Nancy C. Andrews - Publications

Affiliations: 
Harvard University, Cambridge, MA, United States 
Area:
Molecular Biology, Genetics, Cell Biology

22 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2011 Chen W, Huang FW, de Renshaw TB, Andrews NC. Skeletal muscle hemojuvelin is dispensable for systemic iron homeostasis. Blood. 117: 6319-25. PMID 21493799 DOI: 10.1182/blood-2010-12-327957  0.76
2011 Finberg KE, Whittlesey RL, Andrews NC. Tmprss6 is a genetic modifier of the Hfe-hemochromatosis phenotype in mice. Blood. 117: 4590-9. PMID 21355094 DOI: 10.1182/blood-2010-10-315507  0.32
2010 Finberg KE, Whittlesey RL, Fleming MD, Andrews NC. Down-regulation of Bmp/Smad signaling by Tmprss6 is required for maintenance of systemic iron homeostasis. Blood. 115: 3817-26. PMID 20200349 DOI: 10.1182/blood-2009-05-224808  0.32
2009 Carlson ES, Tkac I, Magid R, O'Connor MB, Andrews NC, Schallert T, Gunshin H, Georgieff MK, Petryk A. Iron is essential for neuron development and memory function in mouse hippocampus. The Journal of Nutrition. 139: 672-9. PMID 19211831 DOI: 10.3945/jn.108.096354  0.32
2009 Li JY, Paragas N, Ned RM, Qiu A, Viltard M, Leete T, Drexler IR, Chen X, Sanna-Cherchi S, Mohammed F, Williams D, Lin CS, Schmidt-Ott KM, Andrews NC, Barasch J. Scara5 is a ferritin receptor mediating non-transferrin iron delivery. Developmental Cell. 16: 35-46. PMID 19154717 DOI: 10.1016/j.devcel.2008.12.002  0.4
2008 Finberg KE, Heeney MM, Campagna DR, Aydinok Y, Pearson HA, Hartman KR, Mayo MM, Samuel SM, Strouse JJ, Markianos K, Andrews NC, Fleming MD. Mutations in TMPRSS6 cause iron-refractory iron deficiency anemia (IRIDA). Nature Genetics. 40: 569-71. PMID 18408718 DOI: 10.1038/ng.130  0.32
2008 Wrighting DM, Andrews NC. Iron homeostasis and erythropoiesis. Current Topics in Developmental Biology. 82: 141-67. PMID 18282520 DOI: 10.1016/S0070-2153(07)00006-3  0.64
2007 Wang F, Paradkar PN, Custodio AO, McVey Ward D, Fleming MD, Campagna D, Roberts KA, Boyartchuk V, Dietrich WF, Kaplan J, Andrews NC. Genetic variation in Mon1a affects protein trafficking and modifies macrophage iron loading in mice. Nature Genetics. 39: 1025-32. PMID 17632513 DOI: 10.1038/ng2059  0.32
2007 Babitt JL, Huang FW, Xia Y, Sidis Y, Andrews NC, Lin HY. Modulation of bone morphogenetic protein signaling in vivo regulates systemic iron balance. The Journal of Clinical Investigation. 117: 1933-9. PMID 17607365 DOI: 10.1172/JCI31342  0.76
2007 Gardenghi S, Marongiu MF, Ramos P, Guy E, Breda L, Chadburn A, Liu Y, Amariglio N, Rechavi G, Rachmilewitz EA, Breuer W, Cabantchik ZI, Wrighting DM, Andrews NC, de Sousa M, et al. Ineffective erythropoiesis in beta-thalassemia is characterized by increased iron absorption mediated by down-regulation of hepcidin and up-regulation of ferroportin. Blood. 109: 5027-35. PMID 17299088 DOI: 10.1182/blood-2006-09-048868  0.64
2006 Wrighting DM, Andrews NC. Interleukin-6 induces hepcidin expression through STAT3. Blood. 108: 3204-9. PMID 16835372 DOI: 10.1182/blood-2006-06-027631  0.64
2006 Babitt JL, Huang FW, Wrighting DM, Xia Y, Sidis Y, Samad TA, Campagna JA, Chung RT, Schneyer AL, Woolf CJ, Andrews NC, Lin HY. Bone morphogenetic protein signaling by hemojuvelin regulates hepcidin expression. Nature Genetics. 38: 531-9. PMID 16604073 DOI: 10.1038/ng1777  0.76
2005 Gunshin H, Jin J, Fujiwara Y, Andrews NC, Mims M, Prchal J. Analysis of the E399D mutation in SLC11A2 (mutiple letters) Blood. 106: 2221-2222. PMID 16140868 DOI: 10.1182/blood-2005-03-1192  0.32
2005 Huang FW, Pinkus JL, Pinkus GS, Fleming MD, Andrews NC. A mouse model of juvenile hemochromatosis. The Journal of Clinical Investigation. 115: 2187-91. PMID 16075059 DOI: 10.1172/JCI25049  0.76
2005 Donovan A, Lima CA, Pinkus JL, Pinkus GS, Zon LI, Robine S, Andrews NC. The iron exporter ferroportin/Slc40a1 is essential for iron homeostasis. Cell Metabolism. 1: 191-200. PMID 16054062 DOI: 10.1016/j.cmet.2005.01.003  0.32
2005 Gunshin H, Starr CN, Direnzo C, Fleming MD, Jin J, Greer EL, Sellers VM, Galica SM, Andrews NC. Cybrd1 (duodenal cytochrome b) is not necessary for dietary iron absorption in mice. Blood. 106: 2879-83. PMID 15961514 DOI: 10.1182/blood-2005-02-0716  0.32
2005 Gunshin H, Fujiwara Y, Custodio AO, Direnzo C, Robine S, Andrews NC. Slc11a2 is required for intestinal iron absorption and erythropoiesis but dispensable in placenta and liver. The Journal of Clinical Investigation. 115: 1258-66. PMID 15849611 DOI: 10.1172/JCI24356  0.32
2004 Macedo MF, de Sousa M, Ned RM, Mascarenhas C, Andrews NC, Correia-Neves M. Transferrin is required for early T-cell differentiation. Immunology. 112: 543-9. PMID 15270724 DOI: 10.1111/j.1365-2567.2004.01915.x  0.4
2004 Huang FW, Rubio-Aliaga I, Kushner JP, Andrews NC, Fleming MD. Identification of a novel mutation (C321X) in HJV. Blood. 104: 2176-7. PMID 15138164 DOI: 10.1182/blood-2004-01-0400  0.76
2004 Roy CN, Custodio AO, de Graaf J, Schneider S, Akpan I, Montross LK, Sanchez M, Gaudino A, Hentze MW, Andrews NC, Muckenthaler MU. An Hfe-dependent pathway mediates hyposideremia in response to lipopolysaccharide-induced inflammation in mice. Nature Genetics. 36: 481-5. PMID 15098034 DOI: 10.1038/ng1350  0.32
2003 Ned RM, Swat W, Andrews NC. Transferrin receptor 1 is differentially required in lymphocyte development. Blood. 102: 3711-8. PMID 12881306 DOI: 10.1182/blood-2003-04-1086  0.4
2003 Muckenthaler M, Roy CN, Custodio AO, Miñana B, deGraaf J, Montross LK, Andrews NC, Hentze MW. Regulatory defects in liver and intestine implicate abnormal hepcidin and Cybrd1 expression in mouse hemochromatosis. Nature Genetics. 34: 102-7. PMID 12704390 DOI: 10.1038/ng1152  0.32
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