Search Results - "Courtois, Geneviève"
-
1
An activin receptor IIA ligand trap corrects ineffective erythropoiesis in β-thalassemia
Published in Nature medicine (01-04-2014)“…Michael Dussiot et al . show that an activin receptor IIA ligand trap ameliorates anemia in a mouse model of β-thalassemia by blocking the deleterious effects…”
Get full text
Journal Article -
2
Regulation of globin-heme balance in Diamond-Blackfan anemia by HSP70/GATA1
Published in Blood (21-03-2019)“…Diamond-Blackfan anemia (DBA) is a congenital erythroblastopenia that is characterized by a blockade in erythroid differentiation related to impaired ribosome…”
Get full text
Journal Article -
3
Ineffective Erythropoiesis in β-Thalassemia
Published in TheScientificWorld (01-01-2013)“…In humans, β-thalassemia dyserythropoiesis is characterized by expansion of early erythroid precursors and erythroid progenitors and then ineffective…”
Get full text
Journal Article -
4
XPO1 regulates erythroid differentiation and is a new target for the treatment of β-thalassemia
Published in Haematologica (Roma) (01-09-2020)“…β-thalassemia major (β-TM) is an inherited hemoglobinopathy caused by a quantitative defect in the synthesis of β-globin chains of hemoglobin, leading to the…”
Get full text
Journal Article Web Resource -
5
Biallelic mutations in the SARS2 gene presenting as congenital sideroblastic anemia
Published in Haematologica (Roma) (01-12-2021)Get full text
Journal Article -
6
HSP70 sequestration by free α-globin promotes ineffective erythropoiesis in β-thalassaemia
Published in Nature (London) (09-10-2014)“…In human β-thalassaemiaerythroblasts, HSP70 is sequestered in the cytoplasm by the excess of free α-globin chains and can no longer protect the master…”
Get full text
Journal Article Web Resource -
7
Role of Caspase-10-P13tBID axis in erythropoiesis regulation
Published in Cell death and differentiation (01-01-2023)“…Red blood cell production is negatively controlled by the rate of apoptosis at the stage of CFU-E/pro-erythroblast differentiation, depending on the balance…”
Get full text
Journal Article -
8
Enhanced Renewal of Erythroid Progenitors in Myelodysplastic Anemia by Peripheral Serotonin
Published in Cell reports (Cambridge) (19-03-2019)“…Tryptophan as the precursor of several active compounds, including kynurenine and serotonin, is critical for numerous important metabolic functions. Enhanced…”
Get full text
Journal Article -
9
A deep dive into future therapies for microcytic anemias and clinical considerations
Published in Expert review of hematology (04-05-2023)“…Microcytic anemias (MA) have frequent or rare etiologies. New discoveries in understanding and treatment of microcytic anemias need to be reviewed. Microcytic…”
Get more information
Journal Article -
10
Novel players in β-thalassemia dyserythropoiesis and new therapeutic strategies
Published in Current opinion in hematology (01-05-2016)“…PURPOSE OF REVIEWThe review provides an overview of recent data regarding the molecular players in β-thalassemia dyserythropoiesis and the corresponding…”
Get full text
Journal Article -
11
EKLF-driven PIT1 expression is critical for mouse erythroid maturation in vivo and in vitro
Published in Blood (24-01-2013)“…The PIT1/SLC20A1 protein, a well-described sodium/phosphate cotransporter and retrovirus receptor, has been identified recently as a modular of proliferation…”
Get full text
Journal Article -
12
HSP27 controls GATA-1 protein level during erythroid cell differentiation
Published in Blood (08-07-2010)“…Heat shock protein 27 (HSP27) is a chaperone whose cellular expression increases in response to various stresses and protects the cell either by inhibiting…”
Get full text
Journal Article -
13
OTT-MAL Is a Deregulated Activator of Serum Response Factor-Dependent Gene Expression
Published in Molecular and Cellular Biology (01-10-2008)“…Article Usage Stats Services MCB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
Get full text
Journal Article -
14
Polymeric IgA1 controls erythroblast proliferation and accelerates erythropoiesis recovery in anemia
Published in Nature Medicine (01-11-2011)“…Séverine Coulon et al . identify a new mechanism regulating red blood cell production through transferrin receptor engagement. By binding this receptor on…”
Get full text
Journal Article Magazine Article -
15
Interaction of the tyrosine phosphatase SHP-2 with Gab2 regulates Rho-dependent activation of the c-fos serum response element by interleukin-2
Published in Biochemical journal (01-09-2004)“…Gab2 (Grb2-associated binder-2), a member of the IRS (insulin receptor substrate)/Gab family of adapter proteins, undergoes tyrosine phosphorylation in…”
Get full text
Journal Article -
16
HSP70 regulates ineffective erythropoiesis in beta-thalassaemia
Published in M.S. Médecine sciences (01-01-2015)Get more information
Journal Article -
17
Defective nuclear localization of Hsp70 is associated with dyserythropoiesis and GATA-1 cleavage in myelodysplastic syndromes
Published in Blood (09-02-2012)“…Normal human erythroid cell maturation requests the transcription factor GATA-1 and a transient activation of caspase-3, with GATA-1 being protected from…”
Get full text
Journal Article -
18
Abstract 3293: Leptin induces breast cancer metastasis through a Neuropilin-1 (NRP-1)/OBR complex
Published in Cancer research (Chicago, Ill.) (01-10-2014)“…Several studies have demonstrated Neuropilin-1 (NRP-1) implication in tumor progression independently of its known co-receptors. On the basis of growing…”
Get full text
Journal Article -
19
EKLF-driven PIT1 expression is critical for mouse erythroid maturation in vivo and in vitro
Published in Blood (24-01-2013)“…The PIT1/SLC20A1 protein, a well-described sodium/phosphate cotransporter and retrovirus receptor, has been identified recently as a modular of proliferation…”
Get full text
Journal Article -
20
HSP70 sequestration by free [alpha]-globin promotes ineffective erythropoiesis in [Beta]-thalassaemia
Published in Nature (London) (09-10-2014)“…β-Thalassaemia major (β-TM) is an inherited haemoglobinopathy caused by a quantitative defect in the synthesis of β-globin chains of haemoglobin, leading to…”
Get full text
Journal Article