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240 related items for PubMed ID: 18000384
21. Replication errors in hematological neoplasias: genomic instability in progression of disease is different among different types of leukemia. Ohyashiki JH, Ohyashiki K, Aizawa S, Kawakubo K, Shimamoto T, Iwama H, Hayashi S, Toyama K. Clin Cancer Res; 1996 Sep; 2(9):1583-9. PubMed ID: 9816337 [Abstract] [Full Text] [Related]
27. NPM1 mutations in myelodysplastic syndromes and acute myeloid leukemia with normal karyotype. Zhang Y, Zhang M, Yang L, Xiao Z. Leuk Res; 2007 Jan; 31(1):109-11. PubMed ID: 16678898 [Abstract] [Full Text] [Related]
30. The effectiveness of high-resolution-comparative genomic hybridization in detecting the most common chromosomal abnormalities in pediatric myelodysplastic syndromes. Babicz M, Kowalczyk JR, Winnicka D, Gaworczyk A, Lejman M, Dmowski R, Kaczanowska K. Cancer Genet Cytogenet; 2005 Apr 01; 158(1):49-54. PubMed ID: 15771904 [Abstract] [Full Text] [Related]
31. Genomic gain at 6p21: a new cryptic molecular rearrangement in secondary myelodysplastic syndrome and acute myeloid leukemia. La Starza R, Aventin A, Matteucci C, Crescenzi B, Romoli S, Testoni N, Pierini V, Ciolli S, Sambani C, Locasciulli A, Di Bona E, Lafage-Pochitaloff M, Martelli MF, Marynen P, Mecucci C. Leukemia; 2006 Jun 01; 20(6):958-64. PubMed ID: 16617324 [Abstract] [Full Text] [Related]
32. Myeloid cell differentiation arrest by miR-125b-1 in myelodysplastic syndrome and acute myeloid leukemia with the t(2;11)(p21;q23) translocation. Bousquet M, Quelen C, Rosati R, Mansat-De Mas V, La Starza R, Bastard C, Lippert E, Talmant P, Lafage-Pochitaloff M, Leroux D, Gervais C, Viguié F, Lai JL, Terre C, Beverlo B, Sambani C, Hagemeijer A, Marynen P, Delsol G, Dastugue N, Mecucci C, Brousset P. J Exp Med; 2008 Oct 27; 205(11):2499-506. PubMed ID: 18936236 [Abstract] [Full Text] [Related]
33. CYP2B6 gene single nucleotide polymorphisms and leukemia susceptibility. Yuan ZH, Liu Q, Zhang Y, Liu HX, Zhao J, Zhu P. Ann Hematol; 2011 Mar 27; 90(3):293-9. PubMed ID: 20878158 [Abstract] [Full Text] [Related]
36. Broad copy neutral-loss of heterozygosity regions and rare recurring copy number abnormalities in normal karyotype-acute myeloid leukemia genomes. Barresi V, Romano A, Musso N, Capizzi C, Consoli C, Martelli MP, Palumbo G, Di Raimondo F, Condorelli DF. Genes Chromosomes Cancer; 2010 Nov 27; 49(11):1014-23. PubMed ID: 20725993 [Abstract] [Full Text] [Related]
37. Genome-wide analysis of copy number changes and loss of heterozygosity in myelodysplastic syndrome with del(5q) using high-density single nucleotide polymorphism arrays. Wang L, Fidler C, Nadig N, Giagounidis A, Della Porta MG, Malcovati L, Killick S, Gattermann N, Aul C, Boultwood J, Wainscoat JS. Haematologica; 2008 Jul 27; 93(7):994-1000. PubMed ID: 18508791 [Abstract] [Full Text] [Related]
39. Delineation of yet unknown cryptic subtelomere aberrations in 50% of acute myeloid leukemia with normal GTG-banding karyotype. Gross M, Mkrtchyan H, Glaser M, Fricke HJ, Höffken K, Heller A, Weise A, Liehr T. Int J Oncol; 2009 Feb 27; 34(2):417-23. PubMed ID: 19148476 [Abstract] [Full Text] [Related]
40. Clinical Applications of Chromosomal Microarray Testing in Myeloid Malignancies. Ronaghy A, Yang RK, Khoury JD, Kanagal-Shamanna R. Curr Hematol Malig Rep; 2020 Jun 27; 15(3):194-202. PubMed ID: 32382988 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]