Mineral Micronutrients in Asthma

Selenium, selenoproteins and human health: a review

Brown, K., & Arthur, Jr. (2001) · Public Health Nutrition · doi:10.1079/phn2001143 · Cited by 927 · see citing works

Selenium, Selenoproteins, and Immunity

Avery, J., & Hoffmann, P. R. (2018) · Nutrients · doi:10.3390/nu10091203 · Cited by 913 · see citing works

Iron Homeostasis

Andrews, N. C., & Schmidt, P. J. (2006) · Annual Review of Physiology · doi:10.1146/annurev.physiol.69.031905.164337 · Cited by 640 · see citing works

Superoxide Dismutases in the Lung and Human Lung Diseases

Kinnula, V. L., & Crapo, J. D. (2003) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200212-1479so · Cited by 620 · see citing works

Consequences of excess iodine

Leung, A. M., & Braverman, L. E. (2013) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2013.251 · Cited by 608 · see citing works

The influence of selenium on immune responses

Hoffmann, P. R., & Berry, M. J. (2008) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.200700330 · Cited by 544 · see citing works

Selenium-Dependent Antioxidant Enzymes: Actions and Properties of Selenoproteins

Zoidis, E., Seremelis, I., Kontopoulos, N., & Danezis, G. P. (2018) · Antioxidants · doi:10.3390/antiox7050066 · Cited by 475 · see citing works

Lactoferrin as a natural immune modulator

Actor, J., Hwang, S.-A., & Kruzel, M. (2009) · Current Pharmaceutical Design · doi:10.2174/138161209788453202 · Cited by 455 · see citing works

An increase in selenium intake improves immune function and poliovirus handling in adults with marginal selenium status

Broome, C. S., McArdle, F., Kyle, J. A. M., Andrews, F., Lowe, N. M., Hart, C. A., Arthur, J. R., & Jackson, M. J. (2004) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/80.1.154 · Cited by 402 · see citing works

Exhaled Nitric Oxide in Pulmonary Diseases

Barnes, P. J., Dweik, R. A., Gelb, A. F., Gibson, P. G., George, S. C., Grasemann, H., Pavord, I. D., Ratjen, F. A., Silkoff, P. E., Taylor, D. R., et al. (2010) · CHEST Journal · doi:10.1378/chest.09-2090 · Cited by 393 · see citing works

The Physiological Effects of Dietary Boron

Devirian, T. A., & Volpe, S. L. (2003) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408690390826491 · Cited by 391 · see citing works

Copper, lysyl oxidase, and extracellular matrix protein cross-linking

Rucker, R., Kosonen, T., Clegg, M., Mitchell, A., Rucker, B., Uriu-Hare, J., & Keen, C. (1998) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/67.5.996s · Cited by 371 · see citing works

Eukaryotic selenoproteins and selenoproteomes

Lobanov, A. V., Hatfield, D. L., & Gladyshev, V. N. (2009) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2009.05.014 · Cited by 357 · see citing works

Cell biology of molybdenum

Mendel, R. R., & Bittner, F. (2006) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2006.03.013 · Cited by 356 · see citing works

Vitamin D supplementation to prevent asthma exacerbations: a systematic review and meta-analysis of individual participant data

Jolliffe, D. A., Greenberg, L., Hooper, R., Griffiths, C., Camargo, C. A., Kerley, C. P., Jensen, M. E., Mauger, D. T., Stelmach, I., Urashima, M., et al. (2017) · The Lancet Respiratory Medicine · doi:10.1016/s2213-2600(17)30306-5 · Cited by 344 · see citing works

Lactoferrin in a Context of Inflammation-Induced Pathology

Kruzel, M. L., Zimecki, M., & Actor, J. K. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01438 · Cited by 308 · see citing works

Dietary Antioxidants and Asthma in Adults

SHAHEEN, S. O., Sterne, J. A. C., THOMPSON, R. L., SONGHURST, C. E., Margetts, B., & Burney, P. (2001) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/ajrccm.164.10.2104061 · Cited by 306 · see citing works

Immunomodulation by vitamin B12: augmentation of CD8+ T lymphocytes and natural killer (NK) cell activity in vitamin B12-deficient patients by methyl-B12 treatment

Tamura, J., Kubota, K., Murakami, H., Sawamura, M., Matsushima, T., TAMURA, T., Saitoh, T., Kurabayshi, H., & Naruse, T. (1999) · Clinical & Experimental Immunology · doi:10.1046/j.1365-2249.1999.00870.x · Cited by 295 · see citing works

Zinc: An antioxidant and anti-inflammatory agent: Role of zinc in degenerative disorders of aging

Prasad, A. S. (2014) · Journal of Trace Elements in Medicine and Biology · doi:10.1016/j.jtemb.2014.07.019 · Cited by 295 · see citing works

Macrophages and Systemic Iron Homeostasis

Ganz, T. (2012) · Journal of Innate Immunity · doi:10.1159/000336423 · Cited by 281 · see citing works

Chromium Oligopeptide Activates Insulin Receptor Tyrosine Kinase Activity

Davis, C. M., & Vincent, J. B. (1997) · Biochemistry · doi:10.1021/bi963154t · Cited by 280 · see citing works

Lysyl Oxidase Is Essential for Normal Development and Function of the Respiratory System and for the Integrity of Elastic and Collagen Fibers in Various Tissues

Mäki, J. M., Sormunen, R. T., Lippo, S., Kaarteenaho–Wiik, R., Soininen, R., & Myllyharju, J. (2005) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)61183-2 · Cited by 279 · see citing works

Low Maternal Vitamin E Intake during Pregnancy Is Associated with Asthma in 5-Year-Old Children

Devereux, G. S., Turner, S. W., Craig, L. C. A., McNeill, G., Martindale, S., Harbour, P. J., Helms, P. J. B., & Seaton, A. (2006) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200512-1946oc · Cited by 268 · see citing works

Bronchial reactivity and dietary antioxidants

Soutar, A., Seaton, A., & Brown, K. (1997) · Thorax · doi:10.1136/thx.52.2.166 · Cited by 267 · see citing works

Antioxidant Nutrients and Pulmonary Function: The Third National Health and Nutrition Examination Survey (NHANES III)

Hu, G., & Cassano, P. A. (2000) · American Journal of Epidemiology · doi:10.1093/oxfordjournals.aje.a010141 · Cited by 259 · see citing works

