Regulation of iron homeostasis by the hypoxia-inducible transcription factors (HIFs)

Targeting Hypoxia-Inducible Factors for the Treatment of Anemia in Chronic Kidney Disease Patients

Locatelli, F., Fishbane, S. N., Block, G. A., & Macdougall, I. C. (2017) · American Journal of Nephrology · doi:10.1159/000455166 · Cited by 4,836

Hepcidin Regulates Cellular Iron Efflux by Binding to Ferroportin and Inducing Its Internalization

Nemeth, E., Tuttle, M. S., Powelson, J., Vaughn, M. B., Donovan, A., Ward, D. M., Ganz, T., & Kaplan, J. (2004) · Science · doi:10.1126/science.1104742 · Cited by 4,803

A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis

Feder, J. N., Gnirke, A., Thomas, W., Tsuchihashi, Z., Ruddy, D. A., Basava, A., Dormishian, F., Domingo, R., Ellis, M. C., Fullan, A., et al. (1996) · Nature Genetics · doi:10.1038/ng0896-399 · Cited by 3,664

IL-6 mediates hypoferremia of inflammation by inducing the synthesis of the iron regulatory hormone hepcidin

Nemeth, E., Rivera, S., Gabayan, V., Keller, C., Taudorf, S., Pedersen, B. K., & Ganz, T. (2004) · Journal of Clinical Investigation · doi:10.1172/jci200420945 · Cited by 2,650 · cited 1×

Dysmetabolic Hyperferritinemia: All Iron Overload Is Not Hemochromatosis

Makker, J. S., Hanif, A., Bajantri, B., & Chilimuri, S. S. (2015) · Case Reports in Gastroenterology · doi:10.1159/000373883 · Cited by 1,353

Endothelial PAS domain protein 1 (EPAS1), a transcription factor selectively expressed in endothelial cells.

Tian, H., McKnight, S. L., & Russell, D. W. (1997) · Genes & Development · doi:10.1101/gad.11.1.72 · Cited by 1,351

HIF-1 and mechanisms of hypoxia sensing

Semenza, G. L. (2001) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(00)00194-0 · Cited by 1,301

A Novel Mammalian Iron-regulated Protein Involved in Intracellular Iron Metabolism

Abboud, S., & Haile, D. J. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m000713200 · Cited by 1,267

Lack of hepcidin gene expression and severe tissue iron overload in upstream stimulatory factor 2 ( USF2 ) knockout mice

Nicolas, G., Bennoun, M., Devaux, I., Beaumont, C., Grandchamp, B., Kahn, A., & Vaulont, S. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.151179498 · Cited by 1,233

The gene encoding the iron regulatory peptide hepcidin is regulated by anemia, hypoxia, and inflammation

Nicolas, G., Chauvet, C., Viatte, L., Danan, J. L., Bigard, X., Devaux, I., Beaumont, C., Kahn, A., & Vaulont, S. (2002) · Journal of Clinical Investigation · doi:10.1172/jci0215686 · Cited by 1,214

Hepcidin downregulation by repeated bleeding is not mediated by soluble hemojuvelin.

Krijt, J., Fujikura, Y., Šefc, L., Vokurka, M., Hlobenová, T., & Necas, E. (2010) · PubMed · doi:10.33549/physiolres.931706 · Cited by 16

Impact of hepcidin antimicrobial peptide on iron overload in tuberculosis patients

Javaheri-Kermani, M., Farazmandfar, T., Ajami, A., & Yazdani, Y. (2014) · Scandinavian Journal of Infectious Diseases · doi:10.3109/00365548.2014.929736 · Cited by 15

Hypoxia-inducible factor upregulation by roxadustat attenuates drug reward by altering brain iron homoeostasis

Yan, P., Li, N., Ma, M., Liu, Z., Yang, H., Li, J., Wan, C., Gao, S., Li, S., Zheng, L. T., et al. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01578-2 · Cited by 15

‘3D-QSAR-based, pharmacophore modelling, virtual screening, and molecular docking studies for identification of hypoxia-inducible factor-1 inhibitor with potential bioactivity

Yadav, P. K., Singh, S., & Singh, A. K. (2023) · Computers in Biology and Medicine · doi:10.1016/j.compbiomed.2023.107557 · Cited by 15

Testosterone therapy-induced erythrocytosis: can phlebotomy be justified?

