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Cited by 223

The DOI matches its Crossref record; 17 of the 17 references it cites were found in a registry or an index.

Hepcidin and Anemia: A Tight Relationship

Pagani, Alessia, Nai, Antonella, Silvestri, Laura, Camaschella, Clara·2019·Frontiers in Physiology
DOI 10.3389/fphys.2019.01294
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Citations

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Research works printed but not linked: 30

  1. An, 2012, TMPRSS6, but not TF, TFR2 or BMP2 variants are associated with increased risk of iron-deficiency anemia, Hum. Mol. Genet., 21, 2124, 10.1093/hmg/dds028 · DOI
  2. Beguin, 2003, Soluble transferrin receptor for the evaluation of erythropoiesis and iron status, Clin. Chim. Acta, 329, 9, 10.1016/S0009-8981(03)00005-6 · DOI · Paper page
  3. Camaschella, 2013, How I manage patients with atypical microcytic anaemia, Br. J. Haematol., 160, 12, 10.1111/bjh.12081 · DOI · Paper page
  4. Camaschella, 2019, Iron deficiency, Blood, 133, 30, 10.1182/blood-2018-05-815944 · DOI · Paper page
  5. Camaschella, 2018, Advances in understanding iron metabolism and its crosstalk with erythropoiesis, Br. J. Haematol., 182, 481, 10.1111/bjh.15403 · DOI
  6. Casu, 2018, Hepcidin agonists as therapeutic tools, Blood, 131, 1790, 10.1182/blood-2017-11-737411 · DOI
  7. De Falco, 2013, Iron refractory iron deficiency anemia, Haematologica, 98, 845, 10.3324/haematol.2012.075515 · DOI
  8. De Falco, 2014, Functional and clinical impact of novel TMPRSS6 variants in iron-refractory iron-deficiency anemia patients and genotype-phenotype studies, Hum. Mutat., 35, 1321, 10.1002/humu.22632 · DOI
  9. Donker, 2016, Iron refractory iron deficiency anemia: a heterogeneous disease that is not always iron refractory, Am. J. Hematol., 91, E482, 10.1002/ajh.24561 · DOI
  10. Du, 2008, The serine protease TMPRSS6 is required to sense iron deficiency, Science, 320, 1088, 10.1126/science.1157121 · DOI · Paper page
  11. Finberg, 2008, Mutations in TMPRSS6 cause iron-refractory iron deficiency anemia (IRIDA), Nat. Genet., 40, 569, 10.1038/ng.130 · DOI · Paper page
  12. Ganz, 2019, Anemia of inflammation, N. Engl. J. Med., 381, 1148, 10.1056/NEJMra1804281 · DOI · Paper page
  13. Gupta, 2018, Ineffective erythropoiesis: anemia and iron overload, Hematol. Oncol. Clin. North Am., 32, 213, 10.1016/j.hoc.2017.11.009 · DOI
  14. Heeney, 2014, Iron-refractory iron deficiency anemia (IRIDA), Hematol. Oncol. Clin. North Am., 28, 637, 10.1016/j.hoc.2014.04.009 · DOI
  15. Kovac, 2016, Anti-hemojuvelin antibody corrects anemia caused by inappropriately high hepcidin levels, Haematologica, 101, e173, 10.3324/haematol.2015.140772 · DOI · Paper page
  16. Lakhal, 2011, Regulation of type II transmembrane serine proteinase TMPRSS6 by hypoxia-inducible factors: new link between hypoxia signaling and iron homeostasis, J. Biol. Chem., 286, 4090, 10.1074/jbc.M110.173096 · DOI
  17. Meynard, 2009, Lack of the bone morphogenetic protein BMP6 induces massive iron overload, Nat. Genet., 41, 478, 10.1038/ng.320 · DOI · Paper page
  18. Pagani, 2017, A new form of IRIDA due to combined heterozygous mutations of TMPRSS6 and ACVR1A encoding the BMP receptor ALK2, Blood, 129, 3392, 10.1182/blood-2017-03-773481 · DOI
  19. Pagani, 2015, Regulation of cell surface transferrin receptor-2 by iron-dependent cleavage and release of a soluble form, Haematologica, 100, 458, 10.3324/haematol.2014.118521 · DOI
  20. Pasricha, 2017, Hepcidin is regulated by promoter-associated histone acetylation and HDAC3, Nat. Commun., 8, 403, 10.1038/s41467-017-00500-z · DOI
  21. Piga, 2019, Luspatercept improves hemoglobin levels and blood transfusion requirements in a study of patients with beta-thalassemia, Blood, 133, 1279, 10.1182/blood-2018-10-879247 · DOI · Paper page
  22. Rausa, 2015, Bmp6 expression in murine liver non parenchymal cells: a mechanism to control their high iron exporter activity and protect hepatocytes from iron overload?, PLoS One, 10, e0122696, 10.1371/journal.pone.0122696 · DOI
  23. Sheetz, 2019, Targeting the hepcidin-ferroportin pathway in anaemia of chronic kidney disease, Br. J. Clin. Pharmacol., 85, 935, 10.1111/bcp.13877 · DOI
  24. Shore, 2006, A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva, Nat. Genet., 38, 525, 10.1038/ng1783 · DOI · Paper page
  25. Silvestri, 2008, The serine protease matriptase-2 (TMPRSS6) inhibits hepcidin activation by cleaving membrane hemojuvelin, Cell Metab., 8, 502, 10.1016/j.cmet.2008.09.012 · DOI · Paper page
  26. Silvestri, 2013, How to assess causality of TMPRSS6 mutations?, Hum. Mutat., 34, 1043, 10.1002/humu.22321 · DOI
  27. Sonnweber, 2014, Hypoxia induced downregulation of hepcidin is mediated by platelet derived growth factor BB, Gut, 63, 1951, 10.1136/gutjnl-2013-305317 · DOI · Paper page
  28. Sorensen, 2019, Genetic factors influencing hemoglobin levels in 15,567 blood donors: results from the Danish blood donor study, Transfusion, 59, 226, 10.1111/trf.15075 · DOI
  29. Weinstein, 2002, Inappropriate expression of hepcidin is associated with iron refractory anemia: implications for the anemia of chronic disease, Blood, 100, 3776, 10.1182/blood-2002-04-1260 · DOI · Paper page
  30. Weiss, 2019, Anemia of inflammation, Blood, 133, 40, 10.1182/blood-2018-06-856500 · DOI · Paper page

Cited by

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Metadata

Authors
Pagani, A., Nai, A., Silvestri, L., & Camaschella, C.
Venue
Frontiers in Physiology
Publisher
Frontiers Media SA
Published
2019-10-09
Volume
10
ISSN
1664-042X
DOI
10.3389/fphys.2019.01294
Cited by
223
References
17
Licence
creativecommons.org/licenses/by/4.0/ (vor)

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.