Molecular Mechanisms of Increased Nitric Oxide (NO) in Asthma: Evidence for Transcriptional and Post-Translational Regulation of NO Synthesis

Guo, F. H., COMHAIR, S. A. A., Zheng, S., Dweik, R. A., Eissa, N. T., Thomassen, M. J., Calhoun, W. J., & ERZURUM, S. C. (2000) · The Journal of Immunology · doi:10.4049/jimmunol.164.11.5970 · Cited by 258 · see citing works

Pathophysiology of circulating xanthine oxidoreductase: New emerging roles for a multi-tasking enzyme

Battelli, M. G., Bolognesi, A., & Polito, L. (2014) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2014.05.022 · Cited by 256 · see citing works

Antioxidant Intake in Pregnancy in Relation to Wheeze and Eczema in the First Two Years of Life

Martindale, S., McNeill, G., Devereux, G. S., Campbell, D. M., Russell, G., & Seaton, A. (2004) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200402-220oc · Cited by 249 · see citing works

Early Nutritional Interventions with Zinc, Selenium and Vitamin D for Raising Anti-Viral Resistance Against Progressive COVID-19

Alexander, J., Tinkov, A. A., Strand, T. A., Alehagen, U., Skalny, A. V., & Aaseth, J. (2020) · Nutrients · doi:10.3390/nu12082358 · Cited by 249 · see citing works

Is boron nutritionally relevant?

Nielsen, F. H. (2008) · Nutrition Reviews · doi:10.1111/j.1753-4887.2008.00023.x · Cited by 244 · see citing works

Contemporaneous maturation of immunologic and respiratory functions during early childhood: Implications for development of asthma prevention strategies

Holt, P. G., Upham, J. W., & Sly, P. D. (2005) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2005.04.017 · Cited by 223 · see citing works

Zinc metabolism in airway epithelium and airway inflammation: basic mechanisms and clinical targets. A review

Zalewski, P. D., Truong-Tran, A. Q., Grosser, D., Jayaram, L., Murgia, C., & Ruffin, R. E. (2004) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2004.09.004 · Cited by 196 · see citing works

Superoxide Dismutase Inactivation in Pathophysiology of Asthmatic Airway Remodeling and Reactivity

COMHAIR, S. A. A., Xu, W., Ghosh, S., Thunnissen, E., Almasan, A., Calhoun, W. J., Janocha, A. J., Zheng, L., Hazen, S. L., & ERZURUM, S. C. (2005) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)62288-2 · Cited by 191 · see citing works

Relationship of Serum Antioxidants to Asthma Prevalence in Youth

Rubin, R. N., Navon, L., & Cassano, P. A. (2003) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200301-055oc · Cited by 184 · see citing works

Impact of the discovery of human zinc deficiency on health

Prasad, A. S. (2014) · Journal of Trace Elements in Medicine and Biology · doi:10.1016/j.jtemb.2014.09.002 · Cited by 184 · see citing works

Copper-dependent Inflammation and Nuclear Factor-κ B Activation by Particulate Air Pollution

Kennedy, T. P., Ghio, A. J., Reed, W., Samet, J. M., Zagorski, J., Quay, J., Carter, J., Dailey, L. A., Hoidal, J. R., & Devlin, R. B. (1998) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/ajrcmb.19.3.3042 · Cited by 179 · see citing works

Diet and Asthma: Nutrition Implications from Prevention to Treatment

Allan, K., & Devereux, G. S. (2011) · Journal of the American Dietetic Association · doi:10.1016/j.jada.2010.10.048 · Cited by 179 · see citing works

A comprehensive evaluation of the enzymatic and nonenzymatic antioxidant systems in childhood asthma

Saçkesen, C., Sarıçoban, H. E., Dizdar, E. A., Soyer, Ö., Gümüş, P., Tosun, B. N., Büyüktuncer, Z., Karabulut, E., Besler, H. T., & Kalaycı, Ö. (2008) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2008.03.035 · Cited by 168 · see citing works

Lysyl oxidases regulate fibrillar collagen remodelling in idiopathic pulmonary fibrosis

Tjin, G., White, E. S., Faiz, A., Sicard, D., Tschumperlin, D. J., Mahar, A. M., Kable, E., & Burgess, J. K. (2017) · Disease Models & Mechanisms · doi:10.1242/dmm.030114 · Cited by 161 · see citing works

Anti-inflammatory effects of zinc and alterations in zinc transporter mRNA in mouse models of allergic inflammation

Lang, C. J., Murgia, C., Leong, M., Tan, L., Perozzi, G., Knight, D. A., Ruffin, R. E., & Zalewski, P. D. (2006) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00280.2006 · Cited by 159 · see citing works

Therapeutic Potential of Phosphatidylinositol 3-Kinase Inhibitors in Inflammatory Respiratory Disease

Ito, K., Caramori, G., & Adcock, I. M. (2006) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.106.111674 · Cited by 158 · see citing works

Asthma and sex hormones

Balzano, G., Fuschillo, S., Melillo, G., & Bonini, S. (2001) · Allergy · doi:10.1034/j.1398-9995.2001.00128.x · Cited by 158 · see citing works

Exhaled Metallic Elements and Serum Pneumoproteins in Asymptomatic Smokers and Patients With COPD or Asthma

Mutti, A., Corradi, M., Goldoni, M., Vettori, M. V., Bernard, A., & Apostoli, P. (2006) · Chest · doi:10.1378/chest.129.5.1288 · Cited by 157 · see citing works

Dietary boron as a physiological regulator of the normal inflammatory response: A review and current research progress

Hunt, C. D., & Idso, J. P. (1999) · The Journal of Trace Elements in Experimental Medicine · doi:10.1002/(sici)1520-670x(1999)12:3 · Cited by 155 · see citing works

Copper Ions Strongly Activate the Phosphoinositide-3-Kinase/Akt Pathway Independent of the Generation of Reactive Oxygen Species

Ostrakhovitch, E. A., Lordnejad, M. R., Schliess, F., Sies, H., & Klotz, L. (2002) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.2001.2559 · Cited by 152 · see citing works

Asthma and dietary intake: an overview of systematic reviews

García-Larsen, V., Giacco, S. R. D., Moreira, A. M., Bonini, M., Marshall, D. C., Reeves, T., Carlsen, K. ‐., Haahtela, T., Bonini, S., Fonseca, J., et al. (2015) · Allergy · doi:10.1111/all.12800 · Cited by 147 · see citing works

