On the public citation graph

Redox Balance Keepers and Possible Cell Functions Managed by Redox Homeostasis in Trypanosoma cruzi

https://doi.org/10.3389/fcimb.2019.00435

0 signed · 296 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/cbin.11137openalex-snapshot

Cell death: a review of the major forms of apoptosis, necrosis and autophagy

inferredcites →https://doi.org/10.1002/iub.1602openalex-snapshot

Iron chemistry at the service of life

inferredcites →https://doi.org/10.1002/jcb.21864openalex-snapshot

Natural programmed cell death in T. cruzi epimastigotes maintained in axenic cultures

inferredcites →https://doi.org/10.1002/jms.1267openalex-snapshot

Proteomic analysis of metacyclic trypomastigotes undergoing Trypanosoma cruzi metacyclogenesis

inferredcites →https://doi.org/10.1006/bbrc.1994.2083openalex-snapshot

Reduction of a Trisulfide Derivative of Glutathione by Glutathione Reductase

inferredcites →https://doi.org/10.1006/expr.2001.4615openalex-snapshot

Role of Superoxide and Reactive Nitrogen Intermediates in Rhodnius prolixus (Reduviidae)/Trypanosoma rangeli Interactions

inferredcites →https://doi.org/10.1007/s00018-013-1491-1openalex-snapshot

Mechanisms of cellular invasion by intracellular parasites

inferredcites →https://doi.org/10.1007/s00204-015-1579-5openalex-snapshot

Redox- and non-redox-metal-induced formation of free radicals and their role in human disease

inferredcites →https://doi.org/10.1007/s00281-012-0351-7openalex-snapshot

Current understanding of immunity to Trypanosoma cruzi infection and pathogenesis of Chagas disease

inferredcites →https://doi.org/10.1007/s00384-004-0588-2openalex-snapshot

Effects of iron deprivation or chelation on DNA damage in experimental colitis

inferredcites →https://doi.org/10.1007/s00418-013-1123-8openalex-snapshot

Golgi in copper homeostasis: a view from the membrane trafficking field

inferredcites →https://doi.org/10.1007/s00436-003-0937-zopenalex-snapshot

Microarray analysis of changes in gene expression in a murine model of chronic chagasic cardiomyopathy

inferredcites →https://doi.org/10.1007/s00436-008-1081-6openalex-snapshot

Inhibition of proteasome activity blocks Trypanosoma cruzi growth and metacyclogenesis

inferredcites →https://doi.org/10.1007/s00441-010-0985-5openalex-snapshot

Differential apoptosis-like cell death in amastigote and trypomastigote forms from Trypanosoma cruzi-infected heart cells in vitro

inferredcites →https://doi.org/10.1007/s10863-011-9365-4openalex-snapshot

Role of Trypanosoma cruzi peroxiredoxins in mitochondrial bioenergetics

inferredcites →https://doi.org/10.1007/s10863-011-9369-0openalex-snapshot

O2 consumption rates along the growth curve: new insights into Trypanosoma cruzi mitochondrial respiratory chain

inferredcites →https://doi.org/10.1007/s10863-011-9398-8openalex-snapshot

A comparative assessment of mitochondrial function in epimastigotes and bloodstream trypomastigotes of Trypanosoma cruzi

inferredcites →https://doi.org/10.1007/s11033-016-4022-yopenalex-snapshot

Novel insights into redox system and the mechanism of redox regulation

inferredcites →https://doi.org/10.1007/s40588-018-0081-2openalex-snapshot

Pathogenesis of Chronic Chagas Disease: Macrophages, Mitochondria, and Oxidative Stress

inferredcites →https://doi.org/10.1016/0166-6851(87)90123-xopenalex-snapshot

Aerobic glucose fermentation by Trypanosoma cruzi axenic culture amastigote-like forms during growth and differentiation to epimastigotes

inferredcites →https://doi.org/10.1016/0305-0491(84)90381-xopenalex-snapshot

Protein and amino acid catabolism in Trypanosoma cruzi

inferredcites →https://doi.org/10.1016/0891-5849(91)90192-6openalex-snapshot

Chemistry and biochemistry of 4-hydroxynonenal, malonaldehyde and related aldehydes

inferredcites →https://doi.org/10.1016/0921-8734(95)90004-7openalex-snapshot

Low levels of reactive oxygen species as modulators of cell function

inferredcites →https://doi.org/10.1016/b978-0-12-385895-5.00007-4openalex-snapshot

ROS Signalling of Inflammatory Cytokines During Trypanosoma cruzi Infection

inferredcites →https://doi.org/10.1016/j.abb.2010.12.014openalex-snapshot

Tryparedoxin peroxidases from Trypanosoma cruzi: High efficiency in the catalytic elimination of hydrogen peroxide and peroxynitrite

inferredcites →https://doi.org/10.1016/j.actatropica.2018.09.002openalex-snapshot

Parasitic interactions among Trypanosoma cruzi, triatomine vectors, domestic animals, and wildlife in Big Bend National Park along the Texas-Mexico border

inferredcites →https://doi.org/10.1016/j.actatropica.2019.105168openalex-snapshot

Immunity and vaccine development efforts against Trypanosoma cruzi

inferredcites →https://doi.org/10.1016/j.bbadis.2004.03.005openalex-snapshot

Impaired mitochondrial respiratory chain and bioenergetics during chagasic cardiomyopathy development

inferredcites →https://doi.org/10.1016/j.bbagen.2013.01.013openalex-snapshot

Trypanothione: A unique bis-glutathionyl derivative in trypanosomatids

inferredcites →https://doi.org/10.1016/j.bbamcr.2006.08.019openalex-snapshot

Metabolic functions of glycosomes in trypanosomatids

inferredcites →https://doi.org/10.1016/j.bbamcr.2013.06.028openalex-snapshot

ER stress-induced cell death mechanisms

inferredcites →https://doi.org/10.1016/j.bbamcr.2015.09.015openalex-snapshot

Biogenesis, maintenance and dynamics of glycosomes in trypanosomatid parasites

inferredcites →https://doi.org/10.1016/j.bbapap.2015.10.005openalex-snapshot

Trypanosoma cruzi mitochondrial tryparedoxin peroxidase is located throughout the cell and its pull down provides one step towards the understanding of its mechanism of action

