Reference health
Transferrin-a modulates hepcidin expression in zebrafish embryos
49/49 checkable references clean · checked 2026-07-23
Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.
4 without a DOI — not checked. A reference deposited without a DOI is never matched by title or guessed at; it stays outside the checked set, and this line discloses that.
The 49 checked references that resolve
resolves10.1073/pnas.95.3.1148
<i>Nramp</i>
<i>2</i>
is mutated in the anemic Belgrade (
<i>b</i>
) rat: Evidence of a role for Nramp2 in endosomal iron transport
resolves10.1016/S0021-9258(18)82413-9
Transferrin and the transferrin cycle in Belgrade rat reticulocytes
resolves10.1074/jbc.M908846199
Transferrin Receptor 2-α Supports Cell Growth Both in Iron-chelated Cultured Cells and in Vivo
resolves10.1074/jbc.C000664200
Comparison of the Interactions of Transferrin Receptor and Transferrin Receptor 2 with Transferrin and the Hereditary Hemochromatosis Protein HFE
resolves10.1126/science.1104742
Hepcidin Regulates Cellular Iron Efflux by Binding to Ferroportin and Inducing Its Internalization
resolves10.1172/JCI0215686
The gene encoding the iron regulatory peptide hepcidin is regulated by anemia, hypoxia, and inflammation
resolves10.1016/j.dci.2003.11.009
Organization and expression analysis of the zebrafish hepcidin gene, an antimicrobial peptide gene conserved among vertebrates
resolves10.1074/jbc.M008923200
A New Mouse Liver-specific Gene, Encoding a Protein Homologous to Human Antimicrobial Peptide Hepcidin, Is Overexpressed during Iron Overload
resolves10.1016/S0140-6736(03)12602-5
Disrupted hepcidin regulation in HFE -associated haemochromatosis and the liver as a regulator of body iron homoeostasis
resolves10.1038/ng1053
Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis
resolves10.1038/ng1274
Mutations in HFE2 cause iron overload in chromosome 1q–linked juvenile hemochromatosis
resolves10.1182/blood-2002-04-1169
The zebrafish mutant gene chardonnay (cdy) encodes divalent metal transporter 1 (DMT1)
resolves10.1242/dev.01540
The<i>chianti</i>zebrafish mutant provides a model for erythroid-specific disruption of<i>transferrin receptor 1</i>
resolves10.1038/35001596
Positional cloning of zebrafish ferroportin1 identifies a conserved vertebrate iron exporter
resolves10.1182/blood-2005-05-2049
The N-terminus of hepcidin is essential for its interaction with ferroportin: structure-function study
resolves10.1016/S0092-8674(00)80918-6
Positional Cloning Identifies Zebrafish one-eyed pinhead as a Permissive EGF-Related Ligand Required during Gastrulation
resolves10.1089/oli.1.1997.7.63
Morpholino and Phosphorothioate Antisense Oligomers Compared in Cell-Free and In-Cell Systems
resolves10.1002/1097-0061(200012)17:4<294::AID-YEA54>3.0.CO;2-5
Distinct Requirements for Zebrafish Angiogenesis Revealed by a<i>VEGF-A</i>Morphant
resolves10.1016/j.devcel.2004.12.001
Loss of Gata1 but Not Gata2 Converts Erythropoiesis to Myelopoiesis in Zebrafish Embryos
resolves10.1016/S0091-679X(04)77027-2
Spatial and Temporal Expression of the Zebrafish Genome by Large-Scale In Situ Hybridization Screening
resolves10.1242/dev.123.1.311
Characterization of zebrafish mutants with defects in embryonic hematopoiesis
resolves10.1093/hmg/ddm138
Huntingtin-deficient zebrafish exhibit defects in iron utilization and development
resolves10.1002/jez.1090
Developmental expression of cytochrome P450 aromatase genes (CYP19a and CYP19b) in zebrafish fry (<i>Danio rerio</i>)
resolves10.1002/dvdy.20032
Expression analyses of zebrafish <i>transferrin</i>, <i>ifabp</i>, and <i>elastaseB</i> mRNAs as differentiation markers for the three major endodermal organs: Liver, intestine, and exocrine pancreas
resolves10.1016/S0014-5793(03)00157-1
In vivo studies of liver‐type fatty acid binding protein (L‐FABP) gene expression in liver of transgenic zebrafish (<i>Danio rerio</i>)
resolves10.1177/002215540305100507
Co-localization of the Mammalian Hemochromatosis Gene Product (HFE) and a Newly Identified Transferrin Receptor (TfR2) in Intestinal Tissue and Cells
resolves10.1136/gut.51.5.648
Duodenal mRNA expression of iron related genes in response to iron loading and iron deficiency in four strains of mice
resolves10.1182/blood-2006-06-028787
Suppression of hepcidin during anemia requires erythropoietic activity
resolves10.1152/ajpregu.00673.2001
Influence of hypoxia and of hypoxemia on the development of cardiac activity in zebrafish larvae
resolves10.1038/sj.thj.6200063
Biochemical and genetic defects underlying human congenital hypotransferrinemia
resolves10.3324/haematol.11377
Effects of plasma transfusion on hepcidin production in human congenital hypotransferrinemia
resolves10.1203/01.PDR.0000049513.67410.2D
2002 E. Mead Johnson Award for Research in Pediatrics Lecture: The Molecular Biology of the Anemia of Chronic Disease: A Hypothesis
resolves10.1182/blood-2007-04-087593
Iron transferrin regulates hepcidin synthesis in primary hepatocyte culture through hemojuvelin and BMP2/4
resolves10.1053/j.gastro.2006.11.028
Targeted Disruption of the Hepatic Transferrin Receptor 2 Gene in Mice Leads to Iron Overload
resolves10.1074/jbc.C600197200
Hereditary Hemochromatosis Protein, HFE, Interaction with Transferrin Receptor 2 Suggests a Molecular Mechanism for Mammalian Iron Sensing
resolves10.1006/jmbi.2001.5048
Mutational analysis of the transferrin receptor reveals overlapping HFE and transferrin binding sites
resolves10.1186/1471-2164-6-152
A genome-wide survey of Major Histocompatibility Complex (MHC) genes and their paralogues in zebrafish
The 4 references without a DOI — listed, not checked
no DOI — not checkedThe Zebrafish Book: A Guide for the Laboratory Use of Zebrafish (Brachydanio rerio)
no DOI — not checkedStudies on familial hypotransferrinemia: unique clinical course and molecular pathology.
no DOI — not checkedHereditary hypotransferrinemia with hemosiderosis, a murine disorder resembling human atransferrinemia.
no DOI — not checkedHomozygosity for transferrin receptor-2 Y250X mutation induces early iron overload.
What this badge says. CiteStamped means the CHECKABLE references of this
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