Maturation-Dependent Vulnerability of Oligodendrocytes to Oxidative Stress-Induced Death Caused by Glutathione Depletion

Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays

Mosmann, T. (1983) · Journal of Immunological Methods · doi:10.1016/0022-1759(83)90303-4 · Cited by 56,104

Enzymic method for quantitative determination of nanogram amounts of total and oxidized glutathione: Applications to mammalian blood and other tissues

Tietze, F. (1969) · Analytical Biochemistry · doi:10.1016/0003-2697(69)90064-5 · Cited by 6,077

Bcl-2 functions in an antioxidant pathway to prevent apoptosis

Hockenbery, D. M., Oltvai, Z. N., Yin, X., Milliman, C. L., & Korsmeyer, S. J. (1993) · Cell · doi:10.1016/0092-8674(93)80066-n · Cited by 3,402

Neurology of the newborn.

Volpe, J. J. (1981) · PubMed · Cited by 2,859

Bcl-2 inhibition of neural death: decreased generation of reactive oxygen species

Kane, D. J., Sarafian, T. A., Anton, R., Hahn, H., Gralla, E. B., Valentine, J. S., Örd, T., & Bredesen, D. E. (1993) · Science · doi:10.1126/science.8235659 · Cited by 1,671

Programmed cell death involved in the schizolysigenous formation of the secretory cavity in Citrus sinensis L. (Osbeck)

Chen, Y., & Wu, H. D. (2010) · Chinese Science Bulletin · doi:10.1007/s11434-010-3275-4 · Cited by 1,596

Evaluation of 2′,7′-Dichlorofluorescin and Dihydrorhodamine 123 as Fluorescent Probes for Intracellular H2O2 in Cultured Endothelial Cells

Royall, J. A., & Ischiropoulos, H. (1993) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1993.1222 · Cited by 1,123

Bcl-2 prolongs cell survival after Bax-induced release of cytochrome c

Rossé, T., Olivier, R., Monney, L., Rager, M., Conus, S., Fellay, I., Jansen, B., & Borner, C. (1998) · Nature · doi:10.1038/35160 · Cited by 870

Mitochondrial production of reactive oxygen species in cortical neurons following exposure to N-methyl-D-aspartate

Dugan, L. L., Sensi, S., Canzoniero, L. M. T., Handran, S. D., Rothman, S., Lin, T., Goldberg, M. P., & Choi, D. W. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-10-06377.1995 · Cited by 762

The oligodendrocyte and its many cellular processes

PFEIFFER, S., WARRINGTON, A., & BANSAL, R. (1993) · Trends in Cell Biology · doi:10.1016/0962-8924(93)90213-k · Cited by 737

GYKI-52466: A potential therapeutic agent for glutamate-mediated excitotoxic injury in Cerebral Palsy

Nandhu, M. S., Paul, J., Mathew, J., Kumar, T. P., & Paulose, C. S. (2009) · Medical Hypotheses · doi:10.1016/j.mehy.2009.10.033 · Cited by 3

Trophic factors intervention regenerates the nestin-expressing cell population in a model of perinatal excitotoxicity: Implications for perinatal brain injury and prematurity

Monteros, A. E. D. L. (2016) · Integrative Molecular Medicine · doi:10.15761/imm.1000228 · Cited by 3

Intraventricular Hemorrhage in the Neonate

Inder, T. E., & Volpe, J. J. (2011) · Elsevier eBooks · doi:10.1016/b978-1-4160-3479-7.10166-1 · Cited by 3

The Role of Glutathione and the Glutathione-Linked Enzyme Systems in Brain Tumor Drug Resistance

Backos, D. S., Poerschke, R. L., Franklin, C. C., & Reigan, P. (2013) · Tumors of the central nervous system · doi:10.1007/978-94-007-7217-5_24 · Cited by 3

Transcriptional and neurochemical signatures of cerebral blood flow alterations in schizophrenia and the clinical high-risk state for psychosisPreprint

Knight, S., Abbasova, L., Zeighami, Y., Hansen, J. Y., Martins, D., Zelaya, F. O., Dipasquale, O., Liu, T., Shin, D., Bossong, M. G., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.03.13.583894 · Cited by 3

