpas, 2007, Need of biomarkers of nitrosative stress in plants, Trends Plant Sci., 12, 436, 10.1016/j.tplants.2007.08.013 · DOI
  16. Radi, 2004, Nitric oxide, oxidants, and protein tyrosine nitration, Proc. Natl. Acad. Sci. U. S. A., 101, 4003, 10.1073/pnas.0307446101 · DOI · Paper page
  17. Prolo, 2015, Nitric oxide diffusion to red blood cells limits extracellular but not intraphagosomal, peroxynitrite formation by macrophages, Free Radical Bio. Med., 87, 346, 10.1016/j.freeradbiomed.2015.06.027 · DOI
  18. Wunsche, 2011, S-nitrosoglutathione reductase (GSNOR) mediates the biosynthesis of jasmonic acid and ethylene induced by feeding of the insect herbivore Manduca sexta and is important for jasmonate-elicited responses in Nicotiana attenuate, J. Exp. Bot., 62, 4605, 10.1093/jxb/err171 · DOI
  19. Espunya, 2012, S-nitrosoglutathione is a component of wound- and salicylic acid-induced systemic responses in Arabidopsis thaliana, J. Exp. Bot., 63, 3219, 10.1093/jxb/ers043 · DOI
  20. Díaz, 2003, The gene encoding glutathione-dependent formaldehyde dehydrogenase/GSNO reductase is responsive to wounding, jasmonic acid and salicylic acid, FEBS Lett., 543, 136, 10.1016/S0014-5793(03)00426-5 · DOI
  21. Chaki, 2011, Mechanical wounding induces a nitrosative stress by down-regulation of GSNO reductase and an increase in S-nitrosothiols in sunflower (Helianthus annuus) seedlings, J. Exp. Bot., 62, 1803, 10.1093/jxb/erq358 · DOI · Paper page
  22. Airaki, 2012, Metabolism of reactive oxygen species and reactive nitrogen species in pepper (Capsicum annuum L.) plants under low temperature stress, Plant Cell Environ., 35, 281, 10.1111/j.1365-3040.2011.02310.x · DOI · Paper page
  23. Delledonne, 2001, Signal interactions between nitric oxide and reactive oxygen intermediates in the plant hypersensitive disease resistance response, Proc. Natl. Acad. Sci. U. S. A., 98, 13454, 10.1073/pnas.231178298 · DOI · Paper page
  24. Leterrier, 2012, NADP-dependent isocitrate dehydrogenase from Arabidopsis roots contributes in the mechanism of defence against the nitro-oxidative stress induced by salinity, Sci. World J., 2012, 694, 10.1100/2012/694740 · DOI
  25. Tossi, 2009, An increase in the concentration of abscisic acid is critical for nitric oxide-mediated plant adaptive responses to UV-B irradiation, New Phytol., 181, 871, 10.1111/j.1469-8137.2008.02722.x · DOI · Paper page
  26. Santa-Cruz, 2010, Nitric oxide synthase-like dependent NO production enhances heme oxygenase up-regulation in ultraviolet-B-irradiated soybean plants, Phytochemistry, 71, 1700, 10.1016/j.phytochem.2010.07.009 · doi:10.1016/j.phytochem.2010.07.009
  27. Liu, 2015, Exogenous NO depletes Cd-induced toxicity by eliminating oxidative damage re-establishing ATPase activity, and maintaining stress-related hormone equilibrium in white clover plants, Environ. Sci. Pollut. R., 22, 16843, 10.1007/s11356-015-4888-6 · DOI
  28. Babula, 2015, Lanthanum rather than cadmium induces oxidative stress and metabolite changes in Hypericum perforatum, J. Hazard. Mater., 286, 334, 10.1016/j.jhazmat.2014.12.060 · DOI
  29. Foyer, 2009, Redox regulation in photosynthetic organisms: signaling, acclimation, and practical implications, Antioxid. Redox Sign., 11, 861, 10.1089/ars.2008.2177 · DOI · Paper page
  30. Groβ, 2013, Nitric oxide, antioxidants and prooxidants in plant defence responses, Front. Plant Sci., 4, 419
  31. Liu, 2015, Effects of exogenous NO on the growth, mineral nutrient content, antioxidant system, and ATPase activities of Trifolium repens L. plants under cadmium stress, Acta Physiol. Plant., 37, 172, 10.1007/s11738-014-1721-7 · DOI
  32. Yu, 2014, Nitric oxide function in plant biology: a redox cue in deconvolution, New Phytol., 202, 1142, 10.1111/nph.12739 · DOI · Paper page
  33. Begara-Morales, 2016, Antioxidant systems are regulated by nitric oxide-mediated post-translational modifications (NO-PTMs), Front. Plant Sci., 7, 152, 10.3389/fpls.2016.00152 · DOI · Paper page
