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Journal Articles

Deletion of Sbds from Hematopoietic Progenitors Causes Neutropenia in a Mouse Model of Shwachman-Diamond Syndrome By Specifically Blocking Myeloid Lineage Progression at Late Differentiation Stages

Noemi A. Zambetti, Paulina M.H. Van Strien, Marijke G. Valkhof, Maria N. Adisty, Eric M. J. Bindels, PhD, Remco M. Hoogenboezem, Mathijs A. Sanders, MSc, Johanna M. Rommens, PhD, Ivo P. Touw, PhD, Marc H.G.P. Raaijmakers, MD PhD

Blood (2014) 124 (21): 355.

https://doi.org/10.1182/blood.V124.21.355.355

Published: 2014

Journal Articles

Lessons from the Mouse Model

Johanna M. Rommens, PhD, Marina E. Tourlakis, MSc, Holly Liu, BSc, Rikesh Gandhi, MSc, Peter R. Durie, MD

Blood (2013) 122 (21): SCI-35.

https://doi.org/10.1182/blood.V122.21.SCI-35.SCI-35

Published: 2013

Journal Articles

Quebec Platelet Disorder Is Caused by a Cis-Acting Mutation near the Plasminogen Activator Gene (PLAU) That Increases PLAU Transcription by Megakaryocytes.

Maria Diamandis, Andrew D Paterson, PhD, Johanna M Rommens, PhD, D. Kika Veljkovic, MD, Jessica Blavignac, John S Waye, PhD, Francine Derome, Georges E. Rivard, MD, Catherine PM Hayward, MD, PhD

Blood (2008) 112 (11): 3394.

https://doi.org/10.1182/blood.V112.11.3394.3394

Published: 2008

Journal Articles

Sbds Deficient Neutrophils Exhibit Normal Numbers, Chemotaxis and Phagocytic Functions, but Impaired NADPH Oxidase Activity.

Siyi Zhang, MSc, Chunxian Sun, MSc, Jian Zhong, BSc, Michael Glogauer, DDS,PhD, Johanna M. Rommens, PhD

Blood (2006) 108 (11): 1634.

https://doi.org/10.1182/blood.V108.11.1634.1634

Published: 2006

Journal Articles

Mouse Model for Shwachman-Diamond Syndrome with the R126T Disease Mutation Leads to Severe Growth and Developmental Deficiencies with Impairment of Hematopoiesis.

Siyi Zhang, MSc, Jian Zhong, BSc, Olga I. Gan, PhD, John E. Dick, PhD, Johanna M. Rommens, PhD

Blood (2006) 108 (11): 1283.

https://doi.org/10.1182/blood.V108.11.1283.1283

Published: 2006

NARROW

Deletion of Sbds from Hematopoietic Progenitors Causes Neutropenia in a Mouse Model of Shwachman-Diamond Syndrome By Specifically Blocking Myeloid Lineage Progression at Late Differentiation Stages

Lessons from the Mouse Model

Quebec Platelet Disorder Is Caused by a Cis-Acting Mutation near the Plasminogen Activator Gene (PLAU) That Increases PLAU Transcription by Megakaryocytes.

Sbds Deficient Neutrophils Exhibit Normal Numbers, Chemotaxis and Phagocytic Functions, but Impaired NADPH Oxidase Activity.

Mouse Model for Shwachman-Diamond Syndrome with the R126T Disease Mutation Leads to Severe Growth and Developmental Deficiencies with Impairment of Hematopoiesis.

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ASH Publications

American Society of Hematology

Deletion of Sbds from Hematopoietic Progenitors Causes Neutropenia in a Mouse Model of Shwachman-Diamond Syndrome By Specifically Blocking Myeloid Lineage Progression at Late Differentiation Stages

Lessons from the Mouse Model

Quebec Platelet Disorder Is Caused by a Cis-Acting Mutation near the Plasminogen Activator Gene (PLAU) That Increases PLAU Transcription by Megakaryocytes.

Sbds Deficient Neutrophils Exhibit Normal Numbers, Chemotaxis and Phagocytic Functions, but Impaired NADPH Oxidase Activity.

Mouse Model for Shwachman-Diamond Syndrome with the R126T Disease Mutation Leads to Severe Growth and Developmental Deficiencies with Impairment of Hematopoiesis.

Email alerts

ASH Publications

American Society of Hematology

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