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Oxidative stress is increased in primary and post−polycythemia vera myelofibrosis
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/1096-8652(200010)65:2<136::aid-ajh8>3.0.co;2-6openalex-snapshot
High prevalence of hyperhomocysteinemia due to marginal deficiency of cobalamin or folate in chronic myeloproliferative disorders
inferredcites →https://doi.org/10.1002/cncr.20752openalex-snapshot
New approaches in the treatment of myelofibrosis
inferredcites →https://doi.org/10.1007/s00726-003-0026-8openalex-snapshot
Homocysteine and oxidative stress
inferredcites →https://doi.org/10.1016/0003-2697(90)90595-zopenalex-snapshot
Molecular cloning: A laboratory manual
inferredcites →https://doi.org/10.1016/j.clinbiochem.2003.08.004openalex-snapshot
Significance of elevated cobalamin (vitamin B12) levels in blood
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2007.07.019openalex-snapshot
Production, detection, and adaptive responses to free radicals in exercise
inferredcites →https://doi.org/10.1016/j.lfs.2009.02.026openalex-snapshot
Oxidative stress and metabolic syndrome
inferredcites →https://doi.org/10.1016/s0140-6736(05)71142-9openalex-snapshot
Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders
inferredcites →https://doi.org/10.1016/s0140-6736(84)91886-5openalex-snapshot
LIPID PEROXIDATION, OXYGEN RADICALS, CELL DAMAGE, AND ANTIOXIDANT THERAPY
inferredcites →https://doi.org/10.1016/s0950-3536(98)80037-1openalex-snapshot
3 Pathogenesis and management of idiopathic myelofibrosis
inferredcites →https://doi.org/10.1017/s0007114508076204openalex-snapshot
Glycaemic status in relation to oxidative stress and inflammation in well-controlled type 2 diabetes subjects
inferredcites →https://doi.org/10.1038/nature04634openalex-snapshot
Reactive oxygen species have a causal role in multiple forms of insulin resistance
inferredcites →https://doi.org/10.1038/ng0595-111openalex-snapshot
A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase
inferredcites →https://doi.org/10.1046/j.1365-2141.1997.782714.xopenalex-snapshot
Identification of ‘short‐lived’ and ‘long‐lived’ patients at presentation of idiopathic myelofibrosis
inferredcites →https://doi.org/10.1046/j.1365-2141.1998.00833.xopenalex-snapshot
Myelofibrosis with myeloid metaplasia in young indidviduals: disease characteristics, prognostic factors and identification of risk groups
inferredcites →https://doi.org/10.1056/nejm200004273421706openalex-snapshot
Myelofibrosis with Myeloid Metaplasia
inferredcites →https://doi.org/10.1089/ars.2005.7.547openalex-snapshot
Homocysteine and Redox Signaling
inferredcites →https://doi.org/10.1089/ars.2007.1750openalex-snapshot
Vascular Oxidant Stress and Inflammation in Hyperhomocysteinemia
inferredcites →https://doi.org/10.1089/ars.2007.1771openalex-snapshot
Homocysteine and Glutathione Peroxidase-1
inferredcites →https://doi.org/10.1093/clinchem/45.3.428openalex-snapshot
Development and Multisite Evaluation of an Automated Assay for B12 on the Abbott AxSYM Analyzer
inferredcites →https://doi.org/10.1093/clinchem/48.10.1768openalex-snapshot
Holo-Transcobalamin Is an Early Marker of Changes in Cobalamin Homeostasis. A Randomized Placebo-controlled Study
inferredcites →https://doi.org/10.1093/clinchem/48.3.561openalex-snapshot
Quantification of Holo-Transcobalamin, a Marker of Vitamin B12 Deficiency
inferredcites →https://doi.org/10.1097/01.mat.0000094486.12329.6bopenalex-snapshot
Effect of Incremental Doses of Folate on Homocysteine and Metabolically Related Vitamin Concentrations in Nondiabetic Patients on Peritoneal Dialysis
inferredcites →https://doi.org/10.1097/01.moh.0000203191.99447.98openalex-snapshot
Allogeneic hematopoietic stem cell transplantation for myelofibrosis
