260 related articles for article (PubMed ID: 12237235)
1. Comparative genomic hybridization detects specific cytogenetic abnormalities in pediatric ependymomas and choroid plexus papillomas.
Grill J; Avet-Loiseau H; Lellouch-Tubiana A; Sévenet N; Terrier-Lacombe MJ; Vénuat AM; Doz F; Sainte-Rose C; Kalifa C; Vassal G
Cancer Genet Cytogenet; 2002 Jul; 136(2):121-5. PubMed ID: 12237235
[TBL] [Abstract][Full Text] [Related]
2. Chromosome arm 6q loss is the most common recurrent autosomal alteration detected in primary pediatric ependymoma.
Reardon DA; Entrekin RE; Sublett J; Ragsdale S; Li H; Boyett J; Kepner JL; Look AT
Genes Chromosomes Cancer; 1999 Mar; 24(3):230-7. PubMed ID: 10451703
[TBL] [Abstract][Full Text] [Related]
3. Chromosomal imbalances in choroid plexus tumors.
Rickert CH; Wiestler OD; Paulus W
Am J Pathol; 2002 Mar; 160(3):1105-13. PubMed ID: 11891207
[TBL] [Abstract][Full Text] [Related]
4. Low frequency of chromosomal imbalances in anaplastic ependymomas as detected by comparative genomic hybridization.
Scheil S; Brüderlein S; Eicker M; Herms J; Herold-Mende C; Steiner HH; Barth TF; Möller P
Brain Pathol; 2001 Apr; 11(2):133-43. PubMed ID: 11303789
[TBL] [Abstract][Full Text] [Related]
5. Comparative genomic hybridization detects losses of chromosomes 22 and 16 as the most common recurrent genetic alterations in primary ependymomas.
Zheng PP; Pang JC; Hui AB; Ng HK
Cancer Genet Cytogenet; 2000 Oct; 122(1):18-25. PubMed ID: 11104027
[TBL] [Abstract][Full Text] [Related]
6. Genomic characterization of ependymomas reveals 6q loss as the most common aberration.
Olsen TK; Gorunova L; Meling TR; Micci F; Scheie D; Due-Tønnessen B; Heim S; Brandal P
Oncol Rep; 2014 Aug; 32(2):483-90. PubMed ID: 24939246
[TBL] [Abstract][Full Text] [Related]
7. Specific chromosomal imbalances as detected by array CGH in ependymomas in association with tumor location, histological subtype and grade.
Rousseau A; Idbaih A; Ducray F; Crinière E; Fèvre-Montange M; Jouvet A; Delattre JY
J Neurooncol; 2010 May; 97(3):353-64. PubMed ID: 19865800
[TBL] [Abstract][Full Text] [Related]
8. Gain of 1q and loss of 22 are the most common changes detected by comparative genomic hybridisation in paediatric ependymoma.
Ward S; Harding B; Wilkins P; Harkness W; Hayward R; Darling JL; Thomas DG; Warr T
Genes Chromosomes Cancer; 2001 Sep; 32(1):59-66. PubMed ID: 11477662
[TBL] [Abstract][Full Text] [Related]
9. Human ependymomas reveal frequent deletions on chromosomes 6 and 9.
Huang B; Starostik P; Schraut H; Krauss J; Sörensen N; Roggendorf W
Acta Neuropathol; 2003 Oct; 106(4):357-62. PubMed ID: 12898154
[TBL] [Abstract][Full Text] [Related]
10. High-resolution genomic analysis does not qualify atypical plexus papilloma as a separate entity among choroid plexus tumors.