Bond, P., Verdegaal, T. J., & Smit, D. L. (2024) · Endocrine Connections · doi:10.1530/ec-24-0283 · Cited by 19

Suppression of plasma hepcidin by venesection during steady-state hypoxia

Talbot, N. P., Smith, T. G., Lakhal‐Littleton, S., Gülsever, C. İ., Rivera, M. C., Dorrington, K. L., Mole, D. R., & Robbins, P. A. (2016) · Blood · doi:10.1182/blood-2015-05-647404 · Cited by 15

Anti-Oxidant and Anti-Inflammatory Effects of Lipopolysaccharide from Rhodobacter sphaeroides against Ethanol-Induced Liver and Kidney Toxicity in Experimental Rats

Mehanna, E. T., Ali, A.-S. A., El-shaarawy, F. F., Mesbah, N. M., Abo–Elmatty, D. M., & Aborehab, N. M. (2021) · Molecules · doi:10.3390/molecules26247437 · Cited by 15

Von Hippel-Lindau disease (VHL): a need for a murine model with retinal hemangioblastoma.

Park, S., & Chan, C. (2012) · PubMed · doi:10.14670/hh-27.975 · Cited by 14

Accelerated loss of hypoxia response in zebrafish with familial Alzheimer’s disease-like mutation of presenilin 1

Newman, M., Nik, S. H. M., Sutherland, G. T., Hin, N., Kim, W. S., Halliday, G. M., Jayadev, S., Smith, C., Laird, A. S., Lucas, C. W., et al. (2020) · Human Molecular Genetics · doi:10.1093/hmg/ddaa119 · Cited by 15

Genetic variability of hypoxia‐inducible factor alpha (HIFA) genes in familial erythrocytosis: Analysis of the literature and genome databases

Kristan, A., Debeljak, N., & Kunej, T. (2019) · European Journal Of Haematology · doi:10.1111/ejh.13304 · Cited by 14

Activation of Intestinal HIF2α Ameliorates Iron‐Refractory Anemia

Yu, Y., Su, Y., Yang, S., Liu, Y., Lin, Z., Das, N. K., Wu, Q., Zhou, J., Sun, S., Li, X., et al. (2024) · Advanced Science · doi:10.1002/advs.202307022 · Cited by 14

Parenteral iron polymaltose changes i:c-terminal FGF23 ratios in iron deficiency, but not in dialysis patients

Tan, S.-J., Satake, S., Smith, E. R., Toussaint, N. D., Hewitson, T. D., & Holt, S. G. (2016) · European Journal of Clinical Nutrition · doi:10.1038/ejcn.2016.217 · Cited by 14

Inflammation Mediated Hepcidin-Ferroportin Pathway and Its Therapeutic Window in Breast Cancer

Shibabaw, T., Teferi, B., Molla, M. D., & Ayelign, B. (2020) · Breast Cancer Targets and Therapy · doi:10.2147/bctt.s276404 · Cited by 15

Roxadustat for the treatment of anemia in patients with chronic kidney diseases: a meta-analysis

Zhang, L., Hou, J., Li, J., Su, S., & Xue, S. (2021) · Aging · doi:10.18632/aging.203143 · Cited by 14

Spatial patterns in markers of contaminant exposure, glucose and glycogen metabolism, and immunological response in juvenile winter flounder (Pseudoplueronectes americanus)

McElroy, A. E., Hice, L. A., Frisk, M. G., Purcell, S. L., Phillips, N. C., & Fast, M. D. (2015) · Comparative Biochemistry and Physiology Part D Genomics and Proteomics · doi:10.1016/j.cbd.2015.01.006 · Cited by 14

