497 related articles for article (PubMed ID: 18230666)
41. 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]
42. Ribosomal protein L5 and L11 mutations are associated with cleft palate and abnormal thumbs in Diamond-Blackfan anemia patients.
Gazda HT; Sheen MR; Vlachos A; Choesmel V; O'Donohue MF; Schneider H; Darras N; Hasman C; Sieff CA; Newburger PE; Ball SE; Niewiadomska E; Matysiak M; Zaucha JM; Glader B; Niemeyer C; Meerpohl JJ; Atsidaftos E; Lipton JM; Gleizes PE; Beggs AH
Am J Hum Genet; 2008 Dec; 83(6):769-80. PubMed ID: 19061985
[TBL] [Abstract][Full Text] [Related]
43. Genetic variants in the noncoding region of RPS19 gene in Diamond-Blackfan anemia: potential implications for phenotypic heterogeneity.
Crétien A; Proust A; Delaunay J; Rincé P; Leblanc T; Ducrocq R; Simansour M; Marie I; Tamary H; Meerpohl J; Niemeyer C; Gazda H; Sieff C; Ball S; Tchernia G; Mohandas N; Da Costa L
Am J Hematol; 2010 Feb; 85(2):111-6. PubMed ID: 20054847
[TBL] [Abstract][Full Text] [Related]
44. RPS19 mutations in patients with Diamond-Blackfan anemia.
Campagnoli MF; Ramenghi U; Armiraglio M; Quarello P; Garelli E; Carando A; Avondo F; Pavesi E; Fribourg S; Gleizes PE; Loreni F; Dianzani I
Hum Mutat; 2008 Jul; 29(7):911-20. PubMed ID: 18412286
[TBL] [Abstract][Full Text] [Related]
45. Clinical and genomic heterogeneity of Diamond Blackfan anemia in the Russian Federation.
Smetanina NS; Mersiyanova IV; Kurnikova MA; Ovsyannikova GS; Hachatryan LA; Bobrynina VO; Maschan MA; Novichkova GA; Lipton JM; Maschan AA
Pediatr Blood Cancer; 2015 Sep; 62(9):1597-600. PubMed ID: 25946618
[TBL] [Abstract][Full Text] [Related]
46. Mutations in RPS19 may affect ribosome function and biogenesis in Diamond Blackfan anemia.
Hiregange DG; Rivalta A; Yonath A; Zimmerman E; Bashan A; Yonath H
FEBS Open Bio; 2022 Jul; 12(7):1419-1434. PubMed ID: 35583751
[TBL] [Abstract][Full Text] [Related]
47. Missense mutations associated with Diamond-Blackfan anemia affect the assembly of ribosomal protein S19 into the ribosome.
Angelini M; Cannata S; Mercaldo V; Gibello L; Santoro C; Dianzani I; Loreni F
Hum Mol Genet; 2007 Jul; 16(14):1720-7. PubMed ID: 17517689
[TBL] [Abstract][Full Text] [Related]
48. Erythropoiesis in the Rps19 disrupted mouse: Analysis of erythropoietin response and biochemical markers for Diamond-Blackfan anemia.
Matsson H; Davey EJ; Fröjmark AS; Miyake K; Utsugisawa T; Flygare J; Zahou E; Byman I; Landin B; Ronquist G; Karlsson S; Dahl N
Blood Cells Mol Dis; 2006; 36(2):259-64. PubMed ID: 16458028
[TBL] [Abstract][Full Text] [Related]
49. A novel mutation of ribosomal protein S10 gene in a Japanese patient with diamond-Blackfan anemia.
Yazaki M; Kamei M; Ito Y; Konno Y; Wang R; Toki T; Ito E
J Pediatr Hematol Oncol; 2012 May; 34(4):293-5. PubMed ID: 22510774
[TBL] [Abstract][Full Text] [Related]
50. A novel initiation codon mutation in the ribosomal protein S17 gene (RPS17) in a patient with Diamond-Blackfan anemia.