Zinc fluxes and zinc transporter genes in chronic diseases

Devirgiliis, C., Zalewski, P. D., Perozzi, G., & Murgia, C. (2007) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2007.01.013 · Cited by 144 · see citing works

Decreased Cu,Zn-SOD activity in asthmatic airway epithelium: correction by inhaled corticosteroid in vivo

Raeve, H. R. D., Thunnissen, E., Kaneko, F. T., Guo, F. H., Lewis, M., Kavuru, M. S., Secic, M., Thomassen, M. J., & ERZURUM, S. C. (1997) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.1997.272.1.l148 · Cited by 139 · see citing works

Dietary antioxidants and asthma in adults

Patel, B. D. (2006) · Thorax · doi:10.1136/thx.2004.024935 · Cited by 126 · see citing works

Cellular chromium enhances activation of insulin receptor kinase

Wang, H., Kruszewski, A., & Brautigan, D. L. (2005) · Biochemistry · doi:10.1021/bi0473152 · Cited by 121 · see citing works

Alterations in Plasma Essential Trace Elements Selenium, Manganese, Zinc, Copper, and Iron Concentrations and the Possible Role of these Elements on Oxidative Status in Patients with Childhood Asthma

Kocyigit, A., Armutcu, F., Gurel, A., & Ermis, B. (2004) · Biological Trace Element Research · doi:10.1385/bter:97:1:31 · Cited by 120 · see citing works

Effects of antioxidant supplements and nutrients on patients with asthma and allergies

Moreno-Macías, H., & Romieu, I. (2014) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2014.03.020 · Cited by 120 · see citing works

Dietary micronutrients/antioxidants and their relationship with bronchial asthma severity

Picado, C., Deulofeu, R., Lleonart, R., Agustí, M., Mullol, J., Torra, M., & Quintó, L. (2001) · Allergy · doi:10.1034/j.1398-9995.2001.00793.x · Cited by 118 · see citing works

Role of iron in the pathogenesis of respiratory disease

Ali, M. K., Kim, R., Karim, R., Mayall, J., Martin, K. L., Shahandeh, A., Abbasian, F., Starkey, M. R., Loustaud-Ratti, V., Johnstone, D. M., et al. (2017) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2017.05.003 · Cited by 112 · see citing works

Apoptosis in the normal and inflamed airway epithelium: role of zinc in epithelial protection and procaspase-3 regulation

Truong-Tran, A. Q., Grosser, D., Ruffin, R. E., Murgia, C., & Zalewski, P. D. (2003) · Biochemical Pharmacology · doi:10.1016/s0006-2952(03)00498-2 · Cited by 111 · see citing works

The iron cycle and oxidative stress in the lung

Turi, J. L., Yang, F., Garrick, M. D., Piantadosi, C. A., & Ghio, A. J. (2004) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2003.12.008 · Cited by 108 · see citing works

Sputum Trace Metals Are Biomarkers of Inflammatory and Suppurative Lung Disease

Gray, R. D., Duncan, A., Noble, D., Imrie, M., O'Reilly, D. S. J., Innes, J. A., Porteous, D. J., Greening, A. P., & Boyd, A. C. (2009) · CHEST Journal · doi:10.1378/chest.09-1047 · Cited by 104 · see citing works

Lung Inflammation, Injury, and Proliferative Response after Repetitive Particulate Hexavalent Chromium Exposure

Beaver, L. M., Stemmy, E. J., Schwartz, A. M., Damsker, J. M., Constant, S. L., Ceryak, S. M., & Patierno, S. R. (2009) · Environmental Health Perspectives · doi:10.1289/ehp.0900715 · Cited by 101 · see citing works

A Role for Dietary Selenium and Selenoproteins in Allergic Airway Inflammation

Hoffmann, P. R., Saux, C. J., Hoffmann, F. W., Chang, P. S., Bollt, O., He, Q., Tam, E. K., & Berry, M. J. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.179.5.3258 · Cited by 100 · see citing works

Association Between Atopic Disease and Anemia in US Children

Drury, K. E., Schaeffer, M., & Silverberg, J. I. (2015) · Archives of Pediatrics and Adolescent Medicine · doi:10.1001/jamapediatrics.2015.3065 · Cited by 99 · see citing works

Crucial role for lung iron level and regulation in the pathogenesis and severity of asthma

Ali, M. K., Kim, R., Brown, A. C., Mayall, J., Karim, R., Pinkerton, J., Liu, G., Martin, K. L., Starkey, M. R., Pillar, A. L., et al. (2020) · European Respiratory Journal · doi:10.1183/13993003.01340-2019 · Cited by 98 · see citing works

Is the Pharmacological Mode of Action of Chromium(III) as a Second Messenger?

Vincent, J. B. (2015) · Biological Trace Element Research · doi:10.1007/s12011-015-0231-9 · Cited by 98 · see citing works

Identification of Novel Diagnostic Biomarkers for Asthma and Chronic Obstructive Pulmonary Disease

Verrills, N. M., Irwin, J. A., He, X. Y., Wood, L. G., Powell, H. A., Simpson, J. L., McDonald, V. M., Sim, A. K., & Gibson, P. G. (2011) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201010-1623oc · Cited by 96 · see citing works

Macrophages: central regulators of iron balance

Gammella, E., Buratti, P., Cairo, G., & Recalcati, S. (2014) · Metallomics · doi:10.1039/c4mt00104d · Cited by 95 · see citing works

Protection of Mice from Allergen-induced Asthma by Selenite

Jeong, D., Yoo, M., Kim, T. S., Kim, J.-H., & Kim, I. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m200808200 · Cited by 94 · see citing works

Asthma and oxidant stress: nutritional, environmental, and genetic risk factors.