Exposure to bis(maltolato)oxovanadium(IV) increases levels of hepcidin mRNA and impairs the homeostasis of iron but not that of manganese

Sánchez‐González, C., Rivas‐García, L., López-Chaves, C., Rodríguez‐Nogales, A., Algieri, F., Gálvez, J., Gómez-Aracena, J., Ramírez, L. V., Montes‐Bayón, M., Sanz‐Medel, A., et al. (2014) · Food and Chemical Toxicology · doi:10.1016/j.fct.2014.08.011 · Cited by 14

Structure-based drug design for hypoxia-inducible factor prolyl-hydroxylase inhibitors and its therapeutic potential for the treatment of erythropoiesis-stimulating agent-resistant anemia: raising expectations for exploratory clinical trials

Higashijima, Y., Tanaka, T., & Nangaku, M. (2013) · Expert Opinion on Drug Discovery · doi:10.1517/17460441.2013.796358 · Cited by 14

Regulation of transferrin receptor 2 in human cancer cell lines

Calzolari, A., Finisguerra, V., Oliviero, I., Deaglio, S., Mariani, G., Malavasi, F., & Testa, U. (2009) · Blood Cells Molecules and Diseases · doi:10.1016/j.bcmd.2008.10.001 · Cited by 13

Identification of differentially expressed genes in mouse embryonic stem cell under hypoxia

Hwang, S. J., & Lee, H. (2020) · Genes & Genomics · doi:10.1007/s13258-020-01009-4 · Cited by 13

Hepcidin and its multiple partners: Complex regulation of iron metabolism in health and disease

Ginzburg, Y. Z. (2023) · Vitamins and hormones · doi:10.1016/bs.vh.2023.03.001 · Cited by 15

Therapeutics of managing reduced red cell mass associated with chronic kidney disease – Is there a case for earlier intervention?

Elliott, J. (2023) · Journal of Veterinary Pharmacology and Therapeutics · doi:10.1111/jvp.13127 · Cited by 15

Alcohol exposure increases manganese accumulation in the brain and exacerbates manganese-induced neurotoxicity in mice

Han, M., Böhlke, M., Maher, T. J., & Kim, J. (2021) · Archives of Toxicology · doi:10.1007/s00204-021-03166-1 · Cited by 13

The von Hippel-Lindau Tumor Suppressor Gene Mutations Modulate Lipocalin-2 Expression in Ferroptotic-Inflammatory Pathways

Kuo, C., Hsieh, P., Chiu, V. J.-Y., Lan, C., & Lu, K. (2023) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2023/7736638 · Cited by 15

Effect of Iron Supplementation on the Expression of Hypoxia-Inducible Factor and Antioxidant Status in Rats Exposed to High-Altitude Hypoxia Environment

Xu, C., Dong, C., Xu, C., Han, T., Bao, S., & Gao, X. (2014) · Biological Trace Element Research · doi:10.1007/s12011-014-0166-6 · Cited by 13

PKC-δ inhibitors sustain self-renewal of mouse embryonic stem cells under hypoxiain vitro

Lee, H., Jeong, C., Cha, J., & Kim, K.-W. (2010) · Experimental & Molecular Medicine · doi:10.3858/emm.2010.42.4.028 · Cited by 13

Emerging drugs for the treatment of kidney disease-induced anemia

Małyszko, J., & Małyszko, J. S. (2016) · Expert Opinion on Emerging Drugs · doi:10.1080/14728214.2016.1220537 · Cited by 14

The Molecular Connection Between Aluminum Toxicity, Anemia, Inflammation and Obesity: Therapeutic Cues

Bignucolo, A., Lemire, J. A., Auger, C., Castonguay, Z., Appanna, V. P., & Vasu, D. (2012) · InTech eBooks · doi:10.5772/30273 · Cited by 13

Urinary hepcidin excretion in patients with low grade myelodysplastic syndrome

Murphy, P. T., Mitra, S., Gleeson, M. J., Desmond, R. G., & Swinkels, D. W. (2008) · British Journal of Haematology · doi:10.1111/j.1365-2141.2008.07455.x · Cited by 13

