AAAAAA

   
Results: 1-24 |
Results: 24
Molecular cytogenetics
Authors: Kearney, L
Citation: L. Kearney, Molecular cytogenetics, BEST P R C, 14(3), 2001, pp. 645-NIL_3
Cytogenetics in haematology - Preface
Authors: Buckle, VJ Kearney, L
Citation: Vj. Buckle et L. Kearney, Cytogenetics in haematology - Preface, BEST P R C, 14(3), 2001, pp. VII-VIII
Subtelomeric chromosome rearrangements are detected using an innovative 12-color FISH assay (M-TEL)
Authors: Brown, J Saracoglu, K Uhrig, S Speicher, MR Eils, R Kearney, L
Citation: J. Brown et al., Subtelomeric chromosome rearrangements are detected using an innovative 12-color FISH assay (M-TEL), NAT MED, 7(4), 2001, pp. 497-501
Monosomy for the most telomeric, gene-rich region of the short arm of human chromosome 16 causes minimal phenotypic effects
Authors: Horsley, SW Daniels, RJ Anguita, E Raynham, HA Peden, JF Villegas, A Vickers, MA Green, S Waye, JS Chui, DHK Ayyub, H MacCarthy, AB Buckle, VJ Gibbons, RJ Kearney, L Higgs, DR
Citation: Sw. Horsley et al., Monosomy for the most telomeric, gene-rich region of the short arm of human chromosome 16 causes minimal phenotypic effects, EUR J HUM G, 9(3), 2001, pp. 217-225
Sequence, structure and pathology of the fully annotated terminal 2 Mb of the short arm of human chromosome 16
Authors: Daniels, RJ Peden, JF Lloyd, C Horsley, SW Clark, K Tufarelli, C Kearney, L Buckle, VJ Doggett, NA Flint, J Higgs, DR
Citation: Rj. Daniels et al., Sequence, structure and pathology of the fully annotated terminal 2 Mb of the short arm of human chromosome 16, HUM MOL GEN, 10(4), 2001, pp. 339-352
A mitotically stable marker chromosome negative for whole chromosome libraries, centromere probes and chromosome specific telomere regions: a novel class of supernumerary marker chromosome?
Authors: Ogilvie, CM Harrison, RH Horsley, SW Hodgson, SV Kearney, L
Citation: Cm. Ogilvie et al., A mitotically stable marker chromosome negative for whole chromosome libraries, centromere probes and chromosome specific telomere regions: a novel class of supernumerary marker chromosome?, CYTOG C GEN, 92(1-2), 2001, pp. 69-73
New concepts to improve resolution and sensitivity of molecular cytogenetic diagnostics by multicolor fluorescence in situ hybridization
Authors: Saracoglu, K Brown, J Kearney, L Uhrig, S Azofeifa, J Fauth, C Speicher, MR Eils, R
Citation: K. Saracoglu et al., New concepts to improve resolution and sensitivity of molecular cytogenetic diagnostics by multicolor fluorescence in situ hybridization, CYTOMETRY, 44(1), 2001, pp. 7-15
The paired box domain gene PAX5 is fused to ETV6/TEL in an acute lymphoblastic leukemia case
Authors: Cazzaniga, G Daniotti, M Tosi, S Giudici, G Aloisi, A Pogliani, E Kearney, L Biondi, A
Citation: G. Cazzaniga et al., The paired box domain gene PAX5 is fused to ETV6/TEL in an acute lymphoblastic leukemia case, CANCER RES, 61(12), 2001, pp. 4666-4670
A novel gene, NSD1, is fused to NUP98 in the t(5;11)(q35;p15.5) in de novochildhood acute myeloid leukemia
Authors: Jaju, RJ Fidler, C Haas, OA Strickson, AJ Watkins, F Clark, K Cross, NCP Cheng, JF Aplan, PD Kearney, L Boultwood, J Wainscoat, JS
Citation: Rj. Jaju et al., A novel gene, NSD1, is fused to NUP98 in the t(5;11)(q35;p15.5) in de novochildhood acute myeloid leukemia, BLOOD, 98(4), 2001, pp. 1264-1267
t(7;12)(q36;p13), a new recurrent translocation involving ETV6 in infant leukemia
Authors: Tosi, S Harbott, J Teigler-Schlegel, A Haas, OA Pirc-Danoewinata, H Harrison, CJ Biondi, A Cazzaniga, G Kempski, H Scherer, SW Kearney, L
Citation: S. Tosi et al., t(7;12)(q36;p13), a new recurrent translocation involving ETV6 in infant leukemia, GENE CHROM, 29(4), 2000, pp. 325-332
Combined immunophenotyping and FISH identifies the involvement of B-cells in 5q-syndrome
Authors: Jaju, RJ Jones, M Boultwood, J Kelly, S Mason, DY Wainscoat, JS Kearney, L
Citation: Rj. Jaju et al., Combined immunophenotyping and FISH identifies the involvement of B-cells in 5q-syndrome, GENE CHROM, 29(3), 2000, pp. 276-280
Identification of a subtle t(16;19)(p13.3;p13.3) in an infant with multiple congenital abnormalities using a 12-colour multiplex FISH telomere assay,M-TEL
Authors: Brown, J Horsley, SW Jung, C Saracoglu, K Janssen, B Brough, M Daschner, M Beedgen, B Kerkhoffs, G Eils, R Harris, PC Jauch, A Kearney, L
Citation: J. Brown et al., Identification of a subtle t(16;19)(p13.3;p13.3) in an infant with multiple congenital abnormalities using a 12-colour multiplex FISH telomere assay,M-TEL, EUR J HUM G, 8(12), 2000, pp. 903-910
