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Achille Iolascon

Showing results (141-150 of 290) with videos related to

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Haematologica|December 1, 2020
Apparent recessive inheritance of sideroblastic anemia type 2 due to uniparental isodisomy at the SLC25A38 locusImmacolata Andolfo, Stefania Martone, Michela Ribersani, et al.
Clinical Chemistry and Laboratory Medicine|October 7, 2009
SOCS3 and IRS-1 gene expression differs between genotype 1 and genotype 2 hepatitis C virus-infected HepG2 cellsMarcello Persico, Roberta Russo, Eliana Persico, et al.
Genes|January 21, 2023
A Novel Variant in RAD21 in Cornelia De Lange Syndrome Type 4: Case Report and Bioinformatic AnalysisAlessandro De Falco, Daniele De Brasi, Matteo Della Monica, et al.
Frontiers in Physiology|August 28, 2020
Corrigendum: Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 ProteinRoberta Russo, Roberta Marra, Immacolata Andolfo, et al.
American Journal of Hematology|July 13, 2017
Targeted next generation sequencing identifies a novel β-spectrin gene mutation A2059P in two Omani children with hereditary pyropoikilocytosisArwa Z Al-Riyami, Achille Iolascon, Shoaib Al-Zadjali, et al.
Endocrine, Metabolic & Immune Disorders Drug Targets|February 27, 2023
A New <i>de novo</i> Mosaic Mutation of PHEX Gene: A Case Report of a Boy with Hypophosphatemic RicketsAlessandra Terracciano, Margherita Lucia De Bernardi, Roberto Novizio, et al.
Haematologica|July 14, 2011
Oxidative stress modulates heme synthesis and induces peroxiredoxin-2 as a novel cytoprotective response in β-thalassemic erythropoiesisLucia De Franceschi, Mariarita Bertoldi, Luigia De Falco, et al.
Frontiers in Physiology|June 14, 2019
Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 ProteinRoberta Russo, Roberta Marra, Immacolata Andolfo, et al.
American Journal of Hematology|November 18, 2024
RAS signaling pathway is essential in regulating PIEZO1-mediated hepatic iron overload in dehydrated hereditary stomatocytosisBarbara Eleni Rosato, Vanessa D'Onofrio, Roberta Marra, et al.
Blood|August 30, 2002
Splenectomy prolongs in vivo survival of erythrocytes differently in spectrin/ankyrin- and band 3-deficient hereditary spherocytosisRamune Reliene, Mariagabriella Mariani, Alberto Zanella, et al.
Pageof 29

Showing results (141-150 of 290) with videos related to

Sort By:
Pageof 29
Haematologica|December 1, 2020
Apparent recessive inheritance of sideroblastic anemia type 2 due to uniparental isodisomy at the SLC25A38 locusImmacolata Andolfo, Stefania Martone, Michela Ribersani, et al.
Clinical Chemistry and Laboratory Medicine|October 7, 2009
SOCS3 and IRS-1 gene expression differs between genotype 1 and genotype 2 hepatitis C virus-infected HepG2 cellsMarcello Persico, Roberta Russo, Eliana Persico, et al.
Genes|January 21, 2023
A Novel Variant in RAD21 in Cornelia De Lange Syndrome Type 4: Case Report and Bioinformatic AnalysisAlessandro De Falco, Daniele De Brasi, Matteo Della Monica, et al.
Frontiers in Physiology|August 28, 2020
Corrigendum: Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 ProteinRoberta Russo, Roberta Marra, Immacolata Andolfo, et al.
American Journal of Hematology|July 13, 2017
Targeted next generation sequencing identifies a novel β-spectrin gene mutation A2059P in two Omani children with hereditary pyropoikilocytosisArwa Z Al-Riyami, Achille Iolascon, Shoaib Al-Zadjali, et al.
Endocrine, Metabolic & Immune Disorders Drug Targets|February 27, 2023
A New <i>de novo</i> Mosaic Mutation of PHEX Gene: A Case Report of a Boy with Hypophosphatemic RicketsAlessandra Terracciano, Margherita Lucia De Bernardi, Roberto Novizio, et al.
Haematologica|July 14, 2011
Oxidative stress modulates heme synthesis and induces peroxiredoxin-2 as a novel cytoprotective response in β-thalassemic erythropoiesisLucia De Franceschi, Mariarita Bertoldi, Luigia De Falco, et al.
Frontiers in Physiology|June 14, 2019
Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 ProteinRoberta Russo, Roberta Marra, Immacolata Andolfo, et al.
American Journal of Hematology|November 18, 2024
RAS signaling pathway is essential in regulating PIEZO1-mediated hepatic iron overload in dehydrated hereditary stomatocytosisBarbara Eleni Rosato, Vanessa D'Onofrio, Roberta Marra, et al.
Blood|August 30, 2002
Splenectomy prolongs in vivo survival of erythrocytes differently in spectrin/ankyrin- and band 3-deficient hereditary spherocytosisRamune Reliene, Mariagabriella Mariani, Alberto Zanella, et al.
Pageof 29