Inherited biallelic CSF3R mutations in severe congenital neutropenia
Published 2014 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Inherited biallelic CSF3R mutations in severe congenital neutropenia
Authors
Keywords
-
Journal
BLOOD
Volume 123, Issue 24, Pages 3811-3817
Publisher
American Society of Hematology
Online
2014-04-22
DOI
10.1182/blood-2013-11-535419
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Mutations in SPAG1 Cause Primary Ciliary Dyskinesia Associated with Defective Outer and Inner Dynein Arms
- (2013) Michael R. Knowles et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Loss-of-function mutations in the IL-21 receptor gene cause a primary immunodeficiency syndrome
- (2013) Daniel Kotlarz et al. JOURNAL OF EXPERIMENTAL MEDICINE
- A Congenital Neutrophil Defect Syndrome Associated with Mutations in VPS45
- (2013) Thierry Vilboux et al. NEW ENGLAND JOURNAL OF MEDICINE
- Sequential gain of mutations in severe congenital neutropenia progressing to acute myeloid leukemia
- (2012) R. Beekman et al. BLOOD
- NIH Image to ImageJ: 25 years of image analysis
- (2012) Caroline A Schneider et al. NATURE METHODS
- The WSXWS Motif in Cytokine Receptors Is a Molecular Switch Involved in Receptor Activation: Insight from Structures of the Prolactin Receptor
- (2012) Robert Dagil et al. STRUCTURE
- Genetic Defects in Severe Congenital Neutropenia: Emerging Insights into Life and Death of Human Neutrophil Granulocytes
- (2011) Christoph Klein Annual Review of Immunology
- Automated comparative protein structure modeling with SWISS-MODEL and Swiss-PdbViewer: A historical perspective
- (2010) Nicolas Guex et al. ELECTROPHORESIS
- A method and server for predicting damaging missense mutations
- (2010) Ivan A Adzhubei et al. NATURE METHODS
- Granulocyte colony-stimulating factor receptor: Stimulating granulopoiesis and much more
- (2009) Clifford Liongue et al. INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY
- An activating mutation in theCSF3Rgene induces a hereditary chronic neutrophilia
- (2009) Isabelle Plo et al. JOURNAL OF EXPERIMENTAL MEDICINE
- Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm
- (2009) Prateek Kumar et al. Nature Protocols
- A Syndrome with Congenital Neutropenia and Mutations inG6PC3
- (2009) Kaan Boztug et al. NEW ENGLAND JOURNAL OF MEDICINE
- Granulocyte colony-stimulating factor: Molecular mechanisms of action during steady state and ‘emergency’ hematopoiesis
- (2008) Athanasia D. Panopoulos et al. CYTOKINE
- Crystal Structure of a Prolactin Receptor Antagonist Bound to the Extracellular Domain of the Prolactin Receptor
- (2008) L. Anders Svensson et al. JOURNAL OF BIOLOGICAL CHEMISTRY
Find the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
SearchAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started