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Association of lipid peroxidation with hepatocellular injury in preterm infants

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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/hep.1840220234openalex-snapshot

Reduced antioxidative capacity in liver mitochondria from bile duct ligated rats

inferredcites →https://doi.org/10.1006/bbrc.1993.1927openalex-snapshot

Stimulation of Lipid Peroxidation or 4-Hydroxynonenal Treatment Increases Procollagen α1 (I) Gene Expression in Human Liver Fat-Storing Cells

inferredcites →https://doi.org/10.1007/s000110050649openalex-snapshot

Reactive oxygen intermediates and eicosanoid production by Kupffer cells and infiltrated macrophages in acute and chronic liver injury induced in rats by CCl 4

inferredcites →https://doi.org/10.1007/s11894-000-0069-xopenalex-snapshot

New developments in total parenteral nutrition for children

inferredcites →https://doi.org/10.1016/0009-8981(93)90247-2openalex-snapshot

Changes of lipid peroxide levels in blood and liver tissue of patients with obstructive jaundice

inferredcites →https://doi.org/10.1016/0016-5085(81)90663-6openalex-snapshot

Serial liver biopsies in parenteral nutrition-associated cholestasis of early infancy

inferredcites →https://doi.org/10.1016/0016-5085(94)90822-2openalex-snapshot

Oxidant injury to hepatic mitochondria in patients with Wilson's disease and Bedlington terriers with copper toxicosis

inferredcites →https://doi.org/10.1016/0016-5085(95)90585-5openalex-snapshot

Generation of hydroperoxides in isolated rat hepatocytes and hepatic mitochondria exposed to hydrophobic bile acids

inferredcites →https://doi.org/10.1016/0024-3205(91)90550-uopenalex-snapshot

The biological significance of malondialdehyde determination in the assessment of tissue oxidative stress

inferredcites →https://doi.org/10.1016/0304-4165(92)90073-4openalex-snapshot

Catalase, superoxide dismutase and glutathione peroxidase activities of lung and liver during human development

inferredcites →https://doi.org/10.1016/0378-3782(85)90114-8openalex-snapshot

Creatinine and urea clearances compared to inulin clearance in preterm and mature babies

inferredcites →https://doi.org/10.1016/0891-5849(96)02055-2openalex-snapshot

On the role of lipid peroxidation in the pathogenesis of liver damage induced by long-standing cholestasis

inferredcites →https://doi.org/10.1016/b978-0-08-041749-3.50005-xopenalex-snapshot

OXIDATIVE DAMAGE & REPAIR: INTRODUCTION AND OVERVIEW

inferredcites →https://doi.org/10.1016/s0022-3468(05)80311-2openalex-snapshot

Total parenteral nutrition-associated cholestasis: Clinical and histopathologic correlation

inferredcites →https://doi.org/10.1016/s0022-3468(96)90507-2openalex-snapshot

Parenteral nutrition—Related cholestasis in postsurgical neonates: Multivariate analysis of rick factors

inferredcites →https://doi.org/10.1016/s0022-3476(79)80849-5openalex-snapshot

Parenteral nutrition and neonatal cholestasis

inferredcites →https://doi.org/10.1016/s0022-3476(80)80573-7openalex-snapshot

Prospective controlled study of parenteral nutrition-associated cholestatic jaundice: Effect of protein intake

inferredcites →https://doi.org/10.1016/s0076-6879(78)52032-6openalex-snapshot

[30] Microsomal lipid peroxidation

inferredcites →https://doi.org/10.1016/s0742-8413(00)00102-xopenalex-snapshot

Bile duct ligation and oxidative stress in the rat: effects in liver and kidney

inferredcites →https://doi.org/10.1093/alcalc/28.supplement_1a.111openalex-snapshot

Ethanol and Hydrazine Sulfate Induced Chronic Hepatic Injury in Rats: The Curative Effect Of Administration of Glucogenic Amino Acids

inferredcites →https://doi.org/10.1093/toxsci/65.2.166openalex-snapshot

Mechanisms of Hepatotoxicity

inferredcites →https://doi.org/10.1097/00005176-198909010-00005openalex-snapshot

Decreased Cholestasis with Enteral Instead of Intravenous Protein in the Very Low-Birth-Weight Infant

inferredcites →https://doi.org/10.1136/adc.60.8.774openalex-snapshot

Pathogenesis of liver damage during parenteral nutrition: is lipofuscin a clue?