inferredcites →https://doi.org/10.1016/j.bbrc.2006.12.238openalex-snapshot

Heme requirement and intracellular trafficking in Trypanosoma cruzi epimastigotes

inferredcites →https://doi.org/10.1016/j.bbrc.2007.03.104openalex-snapshot

Evidence of P-body-like structures in Trypanosoma cruzi

inferredcites →https://doi.org/10.1016/j.bbrc.2009.09.135openalex-snapshot

Heme-induced Trypanosoma cruzi proliferation is mediated by CaM kinase II

inferredcites →https://doi.org/10.1016/j.bbrc.2016.10.086openalex-snapshot

Lipid peroxidation in cell death

inferredcites →https://doi.org/10.1016/j.cbi.2017.12.024openalex-snapshot

Oxidative stress, consequences and ROS mediated cellular signaling in rheumatoid arthritis

inferredcites →https://doi.org/10.1016/j.cbpa.2017.06.002openalex-snapshot

Lipid homeostasis and regulated cell death

inferredcites →https://doi.org/10.1016/j.dci.2006.05.008openalex-snapshot

Rhodnius prolixus: Identification of immune-related genes up-regulated in response to pathogens and parasites using suppressive subtractive hybridization

inferredcites →https://doi.org/10.1016/j.ejps.2018.07.005openalex-snapshot

Preclinical pharmacokinetics of benznidazole-loaded interpolyelectrolyte complex-based delivery systems

inferredcites →https://doi.org/10.1016/j.exppara.2007.03.006openalex-snapshot

Trypanosoma cruzi: Treatment with the iron chelator desferrioxamine reduces parasitemia and mortality in experimentally infected mice

inferredcites →https://doi.org/10.1016/j.exppara.2010.05.009openalex-snapshot

Trypanosoma cruzi: Modulation of HSP70 mRNA stability by untranslated regions during heat shock

inferredcites →https://doi.org/10.1016/j.exppara.2012.12.007openalex-snapshot

Release of the cytosolic tryparedoxin peroxidase into the incubation medium and a different profile of cytosolic and mitochondrial peroxiredoxin expression in H2O2-treated Trypanosoma cruzi tissue culture-derived trypomastigotes

inferredcites →https://doi.org/10.1016/j.exppara.2017.10.015openalex-snapshot

Trypanosoma cruzi tryparedoxin II interacts with different peroxiredoxins under physiological and oxidative stress conditions

inferredcites →https://doi.org/10.1016/j.febslet.2005.07.049openalex-snapshot

Inhibitory role of peroxiredoxin II (Prx II) on cellular senescence

inferredcites →https://doi.org/10.1016/j.freeradbiomed.2004.09.011openalex-snapshot

Oxidative modification of mitochondrial respiratory complexes in response to the stress of Trypanosoma cruzi infection

inferredcites →https://doi.org/10.1016/j.freeradbiomed.2006.04.009openalex-snapshot

Increased oxidative stress is correlated with mitochondrial dysfunction in chagasic patients

inferredcites →https://doi.org/10.1016/j.freeradbiomed.2008.05.028openalex-snapshot

Insights into the redox biology of Trypanosoma cruzi: Trypanothione metabolism and oxidant detoxification

inferredcites →https://doi.org/10.1016/j.freeradbiomed.2009.05.026openalex-snapshot

The cell cycle is a redox cycle: Linking phase-specific targets to cell fate

inferredcites →https://doi.org/10.1016/j.freeradbiomed.2009.08.008openalex-snapshot

Trypanosoma cruzi infection disturbs mitochondrial membrane potential and ROS production rate in cardiomyocytes

inferredcites →https://doi.org/10.1016/j.freeradbiomed.2010.09.005openalex-snapshot

The use of thiols by ribonucleotide reductase

inferredcites →https://doi.org/10.1016/j.freeradbiomed.2012.08.001openalex-snapshot

Peroxiredoxin 1 functions as a signal peroxidase to receive, transduce, and transmit peroxide signals in mammalian cells

inferredcites →https://doi.org/10.1016/j.freeradbiomed.2013.04.036openalex-snapshot

Redox metabolism in Trypanosoma cruzi: Functional characterization of tryparedoxins revisited

inferredcites →https://doi.org/10.1016/j.freeradbiomed.2017.03.027openalex-snapshot

Heme modulates Trypanosoma cruzi bioenergetics inducing mitochondrial ROS production

inferredcites →https://doi.org/10.1016/j.freeradbiomed.2018.10.436openalex-snapshot

Trypanothione synthetase confers growth, survival advantage and resistance to anti-protozoal drugs in Trypanosoma cruzi

inferredcites →https://doi.org/10.1016/j.ibmb.2006.01.009openalex-snapshot

Adaptations against heme toxicity in blood-feeding arthropods

inferredcites →https://doi.org/10.1016/j.ibmb.2007.02.001openalex-snapshot

Differential modulation of Rhodnius prolixus nitric oxide activities following challenge with Trypanosoma rangeli, T. cruzi and bacterial cell wall components

inferredcites →https://doi.org/10.1016/j.ijcard.2006.04.046openalex-snapshot

Oxidative stress in chronic cardiopathy associated with Chagas disease

inferredcites →https://doi.org/10.1016/j.ijmm.2012.07.008openalex-snapshot

The trypanothione system and its implications in the therapy of trypanosomatid diseases

inferredcites →https://doi.org/10.1016/j.ijpara.2009.05.010openalex-snapshot

Enzymes of the antioxidant network as novel determiners of Trypanosoma cruzi virulence

inferredcites →https://doi.org/10.1016/j.ijpddr.2016.10.003openalex-snapshot

Effects of a novel β–lapachone derivative on Trypanosoma cruzi: Parasite death involving apoptosis, autophagy and necrosis

inferredcites →https://doi.org/10.1016/j.jinsphys.2006.10.006openalex-snapshot

Exploring the role of insect host factors in the dynamics of Trypanosoma cruzi–Rhodnius prolixus interactions

