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Vascular Endothelial Growth Factor Induces Rapid Phosphorylation of Tight Junction Proteins Occludin and Zonula Occluden 1

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Alcohol, oxidative stress, and free radical damage.

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Possible Involvement of Phosphorylation of Occludin in Tight Junction Formation

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Development of the blood-brain barrier

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Blood-Brain Barrier Tight Junction Disruption in Human Immunodeficiency Virus-1 Encephalitis

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Alcohol-related cerebellar degeneration: not all down to toxicity?

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Lead Intoxication Synergies of the Ethanol-Induced Toxic Responses in Neuronal Cells—PC12

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Effect of blood pressure on early neurological deterioration of acute ischemic stroke patients with intravenous rt-PA thrombolysis may be mediated through oxidative stress induced blood-brain barrier disruption and AQP4 upregulation

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Vascular Oxidative Stress: A Key Factor in the Development of Hypertension Associated with Ethanol Consumption

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Immune activation and neuroinflammation in alcohol use and HIV infection: evidence for shared mechanisms

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Acetyl-L-Carnitine Prevents Methamphetamine-Induced Structural Damage on Endothelial Cells via ILK-Related MMP-9 Activity

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Reduction of Brain Mitochondrial β-Oxidation Impairs Complex I and V in Chronic Alcohol Intake: The Underlying Mechanism for Neurodegeneration

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Acute Alcohol Intoxication‐Induced Microvascular Leakage

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Role of HIF-1α in Alcohol-Mediated Multiple Organ Dysfunction

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Increased Leptin Permeation across the Blood–Brain Barrier after Chronic Alcohol Ingestion

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Thirst sensation and oral dryness following alcohol intake

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The Interplay of Inflammatory Processes and Cognition in Alcohol Use Disorders—A Systematic Review

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Ethanol induces vascular relaxation via redox-sensitive and nitric oxide-dependent pathways

da Rocha, J. T., Hipólito, U. V., Callera, G. E., Yogi, Á., Filho, M. D. A. N., Bendhack, L. M., Touyz, R. M., & Tirapelli, C. R. (2011) · Vascular Pharmacology · doi:10.1016/j.vph.2011.11.006 · Cited by 31

The effects of 17β-estradiol on blood brain barrier integrity in the absence of the estrogen receptor alpha; an in-vitro model

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Protective Effects of Ginsenoside Rb1 against Blood–Brain Barrier Damage Induced by Human Immunodeficiency Virus-1 Tat Protein and Methamphetamine in Sprague-Dawley Rats

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Suppression of PGC-1alpha by Ethanol: Implications of Its Role in Alcohol Induced Liver Injury.

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The influence of physiological and pathological perturbations on blood-brain barrier function

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PCSK9 is Increased in Cerebrospinal Fluid of Individuals With Alcohol Use Disorder

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Associations between major psychiatric disorder polygenic risk scores and blood-based markers in UK biobank

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Innate immune activation: Parallels in alcohol use disorder and Alzheimer’s disease

Ramos, A., Joshi, R., & Szabó, G. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.910298 · Cited by 29

Fluvastatin stabilizes the blood–brain barrier in vitro by nitric oxide-dependent dephosphorylation of myosin light chains

Kuhlmann, C. R. W., Leßmann, V., & Luhmann, H. J. (2006) · Neuropharmacology · doi:10.1016/j.neuropharm.2006.06.004 · Cited by 28

Cryopreservation of Brain Endothelial Cells Derived from Human Induced Pluripotent Stem Cells Is Enhanced by Rho-Associated Coiled Coil-Containing Kinase Inhibition

Wilson, H. K., Faubion, M. G., Hjortness, M. K., Palecek, S. P., & Shusta, E. V. (2016) · Tissue Engineering Part C: Methods · doi:10.1089/ten.tec.2016.0345 · Cited by 29

Long‑term exposure to ethanol downregulates tight junction proteins through the protein kinase Cα signaling pathway in human cerebral microvascular endothelial cells

Yu, H., Wang, C., Wang, X., Wang, H., Zhang, C., You, J., Wang, P., Feng, C.-M., Xu, G., Zhao, R., et al. (2017) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2017.5180 · Cited by 27

