18 results on '"Campagna, Dean R."'
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2. Hepcidin-Mediated Hypoferremia Disrupts Immune Responses to Vaccination and Infection
3. Congenital macrothrombocytopenia with focal myelofibrosis due to mutations in human G6b-B is rescued in humanized mice
4. A recurring mutation in the respiratory complex 1 protein NDUFB11 is responsible for a novel form of X-linked sideroblastic anemia
5. Analysis of novel sph (spherocytosis) alleles in mice reveals allele-specific loss of band 3 and adducin in α-spectrin–deficient red cells
6. hem6: an ENU-induced recessive hypochromic microcytic anemia mutation in the mouse
7. nm1054: a spontaneous, recessive, hypochromic, microcytic anemia mutation in the mouse
8. Normalizing hepcidin predicts TMPRSS6 mutation status in patients with chronic iron deficiency
9. The molecular defect in hypotransferrinemic mice
10. Congenital sideroblastic anemia due to mutations in the mitochondrial HSP70 homologue HSPA9
11. Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, and developmental delay (SIFD)
12. Identification of a Steap3 endosomal targeting motif essential for normal iron metabolism
13. A Novel Conditional Knockout of the Diamond Blackfan Anemia Gene Rpl11 Shows Failure of Erythropoiesis, a Marked Increase in BFU-E Progenitors By Phenotype That Proliferate Poorly in Culture, and Activation of p53 Target Genes
14. Rsp1 Is Indispensable for mRNA Stability during Erythroid Terminal Differentiation
15. Systematic Analysis of Known Candidate Genes in 58 Probands with Previously Uncharacterized Congenital Sideroblastic Anemia: Evidence for Genetic Heterogeneity and Identification of Novel Mutations in ALAS2 and PUS1
16. Response: What's in a name?
17. Identification and Characterization of an Erythrocyte Endosomal Ferrireductase Critical for Transferrin Dependent Iron Uptake.
18. X-Linked Gray Platelet Syndrome Due to a GATA1 Arg216Gln Mutation.
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