Detalhe da pesquisa
1.
Erythroblastic islands foster granulopoiesis in parallel to terminal erythropoiesis.
Blood
; 140(14): 1621-1634, 2022 10 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35862735
2.
Red cell abnormalities characterized by ektacytometry in children with cholestasis.
Pediatr Res
; 95(4): 1035-1040, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38040987
3.
Crosstalk between terminal erythropoiesis and granulopoiesis within their common niche: the erythromyeloblastic island.
Curr Opin Hematol
; 30(4): 99-105, 2023 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37254853
4.
VPS4A Mutations in Humans Cause Syndromic Congenital Dyserythropoietic Anemia due to Cytokinesis and Trafficking Defects.
Am J Hum Genet
; 107(6): 1149-1156, 2020 12 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33186543
5.
Etavopivat, a Pyruvate Kinase Activator in Red Blood Cells, for the Treatment of Sickle Cell Disease.
J Pharmacol Exp Ther
; 380(3): 210-219, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35031585
6.
Congenital dyserythropoietic anemia type I: First report from the Congenital Dyserythropoietic Anemia Registry of North America (CDAR).
Blood Cells Mol Dis
; 87: 102534, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33401150
7.
Alu element insertion in PKLR gene as a novel cause of pyruvate kinase deficiency in Middle Eastern patients.
Hum Mutat
; 39(3): 389-393, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29288557
8.
M-CSF supports medullary erythropoiesis and erythroid iron demand following burn injury through its activity on homeostatic iron recycling.
Sci Rep
; 12(1): 1235, 2022 01 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-35075211
9.
Autism-associated chromatin remodeler CHD8 regulates erythroblast cytokinesis and fine-tunes the balance of Rho GTPase signaling.
Cell Rep
; 40(2): 111072, 2022 07 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-35830790
10.
Automated Oxygen Gradient Ektacytometry: A Novel Biomarker in Sickle Cell Anemia.
Front Physiol
; 12: 636609, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33841173
11.
Corrigendum: The Spectrum of SPTA1-Associated Hereditary Spherocytosis.
Front Physiol
; 10: 1331, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31736770
12.
The Spectrum of SPTA1-Associated Hereditary Spherocytosis.
Front Physiol
; 10: 815, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31333484