inferredcites →https://doi.org/10.1016/j.jinsphys.2010.03.027openalex-snapshot

Phenol oxidases from Rhodnius prolixus: Temporal and tissue expression pattern and regulation by ecdysone

inferredcites →https://doi.org/10.1016/j.jinsphys.2016.11.006openalex-snapshot

Rhodnius prolixus: from physiology by Wigglesworth to recent studies of immune system modulation by Trypanosoma cruzi and Trypanosoma rangeli

inferredcites →https://doi.org/10.1016/j.jprot.2011.04.006openalex-snapshot

Molecular characterization and interactome analysis of Trypanosoma cruzi Tryparedoxin 1

inferredcites →https://doi.org/10.1016/j.jprot.2015.03.001openalex-snapshot

Molecular characterization and interactome analysis of Trypanosoma cruzi tryparedoxin II

inferredcites →https://doi.org/10.1016/j.lab.2004.10.006openalex-snapshot

Is stored iron safe?

inferredcites →https://doi.org/10.1016/j.meegid.2017.01.016openalex-snapshot

Molecular identification and genotyping of Trypanosoma cruzi DNA in autochthonous Chagas disease patients from Texas, USA

inferredcites →https://doi.org/10.1016/j.mib.2009.06.011openalex-snapshot

Fighting the oxidative assault: the Trypanosoma cruzi journey to infection

inferredcites →https://doi.org/10.1016/j.micinf.2008.06.013openalex-snapshot

Tissue-specific oxidative imbalance and mitochondrial dysfunction during Trypanosoma cruzi infection in mice

inferredcites →https://doi.org/10.1016/j.molbiopara.2005.09.001openalex-snapshot

Metacaspases of Trypanosoma cruzi: Possible candidates for programmed cell death mediators

inferredcites →https://doi.org/10.1016/j.molbiopara.2005.12.001openalex-snapshot

Deletion of copies of the gene encoding old yellow enzyme (TcOYE), a NAD(P)H flavin oxidoreductase, associates with in vitro-induced benznidazole resistance in Trypanosoma cruzi

inferredcites →https://doi.org/10.1016/j.molbiopara.2006.03.017openalex-snapshot

Energy metabolism of trypanosomatids: Adaptation to available carbon sources

inferredcites →https://doi.org/10.1016/j.molbiopara.2009.07.006openalex-snapshot

Glucose uptake in the mammalian stages of Trypanosoma cruzi

inferredcites →https://doi.org/10.1016/j.molcel.2004.06.021openalex-snapshot

A 2-Cys Peroxiredoxin Regulates Peroxide-Induced Oxidation and Activation of a Stress-Activated MAP Kinase

inferredcites →https://doi.org/10.1016/j.molcel.2012.05.030openalex-snapshot

Feedback Control of Adrenal Steroidogenesis via H2O2-Dependent, Reversible Inactivation of Peroxiredoxin III in Mitochondria

inferredcites →https://doi.org/10.1016/j.molcel.2017.10.015openalex-snapshot

The Stress Granule Transcriptome Reveals Principles of mRNA Accumulation in Stress Granules

inferredcites →https://doi.org/10.1016/j.mrrev.2015.12.003openalex-snapshot

How Trypanosoma cruzi deals with oxidative stress: Antioxidant defence and DNA repair pathways

inferredcites →https://doi.org/10.1016/j.pt.2010.07.003openalex-snapshot

Interactions between intestinal compounds of triatomines and Trypanosoma cruzi

inferredcites →https://doi.org/10.1016/j.pt.2014.04.003openalex-snapshot

Nitro drugs for the treatment of trypanosomatid diseases: past, present, and future prospects

inferredcites →https://doi.org/10.1016/j.redox.2013.10.005openalex-snapshot

Intracellular glutathione pools are heterogeneously concentrated

inferredcites →https://doi.org/10.1016/j.redox.2017.07.008openalex-snapshot

Proteostasis, oxidative stress and aging

inferredcites →https://doi.org/10.1016/j.redox.2019.101198openalex-snapshot

Metabolic programming of macrophage functions and pathogens control

inferredcites →https://doi.org/10.1016/j.semcdb.2010.03.009openalex-snapshot

Regulation of macroautophagy in Saccharomyces cerevisiae

inferredcites →https://doi.org/10.1016/j.taap.2016.05.007openalex-snapshot

The trypanocidal benznidazole promotes adaptive response to oxidative injury: Involvement of the nuclear factor-erythroid 2-related factor-2 (Nrf2) and multidrug resistance associated protein 2 (MRP2)

inferredcites →https://doi.org/10.1016/j.tcb.2016.05.004openalex-snapshot

Principles and Properties of Stress Granules

inferredcites →https://doi.org/10.1016/j.tibs.2018.06.005openalex-snapshot

Quality Control in the Endoplasmic Reticulum: Crosstalk between ERAD and UPR pathways

inferredcites →https://doi.org/10.1016/j.toxlet.2005.03.004openalex-snapshot

Free heme toxicity and its detoxification systems in human

inferredcites →https://doi.org/10.1016/j.trsl.2017.09.005openalex-snapshot

Reactive oxygen species as signaling molecules in the development of lung fibrosis

inferredcites →https://doi.org/10.1016/s0002-9440(10)62976-8openalex-snapshot

Cardiac Gene Expression Profiling Provides Evidence for Cytokinopathy as a Molecular Mechanism in Chagas' Disease Cardiomyopathy

inferredcites →https://doi.org/10.1016/s0006-2952(02)01663-5openalex-snapshot

Trypanosoma cruzi: effect and mode of action of nitroimidazole and nitrofuran derivatives

inferredcites →https://doi.org/10.1016/s0014-5793(01)03091-5openalex-snapshot

Spermidine is essential for normal proliferation of trypanosomatid protozoa

inferredcites →https://doi.org/10.1016/s0020-7519(02)00283-7openalex-snapshot

Severity of chronic Chagas disease is associated with cytokine/antioxidant imbalance in chronically infected individuals

inferredcites →https://doi.org/10.1016/s0020-7519(03)00107-3openalex-snapshot

Identification of PDZ5, a candidate universal minicircle sequence binding protein of Trypanosoma cruzi

inferredcites →https://doi.org/10.1016/s0021-9258(18)48474-8openalex-snapshot

8-Hydroxyguanine, an abundant form of oxidative DNA damage, causes G-T and A-C substitutions.

