Multiplex ligation-dependent probe amplification and fluorescence in situ hybridization to detect chromosomal abnormalities in Chronic lymphocytic leukemia: A comparative study (Q61039254)

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scientific article published on 02 June 2011

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English	Multiplex ligation-dependent probe amplification and fluorescence in situ hybridization to detect chromosomal abnormalities in Chronic lymphocytic leukemia: A comparative study	scientific article published on 02 June 2011

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scholarly article

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2 February 2020

Multiplex ligation-dependent probe amplification and fluorescence in situ hybridization to detect chromosomal abnormalities in chronic lymphocytic leukemia: a comparative study (English)

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chronic lymphocytic leukemia

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1

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Giovanna Cutrona

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Anna Grazia Recchia

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Manlio Ferrarini

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author name string

Oronzo Scarciolla

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2 February 2020

Fortunato Morabito

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2 February 2020

Rosa Anna Cifarelli

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2 February 2020

Caterina Dininno

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2 February 2020

Serena Matis

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2 February 2020

Massimo Gentile

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2 February 2020

Gabriella Ciceri

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2 February 2020

Angela Ciancio

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Clara Mannarella

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2 February 2020

Alberto Fragasso

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publication date

2 June 2011

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Genes, Chromosomes and Cancer

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9

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2 February 2020

726-734

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2 February 2020

Detection, analysis and clinical validation of chromosomal aberrations by multiplex ligation-dependent probe amplification in chronic leukemia

1 reference

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Inactivation of the lamin A/C gene by CpG island promoter hypermethylation in hematologic malignancies, and its association with poor survival in nodal diffuse large B-cell lymphoma.

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Multiplex ligation-dependent probe amplification versus multiprobe fluorescence in situ hybridization to detect genomic aberrations in chronic lymphocytic leukemia: a tertiary center experience

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Frequent deletions and down-regulation of micro- RNA genes miR15 and miR16 at 13q14 in chronic lymphocytic leukemia

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A MicroRNA signature associated with prognosis and progression in chronic lymphocytic leukemia

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Gain of the short arm of chromosome 2 (2p) is a frequent recurring chromosome aberration in untreated chronic lymphocytic leukemia (CLL) at advanced stages

1 reference

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Chronic lymphocytic leukemia

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Genetic alterations in chronic lymphocytic leukaemia

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Multiplex ligation-dependent probe amplification for detection of genomic alterations in chronic lymphocytic leukaemia

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Clonal heterogeneity in chronic lymphocytic leukemia cells: superior response to surface IgM cross-linking in CD38, ZAP-70-positive cells

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Chromosome anomalies detected by interphase fluorescence in situ hybridization: correlation with significant biological features of B-cell chronic lymphocytic leukaemia

1 reference

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Chronic lymphocytic leukaemia

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Genomic aberrations and survival in chronic lymphocytic leukemia

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Molecular and transcriptional characterization of 17p loss in B-cell chronic lymphocytic leukemia

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Quantitative technologies establish a novel microRNA profile of chronic lymphocytic leukemia

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Novel genomic alterations and clonal evolution in chronic lymphocytic leukemia revealed by representational oligonucleotide microarray analysis (ROMA)

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Guidelines for the diagnosis and treatment of chronic lymphocytic leukemia: a report from the International Workshop on Chronic Lymphocytic Leukemia updating the National Cancer Institute-Working Group 1996 guidelines

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Rb inactivation promotes genomic instability by uncoupling cell cycle progression from mitotic control.

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Multiplex ligation-dependent probe amplification: a diagnostic tool for simultaneous identification of different genetic markers in glial tumors

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Prognostic subgroups in B-cell chronic lymphocytic leukemia defined by specific chromosomal abnormalities

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Screening for subtelomeric rearrangements in 210 patients with unexplained mental retardation using multiplex ligation dependent probe amplification (MLPA).

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Genomic complexity identifies patients with aggressive chronic lymphocytic leukemia

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Definition of progression risk based on combinations of cellular and molecular markers in patients with Binet stage A chronic lymphocytic leukaemia.

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Integrative genomics analyses reveal molecularly distinct subgroups of B-cell chronic lymphocytic leukemia patients with 13q14 deletion.

1 reference

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7 January 2021

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Integrated genomic profiling of chronic lymphocytic leukemia identifies subtypes of deletion 13q14.

1 reference

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Genome-wide analysis of DNA copy number changes and LOH in CLL using high-density SNP arrays.

1 reference

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Chronic lymphocytic leukaemia profiled for prognosis using a fluorescence in situ hybridisation panel

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Multiplex ligation-dependent probe amplification assay for simultaneous detection of Parkinson's disease gene rearrangements

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Spinal muscular atrophy genotyping by gene dosage using multiple ligation-dependent probe amplification

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Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

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Automated array-based genomic profiling in chronic lymphocytic leukemia: development of a clinical tool and discovery of recurrent genomic alterations

1 reference

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Risk stratification in chronic lymphocytic leukemia

1 reference

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7 January 2021

based on heuristic

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Identification of chromosomal abnormalities relevant to prognosis in chronic lymphocytic leukemia using multiplex ligation-dependent probe amplification.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20894

7 January 2021

based on heuristic

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ZAP-70 expression identifies a chronic lymphocytic leukemia subtype with unmutated immunoglobulin genes, inferior clinical outcome, and distinct gene expression profile

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20894

7 January 2021

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Identifiers

10.1002/GCC.20894

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1 reference

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2 February 2020

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