Greene, L. S. (1995) · Journal of the American College of Nutrition · doi:10.1080/07315724.1995.10718516 · Cited by 93 · see citing works

Nutritional immunity: the impact of metals on lung immune cells and the airway microbiome during chronic respiratory disease

Healy, C. M., Muñoz‐Wolf, N., Strydom, J., Faherty, L., Williams, N. C., Kenny, S., Donnelly, S. C., & Cloonan, S. M. (2021) · Respiratory Research · doi:10.1186/s12931-021-01722-y · Cited by 89 · see citing works

Inhibition of airway inflammation and hyperreactivity by an antioxidant mimetic

Chang, L., & Crapo, J. D. (2002) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(02)00919-x · Cited by 88 · see citing works

Altered Zinc Homeostasis and Caspase-3 Activity in Murine Allergic Airway Inflammation

Truong-Tran, A. Q., Ruffin, R. E., Foster, P. S., Koskinen, A. M. L., Coyle, P. V., Philcox, J. C., Rofe, A. M., & Zalewski, P. D. (2002) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2001-0014oc · Cited by 88 · see citing works

Molybdenum in Human Health and Disease

Schwarz, G., & Belaidi, A. A. (2013) · Metal ions in life sciences · doi:10.1007/978-94-007-7500-8_13 · Cited by 86 · see citing works

Inhibition of eosinophil migration by lactoferrin

Bournazou, I., Mackenzie, K. J., Duffin, R., Rossi, A. G., & Gregory, C. D. (2009) · Immunology and Cell Biology · doi:10.1038/icb.2009.86 · Cited by 84 · see citing works

Randomised, double blind, placebo-controlled trial of selenium supplementation in adult asthma

Shaheen, S. O., Newson, R. B., Rayman, M. P., Wong, A., Tumilty, M. K., Phillips, J. A., Potts, J. F., Kelly, F. J., White, P. T., & Burney, P. (2007) · Thorax · doi:10.1136/thx.2006.071563 · Cited by 84 · see citing works

Risk factors for asthma symptoms in Kawerau children.

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Oxidative stress in the pathogenesis of asthma

Bowler, R. P. (2004) · Current Allergy and Asthma Reports · doi:10.1007/s11882-004-0056-7 · Cited by 82 · see citing works

Iron Status is Associated with Asthma and Lung Function in US Women

Brigham, E. P., McCormack, M. C., Takemoto, C. M., & Matsui, E. C. (2015) · PLoS ONE · doi:10.1371/journal.pone.0117545 · Cited by 82 · see citing works

Boric acid inhibits LPS-induced TNF-α formation through a thiol-dependent mechanism in THP-1 cells

Cao, J., Jiang, L., Zhang, X., Yao, X., Geng, C., Xue, X., & Zhong, L. (2008) · Journal of Trace Elements in Medicine and Biology · doi:10.1016/j.jtemb.2008.03.005 · Cited by 80 · see citing works

Selenium status is decreased in patients with intrinsic asthma

Kadrabová, J., Madaric, A., Kovačíková, Z., Podivínsky, F., GINTER, E., & Gazdík, F. (1996) · Biological Trace Element Research · doi:10.1007/bf02789165 · Cited by 80 · see citing works

Linkage of Some Trace Elements, Peripheral Blood Lymphocytes, Inflammation, and Oxidative Stress in Patients Undergoing Either Hemodialysis or Peritoneal Dialysis

Guo, C.-H., Wang, C.-L., Chen, P., & Yang, T.-C. (2010) · Peritoneal Dialysis International · doi:10.3747/pdi.2009.00225 · Cited by 78 · see citing works

Oral health in asthmatic patients: a review: Asthma and its therapy may impact on oral health

Gani, F., Caminati, M., Bellavia, F., Baroso, A., Faccioni, P., Pancera, P., Batani, V., & Senna, G. (2020) · Clinical and Molecular Allergy · doi:10.1186/s12948-020-00137-2 · Cited by 77 · see citing works

Antioxidant Effects of Chromium Supplementation with Type 2 Diabetes Mellitus and Euglycemic Subjects

Cheng, H.-H., Lai, M.-H., Hou, W., & Huang, C. (2004) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf035074j · Cited by 77 · see citing works

Calcium Fructoborate: Plant-Based Dietary Boron for Human Nutrition

Miljkovic, D., Scorei, I. R., Cimpoiasu, V. M., & Scorei, I. D. (2009) · Journal of Dietary Supplements · doi:10.1080/19390210903070772 · Cited by 76 · see citing works

Selenium and selenoproteins in prostanoid metabolism and immunity

Qian, F., Misra, S., & Prabhu, K. S. (2019) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.1080/10409238.2020.1717430 · Cited by 74 · see citing works

Role of certain trace minerals in oxidative stress, inflammation, CD4/CD8 lymphocyte ratios and lung function in asthmatic patients

Guo, C.-H., Liu, P.-J., Hsia, S., Chuang, C.-J., & Chen, P. (2011) · Annals of Clinical Biochemistry International Journal of Laboratory Medicine · doi:10.1258/acb.2011.010266 · Cited by 73 · see citing works

Zinc modulates airway epithelium susceptibility to death receptor-mediated apoptosis

Bao, S., & Knoell, D. L. (2005) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00341.2005 · Cited by 73 · see citing works

Zinc and Copper Status of Allergic Children

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Prenatal exposure to thyroid hormone is necessary for normal postnatal development of murine heart and lungs

van Tuyl, M., Blommaart, P. J. E., de Boer, P. A. J., Wert, S. E., Ruijter, J. M., Islam, S., Schnitzer, J. J., Ellison, A. R., Tibboel, D., Moorman, A. F. M., et al. (2004) · Developmental Biology · doi:10.1016/j.ydbio.2004.03.042 · Cited by 68 · see citing works

Boron and Arthritis: The Results of a Double-blind Pilot Study

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Association between Concentrations of Metals in Urine and Adult Asthma: A Case-Control Study in Wuhan, China

Huang, X., Xie, J., Cui, X., Zhou, Y., Wu, X., Lü, W., Shen, Y., Yuan, J., & Chen, W. (2016) · PLoS ONE · doi:10.1371/journal.pone.0155818 · Cited by 64 · see citing works

Copper supplementation and the maintenance of bone mineral density in middle-aged women

Eaton-Evans, J., Mcllrath, E. M., Jackson, W. E., McCartney, H., & Strain, J. (1996) · The Journal of Trace Elements in Experimental Medicine · doi:10.1002/(sici)1520-670x(1996)9:3 · Cited by 63 · see citing works

Atopy, asthma, and lung function in relation to folate and vitamin B12 in adults

Thuesen, B. H., Husemoen, L. L. N., Ovesen, L., Jørgensen, T., Fenger, M., Gilderson, G., & Linneberg, A. R. (2010) · Allergy · doi:10.1111/j.1398-9995.2010.02378.x · Cited by 61 · see citing works

Immunological and Structural Analysis of IgE-Mediated Cross-Reactivity between Manganese Superoxide Dismutases