inferredcites →https://doi.org/10.1016/s0092-8674(02)01048-6openalex-snapshot

A Thiol Peroxidase Is an H2O2 Receptor and Redox-Transducer in Gene Activation

inferredcites →https://doi.org/10.1016/s0166-6851(01)00285-7openalex-snapshot

Ovothiol and trypanothione as antioxidants in trypanosomatids

inferredcites →https://doi.org/10.1016/s0166-6851(96)02837-xopenalex-snapshot

Effects of Nifurtimox and benznidazole upon glutathione and trypanothione content in epimastigote, trypomastigote and amastigote forms of Trypanosoma cruzi

inferredcites →https://doi.org/10.1016/s0166-6851(97)00032-7openalex-snapshot

Molecular cloning and characterization of two iron superoxide dismutase cDNAs from Trypanosoma cruzi1Note: T. cruzi FeSODA and FeSODB cDNAs have been assigned EMBL/GenBank nucleotide sequence accession numbers U90722 and U90723 respectively.1

inferredcites →https://doi.org/10.1016/s0891-5849(00)00159-3openalex-snapshot

Evidence for a trypanothione-dependent peroxidase system in Trypanosoma cruzi

inferredcites →https://doi.org/10.1016/s0891-5849(00)00224-0openalex-snapshot

Oxidative stress and cell cycle checkpoint function11Both Drs. Paules and Kaufmann received their doctoral degrees in Experimental Pathology from the University of North Carolina at Chapel Hill School of Medicine (in 1984 and 1979, respectively).

inferredcites →https://doi.org/10.1017/s0007485315000504openalex-snapshot

Immune defence mechanisms of triatomines against bacteria, viruses, fungi and parasites

inferredcites →https://doi.org/10.1017/s1462399410001560openalex-snapshot

The endless race betweenTrypanosoma cruziand host immunity: lessons for and beyond Chagas disease

inferredcites →https://doi.org/10.1021/acs.jproteome.6b00208openalex-snapshot

Chromatin Proteomics Reveals Variable Histone Modifications during the Life Cycle of Trypanosoma cruzi

inferredcites →https://doi.org/10.1021/acs.jproteome.6b00655openalex-snapshot

Post-translational Modifications of Trypanosoma cruzi Canonical and Variant Histones

inferredcites →https://doi.org/10.1021/acs.jproteome.7b00603openalex-snapshot

Comparative Proteomic Analysis of Lysine Acetylation in Trypanosomes

inferredcites →https://doi.org/10.1021/ja411006aopenalex-snapshot

Ferrostatins Inhibit Oxidative Lipid Damage and Cell Death in Diverse Disease Models

inferredcites →https://doi.org/10.1021/pr300947gopenalex-snapshot

Proteomic Analysis of Trypanosoma cruzi Secretome: Characterization of Two Populations of Extracellular Vesicles and Soluble Proteins

inferredcites →https://doi.org/10.1038/cdd.2012.12openalex-snapshot

Antagonic activities of Trypanosoma cruzi metacaspases affect the balance between cell proliferation, death and differentiation

inferredcites →https://doi.org/10.1038/nature01819openalex-snapshot

Essential role for the peroxiredoxin Prdx1 in erythrocyte antioxidant defence and tumour suppression

inferredcites →https://doi.org/10.1038/nature05978openalex-snapshot

Base-excision repair of oxidative DNA damage

inferredcites →https://doi.org/10.1038/nature11088openalex-snapshot

Peroxiredoxins are conserved markers of circadian rhythms

inferredcites →https://doi.org/10.1038/ncb1007-1102openalex-snapshot

Autophagosome formation: core machinery and adaptations

inferredcites →https://doi.org/10.1038/nrm.2016.149openalex-snapshot

Necroptosis in development, inflammation and disease

inferredcites →https://doi.org/10.1038/s41419-019-1370-2openalex-snapshot

Cell death pathways in pathogenic trypanosomatids: lessons of (over)kill

inferredcites →https://doi.org/10.1038/s41598-017-10292-3openalex-snapshot

Quantitative proteome and phosphoproteome analyses highlight the adherent population during Trypanosoma cruzi metacyclogenesis

inferredcites →https://doi.org/10.1038/s41598-018-23408-0openalex-snapshot

Modeling the effects of lipid peroxidation during ferroptosis on membrane properties

inferredcites →https://doi.org/10.1038/s41598-018-26532-zopenalex-snapshot

Ubiquitin Proteasome pathway proteins as potential drug targets in parasite Trypanosoma cruzi

inferredcites →https://doi.org/10.1039/c5sc02311dopenalex-snapshot

Effect of lipid peroxidation on membrane permeability of cancer and normal cells subjected to oxidative stress

inferredcites →https://doi.org/10.1039/c7mt00221aopenalex-snapshot

The mitochondrion: a central architect of copper homeostasis

inferredcites →https://doi.org/10.1042/0264-6021:3520755openalex-snapshot

Biochemical characterization of a trypanosome enzyme with glutathione-dependent peroxidase activity

inferredcites →https://doi.org/10.1042/bcj20170698openalex-snapshot

Cardiomyocyte diffusible redox mediators controlTrypanosoma cruziinfection: role of parasite mitochondrial iron superoxide dismutase

inferredcites →https://doi.org/10.1042/bj20020038openalex-snapshot

TcGPXII, a glutathione-dependent Trypanosoma cruzi peroxidase with substrate specificity restricted to fatty acid and phospholipid hydroperoxides, is localized to the endoplasmic reticulum

inferredcites →https://doi.org/10.1042/bj20061281openalex-snapshot

Mitochondrial superoxide radicals mediate programmed cell death in Trypanosoma cruzi : cytoprotective action of mitochondrial iron superoxide dismutase overexpression

inferredcites →https://doi.org/10.1042/bj20061341openalex-snapshot

Depletion of the thioredoxin homologue tryparedoxin impairs antioxidative defence in African trypanosomes

