Ribosomal protein gene deletions in Diamond-Blackfan anemia.
Farrar JE, Vlachos A, Atsidaftos E, Carlson-Donohoe H, Markello TC, Arceci RJ, Ellis SR, Lipton JM, Bodine DM. Blood. 2011 Dec 22;118(26):6943-51. Epub 2011 Nov 1. PMID:22045982[PubMed – indexed for MEDLINE]

Fetal anemia of unknown cause–a diagnostic challenge.
Amann C, Geipel A, Müller A, Heep A, Ritgen J, Stressig R, Kozlowski P, Gembruch U, Berg C. Ultraschall Med. 2011 Dec;32 Suppl 2:E134-40. Epub 2011 Dec 9. PMID: 22161617[PubMed – in process]

Diamond Blackfan anemia.
Ball S.Hematology Am Soc Hematol Educ Program. 2011;2011:487-91. Review.PMID: 22160079 [PubMed – indexed for MEDLINE]

Mice with ribosomal protein S19 deficiency develop bone marrow failure and symptoms like patients with Diamond-Blackfan anemia.
Jaako P, Flygare J, Olsson K, Quere R, Ehinger M, Henson A, Ellis S, Schambach A, Baum C, Richter J, Larsson J, Bryder D, Karlsson S.Blood. 2011 Dec 1;118(23):6087-96. Epub 2011 Oct 11.PMID:21989989[PubMed – indexed for MEDLINE]

Guarding the ‘translation apparatus’: defective ribosome biogenesis and the p53 signaling pathway.
Chakraborty A, Uechi T, Kenmochi N. Wiley Interdiscip Rev RNA. 2011 Jul-Aug;2(4):507-22. doi: 10.1002/wrna.73. Epub 2011 Jan 20. Review.PMID: 21957040 [PubMed – indexed for MEDLINE]

Haploinsufficiency of ribosomal proteins and p53 activation in anemia: Diamond-Blackfan anemia and the 5q- syndrome.
Boultwood J, Pellagatti A, Wainscoat JS. Adv Enzyme Regul. 2011 Sep 12. [Epub ahead of print] No abstract available. PMID: 21930148 [PubMed – as supplied by publisher]

Reduced ribosomal protein gene dosage and p53 activation in low-risk myelodysplastic syndrome.
McGowan KA, Pang WW, Bhardwaj R, Perez MG, Pluvinage JV, Glader BE, Malek R, Mendrysa SM, Weissman IL, Park CY, Barsh GS. Blood. 2011 Sep 29;118(13):3622-33. Epub 2011 Jul 25. PMID: 21788341 [PubMed – in process]

Oral and dental manifestations of diamond-blackfan anemia: case reports.
Ozden FO, Gunduz K, Ozden B, Isci KD, Fisgin T. Eur J Dent. 2011 Jul;5(3):344-8. PMID: 21769279 [PubMed – in process]

Increased frequency of the glucocorticoid receptor A3669G (rs6198) polymorphism in patients with Diamond-Blackfan anemia.
Varricchio L, Godbold J, Scott SA, Whitsett C, Da Costa L, Pospisilova D, Garelli E, Quarello P, Ramenghi U, Migliaccio AR. Blood. 2011 Jul 14;118(2):473-4. No abstract available. PMID: 21757629 [PubMed – indexed for MEDLINE]

Managing the difficult case of fetal anemia.
Zhang EG, Regan F, Layton M, Paramasivam G, Wyatt-Ashmead J, Roberts I, Kumar S. J Matern Fetal Neonatal Med. 2011 Jun 30. [Epub ahead of print] PMID: 21714692 [PubMed – as supplied by publisher]

Neutrophil functions in patients with inherited bone marrow failure syndromes.
Rochowski A, Sun C, Glogauer M, Alter BP. Pediatr Blood Cancer. 2011 Aug;57(2):306-9. doi: 10.1002/pbc.22885. Epub 2010 Nov 5. PMID: 21671367 [PubMed – indexed for MEDLINE]

Genetic analysis of inherited bone marrow failure syndromes from one prospective, comprehensive and population-based cohort and identification of novel mutations.
Tsangaris E, Klaassen R, Fernandez CV, Yanofsky R, Shereck E, Champagne J, Silva M, Lipton JH, Brossard J, Michon B, Abish S, Steele M, Ali K, Dower N, Athale U, Jardine L, Hand JP, Odame I, Canning P, Allen C, Carcao M, Beyene J, Roifman CM, Dror Y. J Med Genet. 2011 Sep;48(9):618-28. Epub 2011 Jun 9. PMID: 21659346 [PubMed – in process]

Successful bone marrow transplantation in a patient with Diamond-Blackfan anemia with co-existing Duchenne muscular dystrophy: a case report.
Nair V, Das S, Sharma A, Sharma S, Kaur J, Mishra D. J Med Case Reports. 2011 Jun 4;5(1):216. PMID: 21639928 [PubMed]