Flückiger, S., Scapozza, L., Mayer, C., Blaser, K., Folkers, G., & Crameri, R. (2002) · International Archives of Allergy and Immunology · doi:10.1159/000063862 · Cited by 61 · see citing works

Intake of antioxidants during pregnancy and the risk of allergies and asthma in the offspring

Nwaru, B. I., Erkkola, M., Ahonen, S., Kaila, M., Kronberg‐Kippilä, C., Ilonen, J., Simell, O., Knip, M., Veijola, R., & Virtanen, S. M. (2011) · European Journal of Clinical Nutrition · doi:10.1038/ejcn.2011.67 · Cited by 59 · see citing works

Dietary Boron Supplementation Enhances the Effects of Estrogen on Bone Mineral Balance in Ovariectomized Rats

Sheng, M. H. ‐., Taper, L. J., Veit, H. P., Thomas, E. A., Ritchey, S. J., & Lau, K. ‐. W. (2001) · Biological Trace Element Research · doi:10.1385/bter:81:1:29 · Cited by 58 · see citing works

An exploratory study of the associations between maternal iron status in pregnancy and childhood wheeze and atopy

Nwaru, B. I., Hayes, H. E., Gambling, L., Craig, L. C. A., Allan, K., Prabhu, N., Turner, S. W., McNeill, G., Erkkola, M., Seaton, A., et al. (2014) · British Journal Of Nutrition · doi:10.1017/s0007114514003122 · Cited by 58 · see citing works

In Vitro Effects of Calcium Fructoborate upon Production of Inflammatory Mediators by LPS-stimulated RAW 264.7 Macrophages

Scorei, I. R., Ciofrangeanu, C. M., Ion, R., Cîmpean, A., Gălățeanu, B., Mitran, V., & Iordãchescu, D. (2009) · Biological Trace Element Research · doi:10.1007/s12011-009-8488-5 · Cited by 58 · see citing works

Effects of vitamin E and selenium on allergic rhinitis and asthma pathophysiology

Jiang, J., Nasab, E. M., Athari, S. M., & Athari, S. S. (2021) · Respiratory Physiology & Neurobiology · doi:10.1016/j.resp.2020.103614 · Cited by 58 · see citing works

Modern diets and diseases: NO–zinc balance

Sprietsma, J. E. (1999) · Medical Hypotheses · doi:10.1054/mehy.1999.0867 · Cited by 57 · see citing works

Asthma, allergy, and responses to methyl donor supplements and nutrients

Sharma, S., & Litonjua, A. A. (2013) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2013.10.039 · Cited by 56 · see citing works

Zinc supplementation alters airway inflammation and airway hyperresponsiveness to a common allergen

Morgan, C. I., Ledford, J. R., Zhou, P. H., & Page, K. (2011) · Journal of Inflammation · doi:10.1186/1476-9255-8-36 · Cited by 56 · see citing works

9. CHROMIUM SUPPLEMENTATION IN HUMAN HEALTH, METABOLIC SYNDROME, AND DIABETES

Maret, W. (2019) · De Gruyter eBooks · doi:10.1515/9783110527872-009 · Cited by 55 · see citing works

Oxidative stress status and plasma trace elements in patients with asthma or allergic rhinitis

Sağdiç, A., Sener, O., Bulucu, F., Karadurmuş, N., Özel, H. E., Yamanel, L., Tasci, C., Naharcı, M. İ., Ocal, R., & Aydın, A. (2011) · Allergologia et Immunopathologia · doi:10.1016/j.aller.2010.07.006 · Cited by 54 · see citing works

Nutritional supplement therapy improves oxidative stress, immune response, pulmonary function, and quality of life in allergic asthma patients: an open-label pilot study.

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Association between concentration of trace elements in serum and bronchial asthma among Japanese general population

Urushidate, S., Matsuzaka, M., Okubo, N., Iwasaki, H., Hasebe, T., Tsuya, R., Iwane, K., Inoüe, R., Yamai, K., Danjo, K., et al. (2010) · Journal of Trace Elements in Medicine and Biology · doi:10.1016/j.jtemb.2010.06.001 · Cited by 53 · see citing works

Lowered platelet glutathione peroxidase activity in patients with intrinsic asthma

Hasselmark, L., Malmgren, R., Unge, G., & ZETTERSTRÖM, O. (1990) · Allergy · doi:10.1111/j.1398-9995.1990.tb00528.x · Cited by 53 · see citing works

Diet and asthma

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Effect of improved zinc status on T helper cell activation and TH1/TH2 ratio in healthy elderly individuals

Kahmann, L., Uciechowski, P., Warmuth, S., Malavolta, M., Mocchegiani, E., & Rink, L. (2006) · Biogerontology · doi:10.1007/s10522-006-9058-2 · Cited by 51 · see citing works

Anemia as a risk factor for childhood asthma

Ramakrishnan, K. G., & Borade, A. (2010) · Lung India · doi:10.4103/0970-2113.63605 · Cited by 49 · see citing works

Role of intracellular zinc in molecular and cellular function in allergic inflammatory diseases

Suzuki, M., Suzuki, T., Watanabe, M., Hatakeyama, S., Kimura, S., Nakazono, A., Honma, A., Nakamaru, Y., Vreugde, S., & Homma, A. (2020) · Allergology International · doi:10.1016/j.alit.2020.09.007 · Cited by 49 · see citing works

Serum level of vitamin D and trace elements in children with recurrent wheezing: a cross-sectional study

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Selenium and asthma

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Association between atopic disease and anemia in pediatrics: a cross-sectional study

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Occupational asthma caused by chromium

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Iron administration reduces airway hyperreactivity and eosinophilia in a mouse model of allergic asthma

Maazi, H., Shirinbak, S., Bloksma, N., Nawijn, M. C., & van Oosterhout, A. J. M. (2011) · Clinical & Experimental Immunology · doi:10.1111/j.1365-2249.2011.04448.x · Cited by 46 · see citing works

Exposure to particulate hexavalent chromium exacerbates allergic asthma pathology

Schneider, B. C., Constant, S. L., Patierno, S. R., Jurjus, R. A., & Ceryak, S. M. (2011) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2011.12.001 · Cited by 44 · see citing works

Airway function and markers of airway inflammation in patients with treated hypothyroidism

Birring, S. S. (2005) · Thorax · doi:10.1136/thx.2004.034900 · Cited by 43 · see citing works