Effects of Consumption of Alcohol on Intraocular Pressure: Korea National Health and Nutrition Examination Survey 2010 to 2011

Song, J. E., Kim, J. M., Lee, M. Y., Jang, H. J., & Park, K. H. (2020) · Nutrients · doi:10.3390/nu12082420 · Cited by 27

Actin Cytoskeleton Remodeling by the Alternatively Spliced Isoform of PDLIM4/RIL Protein

Guryanova, O. A., Drazba, J. A., Frolova, E. I., & Chumakov, P. M. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.241554 · Cited by 27

Adding Fuel to the Fire: Methamphetamine Enhances HIV Infection

Potula, R., & Persidsky, Y. (2008) · American Journal Of Pathology · doi:10.2353/ajpath.2008.080130 · Cited by 26

Alcohol and stress exposure across the lifespan are key risk factors for Alzheimer's Disease and cognitive decline

Seemiller, L. R., Flores-Cuadra, J. A., Griffith, K. R., Smith, G. C., & Crowley, N. A. (2024) · Neurobiology of Stress · doi:10.1016/j.ynstr.2024.100605 · Cited by 25

Chronic paracetamol treatment increases alterations in cerebral vessels in cortical spreading depression model

Yisarakun, W., Supornsilpchai, W., Chantong, C., Srikiatkhachorn, A., & Grand, S. M.-L. (2014) · Microvascular Research · doi:10.1016/j.mvr.2014.04.012 · Cited by 25

Alterations in Synaptic Plasticity and Oxidative Stress Following Long-Term Paracetamol Treatment in Rat Brain

Lalert, L., Ji‐au, W., Srikam, S., Chotipinit, T., Sanguanrungsirikul, S., Srikiatkhachorn, A., & Grand, S. M.-L. (2019) · Neurotoxicity Research · doi:10.1007/s12640-019-00090-2 · Cited by 25

Impact of common ALDH2 inactivating mutation and alcohol consumption on Alzheimer’s disease

Seike, T., Chen, C., & Mochly‐Rosen, D. (2023) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2023.1223977 · Cited by 28

Reactive Oxygen Species Are Central Mediators of Vascular Dysfunction and Hypertension Induced by Ethanol Consumption

Padovan, J. C., Dourado, T. M. H., Pimenta, G. F., Bruder-Nascimento, T. B., & Tirapelli, C. R. (2023) · Antioxidants · doi:10.3390/antiox12101813 · Cited by 27

Effect of status epilepticus and antiepileptic drugs on CYP2E1 brain expression

Boussadia, B., Ghosh, C., Plaud, C., Pascussi, J., de Bock, F., Rousset, M.-C., Janigro, D., & Marchi, N. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.09.055 · Cited by 25

Blocking of P2X7r Reduces Mitochondrial Stress Induced by Alcohol and Electronic Cigarette Exposure in Brain Microvascular Endothelial Cells

Mekala, N. K., Gheewala, N., Rom, S., Sriram, U., & Persidsky, Y. (2022) · Antioxidants · doi:10.3390/antiox11071328 · Cited by 24

Substance abuse, hepatitis C, and aging in HIV: common cofactors that contribute to neurobehavioral disturbances

González, R., & Schuster (2012) · Neurobehavioral HIV Medicine · doi:10.2147/nbhiv.s17408 · Cited by 23

Acute Alcohol Intoxication Aggravates Brain Injury Caused by Intracerebral Hemorrhage in Rats

Liew, H., Cheng, H.-Y., Huang, L., Li, K.-W., Peng, H., Yang, H.-I., Lin, P. B., Kuo, J., & Pang, C. (2015) · Journal of Stroke and Cerebrovascular Diseases · doi:10.1016/j.jstrokecerebrovasdis.2015.08.027 · Cited by 23

Circadian Mechanisms in Alcohol Use Disorder and Tissue Injury

Davis, B. T., Voigt, R. M., Shaikh, M. W., Forsyth, C. B., & Keshavarzian, A. (2018) · Alcoholism Clinical and Experimental Research · doi:10.1111/acer.13612 · Cited by 25

Blood brain barrier inflammation and potential therapeutic role of phytochemicals

Welcome, M. O. (2020) · PharmaNutrition · doi:10.1016/j.phanu.2020.100177 · Cited by 22