inferredcites →https://doi.org/10.1042/bj20071138openalex-snapshot

Peroxiredoxins play a major role in protectingTrypanosoma cruziagainst macrophage- and endogenously-derived peroxynitrite

inferredcites →https://doi.org/10.1042/bj20081981openalex-snapshot

Mitochondrial calcium overload triggers complement-dependent superoxide-mediated programmed cell death inTrypanosoma cruzi

inferredcites →https://doi.org/10.1042/bj20091167openalex-snapshot

Structural insights into the catalytic mechanism of Trypanosoma cruzi GPXI (glutathione peroxidase-like enzyme I)

inferredcites →https://doi.org/10.1042/bj20140213openalex-snapshot

SIRT3 interactions with FOXO3 acetylation, phosphorylation and ubiquitinylation mediate endothelial cell responses to hypoxia

inferredcites →https://doi.org/10.1042/bj20151227openalex-snapshot

Protein oxidation and peroxidation

inferredcites →https://doi.org/10.1042/bj2560861openalex-snapshot

Antioxidant protection by haemopexin of haem-stimulated lipid peroxidation

inferredcites →https://doi.org/10.1042/bse0510031openalex-snapshot

Gene expression regulation in trypanosomatids

inferredcites →https://doi.org/10.1042/bst20160364openalex-snapshot

Post-transcriptional control of gene expression following stress: the role of RNA-binding proteins

inferredcites →https://doi.org/10.1056/nejmoa1507574openalex-snapshot

Randomized Trial of Benznidazole for Chronic Chagas’ Cardiomyopathy

inferredcites →https://doi.org/10.1073/pnas.0504251102openalex-snapshot

Vitamin C biosynthesis in trypanosomes: A role for the glycosome

inferredcites →https://doi.org/10.1073/pnas.0711014105openalex-snapshot

A mechanism for cross-resistance to nifurtimox and benznidazole in trypanosomes

inferredcites →https://doi.org/10.1073/pnas.1216016110openalex-snapshot

Targeting the ERAD pathway via inhibition of signal peptide peptidase for antiparasitic therapeutic design

inferredcites →https://doi.org/10.1073/pnas.1618611114openalex-snapshot

Kinetics, subcellular localization, and contribution to parasite virulence of a Trypanosoma cruzi hybrid type A heme peroxidase ( Tc APx-CcP)

inferredcites →https://doi.org/10.1073/pnas.1821487116openalex-snapshot

Cytosolic Fe-superoxide dismutase safeguards Trypanosoma cruzi from macrophage-derived superoxide radical

inferredcites →https://doi.org/10.1073/pnas.202422899openalex-snapshot

Trypanosoma cruzi expresses a plant-like ascorbate-dependent hemoperoxidase localized to the endoplasmic reticulum

inferredcites →https://doi.org/10.1073/pnas.89.15.6891openalex-snapshot

A single-stranded DNA-binding protein from Crithidia fasciculata recognizes the nucleotide sequence at the origin of replication of kinetoplast DNA minicircles.

inferredcites →https://doi.org/10.1074/jbc.m010352200openalex-snapshot

Trypanothione-dependent Synthesis of Deoxyribonucleotides by Trypanosoma brucei Ribonucleotide Reductase

inferredcites →https://doi.org/10.1074/jbc.m109.090142openalex-snapshot

Peroxiredoxin Ahp1 Acts as a Receptor for Alkylhydroperoxides to Induce Disulfide Bond Formation in the Cad1 Transcription Factor

inferredcites →https://doi.org/10.1074/jbc.m110.167247openalex-snapshot

Intraphagosomal Peroxynitrite as a Macrophage-derived Cytotoxin against Internalized Trypanosoma cruzi

inferredcites →https://doi.org/10.1074/jbc.m111.230847openalex-snapshot

Nifurtimox Activation by Trypanosomal Type I Nitroreductases Generates Cytotoxic Nitrile Metabolites

inferredcites →https://doi.org/10.1074/jbc.m111126200openalex-snapshot

The Trypanosoma cruzi Enzyme TcGPXI Is a Glycosomal Peroxidase and Can Be Linked to Trypanothione Reduction by Glutathione or Tryparedoxin

inferredcites →https://doi.org/10.1074/jbc.m204403200openalex-snapshot

A Single Enzyme Catalyses Formation of Trypanothione from Glutathione and Spermidine in Trypanosoma cruzi

inferredcites →https://doi.org/10.1074/jbc.m302750200openalex-snapshot

Bis(glutathionyl)spermine and Other Novel Trypanothione Analogues in Trypanosoma cruzi

inferredcites →https://doi.org/10.1074/jbc.m708474200openalex-snapshot

Autophagy Is Involved in Nutritional Stress Response and Differentiation in Trypanosoma cruzi

inferredcites →https://doi.org/10.1074/jbc.m804417200openalex-snapshot

Enzymatic Mechanism Controls Redox-mediated Protein-DNA Interactions at the Replication Origin of Kinetoplast DNA Minicircles

inferredcites →https://doi.org/10.1074/jbc.r117.789271openalex-snapshot

Production of superoxide and hydrogen peroxide from specific mitochondrial sites under different bioenergetic conditions

inferredcites →https://doi.org/10.1074/jbc.r117.791962openalex-snapshot

Cytosolic iron chaperones: Proteins delivering iron cofactors in the cytosol of mammalian cells

inferredcites →https://doi.org/10.1080/01926230701320337openalex-snapshot

Apoptosis: A Review of Programmed Cell Death

inferredcites →https://doi.org/10.1080/15548627.2017.1343770openalex-snapshot

Autophagy-monitoring and autophagy-deficient mice

inferredcites →https://doi.org/10.1083/jcb.201810099openalex-snapshot

Autophagosome maturation: An epic journey from the ER to lysosomes

inferredcites →https://doi.org/10.1084/jem.184.5.1909openalex-snapshot

Proteasome activity is required for the stage-specific transformation of a protozoan parasite.

