These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
306 related items for PubMed ID: 19446744
1. Pediatric supratentorial ependymomas show more frequent deletions on chromosome 9 than infratentorial ependymomas: a microsatellite analysis. Schneider D, Monoranu CM, Huang B, Rutkowski S, Gerber NU, Krauss J, Puppe B, Roggendorf W. Cancer Genet Cytogenet; 2009 Jun; 191(2):90-6. PubMed ID: 19446744 [Abstract] [Full Text] [Related]
2. Correlation between 6q25.3 deletion status and survival in pediatric intracranial ependymomas. Monoranu CM, Huang B, Zangen IL, Rutkowski S, Vince GH, Gerber NU, Puppe B, Roggendorf W. Cancer Genet Cytogenet; 2008 Apr 01; 182(1):18-26. PubMed ID: 18328946 [Abstract] [Full Text] [Related]
3. 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 01; 106(4):357-62. PubMed ID: 12898154 [Abstract] [Full Text] [Related]
4. Loss of heterozygosity on chromosome 22 in human ependymomas. Huang B, Starostik P, Kühl J, Tonn JC, Roggendorf W. Acta Neuropathol; 2002 Apr 01; 103(4):415-20. PubMed ID: 11904762 [Abstract] [Full Text] [Related]
5. 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 01; 17(1):37-44. PubMed ID: 8889505 [Abstract] [Full Text] [Related]
6. 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 01; 47(11):1005-22. PubMed ID: 18663750 [Abstract] [Full Text] [Related]
7. [Therapeutic results of eight patients with intracranial ependymomas]. Sasajima T, Takahashi M, Kinouchi H, Suzuki A, Mizoi K. No To Shinkei; 2003 Mar 01; 55(3):233-40. PubMed ID: 12728504 [Abstract] [Full Text] [Related]
8. Trisomy 19 ependymoma, a newly recognized genetico-histological association, including clear cell ependymoma. Rousseau E, Palm T, Scaravilli F, Ruchoux MM, Figarella-Branger D, Salmon I, Ellison D, Lacroix C, Chapon F, Mikol J, Vikkula M, Godfraind C. Mol Cancer; 2007 Jul 12; 6():47. PubMed ID: 17626628 [Abstract] [Full Text] [Related]
9. 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 12; 32(1):59-66. PubMed ID: 11477662 [Abstract] [Full Text] [Related]
10. 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 12; 161(6):2133-41. PubMed ID: 12466129 [Abstract] [Full Text] [Related]
11. 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 10; 27(11):1884-92. PubMed ID: 19289631 [Abstract] [Full Text] [Related]
12. Merlin expression in pediatric anaplastic ependymomas real time PCR study. Buccoliero AM, Castiglione F, Rossi Degl'Innocenti D, Sardi I, Genitori L, Taddei GL. Fetal Pediatr Pathol; 2010 Apr 10; 29(4):245-54. PubMed ID: 20594149 [Abstract] [Full Text] [Related]
13. Supratentorial ependymomas: prognostic factors and outcome analysis in a retrospective series of 46 adult patients. Metellus P, Figarella-Branger D, Guyotat J, Barrie M, Giorgi R, Jouvet A, Chinot O, Club de Neuro-Oncologie de la Société Française de Neurochirurgie and the Association des Neuro-Oncologues d'Expression Française. Cancer; 2008 Jul 01; 113(1):175-85. PubMed ID: 18470910 [Abstract] [Full Text] [Related]
14. Investigation of allelic imbalances on chromosome 3p in nasopharyngeal carcinoma in Tunisia: high frequency of microsatellite instability in patients with early-onset of the disease. Trimeche M, Braham H, Ziadi S, Amara K, Hachana M, Korbi S. Oral Oncol; 2008 Aug 01; 44(8):775-83. PubMed ID: 18206419 [Abstract] [Full Text] [Related]
15. Imbalances of chromosome arm 1p in pediatric and adult germ cell tumors are caused by true allelic loss: a combined comparative genomic hybridization and microsatellite analysis. Zahn S, Sievers S, Alemazkour K, Orb S, Harms D, Schulz WA, Calaminus G, Göbel U, Schneider DT. Genes Chromosomes Cancer; 2006 Nov 01; 45(11):995-1006. PubMed ID: 16897744 [Abstract] [Full Text] [Related]
16. Molecular staging of intracranial ependymoma in children and adults. Korshunov A, Witt H, Hielscher T, Benner A, Remke M, Ryzhova M, Milde T, Bender S, Wittmann A, Schöttler A, Kulozik AE, Witt O, von Deimling A, Lichter P, Pfister S. J Clin Oncol; 2010 Jul 01; 28(19):3182-90. PubMed ID: 20516456 [Abstract] [Full Text] [Related]
17. Infratentorial ependymomas: prognostic factors and outcome analysis in a multi-center retrospective series of 106 adult patients. Guyotat J, Metellus P, Giorgi R, Barrie M, Jouvet A, Fevre-Montange M, Chinot O, Durand A, Figarella-Branger D. Acta Neurochir (Wien); 2009 Aug 01; 151(8):947-60. PubMed ID: 19499166 [Abstract] [Full Text] [Related]
18. Chromosome abnormalities in pediatric brain tumors. Griffin CA, Hawkins AL, Packer RJ, Rorke LB, Emanuel BS. Cancer Res; 1988 Jan 01; 48(1):175-80. PubMed ID: 3334992 [Abstract] [Full Text] [Related]
19. [Prognostic and survival factors among pediatric patients with ependymomas]. López-Aguilar E, Sepúlveda-Vildósola AC, Betanzos-Cabrera Y, Gascón-Lastiri G, Ortiz-Suárez L, Rivera-Márquez H, Cerecedo-Díaz F, Wanzke-Del Angel V, De la Cruz-Yáñez H, Ramírez-Reyes G, Arenas-Aranda D, Siordia-Reyes G. Gac Med Mex; 2009 Jan 01; 145(1):7-13. PubMed ID: 19256405 [Abstract] [Full Text] [Related]