A SNP microarray and FISH-based procedure to detect allelic imbalances in multiple myeloma: an integrated genomics approach reveals a wide gene dosage effect (Q47934995)

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scientific article published in July 2009

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English	A SNP microarray and FISH-based procedure to detect allelic imbalances in multiple myeloma: an integrated genomics approach reveals a wide gene dosage effect	scientific article published in July 2009

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scholarly article

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Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/19396863

A SNP microarray and FISH-based procedure to detect allelic imbalances in multiple myeloma: an integrated genomics approach reveals a wide gene dosage effect (English)

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Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/19396863

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multiple myeloma

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Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/19396863

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6 February 2018

http://europepmc.org/abstract/MED/19396863

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Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/19396863

Francesco Bertoni

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Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/19396863

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Antonino Neri

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Ivo Kwee

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Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/19396863

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Luca Agnelli

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Europe PubMed Central

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6 February 2018

http://europepmc.org/abstract/MED/19396863

Donata Verdelli

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Donata Verdelli

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Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/19396863

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Marta Lionetti

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Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/19396863

Giorgio Lambertenghi-Deliliers

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Giorgio Lambertenghi Deliliers

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Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/19396863

author name string

Adrian Andronache

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Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/19396863

Cristina Battaglia

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Europe PubMed Central

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6 February 2018

http://europepmc.org/abstract/MED/19396863

publication date

1 July 2009

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Europe PubMed Central

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6 February 2018

http://europepmc.org/abstract/MED/19396863

Genes, Chromosomes and Cancer

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6 February 2018

http://europepmc.org/abstract/MED/19396863

48

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http://europepmc.org/abstract/MED/19396863

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http://europepmc.org/abstract/MED/19396863

603-614

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PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/19396863

Molecular classification of multiple myeloma: a distinct transcriptional profile characterizes patients expressing CCND1 and negative for 14q32 translocations.

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Integrative genomic analysis reveals distinct transcriptional and genetic features associated with chromosome 13 deletion in multiple myeloma

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7 January 2021

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Upregulation of translational machinery and distinct genetic subgroups characterise hyperdiploidy in multiple myeloma.

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Molecular pathogenesis and a consequent classification of multiple myeloma

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Metagenes and molecular pattern discovery using matrix factorization

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High-resolution genomic profiles define distinct clinico-pathogenetic subgroups of multiple myeloma patients

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Molecular Dissection of Hyperdiploid Multiple Myeloma by Gene Expression Profiling

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Chromosome abnormalities clustering and its implications for pathogenesis and prognosis in myeloma

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Combined single nucleotide polymorphism-based genomic mapping and global gene expression profiling identifies novel chromosomal imbalances, mechanisms and candidate genes important in the pathogenesis of T-cell prolymphocytic leukemia with inv(14)(q

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Characterization of oncogene dysregulation in multiple myeloma by combined FISH and DNA microarray analyses

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Transcriptional features of multiple myeloma patients with chromosome 1q gain

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Molecular and transcriptional characterization of the novel 17p11.2-p12 amplicon in multiple myeloma.

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Novel definition files for human GeneChips based on GeneAnnot

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Genetics and cytogenetics of multiple myeloma: a workshop report

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Prognostic and biologic significance of chromosomal imbalances assessed by comparative genomic hybridization in multiple myeloma

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Advances in biology of multiple myeloma: clinical applications

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Gene mapping and expression analysis of 16q loss of heterozygosity identifies WWOX and CYLD as being important in determining clinical outcome in multiple myeloma

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Promiscuous mutations activate the noncanonical NF-kappaB pathway in multiple myeloma.

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Chromosome 13q deletion and IgH abnormalities may be both masked by near-tetraploidy in a high proportion of multiple myeloma patients: a combined morphology and I-FISH analysis.

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Multiple myeloma primary cells show a highly rearranged unbalanced genome with amplifications and homozygous deletions irrespective of the presence of immunoglobulin-related chromosome translocations

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Cytogenetics and molecular cytogenetics in multiple myeloma

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Value of comparative genomic hybridization and fluorescence in situ hybridization for molecular diagnostics in multiple myeloma

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Molecular characterization of human multiple myeloma cell lines by integrative genomics: insights into the biology of the disease.

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Gene expression profiling of plasma cell dyscrasias reveals molecular patterns associated with distinct IGH translocations in multiple myeloma

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Circular binary segmentation for the analysis of array-based DNA copy number data

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Integrative analysis of the cancer transcriptome

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An integrative genomic approach reveals coordinated expression of intronic miR-335, miR-342, and miR-561 with deregulated host genes in multiple myeloma

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Prognostic impact of cytogenetic and interphase fluorescence in situ hybridization-defined chromosome 13 deletion in multiple myeloma: early results of total therapy II.

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A validated gene expression model of high-risk multiple myeloma is defined by deregulated expression of genes mapping to chromosome 1.

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Chromosomal analysis in multiple myeloma: cytogenetic evidence of two different diseases

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The costimulation-regulated duration of PKB activation controls T cell longevity

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Use of single nucleotide polymorphism-based mapping arrays to detect copy number changes and loss of heterozygosity in multiple myeloma.

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Integration of global SNP-based mapping and expression arrays reveals key regions, mechanisms, and genes important in the pathogenesis of multiple myeloma

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The molecular classification of multiple myeloma

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7 January 2021

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Identifiers

10.1002/GCC.20668

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/19396863

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/19396863

ResearchGate publication ID

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