184 related articles for article (PubMed ID: 10934139)
1. Losses of chromosomes 1p and 3q are early genetic events in the development of sporadic pheochromocytomas.
Dannenberg H; Speel EJ; Zhao J; Saremaslani P; van Der Harst E; Roth J; Heitz PU; Bonjer HJ; Dinjens WN; Mooi WJ; Komminoth P; de Krijger RR
Am J Pathol; 2000 Aug; 157(2):353-9. PubMed ID: 10934139
[TBL] [Abstract][Full Text] [Related]
2. Microarray-based comparative genomic hybridization of pheochromocytoma cell lines from neurofibromatosis knockout mice reveals genetic alterations similar to those in human pheochromocytomas.
Powers JF; Tischler AS; Mohammed M; Naeem R
Cancer Genet Cytogenet; 2005 May; 159(1):27-31. PubMed ID: 15860353
[TBL] [Abstract][Full Text] [Related]
3. Comparative genomic hybridization reveals frequent losses of chromosomes 1p and 3q in pheochromocytomas and abdominal paragangliomas, suggesting a common genetic etiology.
Edström E; Mahlamäki E; Nord B; Kjellman M; Karhu R; Höög A; Goncharov N; Teh BT; Bäckdahl M; Larsson C
Am J Pathol; 2000 Feb; 156(2):651-9. PubMed ID: 10666394
[TBL] [Abstract][Full Text] [Related]
4. Comparative genomic hybridization reveals frequent losses of 1p and 3q in benign pheochromocytomas of Japanese patients.
Kino M; Suzuki H; Naya Y; Komiya A; Imamoto T; Ichikawa T; Tatsuno I; Ishida H; Shindo T; Seki N
Cancer Genet Cytogenet; 2007 Jun; 175(2):169-72. PubMed ID: 17556075
[No Abstract] [Full Text] [Related]
5. Loss of heterozygosity on the short arm of chromosomes 1 and 3 in sporadic pheochromocytoma and extra-adrenal paraganglioma.
Vargas MP; Zhuang Z; Wang C; Vortmeyer A; Linehan WM; Merino MJ
Hum Pathol; 1997 Apr; 28(4):411-5. PubMed ID: 9104939
[TBL] [Abstract][Full Text] [Related]
6. Molecular cytogenetic characterization in four pediatric pheochromocytomas and paragangliomas.
Vicha A; Holzerova M; Krepelova A; Musil Z; Prochazka P; Sumerauer D; Kodet R; Eckschlager T; Jarosova M
Pathol Oncol Res; 2011 Dec; 17(4):801-8. PubMed ID: 21461997
[TBL] [Abstract][Full Text] [Related]
7. Array-comparative genomic hybridization in sporadic benign pheochromocytomas.
van Nederveen FH; Korpershoek E; deLeeuw RJ; Verhofstad AA; Lenders JW; Dinjens WN; Lam WL; de Krijger RR
Endocr Relat Cancer; 2009 Jun; 16(2):505-13. PubMed ID: 19153209
[TBL] [Abstract][Full Text] [Related]
8. Detailed assessment of chromosome 22 aberrations in sporadic pheochromocytoma using array-CGH.
Jarbo C; Buckley PG; Piotrowski A; Mantripragada KK; Benetkiewicz M; Diaz de Ståhl T; Langford CF; Gregory SG; Dralle H; Gimm O; Bäckdahl M; Geli J; Larsson C; Westin G; Akerström G; Dumanski JP
Int J Cancer; 2006 Mar; 118(5):1159-64. PubMed ID: 16161042
[TBL] [Abstract][Full Text] [Related]
9. Comparative genomic hybridization study of nasal-type NK/T-cell lymphoma.
Ko YH; Choi KE; Han JH; Kim JM; Ree HJ
Cytometry; 2001 Apr; 46(2):85-91. PubMed ID: 11309817
[TBL] [Abstract][Full Text] [Related]
10. Aberrations of chromosomes 5 and 8 as recurrent cytogenetic events in anaplastic carcinoma of the thyroid as detected by fluorescence in situ hybridisation and comparative genomic hybridisation.
Wilkens L; Benten D; Tchinda J; Brabant G; Pötter E; Dralle H; von Wasielewski R
Virchows Arch; 2000 Apr; 436(4):312-8. PubMed ID: 10834532
[TBL] [Abstract][Full Text] [Related]
11. Sporadic and familial pheochromocytomas are associated with loss of at least two discrete intervals on chromosome 1p.