inferredcites →https://doi.org/10.1089/ars.2005.7.327openalex-snapshot

Peroxiredoxin-Mediated Redox Regulation of the Nuclear Localization of Yap1, a Transcription Factor in Budding Yeast

inferredcites →https://doi.org/10.1089/ars.2007.1782openalex-snapshot

Endoplasmic Reticulum Stress and Oxidative Stress: A Vicious Cycle or a Double-Edged Sword?

inferredcites →https://doi.org/10.1089/ars.2016.6831openalex-snapshot

Inhibition of NFE2L2-Antioxidant Response Element Pathway by Mitochondrial Reactive Oxygen Species Contributes to Development of Cardiomyopathy and Left Ventricular Dysfunction in Chagas Disease

inferredcites →https://doi.org/10.1093/acprof:oso/9780198717478.001.0001openalex-snapshot

Free Radicals in Biology and Medicine

inferredcites →https://doi.org/10.1093/carcin/13.7.1227openalex-snapshot

Inhibitory effect of dietary iron deficiency on inductions of putative preneoplastic lesions as well as 8-hydroxydeoxyguanosine in DNA and lipid peroxidation in the livers of rats caused by exposure to a choline-deficient L-amino acid defined diet

inferredcites →https://doi.org/10.1093/clinchem/42.1.64openalex-snapshot

Blood glutathione concentrations in a large-scale human study

inferredcites →https://doi.org/10.1093/femspd/ftv082openalex-snapshot

Immunity and immune modulation in Trypanosoma cruzi infection

inferredcites →https://doi.org/10.1093/jn/131.2.568sopenalex-snapshot

Iron Biology in Immune Function, Muscle Metabolism and Neuronal Functioning

inferredcites →https://doi.org/10.1093/jn/134.11.3171sopenalex-snapshot

Iron, Free Radicals, and Oxidative Injury

inferredcites →https://doi.org/10.1101/cshperspect.a006080openalex-snapshot

Cell Death Signaling

inferredcites →https://doi.org/10.1107/s2053230x15004185openalex-snapshot

Iron superoxide dismutases in eukaryotic pathogens: new insights from Apicomplexa andTrypanosomastructures

inferredcites →https://doi.org/10.1111/j.1365-2958.2007.05833.xopenalex-snapshot

Recruitment of mRNAs to cytoplasmic ribonucleoprotein granules in trypanosomes

inferredcites →https://doi.org/10.1111/j.1600-079x.2007.00427.xopenalex-snapshot

Melatonin treatment reduces the severity of experimental Trypanosoma cruzi infection

inferredcites →https://doi.org/10.1111/j.1742-4658.2010.07747.xopenalex-snapshot

Protein and mRNA content of TcDHH1‐containing mRNPs in Trypanosoma cruzi

inferredcites →https://doi.org/10.1111/j.1742-4658.2012.08557.xopenalex-snapshot

Drug target validation of the trypanothione pathway enzymes through metabolic modelling

inferredcites →https://doi.org/10.1111/jeu.12666openalex-snapshot

The Nuclear RNA ‐binding Protein RBSR 1 Interactome in Trypanosoma cruzi

inferredcites →https://doi.org/10.1111/tmi.12980openalex-snapshot

Development and in vitro/in vivo evaluation of a novel benznidazole liquid dosage form using a quality‐by‐design approach

inferredcites →https://doi.org/10.1126/science.1110289openalex-snapshot

The Trypanosoma cruzi Proteome

inferredcites →https://doi.org/10.1126/science.1112631openalex-snapshot

The Genome Sequence of Trypanosoma cruzi , Etiologic Agent of Chagas Disease

inferredcites →https://doi.org/10.1126/science.1117311openalex-snapshot

A Direct Role for Dual Oxidase in Drosophila Gut Immunity

inferredcites →https://doi.org/10.1126/science.aao3172openalex-snapshot

Redox-sensitive alteration of replisome architecture safeguards genome integrity

inferredcites →https://doi.org/10.1128/aac.00481-12openalex-snapshot

Antiparasitic Effect of Vitamin B 12 on Trypanosoma cruzi

inferredcites →https://doi.org/10.1128/aac.05135-11openalex-snapshot

Activation of Benznidazole by Trypanosomal Type I Nitroreductases Results in Glyoxal Formation

inferredcites →https://doi.org/10.1128/aac.48.1.69-74.2004openalex-snapshot

Anti- Trypanosoma cruzi Activity of Green Tea ( Camellia sinensis ) Catechins

inferredcites →https://doi.org/10.1128/ec.3.2.277-287.2004openalex-snapshot

Redox Potential Regulates Binding of Universal Minicircle Sequence Binding Protein at the Kinetoplast DNA Replication Origin

inferredcites →https://doi.org/10.1128/iai.00193-16openalex-snapshot

TcI Isolates of Trypanosoma cruzi Exploit the Antioxidant Network for Enhanced Intracellular Survival in Macrophages and Virulence in Mice

inferredcites →https://doi.org/10.1128/mspheredirect.00338-18openalex-snapshot

Uptake of l -Alanine and Its Distinct Roles in the Bioenergetics of Trypanosoma cruzi

inferredcites →https://doi.org/10.1134/s0006297919020019openalex-snapshot

Catalytic and Signaling Role of Peroxiredoxins in Carcinogenesis

inferredcites →https://doi.org/10.1146/annurev-cellbio-100616-060748openalex-snapshot

Unconventional Ways to Live and Die: Cell Death and Survival in Development, Homeostasis, and Disease

inferredcites →https://doi.org/10.1146/annurev-pathol-020117-043711openalex-snapshot

Pathology and Pathogenesis of Chagas Heart Disease

inferredcites →https://doi.org/10.1146/annurev.bi.64.070195.000525openalex-snapshot

SUPEROXIDE RADICAL AND SUPEROXIDE DISMUTASES

inferredcites →https://doi.org/10.1146/annurev.mi.46.100192.003403openalex-snapshot

