-
1
-
-
0000477103
-
Enzymatic synthesis of biotin-labeled polynucleotides: Novel nucleic acid affinity probes
-
Langer PR, Waldrop AE, Ward DC. Enzymatic synthesis of biotin-labeled polynucleotides: novel nucleic acid affinity probes. Proc Natl Acad Sci USA 1981; 78, 11: 6633-7.
-
(1981)
Proc Natl Acad Sci USA
, vol.78
, Issue.11
, pp. 6633-6637
-
-
Langer, P.R.1
Waldrop, A.E.2
Ward, D.C.3
-
2
-
-
0023576805
-
Use of whole cosmid cloned genomic sequences for chromosomal localization by non radio-active in situ hybridization
-
Landegent JE, Jansen in de Wal N, Dirks RW, Baas F, van der Ploeg M. Use of whole cosmid cloned genomic sequences for chromosomal localization by non radio-active in situ hybridization. Human Genes 1987; 77: 366-70.
-
(1987)
Human Genes
, vol.77
, pp. 366-370
-
-
Landegent, J.E.1
Jansen In De Wal, N.2
Dirks, R.W.3
Baas, F.4
Van Der Ploeg, M.5
-
3
-
-
0029268926
-
Recent advances in fluorescence in situ hybridization (Fish) in hematology
-
Berger R. Recent advances in fluorescence in situ hybridization (Fish) in hematology. Pathol Biol 1995; 43: 175-80.
-
(1995)
Pathol Biol
, vol.43
, pp. 175-180
-
-
Berger, R.1
-
4
-
-
0027362403
-
In situ hybridization to interphase nuclei in acute leukemia
-
Romana SP, Cherif D, Le Coniat M, Derré J, Flexor MA, Berger R. In situ hybridization to interphase nuclei in acute leukemia. Gene, Chrom Cancer 1993; 8: 98-103.
-
(1993)
Gene, Chrom Cancer
, vol.8
, pp. 98-103
-
-
Romana, S.P.1
Cherif, D.2
Le Coniat, M.3
Derré, J.4
Flexor, M.A.5
Berger, R.6
-
5
-
-
0028334007
-
Detection of monosomy 7 and trisomies 8 and 11 in myelodysplastic disorders by interphase fluorescent in situ hybridization. Comparison with acute non lymphocytic leukemias
-
Brizard F, Brizard A, Guillot F, Tanzer J, Berger R. Detection of monosomy 7 and trisomies 8 and 11 in myelodysplastic disorders by interphase fluorescent in situ hybridization. Comparison with acute non lymphocytic leukemias. Leukemia 1994; 8: 1005-11.
-
(1994)
Leukemia
, vol.8
, pp. 1005-1011
-
-
Brizard, F.1
Brizard, A.2
Guillot, F.3
Tanzer, J.4
Berger, R.5
-
6
-
-
0028216548
-
Fluorescence in situ hybridization improves the detection of monosomy 7 in myelodysplastic syndromes
-
Flactif M, Lai JL, Preudhomme C, Fenaux P. Fluorescence in situ hybridization improves the detection of monosomy 7 in myelodysplastic syndromes. Leukemia 1994; 8: 1012-8.
-
(1994)
Leukemia
, vol.8
, pp. 1012-1018
-
-
Flactif, M.1
Lai, J.L.2
Preudhomme, C.3
Fenaux, P.4
-
7
-
-
0028330771
-
t(12;21): A new recurrent translocation in acute lymphoblastic leukemia
-
Romana SP, Le Coniat M, Berger R. t(12;21): a new recurrent translocation in acute lymphoblastic leukemia. Gene Chrom Cancer 1994; 9: 186-91.
