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Primary hematopoietic cells from DBA patients with mutations in RPL11 and RPS19 genes exhibit distinct erythroid phenotype in vitro.
Moniz H, Gastou M, Leblanc T, Hurtaud C, Crétien A, Lécluse Y, Raslova H, Larghero J, Croisille L, Faubladier M, Bluteau O, Lordier L, Tchernia G, Vainchenker W, Mohandas N, Da Costa L; DBA Group of Société d'Hématologie et d'Immunologie Pédiatrique-SHIP. Moniz H, et al. Among authors: croisille l. Cell Death Dis. 2012 Jul 26;3(7):e356. doi: 10.1038/cddis.2012.88. Cell Death Dis. 2012. PMID: 22833095 Free PMC article.
Autoimmune disorders of erythropoiesis.
Croisille L, Tchernia G, Casadevall N. Croisille L, et al. Curr Opin Hematol. 2001 Mar;8(2):68-73. doi: 10.1097/00062752-200103000-00002. Curr Opin Hematol. 2001. PMID: 11224679 Review.
Dyserythropoiesis associated with a fas-deficient condition in childhood.
Bader-Meunier B, Rieux-Laucat F, Croisille L, Yvart J, Mielot F, Dommergues JP, Ledeist F, Tchernia G. Bader-Meunier B, et al. Among authors: croisille l. Br J Haematol. 2000 Feb;108(2):300-4. doi: 10.1046/j.1365-2141.2000.01862.x. Br J Haematol. 2000. PMID: 10691859 Free article.
36 results