Ethanol Gestational Exposure Impairs Vascular Development and Endothelial Potential to Control BBB-Associated Astrocyte Function in the Developing Cerebral Cortex

Siqueira, M., Araújo, A. P. B., Gomes, F. C. A., & Stipursky, J. (2021) · Molecular Neurobiology · doi:10.1007/s12035-020-02214-8 · Cited by 22

Antioxidant-induced reductive stress has untoward consequences on the brain microvasculature

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Substances of abuse and the blood brain barrier: Interactions with physical exercise

Małkiewicz, M. A., Małecki, A., Toborek, M. J., Szarmach, A., & Winklewski, P. J. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.09.026 · Cited by 21

High concentration of blood cobalt is associated with the impairment of blood-brain barrier permeability

Li, Z., Wang, Z., Xue, K., Wang, Z., Guo, C., Qian, Y., Li, X., & Wei, Y. (2021) · Chemosphere · doi:10.1016/j.chemosphere.2021.129579 · Cited by 21

The role of reactive oxygen species in the regulation of the blood-brain barrier

Shuvalova, M. L., Dmitrieva, A., Belousov, V. V., & Nosov, G. (2024) · Tissue Barriers · doi:10.1080/21688370.2024.2361202 · Cited by 21

Impact of Alcohol Abuse on Susceptibility to Rare Neurodegenerative Diseases

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HIV-1, HCV and Alcohol in the CNS: Potential Interactions and Effects on Neuroinflammation

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Platelet Endothelial Cell Adhesion Molecule-1 and Oligodendrogenesis: Significance in Alcohol Use Disorders

Mandyam, C. D., Villalpando, E. G., Steiner, N. L., Quach, L. W., Fannon, M. J., & Somkuwar, S. S. (2017) · Brain Sciences · doi:10.3390/brainsci7100131 · Cited by 22

The effects of acetaldehyde on nicotine-induced transmitter levels in young and adult brain areas

Sershen, H. W., Shearman, E., Fallon, S. M., Chakraborty, G., Smiley, J. F., & Lajtha, Á. (2009) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2009.04.005 · Cited by 20

Ethanol promotes rat aortic vascular smooth muscle cell proliferation via increase of homocysteine and oxidized-low-density lipoprotein

Shirpoor, A., Salami, S., Ansari, M. H. K., Ilkhanizadeh, B., & Abdollahzadeh, N. (2013) · Journal of Cardiology · doi:10.1016/j.jjcc.2013.06.003 · Cited by 19

Inhibition of Myosin Light-Chain Kinase Attenuates Cerebral Edema after Traumatic Brain Injury in Postnatal Mice

Rossi, J. L., Todd, T., Bazan, N. G., & Belayev, L. (2013) · Journal of Neurotrauma · doi:10.1089/neu.2013.2898 · Cited by 21

Nonmuscle myosin light‐chain kinase mediates microglial migration induced by HIV Tat: Involvement of β1 integrins

Yao, H., Duan, M., Yang, L., & Buch, S. J. (2013) · The FASEB Journal · doi:10.1096/fj.12-219600 · Cited by 19

Estrogen Receptors α and β Play Major Roles in Ethanol‐Evoked Myocardial Oxidative Stress and Dysfunction in Conscious Ovariectomized Rats

Yao, F., & Abdel‐Rahman, A. A. (2016) · Alcoholism Clinical and Experimental Research · doi:10.1111/acer.13290 · Cited by 18

Alcohol Induced Brain and Liver Damage: Advantages of a Porcine Alcohol Use Disorder Model

Shin, S. K., Kaiser, E. E., & West, F. D. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2020.592950 · Cited by 21

Blood Vessels as a Key Mediator for Ethanol Toxicity: Implication for Neuronal Damage

Nakayama, K., & Hasegawa, H. (2022) · Life · doi:10.3390/life12111882 · Cited by 17

CREB Protein Mediates Alcohol‐Induced Circadian Disruption and Intestinal Permeability

Davis, B. T., Voigt, R. M., Shaikh, M. W., Forsyth, C. B., & Keshavarzian, A. (2017) · Alcoholism Clinical and Experimental Research · doi:10.1111/acer.13513 · Cited by 19

p38SJ, a novel DINGG protein protects neuronal cells from alcohol induced injury and death