Ameliorating effect of chromium administration on hepatic glucose metabolism in streptozotocin‐induced experimental diabetes

Sundaram, B., Singhal, K., & Sandhir, R. (2012) · BioFactors · doi:10.1002/biof.194 · Cited by 43 · see citing works

Selenium and asthma: a complex relationship

Hoffmann, P. R. (2008) · Allergy · doi:10.1111/j.1398-9995.2008.01676.x · Cited by 42 · see citing works

Atopic Disease and Anemia in Korean Patients: Cross-Sectional Study with Propensity Score Analysis

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Nutritional supplements and plasma antioxidants in childhood asthma

Fabian, E., Pölöskey, P., Kósa, L., Elmadfa, I., & Réthy, L. A. (2013) · Wiener klinische Wochenschrift · doi:10.1007/s00508-013-0359-6 · Cited by 41 · see citing works

Boron enhances and mimics some effects of estrogen therapy in postmenopausal women

Nielsen, F. H., Gallagher, S. K., Johnson, L. K., & Nielsen, E. J. (1992) · The Journal of Trace Elements in Experimental Medicine · Cited by 41 · see citing works

Iron and Ferritin Concentrations in Exhaled Breath Condensate of Children with Asthma

Vlašić, Ž., Dodig, S., Čepelak, I., Topić, R. Z., Živčić, J., Nogalo, B., & Turkalj, M. (2009) · Journal of Asthma · doi:10.1080/02770900802513007 · Cited by 39 · see citing works

Altered oxidative state in schoolchildren with asthma and allergic rhinitis

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Metabolic reduction of chromium, as related to its carcinogenic properties

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Serum level of zinc in asthmatic patients: A case–control study

Khanbabaee, G., Omidian, A., Imanzadeh, F., Adibeshgh, F., Ashayeripanah, M., & Rezaei, N. (2013) · Allergologia et Immunopathologia · doi:10.1016/j.aller.2012.07.008 · Cited by 39 · see citing works

Association of maternal anemia with increased wheeze and asthma in children

Triche, E. W., Lundsberg, L. S., Wickner, P. G., Belanger, K. D., Leaderer, B. P., & Bracken, M. B. (2011) · Annals of Allergy Asthma & Immunology · doi:10.1016/j.anai.2010.11.007 · Cited by 39 · see citing works

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Zn/Ga−DFO iron–chelating complex attenuates the inflammatory process in a mouse model of asthma

Bibi, H., Vinokur, V., Waisman, D., Elenberg, Y., Landesberg, A., Faingersh, A., Yadid, M., Brod, V., Pesin, J., Berenshtein, E., et al. (2014) · Redox Biology · doi:10.1016/j.redox.2014.06.009 · Cited by 38 · see citing works

Effect of zinc supplementation in children with asthma: a randomized, placebo-controlled trial in northern Islamic Republic of Iran

Ghaffari, J., Khalilian, A., Salehifar, E., Khorasani, E. N., & Rezaii, M. S. (2014) · Eastern Mediterranean Health Journal · doi:10.26719/2014.20.6.391 · Cited by 38 · see citing works

Low Concentrations of Selenium and Zinc in Nails are Associated with Childhood Asthma

Carneiro, M. F. H., Rhoden, C. R., Amantéa, S. L., & Barbosa, F. (2011) · Biological Trace Element Research · doi:10.1007/s12011-011-9080-3 · Cited by 37 · see citing works

Trace Elements Status in Sera of Patients with Allergic Asthma.

Ariaee, N., Farid, R., Shabestari, F., Shabestari, M., & Azad, F. J. (2016) · PubMed Central · Cited by 37 · see citing works

SUBJECT INDEX

Maret, W. (2019) · De Gruyter eBooks · doi:10.1515/9783110527872-015 · Cited by 37 · see citing works

Zinc Deficiency Aggravation of ROS and Inflammatory Injury Leading to Renal Fibrosis in Mice

Xu, R., Chen, M., Wan, L., Chen, Y., & Guo, M. (2020) · Biological Trace Element Research · doi:10.1007/s12011-020-02184-x · Cited by 37 · see citing works

Neonatal folate, homocysteine, vitamin B 12 levels and methylenetetrahydrofolate reductase variants in childhood asthma and eczema

van der Valk, R. J. P., Jong, J. C. K., der Voort, A. M. M. S., Duijts, L., Groen, E. H., Moll, H. A., Tiemeier, H. W., Steegers, E. A. P., Albert Hofman, D., Jaddoe, V. W. V., et al. (2013) · Allergy · doi:10.1111/all.12146 · Cited by 36 · see citing works

Copper Deficiency in the Lungs of TNF-α Transgenic Mice

Liu, L., Geng, X., McDermott, J. R., Shen, J., Corbin, C., Xuan, S. Y., Kim, J. H., Zuo, L., & Liu, Z. (2016) · Frontiers in Physiology · doi:10.3389/fphys.2016.00234 · Cited by 35 · see citing works

Maternal hypothyroidism in the perinatal period and childhood asthma in the offspring

Liu, X., Andersen, S. L., Olsen, J., Agerbo, E., Schlünssen, V., Dharmage, S. C., & Munk‐Olsen, T. (2017) · Allergy · doi:10.1111/all.13365 · Cited by 35 · see citing works

Iron, Nitric Oxide, and Myeloperoxidase in Asthmatic Patients

Ekmekçi, Ö. B., Donma, O., Sardogan, E., Yildirim, N., Uysal, Ö., Demirel, H. S., & Demir, T. (2004) · Biochemistry (Moscow) · doi:10.1023/b:biry.0000026205.89894.25 · Cited by 34 · see citing works

Elevated plasma glutathione peroxidase concentration in acute severe asthma: Comparison with plasma glutathione peroxidase activity, selenium and malondialdehyde

Jacobson, G. A., Yee, K. C., & Ng, C. H. (2007) · Scandinavian Journal of Clinical and Laboratory Investigation · doi:10.1080/00365510601153353 · Cited by 33 · see citing works

Zinc Suppressed the Airway Inflammation in Asthmatic Rats: Effects of Zinc on Generation of Eotaxin, MCP-1, IL-8, IL-4, and IFN-γ

Lu, H., Xin, Y., Tang, Y., & Shao, G. (2012) · Biological Trace Element Research · doi:10.1007/s12011-012-9493-7 · Cited by 32 · see citing works

