Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 96


Amplification of AML1 gene is present in childhood acute lymphoblastic leukemia but not in adult, and is not associated with AML1 gene mutation.

Penther D, Preudhomme C, Talmant P, Roumier C, Godon A, Méchinaud F, Milpied N, Bataille R, Avet-Loiseau H.

Leukemia. 2002 Jun;16(6):1131-4.


AML1 gene over-expression in childhood acute lymphoblastic leukemia.

Mikhail FM, Serry KA, Hatem N, Mourad ZI, Farawela HM, El Kaffash DM, Coignet L, Nucifora G.

Leukemia. 2002 Apr;16(4):658-68.


New mechanisms of AML1 gene alteration in hematological malignancies.

Roumier C, Fenaux P, Lafage M, Imbert M, Eclache V, Preudhomme C.

Leukemia. 2003 Jan;17(1):9-16. Review.


TEL-AML1 translocations with TEL and CDKN2 inactivation in acute lymphoblastic leukemia cell lines.

Kim DH, Moldwin RL, Vignon C, Bohlander SK, Suto Y, Giordano L, Gupta R, Fears S, Nucifora G, Rowley JD.

Blood. 1996 Aug 1;88(3):785-94.


High incidence of biallelic point mutations in the Runt domain of the AML1/PEBP2 alpha B gene in Mo acute myeloid leukemia and in myeloid malignancies with acquired trisomy 21.

Preudhomme C, Warot-Loze D, Roumier C, Grardel-Duflos N, Garand R, Lai JL, Dastugue N, Macintyre E, Denis C, Bauters F, Kerckaert JP, Cosson A, Fenaux P.

Blood. 2000 Oct 15;96(8):2862-9.


Incidence and clinical relevance of TEL/AML1 fusion genes in children with acute lymphoblastic leukemia enrolled in the German and Italian multicenter therapy trials. Associazione Italiana Ematologia Oncologia Pediatrica and the Berlin-Frankfurt-Münster Study Group.

Borkhardt A, Cazzaniga G, Viehmann S, Valsecchi MG, Ludwig WD, Burci L, Mangioni S, Schrappe M, Riehm H, Lampert F, Basso G, Masera G, Harbott J, Biondi A.

Blood. 1997 Jul 15;90(2):571-7.


AML1 gene amplification: a novel finding in childhood acute lymphoblastic leukemia.

Niini T, Kanerva J, Vettenranta K, Saarinen-Pihkala UM, Knuutila S.

Haematologica. 2000 Apr;85(4):362-6.


The 12;21 translocation involving TEL and deletion of the other TEL allele: two frequently associated alterations found in childhood acute lymphoblastic leukemia.

Raynaud S, Cave H, Baens M, Bastard C, Cacheux V, Grosgeorge J, Guidal-Giroux C, Guo C, Vilmer E, Marynen P, Grandchamp B.

Blood. 1996 Apr 1;87(7):2891-9.


High incidence of TEL/AML1 fusion resulting from a cryptic t(12;21) in childhood B-lineage acute lymphoblastic leukemia in Taiwan.

Liang DC, Chou TB, Chen JS, Shurtleff SA, Rubnitz JE, Downing JR, Pui CH, Shih LY.

Leukemia. 1996 Jun;10(6):991-3.


TEL-AML1 fusion RNA as a new target to detect minimal residual disease in pediatric B-cell precursor acute lymphoblastic leukemia.

Cayuela JM, Baruchel A, Orange C, Madani A, Auclerc MF, Daniel MT, Schaison G, Sigaux F.

Blood. 1996 Jul 1;88(1):302-8.


Chromosome 21 abnormalities with AML1 amplification in acute lymphoblastic leukemia.

Busson-Le Coniat M, Nguyen Khac F, Daniel MT, Bernard OA, Berger R.

Genes Chromosomes Cancer. 2001 Nov;32(3):244-9.


Characterization of additional genetic events in childhood acute lymphoblastic leukemia with TEL/AML1 gene fusion: a molecular cytogenetics study.

Ma SK, Wan TS, Cheuk AT, Fung LF, Chan GC, Chan SY, Ha SY, Chan LC.

Leukemia. 2001 Sep;15(9):1442-7.


Amplification of AML1 in childhood acute lymphoblastic leukemias.

Dal Cin P, Atkins L, Ford C, Ariyanayagam S, Armstrong SA, George R, Cleary A, Morton CC.

Genes Chromosomes Cancer. 2001 Apr;30(4):407-9.


Fluorescence in situ hybridization study of TEL/AML1 fusion and other abnormalities involving TEL and AML1 genes. Correlation with cytogenetic findings and prognostic value in children with acute lymphocytic leukemia.

Martínez-Ramírez A, Urioste M, Contra T, Cantalejo A, Tavares A, Portero JA, López-Ibor B, Bernacer M, Soto C, Cigudosa JC, Benítez J.

Haematologica. 2001 Dec;86(12):1245-53.


High frequency of t(12;21) in childhood B-lineage acute lymphoblastic leukemia.

Romana SP, Poirel H, Leconiat M, Flexor MA, Mauchauffé M, Jonveaux P, Macintyre EA, Berger R, Bernard OA.

Blood. 1995 Dec 1;86(11):4263-9.


Amplification of AML1 on a duplicated chromosome 21 in acute lymphoblastic leukemia: a study of 20 cases.

Harewood L, Robinson H, Harris R, Al-Obaidi MJ, Jalali GR, Martineau M, Moorman AV, Sumption N, Richards S, Mitchell C, Harrison CJ.

Leukemia. 2003 Mar;17(3):547-53. Review.


High-level amplification of the RUNX1 gene in two cases of childhood acute lymphoblastic leukemia.

García-Casado Z, Cervera J, Verdeguer A, Tasso M, Valencia A, Pajuelo JC, Mena-Duran AV, Barragán E, Blanes M, Bolufer P, Sanz MA.

Cancer Genet Cytogenet. 2006 Oct 15;170(2):171-4.


Incidence of TEL/AML1 fusion gene analyzed consecutively in children with acute lymphoblastic leukemia in relapse.

Harbott J, Viehmann S, Borkhardt A, Henze G, Lampert F.

Blood. 1997 Dec 15;90(12):4933-7.


AML1/RUNX1 mutations are infrequent, but related to AML-M0, acquired trisomy 21, and leukemic transformation in pediatric hematologic malignancies.

Taketani T, Taki T, Takita J, Tsuchida M, Hanada R, Hongo T, Kaneko T, Manabe A, Ida K, Hayashi Y.

Genes Chromosomes Cancer. 2003 Sep;38(1):1-7.


Supplemental Content

Support Center