  34. Sharma, 2006, The significance of amino acids and amino acid-derived molecules in plant responses and adaptation to heavy metal stress, J. Exp. Bot., 57, 711, 10.1093/jxb/erj073 · DOI · Paper page
  35. Kováčik, 2014, Unexpected behavior of some nitric oxide modulators under cadmium excess in plant tissue, PLoS One, 9, 91685, 10.1371/journal.pone.0091685 · doi:10.1371/journal.pone.0091685
  36. Sandalio, 2001, Cadmium-induced changes in the growth and oxidative metabolism of pea plants, J. Exp. Bot., 52, 2115, 10.1093/jexbot/52.364.2115 · DOI · Paper page
  37. Rodríguez-Serrano, 2006, Cadmium effect on oxidative metabolism of pea (Pisum sativum L.) roots: imaging of reactive oxygen species and nitric oxide accumulation in vivo, Plant Cell Environ., 29, 1532, 10.1111/j.1365-3040.2006.01531.x · DOI · Paper page
  38. Chaki, 2009, Protein targets of tyrosine nitration in sunflower (Helianthus annuus L.) hypocotyls, J. Exp. Bot., 60, 4221, 10.1093/jxb/erp263 · DOI · Paper page
  39. Yamamoto, 2001, Lipid peroxidation is an early symptom triggered by aluminum, but not the primary cause of elongation inhibition in pea roots, Plant Physiol., 125, 199, 10.1104/pp.125.1.199 · DOI · Paper page
  40. Xie, 2013, Roles of NIA/NR/NOA1-dependent nitric oxide production and HY1 expression in the modulation of Arabidopsis salt tolerance, J. Exp. Bot., 64, 3045, 10.1093/jxb/ert149 · DOI
  41. Corpas, 2008, Metabolism of reactive nitrogen species in pea plants under abiotic stress conditions, Plant Cell Physiol., 49, 1711, 10.1093/pcp/pcn144 · DOI · Paper page
  42. Feechan, 2005, A central role for S-nitrosothiols in plant disease resistance, Proc. Natl. Acad. Sci. U. S. A., 102, 8054, 10.1073/pnas.0501456102 · DOI · Paper page
  43. Lea, 2006, Posttranslational regulation of nitrate reductase strongly affects the levels of free amino acids and nitrate, whereas transcriptional regulation has only minor influence, Plant Physiol., 140, 1085, 10.1104/pp.105.074633 · doi:10.1104/pp.105.074633
  44. Liu, 2015, Nitric oxide contributes to minerals absorption, proton pumps and hormone equilibrium under cadmium excess in Trifolium repens L. plants, Ecotox. Environ. Safe., 119, 35, 10.1016/j.ecoenv.2015.04.053 · DOI
  45. Signorelli, 2013, Water stress induces a differential and spatially distributed nitro-oxidative stress response in roots and leaves of Lotus japonicus, Plant Sci., 201–202, 137, 10.1016/j.plantsci.2012.12.004 · DOI
  46. Chomczynski, 1987, Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction, Anal. Biochem., 162, 156, 10.1016/0003-2697(87)90021-2 · DOI · Paper page
  47. Kováčik, 2009, Comparison of cadmium and copper effect on phenolic metabolism, mineral nutrients and stress-related parameters in Matricaria chamomilla plants, Plant Soil, 320, 231, 10.1007/s11104-009-9889-0 · DOI · Paper page
  48. Sun, 2008, Effects of cadmium and arsenic on growth and metal accumulation of Cd-hyperaccumulator Solanum nigrum L, Bioresour. Technol., 99, 1103, 10.1016/j.biortech.2007.02.035 · DOI · Paper page
  49. Uraguchi, 2012, Cadmium transport and tolerance in rice: perspectives for reducing grain cadmium accumulation, Rice, 5, 5, 10.1186/1939-8433-5-5 · DOI · Paper page
  50. Xu, 2012, Comparative physiological responses of Solanum nigrum and Solanum torvum to cadmium stress, New Phytol., 196, 125, 10.1111/j.1469-8137.2012.04236.x · DOI · Paper page
  51. Demidchik, 2015, Mechanisms of oxidative stress in plants: from classical chemistry to cell biology, Environ. Exp. Bot., 109, 212, 10.1016/j.envexpbot.2014.06.021 · DOI · Paper page
  52. Mittler, 2011, ROS signaling: the new wave, Trends Plant Sci., 16, 300, 10.1016/j.tplants.2011.03.007 · DOI · Paper page
  53. Farmer, 2013, ROS-mediated lipid peroxidation and RES-activated signaling, Annu. Rev. Plant Bio., 64, 429, 10.1146/annurev-arplant-050312-120132 · DOI · Paper page
  54. Milone, 2003, Antioxidant responses of wheat treated with realistic concentration of cadmium, Environ. Exp. Bot., 50, 265, 10.1016/S0098-8472(03)00037-6 · DOI · Paper page