Amini, S., Merabova, N., Khalili, K., & Darbinian, N. (2009) · Journal of Cellular Physiology · doi:10.1002/jcp.21903 · Cited by 17

Protective effect of ethyl pyruvate on msP rat leukocytes damaged by alcohol intake

Fedeli, D., Falcioni, G., Olek, R. A., Massi, M., Cifani, C., Polidori, C., & Gabbianelli, R. (2007) · Journal of Applied Toxicology · doi:10.1002/jat.1236 · Cited by 16

Diplomats' Mystery Illness and Pulsed Radiofrequency/Microwave Radiation

Golomb, B. A. (2018) · Neural Computation · doi:10.1162/neco_a_01133 · Cited by 16

Gastroprotective and Antioxidant Properties of Trigonella foenum graecum Seeds Aqueous Extract (Fenugreek) and Omeprazole Against Ethanol-Induced Peptic Ulcer

Selmi, S., Alimi, D., Rtibi, K., Jedidi, S., Grami, D., Marzouki, L., Hosni, K., & Sebaï, H. (2022) · Journal of Medicinal Food · doi:10.1089/jmf.2020.0217 · Cited by 18

Effects of choline supplementation on growth performance, liver histology, nonspecific immunity and related genes expression of hybrid grouper (♀ Epinephelus fuscoguttatus × ♂ E. lanceolatu) fed with high-lipid diets

Li, T., Yan, X., Dong, X., Pan, S., Tan, B., Zhang, S., Suo, X., Huang, W., Zhou, M., & Yang, Y. (2023) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2023.108815 · Cited by 15

The Influence of Experimental Alcohol Load and Alcohol Intoxication on S100B Concentrations

Brin, T., Borucki, K., & Ambrosch, A. (2011) · Shock · doi:10.1097/shk.0b013e31822bd07d · Cited by 15

A case of posterior reversible encephalopathy syndrome associated with acute pancreatitis and chronic alcoholism

Baek, H. S., & Lee, S. (2014) · General Hospital Psychiatry · doi:10.1016/j.genhosppsych.2014.12.004 · Cited by 15

The role of cytochrome P450 2E1 on ethanol-mediated oxidative stress and HIV replication in human monocyte-derived macrophages

Gong, Y., Rao, S., Sinha, N., Ranjit, S., Cory, T. J., & Kumar, S. (2018) · Biochemistry and Biophysics Reports · doi:10.1016/j.bbrep.2018.11.008 · Cited by 15

Endothelial Homeostasis Under the Influence of Alcohol—Relevance to Atherosclerotic Cardiovascular Disease

Gusti, Y., Liu, W., Athar, F., Cahill, P. A., & Redmond, E. M. (2025) · Nutrients · doi:10.3390/nu17050802 · Cited by 14

Posterior reversible encephalopathy syndrome in chronic alcoholism with acute psychiatric symptoms

Kimura, R., Yanagida, M., Kugo, A., Taguchi, S., & Matsunaga, H. (2009) · General Hospital Psychiatry · doi:10.1016/j.genhosppsych.2009.11.006 · Cited by 14

Alcohol use disorder, neuroinflammation, and intake of dietary fibers: a new approach for treatment

Pérez-Reytor, D., & Karahanian, E. (2022) · The American Journal of Drug and Alcohol Abuse · doi:10.1080/00952990.2022.2114005 · Cited by 13

Altered Relation Between Lipopolysaccharide‐Induced Inflammatory Response and Excitotoxicity in Rat Organotypic Hippocampal Slice Cultures During Ethanol Withdrawal

Lutz, J. A., Carter, M., Fields, L., Barron, S., & Littleton, J. M. (2015) · Alcoholism Clinical and Experimental Research · doi:10.1111/acer.12705 · Cited by 12

The role of ethanol on the anticonvulsant effect of valproic acid and cortical microvascular changes after epileptogenesis in mice

Golmohammadi, R., Pejhan, A., Azhdari‐Zarmehri, H., & Mohammad‐Zadeh, M. (2012) · Neurological Sciences · doi:10.1007/s10072-012-1190-y · Cited by 13

Ethanol’s Effects on Transient Receptor Potential Channel Expression in Brain Microvascular Endothelial Cells

Chang, S. L., Huang, W., Mao, X., & Mack, M. L. (2018) · Journal of Neuroimmune Pharmacology · doi:10.1007/s11481-018-9796-3 · Cited by 13

Inflammasome in drug abuse.