Benn DE; Dwight T; Richardson AL; Delbridge L; Bambach CP; Stowasser M; Gordon RD; Marsh DJ; Robinson BG
Cancer Res; 2000 Dec; 60(24):7048-51. PubMed ID: 11156410
[TBL] [Abstract][Full Text] [Related]
12. Increased number of chromosomal imbalances and high-level DNA amplifications in mantle cell lymphoma are associated with blastoid variants.
Beà S; Ribas M; Hernández JM; Bosch F; Pinyol M; Hernández L; García JL; Flores T; González M; López-Guillermo A; Piris MA; Cardesa A; Montserrat E; Miró R; Campo E
Blood; 1999 Jun; 93(12):4365-74. PubMed ID: 10361135
[TBL] [Abstract][Full Text] [Related]
13. Genomic alterations associated with malignancy in head and neck cancer.
Bockmühl U; Wolf G; Schmidt S; Schwendel A; Jahnke V; Dietel M; Petersen I
Head Neck; 1998 Mar; 20(2):145-51. PubMed ID: 9484946
[TBL] [Abstract][Full Text] [Related]
14. Genomic aberrations in carcinomas of the uterine corpus.
Micci F; Teixeira MR; Haugom L; Kristensen G; Abeler VM; Heim S
Genes Chromosomes Cancer; 2004 Jul; 40(3):229-46. PubMed ID: 15139002
[TBL] [Abstract][Full Text] [Related]
15. 1p and 3p deletions in meningiomas without detectable aberrations of chromosome 22 identified by comparative genomic hybridization.
Carlson KM; Bruder C; Nordenskjöld M; Dumanski JP
Genes Chromosomes Cancer; 1997 Dec; 20(4):419-24. PubMed ID: 9408760
[TBL] [Abstract][Full Text] [Related]
16. Regional deletion and amplification on chromosome 6 in a uveal melanoma case without abnormalities on chromosomes 1p, 3 and 8.
van Gils W; Kilic E; Brüggenwirth HT; Vaarwater J; Verbiest MM; Beverloo B; van Til-Berg ME; Paridaens D; Luyten GP; de Klein A
Melanoma Res; 2008 Feb; 18(1):10-5. PubMed ID: 18227702
[TBL] [Abstract][Full Text] [Related]
17. Genetic evidence for early divergence of small functioning and nonfunctioning endocrine pancreatic tumors: gain of 9Q34 is an early event in insulinomas.
Speel EJ; Scheidweiler AF; Zhao J; Matter C; Saremaslani P; Roth J; Heitz PU; Komminoth P
Cancer Res; 2001 Jul; 61(13):5186-92. PubMed ID: 11431358
[TBL] [Abstract][Full Text] [Related]
18. Recurrent genomic alterations in benign and malignant pheochromocytomas and paragangliomas revealed by whole-genome array comparative genomic hybridization analysis.
Sandgren J; Diaz de Ståhl T; Andersson R; Menzel U; Piotrowski A; Nord H; Bäckdahl M; Kiss NB; Brauckhoff M; Komorowski J; Dralle H; Hessman O; Larsson C; Akerström G; Bruder C; Dumanski JP; Westin G
Endocr Relat Cancer; 2010 Sep; 17(3):561-79. PubMed ID: 20410162
[TBL] [Abstract][Full Text] [Related]
19. FISH analyses for alterations in chromosomes 1, 2, 3, and 11 define high-risk groups in neuroblastoma.
Spitz R; Hero B; Ernestus K; Berthold F
Med Pediatr Oncol; 2003 Jul; 41(1):30-5. PubMed ID: 12764740
[TBL] [Abstract][Full Text] [Related]
20. Microarray-based CGH of sporadic and syndrome-related pheochromocytomas using a 0.1-0.2 Mb bacterial artificial chromosome array spanning chromosome arm 1p.
Aarts M; Dannenberg H; deLeeuw RJ; van Nederveen FH; Verhofstad AA; Lenders JW; Dinjens WN; Speel EJ; Lam WL; de Krijger RR
Genes Chromosomes Cancer; 2006 Jan; 45(1):83-93. PubMed ID: 16215979
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