  55. Laspina, 2005, Nitric oxide protects sunflower leaves against Cd-induced oxidative stress, Plant Sci., 169, 323, 10.1016/j.plantsci.2005.02.007 · DOI · Paper page
  56. Romero-Puertas, 2007, S-nitrosylation of peroxiredoxin II E promotes peroxynitrite-mediated tyrosine nitration, Plant Cell, 19, 4120, 10.1105/tpc.107.055061 · DOI · Paper page
  57. Abercrombie, 2008, Transcriptional responses of Arabidopsis thaliana plants to As (V) stress, BMC Plant Biol., 8, 87, 10.1186/1471-2229-8-87 · DOI
  58. Rodríguez-Serrano, 2009, Cellular response of pea plants to cadmium toxicity: cross talk between reactive oxygen species, nitric oxide, and calcium, Plant Physiol., 150, 229, 10.1104/pp.108.131524 · DOI · Paper page
  59. Graziano, 2005, Nitric oxide and iron in plants: an emerging and converging story, Trends Plant Sci., 10, 1, 10.1016/j.tplants.2004.12.004 · DOI · Paper page
  60. Corpas, 2014, Functional implications of peroxisomal nitric oxide (NO) in plants, Front. Plant Sci., 5, 97, 10.3389/fpls.2014.00097 · doi:10.3389/fpls.2014.00097
  61. Corpas, 2014, Peroxynitrite (ONOO−) is endogenously produced in Arabidopsis peroxisomes and is overproduced under cadmium stress, Ann. Bot., 113, 87, 10.1093/aob/mct260 · DOI
  62. Besson-Bard, 2009, Nitric oxide contributes to cadmium toxicity in Arabidopsis by promoting cadmium accumulation in roots and by up-regulating genes related to iron uptake, Plant Physiol., 149, 1302, 10.1104/pp.108.133348 · DOI · Paper page
  63. Xiong, 2009, Cadmium decreases crown root number by decreasing endogenous nitric oxide, which is indispensable for crown root primordia initiation in rice seedlings, Planta, 230, 599, 10.1007/s00425-009-0970-y · DOI
  64. Planchet, 2005, Nitric oxide emission from tobacco leaves and cell suspensions: rate limiting factors and evidence for the involvement of mitochondrial electron transport, Plant J., 732, 10.1111/j.1365-313X.2005.02335.x · DOI · Paper page
  65. del Río, 2004, Nitric oxide and nitric oxide synthase activity in plants, Phytochemistry, 65, 783, 10.1016/j.phytochem.2004.02.001 · DOI · Paper page
  66. Guo, 2005, Arabidopsis nitric oxide synthase1 is targeted to mitochondria and protects against oxidative damage and dark induced senescence, Plant Cell, 17, 3436, 10.1105/tpc.105.037770 · DOI · Paper page
  67. Moreau, 2008, AtNOS/AtNOA1 is a functional Arabidopsis thaliana cGTPase and not a nitric-oxide synthase, J. Biol. Chem., 283, 32957, 10.1074/jbc.M804838200 · DOI · Paper page
  68. Kopyra, 2006, Effect of exogenous nitric oxide on the antioxidant capacity of cadmium-treated soybean cell suspension, Acta Physiol. Plant., 28, 525, 10.1007/s11738-006-0048-4 · doi:10.1007/s11738-006-0048-4
  69. Ma, 2008, Innate immunity signaling: cytosolic Ca2+ elevation is linked to downstream nitric oxide generation through the action of calmodulin or a calmodulin-like protein, Plant Physiol., 148, 818, 10.1104/pp.108.125104 · DOI · Paper page
  70. Leterrier, 2012, Arsenic triggers the nitric oxide (NO) and S-nitrosoglutathione (GSNO) metabolism in Arabidopsis, Environ. Pollut., 166, 136, 10.1016/j.envpol.2012.03.012 · DOI · Paper page
  71. Begara-Morales, 2014, Dual regulation of cytosolic ascorbate peroxidase (APX) by tyrosine nitration and S-nitrosylation, J. Exp. Bot., 65, 527, 10.1093/jxb/ert396 · DOI · Paper page
  72. Ruíz-Torres, 2017, Arsenic-induced stress activates sulfur metabolism in different organs of garlic (Allium sativum L.) plants accompanied by a general decline of the NADPH-generating systems in roots, J. Plant Physiol., 211, 27, 10.1016/j.jplph.2016.12.010 · DOI
  73. Mishra, 2006, Inhibition of ribonuclease and protease activities in arsenic exposed rice seedlings: role of proline as enzyme protectant, J.Plant Physiol., 163, 927, 10.1016/j.jplph.2005.08.003 · DOI · Paper page
  74. Wang, 2002, Inhibitory effects of anthocyanins and other phenolic compounds on nitric oxide production in LPS/IFN-γ-activated RAW 264.7 macrophages, J. Agric. Food Chem., 50, 850, 10.1021/jf010976a · DOI · Paper page

