List of works - Maria Rosaria Esposito

A novel erythroid anion exchange variant (Gly796Arg) of hereditary stomatocytosis associated with dyserythropoiesis

scientific article published on August 2009

Clinical aspects and pathogenesis of congenital dyserythropoietic anemias: from morphology to molecular approach

scientific article

Combating autophagy is a strategy to increase cytotoxic effects of novel ALK inhibitor entrectinib in neuroblastoma cells

scientific article published on 28 December 2015

Congenital dyserythropoietic anaemias: new acquisitions

scientific article published on 13 December 2010

Deregulation of focal adhesion pathway mediated by miR-659-3p is implicated in bone marrow infiltration of stage M neuroblastoma patients.

scientific article

Exome and deep sequencing of clinically aggressive neuroblastoma reveal somatic mutations that affect key pathways involved in cancer progression

scientific article published on 18 March 2016

Genetic abnormalities in adolescents and young adults with neuroblastoma: A report from the Italian Neuroblastoma group

scientific article published on 29 April 2015

Hypomorphic mutations of SEC23B gene account for mild phenotypes of congenital dyserythropoietic anemia type II

scientific article published on March 2013

Inherited hematological disorders due to defects in coat protein (COP)II complex.

scientific article published on 05 July 2012

Missense mutations in the ABCB6 transporter cause dominant familial pseudohyperkalemia.

scientific article

Molecular analysis of 42 patients with congenital dyserythropoietic anemia type II: new mutations in the SEC23B gene and a search for a genotype-phenotype relationship.

scientific article

Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1.

scientific article published on 11 March 2013

Mutational spectrum in congenital dyserythropoietic anemia type II: identification of 19 novel variants in SEC23B gene.

scientific article

Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II.

scientific article

Neuroblastoma treatment in the post-genomic era.

scientific article published on 08 February 2017

Patient-derived organoids (PDOs) as a novel in vitro model for neuroblastoma tumours

scientific article published on 21 October 2019

Somatic mutations in specific and connected subpathways are associated with short neuroblastoma patients' survival and indicate proteins targetable at onset of disease

scientific article published on 17 September 2018

List of works by Maria Rosaria Esposito

A novel erythroid anion exchange variant (Gly796Arg) of hereditary stomatocytosis associated with dyserythropoiesis

Clinical aspects and pathogenesis of congenital dyserythropoietic anemias: from morphology to molecular approach

Combating autophagy is a strategy to increase cytotoxic effects of novel ALK inhibitor entrectinib in neuroblastoma cells

Congenital dyserythropoietic anaemias: new acquisitions

Deregulation of focal adhesion pathway mediated by miR-659-3p is implicated in bone marrow infiltration of stage M neuroblastoma patients.

Exome and deep sequencing of clinically aggressive neuroblastoma reveal somatic mutations that affect key pathways involved in cancer progression

Genetic abnormalities in adolescents and young adults with neuroblastoma: A report from the Italian Neuroblastoma group

Hypomorphic mutations of SEC23B gene account for mild phenotypes of congenital dyserythropoietic anemia type II

Inherited hematological disorders due to defects in coat protein (COP)II complex.

Missense mutations in the ABCB6 transporter cause dominant familial pseudohyperkalemia.

Molecular analysis of 42 patients with congenital dyserythropoietic anemia type II: new mutations in the SEC23B gene and a search for a genotype-phenotype relationship.

Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1.

Mutational spectrum in congenital dyserythropoietic anemia type II: identification of 19 novel variants in SEC23B gene.

Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II.

Neuroblastoma treatment in the post-genomic era.

Patient-derived organoids (PDOs) as a novel in vitro model for neuroblastoma tumours

Somatic mutations in specific and connected subpathways are associated with short neuroblastoma patients' survival and indicate proteins targetable at onset of disease