-
(1994)
Gene Chrom Cancer
, vol.9
, pp. 186-191
-
-
Romana, S.P.1
Le Coniat, M.2
Berger, R.3
-
8
-
-
0030749221
-
Improved sensitivity of BCR-ABL detection: A triple-probe three-color fluorescence in situ hybridization system
-
Sinclair PB, Green AR, Grace C, Nacheva EP. Improved sensitivity of BCR-ABL detection: a triple-probe three-color fluorescence in situ hybridization system. Blood 1997; 90: 1395-402.
-
(1997)
Blood
, vol.90
, pp. 1395-1402
-
-
Sinclair, P.B.1
Green, A.R.2
Grace, C.3
Nacheva, E.P.4
-
9
-
-
0028299948
-
Detection of chimeric BCR-ABL genes on bone marrow samples and blood smears in chronic myeloid and acute lymphoblastic leukemia by in situ hybridization
-
Bentz M, Cabot G, Moos M, Speicher MR, Ganser A, Lichter P, et al. Detection of chimeric BCR-ABL genes on bone marrow samples and blood smears in chronic myeloid and acute lymphoblastic leukemia by in situ hybridization. Blood 1994; 83: 1922-8.
-
(1994)
Blood
, vol.83
, pp. 1922-1928
-
-
Bentz, M.1
Cabot, G.2
Moos, M.3
Speicher, M.R.4
Ganser, A.5
Lichter, P.6
-
10
-
-
0027450689
-
Detecting genetic changes in human tumor cells have scientists «Gone Fishing»
-
Le Beau MM. Detecting genetic changes in human tumor cells have scientists «Gone Fishing». Blood 1993; 8: 1979-3.
-
(1993)
Blood
, vol.8
, pp. 1979-1983
-
-
Le Beau, M.M.1
-
11
-
-
0026655470
-
Detection of minimal residual disease by polymerase chain reaction in Philadelphia chromosome-positive chronic myelogenous leukemia following interferon therapy
-
Lee MS, Kantarjian H, Talpaz M, Freireich EJ, Deisseroth A, Trujillo JM, et al. Detection of minimal residual disease by polymerase chain reaction in Philadelphia chromosome-positive chronic myelogenous leukemia following interferon therapy. Blood 1992; 79: 1920-3.
-
(1992)
Blood
, vol.79
, pp. 1920-1923
-
-
Lee, M.S.1
Kantarjian, H.2
Talpaz, M.3
Freireich, E.J.4
Deisseroth, A.5
Trujillo, J.M.6
-
12
-
-
0027970838
-
Chromosomal translocations in human cancers
-
Rabbitts TH. Chromosomal translocations in human cancers. Nature 1994; 371: 143-9.
-
(1994)
Nature
, vol.371
, pp. 143-149
-
-
Rabbitts, T.H.1
-
13
-
-
0025633261
-
Mapping chromosome band 11q23 in human acute leukemia with biotinylated probes: Identification of 11q23 translocation breakpoints with a yeast artificial chromosome
-
Rowley JD, Diaz MO, Espinosa III R, Patel Y, Van Meile E, Zieminvan der Poel S, et al. Mapping chromosome band 11q23 in human acute leukemia with biotinylated probes: identification of 11q23 translocation breakpoints with a yeast artificial chromosome. Proc Natl Acad Sci USA 1990; 87: 9358-62.
-
(1990)
Proc Natl Acad Sci USA
, vol.87
, pp. 9358-9362
-
-
Rowley, J.D.1
Diaz, M.O.2
Espinosa III, R.3
Patel, Y.4
Van Meile, E.5
Zieminvan Der Poel, S.6
-
14
-
-
0029045087
-
The t(12;21) of acute lymphoblastic leukemia results in a TEL-AML1 gene fusion
-
Romana SP, Machauffé M, Le Coniat M, Chumakov I, Le Paslier D, Berger R, et al. The t(12;21) of acute lymphoblastic leukemia results in a TEL-AML1 gene fusion. Blood 1995; 12: 3662-70.
