115 related articles for article (PubMed ID: 10379869)
1. Mapping of the breakpoints on the short arm of chromosome 17 in neoplasms with an i(17q).
Scheurlen WG; Schwabe GC; Seranski P; Joos S; Harbott J; Metzke S; Döhner H; Poustka A; Wilgenbus K; Haas OA
Genes Chromosomes Cancer; 1999 Jul; 25(3):230-40. PubMed ID: 10379869
[TBL] [Abstract][Full Text] [Related]
2. Isochromosome 17q in blast crisis of chronic myeloid leukemia and in other hematologic malignancies is the result of clustered breakpoints in 17p11 and is not associated with coding TP53 mutations.
Fioretos T; Strömbeck B; Sandberg T; Johansson B; Billström R; Borg A; Nilsson PG; Van Den Berghe H; Hagemeijer A; Mitelman F; Höglund M
Blood; 1999 Jul; 94(1):225-32. PubMed ID: 10381517
[TBL] [Abstract][Full Text] [Related]
3. Interphase FISH screening for the LCR-mediated common rearrangement of isochromosome 17q in primary myelofibrosis.
Bien-Willner GA; Stankiewicz P; Lupski JR; Northup JK; Velagaleti GV
Am J Hematol; 2005 Aug; 79(4):309-13. PubMed ID: 16044457
[TBL] [Abstract][Full Text] [Related]
4. Isochromosome breakpoints on 17p in medulloblastoma are flanked by different classes of DNA sequence repeats.
Mendrzyk F; Korshunov A; Toedt G; Schwarz F; Korn B; Joos S; Hochhaus A; Schoch C; Lichter P; Radlwimmer B
Genes Chromosomes Cancer; 2006 Apr; 45(4):401-10. PubMed ID: 16419060
[TBL] [Abstract][Full Text] [Related]
5. High-resolution deletion mapping of chromosome arm 17p in childhood primitive neuroectodermal tumors reveals a common chromosomal disruption within the Smith-Magenis region, an unstable region in chromosome band 17p11.2.
Scheurlen WG; Seranski P; Mincheva A; Kühl J; Sörensen N; Krauss J; Lichter P; Poustka A; Wilgenbus KK
Genes Chromosomes Cancer; 1997 Jan; 18(1):50-8. PubMed ID: 8993980
[TBL] [Abstract][Full Text] [Related]
6. Molecular characterization of a genetically unstable region containing the SMS critical area and a breakpoint cluster for human PNETs.
Wilgenbus KK; Seranski P; Brown A; Leuchs B; Mincheva A; Lichter P; Poustka A
Genomics; 1997 May; 42(1):1-10. PubMed ID: 9177769
[TBL] [Abstract][Full Text] [Related]
7. Copy number variation at the breakpoint region of isochromosome 17q.
Carvalho CM; Lupski JR
Genome Res; 2008 Nov; 18(11):1724-32. PubMed ID: 18714090
[TBL] [Abstract][Full Text] [Related]
8. Relationship between Charcot-Marie-Tooth 1A and Smith-Magenis regions. snU3 may be a candidate gene for the Smith-Magenis syndrome.
Chevillard C; Le Paslier D; Passage E; Ougen P; Billault A; Boyer S; Mazan S; Bachellerie JP; Vignal A; Cohen D
Hum Mol Genet; 1993 Aug; 2(8):1235-43. PubMed ID: 8401506
[TBL] [Abstract][Full Text] [Related]
9. Comparative genomic hybridisation using a proximal 17p BAC/PAC array detects rearrangements responsible for four genomic disorders.
Shaw CJ; Shaw CA; Yu W; Stankiewicz P; White LD; Beaudet AL; Lupski JR
J Med Genet; 2004 Feb; 41(2):113-9. PubMed ID: 14757858
[TBL] [Abstract][Full Text] [Related]
10. Localization of the 17q breakpoint of a constitutional 1;17 translocation in a patient with neuroblastoma within a 25-kb segment located between the ACCN1 and TLK2 genes and near the distal breakpoints of two microdeletions in neurofibromatosis type 1 patients.
Van Roy N; Vandesompele J; Berx G; Staes K; Van Gele M; De Smet E; De Paepe A; Laureys G; van der Drift P; Versteeg R; Van Roy F; Speleman F
Genes Chromosomes Cancer; 2002 Oct; 35(2):113-20. PubMed ID: 12203774
[TBL] [Abstract][Full Text] [Related]
11. Molecular definition of breakpoints associated with human Xq isochromosomes: implications for mechanisms of formation.