inferredcites →https://doi.org/10.1136/adc.63.7_spec_no.748openalex-snapshot

Serum antioxidant activity in neonates.

inferredcites →https://doi.org/10.1136/jcp.46.4.364openalex-snapshot

Intensity of inflammatory damage and serum lipid peroxide concentrations in liver disease.

inferredcites →https://doi.org/10.1146/annurev.pa.35.040195.003255openalex-snapshot

Macrophages and Inflammatory Mediators in Tissue Injury

inferredcites →https://doi.org/10.1159/000243284openalex-snapshot

Glutathione Peroxidase and Selenium Levels in the Preterm Infant

inferredcites →https://doi.org/10.1177/0148607186010004356openalex-snapshot

Total Parenteral Nutrition‐Related Cholestasis in Infants

inferredcites →https://doi.org/10.1203/00006450-198907000-00008openalex-snapshot

The Total Free Radical Trapping Ability of Cord Blood Plasma in Preterm and Term Babies

inferredcites →https://doi.org/10.1203/00006450-200102000-00017openalex-snapshot

Standard Treatment of α-Tocopherol in Alagille Patients with Severe Cholestasis Is Insufficient

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.4809090openalex-extracted

Response of Red Swamp Crayfish (Procambarus Clarkii) to Abamectin During Nano-Selenium and Sodium Selenite Addition

inferred← citeshttps://doi.org/10.1007/bf02912909openalex-snapshot

Association of plasma level of thiobarbituric acid reactive substances with extent of hepatocellular injury in preterm infants with cholestatic jaundice

inferred← citeshttps://doi.org/10.1007/s00044-022-02892-0openalex-snapshot

Hybrid molecules of scutellarein and 3, 5, 6-trimethylpyrazine-2-formic acid linked with polar amino acid for ischemic stroke

inferred← citeshttps://doi.org/10.1007/s00394-016-1322-xopenalex-snapshot

N-acetylcysteine attenuates intrauterine growth retardation-induced hepatic damage in suckling piglets by improving glutathione synthesis and cellular homeostasis

inferred← citeshttps://doi.org/10.1016/j.apsb.2019.10.012openalex-snapshot

Effects of total parenteral nutrition on drug metabolism gene expression in mice

inferred← citeshttps://doi.org/10.1016/j.biocel.2009.10.006openalex-snapshot

Proliferative retinopathies: Angiogenesis that blinds

inferred← citeshttps://doi.org/10.1016/j.biopha.2020.109841openalex-snapshot

Vitamin E and selenium administration synergistically mitigates ivermectin and doramectin-induced testicular dysfunction in male Wistar albino rats

inferred← citeshttps://doi.org/10.1016/j.chemosphere.2026.144993openalex-snapshot

Comparative toxicity of thiamethoxam and abamectin in red swamp crayfish: Bioaccumulation, oxidative stress, and gut microbiota in a rice-crayfish Co-culture system

inferred← citeshttps://doi.org/10.1016/j.cld.2004.06.003openalex-snapshot

Liver disease due to parenteral and enteral nutrition

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2008.05.016openalex-snapshot

Highlight Commentary on “Influence of lung oxidant and antioxidant status on alveolarization: Role of light-exposed total parenteral nutrition”

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2009.04.026openalex-snapshot

Long-term impact of an antioxidant-deficient neonatal diet on lipid and glucose metabolism

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2019.02.019openalex-snapshot

Non-invasive assessment of oxidative stress in preterm infants

inferred← citeshttps://doi.org/10.1016/j.jnutbio.2023.109432openalex-snapshot

Maternal protein deficiency impairs peroxisome biogenesis and leads to oxidative stress and ferroptosis in liver of fetal growth restriction offspring

inferred← citeshttps://doi.org/10.1016/j.jpedsurg.2006.05.067openalex-snapshot

Oxidative injury and hepatocyte apoptosis in total parenteral nutrition–associated liver dysfunction

inferred← citeshttps://doi.org/10.1016/j.jss.2013.10.002openalex-snapshot

Diverse effects of parenteral arginine on systemic and local oxidant–antioxidant homeostasis and nitrosative stress in rats with subacute peritonitis

