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Items: 1 to 20 of 159

1.

Fusion of the MLL gene with two different genes, AF-6 and AF-5alpha, by a complex translocation involving chromosomes 5, 6, 8 and 11 in infant leukemia.

Taki T, Hayashi Y, Taniwaki M, Seto M, Ueda R, Hanada R, Suzukawa K, Yokota J, Morishita K.

Oncogene. 1996 Nov 21;13(10):2121-30.

PMID:
8950979
3.

Identification of complex genomic breakpoint junctions in the t(9;11) MLL-AF9 fusion gene in acute leukemia.

Super HG, Strissel PL, Sobulo OM, Burian D, Reshmi SC, Roe B, Zeleznik-Le NJ, Diaz MO, Rowley JD.

Genes Chromosomes Cancer. 1997 Oct;20(2):185-95.

PMID:
9331569
4.

The der(11)-encoded MLL/AF-4 fusion transcript is consistently detected in t(4;11)(q21;q23)-containing acute lymphoblastic leukemia.

Downing JR, Head DR, Raimondi SC, Carroll AJ, Curcio-Brint AM, Motroni TA, Hulshof MG, Pullen DJ, Domer PH.

Blood. 1994 Jan 15;83(2):330-5.

5.

Panhandle and reverse-panhandle PCR enable cloning of der(11) and der(other) genomic breakpoint junctions of MLL translocations and identify complex translocation of MLL, AF-4, and CDK6.

Raffini LJ, Slater DJ, Rappaport EF, Lo Nigro L, Cheung NK, Biegel JA, Nowell PC, Lange BJ, Felix CA.

Proc Natl Acad Sci U S A. 2002 Apr 2;99(7):4568-73.

6.

The MYO1F, unconventional myosin type 1F, gene is fused to MLL in infant acute monocytic leukemia with a complex translocation involving chromosomes 7, 11, 19 and 22.

Taki T, Akiyama M, Saito S, Ono R, Taniwaki M, Kato Y, Yuza Y, Eto Y, Hayashi Y.

Oncogene. 2005 Aug 4;24(33):5191-7.

PMID:
15897884
8.

Human LPP gene is fused to MLL in a secondary acute leukemia with a t(3;11) (q28;q23).

Dahéron L, Veinstein A, Brizard F, Drabkin H, Lacotte L, Guilhot F, Larsen CJ, Brizard A, Roche J.

Genes Chromosomes Cancer. 2001 Aug;31(4):382-9.

PMID:
11433529
9.

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.

10.

t(11;22)(q23;q11.2) In acute myeloid leukemia of infant twins fuses MLL with hCDCrel, a cell division cycle gene in the genomic region of deletion in DiGeorge and velocardiofacial syndromes.

Megonigal MD, Rappaport EF, Jones DH, Williams TM, Lovett BD, Kelly KM, Lerou PH, Moulton T, Budarf ML, Felix CA.

Proc Natl Acad Sci U S A. 1998 May 26;95(11):6413-8. Erratum in: Proc Natl Acad Sci U S A 1998 Aug 18;95(17):10344.

11.

Analysis of MLL-derived transcripts in infant acute monocytic leukemia with a complex translocation (1;11;4)(q21;q23;p16).

So CW, Ma SK, Wan TS, Chan GC, Ha SY, Chan LC.

Cancer Genet Cytogenet. 2000 Feb;117(1):24-7.

PMID:
10700861
12.

All patients with the T(11;16)(q23;p13.3) that involves MLL and CBP have treatment-related hematologic disorders.

Rowley JD, Reshmi S, Sobulo O, Musvee T, Anastasi J, Raimondi S, Schneider NR, Barredo JC, Cantu ES, Schlegelberger B, Behm F, Doggett NA, Borrow J, Zeleznik-Le N.

Blood. 1997 Jul 15;90(2):535-41.

13.

t(11;14)(q23;q24) generates an MLL-human gephyrin fusion gene along with a de facto truncated MLL in acute monoblastic leukemia.

Kuwada N, Kimura F, Matsumura T, Yamashita T, Nakamura Y, Wakimoto N, Ikeda T, Sato K, Motoyoshi K.

Cancer Res. 2001 Mar 15;61(6):2665-9.

14.

The biological and clinical significance of MLL abnormalities in haematological malignancies.

Mitterbauer-Hohendanner G, Mannhalter C.

Eur J Clin Invest. 2004 Aug;34 Suppl 2:12-24. Review.

PMID:
15291802
15.

Identification of a MLL-MLLT4 fusion gene resulting from a t(6;11)(q27;q23) presenting as a del(11q) in a child with T-cell acute lymphoblastic leukemia.

De Braekeleer E, Meyer C, Le Bris MJ, Douet-Guilbert N, Basinko A, Morel F, Berthou C, Marschalek R, Férec C, De Braekeleer M.

Leuk Lymphoma. 2010 Aug;51(8):1570-3. doi: 10.3109/10428194.2010.494261. No abstract available.

PMID:
20545580
16.

LCX, leukemia-associated protein with a CXXC domain, is fused to MLL in acute myeloid leukemia with trilineage dysplasia having t(10;11)(q22;q23).

Ono R, Taki T, Taketani T, Taniwaki M, Kobayashi H, Hayashi Y.

Cancer Res. 2002 Jul 15;62(14):4075-80.

18.

GPHN, a novel partner gene fused to MLL in a leukemia with t(11;14)(q23;q24).

Eguchi M, Eguchi-Ishimae M, Seto M, Morishita K, Suzuki K, Ueda R, Ueda K, Kamada N, Greaves M.

Genes Chromosomes Cancer. 2001 Nov;32(3):212-21.

PMID:
11579461
19.

MLL-CBP fusion transcript in a therapy-related acute myeloid leukemia with the t(11;16)(q23;p13) which developed in an acute lymphoblastic leukemia patient with Fanconi anemia.

Sugita K, Taki T, Hayashi Y, Shimaoka H, Kumazaki H, Inoue H, Konno Y, Taniwaki M, Kurosawa H, Eguchi M.

Genes Chromosomes Cancer. 2000 Mar;27(3):264-9.

PMID:
10679915
20.

Near-precise interchromosomal recombination and functional DNA topoisomerase II cleavage sites at MLL and AF-4 genomic breakpoints in treatment-related acute lymphoblastic leukemia with t(4;11) translocation.

Lovett BD, Lo Nigro L, Rappaport EF, Blair IA, Osheroff N, Zheng N, Megonigal MD, Williams WR, Nowell PC, Felix CA.

Proc Natl Acad Sci U S A. 2001 Aug 14;98(17):9802-7. Epub 2001 Aug 7.

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