BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

394 related articles for article (PubMed ID: 25132370)

  • 21. Czech and Slovak Diamond-Blackfan Anemia (DBA) Registry update: Clinical data and novel causative genetic lesions.
    Volejnikova J; Vojta P; Urbankova H; Mojzíkova R; Horvathova M; Hochova I; Cermak J; Blatny J; Sukova M; Bubanska E; Feketeova J; Prochazkova D; Horakova J; Hajduch M; Pospisilova D
    Blood Cells Mol Dis; 2020 Mar; 81():102380. PubMed ID: 31855845
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. [Diagnostic targets and exosome sequence analysis of Diamond-Blackfan anemia in Japan].
    Toki T; Ito E
    Rinsho Ketsueki; 2018; 59(7):945-952. PubMed ID: 30078807
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. Ribosomal protein S19 gene mutations in patients with diamond-blackfan anemia and identification of ribosomal protein S19 pseudogenes.
    Cmejla R; Blafkova J; Stopka T; Zavadil J; Pospisilova D; Mihal V; Petrtylova K; Jelinek J
    Blood Cells Mol Dis; 2000 Apr; 26(2):124-32. PubMed ID: 10753603
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Extensive gene deletions in Japanese patients with Diamond-Blackfan anemia.
    Kuramitsu M; Sato-Otsubo A; Morio T; Takagi M; Toki T; Terui K; Wang R; Kanno H; Ohga S; Ohara A; Kojima S; Kitoh T; Goi K; Kudo K; Matsubayashi T; Mizue N; Ozeki M; Masumi A; Momose H; Takizawa K; Mizukami T; Yamaguchi K; Ogawa S; Ito E; Hamaguchi I
    Blood; 2012 Mar; 119(10):2376-84. PubMed ID: 22262766
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. High frequency of ribosomal protein gene deletions in Italian Diamond-Blackfan anemia patients detected by multiplex ligation-dependent probe amplification assay.
    Quarello P; Garelli E; Brusco A; Carando A; Mancini C; Pappi P; Vinti L; Svahn J; Dianzani I; Ramenghi U
    Haematologica; 2012 Dec; 97(12):1813-7. PubMed ID: 22689679
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Ten novel Diamond-Blackfan anemia mutations and three polymorphisms within the rps19 gene.
    Proust A; Da Costa L; Rince P; Landois A; Tamary H; Zaizov R; Tchernia G; Delaunay J;
    Hematol J; 2003; 4(2):132-6. PubMed ID: 12750732
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Clinical features and pathogenic gene detection of Diamond-Blackfan anemia].
    He X; Xu ZL
    Zhongguo Dang Dai Er Ke Za Zhi; 2017 Feb; 19(2):171-175. PubMed ID: 28202115
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Diamond Blackfan Anemia: A Nonclassical Patient With Diagnosis Assisted by Genomic Analysis.
    Steinberg-Shemer O; Keel S; Dgany O; Walsh T; Noy-Lotan S; Krasnov T; Yacobovich J; Quarello P; Ramenghi U; King MC; Shimamura A; Tamary H
    J Pediatr Hematol Oncol; 2016 Oct; 38(7):e260-2. PubMed ID: 27258031
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Novel deletion of RPL15 identified by array-comparative genomic hybridization in Diamond-Blackfan anemia.
    Landowski M; O'Donohue MF; Buros C; Ghazvinian R; Montel-Lehry N; Vlachos A; Sieff CA; Newburger PE; Niewiadomska E; Matysiak M; Glader B; Atsidaftos E; Lipton JM; Beggs AH; Gleizes PE; Gazda HT
    Hum Genet; 2013 Nov; 132(11):1265-74. PubMed ID: 23812780
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Lentiviral Vectors with Cellular Promoters Correct Anemia and Lethal Bone Marrow Failure in a Mouse Model for Diamond-Blackfan Anemia.
    Debnath S; Jaako P; Siva K; Rothe M; Chen J; Dahl M; Gaspar HB; Flygare J; Schambach A; Karlsson S
    Mol Ther; 2017 Aug; 25(8):1805-1814. PubMed ID: 28434866
    [TBL] [Abstract][Full Text] [Related]  

  • 36. RNA and protein evidence for haplo-insufficiency in Diamond-Blackfan anaemia patients with RPS19 mutations.
    Gazda HT; Zhong R; Long L; Niewiadomska E; Lipton JM; Ploszynska A; Zaucha JM; Vlachos A; Atsidaftos E; Viskochil DH; Niemeyer CM; Meerpohl JJ; Rokicka-Milewska R; Pospisilova D; Wiktor-Jedrzejczak W; Nathan DG; Beggs AH; Sieff CA
    Br J Haematol; 2004 Oct; 127(1):105-13. PubMed ID: 15384984
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Primary hematopoietic cells from DBA patients with mutations in RPL11 and RPS19 genes exhibit distinct erythroid phenotype in vitro.
    Moniz H; Gastou M; Leblanc T; Hurtaud C; Crétien A; Lécluse Y; Raslova H; Larghero J; Croisille L; Faubladier M; Bluteau O; Lordier L; Tchernia G; Vainchenker W; Mohandas N; Da Costa L;
    Cell Death Dis; 2012 Jul; 3(7):e356. PubMed ID: 22833095
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Critical Diamond-Blackfan anemia due to ribosomal protein S19 missense mutation.
    Ozono S; Mitsuo M; Noguchi M; Nakagawa S; Ueda K; Inada H; Ohga S; Ito E
    Pediatr Int; 2016 Sep; 58(9):930-3. PubMed ID: 27601194
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Pediatric Diamond-Blackfan anemia in the Netherlands: An overview of clinical characteristics and underlying molecular defects.
    van Dooijeweert B; van Ommen CH; Smiers FJ; Tamminga RYJ; Te Loo MW; Donker AE; Peters M; Granzen B; Gille HJJP; Bierings MB; MacInnes AW; Bartels M
    Eur J Haematol; 2018 Feb; 100(2):163-170. PubMed ID: 29114930
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 20.