The Percentage of Neutrophils is Independently Associated with Blood-Brain Barrier(BBB) Disruption in Myelin Oligodendrocyte Glycoprotein Antibody Associated Disease (MOGAD)

Cheng, X., Sun, Y., Wang, Y., Cheng, W., Zhang, H., & Jiang, Y. (2025) · Journal of Inflammation Research · doi:10.2147/jir.s501150 · Cited by 2

Pathological Mechanisms of Irradiation‐Induced Neurological Deficits in the Developing Brain

Richard, S. A. (2025) · European Journal of Neuroscience · doi:10.1111/ejn.70070 · Cited by 2

Pain, Analgesia, Sedation, and the Developing Brain

Marshall, C., & McPherson, C. C. (2025) · Pediatric Clinics of North America · doi:10.1016/j.pcl.2025.05.011 · Cited by 2

Neuropeptide CRH prevents premature differentiation of OPCs following CNS injury and in early postnatal development

Ries, C., Štark, T., Boulat, B., Ruhwedel, T., Delling, J. P., Infante, A. M., von Poblotzki, J., Ulivi, A. F., von Mücke-Heim, I.-A., Chang, S., et al. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.116474 · Cited by 3

Perinatal White Matter Injury: Connecting Histology, Pathophysiology and Neurodevelopmental Outcomes

Viaene, A. N. (2026) · Neuropathology and Applied Neurobiology · doi:10.1111/nan.70084 · Cited by 2

Pathophysiology of Hypoxic-Ischemic Brain Injury

McQuillen, P. S., Vannucci, S. J., & Hagberg, H. (2016) · Elsevier eBooks · doi:10.1016/b978-0-323-35214-7.00168-2 · Cited by 3

Mechanistic links between maternal bacterial infection and cerebral palsy

Zhou, H. (2008) · Biotechnology and Molecular Biology Reviews · doi:10.5897/bmbr2008.0005 · Cited by 2

From the Gate-Control Theory to Brain Programs for Neonatal Pain

Anand, K. J. S. (2008) · Springer eBooks · doi:10.1007/978-88-470-0732-1_17 · Cited by 2

Recovery of Human Embryonic Stem Cells-Derived Neural Progenitors Exposed to Hypoxic-Ischemic-Reperfusion Injury by Indirect Exposure to Wharton’s Jelly Mesenchymal Stem Cells Through Phosphatidyl-inositol-3-Kinase Pathway

Sowmithra, S., Jain, N. K., Bhonde, R. R., & Datta, I. (2020) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-020-01007-w · Cited by 2

The Neonate

Rozance, P. J., & Rosenberg, A. A. (2012) · Elsevier eBooks · doi:10.1016/b978-1-4377-1935-2.00021-1 · Cited by 2

Pathophysiology: General Principles

Gunn, A. J., Davidson, J. O., Inder, T. E., & Volpe, J. J. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-10513-5.00016-4 · Cited by 2

Injury to the Developing Preterm Brain

Soul, J. S., & Ment, L. R. (2017) · Elsevier eBooks · doi:10.1016/b978-0-323-37101-8.00022-9 · Cited by 2

Effect of Dexamethasone in the Development of O1 or O4 Immunoreactive Oligodendrocyte of the Neonatal Rat

Kim, M. J., Choi, I. Y., Park, K. S., Maskey, D., Chang, Y. P., & Yoo, Y. B. (2009) · Korean Journal of Physical Anthropology · doi:10.11637/kjpa.2009.22.4.305 · Cited by 2

Respiratory infection with influenza A virus delays remyelination and alters oligodendrocyte metabolism

Louie, A. Y., Drnevich, J. M., Johnson, J. L., Woodard, M., Kukekova, A. V., Johnson, R. W., & Steelman, A. J. (2024) · iScience · doi:10.1016/j.isci.2024.110464 · Cited by 2

The anti-inflammatory effects of vitamin D on offspring brain development during pregnancy: critical review

Kozhevnikova, S. V., Elmes, M. J., Brameld, J. M., & Jethwa, P. H. (2025) · Academia Nutrition and Dietetics · doi:10.20935/acadnutr7573 · Cited by 1

Altered cerebral thyroid hormone, WNT and NOTCH signalling and impaired myelination following intrauterine growth restriction in rats