Prolyl-hydroxylase inhibitors for the treatment of anemia in chronic kidney disease

McMahon, G. M., & Singh, A. K. (2019) · Current Opinion in Nephrology & Hypertension · doi:10.1097/mnh.0000000000000554 · Cited by 12

Estrogen signaling differentially alters iron metabolism in monocytes in an Interleukin 6-dependent manner

Bajbouj, K., Shafarin, J., Muhammad, J. S., Ali, A., Unnikannan, H., Suleiman, B., Al-Jabi, N., Menon, K., & Hamad, M. A. (2020) · Immunobiology · doi:10.1016/j.imbio.2020.151995 · Cited by 12

The Iron Maiden. Cytosolic Aconitase/IRP1 Conformational Transition in the Regulation of Ferritin Translation and Iron Hemostasis

Hognon, C., Bignon, E., Harlé, G., Touche, N., Grandemange, S., & Monari, A. (2021) · Biomolecules · doi:10.3390/biom11091329 · Cited by 14

Quantitative assay of urinary hepcidin using MALDI-TOF mass spectrometry

Gay, M. C. L., Mullaney, I., Trinder, D., Olynyk, J. K., & Trengove, R. D. (2009) · Analytical Methods · doi:10.1039/b9ay00130a · Cited by 12

Hypoxia negatively regulates heparan sulfatase 2 expression in renal cancer cell lines

Khurana, A., Tun, H. W., Marlow, L. A., Copland, J. A., Dredge, K. S., & Shridhar, V. (2011) · Molecular Carcinogenesis · doi:10.1002/mc.20824 · Cited by 15

Iron homeostasis is altered in response to hypoxia and hypothermic preconditioning in brain glial cells

Aral, A., Ergün, M. A., Engin, A. B., Börcek, A. Ö., & Bolay, H. (2020) · TURKISH JOURNAL OF MEDICAL SCIENCES · doi:10.3906/sag-2003-41 · Cited by 12

Hypoxia-inducible factor signaling in vascular calcification in chronic kidney disease patients

Çöpür, S., Uçku, D., Cozzolino, M. G., & Kanbay, M. (2022) · Journal of Nephrology · doi:10.1007/s40620-022-01432-8 · Cited by 14

Molecular basis of hereditary iron homeostasis defects

Horváthová, M., Ponka, P., & Divoký, V. (2010) · Hematology · doi:10.1179/102453310x12583347009810 · Cited by 12

Fibroblast Growth Factor 23 Bone Regulation and Downstream Hormonal Activity

Clinkenbeard, E. L. (2023) · Calcified Tissue International · doi:10.1007/s00223-023-01092-1 · Cited by 12

Physiological focus on the erythropoietin–hepcidin–ferroportin axis

D’Anna, M. C., & Roque, M. E. (2013) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/cjpp-2012-0214 · Cited by 11

Transferrin saturation is independently associated with the severity of obstructive sleep apnea syndrome and hypoxia among obese subjects

Tallec-Estève, N. L., Rousseau, C., Desrues, B., Loréal, O., & Thibault, R. (2020) · Clinical Nutrition · doi:10.1016/j.clnu.2020.06.007 · Cited by 10

Potential Roles of Metals in the Pathogenesis of Pulmonary and Systemic Hypertension

Hopkins, C. D., Wessel, C. R., Chen, O., El‐Kersh, K., Cave, M. C., Cai, L. F., & Huang, J. (2023) · International Journal of Biological Sciences · doi:10.7150/ijbs.85590 · Cited by 11

A Novel Muscle Atrophy Mechanism: Myocyte Degeneration Due to Intracellular Iron Deprivation

Suh, D. K., Lee, W.-Y., Yeo, W. J., Kyung, B. S., Jung, K. W., Seo, H. K., Lee, Y.-S., & Suh, D. W. (2022) · Cells · doi:10.3390/cells11182853 · Cited by 12

