Genome organization and the role of centromeres in evolution of the erythroleukaemia cell line HEL
暂无分享,去创建一个
L. Campbell | M. Wall | J. Peverall | R. MacKinnon | Adrian Zordan | Srilakshmi Nutalapati | Bruce Mercer | Meaghan Wall
[1] L. Campbell,et al. Chromothripsis under the microscope: a cytogenetic perspective of two cases of AML with catastrophic chromosome rearrangement. , 2013, Cancer genetics.
[2] A. Kohlmann,et al. TET2 deletions are a recurrent but rare phenomenon in myeloid malignancies and are frequently accompanied by TET2 mutations on the remaining allele , 2012, British journal of haematology.
[3] L. Campbell,et al. Unbalanced translocations of 20q in AML and MDS often involve interstitial rather than terminal deletions of 20q. , 2011, Cancer genetics.
[4] L. Campbell,et al. The paradox of 20q11.21 amplification in a subset of cases of myeloid malignancy with chromosome 20 deletion , 2010, Genes, chromosomes & cancer.
[5] S. Yu,et al. Telomere Capture as a Frequent Mechanism for Stabilization of the Terminal Chromosomal Deletion Associated with Inverted Duplication , 2010, Cytogenetic and Genome Research.
[6] L. Campbell,et al. Dicentric chromosomes and 20q11.2 amplification in MDS/AML with apparent monosomy 20 , 2008, Cytogenetic and Genome Research.
[7] J. Batanian,et al. Coexistence of neocentromeric marker 3q and trisomy 3 in two different tissues in a 3-year-old boy with peripheral T-cell lymphoma: support for a gene dosage effect hypothesis. , 2006, Cancer genetics and cytogenetics.
[8] Gaëlle Pérot,et al. Molecular cytogenetic characterization of a metastatic lung sarcomatoid carcinoma: 9p23 neocentromere and 9p23-p24 amplification including JAK2 and JMJD2C. , 2006, Cancer genetics and cytogenetics.
[9] H. Drexler,et al. JAK2 V617F tyrosine kinase mutation in cell lines derived from myeloproliferative disorders , 2006, Leukemia.
[10] L. Campbell,et al. A comparison of two contrasting recurrent isochromosomes 20 found in myelodysplastic syndromes suggests that retention of proximal 20q is a significant factor in myeloid malignancies. , 2005, Cancer genetics and cytogenetics.
[11] E. Estey,et al. JAK2 mutation 1849G>T is rare in acute leukemias but can be found in CMML, Philadelphia chromosome-negative CML, and megakaryocytic leukemia. , 2005, Blood.
[12] Sandra A. Moore,et al. Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis. , 2005, Cancer cell.
[13] D. Christiansen,et al. Amplification or duplication of chromosome band 21q22 with multiple copies of the AML1 gene and mutation of the TP53 gene in therapy-related MDS and AML , 2005, Leukemia.
[14] S. Jhanwar,et al. Identification of candidate genes on chromosome band 20q12 by physical mapping of translocation breakpoints found in myeloid leukemia cell lines , 2001, Oncogene.
[15] T. L. Hood,et al. Chromosome 20 deletions in myeloid malignancies: reduction of the common deleted region, generation of a PAC/BAC contig and identification of candidate genes , 2000, Oncogene.
[16] P. Wang,et al. Refinement of the smallest commonly deleted segment of chromosome 20 in malignant myeloid diseases and development of a PAC-based physical and transcription map. , 2000, Genomics.
[17] L. Nagarajan,et al. Deletions of chromosome 5q13.3 and 17p loci cooperate in myeloid neoplasms. , 2000, Blood.
[18] R. Bataille,et al. Amplification of the 11q23 region in acute myeloid leukemia , 1999, Genes, chromosomes & cancer.
[19] T. L. Hood,et al. Identification of multiple copies of a 20q-chromosome in a case of myelodysplastic syndrome: a FISH study. , 1999, Leukemia research.
