123 related articles for article (PubMed ID: 12660032)
1. Detection by fluorescence in situ hybridization of microdeletions at 1p36 in lymphomas, unidentified on cytogenetic analysis.
Rajgopal A; Carr IM; Leek JP; Hodge D; Bell SM; Roberts P; Horgan K; Bonthron DT; Selby PJ; Markham AF; MacLennan KA
Cancer Genet Cytogenet; 2003 Apr; 142(1):46-50. PubMed ID: 12660032
[TBL] [Abstract][Full Text] [Related]
2. Characterization of the recurrent translocation t(1;1)(p36.3;q21.1-2) in non-Hodgkin lymphoma by multicolor banding and fluorescence in situ hybridization analysis.
Lestou VS; Ludkovski O; Connors JM; Gascoyne RD; Lam WL; Horsman DE
Genes Chromosomes Cancer; 2003 Apr; 36(4):375-81. PubMed ID: 12619161
[TBL] [Abstract][Full Text] [Related]
3. Rearrangements of chromosome band 1p36 in non-Hodgkin's lymphoma.
Dave BJ; Hess MM; Pickering DL; Zaleski DH; Pfeifer AL; Weisenburger DD; Armitage JO; Sanger WG
Clin Cancer Res; 1999 Jun; 5(6):1401-9. PubMed ID: 10389925
[TBL] [Abstract][Full Text] [Related]
4. New chromosome abnormalities and lack of BCL-6 gene rearrangements in Argentinean diffuse large B-cell lymphomas.
Cerretini R; Noriega MF; Narbaitz M; Slavutsky I
Eur J Haematol; 2006 Apr; 76(4):284-93. PubMed ID: 16519699
[TBL] [Abstract][Full Text] [Related]
5. An additional segment at 1p36 derived from der(18)t(14;18) in patients with diffuse large B-cell lymphomas transformed from follicular lymphoma.
Nomura K; Kanda-Akano Y; Shimizu D; Okuda T; Yoshida N; Matsumoto Y; Nishida K; Taki T; Yokota S; Horiike S; Taniwaki M
Ann Hematol; 2005 Jul; 84(7):474-6. PubMed ID: 15700138
[TBL] [Abstract][Full Text] [Related]
6. Chromosome band 6q deletion pattern in malignant lymphomas.
Taborelli M; Tibiletti MG; Martin V; Pozzi B; Bertoni F; Capella C
Cancer Genet Cytogenet; 2006 Mar; 165(2):106-13. PubMed ID: 16527604
[TBL] [Abstract][Full Text] [Related]
7. Concomitant 1p36 deletion and TNFRSF14 mutations in primary cutaneous follicle center lymphoma frequently expressing high levels of EZH2 protein.
Gángó A; Bátai B; Varga M; Kapczár D; Papp G; Marschalkó M; Kuroli E; Schneider T; Csomor J; Matolcsy A; Bödör C; Szepesi Á
Virchows Arch; 2018 Oct; 473(4):453-462. PubMed ID: 29858685
[TBL] [Abstract][Full Text] [Related]
8. Fluorescence in situ hybridization analysis of chromosome 1p36 deletions in human MYCN amplified neuroblastoma.
Komuro H; Valentine MB; Rowe ST; Kidd VJ; Makino S; Brodeur GM; Cohn SL; Look AT
J Pediatr Surg; 1998 Nov; 33(11):1695-8. PubMed ID: 9856898
[TBL] [Abstract][Full Text] [Related]
9. A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3.
White PS; Maris JM; Beltinger C; Sulman E; Marshall HN; Fujimori M; Kaufman BA; Biegel JA; Allen C; Hilliard C; Valentine MB; Look AT; Enomoto H; Sakiyama S; Brodeur GM
Proc Natl Acad Sci U S A; 1995 Jun; 92(12):5520-4. PubMed ID: 7777541
[TBL] [Abstract][Full Text] [Related]
10. Comprehensive cytogenetic analysis including multicolor spectral karyotyping and interphase fluorescence in situ hybridization in lymphoma diagnosis. a summary of 154 cases.
Fan YS; Rizkalla K
Cancer Genet Cytogenet; 2003 May; 143(1):73-9. PubMed ID: 12742158
[TBL] [Abstract][Full Text] [Related]
11. High incidence of chromosome 1 abnormalities in a series of 27 renal oncocytomas: cytogenetic and fluorescence in situ hybridization studies.
