[HTML][HTML] Evidence for a lack of a direct transcriptional suppression of the iron regulatory peptide hepcidin by hypoxia-inducible factors
M Volke, DP Gale, U Maegdefrau, G Schley, B Klanke… - PloS one, 2009 - journals.plos.org
Background Hepcidin is a major regulator of iron metabolism and plays a key role in anemia
of chronic disease, reducing intestinal iron uptake and release from body iron stores …
of chronic disease, reducing intestinal iron uptake and release from body iron stores …
Advances in understanding the mechanisms of erythropoiesis in homeostasis and disease
R Liang, S Ghaffari - British journal of haematology, 2016 - Wiley Online Library
Anaemia or decreased blood haemoglobin is the most common blood disorder often
characterized by reduced red blood cell (RBC) numbers. RBC s are produced from …
characterized by reduced red blood cell (RBC) numbers. RBC s are produced from …
Iron-sensing proteins that regulate hepcidin and enteric iron absorption
MD Knutson - Annual review of nutrition, 2010 - annualreviews.org
The human body cannot actively excrete excess iron. As a consequence, iron absorption
must be strictly regulated to ensure adequate iron uptake and prevent toxic iron …
must be strictly regulated to ensure adequate iron uptake and prevent toxic iron …
[PDF][PDF] Role of hepcidin in physiology and pathophysiology. Emerging experimental and clinical evidence.
M Wojciechowska, OW Wisniewski… - Journal of Physiology …, 2021 - jpp.krakow.pl
Normal iron metabolism is an inherent feature of maintaining homeostasis. There is a wide
range of iron disorders, which arise from iron deficiency or overload. In addition …
range of iron disorders, which arise from iron deficiency or overload. In addition …
Cellular iron transport
MD Garrick, LM Garrick - Biochimica et Biophysica Acta (BBA)-General …, 2009 - Elsevier
Iron has a split personality as an essential nutrient that also has the potential to generate
reactive oxygen species. We discuss how different cell types within specific tissues manage …
reactive oxygen species. We discuss how different cell types within specific tissues manage …
The molecular pathogenesis of hereditary hemochromatosis
JL Babitt, HY Lin - Seminars in liver disease, 2011 - thieme-connect.com
Hereditary hemochromatosis is a genetic disorder of iron overload. Over the past 15 years,
significant advances have been made in understanding the molecular pathogenesis of this …
significant advances have been made in understanding the molecular pathogenesis of this …
[HTML][HTML] Nutritional modulation of Hepcidin in the treatment of various anemic states
P D'Andrea, F Giampieri, M Battino - Nutrients, 2023 - mdpi.com
Twenty years after its discovery, hepcidin is still considered the main regulator of iron
homeostasis in humans. The increase in hepcidin expression drastically blocks the flow of …
homeostasis in humans. The increase in hepcidin expression drastically blocks the flow of …
iron disturbances in chronic liver diseases other than haemochromatosis–pathogenic, prognostic, and therapeutic implications
AJ Czaja - Alimentary Pharmacology & Therapeutics, 2019 - Wiley Online Library
Background Disturbances in iron regulation have been described in diverse chronic liver
diseases other than hereditary haemochromatosis, and iron toxicity may worsen liver injury …
diseases other than hereditary haemochromatosis, and iron toxicity may worsen liver injury …
Decreasing TfR1 expression reverses anemia and hepcidin suppression in β-thalassemic mice
H Li, T Choesang, W Bao, H Chen… - Blood, The Journal …, 2017 - ashpublications.org
Iron availability for erythropoiesis and its dysregulation in β-thalassemia are incompletely
understood. We previously demonstrated that exogenous apotransferrin leads to more …
understood. We previously demonstrated that exogenous apotransferrin leads to more …
Transferrin receptor 2 (Tfr2) genetic deletion makes transfusion‐independent a murine model of transfusion‐dependent β‐thalassemia
SM Di Modica, E Tanzi, V Olivari… - American Journal of …, 2022 - Wiley Online Library
Abstract β‐thalassemia is a genetic disorder caused by mutations in the β‐globin gene, and
characterized by anemia, ineffective erythropoiesis and iron overload. Patients affected by …
characterized by anemia, ineffective erythropoiesis and iron overload. Patients affected by …