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Items: 1 to 20 of 122

1.

Karyotyping and analysis of GNAS locus in intramuscular myxomas.

Panagopoulos I, Gorunova L, Lobmaier I, Bjerkehagen B, Heim S.

Oncotarget. 2017 Mar 28;8(13):22086-22094. doi: 10.18632/oncotarget.14986.

2.

Id2 and E Proteins Orchestrate the Initiation and Maintenance of MLL-Rearranged Acute Myeloid Leukemia.

Ghisi M, Kats L, Masson F, Li J, Kratina T, Vidacs E, Gilan O, Doyle MA, Newbold A, Bolden JE, Fairfax KA, de Graaf CA, Firth M, Zuber J, Dickins RA, Corcoran LM, Dawson MA, Belz GT, Johnstone RW.

Cancer Cell. 2016 Jul 11;30(1):59-74. doi: 10.1016/j.ccell.2016.05.019. Epub 2016 Jun 30.

PMID:
27374225
3.

Chromosome 8q24.1/c-MYC abnormality: a marker for high-risk myeloma.

Glitza IC, Lu G, Shah R, Bashir Q, Shah N, Champlin RE, Shah J, Orlowski RZ, Qazilbash MH.

Leuk Lymphoma. 2015 Mar;56(3):602-7. doi: 10.3109/10428194.2014.924116. Epub 2014 Aug 18.

4.

The leucine twenty homeobox (LEUTX) gene, which lacks a histone acetyltransferase domain, is fused to KAT6A in therapy-related acute myeloid leukemia with t(8;19)(p11;q13).

Chinen Y, Taki T, Tsutsumi Y, Kobayashi S, Matsumoto Y, Sakamoto N, Kuroda J, Horiike S, Nishida K, Ohno H, Uike N, Taniwaki M.

Genes Chromosomes Cancer. 2014 Apr;53(4):299-308. doi: 10.1002/gcc.22140. Epub 2014 Jan 21.

PMID:
24446090
5.

miR-9 is a tumor suppressor in pediatric AML with t(8;21).

Emmrich S, Katsman-Kuipers JE, Henke K, Khatib ME, Jammal R, Engeland F, Dasci F, Zwaan CM, den Boer ML, Verboon L, Stary J, Baruchel A, de Haas V, Danen-van Oorschot AA, Fornerod M, Pieters R, Reinhardt D, Klusmann JH, van den Heuvel-Eibrink MM.

Leukemia. 2014 May;28(5):1022-32. doi: 10.1038/leu.2013.357. Epub 2013 Nov 25.

PMID:
24270738
6.

Pediatric acute myeloid leukemia with t(8;16)(p11;p13), a distinct clinical and biological entity: a collaborative study by the International-Berlin-Frankfurt-Munster AML-study group.

Coenen EA, Zwaan CM, Reinhardt D, Harrison CJ, Haas OA, de Haas V, Mihál V, De Moerloose B, Jeison M, Rubnitz JE, Tomizawa D, Johnston D, Alonzo TA, Hasle H, Auvrignon A, Dworzak M, Pession A, van der Velden VH, Swansbury J, Wong KF, Terui K, Savasan S, Winstanley M, Vaitkeviciene G, Zimmermann M, Pieters R, van den Heuvel-Eibrink MM.

Blood. 2013 Oct 10;122(15):2704-13. doi: 10.1182/blood-2013-02-485524. Epub 2013 Aug 23.

7.

Recurrent NCOA2 gene rearrangements in congenital/infantile spindle cell rhabdomyosarcoma.

Mosquera JM, Sboner A, Zhang L, Kitabayashi N, Chen CL, Sung YS, Wexler LH, LaQuaglia MP, Edelman M, Sreekantaiah C, Rubin MA, Antonescu CR.

Genes Chromosomes Cancer. 2013 Jun;52(6):538-50. doi: 10.1002/gcc.22050. Epub 2013 Mar 5.

8.

Molecular cloning of IGλ rearrangements using long-distance inverse PCR (LDI-PCR).

Shimanuki M, Sonoki T, Hosoi H, Watanuki J, Murata S, Kawakami K, Matsuoka H, Hanaoka N, Nakakuma H.

Eur J Haematol. 2013 Jan;90(1):59-67. doi: 10.1111/ejh.12037. Epub 2012 Dec 4.

PMID:
23113889
9.

Prognostic significance of additional cytogenetic aberrations in 733 de novo pediatric 11q23/MLL-rearranged AML patients: results of an international study.

Coenen EA, Raimondi SC, Harbott J, Zimmermann M, Alonzo TA, Auvrignon A, Beverloo HB, Chang M, Creutzig U, Dworzak MN, Forestier E, Gibson B, Hasle H, Harrison CJ, Heerema NA, Kaspers GJ, Leszl A, Litvinko N, Lo Nigro L, Morimoto A, Perot C, Reinhardt D, Rubnitz JE, Smith FO, Stary J, Stasevich I, Strehl S, Taga T, Tomizawa D, Webb D, Zemanova Z, Pieters R, Zwaan CM, van den Heuvel-Eibrink MM.

