textabstractSevere congenital neutropenia (Kostmann syndrome) is characterized by profound absolute neutropenia and a maturation arrest of marrow progenitor cells at the promyelocyte-myelocyte stage. Marrow cells from such patients frequently display a reduced responsiveness to granulocyte-colony-stimulating factor (G-CSF). G-CSF binds to and activates a specific receptor which transduces signals critical for the proliferation and maturation of granulocytic progenitor cells. Here we report the identification of a somatic point mutation in one allele of the G-CSF receptor gene in a patient with severe congenital neutropenia. The mutation result...
Point mutations in the gene for the granu-locyte colony-stimulating factor (G-CSF) receptor CSF3R ha...
We identify an autosomal mutation in the CSF3R gene in a family with a chronic neutrophilia. This T6...
Granulocyte colony-stimulating factor (G-CSF) is a key regulator of granulopoiesis via stimulation o...
textabstractSevere congenital neutropenia (SCN) is a heterogeneous condition characterized...
In severe congenital neutropenia the maturation of myeloid progenitor cells is arrested. The myelody...
Most severe congenital neutropenia (SCN) cases possess constitutive neutrophil elastase mutations; a...
Severe congenital neutropenia (SCN) is characterized by low numbers of peripheral neutrophil granulo...
Neutrophil elastase and granulocyte colony-stimulating factor receptor mutation analyses and leukemi...
To confirm the abnormalities of primitive myeloid progenitor cells in patients withsevere congenital...
Deletion mutants of the intracytoplasmic domain of the granulocyte colony-stimulating factor recepto...
Severe congenital neutropenia (SCN) is a rare disease diagnosed at or soon after birth, characterize...
Severe congenital neutropenia (SCN), Kostmann syndrome is a heterogenous disorder of myelopoiesis ch...
Severe congenital neutropenia (SCN) patients are prone to develop myelodysplastic syndrome (MDS) or ...
Acquired mutations truncating the C-terminal domain of the granulocyte colony-stimulating factor rec...
Congenital neutropenia with autosomal recessive inheritance was first described by the Swedish paedi...
Point mutations in the gene for the granu-locyte colony-stimulating factor (G-CSF) receptor CSF3R ha...
We identify an autosomal mutation in the CSF3R gene in a family with a chronic neutrophilia. This T6...
Granulocyte colony-stimulating factor (G-CSF) is a key regulator of granulopoiesis via stimulation o...
textabstractSevere congenital neutropenia (SCN) is a heterogeneous condition characterized...
In severe congenital neutropenia the maturation of myeloid progenitor cells is arrested. The myelody...
Most severe congenital neutropenia (SCN) cases possess constitutive neutrophil elastase mutations; a...
Severe congenital neutropenia (SCN) is characterized by low numbers of peripheral neutrophil granulo...
Neutrophil elastase and granulocyte colony-stimulating factor receptor mutation analyses and leukemi...
To confirm the abnormalities of primitive myeloid progenitor cells in patients withsevere congenital...
Deletion mutants of the intracytoplasmic domain of the granulocyte colony-stimulating factor recepto...
Severe congenital neutropenia (SCN) is a rare disease diagnosed at or soon after birth, characterize...
Severe congenital neutropenia (SCN), Kostmann syndrome is a heterogenous disorder of myelopoiesis ch...
Severe congenital neutropenia (SCN) patients are prone to develop myelodysplastic syndrome (MDS) or ...
Acquired mutations truncating the C-terminal domain of the granulocyte colony-stimulating factor rec...
Congenital neutropenia with autosomal recessive inheritance was first described by the Swedish paedi...
Point mutations in the gene for the granu-locyte colony-stimulating factor (G-CSF) receptor CSF3R ha...
We identify an autosomal mutation in the CSF3R gene in a family with a chronic neutrophilia. This T6...
Granulocyte colony-stimulating factor (G-CSF) is a key regulator of granulopoiesis via stimulation o...