Xu, E., Liu, J., Wang, X., & Xiong, H. (2017) · PubMed Central · Cited by 12

“Boomerang Neuropathology” of Late-Onset Alzheimer’s Disease is Shrouded in Harmful “BDDS”: Breathing, Diet, Drinking, and Sleep During Aging

Daulatzai, M. A. (2015) · Neurotoxicity Research · doi:10.1007/s12640-015-9528-x · Cited by 12

Combined alcohol and cannabinoid exposure leads to synergistic toxicity by affecting cerebellar Purkinje cells

Zou, G., Xia, J., Luo, H., Xiao, D., Jin, J., Miao, C., Zuo, X., Gao, Q., Zhang, Z., Xue, T., et al. (2022) · Nature Metabolism · doi:10.1038/s42255-022-00633-6 · Cited by 12

A pre-injury high ethanol intake in rats promotes brain edema following traumatic brain injury

Wu, W., Tian, R., Hao, S., Xu, F., Mao, X., & Liu, B. (2014) · British Journal of Neurosurgery · doi:10.3109/02688697.2014.915007 · Cited by 12

The effect of endurance training and testosterone supplementation on the expression of blood spinal cord barrier proteins in rats

Nierwińska, K., Nowacka-Chmielewska, M. M., Bernacki, J., Jagsz, S., Chalimoniuk, M., Langfort, J., & Małecki, A. (2019) · PLoS ONE · doi:10.1371/journal.pone.0211818 · Cited by 12

The Modulatory Effect of Metformin on Ethanol-Induced Anxiety, Redox Imbalance, and Extracellular Matrix Levels in the Brains of Wistar Rats

Bonea, M., Filip, G. A., Toma, V. A., Bâldea, I., Sevastre-Berghian, A., Decea, N., Olteanu, D. E., Moldovan, R., Crivii, C. B., Vinași, R. C., et al. (2020) · Journal of Molecular Neuroscience · doi:10.1007/s12031-020-01593-w · Cited by 13

Aripiprazole in an Animal Model of Chronic Alcohol Consumption and Dopamine D2Receptor Occupancy in Rats

Nirogi, R. V. S., Kandikere, V. N., Jayarajan, P., Bhyrapuneni, G., Saralaya, R., Muddana, N., & Abraham, R. (2013) · The American Journal of Drug and Alcohol Abuse · doi:10.3109/00952990.2012.730590 · Cited by 12

Therapeutic strategies of small molecules in the microbiota–gut–brain axis for alcohol use disorder

Xie, L., Rungratanawanich, W., Yang, Q., Tong, G., Fu, E., Lu, S., Liu, Y., Akbar, M. D., Song, B., & Wang, X. (2023) · Drug Discovery Today · doi:10.1016/j.drudis.2023.103552 · Cited by 11

Acute Pancreatitis and Posterior Reversible Encephalopathy Syndrome: A Case Report

Pereira, V. M., Correia, L. M., Rodrigues, T., & Faria, G. S. (2016) · Acta Médica Portuguesa · doi:10.20344/amp.7368 · Cited by 11

Hyper-oligodendrogenesis at the vascular niche and reduced blood–brain barrier integrity in the prefrontal cortex during protracted abstinence

Somkuwar, S. S., Fannon, M. J., Nguyen, T. B., & Mandyam, C. D. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.08.048 · Cited by 11

Proanthocyanidins prevent ethanol-induced cognitive impairment by suppressing oxidative and inflammatory stress in adult rat brain

Chen, Q., & Hu, P. (2017) · Neuroreport · doi:10.1097/wnr.0000000000000867 · Cited by 11

Biphasic Effects of Ethanol Exposure on Waste Metabolites Clearance in the CNS

Cheng, Y., Ma, X., Belfield, K. D., & Haorah, J. (2021) · Molecular Neurobiology · doi:10.1007/s12035-021-02379-w · Cited by 12

