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Lista de obras de Achille Iolascon

A genomic deletion causes truncation of α-spectrin and ellipto-poikilocytosis ⬇️

artículo científico publicado el 5 de enero de 2011

Advances in understanding the pathogenesis of red cell membrane disorders

artículo científico publicado en 2019

Exploring Shared Susceptibility between Two Neural Crest Cells Originating Conditions: Neuroblastoma and Congenital Heart Disease

scientific article published on 30 August 2019

Gene expression analysis in HBV transgenic mouse liver: a model to study early events related to hepatocarcinogenesis

artículo científico publicado en 2006

Genetic analysis of the novel SARS-CoV-2 host receptor TMPRSS2 in different populations

artículo científico publicado en 2020

Genetic counseling during COVID-19 pandemic: Tuscany experience

artículo científico publicado en 2020

Guidelines for the diagnosis and management of hereditary spherocytosis – 2011 update ⬇️

artículo científico publicado el 5 de noviembre de 2011

Influence of ursodeoxycholate-enriched diet on liver tumor growth in HBV transgenic mice.

artículo científico publicado en 2003

Integrative genomics identifies LMO1 as a neuroblastoma oncogene

artículo científico publicado en 2010

Kinome expression profiling of human neuroblastoma tumors identifies potential drug targets for ultra high-risk patients

artículo científico publicado en 2017

MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness

artículo científico publicado en 2003

MiR-34a targeting of Notch ligand delta-like 1 impairs CD15+/CD133+ tumor-propagating cells and supports neural differentiation in medulloblastoma

artículo científico publicado en 2011

MicroRNA-199b-5p impairs cancer stem cells through negative regulation of HES1 in medulloblastoma

artículo científico publicado en 2009

Oxidative stress modulates heme synthesis and induces peroxiredoxin-2 as a novel cytoprotective response in -thalassemic erythropoiesis ⬇️

artículo científico publicado el 12 de julio de 2011

Phenotype restricted genome-wide association study using a gene-centric approach identifies three low-risk neuroblastoma susceptibility Loci.

artículo científico publicado en 2011

Position of nonmuscle myosin heavy chain IIA (NMMHC-IIA) mutations predicts the natural history of MYH9-related disease

artículo científico publicado en 2008

RAP-011 Rescues the Disease Phenotype in a Cellular Model of Congenital Dyserythropoietic Anemia Type II by Inhibiting the SMAD2-3 Pathway

artículo científico publicado en 2020

RB1CC1 duplication and aberrant overexpression in a patient with schizophrenia: further phenotype delineation and proposal of a pathogenetic mechanism

artículo científico publicado en 2020

Replication of GWAS-identified neuroblastoma risk loci strengthens the role of BARD1 and affirms the cumulative effect of genetic variations on disease susceptibility

artículo científico publicado en 2012

Resolution of sickle cell disease associated inflammation and tissue damage with 17R-Resolvin D1

scientific article published on 07 November 2018

Resveratrol accelerates erythroid maturation by activation of FoxO3 and ameliorates anemia in beta-thalassemic mice

artículo científico publicado en 2013

The Interplay Between Peroxiredoxin-2 and Nuclear Factor-Erythroid 2 Is Important in Limiting Oxidative Mediated Dysfunction in β-Thalassemic Erythropoiesis

artículo científico publicado en 2015

The metallophosphodiesterase Mpped2 impairs tumorigenesis in neuroblastoma.

artículo científico publicado en 2012

The micro-RNA 199b-5p regulatory circuit involves Hes1, CD15, and epigenetic modifications in medulloblastoma.

artículo científico publicado en 2012

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