Japp AS; Gessi M; Messing-Jünger M; Denkhaus D; Zur Mühlen A; Wolff JE; Hartung S; Kordes U; Klein-Hitpass L; Pietsch T
J Neuropathol Exp Neurol; 2015 Feb; 74(2):110-20. PubMed ID: 25575132
[TBL] [Abstract][Full Text] [Related]
11. Genetic abnormalities detected in ependymomas by comparative genomic hybridisation.
Carter M; Nicholson J; Ross F; Crolla J; Allibone R; Balaji V; Perry R; Walker D; Gilbertson R; Ellison DW
Br J Cancer; 2002 Mar; 86(6):929-39. PubMed ID: 11953826
[TBL] [Abstract][Full Text] [Related]
12. Genomic imbalances in pediatric intracranial ependymomas define clinically relevant groups.
Dyer S; Prebble E; Davison V; Davies P; Ramani P; Ellison D; Grundy R
Am J Pathol; 2002 Dec; 161(6):2133-41. PubMed ID: 12466129
[TBL] [Abstract][Full Text] [Related]
13. Fluorescence in situ hybridization determination of 22q12-q13 deletion in two intracerebral ependymomas.
Rousseau-Merck M; Versteege I; Zattara-Cannoni H; Figarella D; Lena G; Aurias A; Vagner-Capodano AM
Cancer Genet Cytogenet; 2000 Sep; 121(2):223-7. PubMed ID: 11063814
[TBL] [Abstract][Full Text] [Related]
14. Molecular genetic alterations on chromosomes 11 and 22 in ependymomas.
Lamszus K; Lachenmayer L; Heinemann U; Kluwe L; Finckh U; Höppner W; Stavrou D; Fillbrandt R; Westphal M
Int J Cancer; 2001 Mar; 91(6):803-8. PubMed ID: 11275983
[TBL] [Abstract][Full Text] [Related]
15. Chromosomal abnormalities subdivide ependymal tumors into clinically relevant groups.
Hirose Y; Aldape K; Bollen A; James CD; Brat D; Lamborn K; Berger M; Feuerstein BG
Am J Pathol; 2001 Mar; 158(3):1137-43. PubMed ID: 11238062
[TBL] [Abstract][Full Text] [Related]
16. Candidate genes on chromosome 9q33-34 involved in the progression of childhood ependymomas.
Puget S; Grill J; Valent A; Bieche I; Dantas-Barbosa C; Kauffmann A; Dessen P; Lacroix L; Geoerger B; Job B; Dirven C; Varlet P; Peyre M; Dirks PB; Sainte-Rose C; Vassal G
J Clin Oncol; 2009 Apr; 27(11):1884-92. PubMed ID: 19289631
[TBL] [Abstract][Full Text] [Related]
17. Real-time quantitative PCR analysis of pediatric ependymomas identifies novel candidate genes including TPR at 1q25 and CHIBBY at 22q12-q13.
Karakoula K; Suarez-Merino B; Ward S; Phipps KP; Harkness W; Hayward R; Thompson D; Jacques TS; Harding B; Beck J; Thomas DG; Warr TJ
Genes Chromosomes Cancer; 2008 Nov; 47(11):1005-22. PubMed ID: 18663750
[TBL] [Abstract][Full Text] [Related]
18. Molecular genetic analysis of chromosome arm 17p and chromosome arm 22q DNA sequences in sporadic pediatric ependymomas.
von Haken MS; White EC; Daneshvar-Shyesther L; Sih S; Choi E; Kalra R; Cogen PH
Genes Chromosomes Cancer; 1996 Sep; 17(1):37-44. PubMed ID: 8889505
[TBL] [Abstract][Full Text] [Related]
19. Methylation of RASSF1A and TRAIL pathway-related genes is frequent in childhood intracranial ependymomas and benign choroid plexus papilloma.
Michalowski MB; de Fraipont F; Michelland S; Entz-Werle N; Grill J; Pasquier B; Favrot MC; Plantaz D
Cancer Genet Cytogenet; 2006 Apr; 166(1):74-81. PubMed ID: 16616114
[TBL] [Abstract][Full Text] [Related]
20. DNA sequences similar to those of simian virus 40 in ependymomas and choroid plexus tumors of childhood.
Bergsagel DJ; Finegold MJ; Butel JS; Kupsky WJ; Garcea RL
N Engl J Med; 1992 Apr; 326(15):988-93. PubMed ID: 1312224
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