inferredcites →https://doi.org/10.1097/01.moh.0000208469.48614.2eopenalex-snapshot
New insights into the pathogenesis and drug treatment of myelofibrosis
inferredcites →https://doi.org/10.1097/01.tp.0000090344.61975.f0openalex-snapshot
Oxidative stress in kidney transplant patients1
inferredcites →https://doi.org/10.1159/000110876openalex-snapshot
Mechanisms of Homocysteine-Induced Glomerular Injury and Sclerosis
inferredcites →https://doi.org/10.1161/01.cir.95.5.1119openalex-snapshot
Hyperhomocyst(e)inemia Is Associated With Impaired Endothelium-Dependent Vasodilation in Humans
inferredcites →https://doi.org/10.1161/hc4501.098925openalex-snapshot
Low Plasma Levels of Vitamin B 6 Are Independently Associated With a Heightened Risk of Deep-Vein Thrombosis
inferredcites →https://doi.org/10.1182/blood-2002-07-2341openalex-snapshot
Both B and T lymphocytes may be clonally involved in myelofibrosis with myeloid metaplasia
inferredcites →https://doi.org/10.1182/blood-2009-04-215848openalex-snapshot
Conditional expression of heterozygous or homozygous Jak2V617F from its endogenous promoter induces a polycythemia vera–like disease
inferredcites →https://doi.org/10.1182/blood.v98.12.3249openalex-snapshot
Diagnostic and clinical relevance of the number of circulating CD34+ cells in myelofibrosis with myeloid metaplasia
inferredcites →https://doi.org/10.1200/jco.1999.17.9.2954openalex-snapshot
Myelofibrosis With Myeloid Metaplasia: Diagnostic Definition and Prognostic Classification for Clinical Studies and Treatment Guidelines
inferredcites →https://doi.org/10.1373/clinchem.2005.054619openalex-snapshot
Holotranscobalamin and Total Transcobalamin in Human Plasma: Determination, Determinants, and Reference Values in Healthy Adults
inferredcites →https://doi.org/10.1373/clinchem.2006.080382openalex-snapshot
Detection of Vitamin B12 Deficiency in Older People by Measuring Vitamin B12 or the Active Fraction of Vitamin B12, Holotranscobalamin
inferredcites →https://doi.org/10.1373/clinchem.2007.096784openalex-snapshot
Active B12: A Rapid, Automated Assay for Holotranscobalamin on the Abbott AxSYM Analyzer
inferredcites →https://doi.org/10.1515/cclm.2004.041openalex-snapshot
Analytical performance and method comparison study of the total homocysteine fluorescence polarization immunoassay (FPIA) on the AxSYM analyzer
inferredcites →https://doi.org/10.1515/cclm.2005.185openalex-snapshot
Evaluation of the technical performance of novel holotranscobalamin (holoTC) assays in a multicenter European demonstration project
inferredcites →https://doi.org/10.1515/cclm.2010.032openalex-snapshot
Determination of serum holotranscobalamin concentrations with the AxSYM active B12 assay: cut-off point evaluation in the clinical laboratory
inferredcites →https://doi.org/10.2174/0929867043365341openalex-snapshot
Role of Oxidant Species in Aging
inferredcites →https://doi.org/10.4161/cc.4.8.1872openalex-snapshot
JAK2 in Myeloproliferative Disorders Is Not Just Another Kinase
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.4670506openalex-extracted
Agent Orange Exposure Enhances the Increased Risk of Cardiovascular Disease in Veterans with Myeloproliferative Neoplasms
inferred← citeshttps://doi.org/10.1002/1878-0261.12387openalex-snapshot
Role of TGF ‐β1/miR‐382‐5p/ SOD 2 axis in the induction of oxidative stress in CD 34+ cells from primary myelofibrosis
inferred← citeshttps://doi.org/10.1002/ajh.27438openalex-snapshot
Risk of myeloproliferative neoplasms among U.S. Veterans from Korean, Vietnam, and Persian Gulf War eras
inferred← citeshttps://doi.org/10.1002/ccr3.281openalex-snapshot
The impact of ruxolitinib treatment on inflammation‐mediated comorbidities in myelofibrosis and related neoplasms