Hepcidin and iron metabolism disorders in patients with chronic kidney disease

Jelic, M., Cvetković, T., Djordjevic, V., Damnjanović, G., Vlahović, P., Kocic, G. M., Djindjić, N., Jovović, B., & Antic, A. (2013) · Vojnosanitetski pregled · doi:10.2298/vsp1304368j · Cited by 10

Inactivation of prolyl hydroxylase domain (PHD) protein by epigallocatechin (EGCG) stabilizes hypoxia-inducible factor (HIF-1α) and induces hepcidin (Hamp) in rat kidney

Manalo, D. J., Baek, J. H., Buehler, P. W., Struble, E. B., Abraham, B., & Alayash, A. I. (2011) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2011.11.085 · Cited by 10

Identification of Ceruloplasmin as a Gene that Affects Susceptibility to Glomerulonephritis Through Macrophage Function

Chen, T., Rotival, M., Chiu, L.-Y., Bagnati, M., Ko, J., Srivastava, P. K., Petretto, E. G., Pusey, C. D., Lai, P., Aitman, T. J., et al. (2017) · Genetics · doi:10.1534/genetics.116.197376 · Cited by 10

The Hepatitis C virus NS5A and core proteins exert antagonistic effects on HAMP gene expression: the hidden interplay with the MTF‐1/MRE pathway

Dimitriadis, A., Foka, P., Kyratzopoulou, E., Karamichali, E., Petroulia, S., Tsitoura, P., Kakkanas, A., Eliadis, P., Georgopoulou, U., & Mamalaki, A. (2020) · FEBS Open Bio · doi:10.1002/2211-5463.13048 · Cited by 10

Expression of Iron Regulatory Protein 1 Is Regulated not only by HIF-1 but also pCREB under Hypoxia

Luo, Q., Qian, Z., Zhou, Y., Zhang, M., Wang, D., Zhu, L., & Ke, Y. (2016) · International Journal of Biological Sciences · doi:10.7150/ijbs.16437 · Cited by 10

Hypoxia and HIF-1α promote lytic de novo KSHV infection

Lee, S.-C., Naik, N. G., Tombácz, D., Gulyás, G. M., Kakuk, B., Boldogkői, Z., Hall, K., Papp, B., Boulant, S., & Tóth, Z. (2023) · Journal of Virology · doi:10.1128/jvi.00972-23 · Cited by 10

Hepcidin mediates the disorder of iron homeostasis and mitochondrial function in mice under hypobaric hypoxia exposure

Liu, J., Zhao, J., He, J., Li, Y., Xu, J., Xiao, C., Zhang, Y., Chen, H., Hu, Y., Fan, C., et al. (2025) · APOPTOSIS · doi:10.1007/s10495-025-02079-z · Cited by 9

The efficacy and safety of roxadustat for anemia in patients with dialysis-dependent chronic kidney disease: a systematic review and meta-analysis

Zhou, Q., Mao, M., Li, J., & Deng, F. (2023) · Renal Failure · doi:10.1080/0886022x.2023.2195011 · Cited by 12

TGF-β-regulated different iron metabolism processes in the development and cisplatin resistance of ovarian cancer

WU, J., Liao, Q., ZHANG, L., WU, S., & LIU, Z. (2023) · Oncology Research Featuring Preclinical and Clinical Cancer Therapeutics · doi:10.32604/or.2023.031404 · Cited by 10

The effect of hemin‐induced oxidative stress on erythropoietin production in HepG2 cells

Nishimura, K., Tokida, M., Katsuyama, H., Nakagawa, H., & Matsuo, S. (2014) · Cell Biology International · doi:10.1002/cbin.10329 · Cited by 9

Estrogen-dependent changes in serum iron levels as a translator of the adverse effects of estrogen during infection: A conceptual framework

Hamad, M. A., & Awadallah, S. M. (2013) · Medical Hypotheses · doi:10.1016/j.mehy.2013.10.019 · Cited by 9

An immunoassay for human serum hepcidin at last: Ganz klar?

