Karin E. Finberg, Ph.D.
Affiliations: | 2002 | Yale University, New Haven, CT |
Area:
GeneticsGoogle:
"Karin Finberg"Parents
Sign in to add mentorRichard P. Lifton | grad student | 2002 | Yale | |
(Genetic dissection of renal mechanisms of systemic pH homeostasis in man and mouse.) | ||||
Nancy C. Andrews | post-doc | 2007-2003 | Children's Hospital Boston / Harvard Medical School (Cell Biology Tree) |
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Publications
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Li X, Lozovatsky L, Sukumaran A, et al. (2020) NCOA4 is Regulated by HIF and Mediates Mobilization of Murine Hepatic Iron Stores After Blood Loss. Blood |
McKnight Q, Jenkins S, Li X, et al. (2020) IL-1β drives production of FGF-23 at the onset of chronic kidney disease in mice. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research |
Finberg KE. (2019) Going solo in iron transport. Blood. 134: 1363-1364 |
Xavier-Ferrucio J, Scanlon V, Li X, et al. (2019) Low Iron Promotes Megakaryocytic Commitment of Megakaryocytic-Erythroid Progenitors in Humans and Mice. Blood |
Stagg DB, Whittlesey RL, Li X, et al. (2019) Genetic loss of Tmprss6 alters terminal erythroid differentiation in a mouse model of β-thalassemia intermedia. Haematologica |
Li X, Lozovatsky L, Finberg KE. (2019) NCOA4 Expression in Hepatic Cells Is Upregulated Under Physiological and Pathophysiological Conditions Associated with Hypoxia Blood. 134: 431-431 |
Stewart T, Finberg K, Walther Z, et al. (2018) Yale Cancer Center Precision Medicine Tumor Board: one tumour, multiple targets. The Lancet. Oncology. 19: 1567-1568 |
Heeney MM, Guo D, De Falco L, et al. (2018) Normalizing hepcidin predicts mutation status in patients with chronic iron deficiency. Blood |
Li X, Lozovatsky L, Liu D, et al. (2018) NCOA4 Mediates Mobilization of Hepatic Iron Stores after Blood Loss Blood. 132: 1046-1046 |
Li X, Lozovatsky L, Sukumaran A, et al. (2017) The Tmprss6-/- Mouse Model of Iron Refractory Iron Deficiency Anemia (IRIDA) Exhibits Disrupted Phosphate Homeostasis, Elevated Circulating FGF23 Levels, and Increased Fgf23 Expression in Bone Marrow Blood. 130: 228-228 |