Search Results - "LILLINGTON, Debra M"
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Genome-wide single nucleotide polymorphism analysis reveals frequent partial uniparental disomy due to somatic recombination in acute myeloid leukemias
Published in Cancer research (Chicago, Ill.) (15-01-2005)“…Genome-wide analysis of single nucleotide polymorphisms in 64 acute myeloid leukemias has revealed that approximately 20% exhibited large regions of…”
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2
Five members of the CEBP transcription factor family are targeted by recurrent IGH translocations in B-cell precursor acute lymphoblastic leukemia (BCP-ALL)
Published in Blood (15-04-2007)“…CCAAT enhancer-binding protein (CEBP) transcription factors play pivotal roles in proliferation and differentiation, including suppression of myeloid…”
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3
Microdeletions are a general feature of adult and adolescent acute lymphoblastic leukemia: Unexpected similarities with pediatric disease
Published in Proceedings of the National Academy of Sciences - PNAS (06-05-2008)“…We present here a genome-wide map of abnormalities found in diagnostic samples from 45 adults and adolescents with acute lymphoblastic leukemia (ALL). A 500K…”
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4
Segmental uniparental disomy is a commonly acquired genetic event in relapsed acute myeloid leukemia
Published in Blood (01-08-2008)“…Despite advances in the curative treatment of acute myeloid leukemia (AML), recurrence will occur in the majority of cases. At diagnosis, acquisition of…”
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5
Differential gene expression in pituitary adenomas by oligonucleotide array analysis
Published in European journal of endocrinology (01-07-2005)“…Objectives: Microarray technology allows for the expression profile of many thousands of genes to be quantified at the same time, and has resulted in novel…”
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6
11q23 balanced chromosome aberrations in treatment-related myelodysplastic syndromes and acute leukemia: Report from an International Workshop
Published in Genes chromosomes & cancer (01-04-2002)“…Among 511 patients with therapy‐related myelodysplastic syndrome or acute leukemia (t‐MDS/t‐AL) and balanced chromosome aberrations, 162 (32%) had…”
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7
Molecular cytogenetic characterization of Sézary syndrome
Published in Genes chromosomes & cancer (01-03-2003)“…Sézary syndrome (SS) is a rare form of erythrodermic cutaneous T‐cell lymphoma with hematological involvement and a poor prognosis. At present little is known…”
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8
Detection of Chromosome Abnormalities Pre–High-Dose Treatment in Patients Developing Therapy-Related Myelodysplasia and Secondary Acute Myelogenous Leukemia After Treatment for Non-Hodgkin’s Lymphoma
Published in Journal of clinical oncology (01-05-2001)“…To assess whether pre-high-dose therapy (HDT)-related factors play a critical role in the development of therapy-related myelodysplasia (tMDS) or secondary…”
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9
Proposals for standardized protocols for cytogenetic analyses of acute leukemias, chronic lymphocytic leukemia, chronic myeloid leukemia, chronic myeloproliferative disorders, and myelodysplastic syndromes
Published in Genes chromosomes & cancer (01-05-2007)“…The impact of cytogenetic characterization based on chromosome banding analyses and fluorescence in situ hybridization on clinical decision making has…”
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10
Amplification and overexpression of JUNB is associated with primary cutaneous T-cell lymphomas
Published in Blood (15-02-2003)“…Primary cutaneous lymphomas (PCLs) represent a heterogeneous group of extranodal T- and B-cell malignancies. The underlying molecular pathogenesis of this…”
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11
Genome-wide analysis of acute myeloid leukemia with normal karyotype reveals a unique pattern of homeobox gene expression distinct from those with translocation-mediated fusion events
Published in Genes chromosomes & cancer (01-06-2003)“…Gene expression profiles were determined from presentation peripheral blood and bone marrow samples of 28 patients with acute myeloid leukemia (AML)…”
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12
Genetic alterations in primary cutaneous CD30+ anaplastic large cell lymphoma
Published in Genes chromosomes & cancer (01-06-2003)“…Primary cutaneous CD30+ anaplastic large cell lymphoma (C‐ALCL) represents a distinct clinical subtype of CD30+ anaplastic large cell lymphomas. The etiology…”
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13
Therapy-Related Myelodysplasia and Secondary Acute Myelogenous Leukemia After High-Dose Therapy With Autologous Hematopoietic Progenitor-Cell Support for Lymphoid Malignancies
Published in Journal of clinical oncology (01-03-2000)“…To evaluate the incidence of and risk factors for therapy-related myelodysplasia (tMDS) and secondary acute myelogenous leukemia (sAML), after high-dose…”
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14
Comparative genomic hybridization of 49 primary retinoblastoma tumors identifies chromosomal regions associated with histopathology, progression, and patient outcome
Published in Genes chromosomes & cancer (01-02-2003)“…Forty‐nine primary retinoblastoma (Rb) tumors were analyzed by the use of comparative genomic hybridization (CGH), and clinical/histological correlations were…”
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15
Genomic Alterations in Blastic Natural Killer/Extranodal Natural Killer-Like T Cell Lymphoma with Cutaneous Involvement
Published in Journal of investigative dermatology (01-09-2003)“…Natural killer and natural killer-like T cell lymphomas represent a rare type of non-Hodgkin's lymphoma originally described to involve the upper aerodigestive…”
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16
Upregulation of lipocortin 1 inhibits tumour necrosis factor-induced apoptosis in human leukaemic cells : a possible mechanism of resistance to immune surveillance
Published in British journal of haematology (01-12-2000)“…The signal transduction pathway through which tumour necrosis factor (TNF) induces apoptosis in leukaemic cells may involve activation of cytosolic…”
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17
Breakpoint heterogeneity in t(10;11) translocation in AML-M4/M5 resulting in fusion of AF10 and MLL is resolved by fluorescent in situ hybridization analysis
Published in Cancer research (Chicago, Ill.) (01-10-1995)“…Ten AML-M4/M5 patients' samples containing a t(10;11) translocation, but with different cytogenetic breakpoints on chromosome 11q (11q13-23), were studied by…”
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18
Molecular cloning of a constitutional t(7;22) translocation associated with risk of hematological malignancy
Published in Genes chromosomes & cancer (01-11-2003)“…We report the molecular characterization of a reciprocal constitutional translocation t(7;22)(p13;q11.2) carried by three family members who have each…”
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19
Cytogenetic and molecular evidence of marrow involvement in extramedullary acute myeloid leukaemia
Published in British journal of haematology (01-09-2000)“…A diagnosis of granulocytic sarcoma was made in a 2‐year‐old child based on the detection of myelomonocytic blasts in tissue obtained from a subcutaneous…”
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20
Upregulation of lipocortin 1 inhibits tumour necrosis factor‐induced apoptosis in human leukaemic cells: a possible mechanism of resistance to immune surveillance
Published in British journal of haematology (01-12-2000)“…The signal transduction pathway through which tumour necrosis factor (TNF) induces apoptosis in leukaemic cells may involve activation of cytosolic…”
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