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168 related items for PubMed ID: 1381950
1. Clinical impact of chromosome 1 aberrations in neuroblastoma: a metaphase and interphase cytogenetic study. Christiansen H, Schestag J, Christiansen NM, Grzeschik KH, Lampert F. Genes Chromosomes Cancer; 1992 Sep; 5(2):141-9. PubMed ID: 1381950 [Abstract] [Full Text] [Related]
2. Interphase cytogenetics of hematological cancer: comparison of classical karyotyping and in situ hybridization using a panel of eleven chromosome specific DNA probes. Poddighe PJ, Moesker O, Smeets D, Awwad BH, Ramaekers FC, Hopman AH. Cancer Res; 1991 Apr 01; 51(7):1959-67. PubMed ID: 2004382 [Abstract] [Full Text] [Related]
3. Rapid interphase and metaphase assessment of specific chromosomal changes in neuroectodermal tumor cells by in situ hybridization with chemically modified DNA probes. Cremer T, Tesin D, Hopman AH, Manuelidis L. Exp Cell Res; 1988 Jun 01; 176(2):199-220. PubMed ID: 3288483 [Abstract] [Full Text] [Related]
4. Detection of Ip36 deletions in paraffin sections of neuroblastoma tissues. Stock C, Ambros IM, Mann G, Gadner H, Amann G, Ambros PF. Genes Chromosomes Cancer; 1993 Jan 01; 6(1):1-9. PubMed ID: 7680215 [Abstract] [Full Text] [Related]
5. 17q gain in neuroblastoma predicts adverse clinical outcome. U.K. Cancer Cytogenetics Group and the U.K. Children's Cancer Study Group. Bown N, Lastowska M, Cotterill S, O'Neill S, Ellershaw C, Roberts P, Lewis I, Pearson AD, U.K. Cancer Cytogenetics Group and the U.K. Children's Cancer Study Group. Med Pediatr Oncol; 2001 Jan 01; 36(1):14-9. PubMed ID: 11464868 [Abstract] [Full Text] [Related]
6. DNA in situ hybridization (interphase cytogenetics) versus comparative genomic hybridization (CGH) in human cancer: detection of numerical and structural chromosome aberrations. Van Dekken H, Krijtenburg PJ, Alers JC. Acta Histochem; 2000 Feb 01; 102(1):85-94. PubMed ID: 10726167 [Abstract] [Full Text] [Related]
7. Flow cytometric quantification of human chromosome specific repetitive DNA sequences by single and bicolor fluorescent in situ hybridization to lymphocyte interphase nuclei. van Dekken H, Arkesteijn GJ, Visser JW, Bauman JG. Cytometry; 1990 Feb 01; 11(1):153-64. PubMed ID: 2307056 [Abstract] [Full Text] [Related]
8. Detection of chromosome aneuploidy in interphase nuclei from human primary breast tumors using chromosome-specific repetitive DNA probes. Devilee P, Thierry RF, Kievits T, Kolluri R, Hopman AH, Willard HF, Pearson PL, Cornelisse CJ. Cancer Res; 1988 Oct 15; 48(20):5825-30. PubMed ID: 3167839 [Abstract] [Full Text] [Related]
9. Sensitive detection of numerical and structural aberrations of chromosome 1 in neuroblastoma by interphase fluorescence in situ hybridization. Comparison with restriction fragment length polymorphism and conventional cytogenetic analyses. Combaret V, Turc-Carel C, Thiesse P, Rebillard AC, Frappaz D, Haus O, Philip T, Favrot MC. Int J Cancer; 1995 Apr 10; 61(2):185-91. PubMed ID: 7705946 [Abstract] [Full Text] [Related]
10. Favorable outcome of triploid neuroblastomas: a contribution to the special oncogenesis of neuroblastoma. Spitz R, Betts DR, Simon T, Boensch M, Oestreich J, Niggli FK, Ernestus K, Berthold F, Hero B. Cancer Genet Cytogenet; 2006 May 10; 167(1):51-6. PubMed ID: 16682287 [Abstract] [Full Text] [Related]
11. Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome-specific library probes. Cremer T, Lichter P, Borden J, Ward DC, Manuelidis L. Hum Genet; 1988 Nov 10; 80(3):235-46. PubMed ID: 3192213 [Abstract] [Full Text] [Related]
12. [Cytogenetic study of 121 patients suffering from various hematologic neoplasms using the in situ hybridization technique]. Pérez Losada A, Solé F, Woessner S, Florensa L, Besses C, Espinet B, Caballín MR, García Eroles L, Sans-Sabrafén J. Sangre (Barc); 1996 Jun 10; 41(3):201-9. PubMed ID: 8755208 [Abstract] [Full Text] [Related]
13. Structural chromosome 1 aberrations in transitional cell carcinoma of the bladder: interphase cytogenetics combining a centromeric, telomeric, and library DNA probe. Poddighe PJ, Ramaekers FC, Smeets AW, Vooijs GP, Hopman AH. Cancer Res; 1992 Sep 15; 52(18):4929-34. PubMed ID: 1516049 [Abstract] [Full Text] [Related]
14. Detection of monosomy in interphase nuclei and identification of marker chromosomes using biotinylated alpha-satellite DNA probes. Kiechle-Schwarz M, Decker HJ, Berger CS, Fiebig HH, Sandberg AA. Cancer Genet Cytogenet; 1991 Jan 15; 51(1):23-33. PubMed ID: 1845850 [Abstract] [Full Text] [Related]
15. Design and validation of DNA probe sets for a comprehensive interphase cytogenetic analysis of acute myeloid leukemia. Fischer K, Scholl C, Sàlat J, Fröhling S, Schlenk R, Bentz M, Stilgenbauer S, Lichter P, Döhner H. Blood; 1996 Nov 15; 88(10):3962-71. PubMed ID: 8916963 [Abstract] [Full Text] [Related]
16. Chromosome 1 interphase-cytogenetics in 32 primary neuroblastomas of different clinical stages. Christiansen H, Schestag J, Bielke W, Schütz B, Rust G, Engel R, Beniers E, Christiansen NM, Lampert F. Prog Clin Biol Res; 1991 Nov 15; 366():99-105. PubMed ID: 2068184 [No Abstract] [Full Text] [Related]
17. Cytogenetic and molecular cytogenetic analysis of B cell chronic lymphocytic leukemia: specific chromosome aberrations identify prognostic subgroups of patients and point to loci of candidate genes. Döhner H, Stilgenbauer S, Fischer K, Bentz M, Lichter P. Leukemia; 1997 Apr 15; 11 Suppl 2():S19-24. PubMed ID: 9178833 [Abstract] [Full Text] [Related]
18. Rapid metaphase and interphase detection of radiation-induced chromosome aberrations in human lymphocytes by chromosomal suppression in situ hybridization. Cremer T, Popp S, Emmerich P, Lichter P, Cremer C. Cytometry; 1990 Apr 15; 11(1):110-8. PubMed ID: 2307051 [Abstract] [Full Text] [Related]
19. Detection of chromosome aberrations in the human interphase nucleus by visualization of specific target DNAs with radioactive and non-radioactive in situ hybridization techniques: diagnosis of trisomy 18 with probe L1.84. Cremer T, Landegent J, Brückner A, Scholl HP, Schardin M, Hager HD, Devilee P, Pearson P, van der Ploeg M. Hum Genet; 1986 Dec 15; 74(4):346-52. PubMed ID: 3793097 [Abstract] [Full Text] [Related]
20. 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 15; 41(1):30-5. PubMed ID: 12764740 [Abstract] [Full Text] [Related] Page: [Next] [New Search]