inferred← citeshttps://doi.org/10.1002/hon.2264openalex-snapshot
Oxidative status in treatment-naïve essential thrombocythemia: a pilot study in a single center
inferred← citeshttps://doi.org/10.1002/jcp.24071openalex-snapshot
Oxidases and reactive oxygen species during hematopoiesis: A focus on megakaryocytes
inferred← citeshttps://doi.org/10.1007/s12288-024-01827-6openalex-snapshot
Oxidant/Antioxidant Status in Patients with BCR-ABL1 Negative Myeloproliferative Neoplasms
inferred← citeshttps://doi.org/10.1007/s12308-022-00488-6openalex-snapshot
Analysis of factors associated with the development of myelofibrosis in polycythemia vera and essential thrombocythemia patients: a single-center experience
inferred← citeshttps://doi.org/10.1007/s44337-025-00278-wopenalex-snapshot
Exploring the interplay between myeloproliferative disorders and atherosclerosis
inferred← citeshttps://doi.org/10.1016/j.advms.2023.03.003openalex-snapshot
Effect of hypoxia on HIF-1α and NOS3 expressions in CD34+ cells of JAK2V617F-positive myeloproliferative neoplasms
inferred← citeshttps://doi.org/10.1016/j.bjhh.2016.04.009openalex-snapshot
Reactive oxygen species overload promotes apoptosis in JAK2V617F-positive cell lines
inferred← citeshttps://doi.org/10.1016/j.clinbiochem.2012.07.100openalex-snapshot
Changes in advanced oxidation protein products, advanced glycation end products, and s-nitrosylated proteins, in patients affected by polycythemia vera and essential thrombocythemia
inferred← citeshttps://doi.org/10.1016/j.euprot.2015.04.001openalex-snapshot
Quantitative analysis of the erythrocyte membrane proteins in polycythemia vera patients treated with hydroxycarbamide
inferred← citeshttps://doi.org/10.1016/j.htct.2020.08.006openalex-snapshot
Exploring redox vulnerabilities in JAK2V617F-positive cellular models
inferred← citeshttps://doi.org/10.1016/j.jaccao.2022.04.002openalex-snapshot
Cardiovascular Disease in Myeloproliferative Neoplasms
inferred← citeshttps://doi.org/10.1016/j.leukres.2016.02.004openalex-snapshot
Myeloid-derived suppressor cells in patients with myeloproliferative neoplasm
inferred← citeshttps://doi.org/10.1016/j.nutres.2025.02.008openalex-snapshot
The combined indicator of vitamin B12 status calculated using 3-parameters (3cB12) is negatively associated with mortality among US adults: NHANES 1999 to 2004
inferred← citeshttps://doi.org/10.1016/j.redox.2021.101895openalex-snapshot
Elevated levels of oxidized nucleosides in individuals with the JAK2V617F mutation from a general population study
inferred← citeshttps://doi.org/10.1038/s41375-019-0629-zopenalex-snapshot
Hypoxia-inducible factor 1 (HIF-1) is a new therapeutic target in JAK2V617F-positive myeloproliferative neoplasms
inferred← citeshttps://doi.org/10.1038/s41388-019-0813-7openalex-snapshot
Addiction to DUSP1 protects JAK2V617F-driven polycythemia vera progenitors against inflammatory stress and DNA damage, allowing chronic proliferation
inferred← citeshttps://doi.org/10.1038/s41598-019-46843-zopenalex-snapshot
Calreticulin Ins5 and Del52 mutations impair unfolded protein and oxidative stress responses in K562 cells expressing CALR mutants
inferred← citeshttps://doi.org/10.1080/10428194.2019.1579323openalex-snapshot
Ruxolitinib treatment reduces monocytic superoxide radical formation without affecting hydrogen peroxide formation or systemic oxidative nucleoside damage in myelofibrosis
inferred← citeshttps://doi.org/10.1080/10428194.2023.2277674openalex-snapshot
Understanding triple negative myeloproliferative neoplasms: pathogenesis, clinical features, and management
inferred← citeshttps://doi.org/10.1080/17474086.2026.2659700openalex-snapshot
Polycythemia vera and metabolic syndrome: is the relationship between the two diseases more than we think?