Selenium serum and urine is associated to mild asthma and atopy. The SUS study

Omland, Ø., Deguchi, Y., Sigsgaard, T., & Hansen, J. C. (2002) · Journal of Trace Elements in Medicine and Biology · doi:10.1016/s0946-672x(02)80039-6 · Cited by 32 · see citing works

Plasma Paraoxonase Activities, Lipoprotein Oxidation, and Trace Element Interaction in Asthmatic Patients

Ekmekçi, Ö. B., Donma, O., Ekmekçi, H., Yıldırım, N., Uysal, Ö., Sardogan, E., Demirel, H., & Demir, T. (2006) · Biological Trace Element Research · doi:10.1385/bter:111:1:41 · Cited by 29 · see citing works

Zinc Supplementation in Children with Asthma Exacerbation

Rerksuppaphol, S., & Rerksuppaphol, L. (2016) · Pediatric Reports · doi:10.4081/pr.2016.6685 · Cited by 28 · see citing works

Maternal iron status during pregnancy and respiratory and atopic outcomes in the offspring: a Mendelian randomisation study

Bédard, A., Lewis, S. J., Burgess, S., Henderson, A. J., & Shaheen, S. O. (2018) · BMJ Open Respiratory Research · doi:10.1136/bmjresp-2018-000275 · Cited by 28 · see citing works

Role of iron and oxidative stress in the exacerbation of allergic inflammation in murine lungs caused by urban particulate matter <2.5 μm and desert dust

He, M., Ichinose, T., Yoshida, S., Nishikawa, M., Sun, G., & Shibamoto, T. (2019) · Journal of Applied Toxicology · doi:10.1002/jat.3773 · Cited by 28 · see citing works

Sputum zinc concentration and clinical outcome in older asthmatics

Jayaram, L., Chunilal, S. D., Pickering, S., Ruffin, R. E., & Zalewski, P. D. (2011) · Respirology · doi:10.1111/j.1440-1843.2011.01932.x · Cited by 27 · see citing works

Airway response to inhaled salbutamol in hyperthyroid and hypothyroid patients before and after treatment.

Harrison, R. N., & Tattersfield, A. (1984) · Thorax · doi:10.1136/thx.39.1.34 · Cited by 27 · see citing works

The Effects of Leucine, Zinc, and Chromium Supplements on Inflammatory Events of the Respiratory System in Type 2 Diabetic Rats

Kolahian, S., Sadri, H., Shahbazfar, A. A., Amani, M., Mazadeh, A., & Mirani, M. (2015) · PLoS ONE · doi:10.1371/journal.pone.0133374 · Cited by 26 · see citing works

Serum Zinc Status and Its Association with Allergic Sensitization: The Fifth Korea National Health and Nutrition Examination Survey

Seo, H., Kim, Y. H., Lee, J. H., Kim, J. S., Park, Y. M., & Lee, J. Y. (2017) · Scientific Reports · doi:10.1038/s41598-017-13068-x · Cited by 26 · see citing works

Lower circulating zinc and selenium levels are associated with an increased risk of asthma: evidence from a meta-analysis

Meng, C., Sun, Y., & Wu, Y. (2019) · Public Health Nutrition · doi:10.1017/s1368980019003021 · Cited by 26 · see citing works

Zinc and vitamin C deficiencies associate with poor pulmonary function in children with persistent asthma

Siripornpanich, S., Chongviriyaphan, N., Manuyakorn, W., & Matangkasombut, P. (2020) · Asian Pacific Journal of Allergy and Immunology · doi:10.12932/ap-100620-0878 · Cited by 26 · see citing works

Intranasal administration of a combination of choline chloride, vitamin C, and selenium attenuates the allergic effect in a mouse model of airway disease

Bansal, P., Saw, S., Govindaraj, D., & Arora, N. (2014) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2014.05.018 · Cited by 25 · see citing works

l -Thyroxine promotes a proliferative airway smooth muscle phenotype in the presence of TGF-β1

Dekkers, B. G. J., Naeimi, S., Bos, I. S. T., Menzen, M. H., Halayko, A. J., Hashjin, G. S., & Meurs, H. (2014) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00071.2014 · Cited by 25 · see citing works

Serum Zinc Level in Asthmatic and Non-Asthmatic School Children

AbdulWahab, A., Zeidan, A., Avades, T. Y., Chandra, P., & Soliman, A. T. (2018) · Children · doi:10.3390/children5030042 · Cited by 25 · see citing works

Long-term exposure to hexavalent chromium inhibits expression of tumor suppressor genes in cultured cells and in mice

Fan, Y., Ovesen, J. L., & Puga, A. (2012) · Journal of Trace Elements in Medicine and Biology · doi:10.1016/j.jtemb.2012.04.009 · Cited by 24 · see citing works

Erythrocyte zinc levels in children with bronchial asthma

Yilmaz, E. A., Özmen, S., Bostancı, İ., Mısırlıoğlu, E. D., & Ertan, Ü. (2011) · Pediatric Pulmonology · doi:10.1002/ppul.21501 · Cited by 24 · see citing works

Pre-natal folic acid and iron supplementation and atopic dermatitis in the first 6 years of life

Fortes, C., Mastroeni, S., Mannooranparampil, T. J., & Lallo, D. D. (2019) · Archives of Dermatological Research · doi:10.1007/s00403-019-01911-2 · Cited by 24 · see citing works

Allergic airway inflammation in hypothyroid rats

Manzolli, S., Macedo-Soares, M. F., Vianna, É. O., & Sannomiya, P. (1999) · Journal of Allergy and Clinical Immunology · doi:10.1016/s0091-6749(99)70329-5 · Cited by 23 · see citing works

The immunomodulatory role of zinc in asthmatic patients

Mohamed, N. A., Rushdy, M., & Abdel-Rehim, A. S. M. (2018) · Cytokine · doi:10.1016/j.cyto.2018.03.007 · Cited by 23 · see citing works

Relationships between Plasma Micronutrients, Serum IgE, and Skin Test Reactivity and Asthma among School Children in Rural Southwest Nigeria

Oluwole, O., Arinola, O. G., Adu, M. D., Adepoju, A., Adedokun, B., Olopade, O. I., & Olopade, C. O. (2014) · Journal of Biomarkers · doi:10.1155/2014/106150 · Cited by 22 · see citing works

Prenatal exposure to selenium may protect against wheezing in children by the age of 3

