-
1
-
-
0242693950
-
Role of RUNX1/Runx1 in the pathogenesis of hematological malignancies
-
Kurokawa M., and Hirai H. Role of RUNX1/Runx1 in the pathogenesis of hematological malignancies. Cancer Sci 94 (2003) 841-846
-
(2003)
Cancer Sci
, vol.94
, pp. 841-846
-
-
Kurokawa, M.1
Hirai, H.2
-
2
-
-
0037265726
-
New mechanisms of RUNX1 gene alteration in hematological malignancies
-
Roumier C., Fenaux P., Lafage M., Imbert M., Eclache V., and Preudhomme C. New mechanisms of RUNX1 gene alteration in hematological malignancies. Leukemia 17 (2003) 9-16
-
(2003)
Leukemia
, vol.17
, pp. 9-16
-
-
Roumier, C.1
Fenaux, P.2
Lafage, M.3
Imbert, M.4
Eclache, V.5
Preudhomme, C.6
-
3
-
-
13544273521
-
Amplification or duplication of chromosome band 21q22 with multiple copies of the RUNX1 gene and mutation of the TP53 gene in therapy-related MDS and AML
-
Andersen M.K., Christiansen D.H., and Pedersen-Bjergaard J. Amplification or duplication of chromosome band 21q22 with multiple copies of the RUNX1 gene and mutation of the TP53 gene in therapy-related MDS and AML. Leukemia 19 (2005) 197-200
-
(2005)
Leukemia
, vol.19
, pp. 197-200
-
-
Andersen, M.K.1
Christiansen, D.H.2
Pedersen-Bjergaard, J.3
-
4
-
-
0036902961
-
Core binding factor genes and human leukemia
-
Hart S.M., and Foroni L. Core binding factor genes and human leukemia. Haematologica 87 (2002) 1307-1323
-
(2002)
Haematologica
, vol.87
, pp. 1307-1323
-
-
Hart, S.M.1
Foroni, L.2
-
5
-
-
33645470588
-
Amplification of RUNX1 gene in association with karyotype, age and diagnosis in acute leukemia patients
-
Kirschnerová G., Tóthová A., and Babusíková O. Amplification of RUNX1 gene in association with karyotype, age and diagnosis in acute leukemia patients. Neoplasma 53 (2006) 150-154
-
(2006)
Neoplasma
, vol.53
, pp. 150-154
-
-
Kirschnerová, G.1
Tóthová, A.2
Babusíková, O.3
-
6
-
-
10744226936
-
Chromosome 21 tandem repetition and RUNX1 (RUNX1) gene amplification
-
Ferro M.T., Hernaez R., Sordo M.T., Garcia-Sagredo J.M., Garcia-Miguel P., Fernández Guijarro M., Lopez J., Villalón C., Vallcorba I., Cabello P., and San Roman C. Chromosome 21 tandem repetition and RUNX1 (RUNX1) gene amplification. Cancer Genet Cytogenet 149 (2004) 11-16
-
(2004)
Cancer Genet Cytogenet
, vol.149
, pp. 11-16
-
-
Ferro, M.T.1
Hernaez, R.2
Sordo, M.T.3
Garcia-Sagredo, J.M.4
Garcia-Miguel, P.5
Fernández Guijarro, M.6
Lopez, J.7
Villalón, C.8
Vallcorba, I.9
Cabello, P.10
San Roman, C.11
-
10
-
-
3042763005
-
Molecular cytogenetic studies in hematological malignancies
-
Finn W., and Peterson L. (Eds), Kluwer Academic Publications, Boston
-
Dewald G., Brockman S.R., and Paternoster S.F. Molecular cytogenetic studies in hematological malignancies. In: Finn W., and Peterson L. (Eds). Hematopathology in Oncology (2004), Kluwer Academic Publications, Boston 69-112
-
(2004)
Hematopathology in Oncology
, pp. 69-112
-
-
Dewald, G.1
Brockman, S.R.2
Paternoster, S.F.3
-
11
-
-
0034995613
-
Spectral karyotyping and fluorescence in situ hybridization detect novel chromosomal aberrations, a recurring involvement of chromosome 21 and amplification of the MYC oncogene in acute myeloid leukaemia M2
-
Hilgenfeld E., Padilla-Nash H., McNeil N., Knutsen T., Montagna C., Tchinda J., Horst J., Ludwig W.D., Serve H., Büchner T., Berdel W.E., Schröck E., and Ried T. Spectral karyotyping and fluorescence in situ hybridization detect novel chromosomal aberrations, a recurring involvement of chromosome 21 and amplification of the MYC oncogene in acute myeloid leukaemia M2. Br J Haematol 113 (2001) 305-317
