| scholarly article | Q13442814 |
| P50 | author | James F Collins | Q89777144 |
| Michael D. Garrick | Q47796123 | ||
| P2093 | author name string | Xiaoyu Wang | |
| P2860 | cites work | The multicopper ferroxidase hephaestin enhances intestinal iron absorption in mice | Q21132022 |
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| Hepcidin as a therapeutic tool to limit iron overload and improve anemia in β-thalassemic mice | Q24633423 | ||
| The flatiron mutation in mouse ferroportin acts as a dominant negative to cause ferroportin disease | Q24678328 | ||
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| Animal models of β-hemoglobinopathies: utility and limitations | Q28067142 | ||
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| Congenital atransferrinemia in a 7-year-old girl | Q28189442 | ||
| Microcytic anaemia mice have a mutation in Nramp2, a candidate iron transporter gene | Q28244982 | ||
| Cloning and characterization of a mammalian proton-coupled metal-ion transporter | Q28245045 | ||
| HFE gene knockout produces mouse model of hereditary hemochromatosis | Q28263309 | ||
| The iron exporter ferroportin/Slc40a1 is essential for iron homeostasis | Q28264540 | ||
| Decreased hephaestin activity in the intestine of copper-deficient mice causes systemic iron deficiency | Q28307150 | ||
| Conditional knockout of the Menkes disease copper transporter demonstrates its critical role in embryogenesis | Q28482175 | ||
| Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformation | Q28505378 | ||
| Phenotypic and genetic characterization of the Atp7a(Mo-Tohm) mottled mouse: a new murine model of Menkes disease | Q28507137 | ||
| Slc11a2 is required for intestinal iron absorption and erythropoiesis but dispensable in placenta and liver | Q28509001 | ||
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| Anti-interleukin 6 (IL-6) receptor antibody suppresses Castleman's disease like symptoms emerged in IL-6 transgenic mice | Q73118585 | ||
| Mutation analysis provides additional proof that mottled is the mouse homologue of Menkes' disease | Q73331948 | ||
| Concentration of iron and distribution of iron and transferrin after experimental iron overload in rat tissues in vivo: study of the liver, the spleen, the central nervous system and other organs | Q73447340 | ||
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| Novel erythropoiesis stimulating protein (darbepoetin alfa) alleviates anemia associated with chronic inflammatory disease in a rodent model | Q74622789 | ||
| Long-term sequelae of HFE deletion in C57BL/6 x 129/O1a mice, an animal model for hereditary haemochromatosis | Q74641886 | ||
| TNF-independent development of transient anemia of chronic disease in a mouse model of protracted septic peritonitis | Q75201824 | ||
| Iron and zinc interactions in humans | Q77077915 | ||
| Effects of prolonged iron loading in the rat using both parenteral and dietary routes | Q78001062 | ||
| Reticulocyte indices in a canine model of nutritional iron deficiency | Q79750465 | ||
| Ctr1 drives intestinal copper absorption and is essential for growth, iron metabolism, and neonatal cardiac function | Q80206847 | ||
| A humanized mouse model for a common beta0-thalassemia mutation | Q81551600 | ||
| Repletion of copper-deficient rats with dietary copper restores duodenal hephaestin protein and iron absorption | Q81690773 | ||
| Antihepcidin antibody treatment modulates iron metabolism and is effective in a mouse model of inflammation-induced anemia | Q82417395 | ||
| Animal models of Wilson disease | Q87856800 | ||
| Hemochromatosis: Evaluation of the dietary iron model and regulation of hepcidin | Q88647676 | ||
| Copper deficiency anemia: review article | Q89357296 | ||
| Copper supplementation reverses dietary iron overload-induced pathologies in mice | Q89362259 | ||
| Intestinal hephaestin potentiates iron absorption in weanling, adult, and pregnant mice under physiological conditions | Q89777147 | ||
| Oral Gavage of Ginger Nanoparticle-Derived Lipid Vectors Carrying Dmt1 siRNA Blunts Iron Loading in Murine Hereditary Hemochromatosis | Q91322260 | ||
| Molecular basis of the brindled mouse mutant (Mo(br)): a murine model of Menkes disease | Q28513437 | ||
| Maternal iron and zinc supplementation during pregnancy affects body weight and iron status in rat pups at weaning | Q28565476 | ||