[20] M. Tschan,et al. Aberrant FHIT mRNA transcripts are present in malignant and normal haematopoiesis, but absence of FHIT protein is restricted to leukaemia , 1999, Oncogene.
[21] M. Seto,et al. Amplification on double‐minute chromosomes and partial‐tandem duplication of the MILL gene in leukemic cells of a patient with acute myelogenous leukemia , 1998, Genes, chromosomes & cancer.
[22] C. Preudhomme,et al. 17p Deletion in acute myeloid leukemia and myelodysplastic syndrome. Analysis of breakpoints and deleted segments by fluorescence in situ. , 1998, Blood.
[23] K. Choo. Centromere DNA dynamics: latent centromeres and neocentromere formation. , 1997, American journal of human genetics.
[24] H. Drexler,et al. Identity of original and late passage Dami megakaryocytes with HEL erythroleukemia cells shown by combined cytogenetics and DNA fingerprinting , 1997, Leukemia.
[25] J. Chang,et al. Aberrant FHIT transcripts in acute myeloid leukaemia , 1997, British journal of haematology.
[26] N. Zhao,et al. dic(5;17): A recurring abnormality in malignant myeloid disorders associated with mutations of TP53 , 1997, Genes, chromosomes & cancer.
[27] H. Drexler,et al. Early contamination of the Dami cell line by HEL. , 1997, Blood.
[28] G. Dewald,et al. Hematologic disorders associated with deletions of chromosome 20q: a clinicopathologic study of 107 patients. , 1996, American journal of clinical pathology.
[29] J. Rowley,et al. The t(10;11)(p13;q14) in the U937 cell line results in the fusion of the AF10 gene and CALM, encoding a new member of the AP-3 clathrin assembly protein family. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[30] T. Manshouri,et al. p16INK4A and p15INK4B gene deletions in primary leukemias. , 1995, Blood.
[31] A. Klein-Szanto,et al. Higher frequency of alterations in the p16/CDKN2 gene in squamous cell carcinoma cell lines than in primary tumors of the head and neck. , 1994, Cancer research.
[32] D. Rosenthal,et al. Characterization of a new megakaryocytic cell line: the Dami cell. , 1988, Blood.
[33] R. Bernstein,et al. Fourth International Workshop on Chromosomes in Leukemia 1982: Abnormalities of chromosome 7 resulting in monosomy 7 or in deletion of the long arm (7q-): review of translocations, breakpoints, and associated abnormalities. , 1984, Cancer genetics and cytogenetics.
[34] T. Papayannopoulou,et al. HEL cells: a new human erythroleukemia cell line with spontaneous and induced globin expression. , 1982, Science.
[35] M. Cohen,et al. Chromosome deletion (46, XY, 20q-) in sideroblastic anemia. , 1974, Israel journal of medical sciences.
[36] P. Nowell,et al. Chromosome preparations of leukocytes cultured from human peripheral blood. , 1960, Experimental cell research.
[37] B. Mcclintock,et al. The Stability of Broken Ends of Chromosomes in Zea Mays. , 1941, Genetics.
[38] M. Seabright. The use of proteolytic enzymes for the mapping of structural rearrangements in the chromosomes of man , 2004, Chromosoma.
[39] T. Manshouri,et al. Loss of heterozygosity on chromosome 5 in adults with acute lymphoblastic leukemia. , 2001, Leukemia research.
[40] A. Look,et al. Amplification of the E2F1 transcription factor gene in the HEL erythroleukemia cell line. , 1995, Genomics.
[41] P. Meltzer,et al. Telomere capture stabilizes chromosome breakage , 1993, Nature Genetics.
[42] C. Morris,et al. Nonrandom cytogenetic changes in New Zealand patients with acute myeloid leukemia. , 1983, Cancer genetics and cytogenetics.
[43] Iscn. International System for Human Cytogenetic Nomenclature , 1978 .
[44] J. Rowley,et al. Deletion of the long arm of chromosome 20 [del(20)(q11)] in myeloid disorders. , 1978, Blood.