-
(1995)
Blood
, vol.12
, pp. 3662-3670
-
-
Romana, S.P.1
Machauffé, M.2
Le Coniat, M.3
Chumakov, I.4
Le Paslier, D.5
Berger, R.6
-
15
-
-
0026495364
-
Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors
-
Kallioniemi A, Kallioniemi OP, Sudar D, Rutovitz D, Gray JW, Waldman F, et al. Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors. Science 1992; 258, 5083: 818-21.
-
(1992)
Science
, vol.258
, Issue.5083
, pp. 818-821
-
-
Kallioniemi, A.1
Kallioniemi, O.P.2
Sudar, D.3
Rutovitz, D.4
Gray, J.W.5
Waldman, F.6
-
16
-
-
0029864105
-
Comparative genomic hybridization: A new tool in cancer pathology
-
Hermsen MAJA, Meijer GA, Baak JPA, Fiac F, Joenje H, Walboomers JJM. Comparative genomic hybridization: a new tool in cancer pathology. Human Pathol 1996; 27, 4: 342-9.
-
(1996)
Human Pathol
, vol.27
, Issue.4
, pp. 342-349
-
-
Hermsen, M.A.J.A.1
Meijer, G.A.2
Baak, J.P.A.3
Fiac, F.4
Joenje, H.5
Walboomers, J.J.M.6
-
17
-
-
0027943920
-
Comparative genomic hybridization: An overview
-
Houldsworth J, Chaganti RSK. Comparative genomic hybridization: an overview. Am J Pathol 1994; 145, 6: 1253-60.
-
(1994)
Am J Pathol
, vol.145
, Issue.6
, pp. 1253-1260
-
-
Houldsworth, J.1
Chaganti, R.S.K.2
-
19
-
-
0027966172
-
Optimizing comparative genomic hybridization for analysis of DNA sequence copy number changes in solid tumors
-
Kallioniemi OP, Kallioniemi A, Piper J, Isola J, Waldman FM, Gray JW, Pinkel D. Optimizing comparative genomic hybridization for analysis of DNA sequence copy number changes in solid tumors. Genes Chrom Cancer 1994; 10: 231-43.
-
(1994)
Genes Chrom Cancer
, vol.10
, pp. 231-243
-
-
Kallioniemi, O.P.1
Kallioniemi, A.2
Piper, J.3
Isola, J.4
Waldman, F.M.5
Gray, J.W.6
Pinkel, D.7
-
20
-
-
0038214755
-
Multicolor spectral karyotyping of human chromosomes
-
Schrök E, Du Manoir SB, Veldman T, Schoell B, Wienberg J, Ferguson-Smith MA, et al. Multicolor spectral karyotyping of human chromosomes. Science 1996; 273: 494-7.
-
(1996)
Science
, vol.273
, pp. 494-497
-
-
Schrök, E.1
Du Manoir, S.B.2
Veldman, T.3
Schoell, B.4
Wienberg, J.5
Ferguson-Smith, M.A.6
-
21
-
-
0029912473
-
Karyotyping human chromosomes by combinatorial multifluor Fish
-
Speicher MR, Ballard SG, Ward DC. Karyotyping human chromosomes by combinatorial multifluor Fish. Nature Genet 1996; 12: 368-75.
-
(1996)
Nature Genet
, vol.12
, pp. 368-375
-
-
Speicher, M.R.1
Ballard, S.G.2
Ward, D.C.3
-
22
-
-
0030909689
-
Hidden chromosome abnormalities in haematological malignancies detected by multicolour spectral karyotyping
-
Veldman T, Vignon C, Schrök E, Rowley JD, Ried T. Hidden chromosome abnormalities in haematological malignancies detected by multicolour spectral karyotyping. Nature Genet 1997; 15: 406-10.
-
(1997)
Nature Genet
, vol.15
, pp. 406-410
-
-
Veldman, T.1
Vignon, C.2
Schrök, E.3
Rowley, J.D.4
Ried, T.5
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