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Journal Articles

Understanding the Transferrin Receptor and Cellular Iron Deficiency Outside the Erythron

Nancy C. Andrews, MD PhD

Blood (2017) 130 (Supplement 1): SCI-42.

https://doi.org/10.1182/blood.V130.Suppl_1.SCI-42.SCI-42

Published: 2017

Journal Articles

Genetic Loss of Tmprss6 Increases Effective Erythropoiesis in a Mouse Model of β-Thalassemia

David B. Stagg, BS, Sara Gardenghi, PhD, Stefano Rivella, PhD, Nancy C. Andrews, MD, PhD, Karin E. Finberg, MD, PhD

Blood (2012) 120 (21): 482.

https://doi.org/10.1182/blood.V120.21.482.482

Published: 2012

Journal Articles

Skeletal muscle hemojuvelin is dispensable for systemic iron homeostasis

Wenjie Chen, Franklin W. Huang, Tomasa Barrientos de Renshaw, Nancy C. Andrews

Blood (2011) 117 (23): 6319–6325.

https://doi.org/10.1182/blood-2010-12-327957

Published: 2011

Includes: Supplemental data

Journal Articles

Tmprss6 is a genetic modifier of the Hfe -hemochromatosis phenotype in mice

Karin E. Finberg, Rebecca L. Whittlesey, Nancy C. Andrews

Blood (2011) 117 (17): 4590–4599.

https://doi.org/10.1182/blood-2010-10-315507

Published: 2011

Includes: Supplemental data

Journal Articles

Transferrin is a major determinant of hepcidin expression in hypotransferrinemic mice

Thomas B. Bartnikas, Nancy C. Andrews, Mark D. Fleming

Blood (2011) 117 (2): 630–637.

https://doi.org/10.1182/blood-2010-05-287359

Published: 2011

Includes: Supplemental data

Journal Articles

Hepcidin induction by transgenic overexpression of Hfe does not require the Hfe cytoplasmic tail, but does require hemojuvelin

Paul J. Schmidt, Nancy C. Andrews, Mark D. Fleming

Blood (2010) 116 (25): 5679–5687.

https://doi.org/10.1182/blood-2010-04-277954

Published: 2010

Includes: Supplemental data

Journal Articles

Tmprss6, An Inhibitor of Hepatic Bmp/Smad Signaling, Is Required for Hepcidin Suppression and Iron Loading In a Mouse Model of β-Thalassemia

Karin E. Finberg, MD, PhD, Rebecca L. Whittlesey, BS, Stefano Rivella, PhD, Nancy C. Andrews, MD, PhD

Blood (2010) 116 (21): 164.

https://doi.org/10.1182/blood.V116.21.164.164

Published: 2010

Journal Articles

The Serine Protease Tmprss6 Regulates Hepcidin Expression, but Its Loss Does Not Cause Systemic Iron Deficiency In the Fetal and Neonatal Periods

Ramsey M. Wehbe, B.S., Rebecca L. Whittlesey, B.S., Nancy C. Andrews, MD, PhD, Karin E. Finberg, MD, PhD

Blood (2010) 116 (21): 4258.

https://doi.org/10.1182/blood.V116.21.4258.4258

Published: 2010

Journal Articles

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

Sara Gardenghi, PhD, Pedro Ramos, Cindy N. Roy, PhD, Nancy C. Andrews, MD, PhD, Elizabeta Nemeth, PhD, Xiuli An, MD, PhD, Mohandas Narla, DSc, Yelena Ginzburg, MD, Eliezer A. Rachmilewitz, MD, Patricia Giardina, MD, Robert W Grady, Stefano Rivella, PhD

Blood (2010) 116 (21): 1009.

https://doi.org/10.1182/blood.V116.21.1009.1009

Published: 2010

Journal Articles

Proinflammatory state, hepcidin, and anemia in older persons

Luigi Ferrucci, Richard D. Semba, Jack M. Guralnik, William B. Ershler, Stefania Bandinelli, Kushang V. Patel, Kai Sun, Richard C. Woodman, Nancy C. Andrews, Robert J. Cotter, Tomas Ganz, Elizabeta Nemeth, Dan L. Longo

Blood (2010) 115 (18): 3810–3816.

https://doi.org/10.1182/blood-2009-02-201087

Published: 2010

Journal Articles

Down-regulation of Bmp/Smad signaling by Tmprss6 is required for maintenance of systemic iron homeostasis

Karin E. Finberg, Rebecca L. Whittlesey, Mark D. Fleming, Nancy C. Andrews

Blood (2010) 115 (18): 3817–3826.

https://doi.org/10.1182/blood-2009-05-224808

Published: 2010

Journal Articles

Tmprss6 Is a Genetic Modifier of the Hfe -Hemochromatosis Phenotype in Mice.

Karin E. Finberg, MD, PhD, Rebecca Whittlesey, B.S., Mark D. Fleming, MD, DPhil, Nancy C. Andrews, MD, PhD

Blood (2009) 114 (22): 625.

https://doi.org/10.1182/blood.V114.22.625.625

Published: 2009

Journal Articles

Inhibited Maturation of Ter119+CD71+ Erythroid Precursors in Mice with Chronic Sterile Abscess.