Song MJ; Yoo EH; Lee KO; Kim GN; Kim HJ; Kim SY; Kim SH
Pediatr Blood Cancer; 2010 Apr; 54(4):629-31. PubMed ID: 19953637
[TBL] [Abstract][Full Text] [Related]
51. Fibroblasts from patients with Diamond-Blackfan anaemia show abnormal expression of genes involved in protein synthesis, amino acid metabolism and cancer.
Avondo F; Roncaglia P; Crescenzio N; Krmac H; Garelli E; Armiraglio M; Castagnoli C; Campagnoli MF; Ramenghi U; Gustincich S; Santoro C; Dianzani I
BMC Genomics; 2009 Sep; 10():442. PubMed ID: 19765279
[TBL] [Abstract][Full Text] [Related]
52. 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]
53. Defective ribosomal protein gene expression alters transcription, translation, apoptosis, and oncogenic pathways in Diamond-Blackfan anemia.
Gazda HT; Kho AT; Sanoudou D; Zaucha JM; Kohane IS; Sieff CA; Beggs AH
Stem Cells; 2006 Sep; 24(9):2034-44. PubMed ID: 16741228
[TBL] [Abstract][Full Text] [Related]
54. Ribosomal protein genes RPS10 and RPS26 are commonly mutated in Diamond-Blackfan anemia.
Doherty L; Sheen MR; Vlachos A; Choesmel V; O'Donohue MF; Clinton C; Schneider HE; Sieff CA; Newburger PE; Ball SE; Niewiadomska E; Matysiak M; Glader B; Arceci RJ; Farrar JE; Atsidaftos E; Lipton JM; Gleizes PE; Gazda HT
Am J Hum Genet; 2010 Feb; 86(2):222-8. PubMed ID: 20116044
[TBL] [Abstract][Full Text] [Related]
55. Exploiting pre-rRNA processing in Diamond Blackfan anemia gene discovery and diagnosis.
Farrar JE; Quarello P; Fisher R; O'Brien KA; Aspesi A; Parrella S; Henson AL; Seidel NE; Atsidaftos E; Prakash S; Bari S; Garelli E; Arceci RJ; Dianzani I; Ramenghi U; Vlachos A; Lipton JM; Bodine DM; Ellis SR
Am J Hematol; 2014 Oct; 89(10):985-91. PubMed ID: 25042156
[TBL] [Abstract][Full Text] [Related]
56. Ribosomal and hematopoietic defects in induced pluripotent stem cells derived from Diamond Blackfan anemia patients.
Garçon L; Ge J; Manjunath SH; Mills JA; Apicella M; Parikh S; Sullivan LM; Podsakoff GM; Gadue P; French DL; Mason PJ; Bessler M; Weiss MJ
Blood; 2013 Aug; 122(6):912-21. PubMed ID: 23744582
[TBL] [Abstract][Full Text] [Related]
57. Systematic transcriptome analysis of the zebrafish model of diamond-blackfan anemia induced by RPS24 deficiency.
Song B; Zhang Q; Zhang Z; Wan Y; Jia Q; Wang X; Zhu X; Leung AY; Cheng T; Fang X; Yuan W; Jia H
BMC Genomics; 2014 Sep; 15(1):759. PubMed ID: 25189322
[TBL] [Abstract][Full Text] [Related]
58. Ribosomal protein S17 gene (RPS17) is mutated in Diamond-Blackfan anemia.
Cmejla R; Cmejlova J; Handrkova H; Petrak J; Pospisilova D
Hum Mutat; 2007 Dec; 28(12):1178-82. PubMed ID: 17647292
[TBL] [Abstract][Full Text] [Related]
59. Human gene mutations. Gene symbol: RPS19. Disease: Diamond-Blackfan anaemia.
Pereira J; Sznajer Y; Ribeiro ML
Hum Genet; 2007 Sep; 122(2):213. PubMed ID: 18386371
[No Abstract] [Full Text] [Related]
60. Human gene mutations. Gene symbol: RPS19. Disease: Diamond-Blackfan anaemia.
Pereira J; Molinés A; Ribeiro ML
Hum Genet; 2007 Sep; 122(2):213. PubMed ID: 18386370
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