-
(2001)
Br J Haematol
, vol.113
, pp. 305-317
-
-
Hilgenfeld, E.1
Padilla-Nash, H.2
McNeil, N.3
Knutsen, T.4
Montagna, C.5
Tchinda, J.6
Horst, J.7
Ludwig, W.D.8
Serve, H.9
Büchner, T.10
Berdel, W.E.11
Schröck, E.12
Ried, T.13
-
12
-
-
0032746867
-
Combined spectral karyotyping and DAPI banding analysis of chromosome abnormalities in myelodysplastic syndrome
-
Kakazu N., Taniwaki M., Horiike S., Nishida K., Tatekawa T., Nagai M., Takahashi T., Akaogi T., Inazawa J., Ohki M., and Abe T. Combined spectral karyotyping and DAPI banding analysis of chromosome abnormalities in myelodysplastic syndrome. Genes Chromosomes Cancer 26 (1999) 336-345
-
(1999)
Genes Chromosomes Cancer
, vol.26
, pp. 336-345
-
-
Kakazu, N.1
Taniwaki, M.2
Horiike, S.3
Nishida, K.4
Tatekawa, T.5
Nagai, M.6
Takahashi, T.7
Akaogi, T.8
Inazawa, J.9
Ohki, M.10
Abe, T.11
-
13
-
-
0034090392
-
RUNX1 gene amplification: a novel finding in childhood acute lymphoblastic leukemia
-
Niini T., Kanerva J., Vettenranta K., Saarinen-Pihkala U.M., and Knuutila S. RUNX1 gene amplification: a novel finding in childhood acute lymphoblastic leukemia. Haematologica 85 (2000) 362-366
-
(2000)
Haematologica
, vol.85
, pp. 362-366
-
-
Niini, T.1
Kanerva, J.2
Vettenranta, K.3
Saarinen-Pihkala, U.M.4
Knuutila, S.5
-
14
-
-
33749179382
-
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 J.C., Mena-Duran A.V., Barragán E., Blanes M., Bolufer P., and Sanz M.A. High-level amplification of the RUNX1 gene in two cases of childhood acute lymphoblastic leukemia. Cancer Genet Cytogenet 170 (2006) 171-174
-
(2006)
Cancer Genet Cytogenet
, vol.170
, pp. 171-174
-
-
García-Casado, Z.1
Cervera, J.2
Verdeguer, A.3
Tasso, M.4
Valencia, A.5
Pajuelo, J.C.6
Mena-Duran, A.V.7
Barragán, E.8
Blanes, M.9
Bolufer, P.10
Sanz, M.A.11
-
15
-
-
33947131584
-
Intrachromosomal amplification of chromosome 21 (iAMP21) may arise from a breakage-fusion-bridge cycle
-
Robinson H.M., Harrison C.J., Moorman A.V., Chudoba I., and Strefford J.C. Intrachromosomal amplification of chromosome 21 (iAMP21) may arise from a breakage-fusion-bridge cycle. Genes Chromosomes Cancer 46 (2007) 318-326
-
(2007)
Genes Chromosomes Cancer
, vol.46
, pp. 318-326
-
-
Robinson, H.M.1
Harrison, C.J.2
Moorman, A.V.3
Chudoba, I.4
Strefford, J.C.5
-
16
-
-
3342936434
-
Insertions generating the 5'RUNX1/3'CBFA2T1 gene in acute myeloid leukemia cases show variable breakpoints
-
Specchia G., Albano F., Anelli L., Zagaria A., Liso A., La Starza R., Mancini M., Sebastio L., Giugliano E., Saglio G., Liso V., and Rocchi M. Insertions generating the 5'RUNX1/3'CBFA2T1 gene in acute myeloid leukemia cases show variable breakpoints. Genes Chromosomes Cancer 41 (2004) 86-91
-
(2004)
Genes Chromosomes Cancer
, vol.41
, pp. 86-91
-
-
Specchia, G.1
Albano, F.2
Anelli, L.3
Zagaria, A.4
Liso, A.5
La Starza, R.6
Mancini, M.7
Sebastio, L.8
Giugliano, E.9
Saglio, G.10
Liso, V.11
Rocchi, M.12
-
17
-
-
38349060647
-
Multiple copies of RUNX1: description of 14 new patients, follow-up, and a review of the literature
-
Pérez-Vera P., Montero-Ruíz O., Frías S., Rivera-Luna R., Valladares A., Arenas D., Paredes-Aguilera R., and Carnevale A. Multiple copies of RUNX1: description of 14 new patients, follow-up, and a review of the literature. Cancer Genet Cytogenet 180 (2008) 129-134
-
(2008)
Cancer Genet Cytogenet
, vol.180
, pp. 129-134
-
-
Pérez-Vera, P.1
Montero-Ruíz, O.2
Frías, S.3
Rivera-Luna, R.4
Valladares, A.5
Arenas, D.6
Paredes-Aguilera, R.7
Carnevale, A.8
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