Literature DB >> 27540014

Increased levels of ERFE-encoding FAM132B in patients with congenital dyserythropoietic anemia type II.

Roberta Russo1,2, Immacolata Andolfo1,2, Francesco Manna2, Gianluca De Rosa2, Luigia De Falco1,2, Antonella Gambale1,2, Mariasole Bruno2,3, Alessandro Mattè3, Paolo Ricchi4, Domenico Girelli3, Lucia De Franceschi3, Achille Iolascon1,2.   

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Year:  2016        PMID： 27540014     DOI： 10.1182/blood-2016-06-724328

Source DB:  PubMed          Journal:  Blood        ISSN： 0006-4971            Impact factor:   22.113


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  9 in total

1.  GATA1 erythroid-specific regulation of SEC23B expression and its implication in the pathogenesis of congenital dyserythropoietic anemia type II.

Authors:  Roberta Russo; Immacolata Andolfo; Antonella Gambale; Gianluca De Rosa; Francesco Manna; Alessandra Arillo; Farooq Wandroo; Maria Grazia Bisconte; Achille Iolascon
Journal:  Haematologica       Date:  2017-05-26       Impact factor: 9.941

Review 2.  Modern iron replacement therapy: clinical and pathophysiological insights.

Authors:  Domenico Girelli; Sara Ugolini; Fabiana Busti; Giacomo Marchi; Annalisa Castagna
Journal:  Int J Hematol       Date:  2017-12-01       Impact factor: 2.490

Review 3.  The pathogenesis, diagnosis and management of congenital dyserythropoietic anaemia type I.

Authors:  Noémi B A Roy; Christian Babbs
Journal:  Br J Haematol       Date:  2019-03-05       Impact factor: 6.998

4.  CoDysAn: A Telemedicine Tool to Improve Awareness and Diagnosis for Patients With Congenital Dyserythropoietic Anemia.

Authors:  Cristian Tornador; Edgar Sánchez-Prados; Beatriz Cadenas; Roberta Russo; Veronica Venturi; Immacolata Andolfo; Ines Hernández-Rodriguez; Achille Iolascon; Mayka Sánchez
Journal:  Front Physiol       Date:  2019-09-13       Impact factor: 4.566

5.  Genetic disarray follows mutant KLF1-E325K expression in a congenital dyserythropoietic anemia patient.

Authors:  Lilian Varricchio; Antanas Planutis; Deepa Manwani; Julie Jaffray; W Beau Mitchell; Anna Rita Migliaccio; James J Bieker
Journal:  Haematologica       Date:  2019-03-14       Impact factor: 9.941

Review 6.  The Interplay between Drivers of Erythropoiesis and Iron Homeostasis in Rare Hereditary Anemias: Tipping the Balance.

Authors:  Simon Grootendorst; Jonathan de Wilde; Birgit van Dooijeweert; Annelies van Vuren; Wouter van Solinge; Roger Schutgens; Richard van Wijk; Marije Bartels
Journal:  Int J Mol Sci       Date:  2021-02-23       Impact factor: 5.923

7.  SEC23B Loss-of-Function Suppresses Hepcidin Expression by Impairing Glycosylation Pathway in Human Hepatic Cells.

Authors:  Barbara Eleni Rosato; Roberta Marra; Vanessa D'Onofrio; Federica Del Giudice; Simone Della Monica; Achille Iolascon; Immacolata Andolfo; Roberta Russo
Journal:  Int J Mol Sci       Date:  2022-01-24       Impact factor: 5.923

8.  Novel Insights and Future Perspective in Iron Metabolism and Anemia.

Authors:  Immacolata Andolfo; Roberta Russo
Journal:  Metabolites       Date:  2022-02-02

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

Authors:  Gianluca De Rosa; Immacolata Andolfo; Roberta Marra; Francesco Manna; Barbara Eleni Rosato; Achille Iolascon; Roberta Russo
Journal:  Int J Mol Sci       Date:  2020-08-04       Impact factor: 5.923
  9 in total

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