Characterization of a highly complex region in Xq13 and mapping of three isodicentric breakpoints associated with preleukemia
Authors: McDonell, N Ramser, J Francis, F Vinet, MC Rider, S Sudbrak, R Riesselman, L Yaspo, ML Reinhardt, R Monaco, AP Ross, F Kahn, A Kearney, L Buckle, V Chelly, J
Citation: N. Mcdonell et al., Characterization of a highly complex region in Xq13 and mapping of three isodicentric breakpoints associated with preleukemia, GENOMICS, 64(3), 2000, pp. 221-229
An integrated map of human 6q22.3-q24 including a 3-Mb high-resolution BAC/PAC contig encompassing a QTL for fetal hemoglobin
Authors: Game, L Close, J Stephens, P Mitchell, J Best, S Rochette, J Louis-dit-Sully, C Riley, J See, CG Sanseau, P Kearney, L Bethel, G Humphray, S Dunham, I Mungall, A Thein, SL
Citation: L. Game et al., An integrated map of human 6q22.3-q24 including a 3-Mb high-resolution BAC/PAC contig encompassing a QTL for fetal hemoglobin, GENOMICS, 64(3), 2000, pp. 264-276
Multiplex fluorescence in situ hybridization and cross species color banding of a case of chronic myeloid leukemia in blastic crisis with a complex Philadelphia translocation
Authors: Harrison, CJ Gibbons, B Yang, FT Butler, T Cheung, KL Kearney, L Dirscherl, L Bray-Ward, P Gregson, M Ferguson-Smith, M
Citation: Cj. Harrison et al., Multiplex fluorescence in situ hybridization and cross species color banding of a case of chronic myeloid leukemia in blastic crisis with a complex Philadelphia translocation, CANC GENET, 116(2), 2000, pp. 105-110
The life of Musorgsky
Authors: Kearney, L
Citation: L. Kearney, The life of Musorgsky, SLAV REV, 59(4), 2000, pp. 945-946
Cytogenetic and molecular evidence of marrow involvement in extramedullaryacute myeloid leukaemia
Authors: Lillington, DM Jaju, RJ Shankar, AG Neat, M Kearney, L Young, BD Saha, V
Citation: Dm. Lillington et al., Cytogenetic and molecular evidence of marrow involvement in extramedullaryacute myeloid leukaemia, BR J HAEM, 110(3), 2000, pp. 547-551
Delineation of multiple deleted regions in 7q in myeloid disorders
Authors: Tosi, S Scherer, SW Giudici, G Czepulkowski, B Biondi, A Kearney, L
Citation: S. Tosi et al., Delineation of multiple deleted regions in 7q in myeloid disorders, GENE CHROM, 25(4), 1999, pp. 384-392
Characterization of the human myeloid leukemia-derived cell line GF-D8 by multiplex fluorescence in situ hybridization, subtelomeric probes, and comparative genomic hybridization
Authors: Tosi, S Giudici, G Rambaldi, A Scherer, SW Bray-Ward, P Dirscherl, L Biondi, A Kearney, L
Citation: S. Tosi et al., Characterization of the human myeloid leukemia-derived cell line GF-D8 by multiplex fluorescence in situ hybridization, subtelomeric probes, and comparative genomic hybridization, GENE CHROM, 24(3), 1999, pp. 213-221
Subtle chromosomal rearrangements in children with unexplained mental retardation
Authors: Knight, SJL Regan, R Nicod, A Horsley, SW Kearney, L Homfray, T Winter, RM Bolton, P Flint, J
Citation: Sjl. Knight et al., Subtle chromosomal rearrangements in children with unexplained mental retardation, LANCET, 354(9191), 1999, pp. 1676-1681
The impact of the new fish technologies on the cytogenetics of haematological malignancies
Authors: Kearney, L
Citation: L. Kearney, The impact of the new fish technologies on the cytogenetics of haematological malignancies, BR J HAEM, 104(4), 1999, pp. 648-658
A new recurrent translocation, t(5;11)(q35;p15.5), associated with del(5q)in childhood acute myeloid leukemia
Authors: Jaju, RJ Haas, OA Neat, M Harbott, J Saha, V Boultwood, J Brown, JM Pirc-Danoewinata, H Krings, BW Muller, U Morris, SW Wainscoat, JS Kearney, L
Citation: Rj. Jaju et al., A new recurrent translocation, t(5;11)(q35;p15.5), associated with del(5q)in childhood acute myeloid leukemia, BLOOD, 94(2), 1999, pp. 773-780
The tyrosine kinase Abl-related gene ARG is fused to ETV6 in an AML-M4Eo patient with a t(1;12)(q25;p13): Molecular cloning of both reciprocal transcripts
Authors: Cazzaniga, G Tosi, S Aloisi, A Giudici, G Daniotti, M Pioltelli, P Kearney, L Biondi, A
Citation: G. Cazzaniga et al., The tyrosine kinase Abl-related gene ARG is fused to ETV6 in an AML-M4Eo patient with a t(1;12)(q25;p13): Molecular cloning of both reciprocal transcripts, BLOOD, 94(12), 1999, pp. 4370-4373
The in-vitro generation of dendritic cells from blast cells in acute leukaemia
Authors: Robinson, SP English, N Jaju, R Kearney, L Knight, SC Reid, CDL
Citation: Sp. Robinson et al., The in-vitro generation of dendritic cells from blast cells in acute leukaemia, BR J HAEM, 103(3), 1998, pp. 763-771
Risultati: 1-24 |