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Journal Articles

A New Genetic Immunodeficiency Syndrome Caused By Autosomal Dominant Mutations in LCP1 Identified By Mosaic Tetraploidy and Severe Neutropenia in Unrelated Pedigrees

Thijs van Bergen, Anna Aalbers, Dennis Bosch, Onno Roovers, Akiko Shimamura, Marc H.G.P. Raaijmakers, Peter E. Newburger, Ivo P Touw

Blood (2022) 140 (Supplement 1): 5463–5464.

https://doi.org/10.1182/blood-2022-165112

Published: 2022

Journal Articles

RUNX1 TAD and RHD Mutations Found in SCN/AML Differentially Affect HSPC Expansion in Conjunction with Truncated CSF3 Receptors

Julia C. Obenauer, M.Sc., Paulina M. H. van Strien, B.Sc., Remco M. Hoogenboezem, M.Sc., Marry M. van den Heuvel-Eibrink, MD PhD, Ivo P. Touw, PhD

Blood (2015) 126 (23): 3606.

https://doi.org/10.1182/blood.V126.23.3606.3606

Published: 2015

Journal Articles

ICL-induced miR139-3p and miR199a-3p have opposite roles in hematopoietic cell expansion and leukemic transformation

Mir Farshid Alemdehy, Jurgen R. Haanstra, Hans W. J. de Looper, Paulina M. H. van Strien, Judith Verhagen-Oldenampsen, Yvette Caljouw, Mathijs A. Sanders, Remco Hoogenboezem, Arnoud H. de Ru, George M. C. Janssen, Stephanie E. Smetsers, Marc B. Bierings, Peter A. van Veelen, Marieke von Lindern, Ivo P. Touw, Stefan J. Erkeland

Blood (2015) 125 (25): 3937–3948.

https://doi.org/10.1182/blood-2014-11-612507

Published: 2015

Includes: Supplemental data

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

Inherited biallelic CSF3R mutations in severe congenital neutropenia

Blood (2014) 123 (24): 3811–3817.

https://doi.org/10.1182/blood-2013-11-535419

Published: 2014

Includes: Supplemental data

Journal Articles

Cooperativity of RUNX1 and CSF3R mutations in severe congenital neutropenia: a unique pathway in myeloid leukemogenesis

Blood (2014) 123 (14): 2229–2237.

https://doi.org/10.1182/blood-2013-11-538025

Published: 2014

Includes: Supplemental data

Journal Articles

Malignant Transformation in Congenital Neutropenia

Ivo P. Touw, PhD

Blood (2013) 122 (21): SCI-44.

https://doi.org/10.1182/blood.V122.21.SCI-44.SCI-44

Published: 2013

Journal Articles

Cooperativity Of RUNX1 and CSF3R Mutations In The Development Of Leukemia In Severe Congenital Neutropenia: A Unique Pathway In Myeloid Leukemogenesis

Blood (2013) 122 (21): 444.

https://doi.org/10.1182/blood.V122.21.444.444

Published: 2013

Journal Articles

The Impact of Novel Molecular Markers on Risk Stratification in Acute Myeloid Leukemia

Bob Löwenberg, MD, PhD, Peter Valk, PhD, Ivo P. Touw, PhD, Ruud Delwel, PhD

Blood (2012) 120 (21): SCI-33.

https://doi.org/10.1182/blood.V120.21.SCI-33.SCI-33

Published: 2012

Journal Articles

Sequential gain of mutations in severe congenital neutropenia progressing to acute myeloid leukemia

Renée Beekman, Marijke G. Valkhof, Mathijs A. Sanders, Paulette M. H. van Strien, Jurgen R. Haanstra, Lianne Broeders, Wendy M. Geertsma-Kleinekoort, Anjo J. P. Veerman, Peter J. M. Valk, Roel G. Verhaak, Bob Löwenberg, Ivo P. Touw

Blood (2012) 119 (22): 5071–5077.

https://doi.org/10.1182/blood-2012-01-406116

Published: 2012

Includes: Supplemental data

Journal Articles

Dicer1 deletion in myeloid-committed progenitors causes neutrophil dysplasia and blocks macrophage/dendritic cell development in mice

Mir Farshid Alemdehy, Nicole G. J. A. van Boxtel, Hans W. J. de Looper, Iris J. van den Berge, Mathijs A. Sanders, Tom Cupedo, Ivo P. Touw, Stefan J. Erkeland

Blood (2012) 119 (20): 4723–4730.

https://doi.org/10.1182/blood-2011-10-386359

Published: 2012

Includes: Supplemental data

Journal Articles

IFNγ induces monopoiesis and inhibits neutrophil development during inflammation

Alexander M. de Bruin, Sten F. Libregts, Marijke Valkhof, Louis Boon, Ivo P. Touw, Martijn A. Nolte

Blood (2012) 119 (6): 1543–1554.

https://doi.org/10.1182/blood-2011-07-367706

Published: 2012

Includes: Supplemental data

Journal Articles

Ribosomal deficiencies in Diamond-Blackfan anemia impair translation of transcripts essential for differentiation of murine and human erythroblasts

Rastislav Horos, Hanna IJspeert, Dagmar Pospisilova, Regine Sendtner, Charlotte Andrieu-Soler, Erdogan Taskesen, Andrzej Nieradka, Radek Cmejla, Michael Sendtner, Ivo P. Touw, Marieke von Lindern

Blood (2012) 119 (1): 262–272.

https://doi.org/10.1182/blood-2011-06-358200

Published: 2012

Includes: Supplemental data

Journal Articles

Interferon-Gamma Induces Monopoiesis and Inhibits Neutrophil Development During Inflammation

Alexander M. de Bruin, Marijke G. Valkhof, Louis Boon, PhD, Ivo P. Touw, PhD, Martijn A. Nolte, PhD

