FLUORESCENCE INSITU HYBRIDIZATION AND CYTOGENETICS OF HEMATOPOIETIC MALIGNANCIES - NEW DEVELOPMENTS

被引:0
作者
CHERIF, D [1 ]
BERGER, R [1 ]
机构
[1] INST GENET MOLEC,CNRS,SDI 15954,INSERM,U301,27 RUE JULIETTE DODU,F-75010 PARIS,FRANCE
来源
NOUVELLE REVUE FRANCAISE D HEMATOLOGIE | 1993年 / 35卷 / 01期
关键词
FLUORESCENCE INSITU HYBRIDIZATION; FISH; CHROMOSOMAL ABNORMALITIES; HEMATOPOIETIC MALIGNANCIES;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Fluorescence in situ hybridization (FISH) is currently developed to analyse chromosomal abnormalities of hemopoietic malignancies in several ways : description of chromosomal rearrangements using specific probes or chromosome painting; delineation of chromosomal breakpoints with probes previously localized to chromosomal bands; hybridization to interphase nuclei to detect numerical changes and, now, some structural abnormalities. Examples of usefulness of FISH to study hemopoietic malignancies are given.
引用
收藏
页码:45 / 47
页数:3
相关论文
共 19 条
[1]  
ANASTASI J, 1992, BLOOD, V79, P1796
[2]   DETECTION OF THE PHILADELPHIA-CHROMOSOME IN INTERPHASE NUCLEI [J].
ARNOLDUS, EPJ ;
WIEGANT, J ;
NOORDERMEER, IA ;
WESSELS, JW ;
BEVERSTOCK, GC ;
GROSVELD, GC ;
VANDERPLOEG, M ;
RAAP, AK .
CYTOGENETICS AND CELL GENETICS, 1990, 54 (3-4) :108-&
[3]   IDENTIFICATION OF A WHOLE-ARM TRANSLOCATION BY INSITU HYBRIDIZATION WITH DIRECTLY FLUOROCHROME-LABELED PROBES IN A MYELODYSPLASTIC SYNDROME [J].
BAJALICA, S ;
BRONDUMNIELSEN, K ;
SORENSEN, AG ;
PEDERSEN, NT ;
HEIM, S .
GENES CHROMOSOMES & CANCER, 1992, 5 (02) :128-131
[4]   THE 11Q23 BREAKPOINT IN ACUTE-LEUKEMIA WITH T(11-19)(Q23-P13) IS DISTAL TO THOSE OF T(4-11), T(6-11) AND T(9-11) [J].
CHERIF, D ;
DERSARKISSIAN, H ;
DERRE, J ;
TOKINO, T ;
NAKAMURA, Y ;
BERGER, R .
GENES CHROMOSOMES & CANCER, 1992, 4 (02) :107-112
[5]  
CHERIF D, 1992, IN PRESS GENES CHROM
[6]   NONRADIOACTIVE INSITU HYBRIDIZATION FOR THE DETECTION AND MONITORING OF TRISOMY-12 IN B-CELL CHRONIC LYMPHOCYTIC-LEUKEMIA [J].
CUNEO, A ;
WLODARSKA, I ;
ALY, MS ;
PIVA, N ;
CARLI, MG ;
FAGIOLI, F ;
TALLARICO, A ;
PAZZI, I ;
FERRARI, L ;
CASSIMAN, JJ ;
VANDENBERGHE, H ;
CASTOLDI, GL .
BRITISH JOURNAL OF HAEMATOLOGY, 1992, 81 (02) :192-196
[7]   RAPID DETECTION OF CHROMOSOME-16 INVERSION IN ACUTE NONLYMPHOCYTIC LEUKEMIA, SUBTYPE M4 - REGIONAL LOCALIZATION OF THE BREAKPOINT IN 16P [J].
DAUWERSE, JG ;
KIEVITS, T ;
BEVERSTOCK, GC ;
VANDERKEUR, D ;
SMIT, E ;
WESSELS, HW ;
HAGEMEIJER, A ;
PEARSON, PL ;
VANOMMEN, GJB ;
BREUNING, MH .
CYTOGENETICS AND CELL GENETICS, 1990, 53 (2-3) :126-&
[8]   INSITU HYBRIDIZATION ASCERTAINS THE PRESENCE OF A TRANSLOCATION T(6-11) IN AN ACUTE MONOCYTIC LEUKEMIA [J].
DERRE, J ;
CHERIF, D ;
LECONIAT, M ;
JULIER, C ;
BERGER, R .
GENES CHROMOSOMES & CANCER, 1990, 2 (04) :341-344
[9]   ISOLATION OF A YEAST ARTIFICIAL CHROMOSOME SPANNING THE 8-21 TRANSLOCATION BREAKPOINT T(8-21)(Q22-Q22.3) IN ACUTE MYELOGENOUS LEUKEMIA [J].
GAO, JZ ;
ERICKSON, P ;
GARDINER, K ;
LEBEAU, MM ;
DIAZ, MO ;
PATTERSON, D ;
ROWLEY, JD ;
DRABKIN, HA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (11) :4882-4886
[10]   DNA-SEQUENCES OF CHROMOSOME 21-SPECIFIC YAC DETECT THE T(8-21) BREAKPOINT OF ACUTE MYELOGENOUS LEUKEMIA [J].
KEARNEY, L ;
WATKINS, PC ;
YOUNG, BD ;
SACCHI, N .
CANCER GENETICS AND CYTOGENETICS, 1991, 57 (01) :109-119