Brugnara, C. (2008) · Blood · doi:10.1182/blood-2008-09-176701 · Cited by 9

Imaging the Rewired Metabolism in Lung Cancer in Relation to Immune Therapy

van Genugten, E. A. J., Weijers, J. A. M., Heskamp, S., Kneilling, M., van den Heuvel, M. M., Piet, B., Bussink, J., Hendriks, L. E. L., & Aarntzen, E. H. J. G. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2021.786089 · Cited by 9

Dietary Iron Absorption: Biochemical and Nutritional Aspects

Frazer, D. M., Anderson, G. J., & Collins, J. F. (2025) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-92033-2_6 · Cited by 8

Iron, the Essential Micronutrient: A Comprehensive Review of Regulatory Pathways of Iron Metabolism

Horváth, A., Tamási, K., Pap, R., Jánosa, G., & Pandur, E. (2025) · Nutrients · doi:10.3390/nu18010109 · Cited by 12

Iron facilitator LS 081 reduces hypoxia‐inducible factor‐1α protein and functions as anticancer agent in hepatocellular carcinoma

Tanaka, H., Li, Z., Ikuta, K., Addo, L., Akutsu, H., Nakamura, M., Sasaki, K., Ohtake, T., Fujiya, M., Torimoto, Y., et al. (2011) · Cancer Science · doi:10.1111/j.1349-7006.2011.02192.x · Cited by 8

The Re-Emerging Role of Iron in Infection and Immunity

Hamad, M. A., & Bajbouj, K. (2016) · Integrative Molecular Medicine · doi:10.15761/imm.1000251 · Cited by 8

HIF1A: A Putative Modifier of Hemochromatosis

Pelucchi, S., Ravasi, G., Arosio, C., Mauri, M., Piazza, R., Mariani, R., & Piperno, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22031245 · Cited by 8

Assessing erythroferrone and iron homeostasis in preeclamptic and normotensive pregnancies: A retrospective study

Masoumi, Z. T., Hansson, L. R., Hansson, E., Ahlm, E., Mezey, É., Erlandsson, L., & Hansson, S. R. (2023) · Placenta · doi:10.1016/j.placenta.2023.01.008 · Cited by 8

Iron Metabolism and Related Disorders

Hoda, K., Bowlus, C. L., Chu, T. W., & Gruen, J. R. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-383834-6.00106-3 · Cited by 8

Serum hepcidin assay in 2011: where do we stand?

Delaby, C., & Beaumont, C. (2012) · Annales de biologie clinique · doi:10.1684/abc.2012.0725 · Cited by 8

Liver iron is a major regulator of hepcidin gene expression via BMP/SMAD pathway in a rat model of chronic renal failure under treatment with high r H u EPO doses

Ribeiro, S., Garrido, P., Fernandes, J. C., Rocha‐Pereira, P., Costa, E. M., Belo, L., Reis, F., & Santos‐Silva, A. (2016) · BioFactors · doi:10.1002/biof.1275 · Cited by 8

Disorders of iron overload

Paterson, A. C., & Pietrangelo, A. (2011) · Elsevier eBooks · doi:10.1016/b978-0-7020-3398-8.00005-2 · Cited by 9

Estrogen-Dependent Downregulation of Hepcidin Synthesis Induces Intracellular Iron Efflux in Cancer Cells In Vitro

Shafarin, J., Bajbouj, K., El-Serafi, A. T., Sandeep, D., & Hamad, M. A. (2016) · Biology and Medicine · doi:10.4172/0974-8369.1000356 · Cited by 8

Regulation of Iron Absorption and Distribution

Latunde-Dada, G. O., & Simpson, R. J. (2009) · Humana Press eBooks · doi:10.1007/978-1-59745-462-9_2 · Cited by 8

Iron metabolism in macrophages from HFE hemochromatosis patients

Jacolot, S., Yang, Y., Paitry, P., Férec, C., & Mura, C. (2010) · Molecular Genetics and Metabolism · doi:10.1016/j.ymgme.2010.07.010 · Cited by 8

