193 related articles for article (PubMed ID: 18326324)
1. [Anemia in children].
Muramatsu H; Kojima S
Nihon Rinsho; 2008 Mar; 66(3):544-7. PubMed ID: 18326324
[TBL] [Abstract][Full Text] [Related]
2. Ribosomal dysfunction and inherited marrow failure.
Ganapathi KA; Shimamura A
Br J Haematol; 2008 May; 141(3):376-87. PubMed ID: 18410571
[TBL] [Abstract][Full Text] [Related]
3. [Diamond-Blackfan anemia reveals the dark side of ribosome biogenesis].
Aguissa-Touré AH; Da Costa L; Leblanc T; Tchernia G; Fribourg S; Gleizes PE
Med Sci (Paris); 2009 Jan; 25(1):69-76. PubMed ID: 19154697
[TBL] [Abstract][Full Text] [Related]
4. Guarding the 'translation apparatus': defective ribosome biogenesis and the p53 signaling pathway.
Chakraborty A; Uechi T; Kenmochi N
Wiley Interdiscip Rev RNA; 2011; 2(4):507-22. PubMed ID: 21957040
[TBL] [Abstract][Full Text] [Related]
5. Ribosomes and marrow failure: coincidental association or molecular paradigm?
Liu JM; Ellis SR
Blood; 2006 Jun; 107(12):4583-8. PubMed ID: 16507776
[TBL] [Abstract][Full Text] [Related]
6. Inherited bone marrow failure syndromes: molecular features.
Shimamura A
Hematology Am Soc Hematol Educ Program; 2006; ():63-71. PubMed ID: 17124042
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. Telomere length in inherited bone marrow failure syndromes.
Alter BP; Giri N; Savage SA; Rosenberg PS
Haematologica; 2015 Jan; 100(1):49-54. PubMed ID: 25304614
[TBL] [Abstract][Full Text] [Related]
10. Ribosomal protein mutations in Diamond-Blackfan anemia: might they operate upstream from protein synthesis?
Pederson T
FASEB J; 2007 Nov; 21(13):3442-5. PubMed ID: 17586729
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Diamond blackfan anemia: New paradigms for a "not so pure" inherited red cell aplasia.
Lipton JM
Semin Hematol; 2006 Jul; 43(3):167-77. PubMed ID: 16822459
[TBL] [Abstract][Full Text] [Related]
13. The genomics of inherited bone marrow failure: from mechanism to the clinic.
Wegman-Ostrosky T; Savage SA
Br J Haematol; 2017 May; 177(4):526-542. PubMed ID: 28211564
[TBL] [Abstract][Full Text] [Related]
14. Inherited bone marrow failure syndromes in adolescents and young adults.
Wilson DB; Link DC; Mason PJ; Bessler M
Ann Med; 2014 Sep; 46(6):353-63. PubMed ID: 24888387
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]
18. 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. PubMed ID: 21435510
[TBL] [Abstract][Full Text] [Related]
19. The genetic basis of bone marrow failure syndromes in children.
Federman N; Sakamoto KM
Mol Genet Metab; 2005; 86(1-2):100-9. PubMed ID: 16125992
[TBL] [Abstract][Full Text] [Related]
20. Mutation of ribosomal protein RPS24 in Diamond-Blackfan anemia results in a ribosome biogenesis disorder.
Choesmel V; Fribourg S; Aguissa-Touré AH; Pinaud N; Legrand P; Gazda HT; Gleizes PE
Hum Mol Genet; 2008 May; 17(9):1253-63. PubMed ID: 18230666
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
