Barbara Eleni Rosato Selected Research

Congenital Dyserythropoietic Anemia (Dyserythropoietic Anemia, Congenital)

1/2022	SEC23B Loss-of-Function Suppresses Hepcidin Expression by Impairing Glycosylation Pathway in Human Hepatic Cells.
11/2020	Uridine treatment normalizes the congenital dyserythropoietic anemia type II-like hematological phenotype in a patient with homozygous mutation in the CAD gene.
8/2020	RAP-011 Rescues the Disease Phenotype in a Cellular Model of Congenital Dyserythropoietic Anemia Type II by Inhibiting the SMAD2-3 Pathway.
1/2020	Corrigendum: Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 Protein.
1/2019	Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 Protein.

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Barbara Eleni Rosato Research Topics

Disease

5	Congenital Dyserythropoietic Anemia (Dyserythropoietic Anemia, Congenital) 01/2022 - 01/2019
4	Anemia 01/2022 - 12/2018
3	Iron Overload 01/2022 - 01/2020
2	COVID-19 01/2022 - 05/2021
2	Infections 01/2022 - 05/2021
1	Hemolysis 01/2022
1	Acute Erythroblastic Leukemia (Erythroleukemia) 08/2020

Drug/Important Bio-Agent (IBA)

3	IronIBA 08/2020 - 11/2019
2	Proteins (Proteins, Gene)FDA Link 01/2020 - 01/2019
1	HepcidinsIBA 01/2022
1	Membrane Proteins (Integral Membrane Proteins)IBA 01/2022
1	Prothrombin (Factor II)IBA 01/2022
1	LectinsIBA 01/2022
1	Complement System Proteins (Complement)IBA 01/2022
1	Biological ProductsIBA 05/2021
1	S- (2- chloro- 1,1,2- trifluoroethyl)cysteine (CTFC)IBA 05/2021
1	UridineIBA 11/2020
1	ACE-011IBA 08/2020
1	Hemin (Panhematin)FDA Link 08/2020
1	GATA1 Transcription FactorIBA 08/2020
1	Differentiation AntigensIBA 08/2020
1	ActRIIA-mIgG2aFc fusion proteinIBA 08/2020
1	PorphyrinsIBA 08/2020
1	CationsIBA 12/2018