Wolff DJ; Miller AP; Van Dyke DL; Schwartz S; Willard HF
Am J Hum Genet; 1996 Jan; 58(1):154-60. PubMed ID: 8554051
[TBL] [Abstract][Full Text] [Related]
12. Transcription mapping in a medulloblastoma breakpoint interval and Smith-Magenis syndrome candidate region: identification of 53 transcriptional units and new candidate genes.
Seranski P; Heiss NS; Dhorne-Pollet S; Radelof U; Korn B; Hennig S; Backes E; Schmidt S; Wiemann S; Schwarz CE; Lehrach H; Poustka A
Genomics; 1999 Feb; 56(1):1-11. PubMed ID: 10036180
[TBL] [Abstract][Full Text] [Related]
13. The breakpoint region of the most common isochromosome, i(17q), in human neoplasia is characterized by a complex genomic architecture with large, palindromic, low-copy repeats.
Barbouti A; Stankiewicz P; Nusbaum C; Cuomo C; Cook A; Höglund M; Johansson B; Hagemeijer A; Park SS; Mitelman F; Lupski JR; Fioretos T
Am J Hum Genet; 2004 Jan; 74(1):1-10. PubMed ID: 14666446
[TBL] [Abstract][Full Text] [Related]
14. Cytogenetic and fluorescence in situ hybridization characterization of chromosome 1 rearrangements in head and neck carcinomas delineate a target region for deletions within 1p11-1p13.
Jin Y; Jin C; Wennerberg J; Mertens F; Höglund M
Cancer Res; 1998 Dec; 58(24):5859-65. PubMed ID: 9865746
[TBL] [Abstract][Full Text] [Related]
15. FISH mapping of i(7q) in acute leukemias and myxoid liposarcoma reveals clustered breakpoints in 7p11.2: implications for formation and pathogenetic outcome of the idic(7)(p11.2).
Schaad K; Strömbeck B; Mandahl N; Andersen MK; Heim S; Mertens F; Johansson B
Cytogenet Genome Res; 2006; 114(2):126-30. PubMed ID: 16825763
[TBL] [Abstract][Full Text] [Related]
16. Characterization of a highly complex region in Xq13 and mapping of three isodicentric breakpoints associated with preleukemia.
McDonell N; Ramser J; Francis F; Vinet MC; Rider S; Sudbrak R; Riesselman L; Yaspo ML; Reinhardt R; Monaco AP; Ross F; Kahn A; Kearney L; Buckle V; Chelly J
Genomics; 2000 Mar; 64(3):221-9. PubMed ID: 10756090
[TBL] [Abstract][Full Text] [Related]
17. Early recurrence in standard-risk medulloblastoma patients with the common idic(17)(p11.2) rearrangement.
Bien-Willner GA; López-Terrada D; Bhattacharjee MB; Patel KU; Stankiewicz P; Lupski JR; Pfeifer JD; Perry A
Neuro Oncol; 2012 Jul; 14(7):831-40. PubMed ID: 22573308
[TBL] [Abstract][Full Text] [Related]
18. A DNA probe combination for improved detection of MLL/11q23 breakpoints by double-color interphase-FISH in acute leukemias.
von Bergh A; Emanuel B; van Zelderen-Bhola S; Smetsers T; van Soest R; Stul M; Vranckx H; Schuuring E; Hagemeijer A; Kluin P
Genes Chromosomes Cancer; 2000 May; 28(1):14-22. PubMed ID: 10738298
[TBL] [Abstract][Full Text] [Related]
19. Cytogenetic evaluation of isochromosome 17q in posterior fossa tumors of children and correlation with clinical outcome in medulloblastoma. Detection of a novel chromosomal abnormality.
DeChiara C; Borghese A; Fiorillo A; Genesio R; Conti A; D'Amore R; Pettinato G; Varone A; Maggi G
Childs Nerv Syst; 2002 Aug; 18(8):380-4. PubMed ID: 12192498
[TBL] [Abstract][Full Text] [Related]
20. Myeloid- and lymphoid-specific breakpoint cluster regions in chromosome band 13q14 in acute leukemia.
Coignet LJ; Lima CS; Min T; Streubel B; Swansbury J; Telford N; Swanton S; Bowen A; Nagai M; Catovsky D; Fonatsch C; Dyer MJ
Genes Chromosomes Cancer; 1999 Jul; 25(3):222-9. PubMed ID: 10379868
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
