BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

512 related articles for article (PubMed ID: 18697920)

  • 21. Ribosomal protein mutations in Korean patients with Diamond-Blackfan anemia.
    Chae H; Park J; Lee S; Kim M; Kim Y; Lee JW; Chung NG; Cho B; Jeong DC; Kim J; Kim JR; Park G
    Exp Mol Med; 2014 Mar; 46(3):e88. PubMed ID: 24675553
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Loss of function mutations in RPL27 and RPS27 identified by whole-exome sequencing in Diamond-Blackfan anaemia.
    Wang R; Yoshida K; Toki T; Sawada T; Uechi T; Okuno Y; Sato-Otsubo A; Kudo K; Kamimaki I; Kanezaki R; Shiraishi Y; Chiba K; Tanaka H; Terui K; Sato T; Iribe Y; Ohga S; Kuramitsu M; Hamaguchi I; Ohara A; Hara J; Goi K; Matsubara K; Koike K; Ishiguro A; Okamoto Y; Watanabe K; Kanno H; Kojima S; Miyano S; Kenmochi N; Ogawa S; Ito E
    Br J Haematol; 2015 Mar; 168(6):854-64. PubMed ID: 25424902
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Ribosomal protein S24 gene is mutated in Diamond-Blackfan anemia.
    Gazda HT; Grabowska A; Merida-Long LB; Latawiec E; Schneider HE; Lipton JM; Vlachos A; Atsidaftos E; Ball SE; Orfali KA; Niewiadomska E; Da Costa L; Tchernia G; Niemeyer C; Meerpohl JJ; Stahl J; Schratt G; Glader B; Backer K; Wong C; Nathan DG; Beggs AH; Sieff CA
    Am J Hum Genet; 2006 Dec; 79(6):1110-8. PubMed ID: 17186470
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [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]  

  • 25. [Molecular mechanisms underlying the pathology of Diamond-Blackfan anemia].
    Toki T; Ito E
    Rinsho Ketsueki; 2015 Jul; 56(7):867-76. PubMed ID: 26251151
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Ribosomal protein S19 and S24 insufficiency cause distinct cell cycle defects in Diamond-Blackfan anemia.
    Badhai J; Fröjmark AS; J Davey E; Schuster J; Dahl N
    Biochim Biophys Acta; 2009 Oct; 1792(10):1036-42. PubMed ID: 19689926
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. 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]  

  • 29. 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]  

  • 30. Depletion of ribosomal protein S19 causes a reduction of rRNA synthesis.
    Juli G; Gismondi A; Monteleone V; Caldarola S; Iadevaia V; Aspesi A; Dianzani I; Proud CG; Loreni F
    Sci Rep; 2016 Oct; 6():35026. PubMed ID: 27734913
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Disorders of sex development and Diamond-Blackfan anemia: is there an association?
    Hoefele J; Bertrand AM; Stehr M; Leblanc T; Tchernia G; Simansour M; Mignot B; Alberer M; Schwarz HP; Da Costa L;
    Pediatr Nephrol; 2010 Jul; 25(7):1255-61. PubMed ID: 20358230
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Untangling the phenotypic heterogeneity of Diamond Blackfan anemia.
    Farrar JE; Dahl N
    Semin Hematol; 2011 Apr; 48(2):124-35. PubMed ID: 21435509
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Analysis of the interactome of ribosomal protein S19 mutants.
    Caterino M; Aspesi A; Pavesi E; Imperlini E; Pagnozzi D; Ingenito L; Santoro C; Dianzani I; Ruoppolo M
    Proteomics; 2014 Oct; 14(20):2286-96. PubMed ID: 25069755
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Mutations in the ribosomal protein genes in Japanese patients with Diamond-Blackfan anemia.
    Konno Y; Toki T; Tandai S; Xu G; Wang R; Terui K; Ohga S; Hara T; Hama A; Kojima S; Hasegawa D; Kosaka Y; Yanagisawa R; Koike K; Kanai R; Imai T; Hongo T; Park MJ; Sugita K; Ito E
    Haematologica; 2010 Aug; 95(8):1293-9. PubMed ID: 20378560
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. The in vivo functions of ARPF2 and ARRS1 in ribosomal RNA processing and ribosome biogenesis in Arabidopsis.
    Choi I; Jeon Y; Yoo Y; Cho HS; Pai HS
    J Exp Bot; 2020 May; 71(9):2596-2611. PubMed ID: 32275312
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Diamond Blackfan anemia and ribosome biogenesis: introduction.
    Ebert B; Lipton JM
    Semin Hematol; 2011 Apr; 48(2):73-4. PubMed ID: 21435502
    [No Abstract]   [Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 26.