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Items: 1 to 20 of 107

1.

A novel t(4;16)(q25;q23.1) associated with EGF and ELOVL6 deregulation in acute myeloid leukemia.

Anelli L, Zagaria A, Coccaro N, Tota G, Impera L, Minervini CF, Pastore D, Minervini A, Casieri P, Specchia G, Albano F.

Gene. 2013 Oct 15;529(1):144-7. doi: 10.1016/j.gene.2013.07.105. Epub 2013 Aug 9.

PMID:
23933272
2.

AML with translocation t(8;16)(p11;p13) demonstrates unique cytomorphological, cytogenetic, molecular and prognostic features.

Haferlach T, Kohlmann A, Klein HU, Ruckert C, Dugas M, Williams PM, Kern W, Schnittger S, Bacher U, Löffler H, Haferlach C.

Leukemia. 2009 May;23(5):934-43. doi: 10.1038/leu.2008.388. Epub 2009 Feb 5.

PMID:
19194466
3.

[Clinical and experimental studies of childhood acute myeloid leukemia with 11q23/MLL rearrangements].

He YX, Xue YQ, Wang HY, Shao XJ, Pan JL, Xu J, Yang NC, Ji ZH, Huang YP, Hu SY.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Dec;29(6):677-82. doi: 10.3760/cma.j.issn.1003-9406.2012.06.011. Chinese.

PMID:
23225048
4.

Complex chromosome abnormality mimicking t(8;21)in an acute myeloblastic leukemia.

Busson-Le Coniat M, Daniel M, Berger R.

Ann Genet. 2001 Jan-Mar;44(1):9-11.

PMID:
11334611
5.

A new recurrent translocation, t(5;11)(q35;p15.5), associated with del(5q) in childhood acute myeloid leukemia. The UK Cancer Cytogenetics Group (UKCCG)

Jaju RJ, Haas OA, Neat M, Harbott J, Saha V, Boultwood J, Brown JM, Pirc-Danoewinata H, Krings BW, Müller U, Morris SW, Wainscoat JS, Kearney L.

Blood. 1999 Jul 15;94(2):773-80.

6.

A cryptic t(5;11)(q35;p15.5) in 2 children with acute myeloid leukemia with apparently normal karyotypes, identified by a multiplex fluorescence in situ hybridization telomere assay.

Brown J, Jawad M, Twigg SR, Saracoglu K, Sauerbrey A, Thomas AE, Eils R, Harbott J, Kearney L.

Blood. 2002 Apr 1;99(7):2526-31.

7.

Incidence and characterization of MLL gene (11q23) rearrangements in acute myeloid leukemia M1 and M5.

Poirel H, Rack K, Delabesse E, Radford-Weiss I, Troussard X, Debert C, Leboeuf D, Bastard C, Picard F, Veil-Buzyn A, Flandrin G, Bernard O, Macintyre E.

Blood. 1996 Mar 15;87(6):2496-505.

8.

t(9;11)(p22;p15) with NUP98-LEDGF fusion gene in pediatric acute myeloid leukemia.

Morerio C, Acquila M, Rosanda C, Rapella A, Tassano E, Micalizzi C, Panarello C.

Leuk Res. 2005 Apr;29(4):467-70. Epub 2004 Dec 9.

PMID:
15725483
9.

Abnormalities of chromosome band 8p11 in leukemia: two clinical syndromes can be distinguished on the basis of MOZ involvement.

Aguiar RC, Chase A, Coulthard S, Macdonald DH, Carapeti M, Reiter A, Sohal J, Lennard A, Goldman JM, Cross NC.

Blood. 1997 Oct 15;90(8):3130-5.

10.

Dual color FISH on CBF primary acute myeloid leukemia.

Sorour A, Nafea D.

Egypt J Immunol. 2008;15(2):25-31.

PMID:
20306685
11.

MLL rearrangement with t(6;11)(q15;q23) as a sole abnormality in a patient with de novo acute myeloid leukemia: conventional cytogenetics, FISH, and multicolor FISH analyses for detection of rare MLL-related chromosome abnormalities.

Park TS, Lee ST, Song J, Lee KA, Lee SG, Kim J, Suh B, Kim SJ, Lee JH, Park R, Choi JR.

Cancer Genet Cytogenet. 2008 Nov;187(1):50-3. doi: 10.1016/j.cancergencyto.2008.07.012.

PMID:
18992643
12.

[Fluorescence in situ hybridization study of acute myeloid leukemia with cryptic chromosome rearrangements].

Bai SX, Xue YQ, Chen SN, Pan JL, Wu YF, Shen J, Wang Y, Zhang J.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Dec;28(6):690-3. doi: 10.3760/cma.j.issn.1003-9406.2011.06.021. Chinese.

PMID:
22161107
14.
15.

Complex three-way translocation involving MLL, ELL, RREB1, and CMAHP genes in an infant with acute myeloid leukemia and t(6;19;11)(p22.2;p13.1;q23.3).

Tuborgh A, Meyer C, Marschalek R, Preiss B, Hasle H, Kjeldsen E.

Cytogenet Genome Res. 2013;141(1):7-15. doi: 10.1159/000351224. Epub 2013 May 30.

PMID:
23735562
16.

Identification of signature genes by microarray for acute myeloid leukemia without maturation and acute promyelocytic leukemia with t(15;17)(q22;q12)(PML/RARalpha).

Morikawa J, Li H, Kim S, Nishi K, Ueno S, Suh E, Dougherty E, Shmulevich I, Shiku H, Zhang W, Kobayashi T.

Int J Oncol. 2003 Sep;23(3):617-25.

PMID:
12888896
17.

The AML1 gene: a transcription factor involved in the pathogenesis of myeloid and lymphoid leukemias.

Lo Coco F, Pisegna S, Diverio D.

Haematologica. 1997 May-Jun;82(3):364-70. Review.

18.

Translocation (8;17;15;21)(q22;q23;q15;q22) in acute myeloid leukemia (M2). a four-way variant of t(8;21).

Vieira L, Oliveira V, Ambrósio AP, Marques B, Pereira AM, Hagemeijer A, Boavida MG.

Cancer Genet Cytogenet. 2001 Jul 15;128(2):104-7.

PMID:
11463447
19.

Translocation (11;13)(q23;q14) as the sole abnormality in a childhood de novo acute myelocytic leukemia.

Tsang KS, Li CK, Lau TT, Wong AP, Leung Y, Ng MH.

Cancer Genet Cytogenet. 2004 Apr 1;150(1):78-80.

PMID:
15041229
20.

RT-PCR analysis of the MOZ-CBP and CBP-MOZ chimeric transcripts in acute myeloid leukemias with t(8;16)(p11;p13).

Panagopoulos I, Isaksson M, Lindvall C, Björkholm M, Ahlgren T, Fioretos T, Heim S, Mitelman F, Johansson B.

Genes Chromosomes Cancer. 2000 Aug;28(4):415-24.

PMID:
10862050
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