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Journal Articles

HAX1 Associated Congenital Neutropenia: A 25 Year Long-Term Analysis of the European Scnir Cohort

Cornelia Zeidler, Sabine Mellor-Heineke, MD, Maksim Klimiankou, Julia Skokowa, Karl Welte, MD PhD

Blood (2017) 130 (Supplement 1): 3566.

https://doi.org/10.1182/blood.V130.Suppl_1.3566.3566

Published: 2017

Journal Articles

BAALC Is a Key Mediator of Leukemia Development in Congenital Neutropenia

Benjamin Dannenmann, Maksim Klimiankou, Anna Solovyeva, Azadeh Zahabi, MSc, Perihan Mir, Masoud Nasri, MSc, Regine Bernhard, Christian Lindner, Tatsuya Morishima, MD PhD, Doris Steinemann, PhD, Cornelia Zeidler, Lothar Kanz, Karl Welte, MD PhD, Julia Skokowa

Blood (2017) 130 (Supplement 1): 541.

https://doi.org/10.1182/blood.V130.Suppl_1.541.541

Published: 2017

Journal Articles

Effects of CSF3R mutations on Myeloid Differentiation and Proliferation of Hematopoietic Cells of Congenital Neutropenia Patients

Maksim Klimiankou, Benjamin Dannenmann, Anna Solovyeva, Regine Bernhard, Diana Amend, Cornelia Zeidler, Sabine Mellor-Heineke, MD, Lothar Kanz, Julia Skokowa, Karl Welte, MD PhD

Blood (2017) 130 (Supplement 1): 2278.

https://doi.org/10.1182/blood.V130.Suppl_1.2278.2278

Published: 2017

Journal Articles

Optimization of CSF3R Mutation Detection in Severe Congenital Neutropenia and Cyclic Neutropenia Patients for Routine Diagnostics Using Next Generation Sequencing

Maksim Klimiankou, PhD, Cornelia Zeidler, MD, Sabine Mellor-Heineke, Ingeborg Steiert, Karin Haehnel, Karl Welte, MD PhD, Julia Skokowa, MD PhD

Blood (2016) 128 (22): 3685.

https://doi.org/10.1182/blood.V128.22.3685.3685

Published: 2016

Journal Articles

Defective Expression of Neutrophil Serine Proteases in Myeloid Progenitors of Congenital Neutropenia Patients Carrying Either ELA2 or HAX1 Mutations.

Julia Skokowa, MD, PhD, John-Paul Fobiwe, Dan Lan, Manuela Germeshausen, PhD, Karl Welte, MD PhD

Blood (2007) 110 (11): 3299.

https://doi.org/10.1182/blood.V110.11.3299.3299

Published: 2007

Journal Articles

Constitutive Activation of STAT5a in Myeloid Progenitors of Severe Congenital Neutropenia Patients Leads to Downregulation of LEF-1.

Julia Skokowa, MD PhD, Kshama Gupta, M.Sc, Annette Mueller Brechlin, Johann Meyer, PhD, Malcolm A.S. Moore, PhD, Karl Welte, MD, PhD

Blood (2007) 110 (11): 663.

https://doi.org/10.1182/blood.V110.11.663.663

Published: 2007

Journal Articles

LEF-1 Regulates C/EBP α Expression and Neutrophil Differentiation in Normal Myelopoiesis and Congenital Neutropenia by a β-Catenin Independent Mechanism.

Julia Skokowa, MD, PhD, Murat Uenalan, MD, Axel Schambach, MD, PhD, Michaela Scherr, PhD, Matthias Eder, MD, Cornelia Zeidler, MD, Christopher Baum, MD, PhD, Martin Stanulla, MD, Gunnar Cario, MD, Karl Welte, MD, PhD

Blood (2006) 108 (11): 500.

https://doi.org/10.1182/blood.V108.11.500.500

Published: 2006

Journal Articles

High Interleukin 15 Expression Characterizes Childhood Acute Lymphoblastic Leukemia with Involvement of the Central Nervous System.

Gunnar Cario, MD, Anja Teichert, Peter Rhein, Andre Schrauder, MD, Julia Skokowa, MD PhD, Wolf-Dieter Ludwig, MD PhD, Shai Izraeli, MD, Karl Welte, MD PhD, Brigitte Schlegelberger, MD PhD, Martin Schrappe, MD PhD, Martin Stanulla, MD MSc

Blood (2006) 108 (11): 2270.

https://doi.org/10.1182/blood.V108.11.2270.2270

Published: 2006

Journal Articles

LEF-1 Transcription Factor Regulates Proliferation and Differentiation of Myeloid Progenitors in Healthy Individuals and in Patients with Severe Congenital Neutropenia (CN).