Cited by

See all 59

Metadata

Authors
Liu, S., Yang, R., Tripathi, D. K., Li, X., He, W., Wu, M., Ali, S., Ma, M., Cheng, Q., & Pan, Y.
Venue
Journal of Hazardous Materials
Publisher
Elsevier BV
Published
2018-02
Volume
344
Pages
1007-1024
ISSN
0304-3894
DOI
10.1016/j.jhazmat.2017.12.004
Cited by
59
References
2
Language
en
Status
Retracted
Update notices
Licence
  • www.elsevier.com/tdm/userlicense/1.0/ (tdm)
  • www.elsevier.com/legal/tdmrep-license (tdm)
Funders
National Natural Science Foundation of China (31670622)

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

How to cite

Cite CoChat for the checks on this page, and the paper for its own findings.

This page
CoChat. (2026). Citation check: RETRACTED: The interplay between reactive oxygen and nitrogen species contributes in the regulatory mechanism of the nitro-oxidative stress induced by cadmium in Arabidopsis. https://app.cochat.ai/papers/10.1016/j.jhazmat.2017.12.004
The paper
Liu, S., Yang, R., Tripathi, D. K., Li, X., He, W., Wu, M., Ali, S., Ma, M., Cheng, Q., & Pan, Y. (2018). RETRACTED: The interplay between reactive oxygen and nitrogen species contributes in the regulatory mechanism of the nitro-oxidative stress induced by cadmium in Arabidopsis. Journal of Hazardous Materials. https://doi.org/10.1016/j.jhazmat.2017.12.004

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.