Azhan, A., Cumberland, A. L., Chincarini, G., Barresi, M., Hale, N., Rowitch, D. H., Wong, F., Walker, D. W., & Tolcos, M. (2025) · Neuroscience · doi:10.1016/j.neuroscience.2025.12.068 · Cited by 1

Putative mechanisms of caffeine as a neuroprotectant in preterm infants

MacNamara, M. A., Colditz, P. B., & Wixey, J. A. (2026) · Pediatric Research · doi:10.1038/s41390-026-04776-0 · Cited by 1

Neuroendocrine-immune perturbations in metabolic disease: pathophysiological mechanisms underlying cognitive impairment

Fraer, A., Saleh, S., Tasabehji, D., Sharma, D. S., & Mokadem, M. (2026) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2026.1857087 · Cited by 1

Neuroprotection in Perinatal Hypoxic-Ischemic Encephalopathy — Pharmacologic Combination Therapy

del Carmen, M., & de Cabo, C. (2014) · InTech eBooks · doi:10.5772/57459 · Cited by 1

Mechanisms Underlying the Selective Vulnerability of Developing Human White Matter

Rosenberg, P. A. (2013) · Springer eBooks · doi:10.1007/978-1-4614-9123-1_6 · Cited by 1

Effet du NO inhalé sur le poumon et le cerveau en développement

Baud, O., Olivier, P., Vottier, G., Pham, H., Mercier, J., & Loron, G. (2009) · Archives de Pédiatrie · doi:10.1016/s0929-693x(09)75295-9 · Cited by 1

Neuroprotective Strategies in Excitotoxic Brain Injury: Potential Applications to the Preterm Brain

Griesmaier, E., & Keller, M. (2009) · Future Neurology · doi:10.2217/fnl.09.28 · Cited by 1

Oxidative Stress and Neurodegeneration

Pasquini, J. M., Pasquini, L. A., & Quintá, H. R. (2016) · Springer eBooks · doi:10.1007/978-3-319-45865-6_20 · Cited by 1

Warfarin-Triggered Renal Toxicity: A Biochemical and Histopathological Study

Abd-Allah, E. A., Mahmoud, H. A., Welson, M., & Atia, M. M. (2021) · Egyptian Academic Journal of Biological Sciences. D, Histology and Histochemistry · doi:10.21608/eajbsd.2021.198267 · Cited by 1

The Neonate

Rozance, P. J., & Rosenberg, A. A. (2017) · Elsevier eBooks · doi:10.1016/b978-0-323-32108-2.00022-6 · Cited by 1

Therapeutic Approaches for the Treatment of Cerebral Palsy and Developmental Disability

Fehlings, M. G., Beldick, S. R., Mailo, J. A., Shaw, O., Almas, S., & Yager, J. Y. (2023) · Springer eBooks · doi:10.1007/978-3-031-20792-1_37 · Cited by 1

Injury to the Developing Preterm Brain: Intraventricular Hemorrhage and White Matter Injury

Soul, J. S., & Ment, L. R. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-10944-7.00031-7 · Cited by 1

The Probable Effects of Cytokines in Intrauterine Infections and Perinatal Brain Injury

Oflaz, M. B. (2014) · The Annals of Clinical and Analytical Medicine · doi:10.4328/jcam.1806 · Cited by 1

Role of magnetic resonance imaging in biometric evaluation of corpus callosum in hypoxic ischemic encephalopathy patients

Garhwal, A., & Patil, A. (2017) · Journal of the Scientific Society · doi:10.4103/jss.jss_30_16 · Cited by 1

Alterations of Both Dendrite Morphology and Weaker Electrical Responsiveness in the Cortex of Hip Area Occur Before Rearrangement of the Motor Map in Neonatal White Matter Injury Model

Ueda, Y., Bandô, Y., Misumi, S., Ogawa, S., Ishida, A., Jung, C., Shimizu, T., & Hida, H. (2018) · Frontiers in Neurology · doi:10.3389/fneur.2018.00443 · Cited by 1

Inflammation and the Insulin-like Growth Factor System at Very Preterm Birth. Implications for Early Morbidity and Development.