| The LEC rat has a deletion in the copper transporting ATPase gene homologous to the Wilson disease gene | Q28575487 | ||
| Lack of hepcidin gene expression and severe tissue iron overload in upstream stimulatory factor 2 (USF2) knockout mice | Q28586797 | ||
| A mouse model for beta 0-thalassemia | Q28587408 | ||
| Targeted disruption of the hepcidin 1 gene results in severe hemochromatosis | Q28588832 | ||
| A mouse model of anemia of inflammation: complex pathogenesis with partial dependence on hepcidin | Q28590264 | ||
| Mouse models of human disease: An evolutionary perspective | Q28602393 | ||
| A novel rat model of hereditary hemochromatosis due to a mutation in transferrin receptor 2 | Q28709084 | ||
| Genomic responses in mouse models poorly mimic human inflammatory diseases | Q29547718 | ||
| The gene encoding the iron regulatory peptide hepcidin is regulated by anemia, hypoxia, and inflammation | Q29620394 | ||
| Urinary hepcidin in congenital chronic anemias | Q33368894 | ||
| Of mice and men, metals and mutations. | Q33672527 | ||
| Anemic copper-deficient rats, but not mice, display low hepcidin expression and high ferroportin levels | Q33727943 | ||
| Mouse model of human beta zero thalassemia: targeted deletion of the mouse beta maj- and beta min-globin genes in embryonic stem cells | Q33895206 | ||
| Iron overload exacerbates age-associated cardiac hypertrophy in a mouse model of hemochromatosis | Q33916265 | ||
| Hereditary hemochromatosis: pathogenesis, diagnosis, and treatment | Q34120394 | ||
| Spontaneous hepatic copper accumulation in Long-Evans Cinnamon rats with hereditary hepatitis. A model of Wilson's disease | Q34190413 | ||
| The effects of the anti-hepcidin Spiegelmer NOX-H94 on inflammation-induced anemia in cynomolgus monkeys | Q34324354 | ||
| Hepcidin-dependent and hepcidin-independent regulation of erythropoiesis in a mouse model of anemia of chronic inflammation | Q34356512 | ||
| Anemia of chronic disease. | Q34401570 | ||
| CRISPR/Cas9 for genome editing: progress, implications and challenges. | Q34411191 | ||
| Mouse strain differences determine severity of iron accumulation in Hfe knockout model of hereditary hemochromatosis | Q34486746 | ||
| Erythroferrone contributes to hepcidin suppression and iron overload in a mouse model of β-thalassemia | Q34489655 | ||
| Copper deficiency leads to anemia, duodenal hypoxia, upregulation of HIF-2α and altered expression of iron absorption genes in mice | Q34651491 | ||
| Molecular and biochemical characterization of Mottled-dappled, an embryonic lethal Menkes disease mouse model | Q34657353 | ||
| Diet-induced iron deficiency anemia and pregnancy outcome in rhesus monkeys | Q34974658 | ||
| Tmprss6 is a genetic modifier of the Hfe-hemochromatosis phenotype in mice | Q34997731 | ||
| DMT1: a mammalian transporter for multiple metals | Q35061952 | ||
| Protracted anemia associated with chronic, relapsing systemic inflammation induced by arthropathic peptidoglycan-polysaccharide polymers in rats | Q35094248 | ||
| Pharmacologic inhibition of hepcidin expression reverses anemia of chronic inflammation in rats | Q35525651 | ||
| First phenotypic description of transferrin receptor 2 knockout mouse, and the role of hepcidin. | Q35597655 | ||
| Gestational-neonatal iron deficiency suppresses and iron treatment reactivates IGF signaling in developing rat hippocampus | Q35780769 | ||
| Nramp2 is mutated in the anemic Belgrade (b) rat: evidence of a role for Nramp2 in endosomal iron transport. | Q35796864 | ||
| Hereditary iron deficiency: X-linked anaemia (sla) in newborn and suckling mice | Q44937943 | ||
| The influence of high iron diet on rat lung manganese absorption | Q45297352 | ||
| Humanized beta-thalassemia mouse model containing the common IVSI-110 splicing mutation | Q45855327 | ||
| A humanized BAC transgenic/knockout mouse model for HbE/beta-thalassemia | Q45857661 | ||
| Not all DMT1 mutations lead to iron overload. | Q45954384 | ||
| Murine models of anaemia of inflammation: extramedullary haematopoiesis represents a species specific difference to human anaemia of inflammation that can be eliminated by splenectomy. | Q46021638 | ||
| Consumption of a High-Iron Diet Disrupts Homeostatic Regulation of Intestinal Copper Absorption in Adolescent Mice | Q46349398 | ||