inferred← citeshttps://doi.org/10.1111/ejh.14081openalex-snapshot
Whole blood transcriptional profiling reveals highly deregulated atherosclerosis genes in Philadelphia‐chromosome negative myeloproliferative neoplasms
inferred← citeshttps://doi.org/10.1136/bcr-2020-240719openalex-snapshot
Acute liver failure after changing oral anticoagulant from apixaban to rivaroxaban
inferred← citeshttps://doi.org/10.1155/2015/648090openalex-snapshot
The Role of Reactive Oxygen Species in Myelofibrosis and Related Neoplasms
inferred← citeshttps://doi.org/10.1155/2024/1827127openalex-snapshot
TLR2 Derangements Likely Play a Significant Role in the Inflammatory Response and Thrombosis in Patients with Ph(−) Classical Myeloproliferative Neoplasm
inferred← citeshttps://doi.org/10.1159/000360102openalex-snapshot
The Thrombotic Events in Polycythemia Vera Patients May Be Related to Increased Oxidative Stress
inferred← citeshttps://doi.org/10.1172/jci124566openalex-snapshot
Erythrocyte-derived microvesicles induce arterial spasms in JAK2V617F myeloproliferative neoplasm
inferred← citeshttps://doi.org/10.1186/s12887-016-0714-7openalex-snapshot
Homocysteine metabolism in children and adolescents with epidermolysis bullosa
inferred← citeshttps://doi.org/10.14744/ejmi.2023.39692openalex-snapshot
Thiol-Disulfide Homeostasis and Ischemia Modified Albumin as a New Oxidative Stress Marker in Patients with Polycythemia Vera
inferred← citeshttps://doi.org/10.1586/ehm.13.21openalex-snapshot
Oxidative stress in oncohematologic diseases: an update
inferred← citeshttps://doi.org/10.3390/antiox11010113openalex-snapshot
The Response to Oxidative Damage Correlates with Driver Mutations and Clinical Outcome in Patients with Myelofibrosis
inferred← citeshttps://doi.org/10.3390/antiox9111037openalex-snapshot
Synergic Crosstalk between Inflammation, Oxidative Stress, and Genomic Alterations in BCR–ABL-Negative Myeloproliferative Neoplasm
inferred← citeshttps://doi.org/10.3390/antiox9121212openalex-snapshot
Protein Carbonylation and Lipid Peroxidation in Hematological Malignancies
inferred← citeshttps://doi.org/10.3390/biomedicines14081837openalex-snapshot
Malondialdehyde at the Crossroads of Oxidative Stress, Lipid Peroxidation, Ferroptosis, and Hematological Malignancies: A Narrative Review
inferred← citeshttps://doi.org/10.3390/cancers15041348openalex-snapshot
Deepening Our Understanding of the Factors Affecting Landscape of Myeloproliferative Neoplasms: What Do We Know about Them?
inferred← citeshttps://doi.org/10.3390/cells10123551openalex-snapshot
Progression of Myeloproliferative Neoplasms (MPN): Diagnostic and Therapeutic Perspectives
inferred← citeshttps://doi.org/10.3390/ijms21217902openalex-snapshot
Clonal Hematopoiesis, Cardiovascular Diseases and Hematopoietic Stem Cells
inferred← citeshttps://doi.org/10.3390/ijms23031013openalex-snapshot
Insights into the Potential Mechanisms of JAK2V617F Somatic Mutation Contributing Distinct Phenotypes in Myeloproliferative Neoplasms
inferred← citeshttps://doi.org/10.3390/ijms23031490openalex-snapshot
Neutrophil Death in Myeloproliferative Neoplasms: Shedding More Light on Neutrophils as a Pathogenic Link to Chronic Inflammation
inferred← citeshttps://doi.org/10.3390/ijms23105837openalex-snapshot
PD-1/PD-L1, MDSC Pathways, and Checkpoint Inhibitor Therapy in Ph(-) Myeloproliferative Neoplasm: A Review
inferred← citeshttps://doi.org/10.3390/ijms25126652openalex-snapshot
Assessment of Total Antioxidant Capacity, 8-Hydroxy-2′-deoxy-guanosine, the Genetic Landscape, and Their Associations in BCR::ABL-1-Negative Chronic and Blast Phase Myeloproliferative Neoplasms
inferred← citeshttps://doi.org/10.3390/ijms25189873openalex-snapshot
The Role of Mutated Calreticulin in the Pathogenesis of BCR-ABL1-Negative Myeloproliferative Neoplasms
inferred← citeshttps://doi.org/10.3390/metabo15090630openalex-snapshot
Metabolomic Profiling Reveals Distinct Signatures in Primary and Secondary Polycythemia
inferred← citeshttps://doi.org/10.3390/nu11020482openalex-snapshot
Vitamin B12 in Relation to Oxidative Stress: A Systematic Review
inferred← citeshttps://doi.org/10.3390/ph16040529openalex-snapshot
Bioactivity of Falkenbergia rufolanosa Methanolic Extract: Assessment of Its Effect on Methyl-Thiophanate Induced Bone and Blood Disorders
inferred← citeshttps://doi.org/10.37506/mlu.v21i1.2556openalex-snapshot
Effect of Polycythemia on Serum Lipid Profile and Oxidative Stress
inferred← citeshttps://doi.org/10.4081/btvb.2022.38openalex-snapshot
Clonal hematopoiesis and inflammation: a link with thrombosis and malignancy
inferred← citeshttps://doi.org/10.70675/d71df373z8cc7z41c1z9896zab996bc5b48eopenalex-snapshot
Pathophysiology of cardiovascular events in Bcr/Abl-negative myeloproliferative neoplasms
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