Pages that link to "Q24646911"
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The following pages link to Molecular basis of inherited microcytic anemia due to defects in iron acquisition or heme synthesis (Q24646911):
Displaying 50 items.
- Mitochondrial Atpif1 regulates haem synthesis in developing erythroblasts (Q24302493) (← links)
- Mechanistic and regulatory aspects of intestinal iron absorption (Q26861531) (← links)
- Involvement of free radicals in breast cancer (Q27027944) (← links)
- ZIP8 zinc transporter: indispensable role for both multiple-organ organogenesis and hematopoiesis in utero (Q27303845) (← links)
- Glycine and Folate Ameliorate Models of Congenital Sideroblastic Anemia (Q27936634) (← links)
- Differential Regulation of the Two Ferrochelatase Paralogues in Shewanella loihica PV-4 in Response to Environmental Stresses (Q28830039) (← links)
- Advances in metal-induced oxidative stress and human disease (Q29615581) (← links)
- Endogenous siderophore 2,5-dihydroxybenzoic acid deficiency promotes anemia and splenic iron overload in mice (Q33743674) (← links)
- Prion protein regulates iron transport by functioning as a ferrireductase (Q33744807) (← links)
- Is Erythrocyte Protoporphyrin a Better Single Screening Test for Iron Deficiency Compared to Hemoglobin or Mean Cell Volume in Children and Women? (Q33851851) (← links)
- Heme metabolism and erythropoiesis (Q33861359) (← links)
- Regulation of divalent metal transporter 1 (DMT1) non-IRE isoform by the microRNA Let-7d in erythroid cells. (Q34032172) (← links)
- Clinical and cytogenetic analysis of human anemias from Jammu region of Jammu and Kashmir state (Q34118831) (← links)
- Iron status predicts malaria risk in Malawian preschool children (Q34390939) (← links)
- Hepcidin-25, mean corpuscular volume, and ferritin as predictors of response to oral iron supplementation in hemodialysis patients (Q35003742) (← links)
- Four variants in transferrin and HFE genes as potential markers of iron deficiency anaemia risk: an association study in menstruating women. (Q35373128) (← links)
- Multivitamin and iron supplementation to prevent periconceptional anemia in rural tanzanian women: a randomized, controlled trial (Q35533039) (← links)
- The long history of iron in the Universe and in health and disease (Q35672646) (← links)
- Iron deficiency protects against severe Plasmodium falciparum malaria and death in young children (Q35845332) (← links)
- Aceruloplasminemia: a rare disease - diagnosis and treatment of two cases (Q36153657) (← links)
- Erythrocyte Catalase Activity in More Frequent Microcytic Hypochromic Anemia: Beta-Thalassemia Trait and Iron Deficiency Anemia (Q36191952) (← links)
- Preoperative mean corpuscular hemoglobin affecting long-term outcomes of hepatectomized patients with hepatocellular carcinoma (Q36523881) (← links)
- Non-invasive detection of iron deficiency by fluorescence measurement of erythrocyte zinc protoporphyrin in the lip. (Q36591261) (← links)
- Iron refractory iron deficiency anemia (Q36892562) (← links)
- An update on iron physiology. (Q37368713) (← links)
- Comparison study of oral iron preparations using a human intestinal model. (Q37401689) (← links)
- Molecular basis of hereditary iron homeostasis defects (Q37737808) (← links)
- Iron-deficiency anemia secondary to mutations in genes controlling hepcidin (Q37810273) (← links)
- Transition metal homeostasis: from yeast to human disease. (Q37863544) (← links)
- Knockout Mouse Models of Iron Homeostasis (Q37872758) (← links)
- β-Thalassemia trait association with autoimmune diseases: β-globin locus proximity to the immunity genes or role of hemorphins? (Q37906684) (← links)
- How I manage patients with atypical microcytic anaemia (Q38051401) (← links)
- Diagnosis of iron-deficient states (Q38566828) (← links)
- A novel type of congenital hypochromic anemia associated with a nonsense mutation in the STEAP3/TSAP6 gene (Q39451929) (← links)
- Application of mathematical modeling for the development and optimization formulation with bioactive copper complex (Q39573123) (← links)
- A mouse model of hereditary coproporphyria identified in an ENU mutagenesis screen (Q41440547) (← links)
- Erythropoietin-driven signaling ameliorates the survival defect of DMT1-mutant erythroid progenitors and erythroblasts (Q41538643) (← links)
- Anemia in children: prevalence, causes, diagnostic work-up, and long-term consequences (Q41986646) (← links)
- Ferroportin and Erythroid Cells: An Update (Q42026727) (← links)
- A novel hemizygous I418S mutation in the ALAS2 gene in a young Korean man with X-linked sideroblastic anemia (Q42415058) (← links)
- Diagnosis of iron deficiency anemia using density-based fractionation of red blood cells. (Q45949916) (← links)
- Dual-wavelength excitation for fluorescence-based quantification of zinc protoporphyrin IX and protoporphyrin IX in whole blood (Q46164287) (← links)
- Mechanism of Developmental Effects in Rats Caused by an N-Phenylimide Herbicide: Transient Fetal Anemia and Sequelae during Mid-to-Late Gestation (Q46597653) (← links)
- Diminished presentation of complement regulatory protein CD55 on red blood cells from patients with hereditary haemolytic anaemias. (Q47722339) (← links)
- Study of Glycine and Folic Acid Supplementation to Ameliorate Transfusion Dependence in Congenital SLC25A38 Mutated Sideroblastic Anemia (Q50246207) (← links)
- [Iron metabolism]. (Q53215770) (← links)
- Effect of heavy metal exposure on blood haemoglobin concentration and methemoglobin percentage in Lumbricus terrestris (Q58416071) (← links)
- Assessment of iron absorption in mice by ICP-MS measurements of 57Fe levels (Q59617576) (← links)
- Unveiling Active Constituents and Potential Targets Related to the Hematinic Effect of Steamed Panax notoginseng Using Network Pharmacology Coupled With Multivariate Data Analyses (Q60916613) (← links)
- Microcytosis in children and adolescents with the sickle cell trait in Basra, Iraq (Q64064182) (← links)