156 related articles for article (PubMed ID: 1333880)
1. Cytogenetic findings in a case of pediatric glioblastoma.
Sawyer JR; Swanson CM; Roloson GJ; Longee DC; Chadduck WM
Cancer Genet Cytogenet; 1992 Nov; 64(1):75-9. PubMed ID: 1333880
[TBL] [Abstract][Full Text] [Related]
2. [Characterization of chromosomal rearrangements by in situ hybridization in glioblastoma].
Bourgeois CA; Kokalj-Vokac N; Dutrillaux AM; Poisson M; Delattre JY; Vega F; Malfoy B; Dutrillaux B
Bull Cancer; 1994 May; 81(5):360-5. PubMed ID: 7538360
[TBL] [Abstract][Full Text] [Related]
3. Multiple structural chromosome rearrangements, including del(7q) and del(10q), in an adenocarcinoma of the prostate.
Lundgren R; Kristoffersson U; Heim S; Mandahl N; Mitelman F
Cancer Genet Cytogenet; 1988 Oct; 35(1):103-8. PubMed ID: 3180000
[TBL] [Abstract][Full Text] [Related]
4. A new der(1;7)(q10;p10) leading to a singular 1p loss in a case of glioblastoma with oligodendroglioma component.
Gadji M; Crous-Tsanaclis AM; Mathieu D; Mai S; Fortin D; Drouin R
Neuropathology; 2014 Apr; 34(2):170-8. PubMed ID: 24118308
[TBL] [Abstract][Full Text] [Related]
5. Molecular cytogenetic analysis of a t(7;10) in a human glioblastoma cell line.
Fults D; Pedone CA; Zhu XL; Williams BJ; Jones E; Brothman AR
Cancer Genet Cytogenet; 1995 Jun; 81(2):118-24. PubMed ID: 7621407
[TBL] [Abstract][Full Text] [Related]
6. Inv dup del(10q): identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements.
Chen CP; Chen M; Su YN; Huang JP; Ma GC; Chang SP; Chern SR; Chen YT; Su JW; Lee CC; Town DD; Wang W
Taiwan J Obstet Gynecol; 2012 Jun; 51(2):245-52. PubMed ID: 22795102
[TBL] [Abstract][Full Text] [Related]
7. Genetic reflection of glioblastoma biopsy material in xenografts: characterization of 11 glioblastoma xenograft lines by comparative genomic hybridization.
Jeuken JW; Sprenger SH; Wesseling P; Bernsen HJ; Suijkerbuijk RF; Roelofs F; Macville MV; Gilhuis HJ; van Overbeeke JJ; Boerman RH
J Neurosurg; 2000 Apr; 92(4):652-8. PubMed ID: 10761656
[TBL] [Abstract][Full Text] [Related]
8. Characterization of double minute chromosomes' DNA content in a human high grade astrocytoma cell line by using comparative genomic hybridization and fluorescence in situ hybridization.
Giollant M; Bertrand S; Verrelle P; Tchirkov A; du Manoir S; Ried T; Mornex F; Doré JF; Cremer T; Malet P
Hum Genet; 1996 Sep; 98(3):265-70. PubMed ID: 8707292
[TBL] [Abstract][Full Text] [Related]
9. Specific subtelomere loss on chromosome der(11)t(3;11)(q23;q23)x2 in anaplastic thyroid cancer cell line OCUT-1.
Kammori M; Onoda N; Nakamura K; Izumiyama N; Ogisawa K; Kurabayashi R; Ogawa T; Kaminishi M; Poon SS; Takubo K
Int J Mol Med; 2006 Jul; 18(1):9-16. PubMed ID: 16786150
[TBL] [Abstract][Full Text] [Related]
10. Telomeric associations in the progression of chromosome aberrations in pediatric solid tumors.
Sawyer JR; Roloson GJ; Bell JM; Thomas JR; Teo C; Chadduck WM
Cancer Genet Cytogenet; 1996 Aug; 90(1):1-13. PubMed ID: 8780739
[TBL] [Abstract][Full Text] [Related]
11. Telomeric fusion as a mechanism for the loss of 1p in meningioma.
Sawyer JR; Husain M; Lukacs JL; Stangeby C; Binz RL; Al-Mefty O
Cancer Genet Cytogenet; 2003 Aug; 145(1):38-48. PubMed ID: 12885461
[TBL] [Abstract][Full Text] [Related]
12. Fluorescence in situ hybridization study of aneuploidy of chromosomes 7, 10, X, and Y in primary and secondary glioblastomas.
Amalfitano G; Chatel M; Paquis P; Michiels JF
Cancer Genet Cytogenet; 2000 Jan; 116(1):6-9. PubMed ID: 10616524
[TBL] [Abstract][Full Text] [Related]
13. Submicroscopic terminal deletion of 1p36.3 and Xp23 hidden in complex chromosome rearrangements: independent mechanism of telomere restitution on the two chromatids.
Reddy KS; Yang X
Am J Med Genet A; 2003 Mar; 117A(3):261-7. PubMed ID: 12599190
[TBL] [Abstract][Full Text] [Related]
14. 47,XY,+der(X)t(X;18)(p11.4;p11.22): A Unique Aneuploidy Associated with Klinefelter Syndrome due to an Extra Derivative X Chromosome Inherited Maternally.
Liang J; Zhang Y; Wang R; Liang Z; Yue J; Liu R
Cytogenet Genome Res; 2015; 146(3):204-10. PubMed ID: 26430900
[TBL] [Abstract][Full Text] [Related]
15. A recurrent 19q11-12 breakpoint suggested by cytogenetic and fluorescence in situ hybridization analysis of three glioblastoma cell lines.
Magnani I; Chiariello E; Conti AM; Finocchiaro G
Cancer Genet Cytogenet; 1999 Apr; 110(2):82-6. PubMed ID: 10214354
[TBL] [Abstract][Full Text] [Related]
16. Molecular and cytogenetic analysis of glioblastoma multiforme.
Mao X; Hamoudi RA
Cancer Genet Cytogenet; 2000 Oct; 122(2):87-92. PubMed ID: 11106817
[TBL] [Abstract][Full Text] [Related]
17. Maternal translocation (9;18) with two abnormal offspring each with different chromosome derivatives.
Pearson M; Riske C; Allanson JE
J Med Genet; 1989 Oct; 26(10):655-8. PubMed ID: 2585464
[TBL] [Abstract][Full Text] [Related]
18. Distribution of epidermal growth factor receptor protein correlates with gain in chromosome 7 revealed by comparative genomic hybridization after microdissection in glioblastoma multiforme.
Romeike BF; Jung V; Feiden W; Moringlane JR; Zang KD; Urbschat SM
Pathol Res Pract; 2001; 197(6):427-31. PubMed ID: 11432670
[TBL] [Abstract][Full Text] [Related]
19. Genetic aberrations in glioblastoma multiforme: translocation of chromosome 10 in an O-2A-like cell line.
Mao X; Jones TA; Tomlinson I; Rowan AJ; Fedorova LI; Zelenin AV; Mao JI; Gutowski NJ; Noble M; Sheer D
Br J Cancer; 1999 Feb; 79(5-6):724-31. PubMed ID: 10070860
[TBL] [Abstract][Full Text] [Related]
20. A role for telomeric and centromeric instability in the progression of chromosome aberrations in meningioma patients.
Sawyer JR; Husain M; Pravdenkova S; Krisht A; Al-Mefty O
Cancer; 2000 Jan; 88(2):440-53. PubMed ID: 10640979
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]