inferred← citeshttps://doi.org/10.1016/j.pepo.2014.03.007openalex-snapshot

Hepatotoksyczność leków stosowanych u noworodków

inferred← citeshttps://doi.org/10.1016/j.preteyeres.2011.11.003openalex-snapshot

From oxygen to erythropoietin: Relevance of hypoxia for retinal development, health and disease

inferred← citeshttps://doi.org/10.1021/acs.jafc.3c02466openalex-snapshot

Oxidized Soybean Oil Evoked Hepatic Fatty Acid Metabolism Disturbance in Rats and their Offspring

inferred← citeshttps://doi.org/10.1038/pr.2012.29openalex-snapshot

Hexapeptides from human milk prevent the induction of oxidative stress from parenteral nutrition in the newborn guinea pig

inferred← citeshttps://doi.org/10.1038/sj.jp.7211686openalex-snapshot

Identifying patients, on the first day of life, at high-risk of developing parenteral nutrition-associated liver disease

inferred← citeshttps://doi.org/10.1039/c9ra09316hopenalex-snapshot

N -Carbamylglutamate and l -arginine supplementation improve hepatic antioxidant status in intrauterine growth-retarded suckling lambs

inferred← citeshttps://doi.org/10.1063/5.0318071openalex-snapshot

Irisin and oxidative stress role in Jaundice of children patients

inferred← citeshttps://doi.org/10.1080/08035250600719713openalex-snapshot

The fear of necrotizing enterocolitis versus achieving optimal growth in preterm infants—an opinion

inferred← citeshttps://doi.org/10.1089/ars.2010.3581openalex-snapshot

Neuronal Death and Oxidative Stress in the Developing Brain

inferred← citeshttps://doi.org/10.1097/01.mpg.0000252193.99331.03openalex-snapshot

Influence of Different Intravenous Lipid Emulsions on Hepatobiliary Dysfunction in a Rabbit Model

inferred← citeshttps://doi.org/10.1097/01.wno.0000161661.29391.0dopenalex-snapshot

Reduced Bile Flow Associated With Parenteral Nutrition Is Independent of Oxidant Load and Parenteral Multivitamins

inferred← citeshttps://doi.org/10.1097/mot.0000000000000277openalex-snapshot

Lipid management in pediatric intestinal failure

inferred← citeshttps://doi.org/10.1097/mpg.0b013e318156113fopenalex-snapshot

Re: Influence of Different Intravenous Lipid Emulsions on Hepatobiliary Dysfunction in a Rabbit Model

inferred← citeshttps://doi.org/10.1111/j.1442-200x.2012.03627.xopenalex-snapshot

Incidence and risk factors of parenteral nutrition‐associated liver disease in newborn infants

inferred← citeshttps://doi.org/10.1177/0148607107031003199openalex-snapshot

Glutathione Decreased Parenteral Nutrition–Induced Hepatocyte Injury in Infant Rabbits

inferred← citeshttps://doi.org/10.1177/0148607111424411openalex-snapshot

Short‐Term Use of Parenteral Nutrition With a Lipid Emulsion Containing a Mixture of Soybean Oil, Olive Oil, Medium‐Chain Triglycerides, and Fish Oil

inferred← citeshttps://doi.org/10.1182/blood-2012-04-396846openalex-snapshot

Eyeing central neurons in vascular growth and reparative angiogenesis

inferred← citeshttps://doi.org/10.1373/clinchem.2005.050427openalex-snapshot

Association between Hydrogen Peroxide-Dependent Byproducts of Ascorbic Acid and Increased Hepatic Acetyl-CoA Carboxylase Activity

inferred← citeshttps://doi.org/10.3390/nu13082631openalex-snapshot

Parenteral Nutrition and Oxidant Load in Neonates

inferred← citeshttps://doi.org/10.4236/jbm.2019.71007openalex-snapshot

The Possible Role Serum Biochemical Analysis Can Play in Predicting an Infant’s Risk of Retinopathy of Prematurity; Elevated Serum Magnesium

inferred← citeshttps://doi.org/10.5897/ajb2013.12014openalex-snapshot

Genotoxicity and mutagenicity of solid waste leachates: A review

inferred← citeshttps://doi.org/10.5923/j.re.20120204.04openalex-snapshot

Liver and Kidney Dysfunction in Wistar Rats Exposed to Municipal Landfill Leachate

inferred← citeshttps://doi.org/10.71781/31537openalex-snapshot

Nutrition parentérale du nouveau-né : modulation du stress oxydant et conséquences hépatiques

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