-
1
-
-
0035306823
-
The application of comparative genomic hybridization as an additional tool in the chromosome analysis of acute myeloid leukemia and myelodysplastic syndrome
-
Kim MH, Stewart J, Devlin C, et al. The application of comparative genomic hybridization as an additional tool in the chromosome analysis of acute myeloid leukemia and myelodysplastic syndrome. Cancer Genet Cytogenet 2001; 126:26-33.
-
(2001)
Cancer Genet Cytogenet
, vol.126
, pp. 26-33
-
-
Kim, M.H.1
Stewart, J.2
Devlin, C.3
-
2
-
-
4644224836
-
Genetic diagnosis by comparative genomic hybridization in adult de novo acute myeloid leukemia
-
Casas S, Aventin A, Fuentes F, et al. Genetic diagnosis by comparative genomic hybridization in adult de novo acute myeloid leukemia. Cancer Genet Cytogenet 2004; 153:16-25.
-
(2004)
Cancer Genet Cytogenet
, vol.153
, pp. 16-25
-
-
Casas, S.1
Aventin, A.2
Fuentes, F.3
-
3
-
-
64549103044
-
Delineation of yet unknown cryptic subtelomere aberrations in 50% of acute myeloid leukemia with normal GTG-banding karyotype
-
Gross M, Mkrtchyan H, Glaser M, et al. Delineation of yet unknown cryptic subtelomere aberrations in 50% of acute myeloid leukemia with normal GTG-banding karyotype. Int J Oncol 2009; 34:417-423.
-
(2009)
Int J Oncol
, vol.34
, pp. 417-423
-
-
Gross, M.1
Mkrtchyan, H.2
Glaser, M.3
-
4
-
-
17044453153
-
Array comparative genomic hybridization analysis of myelodysplastic syndromes with complex karyotypes. A technical evaluation
-
Martinez-Ramerez A, Urioste M, Calasanz MH, et al. Array comparative genomic hybridization analysis of myelodysplastic syndromes with complex karyotypes. A technical evaluation. Cancer Genet Cytogenet 2003; 144:87-89.
-
(2003)
Cancer Genet Cytogenet
, vol.144
, pp. 87-89
-
-
Martinez-Ramerez, A.1
Urioste, M.2
Calasanz, M.H.3
-
5
-
-
34347229790
-
Highly sensitive method for genome-wide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single nucleotide polymorphism genotyping microarrays
-
Yamamoto G, Nannya Y, Kato M, et al. Highly sensitive method for genome-wide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single nucleotide polymorphism genotyping microarrays. Am J Hum Genet 2007; 87:114-126.
-
(2007)
Am J Hum Genet
, vol.87
, pp. 114-126
-
-
Yamamoto, G.1
Nannya, Y.2
Kato, M.3
-
6
-
-
25844451158
-
Frequent loss of heterozygosity without loss of genetic material in acute myeloid leukemia with normal karyotype
-
Gorletta TA, Gasparini P, D'Elios MM, et al. Frequent loss of heterozygosity without loss of genetic material in acute myeloid leukemia with normal karyotype. Genes Chromosomes Cancer 2005; 44:334-337.
-
(2005)
Genes Chromosomes Cancer
, vol.44
, pp. 334-337
-
-
Gorletta, T.A.1
Gasparini, P.2
D'Elios, M.M.3
-
7
-
-
70149093912
-
Recurring mutations found by sequencing an acute myeloid leukemia genome
-
Mardis E, Ding L, Dooling DJ, et al. Recurring mutations found by sequencing an acute myeloid leukemia genome. N Engl J Med 2009; 361:1058-1066.
-
(2009)
N Engl J Med
, vol.361
, pp. 1058-1066
-
-
Mardis, E.1
Ding, L.2
Dooling, D.J.3
-
8
-
-
59449095868
-
Frequent genomic abnormalities in acute myeloid leukemia/myelodysplastic syndrome with normal karyotype
-
Akagi T, Ogawa S, Dugas M, et al. Frequent genomic abnormalities in acute myeloid leukemia/myelodysplastic syndrome with normal karyotype. Haematologica 2008; 94:213-223.
-
(2008)
Haematologica
, vol.94
, pp. 213-223
-
-
Akagi, T.1
Ogawa, S.2
Dugas, M.3
-
9
-
-
69149100639
-
Acquired copy number alterations in adult acute myeloid leukemia genomes
-
Walter MJ, Payton JE, Ries RE, et al. Acquired copy number alterations in adult acute myeloid leukemia genomes. Proc Natl Acad Sci USA 2009; 106: 12950-12955.
