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Journal Articles

SWI/SNF Protein SMARCD2 Orchestrates Transcriptional Networks Controlling Hematopoiesis and Neutrophil Granulocytes in Humans, Mice and Zebrafish

Blood (2016) 128 (22): 2.

https://doi.org/10.1182/blood.V128.22.2.2

Published: 2016

Journal Articles

A Human Bone Marrow Failure Syndrome Caused By a Homozygous Mutation in MYSM1

Ehsan Bahrami, Tomas Racek, PhD, Maximilian Witzel, MD, Jacek Puchalka, PhD, Naschla Greif-Kohistani, MD, Daniel Kotlarz, MD PhD, Michael Orth, PhD, Kirsten Lauber, PhD, Christoph Walz, MD, Waleed Al Herz, MD, Hans-Peter Horny, MD, Heinrich Schmidt, MD, Michael H. Albert, MD, Christoph Klein, MD PhD

Blood (2015) 126 (23): 1204.

https://doi.org/10.1182/blood.V126.23.1204.1204

Published: 2015

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

Inherited Biallelic Loss-Of-Function Mutations In CSF3R Define a Novel Type Of Severe Congenital Neutropenia With Full Myeloid Cell Maturation and Refractoriness To RhG-CSF

Alexa Triot, Päivi M Järvinen, Juan I. Arostegui, MD, Tomas Racek, PhD, Jacek Puchalka, Jose Luis Dapena Díaz, MD, Naschla Kohistani, MD, E. Michael Gertz, PhD, Alejandro A. Schäffer, Cristina Díaz de Heredia Rubio, MD, Mehmet A. Ozdemir, MD, Turkan Patiroglu, MD, Musa Karakukcu, MD, José Sanchez de Toledo Codina, MD, Jordi Yagüe, MD, PhD, Ekrem Unal, Christoph Klein, MD PhD

Blood (2013) 122 (21): 1025.

https://doi.org/10.1182/blood.V122.21.1025.1025

Published: 2013

Journal Articles

Novel NGS-Based Platforms For Molecular Diagnosis Of Severe Congenital Neutropenia

Tomas Racek, PhD, Jacek Puchalka, PhD, Naschla Kohistani, MD, Christoph Klein, MD PhD

Blood (2013) 122 (21): 1034.

https://doi.org/10.1182/blood.V122.21.1034.1034

Published: 2013

Journal Articles

Deficiency Of JAGN1 Causes Severe Congenital Neutropenia Associated With Defective Secretory Pathway and Aberrant Myeloid Cell Homeostasis

Blood (2013) 122 (21): 439.

https://doi.org/10.1182/blood.V122.21.439.439

Published: 2013

NARROW

SWI/SNF Protein SMARCD2 Orchestrates Transcriptional Networks Controlling Hematopoiesis and Neutrophil Granulocytes in Humans, Mice and Zebrafish

A Human Bone Marrow Failure Syndrome Caused By a Homozygous Mutation in MYSM1

Inherited biallelic CSF3R mutations in severe congenital neutropenia

Inherited Biallelic Loss-Of-Function Mutations In CSF3R Define a Novel Type Of Severe Congenital Neutropenia With Full Myeloid Cell Maturation and Refractoriness To RhG-CSF

Novel NGS-Based Platforms For Molecular Diagnosis Of Severe Congenital Neutropenia

Deficiency Of JAGN1 Causes Severe Congenital Neutropenia Associated With Defective Secretory Pathway and Aberrant Myeloid Cell Homeostasis

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ASH Publications

American Society of Hematology

SWI/SNF Protein SMARCD2 Orchestrates Transcriptional Networks Controlling Hematopoiesis and Neutrophil Granulocytes in Humans, Mice and Zebrafish

A Human Bone Marrow Failure Syndrome Caused By a Homozygous Mutation in MYSM1

Inherited biallelic CSF3R mutations in severe congenital neutropenia

Inherited Biallelic Loss-Of-Function Mutations In CSF3R Define a Novel Type Of Severe Congenital Neutropenia With Full Myeloid Cell Maturation and Refractoriness To RhG-CSF

Novel NGS-Based Platforms For Molecular Diagnosis Of Severe Congenital Neutropenia

Deficiency Of JAGN1 Causes Severe Congenital Neutropenia Associated With Defective Secretory Pathway and Aberrant Myeloid Cell Homeostasis

Email alerts

ASH Publications

American Society of Hematology

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