Pages that link to "Q28263309"
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The following pages link to HFE gene knockout produces mouse model of hereditary hemochromatosis (Q28263309):
Displaying 50 items.
- Association of HFE protein with transferrin receptor in crypt enterocytes of human duodenum (Q22001443) (← links)
- The hereditary hemochromatosis protein, HFE, specifically regulates transferrin-mediated iron uptake in HeLa cells (Q22009072) (← links)
- Alcoholic liver disease and hepatitis C: a frequently underestimated combination (Q22305502) (← links)
- Ca2 channel blockers reverse iron overload by a new mechanism via divalent metal transporter-1 (Q24296806) (← links)
- Co-localization of the mammalian hemochromatosis gene product (HFE) and a newly identified transferrin receptor (TfR2) in intestinal tissue and cells (Q24300212) (← links)
- Regulation of transferrin receptor 2 protein levels by transferrin (Q24301632) (← links)
- Hemojuvelin is essential for dietary iron sensing, and its mutation leads to severe iron overload (Q24312272) (← links)
- HFE association with transferrin receptor 2 increases cellular uptake of transferrin-bound iron (Q24312763) (← links)
- The WT hemochromatosis protein HFE inhibits CD8⁺ T-lymphocyte activation (Q24339411) (← links)
- Targeted mutagenesis of the murine transferrin receptor-2 gene produces hemochromatosis (Q24533580) (← links)
- Severe iron deficiency anemia in transgenic mice expressing liver hepcidin (Q24536163) (← links)
- Megalin-dependent cubilin-mediated endocytosis is a major pathway for the apical uptake of transferrin in polarized epithelia (Q24555135) (← links)
- Pathophysiology of hereditary hemochromatosis (Q24654441) (← links)
- Haemochromatosis (Q24685891) (← links)
- Iron overload favors the elimination of Leishmania infantum from mouse tissues through interaction with reactive oxygen and nitrogen species (Q27305261) (← links)
- Transferrin receptor is necessary for development of erythrocytes and the nervous system (Q28118509) (← links)
- Experimental hemochromatosis due to MHC class I HFE deficiency: immune status and iron metabolism (Q28137777) (← links)
- Increased p53 mutation load in nontumorous human liver of wilson disease and hemochromatosis: oxyradical overload diseases (Q28344887) (← links)
- Mechanisms of divalent metal toxicity in affective disorders (Q28384836) (← links)
- A mouse model of familial porphyria cutanea tarda (Q28507743) (← links)
- Transferrin receptor 2: continued expression in mouse liver in the face of iron overload and in hereditary hemochromatosis (Q28508392) (← links)
- Contribution of Hfe expression in macrophages to the regulation of hepatic hepcidin levels and iron loading (Q28512327) (← links)
- Ferroportin-1 is a 'nuclear'-negative acute-phase protein in rat liver: a comparison with other iron-transport proteins (Q28578052) (← links)
- Haemochromatosis protein is expressed on the terminal web of enterocytes in proximal small intestine of the rat (Q28581175) (← links)
- Hepcidin regulates ferroportin expression and intracellular iron homeostasis of erythroblasts (Q28585215) (← links)
- Mechanism of increased iron absorption in murine model of hereditary hemochromatosis: increased duodenal expression of the iron transporter DMT1 (Q28585417) (← links)
- Lack of hepcidin gene expression and severe tissue iron overload in upstream stimulatory factor 2 (USF2) knockout mice (Q28586797) (← links)
- HFE gene: Structure, function, mutations, and associated iron abnormalities. (Q30380172) (← links)
- Expression of hereditary hemochromatosis C282Y HFE protein in HEK293 cells activates specific endoplasmic reticulum stress responses (Q33291582) (← links)
- Global transcriptional response to Hfe deficiency and dietary iron overload in mouse liver and duodenum (Q33507280) (← links)
- Functions of nonclassical MHC and non-MHC-encoded class I molecules. (Q33536532) (← links)
- Cloning of the hereditary hemochromatosis gene: implications for pathogenesis, diagnosis, and screening (Q33540057) (← links)
- Hereditary haemochromatosis: diagnosis and management in the gene era. (Q33603907) (← links)
- Conservation and diversification of MHC class I and its related molecules in vertebrates (Q33630631) (← links)
- Iron overload: molecular clues to its cause (Q33632933) (← links)
- Metal ion transporters in mammals: structure, function and pathological implications (Q33663264) (← links)
- Inherited disorders of iron storage and transport (Q33739304) (← links)
- The hereditary hemochromatosis gene (HFE): a MHC class I-like gene that functions in the regulation of iron homeostasis (Q33784079) (← links)
- Hepatocyte-targeted HFE and TFR2 control hepcidin expression in mice (Q33806074) (← links)
- Human cytomegalovirus protein US2 interferes with the expression of human HFE, a nonclassical class I major histocompatibility complex molecule that regulates iron homeostasis (Q33848523) (← links)
- Taming the elephant: Salmonella biology, pathogenesis, and prevention (Q33877264) (← links)
- Hereditary hemochromatosis (Q33927510) (← links)
- Back to the fold: T cell recognition of HFE, a MHC class Ib molecule that regulates iron metabolism (Q33943959) (← links)
- The major histocompatibility complex-encoded HFE in iron homeostasis and immune function (Q34005737) (← links)
- Expression analysis of the yersiniabactin receptor gene fyuA and the heme receptor hemR of Yersinia enterocolitica in vitro and in vivo using the reporter genes for green fluorescent protein and luciferase (Q34009866) (← links)
- Regulation of transferrin-mediated iron uptake by HFE, the protein defective in hereditary hemochromatosis (Q34016565) (← links)
- Iron uptake from plasma transferrin by the duodenum is impaired in the Hfe knockout mouse. (Q34025772) (← links)
- Role of genetic testing and liver biopsy in the diagnosis of hemochromatosis (Q34027584) (← links)
- The ins and outs of bacterial iron metabolism (Q34055559) (← links)
- Hepatology in the new millennium. Advances in viral hepatitis, hepatic disorders, and liver transplantation (Q34057526) (← links)