Combined Catalase and ADH Inhibition Ameliorates Ethanol-Induced Myocardial Dysfunction Despite Causing Oxidative Stress in Conscious Female Rats

Yao, F., & Abdel‐Rahman, A. A. (2017) · Alcoholism Clinical and Experimental Research · doi:10.1111/acer.13442 · Cited by 9

NADPH oxidase-induced activation of transforming growth factor-beta-1 causes neuropathy by suppressing antioxidant signaling pathways in alcohol use disorder

Bhowmick, S., Alikunju, S., & Muneer, P. M. A. (2022) · Neuropharmacology · doi:10.1016/j.neuropharm.2022.109136 · Cited by 10

The effects of hypoglycemic and alcoholic coma on the blood-brain barrier permeability

Yorulmaz, H., Şeker, F. B., & Öztaş, B. (2011) · Bosnian Journal of Basic Medical Sciences · doi:10.17305/bjbms.2011.2591 · Cited by 9

Correlations Between Trace Elements in Selected Locations of the Human Brain in Individuals with Alcohol Use Disorder

Grochowski, C., Szukała, M., Litak, J., Budny, A., Proch, J., Majerek, D., Blicharska, E., & Niedzielski, P. (2020) · Molecules · doi:10.3390/molecules25020359 · Cited by 9

Purinergic and extracellular vesicle signaling in alcohol-induced blood–brain barrier breakdown and neuroimmune activation

Togre, N. S., Bhoj, P. S., Mekala, N. K., Hancock, R., Trivedi, J., & Persidsky, Y. (2025) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2025.106115 · Cited by 8

Alteration of UCP2 and ZO-1 Expression in Trabecular Meshwork of Neovascular Glaucoma Patients

Yang, J.-G., Zhou, C., Li, X., Sun, P., Li, S., & Ren, B.-C. (2013) · Journal of Glaucoma · doi:10.1097/ijg.0b013e31829d9b91 · Cited by 8

Toxic Effects of Methamphetamine on Perivascular Health: Co-morbid Effects of Stress and Alcohol Use Disorders

Rodriguez, E. A., & Yamamoto, B. K. (2021) · Current Neuropharmacology · doi:10.2174/1570159x19666210803150023 · Cited by 7

Astroglia in the Vulnerability and Maintenance of Alcohol Use Disorders

Miguel-Hidalgo, J. J. (2021) · Advances in neurobiology · doi:10.1007/978-3-030-77375-5_11 · Cited by 8

The ethanol metabolite acetaldehyde induces water and salt intake via two distinct pathways in the central nervous system of rats

Ujihara, I., Hitomi, S., Ono, K., Kakinoki, Y., Hashimoto, H., Ueta, Y., & Inenaga, K. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2015.08.023 · Cited by 8

Oxidative Stress in Fetal Alcohol Spectrum Disorders – Insights for the Development of Antioxidant-Based Therapies

Patten, A. R., Brocardo, P. S., Gil‐Mohapel, J., & Christie, B. R. (2014) · Springer eBooks · doi:10.1007/978-3-642-30018-9_37 · Cited by 8

Acute Ethanol Intake Induces NAD(P)H Oxidase Activation and Rhoa Translocation in Resistance Arteries

Simplicio, J. A., Hipólito, U. V., do Vale, G. T., Callera, G. E., Pereira, C. A., Touyz, R. M., Tostes, R. C., & Tirapelli, C. R. (2016) · Arquivos Brasileiros de Cardiologia · doi:10.5935/abc.20160147 · Cited by 9

The Synergistic and Neuroprotective Effects of Alcohol–Antioxidant Treatment on Blood–Brain Barrier Endothelial Cells

Fisher, D., Thomas, K. A., & Abdul‐Rasool, S. (2020) · Alcoholism Clinical and Experimental Research · doi:10.1111/acer.14433 · Cited by 8

The Influence of Arsenic Co-Exposure in a Model of Alcohol-Induced Neurodegeneration in C57BL/6J Mice

Sides, T. R., Nelson, J. C., Nwachukwu, K. N., Boston, J., & Marshall, S. A. (2023) · Brain Sciences · doi:10.3390/brainsci13121633 · Cited by 7

