BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

241 related articles for article (PubMed ID: 19915364)

  • 21. Gene symbol: RPS19. Disease: Diamond-Blackfan anaemia.
    Gonçalves P; Pereira JC; Kidd AM; Ribeiro ML
    Hum Genet; 2004 Nov; 115(6):534. PubMed ID: 15678589
    [No Abstract]   [Full Text] [Related]  

  • 22. L-Leucine improves the anaemia in models of Diamond Blackfan anaemia and the 5q- syndrome in a TP53-independent way.
    Narla A; Payne EM; Abayasekara N; Hurst SN; Raiser DM; Look AT; Berliner N; Ebert BL; Khanna-Gupta A
    Br J Haematol; 2014 Nov; 167(4):524-528. PubMed ID: 25098371
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. 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]  

  • 25. Activation of the mTOR pathway by the amino acid (L)-leucine in the 5q- syndrome and other ribosomopathies.
    Boultwood J; Yip BH; Vuppusetty C; Pellagatti A; Wainscoat JS
    Adv Biol Regul; 2013 Jan; 53(1):8-17. PubMed ID: 23031788
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [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]  

  • 27. Monolobated megakaryocytes in Diamond-Blackfan anemia with RPL5 mutation at disease presentation mimicking myelodysplastic syndrome.
    Setiadi A; Singh C; Li A; Au N; Amid A
    Pediatr Blood Cancer; 2024 Feb; 71(2):e30771. PubMed ID: 37988264
    [No Abstract]   [Full Text] [Related]  

  • 28. Haploinsufficiency of RPS14 in 5q- syndrome is associated with deregulation of ribosomal- and translation-related genes.
    Pellagatti A; Hellström-Lindberg E; Giagounidis A; Perry J; Malcovati L; Della Porta MG; Jädersten M; Killick S; Fidler C; Cazzola M; Wainscoat JS; Boultwood J
    Br J Haematol; 2008 Jul; 142(1):57-64. PubMed ID: 18477045
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Ribosomapathy: possible roles of ribosomal defects in human disease].
    Kenmochi N
    Tanpakushitsu Kakusan Koso; 2003 Mar; 48(4 Suppl):508-16. PubMed ID: 12696161
    [No Abstract]   [Full Text] [Related]  

  • 30. NRAS, FLT3 and TP53 mutations in patients with myelodysplastic syndrome and a del(5q).
    Fidler C; Watkins F; Bowen DT; Littlewood TJ; Wainscoat JS; Boultwood J
    Haematologica; 2004 Jul; 89(7):865-6. PubMed ID: 15257941
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Revealing the pathogenesis of the 5q- syndrome.
    Valent P
    Eur J Clin Invest; 2008 Aug; 38(8):539-40. PubMed ID: 18717823
    [No Abstract]   [Full Text] [Related]  

  • 32. 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]  

  • 33. Atypical erythroblastosis in a patient with Diamond-Blackfan anemia who developed del(20q) myelodysplasia.
    Sonoda M; Ishimura M; Ichimiya Y; Terashi E; Eguchi K; Sakai Y; Takada H; Hama A; Kanno H; Toki T; Ito E; Ohga S
    Int J Hematol; 2018 Aug; 108(2):228-231. PubMed ID: 29476317
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. L-Leucine improves the anemia and developmental defects associated with Diamond-Blackfan anemia and del(5q) MDS by activating the mTOR pathway.
    Payne EM; Virgilio M; Narla A; Sun H; Levine M; Paw BH; Berliner N; Look AT; Ebert BL; Khanna-Gupta A
    Blood; 2012 Sep; 120(11):2214-24. PubMed ID: 22734070
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Mice with a Mutation in the Mdm2 Gene That Interferes with MDM2/Ribosomal Protein Binding Develop a Defect in Erythropoiesis.
    Kamio T; Gu BW; Olson TS; Zhang Y; Mason PJ; Bessler M
    PLoS One; 2016; 11(4):e0152263. PubMed ID: 27042854
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Diamond Blackfan anemia.
    Ball S
    Hematology Am Soc Hematol Educ Program; 2011; 2011():487-91. PubMed ID: 22160079
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Ribosome defects in disorders of erythropoiesis.
    Narla A; Hurst SN; Ebert BL
    Int J Hematol; 2011 Feb; 93(2):144-149. PubMed ID: 21279816
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Deficiency of ribosomal protein S19 during early embryogenesis leads to reduction of erythrocytes in a zebrafish model of Diamond-Blackfan anemia.
    Uechi T; Nakajima Y; Chakraborty A; Torihara H; Higa S; Kenmochi N
    Hum Mol Genet; 2008 Oct; 17(20):3204-11. PubMed ID: 18653748
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.