METABOLISM AND FUNCTIONS OF TRYPANOTHIONE IN THE KINETOPLASTIDA

inferredcites →https://doi.org/10.1155/2010/131505openalex-snapshot

Improved Label-Free LC-MS Analysis by Wavelet-Based Noise Rejection

inferredcites →https://doi.org/10.1155/2010/525241openalex-snapshot

Gene Expression in Trypanosomatid Parasites

inferredcites →https://doi.org/10.1155/2011/174614openalex-snapshot

The Role of Heme and Reactive Oxygen Species in Proliferation and Survival ofTrypanosoma cruzi

inferredcites →https://doi.org/10.1155/2014/360438openalex-snapshot

Lipid Peroxidation: Production, Metabolism, and Signaling Mechanisms of Malondialdehyde and 4-Hydroxy-2-Nonenal

inferredcites →https://doi.org/10.1155/2015/214878openalex-snapshot

IL-12 Inhibits Lipopolysaccharide Stimulated Osteoclastogenesis in Mice

inferredcites →https://doi.org/10.1155/2015/489758openalex-snapshot

Experimental Vaccines against Chagas Disease: A Journey through History

inferredcites →https://doi.org/10.1155/2017/1809592openalex-snapshot

Relationships between Stress Granules, Oxidative Stress, and Neurodegenerative Diseases

inferredcites →https://doi.org/10.1155/2017/3575348openalex-snapshot

Corrigendum to “Identification of Patients Affected by Mitral Valve Prolapse with Severe Regurgitation: A Multivariable Regression Model”

inferredcites →https://doi.org/10.1155/2017/8459402openalex-snapshot

Redox Regulation of Inflammatory Processes Is Enzymatically Controlled

inferredcites →https://doi.org/10.1155/2018/9603051openalex-snapshot

The Kinetoplast of Trypanosomatids: From Early Studies of Electron Microscopy to Recent Advances in Atomic Force Microscopy

inferredcites →https://doi.org/10.1161/jaha.112.003855openalex-snapshot

Defects of mtDNA Replication Impaired Mitochondrial Biogenesis During Trypanosoma cruzi Infection in Human Cardiomyocytes and Chagasic Patients: The Role of Nrf1/2 and Antioxidant Response

showing the first 200 of 244 · page through all 244

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4765087openalex-extracted

Cross-Species Role of Pip39 in Oxidative Stress Response in Kinetoplastids

inferred← citeshttps://doi.org/10.1007/978-981-16-0691-5_22openalex-snapshot

Metabolomics: A Promising Tool to Study Disease Biomarkers and Host-Pathogen Interactions

inferred← citeshttps://doi.org/10.1007/s00436-021-07400-8openalex-snapshot

Selenium and protozoan parasitic infections: selenocompounds and selenoproteins potential

inferred← citeshttps://doi.org/10.1007/s11686-026-01228-xopenalex-snapshot

Mechanistic and Synergistic Evaluation of Amodiaquine–Isometamidium Combination Against Trypanosoma evansi: Integrated In Silico–In-Vitro Insights

inferred← citeshttps://doi.org/10.1016/bs.apar.2022.04.002openalex-snapshot

Unique thiol metabolism in trypanosomatids: Redox homeostasis and drug resistance

inferred← citeshttps://doi.org/10.1016/j.actatropica.2026.108208openalex-snapshot

L-threonine 3-dehydrogenase overexpression enhances tolerance to oxidative, genotoxic, and drug-induced stress in Trypanosoma cruzi

inferred← citeshttps://doi.org/10.1016/j.bioorg.2026.110059openalex-snapshot

Synthesis of α,γ-disubstituted-β-hydroxy-γ-lactones and evaluation of their anti-trypanosomatid activities

inferred← citeshttps://doi.org/10.1016/j.dnarep.2020.102873openalex-snapshot

Mechanisms of DNA repair in Trypanosoma cruzi: What do we know so far?

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2020.06.035openalex-snapshot

On the functionality of a methionine sulfoxide reductase B from Trypanosoma cruzi

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2026.04.009openalex-snapshot

Role of glutamine metabolism reprogramming in ferroptosis of lens epithelial cells under high-glucose conditions

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2026.05.301openalex-snapshot

Nitric oxide initiates early differentiation events in Leishmania infantum stage transition

inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.144650openalex-snapshot

Targeting antioxidant defense system enzymes for Leishmaniasis treatment

inferred← citeshttps://doi.org/10.1016/j.jprot.2021.104339openalex-snapshot

The thermal proteome stability profile of Trypanosoma cruzi in epimastigote and trypomastigote life stages

inferred← citeshttps://doi.org/10.1016/j.molbiopara.2024.111620openalex-snapshot

Role of PIP39 in oxidative stress response appears conserved in kinetoplastids

inferred← citeshttps://doi.org/10.1016/j.prp.2025.156077openalex-snapshot

Autophagy in disease management: Exploring the potential of natural products as targeted therapies

inferred← citeshttps://doi.org/10.1021/acs.jmedchem.4c01535openalex-snapshot

Synthesis and Biological Evaluation of New Chalcogen Semicarbazone (S, Se) and Their Azole Derivatives against Chagas Disease

inferred← citeshttps://doi.org/10.1039/d6md00631kopenalex-snapshot

Fluorination of amino-quinones enhances anti- Trypanosoma cruzi activity

inferred← citeshttps://doi.org/10.1080/14760584.2021.1969230openalex-snapshot

Oxidative stress implications for therapeutic vaccine development against Chagas disease

inferred← citeshttps://doi.org/10.1080/21505594.2022.2132776openalex-snapshot

Trypanosoma cruzi pathogenicity involves virulence factor expression and upregulation of bioenergetic and biosynthetic pathways

inferred← citeshttps://doi.org/10.1101/2025.09.08.674805openalex-snapshot

The role of the Trypanosoma cruzi enzyme L-threonine 3-dehydrogenase in combating stressful environments

inferred← citeshttps://doi.org/10.1111/mec.17155openalex-snapshot

Long live the host! Proteomic analysis reveals possible strategies for parasitic manipulation of its social host

inferred← citeshttps://doi.org/10.1111/pim.12786openalex-snapshot

Host‐parasite dynamics in Chagas disease from systemic to hyper‐local scales

inferred← citeshttps://doi.org/10.1111/tra.70017openalex-snapshot

Strain‐Dependent Immune Signaling by Small Extracellular Vesicles Derived From Trypanosoma cruzi ‐Infected Macrophages

inferred← citeshttps://doi.org/10.1155/2020/8867701openalex-snapshot

Dual and Opposite Roles of Reactive Oxygen Species (ROS) in Chagas Disease: Beneficial on the Pathogen and Harmful on the Host

inferred← citeshttps://doi.org/10.1155/2022/2849985openalex-snapshot

Mitophagy: A Potential Target for Pressure Overload‐Induced Cardiac Remodelling

inferred← citeshttps://doi.org/10.11606/t.41.2023.tde-09102023-111432openalex-snapshot

