292 related articles for article (PubMed ID: 18410571)
21. Distinct ribosome maturation defects in yeast models of Diamond-Blackfan anemia and Shwachman-Diamond syndrome.
Moore JB; Farrar JE; Arceci RJ; Liu JM; Ellis SR
Haematologica; 2010 Jan; 95(1):57-64. PubMed ID: 19713223
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. Diamond Blackfan anemia: A paradigm for a ribosome-based disease.
Ellis SR; Massey AT
Med Hypotheses; 2006; 66(3):643-8. PubMed ID: 16239073
[TBL] [Abstract][Full Text] [Related]
24. Diamond Blackfan anemia: a disorder of red blood cell development.
Ellis SR; Lipton JM
Curr Top Dev Biol; 2008; 82():217-41. PubMed ID: 18282522
[TBL] [Abstract][Full Text] [Related]
25. p53 in the Molecular Circuitry of Bone Marrow Failure Syndromes.
Rakotopare J; Toledo F
Int J Mol Sci; 2023 Oct; 24(19):. PubMed ID: 37834388
[TBL] [Abstract][Full Text] [Related]
26. Recent insights into the pathogenesis of Diamond-Blackfan anaemia.
Gazda HT; Sieff CA
Br J Haematol; 2006 Oct; 135(2):149-57. PubMed ID: 16942586
[TBL] [Abstract][Full Text] [Related]
27. Inherited aplastic anaemias/bone marrow failure syndromes.
Dokal I; Vulliamy T
Blood Rev; 2008 May; 22(3):141-53. PubMed ID: 18164793
[TBL] [Abstract][Full Text] [Related]
28. Phylogeny, sequence conservation, and functional complementation of the SBDS protein family.
Boocock GR; Marit MR; Rommens JM
Genomics; 2006 Jun; 87(6):758-71. PubMed ID: 16529906
[TBL] [Abstract][Full Text] [Related]
29. The pathology of bone marrow failure.
Leguit RJ; van den Tweel JG
Histopathology; 2010 Nov; 57(5):655-70. PubMed ID: 20727024
[TBL] [Abstract][Full Text] [Related]
30. The human Shwachman-Diamond syndrome protein, SBDS, associates with ribosomal RNA.
Ganapathi KA; Austin KM; Lee CS; Dias A; Malsch MM; Reed R; Shimamura A
Blood; 2007 Sep; 110(5):1458-65. PubMed ID: 17475909
[TBL] [Abstract][Full Text] [Related]
31. Genetic regulation of fetal haemoglobin in inherited bone marrow failure syndromes.
Alter BP; Rosenberg PS; Day T; Menzel S; Giri N; Savage SA; Thein SL
Br J Haematol; 2013 Aug; 162(4):542-6. PubMed ID: 23713742
[TBL] [Abstract][Full Text] [Related]
32. Dyskeratosis congenita: a genetic disorder of many faces.
Kirwan M; Dokal I
Clin Genet; 2008 Feb; 73(2):103-12. PubMed ID: 18005359
[TBL] [Abstract][Full Text] [Related]
33. Inherited bone marrow failure in the pediatric patient.
Dokal I; Tummala H; Vulliamy T
Blood; 2022 Aug; 140(6):556-570. PubMed ID: 35605178
[TBL] [Abstract][Full Text] [Related]
34. Genetic Information-Seeking Behaviors and Knowledge among Family Members and Patients with Inherited Bone Marrow Failure Syndromes.
Hamilton JG; Hutson SP; Frohnmayer AE; Han PK; Peters JA; Carr AG; Alter BP
J Genet Couns; 2015 Oct; 24(5):760-70. PubMed ID: 25540896
[TBL] [Abstract][Full Text] [Related]
35. Advances in understanding the genetic basis for bone-marrow failure.
Lieberman L; Dror Y
Curr Opin Pediatr; 2006 Feb; 18(1):15-21. PubMed ID: 16470156
[TBL] [Abstract][Full Text] [Related]
36. Clinical and genetic analysis of unclassifiable inherited bone marrow failure syndromes.
Teo JT; Klaassen R; Fernandez CV; Yanofsky R; Wu J; Champagne J; Silva M; Lipton JH; Brossard J; Samson Y; Abish S; Steele M; Ali K; Athale U; Jardine L; Hand JP; Tsangaris E; Odame I; Beyene J; Dror Y
Pediatrics; 2008 Jul; 122(1):e139-48. PubMed ID: 18595958
[TBL] [Abstract][Full Text] [Related]
37. Frequency and natural history of inherited bone marrow failure syndromes: the Israeli Inherited Bone Marrow Failure Registry.
Tamary H; Nishri D; Yacobovich J; Zilber R; Dgany O; Krasnov T; Aviner S; Stepensky P; Ravel-Vilk S; Bitan M; Kaplinsky C; Ben Barak A; Elhasid R; Kapelusnik J; Koren A; Levin C; Attias D; Laor R; Yaniv I; Rosenberg PS; Alter BP
Haematologica; 2010 Aug; 95(8):1300-7. PubMed ID: 20435624
[TBL] [Abstract][Full Text] [Related]
38. Ribosomopathies: human disorders of ribosome dysfunction.
Narla A; Ebert BL
Blood; 2010 Apr; 115(16):3196-205. PubMed ID: 20194897
[TBL] [Abstract][Full Text] [Related]
39. Do ribosomopathies explain some cases of common variable immunodeficiency?
Khan S; Pereira J; Darbyshire PJ; Holding S; Doré PC; Sewell WA; Huissoon A
Clin Exp Immunol; 2011 Jan; 163(1):96-103. PubMed ID: 21062271
[TBL] [Abstract][Full Text] [Related]
40. Genomic characterization of the inherited bone marrow failure syndromes.
Khincha PP; Savage SA
Semin Hematol; 2013 Oct; 50(4):333-47. PubMed ID: 24246701
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]