BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

155 related articles for article (PubMed ID: 31574871)

  • 21. Molecular approaches to diagnose Diamond-Blackfan anemia: The EuroDBA experience.
    Da Costa L; O'Donohue MF; van Dooijeweert B; Albrecht K; Unal S; Ramenghi U; Leblanc T; Dianzani I; Tamary H; Bartels M; Gleizes PE; Wlodarski M; MacInnes AW
    Eur J Med Genet; 2018 Nov; 61(11):664-673. PubMed ID: 29081386
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. [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]  

  • 24. Short Stature in Patients with Diamond-Blackfan Anemia: A Cross-Sectional Study.
    Wan Y; Gong X; Cheng S; Yin Z; Gao Y; Li J; Zong S; Zhang Y; Chen Y; Zheng R; Zhu X
    J Pediatr; 2022 Jan; 240():177-185. PubMed ID: 34543620
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. Reduced gene expression of clustered ribosomal proteins in Diamond-Blackfan anemia patients without RPS19 gene mutations.
    Koga Y; Ohga S; Nomura A; Takada H; Hara T
    J Pediatr Hematol Oncol; 2006 Jun; 28(6):355-61. PubMed ID: 16794503
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Diamond-Blackfan anemia: genotype-phenotype correlations in Italian patients with RPL5 and RPL11 mutations.
    Quarello P; Garelli E; Carando A; Brusco A; Calabrese R; Dufour C; Longoni D; Misuraca A; Vinti L; Aspesi A; Biondini L; Loreni F; Dianzani I; Ramenghi U
    Haematologica; 2010 Feb; 95(2):206-13. PubMed ID: 19773262
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. 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]  

  • 30. 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]  

  • 31. 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]  

  • 32. Cells depleted for RPS19, a protein associated with Diamond Blackfan Anemia, show defects in 18S ribosomal RNA synthesis and small ribosomal subunit production.
    Idol RA; Robledo S; Du HY; Crimmins DL; Wilson DB; Ladenson JH; Bessler M; Mason PJ
    Blood Cells Mol Dis; 2007; 39(1):35-43. PubMed ID: 17376718
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. [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]  

  • 35. 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]  

  • 36. Identification of mutations in the ribosomal protein L5 (RPL5) and ribosomal protein L11 (RPL11) genes in Czech patients with Diamond-Blackfan anemia.
    Cmejla R; Cmejlova J; Handrkova H; Petrak J; Petrtylova K; Mihal V; Stary J; Cerna Z; Jabali Y; Pospisilova D
    Hum Mutat; 2009 Mar; 30(3):321-7. PubMed ID: 19191325
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Colorectal cancer screening and surveillance strategy for patients with Diamond Blackfan anemia: Preliminary recommendations from the Diamond Blackfan Anemia Registry.
    Lipton JM; Molmenti CLS; Hussain M; Desai P; Florento M; Atsidaftos E; Vlachos A
    Pediatr Blood Cancer; 2021 Aug; 68(8):e28984. PubMed ID: 34089224
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Variable expressivity and incomplete penetrance in a large family with non-classical Diamond-Blackfan anemia associated with ribosomal protein L11 splicing variant.
    Carlston CM; Afify ZA; Palumbos JC; Bagley H; Barbagelata C; Wooderchak-Donahue WL; Mao R; Carey JC
    Am J Med Genet A; 2017 Oct; 173(10):2622-2627. PubMed ID: 28742285
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.