BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

186 related articles for article (PubMed ID: 26114957)

  • 1. Profound parental bias associated with chromosome 14 acquired uniparental disomy indicates targeting of an imprinted locus.
    Chase A; Leung W; Tapper W; Jones AV; Knoops L; Rasi C; Forsberg LA; Guglielmelli P; Zoi K; Hall V; Chiecchio L; Eder-Azanza L; Bryant C; Lannfelt L; Docherty L; White HE; Score J; Mackay DJ; Vannucchi AM; Dumanski JP; Cross NC
    Leukemia; 2015 Oct; 29(10):2069-74. PubMed ID: 26114957
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Paternal uniparental disomy chromosome 14-like syndrome due a maternal de novo 160 kb deletion at the 14q32.2 region not encompassing the IG- and the MEG3-DMRs: Patient report and genotype-phenotype correlation.
    Corsello G; Salzano E; Vecchio D; Antona V; Grasso M; Malacarne M; Carella M; Palumbo P; Piro E; Giuffrè M
    Am J Med Genet A; 2015 Dec; 167A(12):3130-8. PubMed ID: 26333487
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Epigenetic detection of human chromosome 14 uniparental disomy.
    Murphy SK; Wylie AA; Coveler KJ; Cotter PD; Papenhausen PR; Sutton VR; Shaffer LG; Jirtle RL
    Hum Mutat; 2003 Jul; 22(1):92-7. PubMed ID: 12815599
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical features of maternal uniparental disomy 14 in patients with an epimutation and a deletion of the imprinted DLK1/GTL2 gene cluster.
    Buiting K; Kanber D; Martín-Subero JI; Lieb W; Terhal P; Albrecht B; Purmann S; Gross S; Lich C; Siebert R; Horsthemke B; Gillessen-Kaesbach G
    Hum Mutat; 2008 Sep; 29(9):1141-6. PubMed ID: 18454453
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Acquired uniparental disomy in myeloproliferative neoplasms.
    Score J; Cross NC
    Hematol Oncol Clin North Am; 2012 Oct; 26(5):981-91. PubMed ID: 23009933
    [TBL] [Abstract][Full Text] [Related]  

  • 6. PRR14L mutations are associated with chromosome 22 acquired uniparental disomy, age-related clonal hematopoiesis and myeloid neoplasia.
    Chase A; Pellagatti A; Singh S; Score J; Tapper WJ; Lin F; Hoade Y; Bryant C; Trim N; Yip BH; Zoi K; Rasi C; Forsberg LA; Dumanski JP; Boultwood J; Cross NCP
    Leukemia; 2019 May; 33(5):1184-1194. PubMed ID: 30573780
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Epimutation (hypomethylation) affecting the chromosome 14q32.2 imprinted region in a girl with upd(14)mat-like phenotype.
    Hosoki K; Ogata T; Kagami M; Tanaka T; Saitoh S
    Eur J Hum Genet; 2008 Aug; 16(8):1019-23. PubMed ID: 18478039
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Novel homo- and hemizygous mutations in EZH2 in myeloid malignancies.
    Makishima H; Jankowska AM; Tiu RV; Szpurka H; Sugimoto Y; Hu Z; Saunthararajah Y; Guinta K; Keddache MA; Putnam P; Sekeres MA; Moliterno AR; List AF; McDevitt MA; Maciejewski JP
    Leukemia; 2010 Oct; 24(10):1799-804. PubMed ID: 20724984
    [No Abstract]   [Full Text] [Related]  

  • 9. Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes.
    Kagami M; Sekita Y; Nishimura G; Irie M; Kato F; Okada M; Yamamori S; Kishimoto H; Nakayama M; Tanaka Y; Matsuoka K; Takahashi T; Noguchi M; Tanaka Y; Masumoto K; Utsunomiya T; Kouzan H; Komatsu Y; Ohashi H; Kurosawa K; Kosaki K; Ferguson-Smith AC; Ishino F; Ogata T
    Nat Genet; 2008 Feb; 40(2):237-42. PubMed ID: 18176563
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Isolated imprinting mutation of the DLK1/GTL2 locus associated with a clinical presentation of maternal uniparental disomy of chromosome 14.
    Temple IK; Shrubb V; Lever M; Bullman H; Mackay DJ
    J Med Genet; 2007 Oct; 44(10):637-40. PubMed ID: 17601927
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Frequent CBL mutations associated with 11q acquired uniparental disomy in myeloproliferative neoplasms.
    Grand FH; Hidalgo-Curtis CE; Ernst T; Zoi K; Zoi C; McGuire C; Kreil S; Jones A; Score J; Metzgeroth G; Oscier D; Hall A; Brandts C; Serve H; Reiter A; Chase AJ; Cross NC
    Blood; 2009 Jun; 113(24):6182-92. PubMed ID: 19387008
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genomic imprinting of DIO3, a candidate gene for the syndrome associated with human uniparental disomy of chromosome 14.
    Martinez ME; Cox DF; Youth BP; Hernandez A
    Eur J Hum Genet; 2016 Nov; 24(11):1617-1621. PubMed ID: 27329732
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Molecular mechanisms regulating phenotypic outcome in paternal and maternal uniparental disomy for chromosome 14.
    Ogata T; Kagami M; Ferguson-Smith AC
    Epigenetics; 2008; 3(4):181-7. PubMed ID: 18698157
    [TBL] [Abstract][Full Text] [Related]  

  • 16. SNP array karyotyping allows for the detection of uniparental disomy and cryptic chromosomal abnormalities in MDS/MPD-U and MPD.
    Gondek LP; Dunbar AJ; Szpurka H; McDevitt MA; Maciejewski JP
    PLoS One; 2007 Nov; 2(11):e1225. PubMed ID: 18030353
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prenatal diagnosis of paternal uniparental disomy for chromosome 14 using a single-nucleotide-polymorphism-based microarray analysis: A case report.
    Chen CL; Lee CN; Lin MW; Hsu WW; Tai YY; Lin SY
    J Formos Med Assoc; 2019 Mar; 118(3):739-742. PubMed ID: 30616993
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A multiplex methylation PCR assay for identification of uniparental disomy of chromosome 7.
    Moore MW; Dietz LG; Tirtorahardjo B; Cotter PD
    Hum Mutat; 2003 Jun; 21(6):645-8. PubMed ID: 12754712
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Acquired uniparental disomy of chromosome 9p in hematologic malignancies.
    Wang L; Wheeler DA; Prchal JT
    Exp Hematol; 2016 Aug; 44(8):644-52. PubMed ID: 26646991
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Multiple segmental uniparental disomy associated with abnormal DNA methylation of imprinted Loci in silver-russell syndrome.
    Dias RP; Bogdarina I; Cazier JB; Buchanan C; Donaldson MC; Johnston LB; Hokken-Koelega AC; Clark AJ
    J Clin Endocrinol Metab; 2012 Nov; 97(11):E2188-93. PubMed ID: 22942387
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.