Mechanism of Regio- and Enantioselective Hydroxylation of Arachidonic Acid Catalyzed by Human CYP2E1: A Combined Molecular Dynamics and Quantum Mechanics/Molecular Mechanics Study

Zhang, H., & Hirao, H. (2025) · Journal of Chemical Information and Modeling · doi:10.1021/acs.jcim.5c00115 · Cited by 7

Hepatic and extra-hepatic metabolism of propylene glycol ethers in the context of central nervous system toxicity

Werner, S., Pamies, D., Zurich, M., & Suter‐Dick, L. (2025) · Toxicology · doi:10.1016/j.tox.2025.154081 · Cited by 6

Changes in the brain directly following alcohol consumption—a study of healthy male individuals, with the use of proton magnetic resonance spectroscopy (1HMRS) and diffusion (DWI)

Urbanik, A., Kozub, J., Karcz, P., & Ostrogórska, M. (2020) · Alcohol and Alcoholism · doi:10.1093/alcalc/agaa119 · Cited by 6

Sexually dimorphic prelimbic cortex mechanisms play a role in alcohol dependence: protection by endostatin

Avchalumov, Y., Kreisler, A. D., Xing, N., Shayan, A. A., Bharadwaj, T., Watson, J. R., Sibley, B. D., Somkuwar, S. S., Trenet, W., Olia, S., et al. (2021) · Neuropsychopharmacology · doi:10.1038/s41386-021-01075-6 · Cited by 7

The Endocannabinoid System and Alcohol Dependence: Will Cannabinoid Receptor 2 Agonism be More Fruitful than Cannabinoid Receptor 1 Antagonism?

Oppong‐Damoah, A., Gannon, B. M., & Murnane, K. S. (2021) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/1871527320666210211115007 · Cited by 6

Localization of myosin II regulatory light chain in the cerebral vasculature

Ishmael, J. E., Löhr, C. V., Fischer, K. A., & Kioussi, C. (2007) · Acta Histochemica · doi:10.1016/j.acthis.2007.08.005 · Cited by 6

Cytochrome P450 and Oxidative Stress as Possible Pathways for Alcohol- and Tobacco-Mediated HIV Pathogenesis and NeuroAIDS

Kumar, S., Rao, S., Sinha, N., & Midde, N. M. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-800213-1.00017-1 · Cited by 5

Multivariate analyses of selected trace elements from Kigelia africana (Lam.) Benth. plant by ICP-OES: A chemometrics approach

Fagbohun, O. F., Olawoye, B. T., Oriyomi, O. V., & Joseph, J. S. (2023) · Journal of Trace Elements and Minerals · doi:10.1016/j.jtemin.2023.100081 · Cited by 5

The inflammatory footprints of alcohol-induced oxidative damage in neurovascular components

Alikunju, S., Muneer, P. M. A., Zhang, Y., Szlachetka, A. M., & Haorah, J. (2011) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2011.01.007 · Cited by 53

Ethanol-Induced Activation of Myosin Light Chain Kinase Leads to Dysfunction of Tight Junctions and Blood-Brain Barrier Compromise

Haorah, J., Heilman, D., Knipe, B., Chrastil, J., Leibhart, J., Ghorpade, A., Miller, D. W., & Persidsky, Y. (2005) · Alcoholism Clinical and Experimental Research · doi:10.1097/01.alc.0000166944.79914.0a · Cited by 169

Alcohol-Induced Blood-Brain Barrier Impairment: An In Vitro Study

Carrino, D., Branca, J. J. V., Becatti, M., Paternostro, F., Morucci, G., Gulisano, M., Mannelli, L. D. C., & Pacini, A. (2021) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph18052683 · Cited by 43

Alcohol‐induced blood–brain barrier dysfunction is mediated via inositol 1,4,5‐triphosphate receptor (IP 3 R)‐gated intracellular calcium release

Haorah, J., Knipe, B., Gorantla, S., Zheng, J., & Persidsky, Y. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.04245.x · Cited by 119

Alcohol Induced Oxidative Stress leads to Blood Brain Barrier Dysfunction in an IPSC-derived Model

Borman, W. A., Bell, K. T., Hughes, J. M., & Canfield, S. G. (2019) · Proceedings of IMPRS · doi:10.18060/23424