These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

158 related articles for article (PubMed ID: 15695375)

  • 1. Genome-wide single nucleotide polymorphism analysis reveals frequent partial uniparental disomy due to somatic recombination in acute myeloid leukemias.
    Raghavan M; Lillington DM; Skoulakis S; Debernardi S; Chaplin T; Foot NJ; Lister TA; Young BD
    Cancer Res; 2005 Jan; 65(2):375-8. PubMed ID: 15695375
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukemias.
    Fitzgibbon J; Smith LL; Raghavan M; Smith ML; Debernardi S; Skoulakis S; Lillington D; Lister TA; Young BD
    Cancer Res; 2005 Oct; 65(20):9152-4. PubMed ID: 16230371
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genome-wide single-nucleotide polymorphism analysis in juvenile myelomonocytic leukemia identifies uniparental disomy surrounding the NF1 locus in cases associated with neurofibromatosis but not in cases with mutant RAS or PTPN11.
    Flotho C; Steinemann D; Mullighan CG; Neale G; Mayer K; Kratz CP; Schlegelberger B; Downing JR; Niemeyer CM
    Oncogene; 2007 Aug; 26(39):5816-21. PubMed ID: 17353900
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 93(7):994-1000. PubMed ID: 18508791
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Frequent loss of heterozygosity without loss of genetic material in acute myeloid leukemia with a normal karyotype.
    Gorletta TA; Gasparini P; D'Elios MM; Trubia M; Pelicci PG; Di Fiore PP
    Genes Chromosomes Cancer; 2005 Nov; 44(3):334-7. PubMed ID: 16015648
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of acquired copy number alterations and uniparental disomies in cytogenetically normal acute myeloid leukemia using high-resolution single-nucleotide polymorphism analysis.
    Bullinger L; Krönke J; Schön C; Radtke I; Urlbauer K; Botzenhardt U; Gaidzik V; Carió A; Senger C; Schlenk RF; Downing JR; Holzmann K; Döhner K; Döhner H
    Leukemia; 2010 Feb; 24(2):438-49. PubMed ID: 20016533
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Single nucleotide polymorphism microarray analysis of karyotypically normal acute myeloid leukemia reveals frequent copy number neutral loss of heterozygosity.
    Tyybäkinoja A; Elonen E; Vauhkonen H; Saarela J; Knuutila S
    Haematologica; 2008 Apr; 93(4):631-2. PubMed ID: 18379011
    [No Abstract]   [Full Text] [Related]  

  • 8. Complex and segmental uniparental disomy updated.
    Kotzot D
    J Med Genet; 2008 Sep; 45(9):545-56. PubMed ID: 18524837
    [TBL] [Abstract][Full Text] [Related]  

  • 9. High-density single nucleotide polymorphism array analysis and ASXL1 gene mutation screening in chronic myeloid leukemia during disease progression.
    Boultwood J; Perry J; Zaman R; Fernandez-Santamaria C; Littlewood T; Kusec R; Pellagatti A; Wang L; Clark RE; Wainscoat JS
    Leukemia; 2010 Jun; 24(6):1139-45. PubMed ID: 20410925
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Frequent occurrence of uniparental disomy in colorectal cancer.
    Andersen CL; Wiuf C; Kruhøffer M; Korsgaard M; Laurberg S; Ørntoft TF
    Carcinogenesis; 2007 Jan; 28(1):38-48. PubMed ID: 16774939
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genome-wide DNA-mapping of CD34+ cells from patients with myelodysplastic syndrome using 500K SNP arrays identifies significant regions of deletion and uniparental disomy.
    Nowak D; Nolte F; Mossner M; Nowak V; Baldus CD; Hopfer O; Noll S; Thiel E; Wagner F; Hofmann WK
    Exp Hematol; 2009 Feb; 37(2):215-224. PubMed ID: 19135900
    [TBL] [Abstract][Full Text] [Related]  

  • 12. High-resolution genomic copy number profiling of glioblastoma multiforme by single nucleotide polymorphism DNA microarray.
    Yin D; Ogawa S; Kawamata N; Tunici P; Finocchiaro G; Eoli M; Ruckert C; Huynh T; Liu G; Kato M; Sanada M; Jauch A; Dugas M; Black KL; Koeffler HP
    Mol Cancer Res; 2009 May; 7(5):665-77. PubMed ID: 19435819
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Visualization of uniparental inheritance, Mendelian inconsistencies, deletions, and parent of origin effects in single nucleotide polymorphism trio data with SNPtrio.
    Ting JC; Roberson ED; Miller ND; Lysholm-Bernacchi A; Stephan DA; Capone GT; Ruczinski I; Thomas GH; Pevsner J
    Hum Mutat; 2007 Dec; 28(12):1225-35. PubMed ID: 17661425
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Detection of cryptic chromosomal lesions including acquired segmental uniparental disomy in advanced and low-risk myelodysplastic syndromes.
    Gondek LP; Haddad AS; O'Keefe CL; Tiu R; Wlodarski MW; Sekeres MA; Theil KS; Maciejewski JP
    Exp Hematol; 2007 Nov; 35(11):1728-38. PubMed ID: 17920760
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mitotic recombination and uniparental disomy in Beckwith-Wiedemann syndrome.
    Cooper WN; Curley R; Macdonald F; Maher ER
    Genomics; 2007 May; 89(5):613-7. PubMed ID: 17337339
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Uniparental disomy analysis in trios using genome-wide SNP array and whole-genome sequencing data imply segmental uniparental isodisomy in general populations.
    Sasaki K; Mishima H; Miura K; Yoshiura K
    Gene; 2013 Jan; 512(2):267-74. PubMed ID: 23111162
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Risk assessment in patients with acute myeloid leukemia and a normal karyotype.
    Bienz M; Ludwig M; Leibundgut EO; Mueller BU; Ratschiller D; Solenthaler M; Fey MF; Pabst T
    Clin Cancer Res; 2005 Feb; 11(4):1416-24. PubMed ID: 15746041
    [TBL] [Abstract][Full Text] [Related]  

  • 18. ABL single nucleotide polymorphisms may masquerade as BCR-ABL mutations associated with resistance to tyrosine kinase inhibitors in patients with chronic myeloid leukemia.
    Ernst T; Hoffmann J; Erben P; Hanfstein B; Leitner A; Hehlmann R; Hochhaus A; Müller MC
    Haematologica; 2008 Sep; 93(9):1389-93. PubMed ID: 18603549
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Epimutation at human chromosome 14q32.2 in a boy with a upd(14)mat-like clinical phenotype.
    Zechner U; Kohlschmidt N; Rittner G; Damatova N; Beyer V; Haaf T; Bartsch O
    Clin Genet; 2009 Mar; 75(3):251-8. PubMed ID: 19250383
    [TBL] [Abstract][Full Text] [Related]  

  • 20. SNP-Array genotyping and spectral karyotyping reveal uniparental disomy as early mutational event in MSS- and MSI-colorectal cancer cell lines.
    Melcher R; Al-Taie O; Kudlich T; Hartmann E; Maisch S; Steinlein C; Schmid M; Rosenwald A; Menzel T; Scheppach W; Luhrs H
    Cytogenet Genome Res; 2007; 118(2-4):214-21. PubMed ID: 18000373
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.