MicroRNAs e imunometabolismo em macrófagos e células dendríticas em resposta à infecção com Leishmania spp.

inferred← citeshttps://doi.org/10.1186/s12864-026-12542-zopenalex-snapshot

Integrated analysis of lncRNA-miRNA-mRNA networks reveals stage-specific molecular regulation of oogenesis in Chinese alligator (Alligator sinensis)

inferred← citeshttps://doi.org/10.1371/journal.pntd.0013626openalex-snapshot

Translesion synthesis and microhomology-mediated end-joining repair in trypanosomatids

inferred← citeshttps://doi.org/10.1371/journal.pone.0243855openalex-snapshot

The ubiquinone synthesis pathway is a promising drug target for Chagas disease

inferred← citeshttps://doi.org/10.2139/ssrn.5234358openalex-snapshot

Inference of Chitin Synthase Gene Silencing on Rhodnius Prolixus Vector Competence: Trypanosoma Cruzi Life Cycle and Reactive Oxygen Species Formation

inferred← citeshttps://doi.org/10.2174/1381612826666201211115329openalex-snapshot

Trypanothione Metabolism as Drug Target for Trypanosomatids

inferred← citeshttps://doi.org/10.2174/1568026622666220912101332openalex-snapshot

Mechanism of Action and Implication of Naphthoquinone as Potent Anti-trypanosomal Drugs

inferred← citeshttps://doi.org/10.26434/chemrxiv-2023-2cl8lopenalex-snapshot

In silico screening based on chemoinformatics and molecular docking of trypanothione reductase inhibitors from Trypanosoma cruzi

inferred← citeshttps://doi.org/10.3389/fcimb.2020.00154openalex-snapshot

Trypanosoma brucei and Trypanosoma cruzi DNA Mismatch Repair Proteins Act Differently in the Response to DNA Damage Caused by Oxidative Stress

inferred← citeshttps://doi.org/10.3389/fcimb.2021.669079openalex-snapshot

Comparative Analysis of Virulence Mechanisms of Trypanosomatids Pathogenic to Humans

inferred← citeshttps://doi.org/10.3389/fcimb.2025.1664827openalex-snapshot

Differential antioxidant enzyme profiles reveal early molecular signatures of virulence in Trypanosoma cruzi DTU-TcI and DTU-TcVI strains

inferred← citeshttps://doi.org/10.3389/fimmu.2022.1038332openalex-snapshot

Modulation of STAT-1, STAT-3, and STAT-6 activities in THP-1 derived macrophages infected with two Trypanosoma cruzi strains

inferred← citeshttps://doi.org/10.3389/fimmu.2022.850037openalex-snapshot

Predicting Blood Parasite Load and Influence of Expression of iNOS on the Effect Size of Clinical Laboratory Parameters in Acute Trypanosoma cruzi Infection With Different Inoculum Concentrations in C57BL/6 Mice

inferred← citeshttps://doi.org/10.3389/fmicb.2020.01844openalex-snapshot

TrypOx, a Novel Eukaryotic Homolog of the Redox-Regulated Chaperone Hsp33 in Trypanosoma brucei

inferred← citeshttps://doi.org/10.3389/fmicb.2020.563320openalex-snapshot

Priming Astrocytes With HIV-Induced Reactive Oxygen Species Enhances Their Trypanosoma cruzi Infection

inferred← citeshttps://doi.org/10.3389/fphar.2022.970596openalex-snapshot

Natural phytochemicals that affect autophagy in the treatment of oral diseases and infections: A review

inferred← citeshttps://doi.org/10.3390/antiox14080977openalex-snapshot

LC-MS Evaluation of the Redox Trypanothione Balance in Leishmania infantum Parasites

inferred← citeshttps://doi.org/10.3390/ijms22136883openalex-snapshot

Metabolomic Reprogramming of C57BL/6-Macrophages during Early Infection with L. amazonensis

inferred← citeshttps://doi.org/10.3390/insects13110968openalex-snapshot

Genome-Wide Screening for Pathogenic Proteins and microRNAs Associated with Parasite–Host Interactions in Trypanosoma brucei

inferred← citeshttps://doi.org/10.3390/microorganisms9040759openalex-snapshot

Effects of Visceralising Leishmania on the Spleen, Liver, and Bone Marrow: A Pathophysiological Perspective

inferred← citeshttps://doi.org/10.3390/molecules29102214openalex-snapshot

Targeting Trypanothione Metabolism in Trypanosomatids

inferred← citeshttps://doi.org/10.3390/parasitologia6030024openalex-snapshot

Further Studies on the Antiparasitic Activity of Quinoxaline-1,4-di-N-Oxides Containing a Glycine Side Chain

inferred← citeshttps://doi.org/10.3390/pathogens10111493openalex-snapshot

Molecular and Clinical Aspects of Chronic Manifestations in Chagas Disease: A State-of-the-Art Review

inferred← citeshttps://doi.org/10.3390/pathogens12020282openalex-snapshot

A Review on the Immunological Response against Trypanosoma cruzi

inferred← citeshttps://doi.org/10.3390/ph16030334openalex-snapshot

Recent Advances in the Development of Adenovirus-Vectored Vaccines for Parasitic Infections

inferred← citeshttps://doi.org/10.55810/2789-9136.1109openalex-snapshot

A Comprehensive Review of Current Trends and Future Prospects in Drug Resistance of Leishmania Species

inferred← citeshttps://doi.org/10.5772/intechopen.113762openalex-snapshot

Possible Chemotherapeutic Potential of Inhibiting N-Alpha Terminal Acetylation Activities to Combat Trypanosome Infections

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.