(Q37292779)

19 August 2017

An activating mutation in the CSF3R gene induces a hereditary chronic neutrophilia (English)

1 reference

19 August 2017

Isabelle Plo

0 references

Stéphane de Botton

0 references

Fawzia Louache

0 references

Stefan N Constantinescu

object named as

Stefan N Constantinescu

0 references

William Vainchenker

1 reference

19 August 2017

Yanyan Zhang

1 reference

19 August 2017

Jean-Pierre Le Couédic

1 reference

19 August 2017

Mayuka Nakatake

1 reference

19 August 2017

Jean-Michel Boulet

1 reference

19 August 2017

Miki Itaya

1 reference

19 August 2017

Steven O Smith

1 reference

19 August 2017

Najet Debili

1 reference

19 August 2017

language of work or name

English

0 references

publication date

20 July 2009

1 reference

Journal of Experimental Medicine

19 August 2017

1 reference

19 August 2017

206

1 reference

19 August 2017

1 reference

19 August 2017

1701-1707

1 reference

Granulocyte colony-stimulating factor: molecular mechanisms of action during steady state and 'emergency' hematopoiesis.

19 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2722170

Csf3r mutations in mice confer a strong clonal HSC advantage via activation of Stat5.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2722170

Quantitative comparison of the expression of EVI1 and its presumptive antagonist, MDS1/EVI1, in patients with myeloid leukemia

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2722170

NOD/SCID/gamma(c)(null) mouse: an excellent recipient mouse model for engraftment of human cells

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2722170

An activating mutation in the transmembrane domain of the granulocyte colony-stimulating factor receptor in patients with acute myeloid leukemia

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2722170

Increased granulocyte colony-stimulating factor responsiveness but normal resting granulopoiesis in mice carrying a targeted granulocyte colony-stimulating factor receptor mutation derived from a patient with severe congenital neutropenia

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2722170

Purification of primitive human hematopoietic cells capable of repopulating immune-deficient mice.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2722170

Truncated erythropoietin receptor causes dominantly inherited benign human erythrocytosis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2722170

Active and inactive orientations of the transmembrane and cytosolic domains of the erythropoietin receptor dimer

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2722170

Improved prediction for the structure of the dimeric transmembrane domain of glycophorin A obtained through global searching

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2722170

An activating splice donor mutation in the thrombopoietin gene causes hereditary thrombocythaemia

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2722170

Incidence of CSF3R mutations in severe congenital neutropenia and relevance for leukemogenesis: Results of a long-term survey.

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2722170

Familial essential thrombocythemia associated with a dominant-positive activating mutation of the c-MPL gene, which encodes for the receptor for thrombopoietin

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2722170

Functional CD5+ B cells develop predominantly in the spleen of NOD/SCID/gammac(null) (NOG) mice transplanted either with human umbilical cord blood, bone marrow, or mobilized peripheral blood CD34+ cells

3 September 2018

1 reference

12 December 2020

Two new EPO receptor mutations: truncated EPO receptors are most frequently associated with primary familial and congenital polycythemias

1 reference

12 December 2020

A simple FISH assay for the detection of 3q26 rearrangements in myeloid malignancy

1 reference

12 December 2020

The hematopoietic stem cell compartment of JAK2V617F-positive myeloproliferative disorders is a reflection of disease heterogeneity

1 reference

12 December 2020

New mutations of MPL in primitive myelofibrosis: only the MPL W515 mutations promote a G1/S-phase transition

1 reference

12 December 2020

Identifiers

DOI

10.1084/JEM.20090693

1 reference

19 August 2017

1 reference

19 August 2017

PubMed publication ID

19620628

1 reference