-
(2009)
Proc Natl Acad Sci USA
, vol.106
, pp. 12950-12955
-
-
Walter, M.J.1
Payton, J.E.2
Ries, R.E.3
-
10
-
-
33748450145
-
Disclosure of candidate genes in acute myeloid leukemia with complex karyotypes using microarray based molecular characterization
-
Rucker FG, Bullinger L, Schwaenen C, et al. Disclosure of candidate genes in acute myeloid leukemia with complex karyotypes using microarray based molecular characterization. J Clin Oncol 2006; 24:3887-3894.
-
(2006)
J Clin Oncol
, vol.24
, pp. 3887-3894
-
-
Rucker, F.G.1
Bullinger, L.2
Schwaenen, C.3
-
11
-
-
61849146788
-
Hidden abnormalities and novel classification of t(15; 17) acute promyelocytic leukemia based on genomic alterations
-
Akagi T, Shih LY, Kato M, et al. Hidden abnormalities and novel classification of t(15; 17) acute promyelocytic leukemia based on genomic alterations. Blood 2009; 113:1741-1748.
-
(2009)
Blood
, vol.113
, pp. 1741-1748
-
-
Akagi, T.1
Shih, L.Y.2
Kato, M.3
-
12
-
-
33644783592
-
Genomewide array based comparative genomic hybridization analysis of acute promyelocytic leukemia
-
Karnan S, Tsuzuki S, Kiyoi H, et al. Genomewide array based comparative genomic hybridization analysis of acute promyelocytic leukemia. Genes Chromosomes Cancer 2006; 45:420-425.
-
(2006)
Genes Chromosomes Cancer
, vol.45
, pp. 420-425
-
-
Karnan, S.1
Tsuzuki, S.2
Kiyoi, H.3
-
13
-
-
70349116956
-
Single nucleotide polymorphism genomic array analysis of t(8;21) acute myeloid leukemia cells
-
Akagi T, Shih LY, Ogawa S, et al. Single nucleotide polymorphism genomic array analysis of t(8;21) acute myeloid leukemia cells. Haematologica 2009; 94:1301-1306.
-
(2009)
Haematologica
, vol.94
, pp. 1301-1306
-
-
Akagi, T.1
Shih, L.Y.2
Ogawa, S.3
-
14
-
-
34548329664
-
Chromosomal aberrations in congenital bone marrow failure disorders: An early indicator for leukemo-genesis?
-
Gohring G, Karow A, Steinemann D, et al. Chromosomal aberrations in congenital bone marrow failure disorders: an early indicator for leukemo-genesis? Ann Hematol 2007; 86:733-739.
-
(2007)
Ann Hematol
, vol.86
, pp. 733-739
-
-
Gohring, G.1
Karow, A.2
Steinemann, D.3
-
15
-
-
12544257171
-
Genome-wide single nucleotide polymorphism analysis reveals frequent partial uniparental disomy due to somatic recombination in acute myeloid leukemia
-
Raghavan M, Lillington DM, Skoulakis S, et al. Genome-wide single nucleotide polymorphism analysis reveals frequent partial uniparental disomy due to somatic recombination in acute myeloid leukemia. Cancer Res 2005; 65:375-378.
-
(2005)
Cancer Res
, vol.65
, pp. 375-378
-
-
Raghavan, M.1
Lillington, D.M.2
Skoulakis, S.3
-
16
-
-
50949113696
-
Segmental uniparental disomy is a commonly acquired genetic event in relapsed acute myeloid leukemia
-
Raghavan M, Smith LL, Lillington DM, et al. Segmental uniparental disomy is a commonly acquired genetic event in relapsed acute myeloid leukemia. Blood 2008; 112:814-821.
-
(2008)
Blood
, vol.112
, pp. 814-821
-
-
Raghavan, M.1
Smith, L.L.2
Lillington, D.M.3
-
17
-
-
46749114860
-
Uniparental disomy may be associated with microsatellite instability in acute myeloid leukemia with normal karyotype
-
Serrano E, Carnicer MH, Orantes V, et al. Uniparental disomy may be associated with microsatellite instability in acute myeloid leukemia with normal karyotype. Leuk Lymphoma 2008; 49:1178-1183.
-
(2008)
Leuk Lymphoma
, vol.49
, pp. 1178-1183
-
-
Serrano, E.1
Carnicer, M.H.2
Orantes, V.3
-
18
-
-
27144478643
-
Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leuke-mias
-
Fitzgibbon J, Smith LL, Raghavan M, et al. Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leuke-mias. Cancer Res 2005; 65:9152-9154.
-
(2005)
Cancer Res
, vol.65
, pp. 9152-9154
-
-
Fitzgibbon, J.1
Smith, L.L.2
Raghavan, M.3
|