Julia Skokowa, MD, PhD, Gunnar Cario, MD, Vesna Bucan, Lan Dan, Zheng Wang, PhD, Michaela Scherr, PhD, Axel Schambach, MD, Cornelia Zeidler, MD, Mathias Eder, MD, Christopher Baum, MD, Martin Stanulla, MD, Karl Welte, MD, PhD

Blood (2005) 106 (11): 390.

https://doi.org/10.1182/blood.V106.11.390.390

Published: 2005

Journal Articles

Pre-B-Cell Colony Enhancing Factor (PBEF) Is a New Cytokine Regulating Myeloid Differentiation in Healthy Individuals and Patients with Severe Congenital Neutropenia (CN).

Julia Skokowa, MD, PhD, Lan Dan, Gunnar Cario, MD, Axel Schambach, MD, Cornelia Zeidler, MD, Christopher Baum, MD, Martin Stanulla, MD, Karl Welte, MD, PhD

Blood (2005) 106 (11): 387.

https://doi.org/10.1182/blood.V106.11.387.387

Published: 2005

Journal Articles

The Role of CD4+ T Cells in a Murine Model of Acute Lymphoblastic Leukaemia.

Ahmed N. Hegazy, Mathias Wolenski, PhD, Karl Welte, MD, PhD, Christoph Klein, MD, PhD

Blood (2005) 106 (11): 1838.

https://doi.org/10.1182/blood.V106.11.1838.1838

Published: 2005

Journal Articles

A Variant of Congenital Neutropenia Is Caused by a 3′-UTR Mutation in the Gene Encoding the Endosomal Adaptor Protein p14 ( MAPBPIP ).

Georg Bohn, MD, Anna Allroth, Jens Thiel, MD, Alejandro A. Schäffer, Gudrun Brandes, MD, Erik Glocker, David Teis, PhD, Nicole Taub, Cornelia Zeidler, MD, Robert Geffers, PhD, Jan Buer, MD, Lukas A. Huber, MD/PhD, Karl Welte, MD/PhD, Bodo Grimbacher, MD, Christoph Klein, MD/PhD

Blood (2005) 106 (11): 92.

https://doi.org/10.1182/blood.V106.11.92.92

Published: 2005

Journal Articles

Proto-Oncogenes β- and γ-Catenin in Leukemogenesis in Severe Congenital Neutropenia (CN).

Julia Skokowa, MD, PhD, Gunnar Cario, MD, Lan Dan, Cornelia Zeidler, MD, Vesna Bucan, Karl Welte, MD, PhD

Blood (2005) 106 (11): 94.

https://doi.org/10.1182/blood.V106.11.94.94

Published: 2005

Journal Articles

G-CSF Mobilized Granulocyte Transfusions in 32 Pediatric Patients with Severe Infections after Chemotherapy Induced Neutropenia.

Lorenz Grigull, MD, Nicole Pulver, Lilia Goudeva, MD, Karl W. Sykora, MD, Andreas Beilken, MD, Hansjoerg Schmid, MD, Karl Welte, MD, PhD, Hansgert Heuft, MD

Blood (2004) 104 (11): 2720.

https://doi.org/10.1182/blood.V104.11.2720.2720

Published: 2004

Journal Articles

Fluorescence In Situ Hybridization (FISH) Using a Subtelomeric 11q Probe as a New Diagnostic Tool for Congenital Thrombocytopenia Caused by Deletions in 11q.

Dorothea Gadzicki, MD, Gudrun Michaelsen, MD, Cornelia Rudolph, Doris Steinemann, PhD, Christoph M. Happel, MD, Karl Welte, MD, PhD, Christoph Klein, MD, PhD, Holger Toennies, PhD, Peter Lichter, PhD, Udo Kontny, MD, Charlotte Marie Niemeyer, MD, PhD, Brigitte Schlegelberger, MD, PhD

Blood (2004) 104 (11): 3035.

https://doi.org/10.1182/blood.V104.11.3035.3035

Published: 2004

Journal Articles

Unsupervised Analysis of Human Leukemia Cells Identifies the Valosin-Containing Protein as a Putative Marker for Glucocorticoid Resistance.

Melchior Lauten, MD, Nils v. Neuhoff, PhD, Karl Welte, MD, PhD, Brigitte Schlegelberger, MD, PhD, Martin Schrappe, MD, PhD

Blood (2004) 104 (11): 167.

https://doi.org/10.1182/blood.V104.11.167.167

Published: 2004

Journal Articles

Administration of Granulocyte Colony-Stimulating Factor Does Not Restore Defective Expression of bcl-2 and bcl-2-xL in Myeloid Progenitor Cells of Patients with Severe Congenital Neutropenia (Kostmann Syndrome).

