Regulation of globin-heme balance in Diamond-Blackfan anemia by HSP70/GATA1.
Rio, Sarah; Gastou, Marc; Karboul, Narjesse; Derman, RaphaÑl; Suriyun, Thunwarat; Manceau, Hana; Leblanc, Thierry; El Benna, Jamel; Schmitt, Caroline; Azouzi, Slim; Larghéro, Jérome; Karim, Zoubida; Macias-Garcia, Alejandra; Chen, Jane-Jane; Hermine, Olivier; Courtois, Geneviève; Puy, Hervé; Gouya, Laurent; Mohandas, Narla; Da Costa, Lydie.
; 133(12): 1358-1370, 2019 03 21.
Artigo em Inglês | MEDLINE | ID: mdl-30700418
Functional Selectivity in Cytokine Signaling Revealed Through a Pathogenic EPO Mutation.
Molecular mechanisms of pathology and treatment in Diamond Blackfan Anaemia.
Molecular convergence in ex vivo models of Diamond-Blackfan anemia.
Concise Review: Advanced Cell Culture Models for Diamond Blackfan Anemia and Other Erythroid Disorders.
Critical Diamond-Blackfan anemia due to ribosomal protein S19 missense mutation.
[Molecular mechanisms underlying the pathology of Diamond-Blackfan anemia].
Erythropoiesis failure due to RPS19 deficiency is independent of an activated Tp53 response in a zebrafish model of Diamond-Blackfan anaemia.
Single-cell analyses demonstrate that a heme-GATA1 feedback loop regulates red cell differentiation.
A novel pathogenic mutation in RPL11 identified in a patient diagnosed with diamond Blackfan anemia as a young adult.
Distinct ribosome maturation defects in yeast models of Diamond-Blackfan anemia and Shwachman-Diamond syndrome.