Transduction with BBF2H7/CREB3L2 upregulates SEC23A protein in erythroblasts and partially corrects the hypo-glycosylation phenotype associated with CDAII

Br J Haematol. 2019 Mar;184(5):876-881. doi: 10.1111/bjh.15189. Epub 2018 Mar 14.

Stéphanie Pellegrin^{1

2

3}, Katy L Haydn-Smith^{1

2}, Lea A Hampton-O'Neil^{1

3}, Bethan R Hawley^{1

3}, Kate J Heesom¹, Elisa Fermo⁴, Paola Bianchi⁴, Ashley M Toye^{1

2

3}

¹ School of Biochemistry, Biomedical Sciences Building, University Walk Bristol, Bristol, UK.
² Bristol Institute of Transfusion Sciences, NHSBT Filton, Bristol, UK.
³ National Institute for Health Research (NIHR) Blood and Transplant Unit in Red Blood Cell Products at the University of Bristol, Bristol, UK.
⁴ Haematology Unit, Physiopathology of Anaemia Unit, Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.

No abstract available

Keywords: SEC23; congenital dyserythropoietic anaemia II; erythroid cell differentiation; erythropoiesis; hereditary anaemias.

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