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2. Study of the effects of proteasome inhibitors on ribosomal protein S19 (RPS19) mutants, identified in patients with Diamond-Blackfan anemia. Crétien A; Hurtaud C; Moniz H; Proust A; Marie I; Wagner-Ballon O; Choesmel V; Gleizes PE; Leblanc T; Delaunay J; Tchernia G; Mohandas N; Da Costa L Haematologica; 2008 Nov; 93(11):1627-34. PubMed ID: 18768533 [TBL] [Abstract][Full Text] [Related]
3. The functions of RPS19 and their relationship to Diamond-Blackfan anemia: a review. Morimoto K; Lin S; Sakamoto K Mol Genet Metab; 2007 Apr; 90(4):358-62. PubMed ID: 17178250 [TBL] [Abstract][Full Text] [Related]
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9. Enhanced alternative splicing of the FLVCR1 gene in Diamond Blackfan anemia disrupts FLVCR1 expression and function that are critical for erythropoiesis. Rey MA; Duffy SP; Brown JK; Kennedy JA; Dick JE; Dror Y; Tailor CS Haematologica; 2008 Nov; 93(11):1617-26. PubMed ID: 18815190 [TBL] [Abstract][Full Text] [Related]
10. First de novo mutation in RPS19 gene as the cause of hydrops fetalis in Diamond-Blackfan anemia. Da Costa L; Chanoz-Poulard G; Simansour M; French M; Bouvier R; Prieur F; Couque N; Delezoide AL; Leblanc T; Mohandas N; Touraine R Am J Hematol; 2013 Feb; 88(2):160. PubMed ID: 23349008 [No Abstract] [Full Text] [Related]
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