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Journal Articles

RASA3 Is Essential for Early Mammalian Hematopoiesis and Modulates ERK Signaling in Terminal Erythropoiesis

Elena C. Brindley, BS, Raymond F. Robledo, PhD, Steven L. Ciciotte, MS, Joel H. Graber, PhD, Yue Zhao, Emily Hartman, BS, Julien Papoin, MS, Lionel Blanc, PhD, Luanne L. Peters, PhD

Blood (2019) 134 (Supplement_1): 3505.

https://doi.org/10.1182/blood-2019-130328

Published: 2019

Journal Articles

RASA3 Deficiency Contributes to Anemia By Multiple Mechanisms

Elena C. Brindley, BS, Emily Hartman, BS, Julien Papoin, MS, Brian Dulmovits, MS, Steven L. Ciciotte, MS, Luanne L. Peters, PhD, Lionel Blanc, PhD

Blood (2017) 130 (Supplement 1): 920.

https://doi.org/10.1182/blood.V130.Suppl_1.920.920

Published: 2017

Journal Articles

A Potential Role for Genes within the mTORC1 Pathway in the Regulation of Embryonic Globin Expression Revealed By ChIP-Seq, RNA-Seq and eQTL Mapping in the Nan Anemia Mouse Model

Danitza M. Nebor, PhD, Joel H. Graber, PhD, Kevin R. Gillinder, PhD, Melissa D. Ilsley, BSc, Raymond F. Robledo, PhD, Steven L. Ciciotte, MS, Vivek Philip, PhD, James J. Bieker, PhD, Andrew C Perkins, PhD, Luanne L. Peters, PhD

Blood (2017) 130 (Supplement 1): 2203.

https://doi.org/10.1182/blood.V130.Suppl_1.2203.2203

Published: 2017

Journal Articles

RASA3 Plays a Critical, Conserved Role in Erythroid Differentiation

Lionel Blanc, PhD, Steven L. Ciciotte, MS, Jeffrey Michael Lipton, MD, PhD, Johnson M. Liu, MD, Luanne L. Peters, PhD

Blood (2012) 120 (21): 3186.

https://doi.org/10.1182/blood.V120.21.3186.3186

Published: 2012

Journal Articles

Failure of Erythropoiesis and Megakaryocytopoiesis in RASA3 Mutant Scat Mice

Lionel Blanc, PhD, Babette Gwynn, MS, Steven L. Ciciotte, MS, Luanne L. Peters, PhD

Blood (2011) 118 (21): 680.

https://doi.org/10.1182/blood.V118.21.680.680

Published: 2011

Journal Articles

Positional Cloning of the Mouse Scat Mutation Reveals a Critical Role for RASA3, a Ras GTPase Activating Protein, in Vertebrate Erythropoiesis.

Luanne L. Peters, PhD, Steven L. Ciciotte, MS, E. Ricky Chan, Ph.D, Babette Gwynn, MS, Amy J. Lambert, BS, Eric L. Pierce, BS, Kathleen A. Soltis, BS, Mark D. Adams, PhD, Barry H. Paw, M.D., Ph.D.

Blood (2009) 114 (22): 776.

https://doi.org/10.1182/blood.V114.22.776.776

Published: 2009

Journal Articles

Targeted deletion of α-adducin results in absent β- and γ-adducin, compensated hemolytic anemia, and lethal hydrocephalus in mice

Raymond F. Robledo, Steven L. Ciciotte, Babette Gwynn, Kenneth E. Sahr, Diana M. Gilligan, Narla Mohandas, Luanne L. Peters

Blood (2008) 112 (10): 4298–4307.

https://doi.org/10.1182/blood-2008-05-156000

Published: 2008

Journal Articles

Targeted Deletion of γ-Adducin in Mice.

Kenneth E. Sahr, PhD, Amy J. Lambert, BS, Steven L. Ciciotte, MS, Luanne L. Peters, PhD

Blood (2007) 110 (11): 1723.

https://doi.org/10.1182/blood.V110.11.1723.1723

Published: 2007

Journal Articles

Targeted Deletion of α-Adducin Results in Absent β-Adducin, Compensated Hemolytic Anemia, and Hydrocephalus in Mice.

Raymond F. Robledo, PhD, Steven L. Ciciotte, MS, Babette Gwynn, MS, Kenneth E. Sahr, PhD, Diana M. Gilligan, MD, PhD, Luanne L. Peters, PhD

Blood (2007) 110 (11): 141.

https://doi.org/10.1182/blood.V110.11.141.141

Published: 2007

Journal Articles

Cappuccino, a mouse model of Hermansky-Pudlak syndrome, encodes a novel protein that is part of the pallidin-muted complex (BLOC-1)

Steven L. Ciciotte, Babette Gwynn, Kengo Moriyama, Marjan Huizing, William A. Gahl, Juan S. Bonifacino, Luanne L. Peters

Blood (2003) 101 (11): 4402–4407.

https://doi.org/10.1182/blood-2003-01-0020

Published: 2003

Journal Articles

Defects in the cappuccino ( cno ) gene on mouse chromosome 5 and human 4p cause Hermansky-Pudlak syndrome by an AP-3–independent mechanism

Babette Gwynn, Steven L. Ciciotte, Susan J. Hunter, Linda L. Washburn, Richard S. Smith, Sabra G. Andersen, Richard T. Swank, Esteban C. Dell'Angelica, Juan S. Bonifacino, Eva M. Eicher, Luanne L. Peters

Blood (2000) 96 (13): 4227–4235.

https://doi.org/10.1182/blood.V96.13.4227

Published: 2000

NARROW

RASA3 Is Essential for Early Mammalian Hematopoiesis and Modulates ERK Signaling in Terminal Erythropoiesis

RASA3 Deficiency Contributes to Anemia By Multiple Mechanisms

A Potential Role for Genes within the mTORC1 Pathway in the Regulation of Embryonic Globin Expression Revealed By ChIP-Seq, RNA-Seq and eQTL Mapping in the Nan Anemia Mouse Model

RASA3 Plays a Critical, Conserved Role in Erythroid Differentiation

Failure of Erythropoiesis and Megakaryocytopoiesis in RASA3 Mutant Scat Mice

Positional Cloning of the Mouse Scat Mutation Reveals a Critical Role for RASA3, a Ras GTPase Activating Protein, in Vertebrate Erythropoiesis.

Targeted deletion of α-adducin results in absent β- and γ-adducin, compensated hemolytic anemia, and lethal hydrocephalus in mice

Targeted Deletion of γ-Adducin in Mice.

Targeted Deletion of α-Adducin Results in Absent β-Adducin, Compensated Hemolytic Anemia, and Hydrocephalus in Mice.

Cappuccino, a mouse model of Hermansky-Pudlak syndrome, encodes a novel protein that is part of the pallidin-muted complex (BLOC-1)

Defects in the cappuccino ( cno ) gene on mouse chromosome 5 and human 4p cause Hermansky-Pudlak syndrome by an AP-3–independent mechanism

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American Society of Hematology

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American Society of Hematology

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