Pupp, I. H. (2008) · Lund University Publications (Lund University) · Cited by 1

Less Stress : Oxidative stress and glutathione kinetics in preterm infants

Rook, D. (2013) · Pure Amsterdam UMC · Cited by 1

Perinatal brain damage in very preterm infants : prenatal inflammation and neurologic outcome in children born term and preterm

Kaukola, T. (2005) · Cited by 1

Investigating the Role of In Utero Inflammation on Neurodevelopment in the Fetus and Offspring and the Neuroprotective Properties Afforded by Broccoli Sprouts

Nguyen, A. (2016) · ERA: Education and Research Archive (University of Alberta) · doi:10.7939/r3057d35z · Cited by 1

Broccoli sprout supplementation during placental insufficiency confers structural and functional neuroprotection to the fetal rat

Black, A. M. (2010) · ERA: Education and Research Archive (University of Alberta) · doi:10.7939/r32g8b · Cited by 1

Cell-based therapy for hypoxic-ischemic injury in the preterm brain

Jellema, R. K. (2014) · doi:10.26481/dis.20140923rj · Cited by 1

Neuronal APOE4 drives damaging lipid accumulation via contact-dependent neuron-oligodendrocyte-microglia interaction in Alzheimer’s diseasePreprint

Kim, M. J., Blumenfeld, J. R., Li, Y., Yip, O., Yao, L., Ancheta, S., Leon, S. D., Platow, Z., Liang, Z., Shostak, D. M., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2025.12.04.692390 · Cited by 1

Adrenergic and Glutamergic Receptor Gene Expression and Their Functional regulation in the Cerebral Cortex of Hypoxia Induced Neonatal Rats:Role of Oxygen,Epinephrine and Glucose Supplementation

Chathu, F., & Paulose, C. S. (2007) · Dyuthi Digital Repository (Cochin University of Science and Technology) · Cited by 1

Characterization of System xc -, a Cystine-Glutamate Amino Acid Transporter, as an Effector of Interleukin-1β-Mediated Injury and Neuroprotection

Jackman, N. A. (2013) · OpenCommons at University of Connecticut (University of Connecticut)

Erythropoietin Neuroprotection in the Term and Preterm Infant: Safety and Efficacy

Demers, E. J., & Juul, S. E. (2006) · Springer eBooks · doi:10.1007/978-0-387-30011-5_5

Neonatal Experimental White Matter Injury

Cai, Z. (2013) · Springer eBooks · doi:10.1007/978-1-4614-9123-1_7

Inflammation and neuroprotective strategies in the immature brain after hypoxic-ischemic brain injury

Svedin, P. (2008) · Gothenburg University Publications Electronic Archive (Gothenburg University)

Neuroanatomical and neurofunctional brain basis of cognitive deficits in adolescent subjects who were born preterm. Structural and functional magnetic resonance study

Giménez, M. (2006) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)

Experimental Global Ischemia and White Matter Injury

Seo, J. H., Hayakawa, K., Miyamoto, N., Maki, T., Pham, L. D., Lo, E. H., & Arai, K. (2013) · Springer eBooks · doi:10.1007/978-1-4614-9123-1_10

Periventricular leukomalacia induced by in utero clamping of pregnant rat aorta in fetal rats

Chang, Y. S., Sung, D. K., Kang, S., Park, S. K., Jung, Y. J., Seo, H. J., Choi, S. H., & Park, W. S. (2008) · Korean Journal of Pediatrics · doi:10.3345/kjp.2008.51.8.874

Vascular and non‐vascular risk factors for deep white matter lesions in community‐dwelling elderly subjects

Yao, H., Yuzuriha, T., Koga, H., Takashima, Y., Fukuda, K., Endo, K., Uchino, A., Ibayashi, S., Uchimura, H., Fujishima, M., et al. (2003) · Geriatrics and gerontology international/Geriatrics & gerontology international · doi:10.1046/j.1444-1586.2003.00061.x

Impact of Recurring Technical Pain-Associated Stress in Preterm Infants

Veseli, D., Zavalani, F., Pirushi, R., Shkurti, E., & Shtiza, D. (2015) · Academic Journal of Interdisciplinary Studies · doi:10.5901/mjss.2015.v4n1p411

Brain reorganization in an experimental model of intrauterine growth restriction

Roca, E. E. (2011) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)

Antenatal brain injury and prospects for neuroprotection

Sağlam, B. (2017) · Figshare · doi:10.4225/03/58782b0baacba

Potential neurosteroid replacement therapy following premature birth and fetal growth restriction

Kelleher, M. A. (2012) · NOVA (University of Newcastle Australia)

15 Periventrikuläre Leukomalazie

Feldhaus, B. (. ). (2012) · Thieme eBooks · doi:10.1055/b-0036-136957

Neural Precursor Cells and Toxicant Action: Addressing the Analysis of Low-Level Toxicant Exposure

Noble, M. (2004) · CRC Press eBooks · doi:10.1201/9781420039740.ch1

Oxygen Tension Controls the Expansion an d Differentiation of Normal and Tumor -derived Human Neural Stem Cells.