Olivier D. Prince, M.D., Ian C. Prince, Jeremy Walston, MD, Nancy C. Andrews, MD, PhD, Curt I. Civin, MD, Cindy N. Roy, PhD

Blood (2008) 112 (11): 3844.

https://doi.org/10.1182/blood.V112.11.3844.3844

Published: 2008

Journal Articles

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

Sara Gardenghi, PhD, Maria Franca Marongiu, Kristen Muirhead, Pedro Ramos, Cindy N. Roy, PhD, Nancy C. Andrews, MD, PhD, Elizabeta Nemeth, PhD, Antonia Follenzi, Eliezer Rachmilewitz, M.D, Patricia Giardina, MD, Robert W Grady, PhD, Stefano Rivella, PhD

Blood (2008) 112 (11): 128.

https://doi.org/10.1182/blood.V112.11.128.128

Published: 2008

Journal Articles

Hematopoietic-specific Stat5-null mice display microcytic hypochromic anemia associated with reduced transferrin receptor gene expression

Bing-Mei Zhu, Sara K. McLaughlin, Risu Na, Jie Liu, Yongzhi Cui, Cyril Martin, Akiko Kimura, Gertraud W. Robinson, Nancy C. Andrews, Lothar Hennighausen

Blood (2008) 112 (5): 2071–2080.

https://doi.org/10.1182/blood-2007-12-127480

Published: 2008

Includes: Supplemental data

Journal Articles

Forging a field: the golden age of iron biology

Nancy C. Andrews

Blood (2008) 112 (2): 219–230.

https://doi.org/10.1182/blood-2007-12-077388

Published: 2008

Journal Articles

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

Sara Gardenghi, Maria F. Marongiu, Pedro Ramos, Ella Guy, Laura Breda, Amy Chadburn, YiFang Liu, Ninette Amariglio, Gideon Rechavi, Eliezer A. Rachmilewitz, William Breuer, Z. Ioav Cabantchik, Diedra M. Wrighting, Nancy C. Andrews, Maria de Sousa, Patricia J. Giardina, Robert W. Grady, Stefano Rivella

Blood (2007) 109 (11): 5027–5035.

https://doi.org/10.1182/blood-2006-09-048868

Published: 2007

Includes: Supplemental data

Journal Articles

Of mice and iron: ferroportin disease

Nancy C. Andrews

Blood (2007) 109 (10): 4115.

https://doi.org/10.1182/blood-2007-02-075739

Published: 2007

Journal Articles

Hepcidin antimicrobial peptide transgenic mice exhibit features of the anemia of inflammation

Cindy N. Roy, Howard H. Mak, Imo Akpan, Grigoriy Losyev, David Zurakowski, Nancy C. Andrews

Blood (2007) 109 (9): 4038–4044.

https://doi.org/10.1182/blood-2006-10-051755

Published: 2007

Journal Articles

Hepcidin Expression Is Regulated by a Complex of Hemochromatosis-Associated Proteins.

Paul J. Schmidt, PhD, Franklin W. Huang, BA, Diedra M. Wrighting, BS, Paul T. Toran, BS, Nancy C. Andrews, MD, PhD

Blood (2006) 108 (11): 267.

https://doi.org/10.1182/blood.V108.11.267.267

Published: 2006

NARROW

Understanding the Transferrin Receptor and Cellular Iron Deficiency Outside the Erythron

Genetic Loss of Tmprss6 Increases Effective Erythropoiesis in a Mouse Model of β-Thalassemia

Skeletal muscle hemojuvelin is dispensable for systemic iron homeostasis

Tmprss6 is a genetic modifier of the Hfe -hemochromatosis phenotype in mice

Transferrin is a major determinant of hepcidin expression in hypotransferrinemic mice

Hepcidin induction by transgenic overexpression of Hfe does not require the Hfe cytoplasmic tail, but does require hemojuvelin

Tmprss6, An Inhibitor of Hepatic Bmp/Smad Signaling, Is Required for Hepcidin Suppression and Iron Loading In a Mouse Model of β-Thalassemia

The Serine Protease Tmprss6 Regulates Hepcidin Expression, but Its Loss Does Not Cause Systemic Iron Deficiency In the Fetal and Neonatal Periods

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

Proinflammatory state, hepcidin, and anemia in older persons

Down-regulation of Bmp/Smad signaling by Tmprss6 is required for maintenance of systemic iron homeostasis

Tmprss6 Is a Genetic Modifier of the Hfe -Hemochromatosis Phenotype in Mice.

Inhibited Maturation of Ter119+CD71+ Erythroid Precursors in Mice with Chronic Sterile Abscess.

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

Hematopoietic-specific Stat5-null mice display microcytic hypochromic anemia associated with reduced transferrin receptor gene expression

Forging a field: the golden age of iron biology

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

Of mice and iron: ferroportin disease

Hepcidin antimicrobial peptide transgenic mice exhibit features of the anemia of inflammation

Hepcidin Expression Is Regulated by a Complex of Hemochromatosis-Associated Proteins.

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American Society of Hematology

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American Society of Hematology

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