Search Results - "Oscier, D. G."
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13q deletion anatomy and disease progression in patients with chronic lymphocytic leukemia
Published in Leukemia (01-03-2011)“…Historically, genes targeted by recurrent chromosomal deletions have been identified within the smallest genomic region shared in all patients, the minimally…”
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2
Quantification of subclonal distributions of recurrent genomic aberrations in paired pre-treatment and relapse samples from patients with B-cell chronic lymphocytic leukemia
Published in Leukemia (01-07-2012)“…Genome-wide array approaches and sequencing analyses are powerful tools for identifying genetic aberrations in cancers, including leukemias and lymphomas…”
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3
Telomere length predicts progression and overall survival in chronic lymphocytic leukemia: data from the UK LRF CLL4 trial
Published in Leukemia (01-12-2015)Get full text
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4
A novel functional assay using etoposide plus nutlin-3a detects and distinguishes between ATM and TP53 mutations in CLL
Published in Leukemia (01-07-2008)Get full text
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5
Guidelines on the management of Waldenström macroglobulinaemia
Published in British journal of haematology (01-03-2006)Get full text
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6
Dysregulation of cyclin dependent kinase 6 expression in splenic marginal zone lymphoma through chromosome 7q translocations
Published in Oncogene (04-11-1999)“…The increased or inappropriate expression of genes with oncogenic properties through specific chromosome translocations is an important event in the…”
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7
Proteomic analysis of the cell-surface membrane in chronic lymphocytic leukemia: identification of two novel proteins, BCNP1 and MIG2B
Published in Leukemia (01-08-2003)“…B-cell-specific plasma-membrane proteins are potential targets for either small molecule or antibody-based therapies. We have sought to annotate proteins…”
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8
The configuration of the immunoglobulin genes in B cell chronic lymphocytic leukemia
Published in Leukemia (01-06-2002)“…B cell chronic lymphocytic leukemia (CLL) lacks a consistent genetic abnormality. However, immunoglobulin V(H) gene segment mutation analysis has provided…”
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9
Rapid amplification of immunoglobulin heavy chain switch ( ) translocation breakpoints using long-distance inverse PCR
Published in Leukemia (01-12-2004)“…Molecular cloning of immunoglobulin heavy chain (IGH) translocation breakpoints identifies genes of biological importance in the development of normal and…”
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10
P2X7 polymorphism and chronic lymphocytic leukaemia: lack of correlation with incidence, survival and abnormalities of chromosome 12
Published in Leukemia (01-11-2003)“…The P2X7 receptor, a plasma membrane ATP-gated ion channel that plays a role in lymphocyte apoptosis, has been suggested as an important contributory factor to…”
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11
Non-coding NOTCH1 mutations in chronic lymphocytic leukemia; their clinical impact in the UK CLL4 trial
Published in Leukemia (01-02-2017)Get full text
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12
Atypical lymphocyte morphology: an adverse prognostic factor for disease progression in stage A CLL independent of trisomy 12
Published in British journal of haematology (01-09-1997)“…We studied 270 patients with Binet stage A chronic lymphocytic leukaemia looking for adverse prognostic factors. In a multivariate analysis the following…”
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13
Fludarabine-related autoimmune haemolytic anaemia in patients with chronic lymphocytic leukaemia
Published in British journal of haematology (01-10-1995)“…We have treated 52 patients with chronic lymphocytic leukaemia (CLL) with fludarabine; 12 developed severe autoimmune haemolysis. Only three had a previous…”
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14
Longitudinal copy number, whole exome and targeted deep sequencing of 'good risk' IGHV-mutated CLL patients with progressive disease
Published in Leukemia (01-06-2016)“…The biological features of IGHV-M chronic lymphocytic leukemia responsible for disease progression are still poorly understood. We undertook a longitudinal…”
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15
Lack of somatic hypermutation of IG VH genes in lymphoid malignancies with t(2;14)(p13;q32) translocation involving the BCL11A gene
Published in Leukemia (01-05-2002)“…The t(2;14)(p13;q32.3) involving the BCL11A and IGH genes is a rare but recurrent chromosomal aberration in B-cell malignancies. Hitherto, juxtaposition of…”
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A subset of Binet stage A CLL patients with TP53 abnormalities and mutated IGHV genes have stable disease
Published in Leukemia (01-01-2009)Get full text
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17
Cytogenetic and molecular abnormalities in chronic lymphocytic leukaemia
Published in Blood reviews (01-06-1994)“…Genetic abnormalities are found in 50% of cases of chronic lymphocytic leukaemia (CLL) by cytogenetic analysis and in a higher percentage of patients using…”
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18
Extreme telomere erosion in ATM-mutated and 11q-deleted CLL patients is independent of disease stage
Published in Leukemia (01-04-2012)Get full text
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19
Telomere length in myelodysplastic syndromes
Published in American journal of hematology (01-12-1997)“…We have studied telomere length in the bone marrow cells or the granulocyte and lymphocyte cell fractions of 54 patients with myelodysplastic syndromes (MDS)…”
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20
Cytogenetic studies in splenic lymphoma with villous lymphocytes
Published in British journal of haematology (01-11-1993)“…We report the cytogenetic findings on 31 cases of splenic lymphoma with villous lymphocytes (SLVL). TPA stimulated cells from peripheral blood (28 cases),…”
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