Baïz, N., Chastang, J., Ibañez, G. E., & Annesi‐Maesano, I. (2016) · Immunity Inflammation and Disease · doi:10.1002/iid3.138 · Cited by 22 · see citing works

Impact of thyroid hormones on asthma in older adults

Bingyan, Z., & Dong, W. (2019) · Journal of International Medical Research · doi:10.1177/0300060519856465 · Cited by 21 · see citing works

Serum Zinc, Selenium and Total Antioxidant Contents of Nigerian Children with Asthma: Association with Disease Severity and Symptoms Control

Kuti, B. P., Kuti, D. K., & Smith, O. S. (2019) · Journal of Tropical Pediatrics · doi:10.1093/tropej/fmz078 · Cited by 21 · see citing works

Hyperthyroidism and Asthma

Lương, K. V. Q., & Nguyễn, L. (2000) · Journal of Asthma · doi:10.3109/02770900009055435 · Cited by 19 · see citing works

Chromium alters lipopolysaccharide-induced inflammatory responses both in vivo and in vitro

Jin, Y., Liu, L., Zhang, S., Tao, B., Tao, R., He, X., Qu, L., Huang, J., Wang, X., & Fu, Z. (2016) · Chemosphere · doi:10.1016/j.chemosphere.2016.01.057 · Cited by 19 · see citing works

Asthma as a disruption in iron homeostasis

Ghio, A. J. (2016) · BioMetals · doi:10.1007/s10534-016-9948-y · Cited by 19 · see citing works

Hemopexin: A Novel Anti-inflammatory Marker for Distinguishing COPD From Asthma

Winter, N. A., Gibson, P. G., Fricker, M., Simpson, J. L., Wark, P. A. B., & McDonald, V. M. (2021) · Allergy Asthma and Immunology Research · doi:10.4168/aair.2021.13.3.450 · Cited by 19 · see citing works

Partial Purification of Soluble Lipoxygenase of Sunflower Cotyledons: Action of Boron on the Enzyme and Lipid Constituents

Belver, A., & Donaire, J. P. (1983) · Zeitschrift für Pflanzenphysiologie · doi:10.1016/s0044-328x(83)80114-7 · Cited by 18 · see citing works

Selenium status and allergic disease in a cohort of New Zealand children

Thomson, C. D., Wickens, K. L., Miller, J. C., Ingham, T. R., Lampshire, P., Epton, M., Town, G. I., Pattemore, P., Crane, J., & The year six New Zealand Asthma and Allergy Cohort Study Group (NZAACS6) (2012) · Clinical & Experimental Allergy · doi:10.1111/j.1365-2222.2012.03924.x · Cited by 18 · see citing works

Association between anti-thyroid peroxidase antibody and asthma in women.

Fekri, M. S., Shokoohi, M., Gozashti, M. H., Esmailian, S., Jamshidian, N., Shadkam-Farokhi, M., Lashkarizadeh, M., & Afshar, R. M. (2012) · PubMed · Cited by 18 · see citing works

Zinc-rich inhibitor of apoptosis proteins (IAPs) as regulatory factors in the epithelium of normal and inflamed airways

Roscioli, E., Hamon, R., Lester, S. E., Murgia, C., Grant, J. F., & Zalewski, P. D. (2013) · BioMetals · doi:10.1007/s10534-013-9618-2 · Cited by 18 · see citing works

Relationship Among Manganese, Arginase, and Nitric Oxide in Childhood Asthma

Koçyiğit, A., Zeyrek, D., Keles, H., & Köylü, A. (2004) · Biological Trace Element Research · doi:10.1385/bter:102:1-3:011 · Cited by 17 · see citing works

Selenium status and allergic disease in a cohort of N ew Z ealand children

Thomson, C. D., Wickens, K. L., Miller, J. C., Ingham, T. R., Lampshire, P., Epton, M., Town, G. I., Pattemore, P., & Crane, J. (2012) · Clinical & Experimental Allergy · doi:10.1111/j.1365-2222.2011.03924.x · Cited by 17 · see citing works

Influence of Selenium on Mast Cell Mediator Release

Safaralizadeh, R., Nourizadeh, M., Zare, A., Kardar, G. A., & Pourpak, Z. (2013) · Biological Trace Element Research · doi:10.1007/s12011-013-9712-x · Cited by 16 · see citing works

Maternal selenium status in pregnancy, offspring glutathione peroxidase 4 genotype, and childhood asthma

Shaheen, S. O., Rutterford, C. M., Lewis, S. J., Ring, S. M., Holloway, J. W., Golding, J., & Henderson, A. J. (2014) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2014.10.035 · Cited by 16 · see citing works

Associations of genetic determinants of serum vitamin B12 and folate concentrations with hay fever and asthma: a Mendelian randomization meta-analysis

Skaaby, T., Taylor, A. E., Jacobsen, R. K., Møllehave, L. T., Friedrich, N., Thuesen, B. H., Shabanzadeh, D. M., Paternoster, L., Völker, U., Nauck, M. A., et al. (2017) · European Journal of Clinical Nutrition · doi:10.1038/s41430-017-0037-2 · Cited by 16 · see citing works

Maternal iron status during early pregnancy and school‐age, lung function, asthma, and allergy: The Generation R Study

Quezada‐Pinedo, H. G., Mensink‐Bout, S. M., Reiss, I. K. M., Jaddoe, V. W. V., Vermeulen, M. J., & Duijts, L. (2021) · Pediatric Pulmonology · doi:10.1002/ppul.25324 · Cited by 16 · see citing works

Modulation of mite antigen‐induced immune responses by lecithin‐bound iodine in peripheral blood lymphocytes from patients with bronchial asthma

Kawano, Y., & Noma, T. (1995) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.1995.tb15016.x · Cited by 14 · see citing works

Serum zinc level in bronchial asthma

Yousef, A. M., & Elmorsy, E. M. (2016) · Egyptian Journal of Chest Diseases and Tuberculosis · doi:10.1016/j.ejcdt.2016.10.009 · Cited by 14 · see citing works

A halotyrosine antibody that detects increased protein modifications in asthma patients

Jin, H., Hallstrand, T. S., Daly, D. S., Matzke, M. M., Nair, P. K., Bigelow, D. J., Pounds, J. G., & Zangar, R. C. (2013) · Journal of Immunological Methods · doi:10.1016/j.jim.2013.11.013 · Cited by 13 · see citing works

Association between Chronic Obstructive Pulmonary Disease and Exfoliation Syndrome

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