[The congenital parcial erithroblastopenia–Diamond-Blackfan anemia.]
Kvazireli-Kopadze MA, Pagava KI, Korinteli IA. Georgian Med News. 2011 Apr;(193):81-5. Russian. PMID: 21617281 [PubMed – indexed for MEDLINE]

Dexamethasone and lenalidomide have distinct functional effects on erythropoiesis.
Narla A, Dutt S, McAuley JR, Al-Shahrour F, Hurst S, McConkey M, Neuberg D, Ebert BL. Blood. 2011 Aug 25;118(8):2296-304. Epub 2011 Apr 28. PMID: 21527522 [PubMed – in process]

The central core region of yeast ribosomal protein L11 is important for subunit joining and translational fidelity.
Rhodin MH, Rakauskaite R, Dinman JD. Mol Genet Genomics. 2011 Jun;285(6):505-16. Epub 2011 Apr 26. PMID: 21519857 [PubMed – indexed for MEDLINE]

Non-Diamond Blackfan anemia disorders of ribosome function: Shwachman Diamond syndrome and 5q- syndrome.
Burwick N, Shimamura A, Liu JM. Semin Hematol. 2011 Apr;48(2):136-43. Review. PMID: 21435510 [PubMed – in process]

Untangling the phenotypic heterogeneity of Diamond Blackfan anemia.
Farrar JE, Dahl N. Semin Hematol. 2011 Apr;48(2):124-35. PMID: 21435509 [PubMed – in process]

Diamond Blackfan anemia treatment: past, present, and future.
Narla A, Vlachos A, Nathan DG. Semin Hematol. 2011 Apr;48(2):117-23. PMID: 21435508 [PubMed – in process]

Animal models of Diamond Blackfan anemia.
McGowan KA, Mason PJ. Semin Hematol. 2011 Apr;48(2):106-16. PMID: 21435507 [PubMed – in process]

Diamond Blackfan anemia: ribosomal proteins going rogue.
Ellis SR, Gleizes PE. Semin Hematol. 2011 Apr;48(2):89-96. PMID: 21435505 [PubMed – in process]

Modeling Diamond Blackfan anemia in the zebrafish.
Taylor AM, Zon LI. Semin Hematol. 2011 Apr;48(2):81-8. PMID: 21435504 [PubMed – in process]

Patient advocacy in Diamond Blackfan anemia: facilitating translational research and progress towards the cure of a rare disease.
Arturi MC. Semin Hematol. 2011 Apr;48(2):75-80. No abstract available. PMID: 21435503 [PubMed – in process]

Diamond Blackfan anemia and ribosome biogenesis: introduction.
Ebert B, Lipton JM. Semin Hematol. 2011 Apr;48(2):73-4. No abstract available. PMID: 21435502 [PubMed – in process]

Can mutations in the ribosomal protein S26 (RPS26) gene lead to Klippel-Feil syndrome in Diamond-Blackfan anemia patients? An update from the Czech Diamond-Blackfan Anemia registry.
Cmejla R, Ludikova B, Sukova M, Blatny J, Pospisilova D. Blood Cells Mol Dis. 2011 Apr 15;46(4):300-1. No abstract available. PMID: 21414820 [PubMed – indexed for MEDLINE]

5’UTR variants of ribosomal protein S19 transcript determine translational efficiency: implications for Diamond-Blackfan anemia and tissue variability.
Badhai J, Schuster J, Gidlöf O, Dahl N. PLoS One. 2011 Mar 11;6(3):e17672. PMID: 21412415 [PubMed – indexed for MEDLINE]

Drawing to a Diamond flush.
Ellis SR. Blood. 2011 Mar 3;117(9):2558-9. PMID: 21372157 [PubMed]

Quantification of myocardial iron deposition by two-dimensional speckle tracking in patients with {beta}-thalassaemia major and Blackfan-Diamond anaemia.
Garceau P, Nguyen ET, Carasso S, Ross H, Pendergrast J, Moravsky G, Bruchal-Garbicz B, Rakowski H. Heart. 2011 Mar;97(5):388-93. PMID: 21296782 [PubMed – in process]

Ribosome defects in disorders of erythropoiesis.
Narla A, Hurst SN, Ebert BL. Int J Hematol. 2011 Feb;93(2):144-9. Epub 2011 Feb 1.PMID: 21279816 [PubMed – in process]

Clinical utility gene card for: Diamond Blackfan anemia.
Vlachos A, Dahl N, Dianzani I, Lipton JM. Eur J Hum Genet. 2011 Jan 19. doi: 10.1038/ejhg.2010.247. [Epub ahead of print] No abstract available. PMID: 21248735 [PubMed – as supplied by publisher]

Erythropoiesis failure due to RPS19 deficiency is independent of an activated Tp53 response in a zebrafish model of Diamond-Blackfan anaemia.
Torihara H, Uechi T, Chakraborty A, Shinya M, Sakai N, Kenmochi N. Br J Haematol. 2011 Mar;152(5):648-54. doi: 10.1111/j.1365-2141.2010.08535.x. Epub 2011 Jan 12. PMID: 21223253 [PubMed – in process]