Blood (2011) 118 (21): 1320.

https://doi.org/10.1182/blood.V118.21.1320.1320

Published: 2011

Journal Articles

Ablation of Dicer1 in Myeloid Progenitors Leads to Neutrophil Dysplasia and Depletion of Monocytes, Macrophages, and Myeloid Dendritic Cells

Mir Farshid Alemdehy, Nicole G.J.A. van Boxtel, Hans de Looper, Iris J. van den Berge, Mathijs A. Sanders, Tom Cupedo, PhD, Ivo P. Touw, PhD, Stefan J. Erkeland, PhD

Blood (2011) 118 (21): 43.

https://doi.org/10.1182/blood.V118.21.43.43

Published: 2011

Journal Articles

Methylated Retroviral Integration Mutagenesis (MRIM) in Mice and Comparative Analysis in Human AML Identify Reduced PTP4A3 Expression As a Prognostic Indicator

Renee Beekman, MD, Marijke G. Valkhof, Stefan J. Erkeland, PhD, Erdogan Taskesen, Veronika Rockova, Justine K. Peeters, PhD, Peter Valk, Bob Lowenberg, MD, PhD, Ivo P. Touw, PhD

Blood (2011) 118 (21): 746.

https://doi.org/10.1182/blood.V118.21.746.746

Published: 2011

Journal Articles

MiR-17/20/93/106 promote hematopoietic cell expansion by targeting sequestosome 1–regulated pathways in mice

Annemarie Meenhuis, Peter A. van Veelen, Hans de Looper, Nicole van Boxtel, Iris J. van den Berge, Su M. Sun, Erdogan Taskesen, Patrick Stern, Arnoud H. de Ru, Arjan J. van Adrichem, Jeroen Demmers, Mojca Jongen-Lavrencic, Bob Löwenberg, Ivo P. Touw, Phillip A. Sharp, Stefan J. Erkeland

Blood (2011) 118 (4): 916–925.

https://doi.org/10.1182/blood-2011-02-336487

Published: 2011

Includes: Supplemental data

Journal Articles

Lineage-instructive function of C/EBPα in multipotent hematopoietic cells and early thymic progenitors

Albert Wölfler, Astrid A. Danen-van Oorschot, Jurgen R. Haanstra, Marijke Valkhof, Claudia Bodner, Eric Vroegindeweij, Paulette van Strien, Alexandra Novak, Tom Cupedo, Ivo P. Touw

Blood (2010) 116 (20): 4116–4125.

https://doi.org/10.1182/blood-2010-03-275404

Published: 2010

Includes: Supplemental data

Journal Articles

G-CSF and its receptor in myeloid malignancy

Renée Beekman, Ivo P. Touw

Blood (2010) 115 (25): 5131–5136.

https://doi.org/10.1182/blood-2010-01-234120

Published: 2010

Journal Articles

Lineage Instructive Function of C/EBPα in Multipotent Hematopoietic Progenitor Cells Revealed in a Novel Cebpa -Cre Knock-in Model

Albert Wolfler, Astrid A Danen-van Oorschot, Jurgen Haanstra, Marijke Valkhof, Paulette van Strien, Elwin Rombouts, Ivo P Touw

Blood (2008) 112 (11): 2458.

https://doi.org/10.1182/blood.V112.11.2458.2458

Published: 2008

NARROW

A New Genetic Immunodeficiency Syndrome Caused By Autosomal Dominant Mutations in LCP1 Identified By Mosaic Tetraploidy and Severe Neutropenia in Unrelated Pedigrees

RUNX1 TAD and RHD Mutations Found in SCN/AML Differentially Affect HSPC Expansion in Conjunction with Truncated CSF3 Receptors

ICL-induced miR139-3p and miR199a-3p have opposite roles in hematopoietic cell expansion and leukemic transformation

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

Inherited biallelic CSF3R mutations in severe congenital neutropenia

Cooperativity of RUNX1 and CSF3R mutations in severe congenital neutropenia: a unique pathway in myeloid leukemogenesis

Malignant Transformation in Congenital Neutropenia

Cooperativity Of RUNX1 and CSF3R Mutations In The Development Of Leukemia In Severe Congenital Neutropenia: A Unique Pathway In Myeloid Leukemogenesis

The Impact of Novel Molecular Markers on Risk Stratification in Acute Myeloid Leukemia

Sequential gain of mutations in severe congenital neutropenia progressing to acute myeloid leukemia

Dicer1 deletion in myeloid-committed progenitors causes neutrophil dysplasia and blocks macrophage/dendritic cell development in mice

IFNγ induces monopoiesis and inhibits neutrophil development during inflammation

Ribosomal deficiencies in Diamond-Blackfan anemia impair translation of transcripts essential for differentiation of murine and human erythroblasts

Interferon-Gamma Induces Monopoiesis and Inhibits Neutrophil Development During Inflammation

Ablation of Dicer1 in Myeloid Progenitors Leads to Neutrophil Dysplasia and Depletion of Monocytes, Macrophages, and Myeloid Dendritic Cells

Methylated Retroviral Integration Mutagenesis (MRIM) in Mice and Comparative Analysis in Human AML Identify Reduced PTP4A3 Expression As a Prognostic Indicator

MiR-17/20/93/106 promote hematopoietic cell expansion by targeting sequestosome 1–regulated pathways in mice

Lineage-instructive function of C/EBPα in multipotent hematopoietic cells and early thymic progenitors

G-CSF and its receptor in myeloid malignancy

Lineage Instructive Function of C/EBPα in Multipotent Hematopoietic Progenitor Cells Revealed in a Novel Cebpa -Cre Knock-in Model

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American Society of Hematology

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ASH Publications

American Society of Hematology

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