Sara Gardenghi

发表

Intestinal HIF2α promotes tissue-iron accumulation in disorders of iron overload with anemia

S. Rivella, S. Ramakrishnan, Bryce X. Bredell, 2013, Proceedings of the National Academy of Sciences.

Prospects for a hepcidin mimic to treat β-thalassemia and hemochromatosis

S. Rivella, N. Parrow, Sara Gardenghi, 2011, Expert review of hematology.

Hepcidin as a therapeutic tool to limit iron overload and improve anemia in β-thalassemic mice.

S. Rivella, N. Andrews, N. Mohandas, 2010, The Journal of clinical investigation.

Genetic loss of Tmprss6 alters terminal erythroid differentiation in a mouse model of β-thalassemia intermedia

S. Rivella, K. Finberg, Larisa Lozovatsky, 2019, Haematologica.

Exploring the Role of Hepcidin, an Antimicrobial and Iron Regulatory Peptide, in Increased Iron Absorption in β‐Thalassemia

S. Rivella, K. Adamsky, N. Amariglio, 2005, Annals of the New York Academy of Sciences.

Decreased hepcidin expression in murine β-thalassemia is associated with suppression of Bmp/Smad signaling.

S. Rivella, P. Ramos, R. Grady, 2012, Blood.

Down Regulation of Hepcidin and Haemojuvelin Expression in the Hepatocyte Cell-Line HepG2 Induced by Thalassaemic Sera.

S. Rivella, K. Adamsky, N. Amariglio, 2006 .

Therapeutic Hemoglobin Levels after Gene Transfer in β-Thalassemia Mice and in Hematopoietic Cells of β-Thalassemia and Sickle Cells Disease Patients

S. Rivella, L. Cartegni, R. Gambari, 2012, PloS one.

Macrophages support pathological erythropoiesis in Polycythemia Vera and Beta-Thalassemia

S. Rivella, B. Ebert, O. Abdel-Wahab, 2013, Nature Medicine.

HMGB1 Mediates Anemia of Inflammation in Murine Sepsis Survivors

S. Rivella, B. Volpe, K. Tracey, 2015, Molecular medicine.

Modified activin receptor IIB ligand trap mitigates ineffective erythropoiesis and disease complications in murine β-thalassemia.

S. Rivella, A. Grinberg, R. Suragani, 2014, Blood.

Reducing TMPRSS6 ameliorates hemochromatosis and β-thalassemia in mice.

S. Rivella, Shuling Guo, B. Monia, 2013, The Journal of clinical investigation.

A combined approach for β-thalassemia based on gene therapy-mediated adult hemoglobin (HbA) production and fetal hemoglobin (HbF) induction

S. Rivella, R. Gambari, M. Borgatti, 2012, Annals of Hematology.

Ineffective erythropoiesis in beta-thalassemia is characterized by increased iron absorption mediated by down-regulation of hepcidin and up-regulation of ferroportin.

Yi Fang Liu, S. Rivella, N. Andrews, 2006, Blood.

Anemia, ineffective erythropoiesis, and hepcidin: interacting factors in abnormal iron metabolism leading to iron overload in β-thalassemia.

S. Rivella, R. Grady, Sara Gardenghi, 2010, Hematology/oncology clinics of North America.

β-Thalassemia: HiJAKing Ineffective Erythropoiesis and Iron Overload

S. Rivella, L. Melchiori, Sara Gardenghi, 2010, Advances in hematology.

Surface Plasmon Resonance and Biosensor Technology for Real-Time Molecular Diagnosis of β°39 Thalassemia Mutation

R. Gambari, G. Feriotto, Giulia Breveglieri, 2012, Molecular Diagnosis.

Real-time multiplex analysis of four beta-thalassemia mutations employing surface plasmon resonance and biosensor technology

R. Gambari, A. Finotti, G. Breveglieri, 2004, Laboratory Investigation.

Hepcidin inhibits Smad3 phosphorylation in hepatic stellate cells by impeding ferroportin-mediated regulation of Akt

Ja Hyun Koo, S. Rivella, P. Strnad, 2016, Nature Communications.

Isocitrate ameliorates anemia by suppressing the erythroid iron restriction response.

S. Rivella, K. Tung, D. Kimpel, 2013, The Journal of clinical investigation.

Cranberry A-type proanthocyanidins selectively target acute myeloid leukemia cells.

S. Rivella, M. Guzman, D. Bezerra, 2019, Blood advances.

Distinct roles for hepcidin and interleukin-6 in the recovery from anemia in mice injected with heat-killed Brucella abortus.

S. Rivella, B. Sasu, C. Casu, 2014, Blood.

Enhanced erythropoiesis in Hfe-KO mice indicates a role for Hfe in the modulation of erythroid iron homeostasis.

S. Rivella, N. Van Rooijen, P. Ramos, 2011, Blood.

Iron metabolism and ineffective erythropoiesis in β‐thalassemia mouse models

S. Rivella, S. Gardenghi, P. Ramos, 2010, Annals of the New York Academy of Sciences.

Hepcidin and Hfe in iron overload in β‐thalassemia

S. Rivella, P. Ramos, R. Grady, 2010, Annals of the New York Academy of Sciences.

Increased Hepcidin Expression in Mice Affected by β-Thalassemia Reduces Iron Overload with No Effect on Anemia

S. Rivella, N. Andrews, E. Nemeth, 2008 .

Use of Jak2 Inhibitors to Limit Ineffective Erythropoiesis and Iron Absorption in Mice Affected by β-Thalassemia and Other Disorders of Red Cell Production.

S. Rivella, X. An, L. Melchiori, 2009 .

Treatment With Minihepcidin Peptide Improves Anemia and Iron Overload In a Mouse Model Of Thalassemia Intermedia

S. Rivella, T. Ganz, E. Nemeth, 2013 .

Hepcidin as a Therapeutic Tool to Limit Iron Overload and Improve Anemia In β-Thalassemia

S. Rivella, N. Andrews, X. An, 2010 .

Quantitation of Bt-176 maize genomic sequences by surface plasmon resonance-based biospecific interaction analysis of multiplex polymerase chain reaction (PCR).

Roberto Gambari, Nicoletta Bianchi, R. Gambari, 2003, Journal of agricultural and food chemistry.

Distinct roles for hepcidin and interleukin-6 in the recovery from anemia in mice injected with heat-killed Brucella abortus.

S. Rivella, B. Sasu, C. Casu, 2014, Blood.

Cranberry A

S. Rivella, M. Guzman, D. Bezerra, 2019 .

Enhanced erythropoiesis in Hfe-KO mice indicates a role for Hfe in the modulation of erythroid iron homeostasis.

S. Rivella, N. Van Rooijen, P. Ramos, 2011, Blood.

-Thalassemia: HiJAKing Ineffective Erythropoiesis and Iron Overload

S. Rivella, L. Melchiori, Sara Gardenghi, 2010 .