Paner GP; Lindgren V; Jacobson K; Harrison K; Cao Y; Campbell SC; Flanigan RC; Picken MM
Arch Pathol Lab Med; 2007 Jan; 131(1):81-5. PubMed ID: 17227127
[TBL] [Abstract][Full Text] [Related]
12. Monosomy 1p36 breakpoint junctions suggest pre-meiotic breakage-fusion-bridge cycles are involved in generating terminal deletions.
Ballif BC; Yu W; Shaw CA; Kashork CD; Shaffer LG
Hum Mol Genet; 2003 Sep; 12(17):2153-65. PubMed ID: 12915474
[TBL] [Abstract][Full Text] [Related]
13. Translocation breakpoint mapping and sequence analysis in three monosomy 1p36 subjects with der(1)t(1;1)(p36;q44) suggest mechanisms for telomere capture in stabilizing de novo terminal rearrangements.
Ballif BC; Wakui K; Gajecka M; Shaffer LG
Hum Genet; 2004 Jan; 114(2):198-206. PubMed ID: 14579147
[TBL] [Abstract][Full Text] [Related]
14. Molecular cytogenetic analysis of cutaneous T-cell lymphomas: identification of common genetic alterations in Sézary syndrome and mycosis fungoides.
Mao X; Lillington D; Scarisbrick JJ; Mitchell T; Czepulkowski B; Russell-Jones R; Young B; Whittaker SJ
Br J Dermatol; 2002 Sep; 147(3):464-75. PubMed ID: 12207585
[TBL] [Abstract][Full Text] [Related]
15. Fluorescence in situ hybridization analyses of chromosome band 1p36 in neuroblastoma detect two classes of alterations.
Spitz R; Hero B; Westermann F; Ernestus K; Schwab M; Berthold F
Genes Chromosomes Cancer; 2002 Jul; 34(3):299-305. PubMed ID: 12007190
[TBL] [Abstract][Full Text] [Related]
16. Array comparative genomic hybridization reveals a very high frequency of deletions of the long arm of chromosome 6 in testicular lymphoma.
Bosga-Bouwer AG; Kok K; Booman M; Boven L; van der Vlies P; van den Berg A; van den Berg E; de Jong B; Poppema S; Kluin P
Genes Chromosomes Cancer; 2006 Oct; 45(10):976-81. PubMed ID: 16865685
[TBL] [Abstract][Full Text] [Related]
17. Detection of 14q32.33 translocation and t(11;14) in interphase nuclei of chronic B-cell leukemia/lymphomas by in situ hybridization.
Takashima T; Itoh M; Ueda Y; Nishida K; Tamaki T; Misawa S; Abe T; Seto M; Machii T; Taniwaki M
Int J Cancer; 1997 Jul; 72(1):31-8. PubMed ID: 9212219
[TBL] [Abstract][Full Text] [Related]
18. Molecular analysis of 1p36 breakpoints in two Merkel cell carcinomas.
Van Gele M; Van Roy N; Ronan SG; Messiaen L; Vandesompele J; Geerts ML; Naeyaert JM; Blennow E; Bar-Am I; Das Gupta TK; van der Drift P; Versteeg R; Leonard JH; Speleman F
Genes Chromosomes Cancer; 1998 Sep; 23(1):67-71. PubMed ID: 9713999
[TBL] [Abstract][Full Text] [Related]
19. A novel method of amplified fluorescent in situ hybridization for detection of chromosomal microdeletions in B cell lymphoma.
Mizuno Y; Chinen Y; Tsukamoto T; Takimoto-Shimomura T; Matsumura-Kimoto Y; Fujibayashi Y; Kuwahara-Ota S; Fujino T; Nishiyama D; Shimura Y; Kobayashi T; Horiike S; Taniwaki M; Kuroda J
Int J Hematol; 2019 May; 109(5):593-602. PubMed ID: 30830578
[TBL] [Abstract][Full Text] [Related]
20. Population data suggest that deletions of 1p36 are a relatively common chromosome abnormality.
Heilstedt HA; Ballif BC; Howard LA; Kashork CD; Shaffer LG
Clin Genet; 2003 Oct; 64(4):310-6. PubMed ID: 12974736
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]