Blood. 2011 Jun 30;117(26):7102-11. doi: 10.1182/blood-2010-12-328302. Epub 2011 May 6.

10.

A case of T cell prolymphocytic leukemia involving blast transformation.

Ichikawa K, Noguchi M, Imai H, Sekiguchi Y, Wakabayashi M, Sawada T, Komatsu N.

Int J Hematol. 2011 May;93(5):667-72. doi: 10.1007/s12185-011-0826-7. Epub 2011 Apr 21.

PMID:
21505955
11.

[Cytogenetic and molecular genetic study of a case with 8p inverted duplication deletion syndrome].

Han X, Zhang JM, Jiang WT, Hu Q, Tao J.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010 Aug;27(4):361-6. doi: 10.3760/cma.j.issn.1003-9406.2010.04.001. Chinese.

PMID:
20677137
12.

Isochromosome 5p and related anomalies: a novel recurrent chromosome abnormality in myeloid disorders.

Herry A, Douet-Guilbert N, Morel F, Le Bris MJ, Guéganic N, Berthou C, De Braekeleer M.

Cancer Genet Cytogenet. 2010 Jul 15;200(2):134-9. doi: 10.1016/j.cancergencyto.2010.04.006.

PMID:
20620596
13.

Chromosome 8p11.2 translocations: prevalence, FISH analysis for FGFR1 and MYST3, and clinicopathologic correlates in a consecutive cohort of 13 cases from a single institution.

Patnaik MM, Gangat N, Knudson RA, Keefe JG, Hanson CA, Pardanani A, Ketterling RP, Tefferi A.

Am J Hematol. 2010 Apr;85(4):238-42. doi: 10.1002/ajh.21631.

14.

Recurrent fusion of MYB and NFIB transcription factor genes in carcinomas of the breast and head and neck.

Persson M, Andrén Y, Mark J, Horlings HM, Persson F, Stenman G.

Proc Natl Acad Sci U S A. 2009 Nov 3;106(44):18740-4. doi: 10.1073/pnas.0909114106. Epub 2009 Oct 19.

15.

Multiple recurrent chromosomal breakpoints in mantle cell lymphoma revealed by a combination of molecular cytogenetic techniques.

Salaverria I, Espinet B, Carrió A, Costa D, Astier L, Slotta-Huspenina J, Quintanilla-Martinez L, Fend F, Solé F, Colomer D, Serrano S, Miró R, Beà S, Campo E.

Genes Chromosomes Cancer. 2008 Dec;47(12):1086-97. doi: 10.1002/gcc.20609.

PMID:
18709664
16.

Silencing of unpaired meiotic chromosomes and altered recombination patterns in an azoospermic carrier of a t(8;13) reciprocal translocation.

Ferguson KA, Chow V, Ma S.

Hum Reprod. 2008 Apr;23(4):988-95. doi: 10.1093/humrep/den013. Epub 2008 Feb 12.

PMID:
18270180
17.

The clinical presentation and prognosis of diffuse large B-cell lymphoma with t(14;18) and 8q24/c-MYC rearrangement.

Le Gouill S, Talmant P, Touzeau C, Moreau A, Garand R, Juge-Morineau N, Gaillard F, Gastinne T, Milpied N, Moreau P, Harousseau JL, Avet-Loiseau H.

Haematologica. 2007 Oct;92(10):1335-42.

18.

Cytogenetic patterns in ETV6/RUNX1-positive pediatric B-cell precursor acute lymphoblastic leukemia: A Nordic series of 245 cases and review of the literature.

Forestier E, Andersen MK, Autio K, Blennow E, Borgström G, Golovleva I, Heim S, Heinonen K, Hovland R, Johannsson JH, Kerndrup G, Nordgren A, Rosenquist R, Swolin B, Johansson B; Nordic Society of Pediatric Hematology and Oncology (NOPHO).; Swedish Cytogenetic Leukemia Study Group (SCLSG).; NOPHO Leukemia Cytogenetic Study Group (NLCSG)..

Genes Chromosomes Cancer. 2007 May;46(5):440-50.

PMID:
17285576
19.

Co-amplification of 8p12 and 11q13 in breast cancers is not the result of a single genomic event.

Paterson AL, Pole JC, Blood KA, Garcia MJ, Cooke SL, Teschendorff AE, Wang Y, Chin SF, Ylstra B, Caldas C, Edwards PA.

Genes Chromosomes Cancer. 2007 May;46(5):427-39.

PMID:
17285574
20.

Correlating breakage-fusion-bridge events with the overall chromosomal instability and in vitro karyotype evolution in prostate cancer.

Vukovic B, Beheshti B, Park P, Lim G, Bayani J, Zielenska M, Squire JA.

Cytogenet Genome Res. 2007;116(1-2):1-11.

PMID:
17268171

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