Pediatria, D. D., Dello, M., & Immunologia, I. E. E. (2008)

Impact of repeated invasive procedures during neonatal intensive care on brain microstructure, growth, neurodevelopment and behavior in children born very preterm

Vinall, J. F. (2015) · cIRcle (University of British Columbia) · doi:10.14288/1.0166783

Imaging and Genetics Investigations in Schizophrenia and Aging: A Focus on White Matter

Voineskos, A. N. (2012) · TSpace (University of Toronto)

Propofol-induced changes in neurotrophic signaling in 14-day-old rat forebrain

Popić, J. (2012) · doi:10.2298/bg20120706popic

Novel non-apoptotic cell death: ferroptosis

Woo, S. M., & Kwon, T. K. (2017) · Journal of Yeungnam Medical Science · doi:10.12701/yujm.2017.34.2.174

Hemodynamics and Brain Injury in the Preterm Neonate

du Plessis, A. J. (2012) · Elsevier eBooks · doi:10.1016/b978-1-4377-2763-0.00016-0

Aging exacerbates myelin disruption and axon injury following demyelination

Michaels, N. J. (2019) · doi:10.11575/prism/36466

Long-Term Effects of Premature Birth

Lee, G. E., & Willis, K. A. (2017) · doi:10.1201/9781315382562-23

ffect of Etazolate on ROS Production after tBHP-Induced Oxidative Stress in Oligodendroglial 158N Cell Line

Chierto, E., Cristinziano, G., Sapone, F., Meffre, D., & Jafarian-Tehrani, M. (2020) · doi:10.20455/ros.2020.807

Role of Magnetic Resonance Imaging in Assessing Morphometry of Corpus Callosum in Patients with Hypoxic Ischemic Encephalopathy and Its Ability to Predict the Clinical Outcome

Alemao, N. N., Pahwa, S., & Gowda, S. (2020) · Journal of Evidence Based Medicine and Healthcare · doi:10.18410/jebmh/2020/213

The Oxidative Stress in the Fetus and in the Newborn

Perrone, S., Tataranno, M. L., Santacroce, A., & Buonocore, G. (2014) · Oxidative stress in applied basic research and clinical practice · doi:10.1007/978-1-4939-1405-0_21

The Neonate

Rosenberg, A. A. (2007) · Elsevier eBooks · doi:10.1016/b978-0-443-06930-7.50022-0

Injury to the Developing Preterm Brain

Ment, L. R., & Soul, J. S. (2012) · Elsevier eBooks · doi:10.1016/b978-1-4377-0435-8.00019-6

127 Periventrikuläre Leukomalazie

(2021) · Referenz Radiologie – Kinderradiologie · doi:10.1055/b-0041-181232

The central nervous system

Martin, R. J., Fanaroff, A. A., & Walsh, M. C. (2011) · Elsevier eBooks · doi:10.1016/b978-0-323-06545-0.00049-2

Neuroprotection for Premature Birth and Neonatal Brain Injury

Chang, E. B. (2017) · Oxford University Press eBooks · doi:10.1093/med/9780190280253.003.0014

From the Gate-Control Theory to Brain Programs for Neonatal Pain

Anand, K. J. S. (2017) · Springer eBooks · doi:10.1007/978-3-319-53232-5_18

82 Periventrikuläre Leukomalazie

(2022) · Haug Verlag in Georg Thieme Verlag KG eBooks · doi:10.1055/b-0042-192433

Unlocking the potential of ultra-high dose fractionated radiation for effective treatment of glioblastomaPreprint

Lan, X.-Y., Kalkowski, L., Chu, C., Jabłońska, A., Li, S., Kai, M., Gao, Y., Janowski, M., & Walczak, P. (2023) · Research Square · doi:10.21203/rs.3.rs-3500563/v1

Reduced Expression of Oxidative Stress-Related lncRNAs LINC-PINT and SNHG5 in Schizophrenia: Implications for Biomarker Development

Amirhassani, V., Hussen, B. M., Eslami, S., Sayad, A., & Ghafouri‐Fard, S. (2024) · Biochemical Genetics · doi:10.1007/s10528-024-10986-0

Commentary on: “Delayed necrostatin-1s infusion attenuates cystic white matter injury in preterm fetal sheep.”