| Comeback of the Rat in Biomedical Research. | Q46420544 | ||
| Phlebotomies or erythropoietin injections allow mobilization of iron stores in a mouse model mimicking intensive care anemia | Q46457023 | ||
| A mutation in the TMPRSS6 gene, encoding a transmembrane serine protease that suppresses hepcidin production, in familial iron deficiency anemia refractory to oral iron | Q46500049 | ||
| A new strain of rat for functional analysis of PINA. | Q46541242 | ||
| Membrane-bound serine protease matriptase-2 (Tmprss6) is an essential regulator of iron homeostasis | Q46560159 | ||
| Differences in the effect of iron-deficient diet on tissue weight, hemoglobin concentration and serum triglycerides in Fischer-344, Sprague-Dawley and Wistar rats | Q47255507 | ||
| Influence of Level of Dietary Copper on Weight Gain, Hematology and Liver Copper and Iron Storage of Young Pigs | Q47367841 | ||
| A fully human anti-hepcidin antibody modulates iron metabolism in both mice and nonhuman primates | Q47779816 | ||
| The toxic milk mouse is a murine model of Wilson disease | Q48059534 | ||
| Clinico-pathological study on macular mutant mouse | Q48233201 | ||
| Brain Iron: Persistent Deficiency following Short-term Iron Deprivation in the Young Rat | Q48437097 | ||
| Mutation analysis and expression of the mottled gene in the macular mouse model of Menkes disease | Q48621638 | ||
| Iron deficiency anemia reduces thyroid peroxidase activity in rats | Q48629309 | ||
| A role for divalent metal transporter (DMT1) in mitochondrial uptake of iron and manganese | Q49481733 | ||
| Nutritional Iron Deficiency as a Determinant of Host Resistance in the Rat | Q50232696 | ||
| Mild maternal iron deficiency anemia during pregnancy and lactation in guinea pigs causes abnormal auditory function in the offspring. | Q50433807 | ||
| Pregnancy and maternal iron deficiency stimulate hepatic CRBPII expression in rats. | Q50515983 | ||
| Anemia in monkey collagen-induced arthritis is correlated with serum IL-6, but not TNFalpha. | Q50657758 | ||
| Signs of iron deficiency in copper-deficient rats are not affected by iron supplements administered by diet or by injection. | Q50731441 | ||
| Regulation of iron homeostasis in anemia of chronic disease and iron deficiency anemia: diagnostic and therapeutic implications. | Q51764368 | ||
| Growth in iron-deficient rats. | Q52913960 | ||
| Analysis of IL-22 contribution to hepcidin induction and hypoferremia during the response to LPS in vivo. | Q54433904 | ||
| Liver expression of hepcidin and other iron genes in two mouse models of beta-thalassemia. | Q54578246 | ||
| Anemia of inflammation | Q58605178 | ||
| Constitutive hepcidin expression prevents iron overload in a mouse model of hemochromatosis | Q59512864 | ||
| Kupffer cells and macrophages are not required for hepatic hepcidin activation during iron overload | Q61638660 | ||
| Iron homeostasis in beta-thalassemic mice | Q69418039 | ||
| Pathology of dietary carbonyl iron overload in rats | Q69452056 | ||
| Tissue iron deposition in untransfused beta-thalassemic mice | Q69598979 | ||
| Hepatic zinc in hemochromatosis | Q70168221 | ||
| A mouse model for β-thalassemia | Q70168656 | ||
| Hepatic lipid peroxidation in vivo in rats with chronic dietary iron overload is dependent on hepatic iron concentration | Q71223059 | ||
| Development of a rat model for iron deficiency and toxicological studies: comparison among Fischer 344, Wistar, and Sprague Dawley strains | Q71518325 | ||
| Induction of dietary iron deficiency in rhesus monkeys: sequential changes in serum ferritin and other biochemical indicators of iron status | Q72123709 | ||
| Contrasting effects of a dietary copper deficiency in male and female mice | Q72242817 | ||
| Transferrin and the transferrin cycle in Belgrade rat reticulocytes | Q72816717 | ||
| Manifestation of iron deficiency at various levels of dietary iron intake | Q72843854 | ||
| Dietary iron intake modulates the activity of iron regulatory proteins and the abundance of ferritin and mitochondrial aconitase in rat liver | Q73087930 | ||
| Hepcidin antimicrobial peptide transgenic mice exhibit features of the anemia of inflammation | Q35804433 | ||
| Hepcidin in iron overload disorders | Q35847742 | ||
| High-Iron Consumption Impairs Growth and Causes Copper-Deficiency Anemia in Weanling Sprague-Dawley Rats | Q36106775 | ||
