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Journal Articles

Neutropenia-Associated Mutations of PFAAP5, a Novel Protein Mediating Transcriptional Repressor Interaction between Gfi1 and Neutrophil Elastase.

Stephen J. Salipante, BS, Kathleen F. Benson, PhD, Richard E. Person, PhD, Raffaele Badolato, MD,PhD, Marshall S. Horwitz, MD, PhD

Blood (2006) 108 (11): 501.

https://doi.org/10.1182/blood.V108.11.501.501

Published: 2006

Journal Articles

Acquired Mutation and Reversion of the Neutrophil Elastase Gene, ELA2 , in Kostmann Syndrome and Cyclic Neutropenia Suggest that Some Mutations Cause Neutropenia while Others Paradoxically Suppress It.

Kathleen F. Benson, PhD, Kayleen Williams, BS, Joanna Luty, MD, Valeh Hadavi, MS, Roxana Kariminejad, MS, Mohammad H. Kariminejad, MD, PhD, Marshall Horwitz, MD, PhD

Blood (2004) 104 (11): 781.

https://doi.org/10.1182/blood.V104.11.781.781

Published: 2004

Journal Articles

Low levels of serum elastase are not associated with mutations in ELA-2 elastase encoding gene in chronic idiopathic neutropenia

Helen A. Papadaki, Marshall Horwitz, Stavroula A. Coulocheri, Richard A. Person, Kathleen F. Benson, George D. Eliopoulos

Blood (2003) 101 (7): 2898.

https://doi.org/10.1182/blood-2003-01-0015

Published: 2003

Journal Articles

Mice expressing a neutrophil elastase mutation derived from patients with severe congenital neutropenia have normal granulopoiesis

David S. Grenda, Sonja E. Johnson, Jill R. Mayer, Morgan L. McLemore, Kathleen F. Benson, Marshall Horwitz, Daniel C. Link

Blood (2002) 100 (9): 3221–3228.

https://doi.org/10.1182/blood-2002-05-1372

Published: 2002

Journal Articles

In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: implications for mechanisms of pathogenesis

Joëlle Michaud, Feng Wu, Motomi Osato, Gregory M. Cottles, Masatoshi Yanagida, Norio Asou, Katsuya Shigesada, Yoshiaki Ito, Kathleen F. Benson, Wendy H. Raskind, Colette Rossier, Stylianos E. Antonarakis, Sara Israels, Archie McNicol, Harvey Weiss, Marshall Horwitz, Hamish S. Scott

Blood (2002) 99 (4): 1364–1372.

https://doi.org/10.1182/blood.V99.4.1364

Published: 2002

Journal Articles

Mutations in the gene encoding neutrophil elastase in congenital and cyclic neutropenia

David C. Dale, Richard E. Person, Audrey Anna Bolyard, Andrew G. Aprikyan, Cindy Bos, Mary Ann Bonilla, Laurence A. Boxer, George Kannourakis, Cornelia Zeidler, Karl Welte, Kathleen F. Benson, Marshall Horwitz

Blood (2000) 96 (7): 2317–2322.

https://doi.org/10.1182/blood.V96.7.2317

Published: 2000

NARROW

Neutropenia-Associated Mutations of PFAAP5, a Novel Protein Mediating Transcriptional Repressor Interaction between Gfi1 and Neutrophil Elastase.

Acquired Mutation and Reversion of the Neutrophil Elastase Gene, ELA2 , in Kostmann Syndrome and Cyclic Neutropenia Suggest that Some Mutations Cause Neutropenia while Others Paradoxically Suppress It.

Low levels of serum elastase are not associated with mutations in ELA-2 elastase encoding gene in chronic idiopathic neutropenia

Mice expressing a neutrophil elastase mutation derived from patients with severe congenital neutropenia have normal granulopoiesis

In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: implications for mechanisms of pathogenesis

Mutations in the gene encoding neutrophil elastase in congenital and cyclic neutropenia

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ASH Publications

American Society of Hematology

Neutropenia-Associated Mutations of PFAAP5, a Novel Protein Mediating Transcriptional Repressor Interaction between Gfi1 and Neutrophil Elastase.

Acquired Mutation and Reversion of the Neutrophil Elastase Gene, ELA2 , in Kostmann Syndrome and Cyclic Neutropenia Suggest that Some Mutations Cause Neutropenia while Others Paradoxically Suppress It.

Low levels of serum elastase are not associated with mutations in ELA-2 elastase encoding gene in chronic idiopathic neutropenia

Mice expressing a neutrophil elastase mutation derived from patients with severe congenital neutropenia have normal granulopoiesis

In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: implications for mechanisms of pathogenesis

Mutations in the gene encoding neutrophil elastase in congenital and cyclic neutropenia

Email alerts

ASH Publications

American Society of Hematology

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