Gunnar Cario, MD, Julia Skokowa, MD PhD, Zheng Wang, PhD, Vesna Bucan, Cornelia Zeidler, MD, Martin Stanulla, MD, Martin Schrappe, MD PhD, Karl Welte, MD PhD

Blood (2004) 104 (11): 1456.

https://doi.org/10.1182/blood.V104.11.1456.1456

Published: 2004

Journal Articles

Mutations in the Gene of Neutrophil Elastase Associated with Congenital Neutropenia Lead to Alteration of Intracellular Trafficking and Proteolytic Function of NE Protein.

Carmela Beger, MD, Inga Koellner, Cornelia Zeidler, MD, Manuela Germeshausen, PhD, Nils von Neuhoff, PhD, Brigitte Schlegelberger, MD, PhD, Karl Welte, MD, PhD

Blood (2004) 104 (11): 780.

https://doi.org/10.1182/blood.V104.11.780.780

Published: 2004

Journal Articles

Defective Expression of LEF-1 Transcription Factor mRNA and - Protein in Patients with Severe Congenital Neutropenia (Kostmann’S Syndrome).

Julia Skokowa, MD PhD, Gunnar Cario, MD, Zheng Wang, PhD, Cornelia Zeidler, MD, Martin Stanulla, MD, Karl Welte, MD PhD

Blood (2004) 104 (11): 782.

https://doi.org/10.1182/blood.V104.11.782.782

Published: 2004

NARROW

HAX1 Associated Congenital Neutropenia: A 25 Year Long-Term Analysis of the European Scnir Cohort

BAALC Is a Key Mediator of Leukemia Development in Congenital Neutropenia

Effects of CSF3R mutations on Myeloid Differentiation and Proliferation of Hematopoietic Cells of Congenital Neutropenia Patients

Optimization of CSF3R Mutation Detection in Severe Congenital Neutropenia and Cyclic Neutropenia Patients for Routine Diagnostics Using Next Generation Sequencing

Defective Expression of Neutrophil Serine Proteases in Myeloid Progenitors of Congenital Neutropenia Patients Carrying Either ELA2 or HAX1 Mutations.

Constitutive Activation of STAT5a in Myeloid Progenitors of Severe Congenital Neutropenia Patients Leads to Downregulation of LEF-1.

LEF-1 Regulates C/EBP α Expression and Neutrophil Differentiation in Normal Myelopoiesis and Congenital Neutropenia by a β-Catenin Independent Mechanism.

High Interleukin 15 Expression Characterizes Childhood Acute Lymphoblastic Leukemia with Involvement of the Central Nervous System.

LEF-1 Transcription Factor Regulates Proliferation and Differentiation of Myeloid Progenitors in Healthy Individuals and in Patients with Severe Congenital Neutropenia (CN).

Pre-B-Cell Colony Enhancing Factor (PBEF) Is a New Cytokine Regulating Myeloid Differentiation in Healthy Individuals and Patients with Severe Congenital Neutropenia (CN).

The Role of CD4+ T Cells in a Murine Model of Acute Lymphoblastic Leukaemia.

A Variant of Congenital Neutropenia Is Caused by a 3′-UTR Mutation in the Gene Encoding the Endosomal Adaptor Protein p14 ( MAPBPIP ).

Proto-Oncogenes β- and γ-Catenin in Leukemogenesis in Severe Congenital Neutropenia (CN).

G-CSF Mobilized Granulocyte Transfusions in 32 Pediatric Patients with Severe Infections after Chemotherapy Induced Neutropenia.

Fluorescence In Situ Hybridization (FISH) Using a Subtelomeric 11q Probe as a New Diagnostic Tool for Congenital Thrombocytopenia Caused by Deletions in 11q.

Unsupervised Analysis of Human Leukemia Cells Identifies the Valosin-Containing Protein as a Putative Marker for Glucocorticoid Resistance.

Administration of Granulocyte Colony-Stimulating Factor Does Not Restore Defective Expression of bcl-2 and bcl-2-xL in Myeloid Progenitor Cells of Patients with Severe Congenital Neutropenia (Kostmann Syndrome).

Mutations in the Gene of Neutrophil Elastase Associated with Congenital Neutropenia Lead to Alteration of Intracellular Trafficking and Proteolytic Function of NE Protein.

Defective Expression of LEF-1 Transcription Factor mRNA and - Protein in Patients with Severe Congenital Neutropenia (Kostmann’S Syndrome).

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American Society of Hematology

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ASH Publications

American Society of Hematology

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