Partial uniparental disomy:: a recurrent genetic mechanism alternative to chromosomal deletion in malignant lymphoma

被引:30
作者
Nielaender, I
Martín-Subero, JI
Wagner, F
Martínez-Climent, JA
Siebert, R
机构
[1] Univ Hosp Schleswig Holstein, Inst Human Genet, Kiel, Germany
[2] Deutsch Ressourcesnzentrum Genomforsch, Berlin, Germany
[3] Univ Navarra, Ctr Appl Med Res, Pamplona, Spain
关键词
D O I
10.1038/sj.leu.2404173
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
引用
收藏
页码:904 / 905
页数:3
相关论文
共 7 条
[1]   Comprehensive whole genome array CGH profiling of mantle cell lymphoma model genomes [J].
de Leeuw, RJ ;
Davies, JJ ;
Rosenwald, A ;
Bebb, G ;
Gascoyne, RD ;
Dyer, MJS ;
Staudt, LM ;
Martinez-Climent, JA ;
Lam, WL .
HUMAN MOLECULAR GENETICS, 2004, 13 (17) :1827-1837
[2]   Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukemias [J].
Fitzgibbon, J ;
Smith, LL ;
Raghavan, M ;
Smith, ML ;
Debernardi, S ;
Skoulakis, S ;
Lillington, D ;
Lister, TA ;
Young, BD .
CANCER RESEARCH, 2005, 65 (20) :9152-9154
[3]   Genomic DNA-chip hybridization in t(11;14)-positive mantle cell lymphomas shows a high frequency of aberrations and allows a refined characterization of consensus regions [J].
Kohlhammer, H ;
Schwaenen, C ;
Wessendorf, S ;
Holzmann, K ;
Kestler, HA ;
Kienle, D ;
Barth, TFE ;
Möller, P ;
Ott, G ;
Kalla, J ;
Radlwimmer, B ;
Pscherer, A ;
Stilgenbauer, S ;
Döhner, H ;
Lichter, P ;
Bentz, M .
BLOOD, 2004, 104 (03) :795-801
[4]  
Raghavan M, 2005, CANCER RES, V65, P375
[5]   Mantle-cell lymphoma genotypes identified with CGH to BAC microarrays define a leukemic subgroup of disease and predict patient outcome [J].
Rubio-Moscardo, F ;
Climent, J ;
Siebert, R ;
Piris, MA ;
Martín-Subero, JI ;
Nieländer, I ;
Garcia-Conde, J ;
Dyer, MJS ;
Terol, MJ ;
Pinkel, D ;
Martinez-Climent, JA .
BLOOD, 2005, 105 (11) :4445-4454
[6]   Novel chromosomal imbalances in mantle cell lymphoma detected by genome-wide array-based comparative genomic hybridization [J].
Schraders, M ;
Pfundt, R ;
Straatman, HMP ;
Janssen, IM ;
van Kessel, AG ;
Schoenmakers, EFPM ;
van Krieken, JHJM ;
Groenen, PJTA .
BLOOD, 2005, 105 (04) :1686-1693
[7]   Genomewide single nucleotide polymorphism microarray mapping in basal cell carcinomas unveils uniparental disomy as a key somatic event [J].
Teh, MT ;
Blaydon, D ;
Chaplin, T ;
Foot, NJ ;
Skoulakis, S ;
Raghavan, M ;
Harwood, CA ;
Proby, CM ;
Philpott, MP ;
Young, BD ;
Kelsell, DP .
CANCER RESEARCH, 2005, 65 (19) :8597-8603