Back, S. A. (2025) · Neurotherapeutics · doi:10.1016/j.neurot.2025.e00810

Microglia Pyroptosis-Derived IL-18 Drives White Matter Injury in Developing Brain following Hypothermic Hypoxia-Ischemia

Chen, H., Jin, S. ‐., Liu, M., Zhu, Y., Zhang, L., Li, C., Liu, P., Tong, X., & Zhu, Z. (2026) · Neuroscience Bulletin · doi:10.1007/s12264-026-01602-9

Effets de l'alcoolisation prénatale sur le développement du système GABAergique et de la myélinisation chez l'humain

Marguet, F. (2020) · theses.fr (ABES) · doi:10.70675/7590e822z0aa7z4868z972bz90e8061311fb

Pharmacogenomic identification of small molecules promoting oligodendrogenesis and myelin repair

Huré, J.-B. (2022) · theses.fr (ABES) · doi:10.70675/17691e80z7bacz455fzba89z49fef7be0512

Region- and Cell-Specific Vulnerability to ROS After Global Brain Ischemia-Reperfusion Injury: Molecular and Cellular Mechanisms

Jung, B. H., & Yoo, K. (2026) · Frontiers in Bioscience-Landmark · doi:10.31083/fbl48324

Oligodendrocytes in central nervous system health and disease

Ryan, L. J., & Miron, V. E. (2026) · Cell · doi:10.1016/j.cell.2026.08.003

Neuromodulation as a Potential Strategy to Remodel Brain Parenchyma in Addiction

Limens-Pinaque, J., Selim, M. K., Santis, S. D., Camarena, F., & Canals, S. (2026) · Springer eBooks · doi:10.1007/978-3-031-35658-2_18-1

Dopamine D1 and D2 Receptor Gene Expression and cGMP, IP3 and Ca2+ Regulation in the Brain Regions of Hypoxic Neonatal Rats: Role of Glucose, Oxygen and Epinephrine Supplementation

Joseph, B., & Paulose, C. S. (2008) · Dyuthi Digital Repository (Cochin University of Science and Technology)

Oligodendrocytes as glucocorticoids target cells: functional analysis of the glycerol phosphate dehydrogenase gene

Cheng, J. D., & de Vellis, J. (2000) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(20000201)59:3

12‐Lipoxygenase plays a key role in cell death caused by glutathione depletion and arachidonic acid in rat oligodendrocytes

Wang, H., Li, J., Follett, P. L., Zhang, Y., Cotanche, D. A., Jensen, F. E., Volpe, J. J., & Rosenberg, P. A. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03650.x · Cited by 97

Cystine Deprivation Induces Oligodendroglial Death: Rescue by Free Radical Scavengers and by a Diffusible Glial Factor

Yonezawa, M., Back, S. A., Gan, X., Rosenberg, P. A., & Volpe, J. J. (1996) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1996.67020566.x · Cited by 125

Differential Lipid Peroxidation, Mn Superoxide, and bcl-2 Expression Contribute to the Maturation-Dependent Vulnerability of Oligodendrocytes to Oxidative Stress

Bernardo, A., Greco, A., Levi, G., & Minghetti, L. (2003) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/62.5.509 · Cited by 49

Developmental up‐regulation of MnSOD in rat oligodendrocytes confers protection against oxidative injury

Baud, O., Haynes, R. F., Wang, H., Folkerth, R. D., Li, J., Volpe, J. J., & Rosenberg, P. A. (2004) · European Journal of Neuroscience · doi:10.1111/j.0953-816x.2004.03451.x · Cited by 93

Low Glutathione and High Iron Govern the Susceptibility of Oligodendroglial Precursors to Oxidative Stress

Thorburne, S. K., & Juurlink, B. H. J. (1996) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1996.67031014.x · Cited by 390