The Role of Estrogen Signaling in Cellular Iron Metabolism in Pancreatic β Cells

Taneera, J., Ali, A., & Hamad, M. A. (2022) · Pancreas · doi:10.1097/mpa.0000000000001978 · Cited by 7

Research Translation and Personalized Medicine

Brugarolas, J. (2012) · Springer eBooks · doi:10.1007/978-1-4614-2400-0_8 · Cited by 7

AMP‐activated protein kinase α1 phosphorylates PHD2 to maintain systemic iron homeostasis

Wang, C., Zhang, W., Xu, W., Liu, Z., & Huang, K. (2022) · Clinical and Translational Medicine · doi:10.1002/ctm2.854 · Cited by 9

Hypoxia-inducible factor prolyl hydroxylase inhibitors for anaemia in maintenance dialysis: a meta-analysis

Wu, M., Zang, C., Ma, F., Chen, B., Liu, J., & Xu, Z. (2022) · Clinical and Experimental Nephrology · doi:10.1007/s10157-022-02263-4 · Cited by 7

Deficiency in hereditary hemorrhagic telangiectasia-associated Endoglin elicits hypoxia-driven heart failure in zebrafish

Lelièvre, E., Bureau, C., Bordat, Y., Frétaud, M., Langevin, C., Jopling, C., & Kissa, K. (2023) · Disease Models & Mechanisms · doi:10.1242/dmm.049488 · Cited by 7

Murine mutants in the study of systemic iron metabolism and its disorders: An update on recent advances

Bartnikas, T. B., Fleming, M. D., & Schmidt, P. J. (2012) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2012.01.011 · Cited by 7

Interrelationships between tissue iron status and erythropoiesis during postweaning development following neonatal iron deficiency in rats

Hegde, N. V., Unger, E. L., Jensen, G. L., Hankey, P. A., & Paulson, R. F. (2010) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00463.2010 · Cited by 7

Hypobaric hypoxia-mediated protein expression in plasma of susceptible & tolerant rats.

Kumar, S., Sharma, P., Bansal, A., Sharma, P. C., & Aggarwal, K. K. (2014) · Europe PMC (PubMed Central) · Cited by 7

Cellular and Molecular Defenses Against Hypoxia

Frede, S., & Fandrey, J. (2013) · Springer eBooks · doi:10.1007/978-1-4614-8772-2_2 · Cited by 8

Synthesis of cyanoaminopyridyl enaminoates for their fluorescent “turn off” response towards Fe( iii ) ions

Devi, L., Sasan, S., Changotra, A., & Kapoor, K. K. (2024) · New Journal of Chemistry · doi:10.1039/d4nj01359j · Cited by 6

Cardiomyocyte‐specific overexpression of FPN1 diminishes cardiac hypertrophy induced by chronic intermittent hypoxia

Song, J., Xu, S., Chen, Q., Gou, Y., Zhao, C., Jia, C., Liu, H., Zhang, Z., Li, B., Gao, Y., et al. (2024) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.18543 · Cited by 5

Toxicity of the iron siderophore mycobactin J in mouse macrophages: Evidence for a hypoxia response

McQueen, C. F., & Groves, J. T. (2021) · Journal of Inorganic Biochemistry · doi:10.1016/j.jinorgbio.2021.111669 · Cited by 6

Depletion of HIF-1α by Inducible Cre/loxP Increases the Sensitivity of Cultured Murine Hepatocytes to Ionizing Radiation in Hypoxia

Hamidi, A., Wolf, A., Dueva, R., Kaufmann, M., Göpelt, K., Iliakis, G. E., & Metzen, E. (2022) · Cells · doi:10.3390/cells11101671 · Cited by 6

New Players in Neuronal Iron Homeostasis: Insights from CRISPRi Studies

Bórquez, D. A., Castro, F. B. D., Núñez, M. T., & Urrutia, P. J. (2022) · Antioxidants · doi:10.3390/antiox11091807 · Cited by 6

Idiopathic erythrocytosis: a germline disease?

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