| Intestinal DMT1 is critical for iron absorption in the mouse but is not required for the absorption of copper or manganese | Q36174536 | ||
| Deletion of TMPRSS6 attenuates the phenotype in a mouse model of β-thalassemia. | Q36185297 | ||
| Lethal thalassemia after insertional disruption of the mouse major adult beta-globin gene | Q36225015 | ||
| Iron deficiency anemia and affective response in rhesus monkey infants | Q36236423 | ||
| Late stage erythroid precursor production is impaired in mice with chronic inflammation | Q36366570 | ||
| Modeling the dynamics of mouse iron body distribution: hepcidin is necessary but not sufficient | Q36375897 | ||
| The Menkes and Wilson disease genes counteract in copper toxicosis in Labrador retrievers: a new canine model for copper-metabolism disorders | Q36506584 | ||
| Copper deficient rats and mice both develop anemia but only rats have lower plasma and brain iron levels | Q36542528 | ||
| Effect of dietary iron on fetal growth in pregnant mice | Q36761997 | ||
| A cytosolic iron chaperone that delivers iron to ferritin. | Q36826647 | ||
| Compromised zinc status of experimental rats as a consequence of prolonged iron & calcium supplementation | Q36876796 | ||
| Minihepcidin peptides as disease modifiers in mice affected by β-thalassemia and polycythemia vera | Q37097115 | ||
| Humanized Mouse Model of Cooley's Anemia | Q37099192 | ||
| The pig as an experimental model for elucidating the mechanisms governing dietary influence on mineral absorption | Q37137193 | ||
| Animal models of anemia of inflammation | Q37371412 | ||
| The Regulation of Iron Absorption and Homeostasis | Q37543492 | ||
| Change in serum ferritin concentration in experimentally induced anemia of chronic inflammation in dogs | Q37618325 | ||
| Optimal management of β thalassaemia intermedia. | Q37830724 | ||
| Intestinal brush-border Na+/H+ exchanger-3 drives H+-coupled iron absorption in the mouse. | Q39622458 | ||
| Distinct Wilson's disease mutations in ATP7B are associated with enhanced binding to COMMD1 and reduced stability of ATP7B. | Q40071443 | ||
| Liver iron concentrations and urinary hepcidin in beta-thalassemia | Q40214945 | ||
| Characterization of ferroptosis in murine models of hemochromatosis. | Q40333897 | ||
| Dietary hemoglobin rescues young piglets from severe iron deficiency anemia: Duodenal expression profile of genes involved in heme iron absorption. | Q41042635 | ||
| A common human beta globin splicing mutation modeled in mice. | Q41052265 | ||
| Characterizing the molecular phenotype of an Atp7a(T985I) conditional knock in mouse model for X-linked distal hereditary motor neuropathy (dHMNX). | Q41626358 | ||
| Similar splicing mutations of the Menkes/mottled copper-transporting ATPase gene in occipital horn syndrome and the blotchy mouse. | Q41863725 | ||
| PCBP1 and NCOA4 regulate erythroid iron storage and heme biosynthesis | Q42058946 | ||
| Mutation in the CPC motif-containing 6th transmembrane domain affects intracellular localization, trafficking and copper transport efficiency of ATP7A protein in mosaic mutant mice--an animal model of Menkes disease | Q42723820 | ||
| Rats! | Q43137072 | ||
| Phenotypic diversity of Menkes disease in mottled mice is associated with defects in localisation and trafficking of the ATP7A protein | Q43232414 | ||
| Iron overload can induce mild copper deficiency | Q43632788 | ||
| Maternal iron deficiency identifies critical windows for growth and cardiovascular development in the rat postimplantation embryo | Q44195375 | ||
| A Possible Role of Copper in the Regulation of Heme Biosynthesis Through Ferrochelatase | Q44205034 | ||
| Differences in activation of mouse hepcidin by dietary iron and parenterally administered iron dextran: compartmentalization is critical for iron sensing | Q44320542 | ||
| Diminished iron acquisition by cells and tissues of Belgrade laboratory rats | Q44433031 | ||
| P433 | issue | 12 | |
| P304 | page(s) | 2085-2100 | |
| P577 | publication date | 2019-12-01 | |
| P1433 | published in | Journal of Nutrition | Q3186931 |
| P1476 | title | Animal Models of Normal and Disturbed Iron and Copper Metabolism | |
| P478 | volume | 149 |
| Q92095854 | Identification of The Canidae Iron Regulatory Hormone Hepcidin | cites work | P2860 |
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